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Volumn 624, Issue 1-2, 2001, Pages 259-270

Rhodium-catalysed asymmetric ring opening of oxabicyclic alkenes with heteroatom nucleophiles

Author keywords

Asymmetric ring opening; Heteroatom nucleophiles; Oxabenzonorbornadienes; Rhodium

Indexed keywords


EID: 0001671784     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00904-9     Document Type: Article
Times cited : (86)

References (39)
  • 1
    • 6844254916 scopus 로고    scopus 로고
    • and pertinent refs. therein
    • For a review on allylic alkylation, see: (a) B.M. Trost, D.L. Van Vranken, Chem. Rev. 96 (1996) 395 and pertinent refs. therein. For a review on allylic animation, see: (b) M. Johannsen, K.A. Jorgensen, Chem. Rev. 98 (1998) 1689 and pertinent refs. therein. For a general reference on the chemistry of palladium, see: © J. Tsuji, Palladium Reagents and Catalysis, Wiley, Toronto, 1995.
    • (1996) Chem. Rev. , vol.96 , pp. 395
    • Trost, B.M.1    Van Vranken, D.L.2
  • 2
    • 4243987144 scopus 로고    scopus 로고
    • and pertinent refs. therein
    • For a review on allylic alkylation, see: (a) B.M. Trost, D.L. Van Vranken, Chem. Rev. 96 (1996) 395 and pertinent refs. therein. For a review on allylic animation, see: (b) M. Johannsen, K.A. Jorgensen, Chem. Rev. 98 (1998) 1689 and pertinent refs. therein. For a general reference on the chemistry of palladium, see: © J. Tsuji, Palladium Reagents and Catalysis, Wiley, Toronto, 1995.
    • (1998) Chem. Rev. , vol.98 , pp. 1689
    • Johannsen, M.1    Jorgensen, K.A.2
  • 3
    • 6844254916 scopus 로고    scopus 로고
    • Wiley, Toronto
    • For a review on allylic alkylation, see: (a) B.M. Trost, D.L. Van Vranken, Chem. Rev. 96 (1996) 395 and pertinent refs. therein. For a review on allylic animation, see: (b) M. Johannsen, K.A. Jorgensen, Chem. Rev. 98 (1998) 1689 and pertinent refs. therein. For a general reference on the chemistry of palladium, see: © J. Tsuji, Palladium Reagents and Catalysis, Wiley, Toronto, 1995.
    • (1995) Palladium Reagents and Catalysis
    • Tsuji, J.1
  • 30
    • 0002838169 scopus 로고
    • For palladium catalyzed allylic etherification reactions, see: (a) J. Muzart, J.P. Genet, A. Denis, J. Organomet. Chem. 326 (1987) C23. For enantioselective ring opening of epoxides with Cr(-salen) complexes, see: (b) J.M. Ready, E.N. Jacobsen, J. Am. Chem. Soc. 121 (1999) 6086. For the enantioselective ring opening of epoxides with Ga heterobimetallic complexes, see: © T. Iida, N. Yamamoto, S. Matsunaga, H.-G. Woo, M. Shibasaki, Angew. Chem. Int. Ed. 37 (1998) 2223. For desymmetrization of Baylis-Hillman adducts with palladium, see: (d) B.M. Trost, H.C. Tsui, F.D. Toste, J. Am. Chem. Soc. 122 (2000) 3534.
    • (1987) J. Organomet. Chem. , vol.326 , pp. C23
    • Muzart, J.1    Genet, J.P.2    Denis, A.3
  • 31
    • 0033618105 scopus 로고    scopus 로고
    • For palladium catalyzed allylic etherification reactions, see: (a) J. Muzart, J.P. Genet, A. Denis, J. Organomet. Chem. 326 (1987) C23. For enantioselective ring opening of epoxides with Cr(- salen) complexes, see: (b) J.M. Ready, E.N. Jacobsen, J. Am. Chem. Soc. 121 (1999) 6086. For the enantioselective ring opening of epoxides with Ga heterobimetallic complexes, see: © T. Iida, N. Yamamoto, S. Matsunaga, H.-G. Woo, M. Shibasaki, Angew. Chem. Int. Ed. 37 (1998) 2223. For desymmetrization of Baylis-Hillman adducts with palladium, see: (d) B.M. Trost, H.C. Tsui, F.D. Toste, J. Am. Chem. Soc. 122 (2000) 3534.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6086
    • Ready, J.M.1    Jacobsen, E.N.2
  • 32
    • 0031704998 scopus 로고    scopus 로고
    • For palladium catalyzed allylic etherification reactions, see: (a) J. Muzart, J.P. Genet, A. Denis, J. Organomet. Chem. 326 (1987) C23. For enantioselective ring opening of epoxides with Cr(- salen) complexes, see: (b) J.M. Ready, E.N. Jacobsen, J. Am. Chem. Soc. 121 (1999) 6086. For the enantioselective ring opening of epoxides with Ga heterobimetallic complexes, see: © T. Iida, N. Yamamoto, S. Matsunaga, H.-G. Woo, M. Shibasaki, Angew. Chem. Int. Ed. 37 (1998) 2223. For desymmetrization of Baylis-Hillman adducts with palladium, see: (d) B.M. Trost, H.C. Tsui, F.D. Toste, J. Am. Chem. Soc. 122 (2000) 3534.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2223
    • Iida, T.1    Yamamoto, N.2    Matsunaga, S.3    Woo, H.-G.4    Shibasaki, M.5
  • 33
    • 0034639986 scopus 로고    scopus 로고
    • For palladium catalyzed allylic etherification reactions, see: (a) J. Muzart, J.P. Genet, A. Denis, J. Organomet. Chem. 326 (1987) C23. For enantioselective ring opening of epoxides with Cr(- salen) complexes, see: (b) J.M. Ready, E.N. Jacobsen, J. Am. Chem. Soc. 121 (1999) 6086. For the enantioselective ring opening of epoxides with Ga heterobimetallic complexes, see: © T. Iida, N. Yamamoto, S. Matsunaga, H.-G. Woo, M. Shibasaki, Angew. Chem. Int. Ed. 37 (1998) 2223. For desymmetrization of Baylis-Hillman adducts with palladium, see: (d) B.M. Trost, H.C. Tsui, F.D. Toste, J. Am. Chem. Soc. 122 (2000) 3534.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 3534
    • Trost, B.M.1    Tsui, H.C.2    Toste, F.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.