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Enantioselective Access to Key Intermediates for Salvinorin A and Analogues
Author(s) -
Lanfranchi Don Antoine,
Bour Christophe,
Hanquet Gilles
Publication year - 2011
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201100207
Subject(s) - enantiopure drug , chemistry , enantioselective synthesis , key (lock) , cycloaddition , stereochemistry , combinatorial chemistry , organic chemistry , catalysis , computer science , computer security
Access to enantiopure synthetic platforms that can generate key intermediates for salvinorin A analogues through diastereoselective Diels–Alder cycloaddition between an enantiopure sulfinylquinone and semicyclic dienes is described.