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Volumn 10, Issue 20, 2008, Pages 4445-4447

Ynol ethers from dichloroenol ethers: Mechanistic elucidation through 35Cl labeling

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EID: 61349155548     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801704u     Document Type: Article
Times cited : (25)

References (32)
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    • For reviews, see: a, Raphael, R. A, Taylor, E. C, Wynberg, H, Eds, Interscience Publishers, Ltd: New York
    • For reviews, see: (a) Arens, J. F. In Advances in Organic Chemistry; Raphael, R. A., Taylor, E. C., Wynberg, H., Eds.; Interscience Publishers, Ltd: New York, 1960; Vol. II, pp 117-212.
    • (1960) Advances in Organic Chemistry , vol.2 , pp. 117-212
    • Arens, J.F.1
  • 2
    • 84956064688 scopus 로고
    • For more recent publications, see refs 3a-g
    • (b) Rachenko, S. I.; Petrov, A. A. Russ. Chem. Rev. 1989, 58, 1671-1702. For more recent publications, see refs 3a-g.
    • (1989) Russ. Chem. Rev , vol.58 , pp. 1671-1702
    • Rachenko, S.I.1    Petrov, A.A.2
  • 6
    • 18844386511 scopus 로고    scopus 로고
    • There are over 100 citations of refs 2a-c. For selected recent papers, see: (a) Harmata, M.; Lee, D. R.; Barnes, C. L. Org. Lett. 2005, 7, 1881-1883.
    • There are over 100 citations of refs 2a-c. For selected recent papers, see: (a) Harmata, M.; Lee, D. R.; Barnes, C. L. Org. Lett. 2005, 7, 1881-1883.
  • 15
    • 0009545745 scopus 로고
    • For reviews, see
    • (c) Wiechell, H. Liebigs Ann. Chem. 1894, 279, 337. For reviews, see:
    • (1894) Liebigs Ann. Chem , vol.279 , pp. 337
    • Wiechell, H.1
  • 16
    • 4644275985 scopus 로고    scopus 로고
    • (d) Knorr, R. Chem. Rev. 2004, 104, 3795-3849.
    • (2004) Chem. Rev , vol.104 , pp. 3795-3849
    • Knorr, R.1
  • 20
    • 61349131936 scopus 로고    scopus 로고
    • 3b,c,f was also found to be E.
    • 3b,c,f was also found to be E.
  • 21
    • 61349192155 scopus 로고    scopus 로고
    • Baldwin, J. E, Williams, R. M, Eds, Pergamon Press: Oxford, Chapter 3
    • Clayden, J. In Organolihtiums: selectivity for synthesis; Baldwin, J. E., Williams, R. M., Eds.; Pergamon Press: Oxford", 2002; Chapter 3.
    • (2002) Organolihtiums: Selectivity for synthesis
    • Clayden, J.1
  • 23
    • 61349116708 scopus 로고    scopus 로고
    • The choroynol ether obtained from the stericol derivative 3b,c,f proved to be unstable
    • 3b,c,f proved to be unstable.
  • 27
    • 0034638381 scopus 로고    scopus 로고
    • For the hydrochlorination of simple ynol ethers, see
    • For the hydrochlorination of simple ynol ethers, see: Yu, W.; Jin, Z. J. Am. Chem. Soc. 2000, 122, 9840-9841.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 9840-9841
    • Yu, W.1    Jin, Z.2
  • 28
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    • This measurement was realized in the mass spectrometry laboratory of the Université Pierre et Marie Curie Paris VI, The major isotope had a relative intensity of 100, the precision of the result is within 1, of the intensity of the minor mass. This same technique could not be applied to compound 3 due to a lack of ionization
    • This measurement was realized in the mass spectrometry laboratory of the Université Pierre et Marie Curie (Paris VI). The major isotope had a relative intensity of 100%; the precision of the result is within 1 % of the intensity of the minor mass. This same technique could not be applied to compound 3 due to a lack of ionization.


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