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Volumn , Issue 14, 2008, Pages 2344-2349

Silylene and germylene intermediates in the reactions of silole and germole dianions with N,N′-Di-tert-butylethylenediimine

Author keywords

Germole dianion; Germylene; Metallation; N,N Di tert butylethylenediimine; Silole dianion; Silylene

Indexed keywords

REACTION INTERMEDIATES;

EID: 53249092240     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200800083     Document Type: Article
Times cited : (12)

References (34)
  • 11
    • 85153187613 scopus 로고    scopus 로고
    • 2SiH: M. Kako, S. Oba, R. Uesugi, S. Sumiishi, Y. Nakadaira, K. Tanaka, T. Takada, J. Chem. Soc. Perkin Trans. 2 1997, 1251-1253. This mode of trapping was unsuccessful in our experiments, evidently because addition of 6a to the diimine was more rapid than Si-H bond insertion.
    • 2SiH: M. Kako, S. Oba, R. Uesugi, S. Sumiishi, Y. Nakadaira, K. Tanaka, T. Takada, J. Chem. Soc. Perkin Trans. 2 1997, 1251-1253. This mode of trapping was unsuccessful in our experiments, evidently because addition of 6a to the diimine was more rapid than Si-H bond insertion.
  • 13
    • 53249132363 scopus 로고    scopus 로고
    • Eds: Z. Rappoport, I. Marek, Wiley Interscience, chapter 1, p
    • a) G. Fraenkel in The Chemistry of Organolithium Compounds (Eds: Z. Rappoport, I. Marek), Wiley Interscience, 2005, vol. 2, chapter 1, p. 1;
    • (2005) The Chemistry of Organolithium Compounds , vol.2 , pp. 1
    • Fraenkel, G.1
  • 26
    • 85153278009 scopus 로고    scopus 로고
    • All computations were done with Gaussian 03 Revision B.03, Gaussian, Inc., Pittsburgh PA, 2003.
    • All computations were done with Gaussian 03 Revision B.03, Gaussian, Inc., Pittsburgh PA, 2003.
  • 27


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.