Literature DB >> 22615199

Mg-catalyzed enantioselective benzylic C-H bond functionalization of isoindolinones: addition to imines.

Yudai Suzuki1, Motomu Kanai, Shigeki Matsunaga.   

Abstract

Access to chiral isoindolinones: The Mg-catalyzed enantioselective benzylic C-H bond functionalization of isoindolinones is described. A Bu(2) Mg/Schiff base catalyst (1:1) promoted the enantioselective addition of N-Boc-isoindolinones to aryl, heteroaryl, alkenyl, and alkyl imines, giving 3-substituted isoindolinones in 84-99 % ee and 50:50-91:9 d.r. (see scheme).
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22615199     DOI: 10.1002/chem.201200821

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


  1 in total

1.  Magnesium-mediated sp3 C-H activation in cascade cyclization of 1-arylethynyl-2-alkyl-o-carboranes: efficient synthesis of carborane-fused cyclopentanes.

Authors:  Jie Zhang; Cen Tang; Zuowei Xie
Journal:  Chem Sci       Date:  2020-09-02       Impact factor: 9.825

  1 in total

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