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- W2073246370 abstract "The tosylation of 1-t-butyl-3-azetidinol in pyridine gave 1-t-butylazetidinyl-3 tosylate, but 1-cyclohexyl-3-azetidinol gave mainly N-tosyl-1-cyclohexylamino-3-chloro-2-propanol. The reaction of both the azetidinols with p-nitrobenzoyl chloride in pyridine gave the 3-nitrobenzoates, while in acetone 1-cyclohexyl-3-azetidinol gave a ring cleavage product. The preparation of 1-t-butylazetidine-3-carboxylic acid is described." @default.
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- W2073246370 date "1967-10-01" @default.
- W2073246370 modified "2023-10-01" @default.
- W2073246370 title "Azetidines. III. The Tosylation and Acylation of 1-Substituted 3-Azetidinols. The Preparation of 1-t-Butylazetidine-3-carboxylic Acid" @default.
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- W2073246370 doi "https://doi.org/10.1246/bcsj.40.2401" @default.
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