메뉴 건너뛰기




Volumn 26, Issue 20, 2007, Pages 4869-4871

Carbon-carbon bond formation through double sp2 C-H activations: Synthesis of ferrocenyl oxazoline derivatives

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CHEMICAL ACTIVATION; OXIDANTS; PALLADIUM COMPOUNDS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 34948824004     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om700806e     Document Type: Article
Times cited : (179)

References (43)
  • 3
    • 0035753429 scopus 로고    scopus 로고
    • Bringmann. G.; Günther, C.; Ochse, M.; Schupp, O.; Tasler, S. Biaryls in Nature: A Multi-Facetted Class of Stereochemically, Biosynthetically, and Pharmacologically Intriguing Secondary Metabolites. In Progress in the Chemistry of Organic Natural Products; Herz. W., Falk, H., Kirby, G. W., Moore, R. E., Eds.; Springer-Verlag: New York, 2001; 82.
    • (c) Bringmann. G.; Günther, C.; Ochse, M.; Schupp, O.; Tasler, S. Biaryls in Nature: A Multi-Facetted Class of Stereochemically, Biosynthetically, and Pharmacologically Intriguing Secondary Metabolites. In Progress in the Chemistry of Organic Natural Products; Herz. W., Falk, H., Kirby, G. W., Moore, R. E., Eds.; Springer-Verlag: New York, 2001; Vol. 82.
  • 13
    • 34247489285 scopus 로고    scopus 로고
    • For selected recent examples: a
    • For selected recent examples: (a) Chiong, H. A.; Daugulis, O. Org. Lett. 2007, 9, 1449.
    • (2007) Org. Lett , vol.9 , pp. 1449
    • Chiong, H.A.1    Daugulis, O.2
  • 23
    • 33846396118 scopus 로고    scopus 로고
    • and references therein
    • (b) Li, R.; Jiang. L.; Lu, W. Organometallics 2006, 25, 5973, and references therein.
    • (2006) Organometallics , vol.25 , pp. 5973
    • Li, R.1    Jiang, L.2    Lu, W.3
  • 24
    • 0004221231 scopus 로고
    • Hayashi, T, Togni, A, Eds, VCH: Weinheim
    • (a) Hayashi, T., Togni, A., Eds. Ferrocenes; VCH: Weinheim, 1995.
    • (1995) Ferrocenes
  • 29
    • 17044366225 scopus 로고    scopus 로고
    • For utilization of oxazoline as a directing group in C-H activation, see: a
    • For utilization of oxazoline as a directing group in C-H activation, see: (a) Giri, R.; Chen, X.; Yu, J.-Q. Angew. Chem., Int. Ed. 2005, 44, 2112.
    • (2005) Angew. Chem., Int. Ed , vol.44 , pp. 2112
    • Giri, R.1    Chen, X.2    Yu, J.-Q.3
  • 32
    • 0040140745 scopus 로고    scopus 로고
    • Selected examples for applications of ferrocenyl oxazolines: (a) Bolm, C.; Muñiz-Fernández, K.; Seger, A.; Raabe, G.; Günther, K. J. Org. Chem. 1998, 63, 7860.
    • Selected examples for applications of ferrocenyl oxazolines: (a) Bolm, C.; Muñiz-Fernández, K.; Seger, A.; Raabe, G.; Günther, K. J. Org. Chem. 1998, 63, 7860.
  • 40
    • 34249936878 scopus 로고    scopus 로고
    • During the preparation of the manuscript, two reports on the Pd-catalyzed C-C bond formation via double C-H activations appeared; see: a
    • During the preparation of the manuscript, two reports on the Pd-catalyzed C-C bond formation via double C-H activations appeared; see: (a) Stuart, D. R.; Fagnou, K. Science 2007, 316, 1172.
    • (2007) Science , vol.316 , pp. 1172
    • Stuart, D.R.1    Fagnou, K.2
  • 42
    • 34948878766 scopus 로고    scopus 로고
    • For details, see the Supporting Information
    • For details, see the Supporting Information.
  • 43
    • 17044397325 scopus 로고    scopus 로고
    • For 4-ferrocenyl-1,3-oxazoline, a different palladium complex, palladation on a different Cp ring, is formed; see: Moyano, A.; Rosol, M.; Moreno, R. M.; López, C.; Maestro, M. A. Angew. Chem., Int. Ed. 2005, 44, 1865.
    • For 4-ferrocenyl-1,3-oxazoline, a different palladium complex, palladation on a different Cp ring, is formed; see: Moyano, A.; Rosol, M.; Moreno, R. M.; López, C.; Maestro, M. A. Angew. Chem., Int. Ed. 2005, 44, 1865.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.