The carbocyclic compound (4R,5R)-(-)-3-[(benzyloxy)methyl]-4,5-O- isopropylidene-2-cyclopentenone 1 is an important synthetic intermediate to access a variety of carbanucleosides. Herein, synthetic studies that lead to this valuable compound employing inexpensive d-ribose as the chiral source are presented.Fil: Elhalem, Eleonora. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Orgánica; ArgentinaFil: Comin, Maria Julieta. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Orgánica; ArgentinaFil: Leitofuter, Juli...
The area of carbocyclic nucleosides (carbanucleosides) has developed after the isolation of (-)-ari...
The natural nucleoside antibiotic, bredinin, exhibits antiviral and other biological activities. Whi...
The area of carbocyclic nucleosides has developed after the isolation of (-)-aristeromycin (1) and ...
Carbocyclic nucleosides (carbanucleosides) are mimetics of natural nucleosides and have been the sub...
The recent advances in the chemistry of carbocyclic nucleosides focused on different synthetic appro...
The key intermediate 1,2:5,6-di-O-isopropylidene-3-deoxy-3 beta-allyl-alpha-D-glucofuranose (8) coul...
A regio- and stereo-specific synthesis of cis-(±)-3-acetoxy-5- (acetoxymethyl)cyclopentene 3 from cy...
A regio- and stereo-specific synthesis of cis-(±)-3-acetoxy-5- (acetoxymethyl)cyclopentene 3 from cy...
A novel and stereoselective synthetic route towards carba-C-nucleosides was investigated applying an...
Removal of silyl protection from D-glucose derived substrate 6 afforded 7, which upon acetonide dep...
Removal of silyl protection from D-glucose derived substrate 6 afforded 7, which upon acetonide depr...
Copyright © 2018, Georg Thieme Verlag. All rights reserved. We describe a short and stereospecific s...
A practical and convenient methodology for the synthesis of chiral cyclopentenol derivative (+)-12a ...
A convergent and stereoselective synthesis of chiral cyclopentyl- and cyclohexylamine derivatives of...
The synthesis of prototype models of purine and pyrimidine carbanucleosides built on a 6-thiabicyclo...
The area of carbocyclic nucleosides (carbanucleosides) has developed after the isolation of (-)-ari...
The natural nucleoside antibiotic, bredinin, exhibits antiviral and other biological activities. Whi...
The area of carbocyclic nucleosides has developed after the isolation of (-)-aristeromycin (1) and ...
Carbocyclic nucleosides (carbanucleosides) are mimetics of natural nucleosides and have been the sub...
The recent advances in the chemistry of carbocyclic nucleosides focused on different synthetic appro...
The key intermediate 1,2:5,6-di-O-isopropylidene-3-deoxy-3 beta-allyl-alpha-D-glucofuranose (8) coul...
A regio- and stereo-specific synthesis of cis-(±)-3-acetoxy-5- (acetoxymethyl)cyclopentene 3 from cy...
A regio- and stereo-specific synthesis of cis-(±)-3-acetoxy-5- (acetoxymethyl)cyclopentene 3 from cy...
A novel and stereoselective synthetic route towards carba-C-nucleosides was investigated applying an...
Removal of silyl protection from D-glucose derived substrate 6 afforded 7, which upon acetonide dep...
Removal of silyl protection from D-glucose derived substrate 6 afforded 7, which upon acetonide depr...
Copyright © 2018, Georg Thieme Verlag. All rights reserved. We describe a short and stereospecific s...
A practical and convenient methodology for the synthesis of chiral cyclopentenol derivative (+)-12a ...
A convergent and stereoselective synthesis of chiral cyclopentyl- and cyclohexylamine derivatives of...
The synthesis of prototype models of purine and pyrimidine carbanucleosides built on a 6-thiabicyclo...
The area of carbocyclic nucleosides (carbanucleosides) has developed after the isolation of (-)-ari...
The natural nucleoside antibiotic, bredinin, exhibits antiviral and other biological activities. Whi...
The area of carbocyclic nucleosides has developed after the isolation of (-)-aristeromycin (1) and ...