A versatile indium trichloride mediated Prins-type reaction to unsaturated heterocycles
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Dobbs, Adrian P. ORCID: https://orcid.org/0000-0002-7241-7118, Guesné, Sebastien J. J., Martinović, Saša, Coles, Simon J. and Hursthouse, Michael B. (2003) A versatile indium trichloride mediated Prins-type reaction to unsaturated heterocycles. The Journal of Organic Chemistry, 68 (20). pp. 7880-7883. ISSN 0022-3263 (Print), 1520-6904 (Online) (doi:10.1021/jo034981k)
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Official URL: http://dx.doi.org/10.1021/jo034981k
Abstract
A versatile and high-yielding indium trichloride mediated cyclization reaction of silylated homoallylic alcohols, thiols, or amines with aldehydes or epoxides is described as a rapid route to a range of unsaturated heterocycles. The excellent diastereoselectivity observed offers a method of wide scope and generality.
Item Type: | Article |
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Uncontrolled Keywords: | indium trichloride, Prins reaction, silyl-Prins reaction |
Subjects: | Q Science > QD Chemistry |
Faculty / School / Research Centre / Research Group: | Faculty of Engineering & Science > School of Science (SCI) |
Related URLs: | |
Last Modified: | 21 Oct 2020 22:31 |
URI: | http://gala.gre.ac.uk/id/eprint/10582 |
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