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- W2144211102 abstract "Sodium borohydride reduction of 6-benzylideneoctahydropyrrolo[1,2-a]pyrimidines and 5-benzylidenehexahydropyrrolo[1,2-a]imidazoles affords N-(w-aminoalkyl)pyrrolidines, whereas these substrates react with H2 or cyclohexene in the presence of catalytic amounts of Pd/C to give benzyl- or benzylidene-substituted bicyclic amidines, respectively." @default.
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- W2144211102 date "2013-01-01" @default.
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- W2144211102 title "Selective Reduction and Dehydrogenation of 6-Benzylideneoctahydropyrrolo[1,2-a]Pyrimidines and 5-Benzylidenehexahydropyrrolo[1,2-a]Imidazoles as New Approaches to N-(ω-Aminoalkyl)Pyrrolidines and Bicyclic Amidines" @default.
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- W2144211102 doi "https://doi.org/10.1016/j.mencom.2013.01.011" @default.
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