INTRAMOLECULAR DOUBLE MICHAEL REACTION. PART II. SYNTHESIS OF ISOATISIRENE TYPE COMPOUND

DOI: 10.1016/S0040-4039(01)91019-6

Source and publish data:

Tetrahedron Letters p. 3235 - 3238 (1984)

Update date:2022-08-03

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Authors:

Ihara, Masataka

Toyota, Masahiro

Fukumoto, Keiichiro

Kametani, Tetsuji

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Article abstract of DOI:10.1016/S0040-4039(01)91019-6

Intramolecular double Michael reaction of the α,β-unsaturated enone ester (16), prepared from the dienone (5), stereoselectively gave the tetracyclic product (17), which was converted into the isoatisirene type compound (20).

Full text of DOI:10.1016/S0040-4039(01)91019-6

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