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'3 Dipolar Cycloadditions' in keywords Facet   section ZfN Section B  [X]
Facet   Publication Year 1997  [X]
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1Author    Z. Ah Id, M. Aq, L+-, M. Ashooda, H. Asan, KevinT. Pott, M. Alik++, C., T. Anveer, A., N. Izam Ic, W. OlfgangRequires cookie*
 Title    Syntheses of Anomeric Pairs of New C-Nucleosides via 1,3-Dipolar Cycloaddition Reaction, Part I  
 Abstract    A convenient pathway to a variety of ß-and a-C-nucleosides has been developed by utiliz­ ing 1,3-dipolar cycloaddition reactions of various exocyclic and endocyclic heterocyclic ylides with ß (5a) and a (5b) anomers of ethyl 3-(2',3'-0-isopropylidene-5'-0-trityl-D-ribofurano-syl) propiolate, respectively. Assignment of configuration at exposition of the C-nucleosides could be made by a comparative study of the properties of corresponding a and ß anomers with a reasonable degree of certainity. 
  Reference    Z. Naturforsch. 52b, 1383—1392 (1997); received July 21 1997 
  Published    1997 
  Keywords    C-Nucleosides, 1, 3-Dipolar Cycloadditions 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-1383.pdf 
 Identifier    ZNB-1997-52b-1383 
 Volume    52