Literature DB >> 23884088

Catalytic asymmetric exo-selective [6+3] cycloaddition of iminoesters with fulvenes.

Marco Potowski1, Andrey P Antonchick, Herbert Waldmann.   

Abstract

A novel exo-selective [6+3] cycloaddition approach for the highly enantioselective synthesis of polysubstituted piperidines was developed. The developed methodology was applied in a one-pot [6+3]-[4+2] dicycloaddition, allowing the construction of structurally and stereochemically rich polycyclic compounds from simple building blocks.

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Year:  2013        PMID: 23884088     DOI: 10.1039/c3cc43824d

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


  3 in total

Review 1.  An overview of the cycloaddition chemistry of fulvenes and emerging applications.

Authors:  Ellen Swan; Kirsten Platts; Anton Blencowe
Journal:  Beilstein J Org Chem       Date:  2019-09-06       Impact factor: 2.883

2.  Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis.

Authors:  Rishikesh Narayan; Marco Potowski; Zhi-Jun Jia; Andrey P Antonchick; Herbert Waldmann
Journal:  Acc Chem Res       Date:  2014-03-22       Impact factor: 22.384

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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