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- W1996543192 abstract "The electron donor-acceptor photo-reaction of norbornadiene (N)dN with 1-cyano-naphthalene (CNN) in benzene yields four [2+2] cycloadducts, 1–4. The addition occurs exclusively on the exo-face of N, on either ring of the acceptor, either at or adjacent to the cyano group, and shows limited preference for anti- vs. syn-addition. In more polar solvents, the reaction becomes more selective, favoring anti-addition to the substituted ring. The formation of the products is rationalized via the “collapse” of short-lived encounter complexes of different geometries." @default.
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- W1996543192 title "Electron donor-acceptor photochemistry of 1-cyano-naphthalene with norbornadiene: Stereospecific regiorandom [2 + 2] cycloaddition" @default.
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- W1996543192 doi "https://doi.org/10.1016/0040-4039(96)01004-0" @default.
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