@article{12919,
  abstract     = {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.},
  author       = {Murakami, Sho and Brudy, Cosima and Bachmann, Moritz and Takemoto, Yoshiji and Pieber, Bartholomäus},
  issn         = {1437-210X},
  journal      = {Synthesis},
  keywords     = {Organic Chemistry, Catalysis},
  number       = {09},
  pages        = {1367--1374},
  publisher    = {Georg Thieme Verlag},
  title        = {{Photocatalytic cleavage of trityl protected thiols and alcohols}},
  doi          = {10.1055/a-1979-5933},
  volume       = {55},
  year         = {2023},
}