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Volumn 60, Issue 16, 2004, Pages 3605-3610

An electrochemical interpretation of the mechanism of the chemical decarboxylation of 6-carboxyperhydropyrimidin-4-ones

Author keywords

Non Kolbe electrochemical reaction; Oxidative decarboxylation; Pyrimidinone carboxylic acid; Ritter reaction

Indexed keywords

1 BENZOYL 2 TERT BUTYL 6 CARBOXYPERHYDROPYRIMIDIN 4 ONE; ACETONITRILE; ALUMINUM DERIVATIVE; AMINO ACID DERIVATIVE; CARBON; CARBOXYL GROUP; CHLORIDE; HYDROGEN; HYDROXYL GROUP; KETONE DERIVATIVE; PYRIMIDINE DERIVATIVE; SOLVENT; TETRABUTYLAMMONIUM; UNCLASSIFIED DRUG;

EID: 1842420404     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.02.052     Document Type: Article
Times cited : (10)

References (36)
  • 17
    • 0002497398 scopus 로고
    • For general reviews on the enantioselective synthesis of β-amino acids, see: (a)
    • For general reviews on the enantioselective synthesis of β-amino acids, see: (a) Juaristi E., Quintana D., Escalante J. Aldrichimica Acta. 27:1994;3.
    • (1994) Aldrichimica Acta , vol.27 , pp. 3
    • Juaristi, E.1    Quintana, D.2    Escalante, J.3
  • 27
    • 1842513423 scopus 로고    scopus 로고
    • note
    • P/∂log ν) is expected to be smaller than the observed value, which approaches those reported for an electrochemical-chemical mechanism where the chemical step corresponds totally or partially to the rate determining step (Ref. 9a).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.