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Volumn 20, Issue 6-8, 2009, Pages 773-780

Stereoselective synthesis of α-glucosides by neighbouring group participation via an intermediate thiophenium ion

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSIDE; THIOPHENE DERIVATIVE; THIOPHENIUM ION; TRICHLOROACETIMIDIC ACID; UNCLASSIFIED DRUG;

EID: 65549115350     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.02.018     Document Type: Article
Times cited : (52)

References (53)
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    • Angew. Chem. 86 (1974) 173-187
    • (1974) Angew. Chem. , vol.86 , pp. 173-187
  • 9
    • 0342936076 scopus 로고    scopus 로고
    • For a review of intramolecular glycosylation see:
    • For a review of intramolecular glycosylation see:. Jung K.-H., Müller M., and Schmidt R.R. Chem. Rev. 100 (2000) 4423-4442
    • (2000) Chem. Rev. , vol.100 , pp. 4423-4442
    • Jung, K.-H.1    Müller, M.2    Schmidt, R.R.3
  • 17
    • 0027437186 scopus 로고
    • Bols M. Tetrahedron 44 (1993) 10049-10060
    • (1993) Tetrahedron , vol.44 , pp. 10049-10060
    • Bols, M.1
  • 28
    • 0001325832 scopus 로고
    • Angew. Chem. 106 (1994) 1843-1845
    • (1994) Angew. Chem. , vol.106 , pp. 1843-1845
  • 40
    • 27744505650 scopus 로고    scopus 로고
    • Esters are not the only protecting groups that participate during glycosylation reactions. For example see:
    • Esters are not the only protecting groups that participate during glycosylation reactions. For example see:. Smoot J.T., Pornsuriyasak P., and Demchenko A.V. Angew. Chem., Int. Ed. 44 (2005) 7123-7126
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 7123-7126
    • Smoot, J.T.1    Pornsuriyasak, P.2    Demchenko, A.V.3
  • 45
    • 65549171744 scopus 로고    scopus 로고
    • note
    • 2SPh moiety, and an 8:1 α:β selectivity was observed. See Ref. 17b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.