---
_id: '14776'
abstract:
- lang: eng
text: Soluble chaperones residing in the endoplasmic reticulum (ER) play vitally
important roles in folding and quality control of newly synthesized proteins that
transiently pass through the ER en route to their final destinations. These soluble
residents of the ER are themselves endowed with an ER retrieval signal that enables
the cell to bring the escaped residents back from the Golgi. Here, by using purified
proteins, we showed that Nicotiana tabacum phytaspase, a plant aspartate-specific
protease, introduces two breaks at the C-terminus of the N. tabacum ER resident
calreticulin-3. These cleavages resulted in removal of either a dipeptide or a
hexapeptide from the C-terminus of calreticulin-3 encompassing part or all of
the ER retrieval signal. Consistently, expression of the calreticulin-3 derivative
mimicking the phytaspase cleavage product in Nicotiana benthamiana cells demonstrated
loss of the ER accumulation of the protein. Notably, upon its escape from the
ER, calreticulin-3 was further processed by an unknown protease(s) to generate
the free N-terminal (N) domain of calreticulin-3, which was ultimately secreted
into the apoplast. Our study thus identified a specific proteolytic enzyme capable
of precise detachment of the ER retrieval signal from a plant ER resident protein,
with implications for the further fate of the escaped resident.
acknowledgement: "We thank C.U.T. Hellen for critically reading the manuscript. The
MALDI MS facility and CLSM became available to us in the framework of Moscow State
University Development Programs PNG 5.13 and PNR 5.13.\r\nThis work was funded by
the Russian Science Foundation, grant numbers 19-14-00010 and 22-14-00071."
article_number: '16527'
article_processing_charge: Yes
article_type: original
author:
- first_name: Anastasiia
full_name: Teplova, Anastasiia
id: e3736151-106c-11ec-b916-c2558e2762c6
last_name: Teplova
- first_name: Artemii A.
full_name: Pigidanov, Artemii A.
last_name: Pigidanov
- first_name: Marina V.
full_name: Serebryakova, Marina V.
last_name: Serebryakova
- first_name: Sergei A.
full_name: Golyshev, Sergei A.
last_name: Golyshev
- first_name: Raisa A.
full_name: Galiullina, Raisa A.
last_name: Galiullina
- first_name: Nina V.
full_name: Chichkova, Nina V.
last_name: Chichkova
- first_name: Andrey B.
full_name: Vartapetian, Andrey B.
last_name: Vartapetian
citation:
ama: Teplova A, Pigidanov AA, Serebryakova MV, et al. Phytaspase Is capable of detaching
the endoplasmic reticulum retrieval signal from tobacco calreticulin-3. International
Journal of Molecular Sciences. 2023;24(22). doi:10.3390/ijms242216527
apa: Teplova, A., Pigidanov, A. A., Serebryakova, M. V., Golyshev, S. A., Galiullina,
R. A., Chichkova, N. V., & Vartapetian, A. B. (2023). Phytaspase Is capable
of detaching the endoplasmic reticulum retrieval signal from tobacco calreticulin-3.
International Journal of Molecular Sciences. MDPI. https://doi.org/10.3390/ijms242216527
chicago: Teplova, Anastasiia, Artemii A. Pigidanov, Marina V. Serebryakova, Sergei
A. Golyshev, Raisa A. Galiullina, Nina V. Chichkova, and Andrey B. Vartapetian.
“Phytaspase Is Capable of Detaching the Endoplasmic Reticulum Retrieval Signal
from Tobacco Calreticulin-3.” International Journal of Molecular Sciences.
MDPI, 2023. https://doi.org/10.3390/ijms242216527.
ieee: A. Teplova et al., “Phytaspase Is capable of detaching the endoplasmic
reticulum retrieval signal from tobacco calreticulin-3,” International Journal
of Molecular Sciences, vol. 24, no. 22. MDPI, 2023.
ista: Teplova A, Pigidanov AA, Serebryakova MV, Golyshev SA, Galiullina RA, Chichkova
NV, Vartapetian AB. 2023. Phytaspase Is capable of detaching the endoplasmic reticulum
retrieval signal from tobacco calreticulin-3. International Journal of Molecular
Sciences. 24(22), 16527.
mla: Teplova, Anastasiia, et al. “Phytaspase Is Capable of Detaching the Endoplasmic
Reticulum Retrieval Signal from Tobacco Calreticulin-3.” International Journal
of Molecular Sciences, vol. 24, no. 22, 16527, MDPI, 2023, doi:10.3390/ijms242216527.
short: A. Teplova, A.A. Pigidanov, M.V. Serebryakova, S.A. Golyshev, R.A. Galiullina,
N.V. Chichkova, A.B. Vartapetian, International Journal of Molecular Sciences
24 (2023).
date_created: 2024-01-10T09:24:35Z
date_published: 2023-11-01T00:00:00Z
date_updated: 2024-01-10T13:41:10Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.3390/ijms242216527
external_id:
isi:
- '001113792600001'
pmid:
- '38003717'
file:
- access_level: open_access
checksum: 4df7d206ba022b7f54eff1f0aec1659a
content_type: application/pdf
creator: dernst
date_created: 2024-01-10T13:39:42Z
date_updated: 2024-01-10T13:39:42Z
file_id: '14791'
file_name: 2023_IJMS_Teplova.pdf
file_size: 2637784
relation: main_file
success: 1
file_date_updated: 2024-01-10T13:39:42Z
has_accepted_license: '1'
intvolume: ' 24'
isi: 1
issue: '22'
keyword:
- Inorganic Chemistry
- Organic Chemistry
- Physical and Theoretical Chemistry
- Computer Science Applications
- Spectroscopy
- Molecular Biology
- General Medicine
- Catalysis
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
publication: International Journal of Molecular Sciences
publication_identifier:
issn:
- 1422-0067
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: Phytaspase Is capable of detaching the endoplasmic reticulum retrieval signal
from tobacco calreticulin-3
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2023'
...
---
_id: '12919'
abstract:
- lang: eng
text: We report the visible light photocatalytic cleavage of trityl thioethers or
ethers under pH-neutral conditions. The method results in the formation of the
respective symmetrical disulfides and alcohols in moderate to excellent yield.
