Recent Publications on Carbasugars: |  |
| Biomimetic organocatalytic C-C-bond formations.
| 15th August, 2008
| Institute of Organic Chemistry, RWTH Aachen University, Aachen, Germany.
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D-glucosamine trimethylene dithioacetal derivatives: formation of six- and seven-membered ring amino carbasugars. Synthesis of (-)-calystegine B3.
By virtue of carefully chosen protecting groups, d-glucosamine...
Direct Link | 21st December, 2007
| Organisch-Chemisches Institut, Westfalische Wilhelms-Universitat Munster,
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gem-Difluoro-carbasugars, the cases of mannopyranose and galactopyranose.
5a-Difluoro-5a-carbamannopyranose (gem-difluoro-carbamannopyranose) and...
Direct Link | 28th September, 2007
| Universite Pierre et Marie Curie-Paris 6, Institut de Chimie Moleculaire
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Synthesis and conformational and biological aspects of carbasugars.
5a-Difluoro-5a-carbamannopyranose (gem-difluoro-carbamannopyranose) and...
Direct Link | 19th August, 2007
| Departamento de Quimica Organica, Facultad de Quimica, Universidad
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A convenient approach for access to both carbapentofuranoses and carbahexopyranoses. Stereocontrolled synthesis of enantiopure carba-D-ribofuranoses, carba-D-arabinofuranoses and carba-L-gulopyranose.
A new approach to carbasugars in enantiomerically pure form is reported....
Direct Link | 27th February, 2007
| Department of Organic Chemistry, Indian Association for the Cultivation of
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Chemoenzymatic synthesis of carbasugars from iodobenzene.
The versatile enantiopure cis-dihydrodiol metabolite 1, formed by...
Direct Link | 18th July, 2006
| Centre for Theory and Application of Catalysis, School of Chemistry, The
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Ring fission of chiral cyclic acetals plus intramolecular [4 + 2] cycloaddition: a sequential access to medium-size lactones. Application to the synthesis of carbasugars.
A set of alpha,beta-unsaturated cyclic acetals were reacted with...
Direct Link | 11th July, 2006
| Laboratoire des Fonctions Azotees & Oxygenees Complexes, IRCOF, UMR 6014
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| Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides.
| 16th December, 2005
| WonJun Choi Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha
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Synthesis of novel apio carbocyclic nucleoside analogues as selective a(3) adenosine receptor agonists.
On the basis of the biological activity of neplanocin A and...
Direct Link | 21st July, 2005
| Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans
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| Recent advances in the synthesis of the carbocyclic nucleosides as potential antiviral agents.
| 30th March, 2005
| Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans
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Sensible improvements induced by ionic liquids in the reaction of modified carbasugars with bases for the building of constrained carbanucleosides.
Starting from racemic 4-hydroxy-4-methyl-2-cyclopentenone, a family of...
Direct Link | 29th September, 2004
| Dipartimento Farmaco-Chimico-Tecnologico, Universita degli Studi di Siena,
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Variable strategy toward carbasugars and relatives. 6. Diastereoselective synthesis of 2-deoxy-2-amino-5a-carba-beta-L-mannopyranuronic acid and 2-deoxy-2-amino-5a-carba-beta-L-mannopyranose.
Efficient, total syntheses of novel...
Direct Link | 5th May, 2004
| Istituto di Chimica Biomolecolare del CNR, Sezione di Sassari, Traversa La
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(S,S)-2,3-Dihydroxy-2,3-dihydrobenzoic acid: microbial access with engineered cells of Escherichia coli and application as starting material in natural-product synthesis.
Cyclohexadiene-trans-5,6-diols such as...
Direct Link | 19th February, 2004
| Institut fur Biotechnologie 2, Forschungszentrum Julich GmbH 52425 Julich,
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