Issue 24, 2008

Indium and zinc-mediated Barbier-type addition reaction of 2,3-allenals with allyl bromide: an efficient synthesis of 1,5,6-alkatrien-4-ols

Abstract

A zinc or indium-mediated Barbier-type addition reaction of 2,3-allenals with allyl bromide in a mixed medium of aqueous NH4Cl and THF (5 : 2) was developed to provide an efficient route to 1,5,6-alkatrien-4-ols, which is synthetically very useful. No 1,4-addition reaction was observed. Depending on the substrates, both indium and activated zinc afforded the 1,2-addition products in moderate to excellent yields: for terminal allenals, activated zinc was better while in other cases the yields with indium were relatively higher.

Graphical abstract: Indium and zinc-mediated Barbier-type addition reaction of 2,3-allenals with allyl bromide: an efficient synthesis of 1,5,6-alkatrien-4-ols

Supplementary files

Article information

Article type
Paper
Submitted
01 Aug 2008
Accepted
26 Aug 2008
First published
27 Oct 2008

Org. Biomol. Chem., 2008,6, 4587-4592

Indium and zinc-mediated Barbier-type addition reaction of 2,3-allenals with allyl bromide: an efficient synthesis of 1,5,6-alkatrien-4-ols

W. Kong, C. Fu and S. Ma, Org. Biomol. Chem., 2008, 6, 4587 DOI: 10.1039/B812869C

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