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Electronic control of stereoselectivity. 30. X-ray analysis of the effect of apical substitution on the three-dimensional features of isodicyclopentafulvenes. Experimental demonstration of minimal bridgehead C-H angle deformation accompanying substantial hybridization change at the apical center

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Electronic control of stereoselectivity. 31. .pi.-Facial course of Diels-Alder cycloadditions to 10-isopropylideneisodicyclopentadiene

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The 1,7-cyclohexenonorbornadiene system

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Electronic control of stereoselectivity. 13. Stereochemically specific Diels-Alder additions to norbornyl- and norbornenyl-fused fulvene systems

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Organolithium reagent-promoted conversion of a functionalized 7-oxanorbornane to annulated fulvenes. An expedient route to 1,7-cyclohexenonorbornadienes

L. Paquette, T. Kravetz, 1985 .

Chemistry of 8-chloroberberine.

A. H. Abd el Rahman, M. Shamma, J. L. Moniot, 1979, Journal of pharmaceutical sciences.