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Volumn 23, Issue 23, 2004, Pages 5386-5388

Group-6 imido activation by a ring-strained alkyne

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDITION; LIGANDS; METAL COMPLEXES; THERMOLYSIS;

EID: 9144260135     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om049262q     Document Type: Article
Times cited : (33)

References (22)
  • 3
    • 0000315733 scopus 로고
    • Other methods for readily prepared group-6 alkylidene complexes have appeared. For examples see: (a) Nugent, W. A.; Feldman, J.; Calabrese, J. C. J. Am. Chem. Soc. 1995, 117, 8992. (b) Johnson, L. K.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1993, 115, 8130.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8992
    • Nugent, W.A.1    Feldman, J.2    Calabrese, J.C.3
  • 4
    • 0043199564 scopus 로고
    • Other methods for readily prepared group-6 alkylidene complexes have appeared. For examples see: (a) Nugent, W. A.; Feldman, J.; Calabrese, J. C. J. Am. Chem. Soc. 1995, 117, 8992. (b) Johnson, L. K.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1993, 115, 8130.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 8130
    • Johnson, L.K.1    Grubbs, R.H.2    Ziller, J.W.3
  • 12
    • 0000959461 scopus 로고
    • For seminal mechanistic studies on group-4 metal catalyzed hydroamination see: (a) Baranger, A. M.; Walsh, P. J.; Bergman, R. G. J. Am. Chem. Soc. 1993, 115, 2753. (b) Walsh, P. J.; Baranger, A. M.; Bergman, R. G. J. Am. Chem. Soc. 1992, 114, 1708.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 2753
    • Baranger, A.M.1    Walsh, P.J.2    Bergman, R.G.3
  • 13
    • 0000239830 scopus 로고
    • For seminal mechanistic studies on group-4 metal catalyzed hydroamination see: (a) Baranger, A. M.; Walsh, P. J.; Bergman, R. G. J. Am. Chem. Soc. 1993, 115, 2753. (b) Walsh, P. J.; Baranger, A. M.; Bergman, R. G. J. Am. Chem. Soc. 1992, 114, 1708.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1708
    • Walsh, P.J.1    Baranger, A.M.2    Bergman, R.G.3
  • 17
    • 0041487865 scopus 로고
    • The ring-strain in the triple bond of cyclooctyne is estimated by hydrogenation (cyclooctyne to cis-cyclooctene versus 4-octyne to cis-4-octene) to be ∼10 kcal/mol. Turner, R. B.; Jarret, A. D.; Goebel, P.; Mallon, B. J. J. Am. Chem. Soc. 1973, 95, 790.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 790
    • Turner, R.B.1    Jarret, A.D.2    Goebel, P.3    Mallon, B.J.4
  • 18
    • 84988066108 scopus 로고
    • Cyclooctyne is readily prepared on > 10 g scales. Brandsma, L.; Verkruijsse, H. D. Synthesis 1978, 290. At -35°C under an inert atmosphere, pure cyclooctyne has been stored without noticeable decomposition for months.
    • (1978) Synthesis , pp. 290
    • Brandsma, L.1    Verkruijsse, H.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.