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Volumn 118, Issue 28, 1996, Pages 6698-6706

Synthesis of η3-propargyl rhenium complexes

Author keywords

[No Author keywords available]

Indexed keywords

RHENIUM COMPLEX;

EID: 0029889914     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja960375d     Document Type: Article
Times cited : (41)

References (54)
  • 4
    • 8944262888 scopus 로고
    • For other examples of hydride abstraction from metal π-complexes, see: (a) Casey, C. P.; Yi, C. S. Organometallics 1990, 9, 2143. (b) Batchelor, R. J.; Einstein, F. W. B.; Zhuang, J.-M.; Sutton, D. J. Organomet. Chem. 1990, 397, 69-80. (c) Margulis, T. N.; Schiff, L.; Rosenblum, M. J. Am. Chem. Soc. 1965, 87, 3269. (d) Fischer, E. O.; Fischer, R. D. Angew. Chem. 1960, 72, 919.
    • (1990) Organometallics , vol.9 , pp. 2143
    • Casey, C.P.1    Yi, C.S.2
  • 5
    • 0001840528 scopus 로고
    • For other examples of hydride abstraction from metal π-complexes, see: (a) Casey, C. P.; Yi, C. S. Organometallics 1990, 9, 2143. (b) Batchelor, R. J.; Einstein, F. W. B.; Zhuang, J.-M.; Sutton, D. J. Organomet. Chem. 1990, 397, 69-80. (c) Margulis, T. N.; Schiff, L.; Rosenblum, M. J. Am. Chem. Soc. 1965, 87, 3269. (d) Fischer, E. O.; Fischer, R. D. Angew. Chem. 1960, 72, 919.
    • (1990) J. Organomet. Chem. , vol.397 , pp. 69-80
    • Batchelor, R.J.1    Einstein, F.W.B.2    Zhuang, J.-M.3    Sutton, D.4
  • 6
    • 0041824955 scopus 로고
    • For other examples of hydride abstraction from metal π-complexes, see: (a) Casey, C. P.; Yi, C. S. Organometallics 1990, 9, 2143. (b) Batchelor, R. J.; Einstein, F. W. B.; Zhuang, J.-M.; Sutton, D. J. Organomet. Chem. 1990, 397, 69-80. (c) Margulis, T. N.; Schiff, L.; Rosenblum, M. J. Am. Chem. Soc. 1965, 87, 3269. (d) Fischer, E. O.; Fischer, R. D. Angew. Chem. 1960, 72, 919.
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 3269
    • Margulis, T.N.1    Schiff, L.2    Rosenblum, M.3
  • 7
    • 0001747404 scopus 로고
    • For other examples of hydride abstraction from metal π-complexes, see: (a) Casey, C. P.; Yi, C. S. Organometallics 1990, 9, 2143. (b) Batchelor, R. J.; Einstein, F. W. B.; Zhuang, J.-M.; Sutton, D. J. Organomet. Chem. 1990, 397, 69-80. (c) Margulis, T. N.; Schiff, L.; Rosenblum, M. J. Am. Chem. Soc. 1965, 87, 3269. (d) Fischer, E. O.; Fischer, R. D. Angew. Chem. 1960, 72, 919.
    • (1960) Angew. Chem. , vol.72 , pp. 919
    • Fischer, E.O.1    Fischer, R.D.2
  • 23
    • 0001524493 scopus 로고
    • (c) McMullen, A. K.; Selegue, J. P.; Wang, J.-G. Organometallics 1991, 10, 3421-3; Jia, G.; Rheingold, A. L.; Meek, D. W. Organomelallics 1989, 8, 1378-80.
    • (1989) Organomelallics , vol.8 , pp. 1378-1380
    • Jia, G.1    Rheingold, A.L.2    Meek, D.W.3
  • 36
    • 37049091255 scopus 로고
    • For related syntheses of π-allyl metal complexes by protonation of allyl alcohol complexes, see: (a) Rosan, A. M. J. Chem. Soc., Chem. Commun. 1981, 311. (b) Krivykh, V. V.; Gusev, O. V.; Rybinskaya, M. I. J. Organomet. Chem. 1989, 362, 351-362. (c) Rosan, A. M.; Romano, D. M. Organometallics 1990, 9, 1048-1052.
    • (1981) J. Chem. Soc., Chem. Commun. , pp. 311
    • Rosan, A.M.1
  • 37
    • 0000362195 scopus 로고
    • For related syntheses of π-allyl metal complexes by protonation of allyl alcohol complexes, see: (a) Rosan, A. M. J. Chem. Soc., Chem. Commun. 1981, 311. (b) Krivykh, V. V.; Gusev, O. V.; Rybinskaya, M. I. J. Organomet. Chem. 1989, 362, 351-362. (c) Rosan, A. M.; Romano, D. M. Organometallics 1990, 9, 1048-1052.
    • (1989) J. Organomet. Chem. , vol.362 , pp. 351-362
    • Krivykh, V.V.1    Gusev, O.V.2    Rybinskaya, M.I.3
  • 38
    • 0345621759 scopus 로고
    • For related syntheses of π-allyl metal complexes by protonation of allyl alcohol complexes, see: (a) Rosan, A. M. J. Chem. Soc., Chem. Commun. 1981, 311. (b) Krivykh, V. V.; Gusev, O. V.; Rybinskaya, M. I. J. Organomet. Chem. 1989, 362, 351-362. (c) Rosan, A. M.; Romano, D. M. Organometallics 1990, 9, 1048-1052.
    • (1990) Organometallics , vol.9 , pp. 1048-1052
    • Rosan, A.M.1    Romano, D.M.2
  • 46
    • 8944260955 scopus 로고    scopus 로고
    • 3COH. We cannot rule out the water from the glassware as the proton source, despite our best efforts to maintain dry conditions
    • 3COH. We cannot rule out the water from the glassware as the proton source, despite our best efforts to maintain dry conditions.
  • 47
    • 8944244583 scopus 로고    scopus 로고
    • The net 1,2-hydride shift might also occur by β-hydride elimination from the vinyl intermediate to form a metal-hydride-allene complex, followed by addition of hydride to the central carbon
    • The net 1,2-hydride shift might also occur by β-hydride elimination from the vinyl intermediate to form a metal-hydride-allene complex, followed by addition of hydride to the central carbon.
  • 53
    • 0004150157 scopus 로고    scopus 로고
    • 1994, Siemens Analytical X-ray Instruments: 6300 Enterprise Dr., Madison, WI 53719-1173
    • Sheldrick, G. M., 1994, SHELXTL Version 5 Reference Manual. Siemens Analytical X-ray Instruments: 6300 Enterprise Dr., Madison, WI 53719-1173.
    • SHELXTL Version 5 Reference Manual
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.