메뉴 건너뛰기




Volumn 9, Issue 18, 2007, Pages 3651-3653

A new efficient synthesis of pyranoquinolines from 1-acetyl N-aryl cyclopentanecarboxamides

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTANE DERIVATIVE; PYRAN DERIVATIVE; QUINOLINE DERIVATIVE;

EID: 34548530099     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol701536q     Document Type: Article
Times cited : (50)

References (44)
  • 12
    • 0043104432 scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Danishefsky, S. Acc. Chem. Res. 1979, 12, 66-72.
    • (1979) Acc. Chem. Res , vol.12 , pp. 66-72
    • Danishefsky, S.1
  • 18
    • 0037509951 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Namyslo, J. C.; Kaufmann, D. E. Chem. Rev. 2003, 103, 1485-1538.
    • (2003) Chem. Rev , vol.103 , pp. 1485-1538
    • Namyslo, J.C.1    Kaufmann, D.E.2
  • 30
    • 7044235263 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Tietze, L. F. Chem. Rev. 1996, 96, 115-136.
    • (1996) Chem. Rev , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 34
    • 34248220941 scopus 로고    scopus 로고
    • Zhang, Z.; Zhang, Q.; Sun, S.; Xiong, T.; Liu, Q. Angew. Chem., Int. Ed. 2007, 46, 1726-1729 and references cited therein. A proposed mechanism as follows:
    • Zhang, Z.; Zhang, Q.; Sun, S.; Xiong, T.; Liu, Q. Angew. Chem., Int. Ed. 2007, 46, 1726-1729 and references cited therein. A proposed mechanism as follows:
  • 35
    • 34548540281 scopus 로고    scopus 로고
    • For the reaction procedure in detail please see the Supporting Information
    • For the reaction procedure in detail please see the Supporting Information.
  • 39
    • 0009535922 scopus 로고
    • Wiley: New York
    • (d) Jones, G. Quinolines; Wiley: New York, 1977; pp 151-158.
    • (1977) Quinolines , pp. 151-158
    • Jones, G.1
  • 40
    • 12044254693 scopus 로고    scopus 로고
    • For reviews on how the C-ring cyclization process overcomes the energy barrier required to expand the tertiary cyclopentyl carbocation to the less stable secondary cyclohexyl carbocation in the transformation from squalene to lanosterol and related transformations, see: (a) Abe, I, Rohmer, M, Restwich, G. D. Chem. Rev. 1993, 93, 2189-2206
    • For reviews on how the C-ring cyclization process overcomes the energy barrier required to expand the tertiary cyclopentyl carbocation to the less stable secondary cyclohexyl carbocation in the transformation from squalene to lanosterol and related transformations, see: (a) Abe, I.; Rohmer, M.; Restwich, G. D. Chem. Rev. 1993, 93, 2189-2206.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.