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2000 (1)
1Author    Z. NaturforschRequires cookie*
 Title    An Expeditious Approach to Trisubstituted Chiral Tetrahydrofurans  
 Abstract    F azila Iq b a l3, M o h a m m e d Saleh S h e k h a n i3*, A b d u l M a lik 3 *, M a so o d P a rv e z b, U z m a R ia z 3, Z u lfiq a r A li3, an d K halid M o h a m m e d K h a n 3 Ozonolysis of 3,6-anhydro-4-0-(/?-toluenesulphonyl)-D-glucal (9), obtained in four steps from D-glucose, provided the target compound 11. The structure and configurations of 9 and 11 have been determined by spectral studies and X-ray crystallography. Similar strategy with D-galactose provided the corresponding derivatives 10 and 12, respectively. 
  Reference    Z. Naturforsch. 55b, 317—320 (2000); received September 20 1999 
  Published    2000 
  Keywords    Chiral Tetrahydrofurans, Asymmetric Synthesis, D-Glucose, D-Galactose 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0317.pdf 
 Identifier    ZNB-2000-55b-0317 
 Volume    55