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- W2952890275 abstract "In the presence of triethyl amine, the reaction of 2,4-disubstituted-2,3-dihydro-1,5-benzothiazepine with chloro and dichloroacetyl chlorides produced not only the expected β-lactam derivative of the benzo-thiazepine, but also the ring opening product. Different results were obtained when the substituent at 2-position of the benxothiazepine varied from methyl to aryl, and the substituent on the chloroacetyl chloride varied from H to Cl, or when carrying out the reaction at different temperatures. The structures of the obtained products and the reaction mechanism are discussed." @default.
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- W2952890275 date "2001-05-01" @default.
- W2952890275 modified "2023-10-14" @default.
- W2952890275 title "A study of the reaction between 2,4-disubstituted-2,3-dihydro-1,5-benzothiazepines and ketenes generatedin situfrom chloro and dichloroacetyl chlorides" @default.
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- W2952890275 doi "https://doi.org/10.1002/jhet.5570380302" @default.
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