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Showing papers by "Keiichiro Fukumoto published in 1984"


Journal ArticleDOI
TL;DR: In this article, 1-acyl-1-alkylbenzocyclobutenes was found to give predominantly the corresponding isochromenes via Z-conformer of the o-quinodimethane in the transition state.
Abstract: Thermolysis of 1-acyl-1-alkylbenzocyclobutenes was found to give predominantly the corresponding isochromenes via Z-conformer of the o-quinodimethane in the transition state.

24 citations


Journal ArticleDOI
TL;DR: In this paper, it was shown that the stereoselectivity of the transformations could be attributed to a predominance of the endo conformer (e.g. 12) in the transition state.
Abstract: cis-9b-Cyano-3a-methyl-2, 3, 3a, 4, 5, 9b-hexahydro-1H-benz [e] indene derivatives (14, 20) were synthesized stereoselectively via the intramolecular Diels-Alder reaction of 1, 2-dihydrobenzocyclobutenes (11, 19). The cis stereochemistry in the cycloadducts was confirmed by nuclear Overhauser effect (NOE) experiments. Examination of CPK molecular models revealed that the stereoselectivity of the transformations could be attributed to a predominance of the endo conformer (e.g. 12) in the transition state. Moreover, the stereochemical outcome of the decyanation of 14 by dissolving metal reduction is also considered.

6 citations


Journal ArticleDOI
TL;DR: In this article, it was shown that the stereoselectivity of the transformations could be attributed to a predominance of the endo conformer (e.g. 12) in the transition state.
Abstract: cis-9b-Cyano-3a-methyl-2, 3, 3a, 4, 5, 9b-hexahydro-1H-benz [e] indene derivatives (14, 20) were synthesized stereoselectively via the intramolecular Diels-Alder reaction of 1, 2-dihydrobenzocyclobutenes (11, 19). The cis stereochemistry in the cycloadducts was confirmed by nuclear Overhauser effect (NOE) experiments. Examination of CPK molecular models revealed that the stereoselectivity of the transformations could be attributed to a predominance of the endo conformer (e.g. 12) in the transition state. Moreover, the stereochemical outcome of the decyanation of 14 by dissolving metal reduction is also considered.