Highly Enantioselective Aldol Reactions Using a tropos Dibenz[c,e]azepine Organocatalyst.
ChemInform(2012)
Abstract
A newly synthesized chiral primary tertiary diamine salt possessing a dibenz[c,e]azepine ring, promotes highly enantioselective crossed-aldol reactions between cyclohexanone (I) and a series of aromatic aldehydes.
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Key words
enantioselective aldol reactions,organocatalyst,cheminform abstract
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