USE OF THE ELECTROPHILIC C-ARYLATION BY ARYLLEAD TRIACETATES IN THE CONSTRUCTION OF SYNTHONS FOR AIZOACEAE AND AMARYLLIDACEAE ALKALOID SYNTHESIS

DOI: 10.1016/S0040-4039(00)95031-7

Source and publish data:

Tetrahedron Letters p. 5331 - 5334 (1985)

Update date:2022-08-02

Topics:

Authors:

Ackland, Darren J.

Pinhey, John T.

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Article abstract of DOI:10.1016/S0040-4039(00)95031-7

The vinylogous β-keto esters, ethyl 2-methyl-4-oxocyclohex-2-ene-carboxylate (Hagemann's Ester) (4), ethyl 4-oxocyclohex-1-ene-carboxylate (7a) and its double bond isomer (7b), undergo regiospecific arylation with aryllead triacetates at C1; reaction of t

Full text of DOI:10.1016/S0040-4039(00)95031-7

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