Unknown

Dataset Information

0

Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues.


ABSTRACT: The racemic synthesis of new carbocyclic nucleoside methylphosphonate analogues bearing purine bases (adenine and guanine) was accomplished using bio-sourced furfuryl alcohol derivatives. All compounds were prepared using a Mitsunobu coupling between the heterocyclic base and an appropriate carbocyclic precursor. After deprotection, the compounds were evaluated for their activity against a large number of viruses. However, none of them showed significant antiviral activity or cytotoxicity.

SUBMITTER: Sidi Mohamed B 

PROVIDER: S-EPMC5331271 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

altmetric image

Publications

Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues.

Sidi Mohamed Bemba B   Périgaud Christian C   Mathé Christophe C  

Beilstein journal of organic chemistry 20170209


The racemic synthesis of new carbocyclic nucleoside methylphosphonate analogues bearing purine bases (adenine and guanine) was accomplished using bio-sourced furfuryl alcohol derivatives. All compounds were prepared using a Mitsunobu coupling between the heterocyclic base and an appropriate carbocyclic precursor. After deprotection, the compounds were evaluated for their activity against a large number of viruses. However, none of them showed significant antiviral activity or cytotoxicity. ...[more]

Similar Datasets

| S-EPMC7756257 | biostudies-literature
| S-EPMC4077357 | biostudies-literature
| S-EPMC7994825 | biostudies-literature
| S-EPMC2721324 | biostudies-literature
| S-EPMC6767184 | biostudies-literature
| S-EPMC7582934 | biostudies-literature
| S-EPMC6630956 | biostudies-literature
| S-EPMC1186092 | biostudies-other
| S-EPMC6278576 | biostudies-literature