The protocol only requires the addition of a suitable photocatalyst and light
rendering it orthogonal to several functionalities, including acid labile protective
groups. The same conditions can be used to directly convert trityl-protected thiols
into unsymmetrical disulfides or selenosulfides, and to cleave trityl resins in
solid phase organic synthesis.
article_processing_charge: No
article_type: original
author:
- first_name: Sho
full_name: Murakami, Sho
last_name: Murakami
- first_name: Cosima
full_name: Brudy, Cosima
last_name: Brudy
- first_name: Moritz
full_name: Bachmann, Moritz
last_name: Bachmann
- first_name: Yoshiji
full_name: Takemoto, Yoshiji
last_name: Takemoto
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
citation:
ama: Murakami S, Brudy C, Bachmann M, Takemoto Y, Pieber B. Photocatalytic cleavage
of trityl protected thiols and alcohols. Synthesis. 2023;55(09):1367-1374.
doi:10.1055/a-1979-5933
apa: Murakami, S., Brudy, C., Bachmann, M., Takemoto, Y., & Pieber, B. (2023).
Photocatalytic cleavage of trityl protected thiols and alcohols. Synthesis.
Georg Thieme Verlag. https://doi.org/10.1055/a-1979-5933
chicago: Murakami, Sho, Cosima Brudy, Moritz Bachmann, Yoshiji Takemoto, and Bartholomäus
Pieber. “Photocatalytic Cleavage of Trityl Protected Thiols and Alcohols.” Synthesis.
Georg Thieme Verlag, 2023. https://doi.org/10.1055/a-1979-5933.
ieee: S. Murakami, C. Brudy, M. Bachmann, Y. Takemoto, and B. Pieber, “Photocatalytic
cleavage of trityl protected thiols and alcohols,” Synthesis, vol. 55,
no. 09. Georg Thieme Verlag, pp. 1367–1374, 2023.
ista: Murakami S, Brudy C, Bachmann M, Takemoto Y, Pieber B. 2023. Photocatalytic
cleavage of trityl protected thiols and alcohols. Synthesis. 55(09), 1367–1374.
mla: Murakami, Sho, et al. “Photocatalytic Cleavage of Trityl Protected Thiols and
Alcohols.” Synthesis, vol. 55, no. 09, Georg Thieme Verlag, 2023, pp. 1367–74,
doi:10.1055/a-1979-5933.
short: S. Murakami, C. Brudy, M. Bachmann, Y. Takemoto, B. Pieber, Synthesis 55
(2023) 1367–1374.
date_created: 2023-05-08T08:25:08Z
date_published: 2023-05-01T00:00:00Z
date_updated: 2023-05-15T08:43:50Z
day: '01'
doi: 10.1055/a-1979-5933
extern: '1'
intvolume: ' 55'
issue: '09'
keyword:
- Organic Chemistry
- Catalysis
language:
- iso: eng
month: '05'
oa_version: None
page: 1367-1374
publication: Synthesis
publication_identifier:
eissn:
- 1437-210X
issn:
- 0039-7881
publication_status: published
publisher: Georg Thieme Verlag
quality_controlled: '1'
scopus_import: '1'
status: public
title: Photocatalytic cleavage of trityl protected thiols and alcohols
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 55
year: '2023'
...
---
_id: '12920'
abstract:
- lang: eng
text: The multicomponent approach allows to incorporate several functionalities
into a single covalent organic framework (COF) and consequently allows the construction
of bifunctional materials for cooperative catalysis. The well-defined structure
of such multicomponent COFs is furthermore ideally suited for structure-activity
relationship studies. We report a series of multicomponent COFs that contain acridine-
and 2,2’-bipyridine linkers connected through 1,3,5-benzenetrialdehyde derivatives.
The acridine motif is responsible for broad light absorption, while the bipyridine
unit enables complexation of nickel catalysts. These features enable the usage
of the framework materials as catalysts for light-mediated carbon−heteroatom cross-couplings.
Variation of the node units shows that the catalytic activity correlates to the
keto-enamine tautomer isomerism. This allows switching between high charge-carrier
mobility and persistent, localized charge-separated species depending on the nodes,
a tool to tailor the materials for specific reactions. Moreover, nickel-loaded
COFs are recyclable and catalyze cross-couplings even using red light irradiation.
article_number: e202202967
article_processing_charge: No
article_type: original
author:
- first_name: Michael
full_name: Traxler, Michael
last_name: Traxler
- first_name: Susanne
full_name: Reischauer, Susanne
last_name: Reischauer
- first_name: Sarah
full_name: Vogl, Sarah
last_name: Vogl
- first_name: Jérôme
full_name: Roeser, Jérôme
last_name: Roeser
- first_name: Jabor
full_name: Rabeah, Jabor
last_name: Rabeah
- first_name: Christopher
full_name: Penschke, Christopher
last_name: Penschke
- first_name: Peter
full_name: Saalfrank, Peter
last_name: Saalfrank
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Arne
full_name: Thomas, Arne
last_name: Thomas
citation:
ama: Traxler M, Reischauer S, Vogl S, et al. Programmable photocatalytic activity
of multicomponent covalent organic frameworks used as metallaphotocatalysts. Chemistry
– A European Journal. 2023;29(4). doi:10.1002/chem.202202967
apa: Traxler, M., Reischauer, S., Vogl, S., Roeser, J., Rabeah, J., Penschke, C.,
… Thomas, A. (2023). Programmable photocatalytic activity of multicomponent covalent
organic frameworks used as metallaphotocatalysts. Chemistry – A European Journal.
Wiley. https://doi.org/10.1002/chem.202202967
chicago: Traxler, Michael, Susanne Reischauer, Sarah Vogl, Jérôme Roeser, Jabor
Rabeah, Christopher Penschke, Peter Saalfrank, Bartholomäus Pieber, and Arne Thomas.
