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Volumn , Issue 15, 2007, Pages 2470-2476

Stereoselective synthesis of 2-deoxyglycosides from sulfanyl alkenes by consecutive "one pot" cyclization and glycosylation reactions

Author keywords

Carbohydrates; Cyclization; Glycosides; Glycosylation; Oligosaccharides

Indexed keywords


EID: 34250665130     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200601115     Document Type: Article
Times cited : (15)

References (36)
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    • H. P. Albrecht, Cardiac Glycosides in Naturally Occurring Glycosides, R. Ikan, Wiley, Chichester, 1999;
    • b) H. P. Albrecht, Cardiac Glycosides in Naturally Occurring Glycosides, R. Ikan, Wiley, Chichester, 1999;
  • 12
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    • For glycosylation methods that involve the use of 2-iododeoxy glycosyl donors, see: a
    • For glycosylation methods that involve the use of 2-iododeoxy glycosyl donors, see: a) T. B. Durham, W. R. Roush, Org. Lett. 2003, 5, 1871-1874;
    • (2003) Org. Lett , vol.5 , pp. 1871-1874
    • Durham, T.B.1    Roush, W.R.2
  • 21
    • 2142850939 scopus 로고
    • For a procedure of synthesis of glycosides involving a mercury-induced cyclization of enol ethers, see
    • For a procedure of synthesis of glycosides involving a mercury-induced cyclization of enol ethers, see: F. Paquet, P. Sinaÿ, Tetrahedron Lett. 1984, 25, 3071-3074.
    • (1984) Tetrahedron Lett , vol.25 , pp. 3071-3074
    • Paquet, F.1    Sinaÿ, P.2
  • 22
    • 33644751581 scopus 로고    scopus 로고
    • The 2-deoxy-2-iodo-1-thiopyranosides are useful starting materials for preparing glycals of all configurations; O. Boutureira, M. A. Rodríguez, M. I. Matheu, Y Díaz, S. Castillón, Org. Lett. 2006, 8, 673-675.
    • The 2-deoxy-2-iodo-1-thiopyranosides are useful starting materials for preparing glycals of all configurations; O. Boutureira, M. A. Rodríguez, M. I. Matheu, Y Díaz, S. Castillón, Org. Lett. 2006, 8, 673-675.
  • 26
    • 2542475310 scopus 로고    scopus 로고
    • For a review about glycosylation of steroids, see
    • For a review about glycosylation of steroids, see: H. Pellisier, Tetrahedron 2004, 60, 5123-5162.
    • (2004) Tetrahedron , vol.60 , pp. 5123-5162
    • Pellisier, H.1
  • 27
    • 34250627139 scopus 로고    scopus 로고
    • For a discussion on the different reactivities of the Z and E alkenyl sulfides towards cyclization, see ref.[3
    • [3]
  • 28
    • 0035067443 scopus 로고    scopus 로고
    • For reviews about synthesis of 2-deoxyglycosides, see: a
    • For reviews about synthesis of 2-deoxyglycosides, see: a) A. Kirschning, M. Jesberger, K.-U. Schöning, Synthesis 2001, 507-540;
    • (2001) Synthesis , pp. 507-540
    • Kirschning, A.1    Jesberger, M.2    Schöning, K.-U.3
  • 29
    • 0000562875 scopus 로고    scopus 로고
    • Eds, B. Ernst, G. W. Hart, P. Sinaÿ, Wiley-VCH, Weinheim
    • b) A. Veyrières, in Carbohydrates in Chemistry and Biology (Eds.: B. Ernst, G. W. Hart, P. Sinaÿ), Wiley-VCH, Weinheim, 2000, part I, vol. I, p. 367;
    • (2000) Carbohydrates in Chemistry and Biology , vol.1 , Issue.PART I , pp. 367
    • Veyrières, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.