Efficient Synthetic Method of Multisubstituted Allenes from the Reactions of Allylindium Reagents with 3°-Propargyl Alcohols

Kooyeon Lee and Phil Ho Lee
National Research Laboratory for Catalytic Organic Reaction, Department of Chemistry and Institute for Molecular Science & Fusion Technology, Kangwon National University, Chunchon 200-701, Republic of Korea
Org. Lett., 2008, 10 (12), pp 2441–2444
DOI: 10.1021/ol800719g
Publication Date (Web): May 14, 2008
Copyright © 2008 American Chemical Society

Abstract

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An efficient synthetic method of tri- and tetra-substituted allenes having an allyl and methallyl group was developed by the reactions of allylindium reagents generated in situ from indium and allyl bromides with 3°-propargyl alcohols.

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History

  • Published In Issue June 19, 2008
  • Article ASAPMay 14, 2008
  • Received: March 31, 2008

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