Indium-mediated consecutive 1,2-shift reaction and regioselective allylation of vinyl epoxides
- Authors
- Oh, BK; Cha, JH; Cho, YS; Choi, KI; Koh, HY; Chang, MH; Pae, 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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