Literature DB >> 24875953

Synergistic catalysis: highly diastereoselective benzoxazole addition to Morita-Baylis-Hillman carbonates.

Victor Ceban1, Piotr Putaj, Marta Meazza, Mateusz B Pitak, Simon J Coles, Jan Vesely, Ramon Rios.   

Abstract

An expedited method has been developed for the diastereoselective synthesis of highly functionalized alkyl-azaarene systems with good yields and high diastereoselectivities (>15 : 1 dr). The methodology includes a synergistic catalysis event involving organometallic (10 mol% AgOAc) activation of an alkyl azaarene and Lewis base (10 mol% DABCO) activation of a Morita-Baylis-Hillman carbonate. The structure and relative configuration of a representative product were confirmed by X-ray analysis.

Entities:  

Year:  2014        PMID: 24875953     DOI: 10.1039/c4cc00728j

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


  1 in total

1.  Expanding the scope of Metal-Free enantioselective allylic substitutions: Anthrones.

Authors:  Victor Ceban; Jiří Tauchman; Marta Meazza; Greg Gallagher; Mark E Light; Ivana Gergelitsová; Jan Veselý; Ramon Rios
Journal:  Sci Rep       Date:  2015-11-23       Impact factor: 4.379

  1 in total

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