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Volumn 46, Issue 20, 2005, Pages 3521-3524

High throughput screening of O-glycosylation conditions

Author keywords

1H NMR; Deuterium labeled compound; MALDI TOF MS; Rapid and quantitative screening; Stereoselective glycosylation

Indexed keywords

ETHER DERIVATIVE;

EID: 17844391804     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.03.066     Document Type: Article
Times cited : (24)

References (25)
  • 10
    • 0242585395 scopus 로고    scopus 로고
    • Recent methods for quantitative analysis using deuterium-labeled amino acid T. Nakanishi, K. Iguchi, and A. Shimizu Clin. Chem. 49 2003 829 831
    • (2003) Clin. Chem. , vol.49 , pp. 829-831
    • Nakanishi, T.1    Iguchi, K.2    Shimizu, A.3
  • 12
    • 0038103867 scopus 로고    scopus 로고
    • Recent review for the synthesis of 1,2-cis glycoside, see A.V. Demchenko Synlett 2003 1225 1240
    • (2003) Synlett , pp. 1225-1240
    • Demchenko, A.V.1
  • 15
    • 85030796290 scopus 로고    scopus 로고
    • note
    • 8 following the procedure in Ref. 6
  • 17
    • 85030796441 scopus 로고    scopus 로고
    • note
    • 6, 400 MHz) δ 0.90-1.95 (10H, m, cyclohexyl × 2), 3.10-3.20 (1H, m, Glc1C5H), 3.19-3.27 (1H, m, Glc2C5H), 3.27 (1H, s, MeO), 3.68-3.74 (4H, m, Glc1C6H, Glc2C2H, Glc2C3H, Glc2C6H), 3.78-3.85 (3H, m, Glc1C42H, Glc1C6H, Glc2C4H), 3.89 (1H, t, J = 8.0 Hz, Glc1C2H), 3.94 (1H, dd, J = 9.2, 5.2 Hz, Glc2C6H), 4.17 (1H, t, J = 8.8 Hz, Glc1C3H), 4.91 (1H, d, J = 7.6 Hz, Glc1C1H), 5.26 (1H, d, J = 7.2 Hz, Glc2C1H), 6.69 (2H, d, J = 9.2 Hz, MPM), 7.00 (2H, d, J = 9.2 Hz, MPM)
  • 18
    • 85030799240 scopus 로고    scopus 로고
    • note
    • We checked the ionization ratio of labeled to non-labeled compound by comparing the apex values (mV) of the MALDI-TOF MS peaks; for (3H-α)/(3D-α), y = 1.04×; for (3H-α)/(3D-β), y = 0.967×
  • 19
    • 85030795149 scopus 로고    scopus 로고
    • note
    • +


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.