Diels-alder reactions of chiral 5,5-dimethyl-4,6-methano-2-methoxycarbonyl-2-cyclohexenone

DOI: 10.1016/S0040-4039(00)78893-9

Source and publish data:

Tetrahedron Letters p. 2005 - 2008 (1991)

Update date:2022-08-05

Topics:

Authors:

Liu, Hsing-Jang

Chew, Sew Yeu

Browne, Eric N.C.

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Article abstract of DOI:10.1016/S0040-4039(00)78893-9

Diels-Alder reactions of the chiral enone ester 1 proceed in high yield with addition exclusively to the less hindred Si-face to give adducts of type 5.

Full text of DOI:10.1016/S0040-4039(00)78893-9

Products guided by the article

Product name:(1R,3R,4S,8S,9R)-(+)-3-carbomethoxy-4,6,10,10-tetramethyltricyclo<7.1.1.0^3,8>undec-5-en-2-one

Cas No:135356-72-8

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