Literature DB >> 29513404

Enantioselective Alkylation of 2-Oxindoles Catalyzed by a Bifunctional Phase-Transfer Catalyst: Synthesis of (-)-Debromoflustramine B.

Ryan Craig1, Emiliano Sorrentino1, Stephen J Connon1.   

Abstract

A new bifunctional phase-transfer catalyst that employs hydrogen bonding as a control element was developed to promote efficient enantioselective SN 2 reactions for the construction all-carbon quaternary stereocenters in high yield and excellent enantioselectivity (up to 97 % ee) utilizing the alkylation of a malleable oxindole substrate. The utility of the methodology was demonstrated through a concise and highly enantioselective synthesis of (-)-debromoflustramine B.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkylation; enolates; oxindoles; phase-transfer catalysis; pyrroloindoline

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Substances:

Year:  2018        PMID: 29513404     DOI: 10.1002/chem.201800313

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


  1 in total

1.  Synthesis of 2-Mercapto-(2-Oxoindolin-3-Ylidene)Acetonitriles from 3-(4-Chloro-5H-1,2,3-Dithiazol-5-Ylidene)Indolin-2-ones.

Authors:  Boris Letribot; Régis Delatouche; Hervé Rouillard; Antoine Bonnet; Jean-René Chérouvrier; Lisianne Domon; Thierry Besson; Valérie Thiéry
Journal:  Molecules       Date:  2018-06-08       Impact factor: 4.411

  1 in total

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