SYNTHESIS OF (+/-)-α-CHAMIGRENE

DOI: 10.1016/S0040-4039(00)74834-9

Source and publish data:

Tetrahedron Letters p. 589 - 592 (1991)

Update date:2022-08-04

Topics:

Authors:

Plamondon, Josee

Canonne, Persephone

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Article abstract of DOI:10.1016/S0040-4039(00)74834-9

Regiospecific spiroalkylation of the selectively generated enolate arising from the 1,4-addition of lithium dimethylcuprate to 3-methylcyclohex-2-en-1-one allows an efficient preparation of spiroketones, including a key intermediate for the synthesis of (+/-)-α-Chamigrene.

Full text of DOI:10.1016/S0040-4039(00)74834-9

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