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Volumn 5, Issue 24, 2003, Pages 4545-4548

Glycosidation with a Disarmed Glycosyl Iodide: Promotion and Scope

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; GLUCURONIDE; GLUCURONYL IODIDE; GLYCOSYL IODIDE; IODINE DERIVATIVE; MESYLIC ACID DERIVATIVE; METAL; PHENETHYL ALCOHOL; SUCCINIMIDE DERIVATIVE; TRIMETHYLSILYL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0347411088     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol035475k     Document Type: Article
Times cited : (23)

References (25)
  • 1
    • 0040657616 scopus 로고
    • For example: Paulsen, H. Angew. Chem., Int. Ed. Engl. 1982, 21, 155-173. Boons, G. J. Tetrahedron 1996, 52, 1095-1121. Davis, B. G. J. Chem. Soc., Perkin Trans. 1 2000, 2137-2160.
    • (1982) Angew. Chem., Int. Ed. Engl. , vol.21 , pp. 155-173
    • Paulsen, H.1
  • 2
    • 0030058793 scopus 로고    scopus 로고
    • For example: Paulsen, H. Angew. Chem., Int. Ed. Engl. 1982, 21, 155-173. Boons, G. J. Tetrahedron 1996, 52, 1095-1121. Davis, B. G. J. Chem. Soc., Perkin Trans. 1 2000, 2137-2160.
    • (1996) Tetrahedron , vol.52 , pp. 1095-1121
    • Boons, G.J.1
  • 3
    • 0034698451 scopus 로고    scopus 로고
    • For example: Paulsen, H. Angew. Chem., Int. Ed. Engl. 1982, 21, 155-173. Boons, G. J. Tetrahedron 1996, 52, 1095-1121. Davis, B. G. J. Chem. Soc., Perkin Trans. 1 2000, 2137-2160.
    • (2000) J. Chem. Soc., Perkin Trans. 1 , pp. 2137-2160
    • Davis, B.G.1
  • 5
    • 0000623379 scopus 로고    scopus 로고
    • Glycosyl iodides in organic synthesis
    • JAI Press, Inc.
    • (a) Gervay, J. Glycosyl Iodides in Organic Synthesis. In Organic Synthesis: Theory and Applications; JAI Press, Inc.: 1998; Vol. 4, pp 121-153.
    • (1998) Organic Synthesis: Theory and Applications , vol.4 , pp. 121-153
    • Gervay, J.1
  • 13
    • 0347778765 scopus 로고    scopus 로고
    • note
    • Spherical 3 Å molecular sieves of 1/16 in. diameter were used, activated by drying at 130 °C.
  • 14
    • 0346518287 scopus 로고    scopus 로고
    • note
    • 3) 4.29 (1 H, approximately t, 2-H) and 5.91 (1 H, d, J = 4.8 Hz, 1-H).
  • 18
    • 0345887414 scopus 로고    scopus 로고
    • note
    • 3), inter alia, 4.40 (d, J = 9.9 Hz, 5-H), 4.78 (dd, J = 9.8 and 3.9 Hz, 2-H), and 5.57 (t, J = 9.8 Hz).
  • 24
    • 0345887413 scopus 로고    scopus 로고
    • note
    • A referee suggested that the α-anomers may be formed by rearrangement from the ortho ester stage.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.