4.4 Article

Enantioselective formal total synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol-Eschenmoser/Claisen rearrangement

期刊

TETRAHEDRON
卷 66, 期 27-28, 页码 5053-5058

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.04.134

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资金

  1. Japan Society for the Promotion of Science (JSPS)
  2. Uehara Memorial Foundation
  3. Program for Promotion of Basic and Applied Research for Innovations in the Bio-oriented Industry (BRAIN)

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The enantioselective formal total synthesis of aplysin has been achieved utilizing a palladium-catalyzed addition of arylboronic acid to the allenic alcohol followed by the Eschenmoser/Claisen rearrangement as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.

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