4.4 Article

A general preparation of (Z)-1-fluorostilbene derivatives for the design of conformationally restricted peptidomimetics

Journal

TETRAHEDRON LETTERS
Volume 51, Issue 1, Pages 121-124

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.10.099

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Funding

  1. Indiana University
  2. the National Institutes of Health [GM42897]

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The preparation of (Z)-1-fluoro-2-bromostyrenes provides a general route for the formation of (Z)-1-fluorostilbene derivatives as configurationally stable spacial linkers for the design of conformationally restricted peptidomimetics. Palladium-catalyzed aryl Suzuki and Stille cross-coupling reactions have been surveyed to proceed with complete retention of fluoroalkene geometry, and permit the direct incorporation of a variety of aryl and heteroaromatic substituents. (C) 2009 Elsevier Ltd. All rights reserved.

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