Literature DB >> 20429598

Asymmetric synthesis of spiro-3,4-dihydropyrans via a domino organocatalytic sequence.

Weijun Yao1, Lianjie Pan, Yihua Wu, Cheng Ma.   

Abstract

A cinchona alkaloid-catalyzed domino Michael/hemiacetalization reaction of cyclic beta-oxo aldehydes and aromatic beta,gamma-unsaturated alpha-keto esters, resulting in the formation of spiro-dihydropyran architectures in good yield with high stereoselectivity (up to 97% ee), is presented.

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Year:  2010        PMID: 20429598     DOI: 10.1021/ol1007873

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Asymmetric aldol reactions of α,β-unsaturated ketoester substrates catalyzed by chiral diamines.

Authors:  Sha-Sha Kan; Jian-Zhen Li; Cheng-Yan Ni; Quan-Zhong Liu; Tai-Ran Kan
Journal:  Molecules       Date:  2011-05-04       Impact factor: 4.411

  1 in total

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