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- W2007474221 abstract "Acetone sensitized irradiation of novel 5,6-benzo-2-azabarrelenols were performed to afford di-π-methane photoproducts whose structures and ratios depended on the structural features and substituents; the phenyl substituent at C-8 rendered the pronounced effect on the formation of novel “cross-bonding” product through the imino-ether bridge, and importance of the product forming step for the observed regioselectivity was pointed out." @default.
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- W2007474221 date "1983-01-01" @default.
- W2007474221 modified "2023-10-03" @default.
- W2007474221 title "Photochemistry of novel azabicyclic compounds; concerning the site- and regio-selectivity of di-π-methane transformations of 5,6-benzo-2-azabarrelenes" @default.
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- W2007474221 doi "https://doi.org/10.1016/s0040-4039(00)81901-2" @default.
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