Literature DB >> 24756902

Highly diastereo- and enantioselective silver-catalyzed double [3+2] cyclization of α-imino esters with isocyanoacetate.

Pan-Lin Shao1, Jia-Yu Liao, Yee Ann Ho, Yu Zhao.   

Abstract

Presented herein is a new complexity-generating method in which both functionalities of α-imino esters undergo stereoselective cyclization with isocyanoacetates to produce directly linked oxazole-imidazolines, which can be transformed into highly functionalized α,β-diamino esters and imidazolinium salts in high diastereo- and enantiopurity.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric catalysis; cyclization; enantioselectivity; heterocycles; multicomponent reaction

Mesh:

Substances:

Year:  2014        PMID: 24756902     DOI: 10.1002/anie.201402788

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Direct catalytic enantio- and diastereoselective ketone aldol reactions of isocyanoacetates.

Authors:  Raquel de la Campa; Irene Ortín; Darren J Dixon
Journal:  Angew Chem Int Ed Engl       Date:  2015-03-03       Impact factor: 15.336

2.  A mild catalytic synthesis of 2-oxazolines via oxetane ring-opening: rapid access to a diverse family of natural products.

Authors:  Hai Huang; Wen Yang; Zuliang Chen; Zengwei Lai; Jianwei Sun
Journal:  Chem Sci       Date:  2019-08-26       Impact factor: 9.825

  2 in total

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