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Volumn 125, Issue 14, 2003, Pages 4020-4021

The niobaziridinee-hydride functional group: Synthesis and divergent reactivity

Author keywords

[No Author keywords available]

Indexed keywords

LIGAND; NIOBAZIRIDINE; NIOBIUM; UNCLASSIFIED DRUG;

EID: 0037427335     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja028446y     Document Type: Article
Times cited : (108)

References (22)
  • 10
    • 0242528132 scopus 로고    scopus 로고
    • note
    • We attribute the low isolated yield of 1 to its high lipophilicity.
  • 11
    • 84989111368 scopus 로고
    • Such downfield shifts are typical for high valent early T.M. hydride complexes, and the broadness of the signal can be attributed to coupling to the quadrupolar Nb nucleus. For instance, see: (a) Templeton, J. C.; Craig, P. C.; Pregosin, P. S.; Ruegger, H. Magn. Reson. Chem. 1993, 31, 58. (b) Besescker, C. J.; Klemperer, W. G.; Maltbie, D. J.; Write, D. A. Inorg. Chem. 1985, 24, 1027.
    • (1993) Magn. Reson. Chem. , vol.31 , pp. 58
    • Templeton, J.C.1    Craig, P.C.2    Pregosin, P.S.3    Ruegger, H.4
  • 12
    • 0000164276 scopus 로고
    • Such downfield shifts are typical for high valent early T.M. hydride complexes, and the broadness of the signal can be attributed to coupling to the quadrupolar Nb nucleus. For instance, see: (a) Templeton, J. C.; Craig, P. C.; Pregosin, P. S.; Ruegger, H. Magn. Reson. Chem. 1993, 31, 58. (b) Besescker, C. J.; Klemperer, W. G.; Maltbie, D. J.; Write, D. A. Inorg. Chem. 1985, 24, 1027.
    • (1985) Inorg. Chem. , vol.24 , pp. 1027
    • Besescker, C.J.1    Klemperer, W.G.2    Maltbie, D.J.3    Write, D.A.4
  • 14
  • 22
    • 0242696988 scopus 로고    scopus 로고
    • note
    • 6, 100 °C, 3 d).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.