New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.

The recent advances in the chemistry of carbocyclic nucleosides focused on different synthetic approaches that lead to optically pure products as well as a comprehensive overview of their biological properties are discussed. In the latter aspect, molecular recognition of enzymes of pharmacological i...

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Autores principales: Rodríguez, J.B., Comin, M.J.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_13895575_v3_n2_p95_Rodriguez
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spelling todo:paper_13895575_v3_n2_p95_Rodriguez2023-10-03T16:12:45Z New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides. Rodríguez, J.B. Comin, M.J. 2',3' dideoxynucleoside derivative alkanone anti human immunodeficiency virus agent antineoplastic agent carbovir cyclohexane derivative cyclopentane derivative cyclopropane derivative glyceraldehyde glycoside nucleoside chemistry conformation cyclization human review stereoisomerism synthesis Anti-HIV Agents Antineoplastic Agents Butanones Cyclization Cyclohexanes Cyclopentanes Cyclopropanes Dideoxynucleosides Glyceraldehyde Glycosides Humans Molecular Conformation Nucleosides Stereoisomerism The recent advances in the chemistry of carbocyclic nucleosides focused on different synthetic approaches that lead to optically pure products as well as a comprehensive overview of their biological properties are discussed. In the latter aspect, molecular recognition of enzymes of pharmacological importance such as: reverse transcriptase, adenosine deaminase, thymidine kinase, DNA cytosine-C5 methyl transferase, S-adenosylhomocysteine hydrolase, etc are considered. The role of conformation and puckering of the glycon moiety in modulating the biological activity and also the use of carbanucleosides as building blocks to prepare oligonucleotides are carefully illustrated. Fil:Rodríguez, J.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Comin, M.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_13895575_v3_n2_p95_Rodriguez
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 2',3' dideoxynucleoside derivative
alkanone
anti human immunodeficiency virus agent
antineoplastic agent
carbovir
cyclohexane derivative
cyclopentane derivative
cyclopropane derivative
glyceraldehyde
glycoside
nucleoside
chemistry
conformation
cyclization
human
review
stereoisomerism
synthesis
Anti-HIV Agents
Antineoplastic Agents
Butanones
Cyclization
Cyclohexanes
Cyclopentanes
Cyclopropanes
Dideoxynucleosides
Glyceraldehyde
Glycosides
Humans
Molecular Conformation
Nucleosides
Stereoisomerism
spellingShingle 2',3' dideoxynucleoside derivative
alkanone
anti human immunodeficiency virus agent
antineoplastic agent
carbovir
cyclohexane derivative
cyclopentane derivative
cyclopropane derivative
glyceraldehyde
glycoside
nucleoside
chemistry
conformation
cyclization
human
review
stereoisomerism
synthesis
Anti-HIV Agents
Antineoplastic Agents
Butanones
Cyclization
Cyclohexanes
Cyclopentanes
Cyclopropanes
Dideoxynucleosides
Glyceraldehyde
Glycosides
Humans
Molecular Conformation
Nucleosides
Stereoisomerism
Rodríguez, J.B.
Comin, M.J.
New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
topic_facet 2',3' dideoxynucleoside derivative
alkanone
anti human immunodeficiency virus agent
antineoplastic agent
carbovir
cyclohexane derivative
cyclopentane derivative
cyclopropane derivative
glyceraldehyde
glycoside
nucleoside
chemistry
conformation
cyclization
human
review
stereoisomerism
synthesis
Anti-HIV Agents
Antineoplastic Agents
Butanones
Cyclization
Cyclohexanes
Cyclopentanes
Cyclopropanes
Dideoxynucleosides
Glyceraldehyde
Glycosides
Humans
Molecular Conformation
Nucleosides
Stereoisomerism
description The recent advances in the chemistry of carbocyclic nucleosides focused on different synthetic approaches that lead to optically pure products as well as a comprehensive overview of their biological properties are discussed. In the latter aspect, molecular recognition of enzymes of pharmacological importance such as: reverse transcriptase, adenosine deaminase, thymidine kinase, DNA cytosine-C5 methyl transferase, S-adenosylhomocysteine hydrolase, etc are considered. The role of conformation and puckering of the glycon moiety in modulating the biological activity and also the use of carbanucleosides as building blocks to prepare oligonucleotides are carefully illustrated.
format JOUR
author Rodríguez, J.B.
Comin, M.J.
author_facet Rodríguez, J.B.
Comin, M.J.
author_sort Rodríguez, J.B.
title New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
title_short New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
title_full New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
title_fullStr New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
title_full_unstemmed New progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
title_sort new progresses in the enantioselective synthesis and biological properties of carbocyclic nucleosides.
url http://hdl.handle.net/20.500.12110/paper_13895575_v3_n2_p95_Rodriguez
work_keys_str_mv AT rodriguezjb newprogressesintheenantioselectivesynthesisandbiologicalpropertiesofcarbocyclicnucleosides
AT cominmj newprogressesintheenantioselectivesynthesisandbiologicalpropertiesofcarbocyclicnucleosides
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