4.4 Article

Preparation of α,β-unsaturated esters and amides via external-CO-free palladium-catalyzed carbonylation of alkenyl tosylates

Journal

TETRAHEDRON LETTERS
Volume 53, Issue 38, Pages 5171-5175

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2012.07.057

Keywords

Carbonylation; Alkenyl tosylates; Phenyl formate; Palladium

Funding

  1. Daiichi-Sankyo Co., Ltd.
  2. Grants-in-Aid for Scientific Research [23790016] Funding Source: KAKEN

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Palladium-catalyzed carbonylation of tosylates with phenyl formate is described. This procedure needs neither external carbon monoxide nor any pressure-resistant apparatus. A variety of cyclic and acyclic alkenyl tosylates can be converted into the corresponding phenyl esters in good yields. Furthermore, this method is effective for the one-pot synthesis of alpha,beta-unsaturated amides. (C) 2012 Elsevier Ltd. All rights reserved.

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