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Recent Developments in Enantioselective Deprotonation Mediated by Sub‐Stoichiometric Quantities of Chiral Bases
Author(s) -
Eames Jason
Publication year - 2002
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 - 10.1002/1099-0690(20022)2002:3<393::aid-ejoc393>3.0.co;2-f
Subject(s) - enantioselective synthesis , deprotonation , chemistry , stereoselectivity , stoichiometry , solvent , organic chemistry , computational chemistry , combinatorial chemistry , catalysis , ion
Recent developments in the enantioselective deprotonation of prostereogenic substrates by use of substoichiometric quantities of chiral bases are discussed. The effect that reaction parameters (such as solvent, temperature and additive) have on the stereoselectivity are outlined.