“Programmable Photocatalytic Activity of Multicomponent Covalent Organic Frameworks
Used as Metallaphotocatalysts.” Chemistry – A European Journal. Wiley,
2023. https://doi.org/10.1002/chem.202202967.
ieee: M. Traxler et al., “Programmable photocatalytic activity of multicomponent
covalent organic frameworks used as metallaphotocatalysts,” Chemistry – A European
Journal, vol. 29, no. 4. Wiley, 2023.
ista: Traxler M, Reischauer S, Vogl S, Roeser J, Rabeah J, Penschke C, Saalfrank
P, Pieber B, Thomas A. 2023. Programmable photocatalytic activity of multicomponent
covalent organic frameworks used as metallaphotocatalysts. Chemistry – A European
Journal. 29(4), e202202967.
mla: Traxler, Michael, et al. “Programmable Photocatalytic Activity of Multicomponent
Covalent Organic Frameworks Used as Metallaphotocatalysts.” Chemistry – A European
Journal, vol. 29, no. 4, e202202967, Wiley, 2023, doi:10.1002/chem.202202967.
short: M. Traxler, S. Reischauer, S. Vogl, J. Roeser, J. Rabeah, C. Penschke, P.
Saalfrank, B. Pieber, A. Thomas, Chemistry – A European Journal 29 (2023).
date_created: 2023-05-08T08:25:34Z
date_published: 2023-01-18T00:00:00Z
date_updated: 2023-05-15T08:39:24Z
day: '18'
doi: 10.1002/chem.202202967
extern: '1'
intvolume: ' 29'
issue: '4'
keyword:
- General Chemistry
- Catalysis
- Organic Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/chem.202202967
month: '01'
oa: 1
oa_version: Published Version
publication: Chemistry – A European Journal
publication_identifier:
eissn:
- 1521-3765
issn:
- 0947-6539
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Programmable photocatalytic activity of multicomponent covalent organic frameworks
used as metallaphotocatalysts
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 29
year: '2023'
...
---
_id: '12921'
abstract:
- lang: eng
text: Visible-light photocatalysis provides numerous useful methodologies for synthetic
organic chemistry. However, the mechanisms of these reactions are often not fully
understood. Common mechanistic experiments mainly aim to characterize excited
state properties of photocatalysts and their interaction with other species. Recently,
in situ reaction monitoring using dedicated techniques was shown to be well-suited
for the identification of intermediates and to obtain kinetic insights, thereby
providing more holistic pictures of the reactions of interest. This minireview
surveys these technologies and discusses selected examples where reaction monitoring
was used to elucidate the mechanism of photocatalytic reactions.
article_number: e202201583
article_processing_charge: No
article_type: original
author:
- first_name: Amiera
full_name: Madani, Amiera
last_name: Madani
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
citation:
ama: Madani A, Pieber B. In situ reaction monitoring in photocatalytic organic synthesis.
ChemCatChem. 2023;15(7). doi:10.1002/cctc.202201583
apa: Madani, A., & Pieber, B. (2023). In situ reaction monitoring in photocatalytic
organic synthesis. ChemCatChem. Wiley. https://doi.org/10.1002/cctc.202201583
chicago: Madani, Amiera, and Bartholomäus Pieber. “In Situ Reaction Monitoring in
Photocatalytic Organic Synthesis.” ChemCatChem. Wiley, 2023. https://doi.org/10.1002/cctc.202201583.
ieee: A. Madani and B. Pieber, “In situ reaction monitoring in photocatalytic organic
synthesis,” ChemCatChem, vol. 15, no. 7. Wiley, 2023.
ista: Madani A, Pieber B. 2023. In situ reaction monitoring in photocatalytic organic
synthesis. ChemCatChem. 15(7), e202201583.
mla: Madani, Amiera, and Bartholomäus Pieber. “In Situ Reaction Monitoring in Photocatalytic
Organic Synthesis.” ChemCatChem, vol. 15, no. 7, e202201583, Wiley, 2023,
doi:10.1002/cctc.202201583.
short: A. Madani, B. Pieber, ChemCatChem 15 (2023).
date_created: 2023-05-08T08:25:55Z
date_published: 2023-04-06T00:00:00Z
date_updated: 2023-05-15T08:35:48Z
day: '06'
doi: 10.1002/cctc.202201583
extern: '1'
intvolume: ' 15'
issue: '7'
keyword:
- Inorganic Chemistry
- Organic Chemistry
- Physical and Theoretical Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/cctc.202201583
month: '04'
oa: 1
oa_version: Published Version
publication: ChemCatChem
publication_identifier:
eissn:
- 1867-3899
issn:
- 1867-3880
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: In situ reaction monitoring in photocatalytic organic synthesis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2023'
...
---
_id: '12939'
abstract:
- lang: eng
text: 'Linear tetrapyrroles, called phyllobilins, are obtained as major catabolites
upon chlorophyll degradation. Primarily, colorless phylloleucobilins featuring
four deconjugated pyrrole units were identified. Their yellow counterparts, phylloxanthobilins,
were discovered more recently. Although the two catabolites differ only by one
double bond, physicochemical properties are very distinct. Moreover, the presence
of the double bond seems to enhance physiologically relevant bioactivities: in
contrast to phylloleucobilin, we identified a potent anti-proliferative activity
for a phylloxanthobilin, and show that this natural product induces apoptotic
cell death and a cell cycle arrest in cancer cells. Interestingly, upon modifying
inactive phylloleucobilin by esterification, an anti-proliferative activity can
be observed that increases with the chain lengths of the alkyl esters. We provide
first evidence for anti-cancer activity of phyllobilins, report a novel plant
source for a phylloxanthobilin, and by using paper spray MS, show that these bioactive
yellow chlorophyll catabolites are more prevalent in Nature than previously assumed.'
article_processing_charge: No
article_type: original
author:
- first_name: Cornelia A.
full_name: Karg, Cornelia A.
last_name: Karg
- first_name: Pengyu
full_name: Wang, Pengyu
last_name: Wang
- first_name: Florian
full_name: Kluibenschedl, Florian
id: 7499e70e-eb2c-11ec-b98b-f925648bc9d9
last_name: Kluibenschedl
- first_name: Thomas
full_name: Müller, Thomas
last_name: Müller
- first_name: Lars
full_name: Allmendinger, Lars
last_name: Allmendinger
- first_name: Angelika M.
full_name: Vollmar, Angelika M.
last_name: Vollmar
- first_name: Simone
full_name: Moser, Simone
last_name: Moser
citation:
ama: Karg CA, Wang P, Kluibenschedl F, et al. Phylloxanthobilins are abundant linear
tetrapyrroles from chlorophyll breakdown with activities against cancer cells.
