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Guanidine-catalyzed enantioselective desymmetrization of meso-aziridines
- TCHLab
- Feb 21, 2011
- 1 min read
Yan Zhang, Choon Wee Kee, Richmond Lee, Xiao Fu, Julian Ying-Teck Soh, Esther Mun Foong Loh, Kuo-Wei Huang and Choon-Hong Tan
Chemical Communications, 47, 3897–3899.
Abstract: An amino-indanol derived chiral guanidine was developed as an efficient Brønsted base catalyst for the desymmetrization of meso-aziridines with both thiols and carbamodithioic acids as nucleophiles, which provided 1,2-difunctionalized ring-opened products in high yields and enantioselectivities.
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