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Volumn 60, Issue 10, 2003, Pages 2259-2271

Investigation of the intermolecular Pauson-Khand reaction of various 1-alkynes with cyclic exo-methylene compounds

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE DERIVATIVE; BENZENE DERIVATIVE; CARBENOID; CYCLOPENTENONE DERIVATIVE; SPIROCYCLOPENTENONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0142027854     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-03-9849     Document Type: Article
Times cited : (16)

References (41)
  • 23
    • 0142136470 scopus 로고
    • Organic Reactions, John Wiley & Sons Inc., New York
    • N. E. Shore, 'The Pauson-Khand Cycloaddition Reaction for Synthesis of Cyclopentanones' in Organic Reactions, Vol. 40, John Wiley & Sons Inc., New York, 1991, p. 6: The reaction of phenylacetylene with simple alkene such as cyclohexene (2 eq.) in boiling toluene gave the corresponding adduct in only 3% yield; I. U. Khand and P. L. Pauson, J. Chem. Res. (M), 1977, 168.
    • (1991) 'The Pauson-Khand Cycloaddition Reaction for Synthesis of Cyclopentanones' , vol.40 , pp. 6
    • Shore, N.E.1
  • 24
    • 0000134235 scopus 로고
    • N. E. Shore, 'The Pauson-Khand Cycloaddition Reaction for Synthesis of Cyclopentanones' in Organic Reactions, Vol. 40, John Wiley & Sons Inc., New York, 1991, p. 6: The reaction of phenylacetylene with simple alkene such as cyclohexene (2 eq.) in boiling toluene gave the corresponding adduct in only 3% yield; I. U. Khand and P. L. Pauson, J. Chem. Res. (M), 1977, 168.
    • (1977) J. Chem. Res. (M) , pp. 168
    • Khand, I.U.1    Pauson, P.L.2
  • 27
    • 0000800296 scopus 로고
    • To the best of our knowledge, it is the first example to use nitroarylacetylenes in Pauson-Khand reaction: For previous reports on Pauson-Khand reaction using electron-defficient alkynes; (a) M. E. Krafft, R. H. Romulo, and I. L. Scott, J. Org. Chem., 1992, 57, 5277.
    • (1992) J. Org. Chem. , vol.57 , pp. 5277
    • Krafft, M.E.1    Romulo, R.H.2    Scott, I.L.3
  • 30
    • 0142041204 scopus 로고    scopus 로고
    • note
    • Unfortunately, the reaction of sterically hindered trimethylsilylacetylene with 2a did not give desired adduct at all.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.