Literature DB >> 23302762

3-Bromooxindoles as nucleophiles in asymmetric organocatalytic Mannich reactions with N-Ts-imines.

Jianhao Li1, Taiping Du, Gang Zhang, Yungui Peng.   

Abstract

A direct asymmetric Mannich reaction of N-unprotected 3-bromooxindoles with N-Ts-imines catalyzed by bifunctional thiourea derived from 2-substituted cinchona alkaloid was developed. Products with vicinal chiral tertiary and brominated quaternary stereogenic centers were achieved in excellent diastereo- and enantioselectivity (up to 99 : 1 dr, 99% ee).

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Year:  2013        PMID: 23302762     DOI: 10.1039/c2cc38475b

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


  1 in total

1.  Ring-opening cyclization of activated spiro-aziridine oxindoles with heteroarenes: a facile synthetic approach to spiro-oxindole-fused pyrroloindolines.

Authors:  Sonal Bhandari; Sravani Sana; Vandana Lahoti; Ramya Tokala; Nagula Shankaraiah
Journal:  RSC Adv       Date:  2020-04-24       Impact factor: 4.036

  1 in total

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