메뉴 건너뛰기




Volumn 129, Issue 41, 2007, Pages 12392-12393

Chiral tetraaminophosphonium salt-mediated asymmetric direct henry reaction

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHONIUM DERIVATIVE; TETRAAMINOPHOSPHONIUM; UNCLASSIFIED DRUG;

EID: 35349001124     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja075152+     Document Type: Article
Times cited : (233)

References (43)
  • 2
    • 0004231121 scopus 로고    scopus 로고
    • Quin, L. D, Ed, John Wiley & Sons: New York
    • (b) A Guide to Organophosphorus Chemistry; Quin, L. D., Ed.; John Wiley & Sons: New York, 2000.
    • (2000) A Guide to Organophosphorus Chemistry
  • 4
    • 35349026573 scopus 로고    scopus 로고
    • Phase-transfer catalyst: (a) Handbook of Phase Transfer Catalysis, Sasson, Y., Neumann, R., Eds.; Blackie Academic & Professional: London, 1997.
    • Phase-transfer catalyst: (a) Handbook of Phase Transfer Catalysis, Sasson, Y., Neumann, R., Eds.; Blackie Academic & Professional: London, 1997.
  • 6
    • 0007200681 scopus 로고    scopus 로고
    • Organic fluoride-ion source: (c) Bohsako, A.; Asakura, C.; Shioiri, T. Synlett 1995, 1033.
    • Organic fluoride-ion source: (c) Bohsako, A.; Asakura, C.; Shioiri, T. Synlett 1995, 1033.
  • 7
    • 35348958797 scopus 로고    scopus 로고
    • Lewis acidic promoter: (d) Mukaiyama, T.; Matsui, S.; Kashiwagi, K. Chem. Lett. 1989, 993.
    • Lewis acidic promoter: (d) Mukaiyama, T.; Matsui, S.; Kashiwagi, K. Chem. Lett. 1989, 993.
  • 9
    • 35348989096 scopus 로고    scopus 로고
    • Cornils, B, Herrmann, W. A, Horvath, I. T, Leitner, W, Mecking, S, Olivier-Bourbigou, H, Vogt, D, Eds, Wiley-VCH: New York, Chapter 5.2.2.7, p
    • (f) McNulty, J. In Multiphase Homogeneous Catalysis; Cornils, B., Herrmann, W. A., Horvath, I. T., Leitner, W., Mecking, S., Olivier-Bourbigou, H., Vogt, D., Eds.; Wiley-VCH: New York, 2005; Vol. 2, Chapter 5.2.2.7, p 542-546.
    • (2005) Multiphase Homogeneous Catalysis , vol.2 , pp. 542-546
    • McNulty, J.1
  • 12
    • 35348957199 scopus 로고    scopus 로고
    • Beil, W.; Hoeppener, A.; Wolf, H. J.; Beil, H. C. NL-6407501-19650111.
    • (a) Beil, W.; Hoeppener, A.; Wolf, H. J.; Beil, H. C. NL-6407501-19650111.
  • 13
    • 35348960844 scopus 로고    scopus 로고
    • Shomova, E. A.; Rudavskii, V. P.; Derkach, G. I.; SU-195785-19670504.
    • (b) Shomova, E. A.; Rudavskii, V. P.; Derkach, G. I.; SU-195785-19670504.
  • 15
    • 27744463253 scopus 로고    scopus 로고
    • 4PX-type tetraaminophosphonium salts: (a) Cameron, T. B.; Hanson, H. N.; de la Fuente, G. F.; Huheey, J. E. Phosphorus, Sulfur, Silicon 1993, 78, 37.
    • 4PX-type tetraaminophosphonium salts: (a) Cameron, T. B.; Hanson, H. N.; de la Fuente, G. F.; Huheey, J. E. Phosphorus, Sulfur, Silicon 1993, 78, 37.
  • 19
    • 13244273568 scopus 로고    scopus 로고
    • Basicity of iminophosphoranes: (a) Kaljurand, I.; Kütt, A.; Sooväli, L.; Rodima, T.; Mäemets, V.; Leito, I.; Koppel, I. A. J. Org. Chem. 2005, 70, 1019.
    • Basicity of iminophosphoranes: (a) Kaljurand, I.; Kütt, A.; Sooväli, L.; Rodima, T.; Mäemets, V.; Leito, I.; Koppel, I. A. J. Org. Chem. 2005, 70, 1019.
  • 21
    • 2342550664 scopus 로고    scopus 로고
    • Synthetic application of a phosphazene as a base catalyst: (a) Bensa, D.; Constantieux, T.; Rodriguez, J. Synthesis 2004, 923.
    • Synthetic application of a phosphazene as a base catalyst: (a) Bensa, D.; Constantieux, T.; Rodriguez, J. Synthesis 2004, 923.
  • 23
    • 0033597638 scopus 로고    scopus 로고
    • Chiral variants: (a) Brunel, J. M.; Legrand, O.; Reymond, S.; Buono, G. J. Am. Chem. Soc. 1999, 121, 5807.
    • Chiral variants: (a) Brunel, J. M.; Legrand, O.; Reymond, S.; Buono, G. J. Am. Chem. Soc. 1999, 121, 5807.
  • 30
    • 35348942196 scopus 로고    scopus 로고
    • Although a minor diastereomer, P,S-3a, has not been isolated in its pure form, a preliminary experiment indicated that the (M,S)-isomer is more effective in this reaction. Relative stereochemistries of 3b-d were determined by the chemical shifts of 1H NMR spectra by analogy
    • 1H NMR spectra by analogy.
  • 32
    • 33846593979 scopus 로고    scopus 로고
    • Recent reviews on the asymmetric Henry reaction: (a) Boruwa, J.; Gogoi, N.; Saikia, P. P.; Barua, N. C. Tetrahedron: Asymmetry 2006, 17, 3315.
    • Recent reviews on the asymmetric Henry reaction: (a) Boruwa, J.; Gogoi, N.; Saikia, P. P.; Barua, N. C. Tetrahedron: Asymmetry 2006, 17, 3315.
  • 42
    • 34250632623 scopus 로고
    • and references therein
    • (i) Ma, K.; You, J. Chem. Eur. J. 2007, 13, 1863 and references therein.
    • (1863) Chem. Eur. J , vol.13
    • Ma, K.1    You, J.2
  • 43
    • 35348989620 scopus 로고    scopus 로고
    • See Supporting Information for details of the NMR experiment
    • See Supporting Information for details of the NMR experiment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.