Tetrahedron Letters p. 3235 - 3238 (1984)
Update date:2022-08-03
Topics:
Ihara, Masataka
Toyota, Masahiro
Fukumoto, Keiichiro
Kametani, Tetsuji
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).
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Doi:10.1039/c1gc16162h
(2012)Doi:10.1016/j.ejmech.2011.10.055
(2012)Doi:10.1021/ja209135t
(2012)Doi:10.1021/acs.orglett.9b01437
(2019)Doi:10.1021/acscatal.8b03169
(2018)Doi:10.1039/DT9850002277
(1985)
