1967
DOI: 10.1007/bf01176026
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Reactivity of nitrocompounds

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1970
1970
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1970

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“…Spectra of naphthoxazolium iodides were similar to the corresponding hydrolyzed products, indicating ring cleavage (144)• Absorbance at 310 to 350 mp increased continuously, showing the release of p-nitrophenyl phosphate from deoxythymidine 5'phosphate by hydrolysis by staphylococcal nuclease (78). The hydration of -nitrocrotonic ester was shown to produce nitroacetic acid and acetaldehyde at pH 4 (31).…”
Section: Reaction Mechanismsmentioning
confidence: 90%
“…Spectra of naphthoxazolium iodides were similar to the corresponding hydrolyzed products, indicating ring cleavage (144)• Absorbance at 310 to 350 mp increased continuously, showing the release of p-nitrophenyl phosphate from deoxythymidine 5'phosphate by hydrolysis by staphylococcal nuclease (78). The hydration of -nitrocrotonic ester was shown to produce nitroacetic acid and acetaldehyde at pH 4 (31).…”
Section: Reaction Mechanismsmentioning
confidence: 90%