Scientific article
English

Boron trifluoride assisted opening of epoxides by lithium alkenyl aluminate reagents

Published inTetrahedron, vol. 45, no. 19, p. 6197-6202
Publication date1989
Abstract

Alkenyl aluminate reagents, obtained by hydroalumination of terminal alkynes followed by Image complexation with Meli, react readily with poorly reactive cyclic ethers such as cyclohexene oxide and oxetane, in the presence of BF3·Et2O. Alkenyl aluminate reagents obtained by reaction of an alkenyl tithium reagent and Me3Al behave similarly.

Affiliation entities Not a UNIGE publication
Citation (ISO format)
ALEXAKIS, Alexandre, JACHIET, D. Boron trifluoride assisted opening of epoxides by lithium alkenyl aluminate reagents. In: Tetrahedron, 1989, vol. 45, n° 19, p. 6197–6202. doi: 10.1016/S0040-4020(01)85130-9
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Journal ISSN0040-4020
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