메뉴 건너뛰기




Volumn , Issue 5, 2005, Pages 663-665

New catalytic route to functionalized vinylboronates

Author keywords

[No Author keywords available]

Indexed keywords

BORANE DERIVATIVE; BORON DERIVATIVE; BORONIC ACID DERIVATIVE; RUBIDIUM; UNCLASSIFIED DRUG; VINYLBORONATE DERIVATIVE; VINYLDIOXABORINANE; VINYLDIOXABOROLANE;

EID: 14544294885     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b414644a     Document Type: Article
Times cited : (69)

References (27)
  • 1
    • 9644304824 scopus 로고    scopus 로고
    • Organoboranes for Synthesis, ACS Symposium Series 783, ed. P. V. Ramachandran and H. C. Brown, American Chemical Society, Washington, DC
    • P. V. Ramachandran and H. C. Brown in Recent Advances in Borane Chemistry. Organoboranes for Synthesis, ACS Symposium Series 783, ed. P. V. Ramachandran and H. C. Brown, American Chemical Society, Washington, DC, 2001, p. 1-15.
    • (2001) Recent Advances in Borane Chemistry , pp. 1-15
    • Ramachandran, P.V.1    Brown, H.C.2
  • 6
    • 0000078067 scopus 로고
    • A. R. Katritzky, O. Methcohn and C. W. Rees, eds., Elsevier Science, Oxford, ch. 2.18
    • L. Hevesi in Comprehensive Organic Functional Group Transformations, A. R. Katritzky, O. Methcohn and C. W. Rees, eds., Elsevier Science, Oxford, 1995, vol 2, ch. 2.18.
    • (1995) Comprehensive Organic Functional Group Transformations , vol.2
    • Hevesi, L.1
  • 19
    • 0037405684 scopus 로고    scopus 로고
    • For recent reviews on silylative coupling and cross-metathesis of vinylsilicon functionality see B. Marciniec and C. Pietraszuk, Curr. Org. Chem., 2003, 7, 691.
    • (2003) Curr. Org. Chem. , vol.7 , pp. 691
    • Marciniec, B.1    Pietraszuk, C.2
  • 23
    • 14544288391 scopus 로고    scopus 로고
    • note
    • 2 (0.0032 g, 0.0044 mmol) was added and the reaction was carried out for 3 h.
  • 24
    • 14544287501 scopus 로고    scopus 로고
    • note
    • For similar experiment see: ref. 7a.
  • 27
    • 14544272072 scopus 로고    scopus 로고
    • note
    • It was found that a small (threefold in relation to catalyst) excess of free phosphine strongly retards the process.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.