European Journal of Organic Chemistry. 2020;2020(29):4499-4509. doi:10.1002/ejoc.202000692
apa: Karg, C. A., Wang, P., Kluibenschedl, F., Müller, T., Allmendinger, L., Vollmar,
A. M., & Moser, S. (2020). Phylloxanthobilins are abundant linear tetrapyrroles
from chlorophyll breakdown with activities against cancer cells. European Journal
of Organic Chemistry. Wiley. https://doi.org/10.1002/ejoc.202000692
chicago: Karg, Cornelia A., Pengyu Wang, Florian Kluibenschedl, Thomas Müller, Lars
Allmendinger, Angelika M. Vollmar, and Simone Moser. “Phylloxanthobilins Are Abundant
Linear Tetrapyrroles from Chlorophyll Breakdown with Activities against Cancer
Cells.” European Journal of Organic Chemistry. Wiley, 2020. https://doi.org/10.1002/ejoc.202000692.
ieee: C. A. Karg et al., “Phylloxanthobilins are abundant linear tetrapyrroles
from chlorophyll breakdown with activities against cancer cells,” European
Journal of Organic Chemistry, vol. 2020, no. 29. Wiley, pp. 4499–4509, 2020.
ista: Karg CA, Wang P, Kluibenschedl F, Müller T, Allmendinger L, Vollmar AM, Moser
S. 2020. Phylloxanthobilins are abundant linear tetrapyrroles from chlorophyll
breakdown with activities against cancer cells. European Journal of Organic Chemistry.
2020(29), 4499–4509.
mla: Karg, Cornelia A., et al. “Phylloxanthobilins Are Abundant Linear Tetrapyrroles
from Chlorophyll Breakdown with Activities against Cancer Cells.” European
Journal of Organic Chemistry, vol. 2020, no. 29, Wiley, 2020, pp. 4499–509,
doi:10.1002/ejoc.202000692.
short: C.A. Karg, P. Wang, F. Kluibenschedl, T. Müller, L. Allmendinger, A.M. Vollmar,
S. Moser, European Journal of Organic Chemistry 2020 (2020) 4499–4509.
date_created: 2023-05-10T14:49:30Z
date_published: 2020-08-09T00:00:00Z
date_updated: 2023-05-15T07:57:14Z
day: '09'
doi: 10.1002/ejoc.202000692
extern: '1'
intvolume: ' 2020'
issue: '29'
keyword:
- Organic Chemistry
- Physical and Theoretical Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/ejoc.202000692
month: '08'
oa: 1
oa_version: Published Version
page: 4499-4509
publication: European Journal of Organic Chemistry
publication_identifier:
issn:
- 1434-193X
- 1099-0690
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Phylloxanthobilins are abundant linear tetrapyrroles from chlorophyll breakdown
with activities against cancer cells
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2020
year: '2020'
...
---
_id: '13369'
abstract:
- lang: eng
text: Arylazopyrazoles represent a new family of molecular photoswitches characterized
by a near-quantitative conversion between two states and long thermal half-lives
of the metastable state. Here, we investigated the behavior of a model arylazopyrazole
in the presence of a self-assembled cage based on Pd–imidazole coordination. Owing
to its high water solubility, the cage can solubilize the E isomer of arylazopyrazole,
which, by itself, is not soluble in water. NMR spectroscopy and X-ray crystallography
have independently demonstrated that each cage can encapsulate two molecules of
E-arylazopyrazole. UV-induced switching to the Z isomer was accompanied by the
release of one of the two guests from the cage and the formation of a 1:1 cage/Z-arylazopyrazole
inclusion complex. DFT calculations suggest that this process involves a dramatic
change in the conformation of the cage. Back-isomerization was induced with green
light and resulted in the initial 1:2 cage/E-arylazopyrazole complex. This back-isomerization
reaction also proceeded in the dark, with a rate significantly higher than in
the absence of the cage.
article_processing_charge: No
article_type: original
author:
- first_name: Anton I
full_name: Hanopolskyi, Anton I
last_name: Hanopolskyi
- first_name: Soumen
full_name: De, Soumen
last_name: De
- first_name: Michał J
full_name: Białek, Michał J
last_name: Białek
- first_name: Yael
full_name: Diskin-Posner, Yael
last_name: Diskin-Posner
- first_name: Liat
full_name: Avram, Liat
last_name: Avram
- first_name: Moran
full_name: Feller, Moran
last_name: Feller
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Hanopolskyi AI, De S, Białek MJ, et al. Reversible switching of arylazopyrazole
within a metal–organic cage. Beilstein Journal of Organic Chemistry. 2019;15:2398-2407.
doi:10.3762/bjoc.15.232
apa: Hanopolskyi, A. I., De, S., Białek, M. J., Diskin-Posner, Y., Avram, L., Feller,
M., & Klajn, R. (2019). Reversible switching of arylazopyrazole within a metal–organic
cage. Beilstein Journal of Organic Chemistry. Beilstein Institut. https://doi.org/10.3762/bjoc.15.232
chicago: Hanopolskyi, Anton I, Soumen De, Michał J Białek, Yael Diskin-Posner, Liat
Avram, Moran Feller, and Rafal Klajn. “Reversible Switching of Arylazopyrazole
within a Metal–Organic Cage.” Beilstein Journal of Organic Chemistry. Beilstein
Institut, 2019. https://doi.org/10.3762/bjoc.15.232.
ieee: A. I. Hanopolskyi et al., “Reversible switching of arylazopyrazole
within a metal–organic cage,” Beilstein Journal of Organic Chemistry, vol.
