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Volumn 94, Issue 11, 1972, Pages 3877-3883

Oxidation of a-Ketoacyl Derivatives. Rearrangement of Pyruvates to Malonates

Author keywords

[No Author keywords available]

Indexed keywords

MALONIC ACID DERIVATIVE; PYRUVIC ACID DERIVATIVE;

EID: 0015530816     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00766a036     Document Type: Article
Times cited : (41)

References (30)
  • 20
    • 85012332331 scopus 로고
    • Purchased from International Chemical and Nuclear Corporation. Purity was established by thin-1ayer chromatography and radioautography and integrity of label at C-7 of nicotinic acid was established by conversion to 3-benzoylpyridine, then to a mixture of stereoisomeric phenyl 3-pyridylketoximes, mp 135-155°
    • Purchased from International Chemical and Nuclear Corporation. Purity was established by thin-1ayer chromatography and radioautography and integrity of label at C-7 of nicotinic acid was established by conversion to 3-benzoylpyridine [F. J. Villani and M. S. King, Org. Syn., 37, 6 (1957)], then to a mixture of stereoisomeric phenyl 3-pyridylketoximes, mp 135-155°
    • (1957) Org. Syn. , vol.37 , pp. 6
    • Villani, F.J.1    King, M.S.2
  • 21
    • 85012424369 scopus 로고
    • which was Beckmann rearranged using thionyl chloride. Hydrolysis of the rearranged products gave benzoic acid and nicotinic acid, both of equal specific activity, and 3-aminopyridine and aniline, both inactive
    • B. Jeiteles, Monatsh., 17, 575 (1896)] which was Beckmann rearranged using thionyl chloride. Hydrolysis of the rearranged products gave benzoic acid and nicotinic acid, both of equal specific activity, and 3-aminopyridine and aniline, both inactive.
    • (1896) Monatsh. , vol.17 , pp. 575
    • Jeiteles, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.