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Volumn , Issue 21, 2009, Pages 3595-3604

Alkoxyallene-based de novo synthesis of rare deoxy sugars: New routes to L-cymarose, L-sarmentose, L-diginose and L-oleandrose

Author keywords

Allenes; Carbohydrates; Deoxy sugars; Furans; Glycosylation; Gold catalysis; Oxygen heterocycles; Total synthesis

Indexed keywords


EID: 67650671014     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200900450     Document Type: Article
Times cited : (31)

References (76)
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    • X. Y. Zhao. M. Ono, H. Akita, Y. M. Chi, Chin. Chem. Lett. 2006, 17, 730-732. Sarmentose (2):
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    • T. Mukaiyama, K. Suzuki, T. Yamada, F. Tabusa, Tetrahedron 1990, 46, 265-276. Oleandrose (4):
    • l) T. Mukaiyama, K. Suzuki, T. Yamada, F. Tabusa, Tetrahedron 1990, 46, 265-276. Oleandrose (4):
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    • For further examples of this oxidative cleavage and for a preliminary communication of part of the work presented here see: M. Brasholz, H.-U. Reißig, Angew. Chem. 2007, 119, 1659-1662;
    • b) For further examples of this oxidative cleavage and for a preliminary communication of part of the work presented here see: M. Brasholz, H.-U. Reißig, Angew. Chem. 2007, 119, 1659-1662;
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    • No side products have been isolated in this reaction
    • No side products have been isolated in this reaction.
  • 62
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    • For an account dealing with the preferred conformation of compounds analogous to arabino-configuvsd lactone 22, please refer to ref. 16d;
    • a) For an account dealing with the preferred conformation of compounds analogous to arabino-configuvsd lactone 22, please refer to ref. 16d;
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    • 4 form. This is in agreement with NMR spectro-scopic data previously reported for related systems: J. S. D. Kumar, F.-Y. Dupradeau, M. J. Strouse, M. E. Phelps, T. Toyokuni, J. Org. Chem., 2001, 66, 3220-3223.
    • 4 form. This is in agreement with NMR spectro-scopic data previously reported for related systems: J. S. D. Kumar, F.-Y. Dupradeau, M. J. Strouse, M. E. Phelps, T. Toyokuni, J. Org. Chem., 2001, 66, 3220-3223.
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    • Assignment of the diastereomers was based on NMR and made according to the literature
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    • Landmann, B.1    Hoffmann, R.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.