15. Beilstein Institut, pp. 2398–2407, 2019.
ista: Hanopolskyi AI, De S, Białek MJ, Diskin-Posner Y, Avram L, Feller M, Klajn
R. 2019. Reversible switching of arylazopyrazole within a metal–organic cage.
Beilstein Journal of Organic Chemistry. 15, 2398–2407.
mla: Hanopolskyi, Anton I., et al. “Reversible Switching of Arylazopyrazole within
a Metal–Organic Cage.” Beilstein Journal of Organic Chemistry, vol. 15,
Beilstein Institut, 2019, pp. 2398–407, doi:10.3762/bjoc.15.232.
short: A.I. Hanopolskyi, S. De, M.J. Białek, Y. Diskin-Posner, L. Avram, M. Feller,
R. Klajn, Beilstein Journal of Organic Chemistry 15 (2019) 2398–2407.
date_created: 2023-08-01T09:38:06Z
date_published: 2019-10-10T00:00:00Z
date_updated: 2023-08-07T10:34:56Z
day: '10'
doi: 10.3762/bjoc.15.232
extern: '1'
external_id:
pmid:
- '31666874'
intvolume: ' 15'
keyword:
- Organic Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.3762/bjoc.15.232
month: '10'
oa: 1
oa_version: Published Version
page: 2398-2407
pmid: 1
publication: Beilstein Journal of Organic Chemistry
publication_identifier:
eissn:
- 1860-5397
publication_status: published
publisher: Beilstein Institut
quality_controlled: '1'
scopus_import: '1'
status: public
title: Reversible switching of arylazopyrazole within a metal–organic cage
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2019'
...
---
_id: '13379'
article_number: '1700827'
article_processing_charge: No
article_type: letter_note
author:
- first_name: David
full_name: Bléger, David
last_name: Bléger
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Bléger D, Klajn R. Integrating macromolecules with molecular switches. Macromolecular
Rapid Communications. 2018;39(1). doi:10.1002/marc.201700827
apa: Bléger, D., & Klajn, R. (2018). Integrating macromolecules with molecular
switches. Macromolecular Rapid Communications. Wiley. https://doi.org/10.1002/marc.201700827
chicago: Bléger, David, and Rafal Klajn. “Integrating Macromolecules with Molecular
Switches.” Macromolecular Rapid Communications. Wiley, 2018. https://doi.org/10.1002/marc.201700827.
ieee: D. Bléger and R. Klajn, “Integrating macromolecules with molecular switches,”
Macromolecular Rapid Communications, vol. 39, no. 1. Wiley, 2018.
ista: Bléger D, Klajn R. 2018. Integrating macromolecules with molecular switches.
Macromolecular Rapid Communications. 39(1), 1700827.
mla: Bléger, David, and Rafal Klajn. “Integrating Macromolecules with Molecular
Switches.” Macromolecular Rapid Communications, vol. 39, no. 1, 1700827,
Wiley, 2018, doi:10.1002/marc.201700827.
short: D. Bléger, R. Klajn, Macromolecular Rapid Communications 39 (2018).
date_created: 2023-08-01T09:40:48Z
date_published: 2018-01-08T00:00:00Z
date_updated: 2023-08-07T11:16:49Z
day: '08'
doi: 10.1002/marc.201700827
extern: '1'
external_id:
pmid:
- '29314396'
intvolume: ' 39'
issue: '1'
keyword:
- Materials Chemistry
- Polymers and Plastics
- Organic Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/marc.201700827
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Macromolecular Rapid Communications
publication_identifier:
eissn:
- 1521-3927
issn:
- 1022-1336
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Integrating macromolecules with molecular switches
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 39
year: '2018'
...
---
_id: '13383'
abstract:
- lang: eng
text: Two novel donor–acceptor Stenhouse adducts (DASAs) featuring the catechol
moiety were synthesized and characterized. Both compounds bind strongly to the
surfaces of magnetite nanoparticles. An adrenaline-derived DASA renders the particles
insoluble in all common solvents, likely because of poor solvation of the zwitterionic
isomer generated on the nanoparticle surfaces. Well-soluble nanoparticles were
successfully obtained using dopamine-derived DASA equipped with a long alkyl chain.
Upon its attachment to nanoparticles, this DASA undergoes an irreversible decoloration
reaction owing to the formation of the zwitterionic form. The reaction follows
first-order kinetics and proceeds more rapidly on large nanoparticles. Interestingly,
decoloration can be suppressed in the presence of free DASA molecules in solution
or at high nanoparticle concentrations.
article_processing_charge: No
article_type: original
author:
- first_name: Johannes
full_name: Ahrens, Johannes
last_name: Ahrens
- first_name: Tong
full_name: Bian, Tong
last_name: Bian
- first_name: Tom
full_name: Vexler, Tom
last_name: Vexler
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Ahrens J, Bian T, Vexler T, Klajn R. Irreversible bleaching of donor-acceptor
stenhouse adducts on the surfaces of magnetite nanoparticles. ChemPhotoChem.
2017;1(5):230-236. doi:10.1002/cptc.201700009
apa: Ahrens, J., Bian, T., Vexler, T., & Klajn, R. (2017). Irreversible bleaching
of donor-acceptor stenhouse adducts on the surfaces of magnetite nanoparticles.
ChemPhotoChem. Wiley. https://doi.org/10.1002/cptc.201700009
chicago: Ahrens, Johannes, Tong Bian, Tom Vexler, and Rafal Klajn. “Irreversible
Bleaching of Donor-Acceptor Stenhouse Adducts on the Surfaces of Magnetite Nanoparticles.”
ChemPhotoChem. Wiley, 2017. https://doi.org/10.1002/cptc.201700009.
ieee: J. Ahrens, T. Bian, T. Vexler, and R. Klajn, “Irreversible bleaching of donor-acceptor
stenhouse adducts on the surfaces of magnetite nanoparticles,” ChemPhotoChem,
vol. 1, no. 5. Wiley, pp. 230–236, 2017.
ista: Ahrens J, Bian T, Vexler T, Klajn R. 2017. Irreversible bleaching of donor-acceptor
stenhouse adducts on the surfaces of magnetite nanoparticles. ChemPhotoChem. 1(5),
230–236.
mla: Ahrens, Johannes, et al. “Irreversible Bleaching of Donor-Acceptor Stenhouse
Adducts on the Surfaces of Magnetite Nanoparticles.” ChemPhotoChem, vol.
