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- W2013759769 abstract "3-Substituted hexahydroindeno[2,1-b]pyrroles were prepared in a stereoselective manner in high yield via an intramolecular azomethine ylide cycloaddition. Olefin geometry in the ylide precursor controlled the stereochemistry at the 3-position." @default.
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- W2013759769 title "A stereoselective synthesis of 3-substituted hexahydroindeno[2,1-b]pyrroles via an intramolecular azomethine ylide cycloaddition" @default.
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- W2013759769 doi "https://doi.org/10.1016/s0040-4020(98)00932-6" @default.
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