An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular Baylis–Hillman reaction
摘要:
A highly enantioselective proline catalyzed intramolecular Baylis-Hillman reaction of hept-2-enedial is reported. Addition of imidazole to the mixture results in art unusual inversion of enantioselectivity. (c) 2005 Elsevier Ltd. All rights reserved.
The intramolecular Baylis–Hillman reaction: easy preparation of versatile substrates, facile reactions, and synthetic applications
作者:Jung Eun Yeo、Xiuling Yang、Hee Jin Kim、Sangho Koo
DOI:10.1039/b311951c
日期:——
We have developed a general and highly efficient method for the preparation of diverse [small omega]-formyl-[small alpha],[small beta]-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis-Hillman reactions of these compounds to provide various biologically important polycyclic compounds.