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Volumn 122, Issue 14, 2000, Pages 3534-3535

Deracemization of Baylis-Hillman adducts [7]

Author keywords

[No Author keywords available]

Indexed keywords

ORGANIC COMPOUND;

EID: 0034639986     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja994326n     Document Type: Letter
Times cited : (167)

References (25)
  • 10
    • 0000276556 scopus 로고
    • Trost, B. M., Fleming, I., Semmelhack, M. F., Eds., Pergamon Press: Oxford
    • Godleski, S. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Semmelhack, M. F., Eds., Pergamon Press: Oxford, 1991; Vol. 4, pp 585-662.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 585-662
    • Godleski, S.A.1
  • 21
    • 33646274026 scopus 로고    scopus 로고
    • New compounds have been fully characterized by spectroscopic methods and elemental composition established by high-resolution mass spectroscopy or combustion analysis
    • New compounds have been fully characterized by spectroscopic methods and elemental composition established by high-resolution mass spectroscopy or combustion analysis.
  • 22
    • 33646318809 scopus 로고    scopus 로고
    • For eq 3. the ralios of 15 to its regioisomer in the crude reactions are as follows: a. 93:7, b. 93:7, c. 87:13. d. 68:32, e. 86:14, f. 76:24. For eq 4, the ratios of 16 to its regioisomer in the crude reactions are as follows: a. 90:10. h. 87:13. c. 91:9, d. 86:14
    • For eq 3. the ralios of 15 to its regioisomer in the crude reactions are as follows: a. 93:7, b. 93:7, c. 87:13. d. 68:32, e. 86:14, f. 76:24. For eq 4, the ratios of 16 to its regioisomer in the crude reactions are as follows: a. 90:10. h. 87:13. c. 91:9, d. 86:14.


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