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Volumn 63, Issue 23, 1998, Pages 8247-8258

Alkyl galactopyranosides: Rotational population dependence of the hydroxymethyl group on the aglycon and its absolute configuration and on the anomeric configuration

Author keywords

[No Author keywords available]

Indexed keywords

GALACTOPYRANOSIDE DERIVATIVE; PYRANOSIDE; UNCLASSIFIED DRUG;

EID: 0032514999     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo981002t     Document Type: Article
Times cited : (31)

References (30)
  • 13
    • 15444342162 scopus 로고    scopus 로고
    • note
    • Software for the calculation of rotameric populations, by using any of the four sets of equations mentioned in the text, is available upon request from E.Q.M.
  • 18
    • 0003658865 scopus 로고
    • University Science Books: California
    • For a monograph on exciton CD spectroscopy see: (a) Harada, N.; Nakanishi, K. Circular Dichroic Spectroscopy Exciton Coupling in Organic Stereochemistry; University Science Books: California, 1983. (b) Nakanishi, K.; Berova, N. The Exciton Chirality Method in Circular Dichroism, Principles and Applications; Nakanishi, K., Berova, N., Woody, R. W., Eds.; VCH Publishers: New York, 1994.
    • (1983) Circular Dichroic Spectroscopy Exciton Coupling in Organic Stereochemistry
    • Harada, N.1    Nakanishi, K.2
  • 19
    • 0038816390 scopus 로고
    • Nakanishi, K., Berova, N., Woody, R. W., Eds.; VCH Publishers: New York
    • For a monograph on exciton CD spectroscopy see: (a) Harada, N.; Nakanishi, K. Circular Dichroic Spectroscopy Exciton Coupling in Organic Stereochemistry; University Science Books: California, 1983. (b) Nakanishi, K.; Berova, N. The Exciton Chirality Method in Circular Dichroism, Principles and Applications; Nakanishi, K., Berova, N., Woody, R. W., Eds.; VCH Publishers: New York, 1994.
    • (1994) The Exciton Chirality Method in Circular Dichroism, Principles and Applications
    • Nakanishi, K.1    Berova, N.2
  • 20
    • 15444347730 scopus 로고    scopus 로고
    • note
    • 2 are the intensities of the first and the second Cotton effect, respectively.
  • 21
    • 15444352929 scopus 로고    scopus 로고
    • note
    • Occasionally, the presence of a background ellipticity alters the intensity of the Cotton effects at short wavelengths. Thus, the intensities of the second Cotton effect and, therefore, the amplitudes (A value) of the CD spectra of our model compounds may not be precise, the intensities of the first Cotton effect therefore being more accurate for comparative analysis.
  • 24
    • 0001339474 scopus 로고
    • The stereoelectronic exo anomeric effect is the preference for the gauche (sc) conformation about the glycosidic C-OR bond of sugar derivatives. Lemieux, R. U.; Pavia, A. A.; Martin, J. C.; Watanabe, K. A. Can. J. Chem. 1969, 47, 4427.
    • (1969) Can. J. Chem. , vol.47 , pp. 4427
    • Lemieux, R.U.1    Pavia, A.A.2    Martin, J.C.3    Watanabe, K.A.4
  • 26
    • 0001876290 scopus 로고
    • Anomeric and Associated Stereoelectronic Effects. Scope and Controversy
    • Thatcher, G. R. J., Ed.; ACS Symposium Series 539; American Chemical Society: Washington, DC
    • (b) Thatcher, G. R. J. Anomeric and Associated Stereoelectronic Effects. Scope and Controversy. In The Anomeric Effect and Associated Stereoelectronic Effects; Thatcher, G. R. J., Ed.; ACS Symposium Series 539; American Chemical Society: Washington, DC, 1993.
    • (1993) The Anomeric Effect and Associated Stereoelectronic Effects
    • Thatcher, G.R.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.