Literature DB >> 24789674

A concise approach to polysubstituted oxazoles from N-acyl-2-bromo enamides via a copper(I)/amino acid-catalyzed intramolecular C-O bond formation.

Bingjie Liu1, Yueteng Zhang, Gang Huang, Xinting Zhang, Pengfei Niu, Jie Wu, Wenquan Yu, Junbiao Chang.   

Abstract

A straightforward and efficient copper(I)/amino acid-catalyzed intramolecular Ullmann-type C-O coupling reaction has been developed. This protocol affords a facile methodology for the synthesis of a series of novel 2,4,5-substituted oxazoles from readily accessible N-acyl-2-bromo enamides under mild conditions.

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Year:  2014        PMID: 24789674     DOI: 10.1039/c4ob00309h

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


  1 in total

1.  Crystal structure of N-(tert-but-oxy-carbon-yl)glycyl-(Z)-β-bromo-dehydro-alanine methyl ester [Boc-Gly-(β-Br)((Z))ΔAla-OMe].

Authors:  Paweł Lenartowicz; Maciej Makowski; Bartosz Zarychta; Krzysztof Ejsmont
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-11-29
  1 in total

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