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Volumn 77, Issue 18, 2012, Pages 8220-8230

Preparation of N-alkyl 2-pyridones via a lithium iodide promoted oto N-alkyl migration: Scope and mechanism

Author keywords

[No Author keywords available]

Indexed keywords

2-PYRIDONES; HETEROCYCLES; LITHIUM CATIONS; LITHIUM IODIDE; SOLVENT FREE CONDITIONS;

EID: 84868159281     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3015424     Document Type: Article
Times cited : (32)

References (42)
  • 27
    • 18844460949 scopus 로고
    • Benzylacetamide is presumed to form via a Ritter process see: Ritter, J. J.; Minieri, P. P. J. Am. Chem. Soc. 1948, 70, 4045-4048.
    • (1948) J. Am. Chem. Soc. , vol.70 , pp. 4045-4048
    • Ritter, J.J.1    Minieri, P.P.2
  • 29
    • 0043284167 scopus 로고    scopus 로고
    • The incomplete thermal rearrangement of alkoxypyridines to give the corresponding N-alkyl pyridones using flash vacuum pyrolysis at 600 °C has been observed previously see: Lister, T.; Prager, R. H.; Tsaconas, M.; Wilkinson, K. L. Aust. J. Chem. 2003, 56, 913-916.
    • (2003) Aust. J. Chem. , vol.56 , pp. 913-916
    • Lister, T.1    Prager, R.H.2    Tsaconas, M.3    Wilkinson, K.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.