1, no. 5, Wiley, 2017, pp. 230–36, doi:10.1002/cptc.201700009.
short: J. Ahrens, T. Bian, T. Vexler, R. Klajn, ChemPhotoChem 1 (2017) 230–236.
date_created: 2023-08-01T09:41:43Z
date_published: 2017-05-01T00:00:00Z
date_updated: 2023-08-07T12:08:05Z
day: '01'
doi: 10.1002/cptc.201700009
extern: '1'
intvolume: ' 1'
issue: '5'
keyword:
- Organic Chemistry
- Physical and Theoretical Chemistry
- Analytical Chemistry
language:
- iso: eng
month: '05'
oa_version: None
page: 230-236
publication: ChemPhotoChem
publication_identifier:
eissn:
- 2367-0932
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Irreversible bleaching of donor-acceptor stenhouse adducts on the surfaces
of magnetite nanoparticles
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 1
year: '2017'
...
---
_id: '13405'
abstract:
- lang: eng
text: We report a method for preparing electrode–molecule–electrode junctions that
incorporate nonsymmetrical azobenzene dithiols. Our approach is based on sequential
deprotection of thiol moieties originally carrying two different protecting groups.
The azobenzene derivatives retained their switching properties within monolayers
and permitted the photocontrol of electrical conductance.
article_processing_charge: No
article_type: original
author:
- first_name: Tal
full_name: Ely, Tal
last_name: Ely
- first_name: Sanjib
full_name: Das, Sanjib
last_name: Das
- first_name: Wenjie
full_name: Li, Wenjie
last_name: Li
- first_name: Pintu
full_name: Kundu, Pintu
last_name: Kundu
- first_name: Einat
full_name: Tirosh, Einat
last_name: Tirosh
- first_name: David
full_name: Cahen, David
last_name: Cahen
- first_name: Ayelet
full_name: Vilan, Ayelet
last_name: Vilan
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Ely T, Das S, Li W, et al. Photocontrol of electrical conductance with a nonsymmetrical
azobenzene dithiol. Synlett. 2013;24(18):2370-2374. doi:10.1055/s-0033-1340087
apa: Ely, T., Das, S., Li, W., Kundu, P., Tirosh, E., Cahen, D., … Klajn, R. (2013).
Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol.
Synlett. Georg Thieme Verlag. https://doi.org/10.1055/s-0033-1340087
chicago: Ely, Tal, Sanjib Das, Wenjie Li, Pintu Kundu, Einat Tirosh, David Cahen,
Ayelet Vilan, and Rafal Klajn. “Photocontrol of Electrical Conductance with a
Nonsymmetrical Azobenzene Dithiol.” Synlett. Georg Thieme Verlag, 2013.
https://doi.org/10.1055/s-0033-1340087.
ieee: T. Ely et al., “Photocontrol of electrical conductance with a nonsymmetrical
azobenzene dithiol,” Synlett, vol. 24, no. 18. Georg Thieme Verlag, pp.
2370–2374, 2013.
ista: Ely T, Das S, Li W, Kundu P, Tirosh E, Cahen D, Vilan A, Klajn R. 2013. Photocontrol
of electrical conductance with a nonsymmetrical azobenzene dithiol. Synlett. 24(18),
2370–2374.
mla: Ely, Tal, et al. “Photocontrol of Electrical Conductance with a Nonsymmetrical
Azobenzene Dithiol.” Synlett, vol. 24, no. 18, Georg Thieme Verlag, 2013,
pp. 2370–74, doi:10.1055/s-0033-1340087.
short: T. Ely, S. Das, W. Li, P. Kundu, E. Tirosh, D. Cahen, A. Vilan, R. Klajn,
Synlett 24 (2013) 2370–2374.
date_created: 2023-08-01T09:47:17Z
date_published: 2013-10-22T00:00:00Z
date_updated: 2023-08-08T07:47:35Z
day: '22'
doi: 10.1055/s-0033-1340087
extern: '1'
intvolume: ' 24'
issue: '18'
keyword:
- Organic Chemistry
language:
- iso: eng
month: '10'
oa_version: None
page: 2370-2374
publication: Synlett
publication_identifier:
eissn:
- 1437-2096
issn:
- 0936-5214
publication_status: published
publisher: Georg Thieme Verlag
quality_controlled: '1'
scopus_import: '1'
status: public
title: Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2013'
...
---
_id: '10392'
abstract:
- lang: eng
text: Protonated formylmetallocenes [M(C5H5)(C5H4-CHOH)]+ (M = Fe, Ru) and their
isomers have been studied at the BP86 and B3LYP levels of density functional theory.
Oxygen-protonated isomers are the most stable forms in each case, with a plethora
of ring- or metal-protonated species at least ca. 14 and 10 kcal/mol higher in
energy for M = Fe and Ru, respectively. The computed rotational barriers around
the C−C bond connecting the cyclopentadienyl and protonated formyl moieties, ca.
18 kcal/mol, are indicative of substantial conjugation between these moieties.
Some of the ring- and iron-protonated species are models for possible intermediates
in Friedel–Crafts acylation of ferrocene, and the computations provide further
evidence that exo attack is clearly favored over endo attack of the electrophile
in this reaction. The structures of the most stable mono- and diprotonated formylferrocenes
are corroborated by the good agreement between GIAO-B3LYP-computed and experimental
NMR chemical shifts.
acknowledgement: M.B. wishes to thank Prof. W. Thiel and the Max-Planck-Institut für
Kohlenforschung for continuing support. A Humboldt fellowship for V.V. is gratefully
acknowledged. Computations were performed on Compaq XP1000 and ES40 workstations
as well as on an Intel Xeon PC cluster at the MPI Mülheim. A.S. thanks the Computing
Center of the University of Zagreb SRCE for allocating computer time on the Isabella
cluster.
article_processing_charge: No
article_type: original
author:
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Valerije
full_name: Vrček, Valerije
last_name: Vrček
- first_name: Michael
full_name: Bühl, Michael
last_name: Bühl
citation:
ama: Šarić A, Vrček V, Bühl M. Density functional study of protonated formylmetallocenes.
