Indium-mediated consecutive 1,2-shift reaction and regioselective allylation of vinyl epoxides

Authors
Oh, BKCha, JHCho, YSChoi, KIKoh, HYChang, MHPae, AN
Issue Date
2003-03-31
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON LETTERS, v.44, no.14, pp.2911 - 2913
Abstract
Allyl indium, prepared from allyl bromide and indium metal in aprotic solvent, reacts with terminal vinyl epoxides at room temperature to afford various bishomoallyl alcohols in moderate to high yields via consecutive 1,2-shift reaction and regioselective allylation. (C) 2003 Elsevier Science Ltd. All rights reserved.
Keywords
TERMINAL EPOXIDES; TERMINAL EPOXIDES; indum
ISSN
0040-4039
URI
https://pubs.kist.re.kr/handle/201004/138733
DOI
10.1016/S0040-4039(03)00418-0
Appears in Collections:
KIST Article > 2003
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