AbstractAcyclic nucleosides and their phosphonates possess significantly antiviral and cytostatic activities. For acyclic nucleosides and their phosphonates, the introduction of a chiral group to their side chain or the absolute configuration of the chiral atom could affect their biological activities obviously. Thus, the asymmetric synthesis of chiral acyclic nucleosides and their phosphonates has received continuous attention. The previous reports mainly focus on employing the chiral pool and chiral auxiliary methods for the synthesis of chiral acyclic nucleosides and their phosphonates. In contrast, the asymmetric catalysis methods for the synthesis of acyclic nucleosides and their phosphonates are still in the beginning. This digest pap...
The present review is focused on the description of synthesis and antiviral activities of both acyc...
The synthesis of novel nucleotide analogues on the basis of ethylphosphonic acid was described. A ri...
An efficient method to construct chiral acyclic nucleosides via Sharpless asymmetric dihydroxylation...
AbstractAcyclic nucleosides and their phosphonates possess significantly antiviral and cytostatic ac...
A synthetic approach to phosphonate derivatives of 2,5-cis-substituted dihydro-2H-pyranyl nucleoside...
First part of this thesis was focused on the previously overlooked field of C1'-branched acyclic nuc...
Charles University, Faculty of Science Department of Organic and Nuclear Chemistry Synthesis and Pro...
The current review is devoted to the achievements in the development of methods for the catalytic as...
Chiral vinyl phosphonates, homomorphous with natural nucleotides, have been prepared starting from (...
Chiral vinyl phosphonates, homomorphous with natural nucleotides, have been prepared starting from (...
Chiral vinyl phosphonates, homomorphous with natural nucleotides, have been prepared starting from (...
A diastereoselective synthesis of cycloSal-phosphotriesters (cycloSal=cycloSaligenyl) based on chira...
The area of carbocyclic nucleosides has developed after the isolation of (-)-aristeromycin (1) and ...
An efficient route to construct chiral acyclic purine nucleosides containing a hemiaminal ester moie...
The present review is focused on the description of synthesis and antiviral activities of both acyc...
The present review is focused on the description of synthesis and antiviral activities of both acyc...
The synthesis of novel nucleotide analogues on the basis of ethylphosphonic acid was described. A ri...
An efficient method to construct chiral acyclic nucleosides via Sharpless asymmetric dihydroxylation...
AbstractAcyclic nucleosides and their phosphonates possess significantly antiviral and cytostatic ac...
A synthetic approach to phosphonate derivatives of 2,5-cis-substituted dihydro-2H-pyranyl nucleoside...
First part of this thesis was focused on the previously overlooked field of C1'-branched acyclic nuc...
Charles University, Faculty of Science Department of Organic and Nuclear Chemistry Synthesis and Pro...
The current review is devoted to the achievements in the development of methods for the catalytic as...
Chiral vinyl phosphonates, homomorphous with natural nucleotides, have been prepared starting from (...
Chiral vinyl phosphonates, homomorphous with natural nucleotides, have been prepared starting from (...
Chiral vinyl phosphonates, homomorphous with natural nucleotides, have been prepared starting from (...
A diastereoselective synthesis of cycloSal-phosphotriesters (cycloSal=cycloSaligenyl) based on chira...
The area of carbocyclic nucleosides has developed after the isolation of (-)-aristeromycin (1) and ...
An efficient route to construct chiral acyclic purine nucleosides containing a hemiaminal ester moie...
The present review is focused on the description of synthesis and antiviral activities of both acyc...
The present review is focused on the description of synthesis and antiviral activities of both acyc...
The synthesis of novel nucleotide analogues on the basis of ethylphosphonic acid was described. A ri...
An efficient method to construct chiral acyclic nucleosides via Sharpless asymmetric dihydroxylation...