Facile Synthesis of Enantiopure 1,2-Diols and Terminal Epoxides from Chiral β-Hydroxy Sulfides | Zendy

Byung-Tae Choi Cho | Zendy

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Facile Synthesis of Enantiopure 1,2-Diols and Terminal Epoxides from Chiral β-Hydroxy Sulfides

Author(s) -

Byung-Tae Choi Cho

Publication year - 2003

Publication title -

bulletin of the korean chemical society

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.237

H-Index - 59

eISSN - 1229-5949

pISSN - 0253-2964

DOI - 10.5012/bkcs.2003.24.7.1023

Subject(s) - enantiopure drug , terminal (telecommunication) , epoxide , chemistry , organic chemistry , stereochemistry , combinatorial chemistry , enantioselective synthesis , catalysis , computer science , telecommunications

In recent years, manychemical and biological methods for the synthesis ofoptically active epoxides, such as asymmetric epoxidation ofolefins, resolution of racemic epoxides and indirect chemicaltransformation, have been reported. However, the directasymmetric epoxidation of terminal olefins such as styreneanalogues catalyzed by salen and porphyrin ligands,

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