Organometallics. 2008;27(3):394-401. doi:10.1021/om700916f
apa: Šarić, A., Vrček, V., & Bühl, M. (2008). Density functional study of protonated
formylmetallocenes. Organometallics. American Chemical Society. https://doi.org/10.1021/om700916f
chicago: Šarić, Anđela, Valerije Vrček, and Michael Bühl. “Density Functional Study
of Protonated Formylmetallocenes.” Organometallics. American Chemical Society,
2008. https://doi.org/10.1021/om700916f.
ieee: A. Šarić, V. Vrček, and M. Bühl, “Density functional study of protonated formylmetallocenes,”
Organometallics, vol. 27, no. 3. American Chemical Society, pp. 394–401,
2008.
ista: Šarić A, Vrček V, Bühl M. 2008. Density functional study of protonated formylmetallocenes.
Organometallics. 27(3), 394–401.
mla: Šarić, Anđela, et al. “Density Functional Study of Protonated Formylmetallocenes.”
Organometallics, vol. 27, no. 3, American Chemical Society, 2008, pp. 394–401,
doi:10.1021/om700916f.
short: A. Šarić, V. Vrček, M. Bühl, Organometallics 27 (2008) 394–401.
date_created: 2021-11-29T15:31:06Z
date_published: 2008-01-15T00:00:00Z
date_updated: 2021-11-30T08:04:44Z
day: '15'
doi: 10.1021/om700916f
extern: '1'
intvolume: ' 27'
issue: '3'
keyword:
- Inorganic Chemistry
- Organic Chemistry
- Physical and Theoretical Chemistry
language:
- iso: eng
main_file_link:
- url: https://pubs.acs.org/doi/10.1021/om700916f
month: '01'
oa_version: None
page: 394-401
publication: Organometallics
publication_identifier:
eissn:
- 1520-6041
issn:
- 0276-7333
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Density functional study of protonated formylmetallocenes
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 27
year: '2008'
...
---
_id: '13433'
abstract:
- lang: eng
text: Self-assembled monolayers (SAMs) of alkane thiols on gold and other metals
are versatile constructs with which to study interfacial phenomena and reactions
at surfaces. Surface properties of SAMs - e.g., wettability, stability in diverse
environments, propensity to interact with or to resist adsorption of macromolecules
-- depend on and can be controlled flexibly by the properties of the functional
(head) groups in the w position of the alkyl chain. SAMs provide a basis for many
important scientific and technological applications, ranging from micropatterning
methods, through sensing, to biological recognition. Despite their importance,
the literature on SAMs and the synthesis of molecules that constitute them remains
scattered and often conflicting. The purpose of this Review is (i) to summarize
the applications and physical properties of SAMs and (ii) to systematize the strategies
of synthesis of ω-functionalized alkane thiols. Generic retrosynthetic scheme
is developed that allows efficient synthetic planning. Issues related to the selection
of appropriate protecting groups and the ways of introduction of the thiol functionality
are discussed in detail, and illustrated with examples of syntheses of several
complex alkane thiols.
article_processing_charge: No
article_type: original
author:
- first_name: Dariusz
full_name: Witt, Dariusz
last_name: Witt
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Piotr
full_name: Barski, Piotr
last_name: Barski
- first_name: Bartosz
full_name: Grzybowski, Bartosz
last_name: Grzybowski
citation:
ama: Witt D, Klajn R, Barski P, Grzybowski B. Applications, properties and synthesis
of w-functionalized n-alkanethiols and disulfides - the building blocks of self-assembled
monolayers. Current Organic Chemistry. 2005;8(18):1763-1797. doi:10.2174/1385272043369421
apa: Witt, D., Klajn, R., Barski, P., & Grzybowski, B. (2005). Applications,
properties and synthesis of w-functionalized n-alkanethiols and disulfides - the
building blocks of self-assembled monolayers. Current Organic Chemistry.
Bentham Science. https://doi.org/10.2174/1385272043369421
chicago: Witt, Dariusz, Rafal Klajn, Piotr Barski, and Bartosz Grzybowski. “Applications,
Properties and Synthesis of w-Functionalized n-Alkanethiols and Disulfides - the
Building Blocks of Self-Assembled Monolayers.” Current Organic Chemistry.
Bentham Science, 2005. https://doi.org/10.2174/1385272043369421.
ieee: D. Witt, R. Klajn, P. Barski, and B. Grzybowski, “Applications, properties
and synthesis of w-functionalized n-alkanethiols and disulfides - the building
blocks of self-assembled monolayers,” Current Organic Chemistry, vol. 8,
no. 18. Bentham Science, pp. 1763–1797, 2005.
ista: Witt D, Klajn R, Barski P, Grzybowski B. 2005. Applications, properties and
synthesis of w-functionalized n-alkanethiols and disulfides - the building blocks
of self-assembled monolayers. Current Organic Chemistry. 8(18), 1763–1797.
mla: Witt, Dariusz, et al. “Applications, Properties and Synthesis of w-Functionalized
n-Alkanethiols and Disulfides - the Building Blocks of Self-Assembled Monolayers.”
Current Organic Chemistry, vol. 8, no. 18, Bentham Science, 2005, pp. 1763–97,
doi:10.2174/1385272043369421.
short: D. Witt, R. Klajn, P. Barski, B. Grzybowski, Current Organic Chemistry 8
(2005) 1763–1797.
date_created: 2023-08-01T10:38:58Z
date_published: 2005-12-01T00:00:00Z
date_updated: 2023-08-08T12:39:52Z
day: '01'
doi: 10.2174/1385272043369421
extern: '1'
intvolume: ' 8'
issue: '18'
keyword:
- Organic Chemistry
language:
- iso: eng
month: '12'
oa_version: None
page: 1763-1797
publication: Current Organic Chemistry
publication_identifier:
eissn:
- 1875-5348
issn:
- 1385-2728
publication_status: published
publisher: Bentham Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Applications, properties and synthesis of w-functionalized n-alkanethiols and
disulfides - the building blocks of self-assembled monolayers
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2005'
...
---
_id: '13436'
abstract:
- lang: eng
text: Cross-metathesis reactions of α,β-unsaturated sulfones and sulfoxides in the
presence of molybdenum and ruthenium pre-catalysts were tested. A selective metahesis
reaction was achieved between functionalized terminal olefins and vinyl sulfones
by using the ‘second generation’ ruthenium catalysts 1c–h while the highly active
Schrock catalyst 1b was found to be functional group incompatible with vinyl sulfones.
