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Volumn 16, Issue 41, 2010, Pages 12454-12461

Dicationic tellurium analogues of the classic N-heterocyclic carbene

Author keywords

carbene analogues; heterocycles; N ligands; polycations; tellurium

Indexed keywords

CARBENE ANALOGUES; CENTRAL ELEMENTS; COUPLING REACTION; DICATIONS; DIIMINE LIGAND; DIIMINES; HALIDE ABSTRACTION; HETEROCYCLES; ISOSTRUCTURAL; LONE PAIR; N LIGANDS; N-HETEROCYCLIC CARBENES; OXIDATION STATE; POLYCATIONS; SOLID-STATE STRUCTURES; STARTING MATERIALS; STEREOCHEMICALLY ACTIVE LONE PAIR OF ELECTRONS;

EID: 77956195654     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001447     Document Type: Article
Times cited : (37)

References (55)
  • 2
    • 33845279754 scopus 로고
    • Bertrand's isolation of a stable carbene slightly predates Arduengo's, see:
    • Bertrand's isolation of a stable carbene slightly predates Arduengo's, see:, A. Igaur, H. Grutzmacher, A. Baceiredor, G. Bertrand, J. Am. Chem. Soc. 1988, 110, 6463 - 6466.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 6463-6466
    • Igaur, A.1    Grutzmacher, H.2    Baceiredor, A.3    Bertrand, G.4
  • 22
    • 78249255608 scopus 로고    scopus 로고
    • The observed differences in the mertrical parameters found in, for example, the imidazolium or chlorophosphine and the corresponding NHC or N-heterocyclic phosphenium cation are quite subtle.
    • The observed differences in the mertrical parameters found in, for example, the imidazolium or chlorophosphine and the corresponding NHC or N-heterocyclic phosphenium cation are quite subtle.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.