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Repairing the Thiol‐Ene Coupling Reaction
Author(s) -
Povie Guillaume,
Tran AnhTuan,
Bonnaffé David,
Habegger Jacqueline,
Hu Zhaoyu,
Le Narvor Christine,
Renaud Philippe
Publication year - 2014
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201309984
Subject(s) - ene reaction , allylic rearrangement , chemistry , coupling reaction , thiol , catechol , triethylborane , photochemistry , stereochemistry , organic chemistry , catalysis
Thiol‐ene coupling (TEC) reactions emerged as one of the most useful processes for coupling different molecular units under reaction mild conditions. However, TEC reactions involving weak CH bonds (allylic and benzylic fragments) are difficult to run and often low yielding. Mechanistic studies demonstrate that hydrogen‐atom transfer processes at allylic and benzylic positions are responsible for the lack of efficiency of the radical‐chain process. These competing reactions cannot be prevented, but reported herein is a method to repair the chain process by running the reaction in the presence of triethylborane and catechol. Under these reaction conditions, a unique repair mechanism leads to an efficient chain reaction, which is demonstrated with a broad range of anomeric O‐allyl sugar derivatives including mono‐, di‐, and tetrasaccharides bearing various functionalities and protecting groups.

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