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Volumn 29, Issue 12, 2005, Pages 1581-1584

Highly reactive oligosilyltriflates - Synthesis, structure and rearrangement

Author keywords

[No Author keywords available]

Indexed keywords

1,1,1,3,3,4,4,6,6,6 DECAMETHYL 2,5 BIS(TRIFLUOROMETHANESULFONATO) 2,5 BIS(TRIMETHYLSILYL)HEXASILANE; 1,1,1,3,3,4,5,5,7,7,7 UNDECAMETHYL 2,6 TRIFLUOROMETHANESULFONATO 2,6 BIS(TRIMETHYLSILYL) 4 (1,1,3,3,3 PENTAMETHYL 2 TRIFLUOROMETHANESULFONATO 2 TRIMETHYLSILYLTRISILANYL)HEPTASILANE; 1,1,1,3,3,5,5 HEPTAMETHYL 2,5 BIS(TRIFLUOROMETHANESULFONATO) 2,4,4 TRIS(TRIMETHYLSILYL)PENTASILANE; 1,1,1,3,3,5,5,5 OCTAMETHYL 2,4 BIS(TRIFLUOROMETHANESULFONATO) 2,4 BIS(TRIMETHYLSILYL) 3 GERMAPENTASILANE; 1,1,1,3,3,5,5,5 OCTAMETHYL 2,4 BIS(TRIFLUOROMETHANESULFONATO) 2,4 BIS(TRIMETHYLSILYL)PENTASILANE; 1,1,1,4,4,4 HEXAMETHYL 2,3 BIS(TRIFLUOROMETHANESULFONATO) 2,3 BIS(TRIMETHYLSILYL)TETRASILANE; SILANE DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

EID: 29144452942     PISSN: 11440546     EISSN: 13699261     Source Type: Journal    
DOI: 10.1039/b408573f     Document Type: Article
Times cited : (11)

References (54)
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    • Uhlig, W.1
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    • In a previous work 2a was produced analogously using toluene as solvent, but neither was the compound isolated nor were analytical data given, except for the Si-NMR spectrum which is in agreement with our data. U. Baumeister, K. Schenzel, R. Zink and K. Hassler, J. Organomet. Chem., 1997, 543, 117.
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    • Baumeister, U.1    Schenzel, K.2    Zink, R.3    Hassler, K.4
  • 34
    • 29144455715 scopus 로고    scopus 로고
    • note
    • The conformations are roughly classified as cis (C) and trans (T) by dihedral angles of 0-30° and 150-180°, respectively.
  • 36
    • 0024875875 scopus 로고
    • ed. S. Patai and Z. Rappoport, Wiley, Chichester, UK
    • (b) R. West, in The Chemistry of Organic Silicon Compounds, ed. S. Patai and Z. Rappoport, Wiley, Chichester, UK, 1989, p. 1207.
    • (1989) The Chemistry of Organic Silicon Compounds , pp. 1207
    • West, R.1
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    • 0000879050 scopus 로고    scopus 로고
    • ed. Z. Rappoport and Y. Apeloig, Wiley, Chichester, UK, Ch. 11
    • P. D. Lickiss, The Chemistry of Organic Silicon Compounds, ed. Z. Rappoport and Y. Apeloig, Wiley, Chichester, UK, 1998, Vol. 2, Part 1, Ch. 11.
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    • note
    • 15 The Si-OTf distances in pentacoordinate Organosilicon structures are usually longer than in tetracoordinate derivatives.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.