Synthesis of α- and β-D-carbaribofuranose from (+)-norborn-5-en-2-one
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Synthetic ventures in pseudo-sugar chemistry
2. Syntheses of (1S,2S,3S,4R)- and (1R,2R,3S,4R)-2,3,4-trihydroxycyclopentane-1-methanol, carbocyclic analogs of .alpha.-L-arabinofuranose and .beta.-D-ribofuranose
3. Transformation of D-erythrose to some pseudoaldopentofuranoses. Syntheses of (1S,2R,3S,4S)-, (1R,2R,3S,4S)-, and (1R,2S,3S,4S)-2,3,4-trihydroxy-1-(hydroxymethyl)cyclopentanes and (1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)-1-cyclopentanamine
4. New approaches to enzyme regulators. Synthesis and enzymological activity of carbocyclic analogs of D-fructofuranose and D-fructofuranose-6-phosphate
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2. Highly Substituted Cyclopentane–CMP Conjugates as Potent Sialyltransferase Inhibitors;Journal of Medicinal Chemistry;2015-10-07
3. ChemInform Abstract: Synthesis of α- and β-D-Carbaribofuranose from (+)-Norborn- 5-en-2-one.;ChemInform;2010-08-23
4. Synthesis and Conformational and Biological Aspects of Carbasugars;Chemical Reviews;2007-05-01
5. A Convenient Approach for Access to Both Carbapentofuranoses and Carbahexopyranoses. Stereocontrolled Synthesis of Enantiopure Carba-d-ribofuranoses, Carba-d-arabinofuranoses and Carba-l-gulopyranose;The Journal of Organic Chemistry;2006-11-29
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