The cross-metathesis products were isolated in good yields with an excellent (E)-selectivity.
Both the molybdenum and ruthenium-based complexes were, however, incompatible
with α,β- and β,γ-unsaturated sulfoxides.
article_processing_charge: No
article_type: original
author:
- first_name: Anna
full_name: Michrowska, Anna
last_name: Michrowska
- first_name: Michał
full_name: Bieniek, Michał
last_name: Bieniek
- first_name: Mikhail
full_name: Kim, Mikhail
last_name: Kim
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Karol
full_name: Grela, Karol
last_name: Grela
citation:
ama: Michrowska A, Bieniek M, Kim M, Klajn R, Grela K. Cross-metathesis reaction
of vinyl sulfones and sulfoxides. Tetrahedron. 2003;59(25):4525-4531. doi:10.1016/s0040-4020(03)00682-3
apa: Michrowska, A., Bieniek, M., Kim, M., Klajn, R., & Grela, K. (2003). Cross-metathesis
reaction of vinyl sulfones and sulfoxides. Tetrahedron. Elsevier. https://doi.org/10.1016/s0040-4020(03)00682-3
chicago: Michrowska, Anna, Michał Bieniek, Mikhail Kim, Rafal Klajn, and Karol Grela.
“Cross-Metathesis Reaction of Vinyl Sulfones and Sulfoxides.” Tetrahedron.
Elsevier, 2003. https://doi.org/10.1016/s0040-4020(03)00682-3.
ieee: A. Michrowska, M. Bieniek, M. Kim, R. Klajn, and K. Grela, “Cross-metathesis
reaction of vinyl sulfones and sulfoxides,” Tetrahedron, vol. 59, no. 25.
Elsevier, pp. 4525–4531, 2003.
ista: Michrowska A, Bieniek M, Kim M, Klajn R, Grela K. 2003. Cross-metathesis reaction
of vinyl sulfones and sulfoxides. Tetrahedron. 59(25), 4525–4531.
mla: Michrowska, Anna, et al. “Cross-Metathesis Reaction of Vinyl Sulfones and Sulfoxides.”
Tetrahedron, vol. 59, no. 25, Elsevier, 2003, pp. 4525–31, doi:10.1016/s0040-4020(03)00682-3.
short: A. Michrowska, M. Bieniek, M. Kim, R. Klajn, K. Grela, Tetrahedron 59 (2003)
4525–4531.
date_created: 2023-08-01T10:39:34Z
date_published: 2003-06-16T00:00:00Z
date_updated: 2023-08-08T12:44:17Z
day: '16'
doi: 10.1016/s0040-4020(03)00682-3
extern: '1'
intvolume: ' 59'
issue: '25'
keyword:
- Organic Chemistry
- Drug Discovery
- Biochemistry
language:
- iso: eng
month: '06'
oa_version: None
page: 4525-4531
publication: Tetrahedron
publication_identifier:
eissn:
- 1464-5416
issn:
- 0040-4020
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cross-metathesis reaction of vinyl sulfones and sulfoxides
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 59
year: '2003'
...
---
_id: '13437'
abstract:
- lang: eng
text: Liquid/liquid Phase Transfer Catalysis (PTC) reaction of 4-chlorobutyronitrile
with nonenolisable aldehydes leads via an addition-cyclisation reaction sequence
to derivatives of tetrahydrofuran-3-carbonitrile.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Mieczysław
full_name: Macogonkosza, Mieczysław
last_name: Macogonkosza
- first_name: Jacek
full_name: Przyborowski, Jacek
last_name: Przyborowski
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Andrzej
full_name: Kwast, Andrzej
last_name: Kwast
citation:
ama: Macogonkosza M, Przyborowski J, Klajn R, Kwast A. Simple synthesis of 2-substituted
Tetrahydrofuran-3-carbonitriles. Synlett. 2000;2000(12):1773-1774. doi:10.1055/s-2000-8670
apa: Macogonkosza, M., Przyborowski, J., Klajn, R., & Kwast, A. (2000). Simple
synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles. Synlett. Georg
Thieme Verlag. https://doi.org/10.1055/s-2000-8670
chicago: Macogonkosza, Mieczysław, Jacek Przyborowski, Rafal Klajn, and Andrzej
Kwast. “Simple Synthesis of 2-Substituted Tetrahydrofuran-3-Carbonitriles.” Synlett.
Georg Thieme Verlag, 2000. https://doi.org/10.1055/s-2000-8670.
ieee: M. Macogonkosza, J. Przyborowski, R. Klajn, and A. Kwast, “Simple synthesis
of 2-substituted Tetrahydrofuran-3-carbonitriles,” Synlett, vol. 2000,
no. 12. Georg Thieme Verlag, pp. 1773–1774, 2000.
ista: Macogonkosza M, Przyborowski J, Klajn R, Kwast A. 2000. Simple synthesis of
2-substituted Tetrahydrofuran-3-carbonitriles. Synlett. 2000(12), 1773–1774.
mla: Macogonkosza, Mieczysław, et al. “Simple Synthesis of 2-Substituted Tetrahydrofuran-3-Carbonitriles.”
Synlett, vol. 2000, no. 12, Georg Thieme Verlag, 2000, pp. 1773–74, doi:10.1055/s-2000-8670.
short: M. Macogonkosza, J. Przyborowski, R. Klajn, A. Kwast, Synlett 2000 (2000)
1773–1774.
date_created: 2023-08-01T10:39:48Z
date_published: 2000-12-01T00:00:00Z
date_updated: 2023-08-02T07:54:46Z
day: '01'
doi: 10.1055/s-2000-8670
extern: '1'
intvolume: ' 2000'
issue: '12'
keyword:
- Organic Chemistry
language:
- iso: eng
month: '12'
oa_version: None
page: 1773-1774
publication: Synlett
publication_identifier:
eissn:
- 1437-2096
issn:
- 0936-5214
publication_status: published
publisher: Georg Thieme Verlag
quality_controlled: '1'
scopus_import: '1'
status: public
title: Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2000
year: '2000'
...