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The major product, N-(1,3,4-triphenyl-azetidin-2-ylidene)- benzenesulfonamide, was obtained in 71 % yield as a 90:10 mixture of isomers in favor of the trans product. The regiochemistry of the triazole by-product was confirmed by unambiguous synthesis of the 1,5-regioisomer and comparison of their spectral data. See the Supporting Information for further details.
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