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Volumn 66, Issue 15, 2010, Pages 2830-2834

Synthesis of eight-membered iminocyclitols from d-glucose

Author keywords

Baylis Hillman reaction; Conjugate addition; Diastereoselectivity; Iminosugars

Indexed keywords

3 O BENZYL 6 DEOXY (N BENZYLAMINOMETHYL) 1,2 O ISOPROPYLIDENE ALPHA DEXTRO GLUCO 1,4 HEPTOFURANOATE; 3 O BENZYL ALPHA DEXTRO XYLOPENTODIALDO 1,4 FURANOSE; ALCOHOL DERIVATIVE; ALPHA METHYLENE BETA HYDROXY ESTER DERIVATIVE; AZOCANE 7 (HYDROXYMETHYL) 2,3,4,5,6 PENTANOL; BENZYL DERIVATIVE; BENZYLAMINE; CYCLITOL; ESTER DERIVATIVE; ETHYL 3 O BENZYL 6 DEOXY (N BENZYLAMINOMETHYL) 1,2 O ISOPROPYLIDENE ALPHA LEVO IDO 1,4 HEPTOFURANOATE; FURAN DERIVATIVE; GLUCOSE; IMINOSUGAR; UNCLASSIFIED DRUG;

EID: 77949262323     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.02.044     Document Type: Article
Times cited : (7)

References (24)
  • 19
    • 77949276043 scopus 로고    scopus 로고
    • 4,5=5.9 Hz) was assigned the d-gluco-configuration see:
    • 4,5=5.9 Hz) was assigned the d-gluco-configuration see:
  • 22
    • 77949269243 scopus 로고    scopus 로고
    • note
    • The minor isomer was all the time contaminated with the major compound.
  • 23
    • 77949269241 scopus 로고    scopus 로고
    • note
    • The crystallographic data have been deposited with the Cambridge Crystallographic Data Centre as deposition no. CCDC-761145 (4a). Copies of the data can be obtained, free of charge, on application to the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44 1223 336033; e-mail: deposit@ccdc.cam.ac.uk].
  • 24
    • 77949272993 scopus 로고
    • Application of nuclear magnetic resonance spectroscopy in organic chemistry
    • 1H NMR analogy of six-membered chair conformation system wherein; equatorial proton is deshielded as compared to the axial proton and the axial-axial proton coupling is larger than the axial-equatorial or equatorial-equatorial., University of California, Pergamon pp 238-248 and 280-300
    • 1H NMR analogy of six-membered chair conformation system wherein; equatorial proton is deshielded as compared to the axial proton and the axial-axial proton coupling is larger than the axial-equatorial or equatorial-equatorial. Jackman L.M., and Sternehell S. Application of nuclear magnetic resonance spectroscopy in organic chemistry. International Series in Organic Chemistry. 2nd ed. Vol. 10 (1969), University of California, Pergamon pp 238-248 and 280-300
    • (1969) International Series in Organic Chemistry. 2nd ed. , vol.10
    • Jackman, L.M.1    Sternehell, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.