메뉴 건너뛰기




Volumn 6, Issue 3, 2008, Pages 577-585

Electron-rich heteroaroylphosphonates and their reaction with trimethyl phosphite

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYGENATION; ELECTRON-RICH HETEROAROYLPHOSPHONATES; FURAN-3-OYLPHOSPHONATES; INTERMOLECULAR TRAPPING; TRIMETHYL PHOSPHITES;

EID: 38549093539     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b717130g     Document Type: Article
Times cited : (14)

References (21)
  • 11
    • 38549091147 scopus 로고    scopus 로고
    • University of Ulm, Germany, personal communication
    • D. M. Benoit, University of Ulm, Germany, personal communication
    • Benoit, D.M.1
  • 12
    • 0006258854 scopus 로고    scopus 로고
    • Data have been deposited with the Cambridge Crystallographic Data Centre as CCDC 648419; for crystallographic data in CIF or other electronic format, see DOI:
    • R. Albers W. Sander Liebigs Ann./Recl. 1997 897
    • (1997) Liebigs Ann./Recl. , pp. 897
    • Albers, R.1    Sander, W.2
  • 15
    • 0032515429 scopus 로고    scopus 로고
    • Our studies of the carbenes generated from dialkyl benzoylphosphonates have shown that intermolecular trapping by trialkyl phosphites can even compete effectively with intramolecular insertion into an adjacent substituent if the quantity of solvent present is limited
    • T. Khasanova R. S. Sheridan J. Am. Chem. Soc. 1998 120 233
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 233
    • Khasanova, T.1    Sheridan, R.S.2
  • 16
    • 38549181646 scopus 로고    scopus 로고
    • D. V. Griffiths, Y.-K. Cheong, P. Duncanson, J. E. Harris, H. V. Taylor, manuscript in preparation
    • D. V. Griffiths, Y.-K. Cheong, P. Duncanson, J. E. Harris, H. V. Taylor, manuscript in preparation
  • 21
    • 0034060280 scopus 로고    scopus 로고
    • Further relevant information available in ESI Several of these components require the presence of traces of moisture in the reaction mixture so their formation can be suppressed by the rigorous exclusion of moisture Signal partially obscured
    • M. Curini F. Epifano M. Marcotullio O. Rosati Y. Guan E. Wenkert Helv. Chim. Acta 2000 83 755
    • (2000) Helv. Chim. Acta , vol.83 , pp. 755
    • Curini, M.1    Epifano, F.2    Marcotullio, M.3    Rosati, O.4    Guan, Y.5    Wenkert, E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.