Literature DB >> 24730463

Enantio- and diastereoselective synthesis of spiro-epoxyoxindoles.

Amina Boucherif1, Qing-Qing Yang, Qiang Wang, Jia-Rong Chen, Liang-Qiu Lu, Wen-Jing Xiao.   

Abstract

An asymmetric synthesis of epoxyoxindoles from isatins has been developed by employing chiral sulfur ylides generated in situ from camphor-derived sulfonium salts. This reaction allows an efficient access to enantioenriched spiro-epoxyoxindoles under mild reaction conditions, featuring high yields and excellent enantio- and diastereoselectivities.

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Year:  2014        PMID: 24730463     DOI: 10.1021/jo5003856

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Asymmetric Synthesis of Spirooxindoles via Nucleophilic Epoxidation Promoted by Bifunctional Organocatalysts.

Authors:  Martina Miceli; Andrea Mazziotta; Chiara Palumbo; Elia Roma; Eleonora Tosi; Giovanna Longhi; Sergio Abbate; Paolo Lupattelli; Giuseppe Mazzeo; Tecla Gasperi
Journal:  Molecules       Date:  2018-02-16       Impact factor: 4.411

  1 in total

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