Literature DB >> 16320987

A formal [3+2] cycloaddition process with nonactivated aziridines to polysubstituted indolizidines.

Wei Zhu1, Guorong Cai, Dawei Ma.   

Abstract

[chemical reaction: see text]. Heating a mixture of ethyl 7-iodo-2-heptynoate (or its analogues), 2-aryl aziridines, and K2CO3 in dry CH(3)CN delivers polysubstituted indolizidines. This reaction goes through an S(N)2/formal [3+2] cycloaddition process and represents the first synthetically useful example of the formal [3+2] cycloaddition process through a C-N bond cleavage of nonactivated aziridines.

Entities:  

Year:  2005        PMID: 16320987     DOI: 10.1021/ol0513692

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


  3 in total

1.  Stereoselective Lewis acid mediated (3+2) cycloadditions of N-H- and N-sulfonylaziridines with heterocumulenes.

Authors:  Robert A Craig; Nicholas R O'Connor; Alexander F G Goldberg; Brian M Stoltz
Journal:  Chemistry       Date:  2014-03-06       Impact factor: 5.236

2.  Oxidative β-C-H sulfonylation of cyclic amines.

Authors:  R J Griffiths; W C Kong; S A Richards; G A Burley; M C Willis; E P A Talbot
Journal:  Chem Sci       Date:  2018-01-22       Impact factor: 9.825

3.  Efficient Synthesis of Fully Substituted Pyrrolidine-Fused 3-Spirooxindoles via 1,3-Dipolar Cycloaddition of Aziridine and 3-Ylideneoxindole.

Authors:  Wen Ren; Qian Zhao; Chuan Zheng; Qiong Zhao; Li Guo; Wei Huang
Journal:  Molecules       Date:  2016-08-24       Impact factor: 4.411

  3 in total

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