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Volumn 301, Issue 5637, 2003, Pages 1223-1225

Synthesis of carbenes through substitution reactions at a carbene center

Author keywords

[No Author keywords available]

Indexed keywords

SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 0041821739     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1086860     Document Type: Article
Times cited : (58)

References (23)
  • 1
    • 0003428791 scopus 로고
    • Wiley, New York
    • M. Jones, R. A. Moss, Eds., Carbenes (Wiley, New York, vols. 1 and 2, 1973 and 1975).
    • (1973) Carbenes , vol.1-2
    • Jones, M.1    Moss, R.A.2
  • 5
    • 0041705223 scopus 로고    scopus 로고
    • note
    • Persistent triplet carbenes have also been characterized, but not isolated (6).
  • 10
    • 0041705222 scopus 로고    scopus 로고
    • note
    • Their efficiency is largely due to their strong δ-donor property, which can be superior to that of the best phosphine donor ligands (11). To date, the bis(diisopropylamino)carbene (12) is the most basic known carbene ligand (13).
  • 15
    • 0042205742 scopus 로고    scopus 로고
    • note
    • A mechanism involving a substitution reaction at a transient dichlorocarbene has been postulated in the basic hydrolysis of chloroform (16).
  • 22
    • 0042706871 scopus 로고    scopus 로고
    • note
    • The position of the aromatic tert-butyl groups of carbene 8 has been ascertained by a single crystal x-ray diffraction study of the derivative 9 that results from the thiolation of both the phosphine and carbene center of 8.
  • 23
    • 0041705221 scopus 로고    scopus 로고
    • note
    • We are grateful to the American Chemical Society-Petroleum Research Fund (grant no. 38192-AC4) and to Rhodia, Inc. for financial support.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.