Literature DB >> 24670223

(DHQ)2AQN-catalyzed asymmetric substitution of isatin-derived hydrazones with O-Boc-protected Morita-Baylis-Hillman adducts: A strategy for synthesizing enantioenriched azo compounds incorporating an oxindole scaffold.

Hai-Bin Yang1, Yun-Zhou Zhao, Rui Sang, Min Shi.   

Abstract

The first example for the preparation of enantioenriched azo compounds from hydrazones and Morita-Baylis-Hillman adducts has been developed, affording azo compounds incorporating an oxindole scaffold in up to 91% yield along with a 93% ee value under the catalysis of (DHQ)2AQN.

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Year:  2014        PMID: 24670223     DOI: 10.1021/jo5003246

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction.

Authors:  Liang-Hua Zou; Arne R Philipps; Gerhard Raabe; Dieter Enders
Journal:  Chemistry       Date:  2014-12-02       Impact factor: 5.236

  1 in total

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