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- W2070366323 abstract "The ring-opening of cyclopropenes (1) to carbenes (3) occurs more readily when X is an electron releasing group, and in the case of (1, X = C6H44Y) the rate of cyclopropanation of alkenes correlates with σI for Y. The selectivity of carbenes (3, X = H, OMe) towards alkenes correlates well with that for tetrachloroprop2en1ylidene." @default.
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- W2070366323 title "Substituent effects in the generation and trapping of 1,2-dichloro-3,3-dialkylbut-2-en-1-ylidenes" @default.
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- W2070366323 doi "https://doi.org/10.1016/s0040-4039(00)99637-0" @default.
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