Synfacts 2006(11): 1158-1158  
DOI: 10.1055/s-2006-949482
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York

trans-Hydroalumination-Alkylation of Propargylic Alcohols

Contributor(s): Paul Knochel, Andrei Gavryushin
N. F. Langille, T. F. Jamison*
Massachusetts Institute of Technology, Cambridge, USA
Further Information

Publication History

Publication Date:
24 October 2006 (online)

Significance

This is a simple method for the trans-hydroalumination-alkylation of propargylic alcohols, giving stereochemically defined trisubstituted allylic alcohols. This method complements the known procedure for the cis-hydroalumination-alkylation of allylic alcohols with DIBAL-H. The method uses inexpensive and relatively safe Vitride (Red-Al) as the hydroalumination agent. The method is not sensitive to the steric hindrance in the allylic alcohol. Only reactive electrophiles like allylic, benzylic and propargylic halides afford good yields of products.