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Volumn 50, Issue 31, 2009, Pages 4427-4429

Synthesis of a constrained polyfunctional bicyclic iminocyclitol scaffold from l-sorbose via a tandem sequence including stereoselective intramolecular Huisgen cycloaddition

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND; AMINO ACID; AZIDE; AZIRIDINE; CYCLITOL; OCTANE; SORBOSE;

EID: 66949120720     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.060     Document Type: Article
Times cited : (9)

References (44)
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    • (2007) Iminosugars , pp. 295-326
    • Cox, T.M.1    Platt, F.M.2    Aerts, J.M.F.G.3
  • 15
    • 35548985408 scopus 로고    scopus 로고
    • For reviews on intramolecular 1,3-dipolar cycloaddition in targeted synthesis, see:
    • For reviews on intramolecular 1,3-dipolar cycloaddition in targeted synthesis, see:. Nair V., and Suja T.D. Tetrahedron 63 (2007) 12247-12275
    • (2007) Tetrahedron , vol.63 , pp. 12247-12275
    • Nair, V.1    Suja, T.D.2
  • 16
    • 66949127641 scopus 로고
    • Padwa A. (Ed), Wiley-Interscience, New York
    • Padwa A. In: Padwa A. (Ed). 1,3-Dipolar Cycloaddition Chemistry. Vol. 2 (1984), Wiley-Interscience, New York 316
    • (1984) Vol. 2 , pp. 316
    • Padwa, A.1
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    • For a review on applications of organic azides including alkene-azide cycloadditions, see:
    • For a review on applications of organic azides including alkene-azide cycloadditions, see:. Bräse S., Gil C., Knepper K., and Zimmermann V. Angew. Chem., Int. Ed. 44 (2005) 5188-5240
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 5188-5240
    • Bräse, S.1    Gil, C.2    Knepper, K.3    Zimmermann, V.4
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    • 0033593268 scopus 로고    scopus 로고
    • Herein is described a tandem azide substitution-cycloaddition reaction. For examples of tandem alkene formation-cycloaddition sequences using sugar derivatives, see:
    • Herein is described a tandem azide substitution-cycloaddition reaction. For examples of tandem alkene formation-cycloaddition sequences using sugar derivatives, see:. Herdeis C., and Schiffer T. Tetrahedron 55 (1999) 1043-1056
    • (1999) Tetrahedron , vol.55 , pp. 1043-1056
    • Herdeis, C.1    Schiffer, T.2
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    • Morpholine based scaffolds have recently been of interest, see:
    • Morpholine based scaffolds have recently been of interest, see:. Sladojevich F., Trabocchi A., and Guarna A. Org. Biomol. Chem. 6 (2008) 3328-3336
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 3328-3336
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  • 38
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    • The generation of polyfunctional scaffolds from a monosaccharide is a means of further increasing the diversity of scaffolds, see:
    • The generation of polyfunctional scaffolds from a monosaccharide is a means of further increasing the diversity of scaffolds, see:. Holt D.J., Barker W.D., Jenkins P.R., Panda J., and Ghosh S. J. Org. Chem. 65 (2000) 482-493
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.