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- W2023282575 abstract "Treatment of 2-pivaloyl-1,3-indandione with hydroxylamine leads to the formation of a pair of isomeric indenoisoxazoles, the product formed dependent upon the cyclization conditions. Under acidic conditions, 8-t-butylindeno[1,2-c]isoxazol-7-one (5) is formed while under neutral or basic conditions, an oxime, 2, is generated which may then be cyclized under acidic conditions to give 3-t-butylindeno[1,2-c]isoxazol-4-one (4). Although these isomeric indenoisoxazoles may be discriminated by chemical means, we were interested in developing an unequivocal method for distinguishing these and potentially other isomeric pairs by spectroscopic means. A 13C-nmr based method for the discrimination of these isomers which is based on the utilization of chemical shift arguments and spin-lattice relaxation data is thus presented." @default.
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- W2023282575 date "1982-09-01" @default.
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- W2023282575 title "The utilization of chemical shift and spin-lattice (T<sub>1</sub>) relaxation time data for the discrimination of isomeric indenoisoxazoles" @default.
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- W2023282575 doi "https://doi.org/10.1002/jhet.5570190524" @default.
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