Literature DB >> 19034940

A highly site-, regio-, and stereoselective Lewis acid catalyzed formal [3+3] cycloaddition of methylenecyclopropane-1,1-diesters with C,N-diarylnitrones.

Bao Hu1, Jianlin Zhu, Siyang Xing, Jie Fang, Ding Du, Zhongwen Wang.   

Abstract

Entities:  

Year:  2009        PMID： 19034940     DOI： 10.1002/chem.200801990

Source DB:  PubMed          Journal:  Chemistry        ISSN： 0947-6539            Impact factor:   5.236


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  3 in total

Review 1.  Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis.

Authors:  Bao Hu; Stephen G DiMagno
Journal:  Org Biomol Chem       Date:  2015-04-07       Impact factor: 3.876

2.  Stereospecific synthesis of alkylidenecyclopropanes via sequential cyclopropene carbomagnesation/1,3-carbon shift.

Authors:  Xiaocong Xie; Zhe Yang; Joseph M Fox
Journal:  J Org Chem       Date:  2010-06-04       Impact factor: 4.354

3.  The [3 + 3]-cycloaddition alternative for heterocycle syntheses: catalytically generated metalloenolcarbenes as dipolar adducts.

Authors:  Xinfang Xu; Michael P Doyle
Journal:  Acc Chem Res       Date:  2014-03-20       Impact factor: 22.384
  3 in total

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