Literature DB >> 12240070

First chiral selenium ylides used for asymmetric conversion of aldehydes into epoxides.

H Takada1, P Metzner, C Philouze.   

Abstract

Enantioenriched selenonium ylides have been generated by addition of benzyl bromide to C2 symmetric (2R,5R)-2,5-dimethylselenolane in the presence of NaOH, and subsequently reacted with a variety of aldehydes to give oxiranes with excellent enantiomeric excesses (a catalytic version has been achieved); also, an aliphatic cyclic hypervalent dibromoselenurane structure has been demonstrated by X-ray analysis.

Entities:  

Year:  2001        PMID: 12240070     DOI: 10.1039/b106063p

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


  2 in total

Review 1.  Selenonium Ylides: Syntheses, Structural Aspects, and Synthetic Applications.

Authors:  Józef Drabowicz; Aneta Rzewnicka; Remigiusz Żurawiński
Journal:  Molecules       Date:  2020-05-22       Impact factor: 4.411

2.  The nature of the chemical bond in linear three-body systems: from i3- to mixed chalcogen/halogen and trichalcogen moieties.

Authors:  M Carla Aragoni; Massimiliano Arca; Francesco A Devillanova; Alessandra Garau; Francesco Isaia; Vito Lippolis; Annalisa Mancini
Journal:  Bioinorg Chem Appl       Date:  2007       Impact factor: 7.778

  2 in total

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