메뉴 건너뛰기




Volumn 72, Issue 9, 2007, Pages 3207-3210

Rhodium-catalyzed intramolecular C-H insertion of α-aryl-α- diazo ketones

Author keywords

[No Author keywords available]

Indexed keywords

ARYL CYCLOPENTANONES; DIAZO KETONES; INTRAMOLECULAR C-H INSERTION;

EID: 34247621671     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0624694     Document Type: Article
Times cited : (29)

References (49)
  • 24
    • 0041878773 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: (a) Davies, H. M. L.; Beckwith, R. E. J. Chem. Rev. 2003, 103, 2861.
    • (2003) Chem. Rev , vol.103 , pp. 2861
    • Davies, H.M.L.1    Beckwith, R.E.J.2
  • 26
    • 34247554476 scopus 로고    scopus 로고
    • For the cyclization of α-diazo-α-aryl ketones with an alkene tether between the ketone and the target C-H, see: (a) Fernández-Mateos, T. A, Pascual, Coca, G, Pérez Alonso, J. J, Rubio González, R, Simmonds, M. S. J, Blaney, W. M. Tetrahedron 1988, 54, 14989
    • For the cyclization of α-diazo-α-aryl ketones with an alkene tether between the ketone and the target C-H, see: (a) Fernández-Mateos, T. A.; Pascual, Coca, G.; Pérez Alonso, J. J.; Rubio González, R.; Simmonds, M. S. J.; Blaney, W. M. Tetrahedron 1988, 54, 14989.
  • 27
    • 0342881493 scopus 로고    scopus 로고
    • Fernández-Mateos, A.; Pascual, Coca, G.; Pérez Alonso, J. J.; Rubio González, R.; Hernández, C. T. Synlett 1996, 1134.
    • (b) Fernández-Mateos, A.; Pascual, Coca, G.; Pérez Alonso, J. J.; Rubio González, R.; Hernández, C. T. Synlett 1996, 1134.
  • 28
    • 40849085240 scopus 로고    scopus 로고
    • Several general methods have been developed for the preparation of α-aryl ketones. For example: (a) Abramovitch, R. A.; Barton, D. H. R.; Finet, J. P. Tetrahedron 1988, 44, 3039.
    • Several general methods have been developed for the preparation of α-aryl ketones. For example: (a) Abramovitch, R. A.; Barton, D. H. R.; Finet, J. P. Tetrahedron 1988, 44, 3039.
  • 34
    • 31944441649 scopus 로고    scopus 로고
    • Several of the substances reported here were previously described. (a) 1a: Taber, D. F.; Tian, W. J. Am. Chem. Soc. 2006, 128, 1058.
    • Several of the substances reported here were previously described. (a) 1a: Taber, D. F.; Tian, W. J. Am. Chem. Soc. 2006, 128, 1058.
  • 35
    • 34247585259 scopus 로고    scopus 로고
    • 1b: Utimoto, K.; Takai, K. NATO AS1 Series, Series, C 1989, 269, 379.
    • (b) 1b: Utimoto, K.; Takai, K. NATO AS1 Series, Series, C 1989, 269, 379.
  • 36
    • 34247560355 scopus 로고    scopus 로고
    • 2b: ref. 9b
    • (c) 2b: ref. 9b.
  • 37
    • 34247614160 scopus 로고    scopus 로고
    • 4c: Quelet, R. Bull. Soc. Chim. Fr. 1929, 75.
    • (d) 4c: Quelet, R. Bull. Soc. Chim. Fr. 1929, 75.
  • 49
    • 34247596924 scopus 로고    scopus 로고
    • 13C multiplicities were determined with the aid of a JVERT pulse sequence, differentiating the signals for methyl and methine carbons as d and for methylene and quaternary carbons as u.
    • 13C multiplicities were determined with the aid of a JVERT pulse sequence, differentiating the signals for methyl and methine carbons as "d" and for methylene and quaternary carbons as "u".


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.