Scientific article
English

Alkenyl copper reagents 26. Carbocupration of alkynes by reagents bearing a protected hydroxy or thiol function

Published inTetrahedron, vol. 41, no. 24, p. 5887-5899
Publication date1985
Abstract

Halohydrins, protected as ethers, acetals or chloro-magnesium alcoholates are sequentially transformed into the Li or Mg reagents and then into copper or cuprate derivatives. Addition to acetylene or propyne is discussed according to various parameters. The alkenyl copper or cuprate species, thus obtained, may react further with various electrophiles, leading to difunctionalized alkenes.

Affiliation entities Not a UNIGE publication
Citation (ISO format)
GARDETTE, M., ALEXAKIS, Alexandre, NORMANT, Jean F. Alkenyl copper reagents 26. Carbocupration of alkynes by reagents bearing a protected hydroxy or thiol function. In: Tetrahedron, 1985, vol. 41, n° 24, p. 5887–5899. doi: 10.1016/S0040-4020(01)91428-0
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Journal ISSN0040-4020
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