Literature DB >> 22434093

An organocatalytic Michael-aldol cascade: formal [3+2] annulation to construct enantioenriched spirocyclic oxindole derivatives.

Shu-Wen Duan1, Yang Li, Yi-Yin Liu, You-Quan Zou, De-Qing Shi, Wen-Jing Xiao.   

Abstract

An efficient organocatalytic Michael-aldol cascade reaction for the asymmetric synthesis of spirocyclic oxindole derivatives fused with tetrahydrothiophenes has been developed through a formal [3+2] annulation strategy. This journal is © The Royal Society of Chemistry 2012

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Year:  2012        PMID: 22434093     DOI: 10.1039/c2cc30931a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Synthesis of spiro[indoline-3,1'-quinolizines] and spiro[indoline-3, 4'-pyrido[1,2-a]quinolines] via three-component reactions of azaarenes, acetylenedicarboxylate, and 3-methyleneoxindoles.

Authors:  Jing Sun; Hui Gong; Yan Sun; Chao-Guo Yan
Journal:  Mol Divers       Date:  2013-07-19       Impact factor: 2.943

  1 in total

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