STEREOSPECIFIC TRIPLE MICHAEL ADDITION

DOI: 10.1016/S0040-4039(00)84512-8

Source and publish data:

Tetrahedron Letters p. 2295 - 2298 (1986)

Update date:2022-08-16

Topics:

Authors:

Thanupran, Chatchai

Thebtaranonth, Chachanat

Thebtaranonth, Yodhathai

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Article abstract of DOI:10.1016/S0040-4039(00)84512-8

The consecutive Michael addition of a nucleophile to an α-methylene cyclopentenone, thence to methyl acrylate, occurs readily and stereospecifically, yielding bicyclo-<2,2,1>-heptanone.The reaction represents the first example of a three-component triple conjugate addition process.

Full text of DOI:10.1016/S0040-4039(00)84512-8

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