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Volumn 73, Issue 13, 2008, Pages 5064-5068

A general synthetic route to differentially functionalized angularly and linearly fused [6-7-5] ring systems: A Rh(I)-catalyzed cyclocarbonylation reaction

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CHEMICAL BONDS; REACTION KINETICS; RHODIUM;

EID: 46849109760     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8007258     Document Type: Article
Times cited : (31)

References (33)
  • 4
    • 4243431054 scopus 로고    scopus 로고
    • For a review of metal-catalyzed cascade reactions, see
    • (a) For a review of metal-catalyzed cascade reactions, see: Malacria, M. Chem. Rev. 1996, 96, 286-306.
    • (1996) Chem. Rev , vol.96 , pp. 286-306
    • Malacria, M.1
  • 5
    • 84906438197 scopus 로고    scopus 로고
    • Bond Formation (Part 1) by Addition Reactions: Alder-ene Reaction
    • For a recent review on transition metal-catalyzed Alder-ene reactions, see: c, 3rd ed, Crabtree, R, Mungos, M, Eds, Elsevier Science: New York
    • (b) For a recent review on transition metal-catalyzed Alder-ene reactions, see: (c) Brummond, K. M.; Loyer-Drew, J. A. C-C Bond Formation (Part 1) by Addition Reactions: Alder-ene Reaction. In Comprehensive Organometallic Chemistry, 3rd ed.; Crabtree, R., Mungos, M., Eds.; Elsevier Science: New York, 2006; Vol. 10, pp 557-601.
    • (2006) Comprehensive Organometallic Chemistry , vol.10 , pp. 557-601
    • Brummond, K.M.1    Loyer-Drew, J.A.C.-C.2
  • 9
    • 24144488325 scopus 로고    scopus 로고
    • Similar observations were reported independently: (d) Mukai, C.; Inagaki, F.; Yoshida, T.; Yoshitani, K.; Hara, Y.; Kitagaki, S. J. Org. Chem. 2005, 70, 7159-7171.
    • Similar observations were reported independently: (d) Mukai, C.; Inagaki, F.; Yoshida, T.; Yoshitani, K.; Hara, Y.; Kitagaki, S. J. Org. Chem. 2005, 70, 7159-7171.
  • 12
    • 4644324093 scopus 로고    scopus 로고
    • and references therein
    • (a) Bonaga, L. V. R.; Krafft, M. Tetrahedron 2004, 60, 9795-9833, and references therein.
    • (2004) Tetrahedron , vol.60 , pp. 9795-9833
    • Bonaga, L.V.R.1    Krafft, M.2
  • 20
    • 0000203834 scopus 로고    scopus 로고
    • Homoallenic iodides were prepared by a modified four-step reaction sequence on multigram scale and were freshly purified via flash chromatography prior to the alkylation reaction. Dauben, W. G, Shapiro, G. J. Org. Chem. 1984, 49, 4252-4258
    • Homoallenic iodides were prepared by a modified four-step reaction sequence on multigram scale and were freshly purified via flash chromatography prior to the alkylation reaction. Dauben, W. G.; Shapiro, G. J. Org. Chem. 1984, 49, 4252-4258.
  • 29
    • 34247869546 scopus 로고    scopus 로고
    • Mukai and co-workers have found that electronically tuning the allene gives mixtures of cyclocarbonylation products with both the distal and proximal olefin reacting; the reaction with the distal olefin predominates in all cases. Inagaki, F, Kawamura, T, Mukai, C. Tetrahedron 2007, 63, 5154-5160
    • Mukai and co-workers have found that electronically tuning the allene gives mixtures of cyclocarbonylation products with both the distal and proximal olefin reacting; the reaction with the distal olefin predominates in all cases. Inagaki, F.; Kawamura, T.; Mukai, C. Tetrahedron 2007, 63, 5154-5160.
  • 33
    • 46849106367 scopus 로고    scopus 로고
    • For crystallographic data, see the Supporting Information. This data (CCDC 629739) may also be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
    • For crystallographic data, see the Supporting Information. This data (CCDC 629739) may also be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.