Literature DB >> 24469542

First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines derived from isatins.

Jimil George1, B Sridhar, B V Subba Reddy.   

Abstract

A highly enantioselective addition of diphenyl phosphite to ketimines derived from isatins has been achieved using a bifunctional organocatalyst, quinine-derived squaramide catalyst. This method works efficiently with several ketimines to produce the corresponding 3-amino-2-oxoindolin-3-yl-phosphonates in excellent yields with high enantioselectivity (up to 98% ee).

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24469542     DOI: 10.1039/c3ob42026d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Enantioselective addition of diphenyl phosphonate to ketimines derived from isatins catalyzed by binaphthyl-modified organocatalysts.

Authors:  Hee Seung Jang; Yubin Kim; Dae Young Kim
Journal:  Beilstein J Org Chem       Date:  2016-07-20       Impact factor: 2.883

2.  Investigations towards the stereoselective organocatalyzed Michael addition of dimethyl malonate to a racemic nitroalkene: possible route to the 4-methylpregabalin core structure.

Authors:  Denisa Vargová; Rastislav Baran; Radovan Šebesta
Journal:  Beilstein J Org Chem       Date:  2018-03-05       Impact factor: 2.883

Review 3.  Asymmetric Synthesis of Tetrasubstituted α-Aminophosphonic Acid Derivatives.

Authors:  Aitor Maestro; Xabier Del Corte; Adrián López-Francés; Edorta Martínez de Marigorta; Francisco Palacios; Javier Vicario
Journal:  Molecules       Date:  2021-05-27       Impact factor: 4.411

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.