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From α,β-Epoxyaldehydes to Peptidonucleosides and Iminosugars

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摘要 1 Introduction The primary objectives of the group“Natural products and bioactive molecules”,are the development of synthetic methods,their application in the elaboration of natural compounds and analogues and the translation of this know-how through an integrated approach to the identification of attractive leads in order to confront some of the major diseases in the developed and developing countries.
出处 《复旦学报(自然科学版)》 CAS CSCD 北大核心 2005年第5期648-649,共2页 Journal of Fudan University:Natural Science
基金 We are grateful to the CNRS and the“Université Paul Sabatier”for finan cial support and the“Ministére de la Recherche et des Technologies”for grants(M.C.,T.A.,V.F.).
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  • 1Collet M, Baltas M, Martinez A, et al. Addition of lithium ethyl fluoroaeetate to cis and trans alpha-beta epoxyaldehydes. Access to C2 fluorinated butyrolactones[ J ]. Tetrahedron Letters,2003,44 : 1891-1894.
  • 2Ayad T, Faugeroux V, C-enisson Y, et al. Stereoselective access to the versatile 4-aminohex-5-ene-1,2,3-triol pattern[J ]. J Org Chem, 2004,69 : 8775-8779.
  • 3Marotte K, Ayad T, Genisson Y, et al. Synthesis and biological evaluation of imino-oligoarabinofuranoside hybrids, a new class of mycobacterial arabinofuranosyltransferase inhibitors[J]. Eur J Org Chem, 2003,14:2557-2565.
  • 4Dehoux C, Fontaine E, Escudier J M, et al. Total Synthesis of a Thymidine 2-deoxypolyoxin C analogue[ J ]. J Org Ckem, 1998,63:2601-2608.

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