Journal of Organic Chemistry p. 3999 - 4001 (1980)
Update date:2022-07-30
Topics:
Cargill, Robert L.
Peet, Norton P.
Pond, David M.
Bundy, William A.
Sears, A. Bradford
The irradiation of the tricyclo<4.3.2.0>undecenones 6a-c, even in cyclohexene as solvent, results only in a quantitative isomerization to 7a-c, whereas irradiation of the tricyclo<3.3.3.0>undecenones 11 and 18 in cyclohexene gives primarily cycloadducts and products of "frustrated" cycloaddition.
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Doi:10.1039/P29800000860
(1980)Doi:10.1021/ja01183a018
(1948)Doi:10.1021/jo01052a501
(1962)Doi:10.1071/CH9800451
(1980)Doi:10.1021/jm00185a015
(1980)Doi:10.1016/S0022-1139(00)82509-9
(1974)
