4.8 Article

Enantioselective imidazole-directed allylation of aldimines and ketimines

Journal

ORGANIC LETTERS
Volume 9, Issue 18, Pages 3699-3701

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol701723w

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A new chiral allylchlorosilane has been developed that allows the highly enantioselective allylation and crotylation of a range of 2-imidazolylaldimines and ketimines. The method may be exploited for the protecting group-free synthesis of a diverse array of imidazole-bearing chiral carbinamines and, when coupled with ring-closing metathesis reactions, allows the one-pot synthesis of unusual heterocyclic motifs with potential relevance in medicinal chemistry.

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