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Volumn 121, Issue 47, 1999, Pages 10924-10927

Cobaloxime π-cation steric and stereoelectronic effects: The amazing effect of a single methyl group adjacent to the site of reaction

Author keywords

[No Author keywords available]

Indexed keywords

OXIME DERIVATIVE; SULFONIC ACID DERIVATIVE;

EID: 0033486056     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja993556z     Document Type: Article
Times cited : (11)

References (21)
  • 4
    • 0001352093 scopus 로고    scopus 로고
    • Grubb, L. M.; Branchaud, B. P. J. Org. Chem. 1997, 62, 2, 242-243. See also Grubb, L. M.; Brown, K. A.; Branchaud, B. P. Tetrahedron Lett. 1998, 39, 3447-3448
    • (1997) J. Org. Chem. , vol.62 , Issue.2 , pp. 242-243
    • Grubb, L.M.1    Branchaud, B.P.2
  • 13
    • 0001650268 scopus 로고    scopus 로고
    • 2py group has a large steric effect in Diels-Alder reactions, shifting endo-selective reactions into exo-selective ones: (a) Richardson, B. M., Welker, M. E. J. Org. Chem. 1997, 62, 1299-1304. (b) Chapman, J. J.; Welker, M. E. Organometallics 1997, 7477-755. Adams, T. A.; Welker, M. E.; Day, C. S. J. Org. Chem. 1998, 63, 3683-3686.
    • (1997) J. Org. Chem. , vol.62 , pp. 1299-1304
    • Richardson, B.M.1    Welker, M.E.2
  • 14
    • 0001650268 scopus 로고    scopus 로고
    • 2py group has a large steric effect in Diels-Alder reactions, shifting endo-selective reactions into exo-selective ones: (a) Richardson, B. M., Welker, M. E. J. Org. Chem. 1997, 62, 1299-1304. (b) Chapman, J. J.; Welker, M. E. Organometallics 1997, 7477-755. Adams, T. A.; Welker, M. E.; Day, C. S. J. Org. Chem. 1998, 63, 3683-3686.
    • (1997) Organometallics , pp. 7477-7755
    • Chapman, J.J.1    Welker, M.E.2
  • 15
    • 0001668573 scopus 로고    scopus 로고
    • 2py group has a large steric effect in Diels-Alder reactions, shifting endo-selective reactions into exo-selective ones: (a) Richardson, B. M., Welker, M. E. J. Org. Chem. 1997, 62, 1299-1304. (b) Chapman, J. J.; Welker, M. E. Organometallics 1997, 7477-755. Adams, T. A.; Welker, M. E.; Day, C. S. J. Org. Chem. 1998, 63, 3683-3686.
    • (1998) J. Org. Chem. , vol.63 , pp. 3683-3686
    • Adams, T.A.1    Welker, M.E.2    Day, C.S.3
  • 19
    • 33947087984 scopus 로고
    • 1,2-Epoxylinalool was prepared by a literature procedure by vanadium-catalyzed epoxidation of linalool: Sharpless, K. B.; Michaelson, R. C. J. Am. Chem. Soc. 1973, 95, 6136-6137.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 6136-6137
    • Sharpless, K.B.1    Michaelson, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.