4.4 Article

Synthesis of 2,3,5-trisubstituted furans from α-formylaroylketene dithioacetals

Journal

TETRAHEDRON LETTERS
Volume 52, Issue 14, Pages 1667-1669

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2011.01.128

Keywords

Furan; alpha-Formylketene dithioacetal; Vinylketene dithioacetal; N-Bromosuccinimide; Bromination

Funding

  1. KSCSTE Trivandrum

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A new strategy for the synthesis of 2,3,5-trisbustituted furans from alpha-formylketene dithioacetals is described. The protocol involves a facile conversion of alpha-formylketene dithioacetals to vinylketene dithioacetals via Wittig reaction and subsequent N-bromosuccinimide-mediated cyclization to 2,3,5-trisbustituted furans. Further conversion of the 2-thioalkylfurans thus obtained to 2-aminofurans shows the potential synthetic utility of this new approach. (c) 2011 Elsevier Ltd. All rights reserved.

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