Abstract
AbstractAn aza-Peterson olefination methodology to access 1,3-dienes and stilbene derivatives from the corresponding allyl- or benzyltrimethylsilane is described. Silanes can be deprotonated using Schlosser’s base and added to N-phenyl imines or ketones to directly give the desired products in high yields.
Funder
Manchester Metropolitan University
Royal Society of Chemistry
Medical Research Council
Subject
Organic Chemistry,Catalysis
Cited by
7 articles.
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