Literature DB >> 18429630

A novel polymer supported approach to nucleoside modification.

Suyeal Bae1, Mahesh K Lakshman.   

Abstract

Polymer-supported O(6)-(benzotriazol-1-yl)inosine derivatives (Pol-I and Pol-dI) have been synthesized reasonably effectively via reaction of nucleoside phosphonium salts with polymer-linked HOBt (Pol-HOBt). In constast to solution chemistry, use of polymer-supported BOP (Pol-BOP) did not lead to efficient nucleoside loading. Presence of the nucleosides on the support could be readily detected by MAS NMR. Exposure of the polymer-supported nucleosides, Pol-I and Pol-dI, to alcohol, phenol, thiol and amine nucleophiles caused cleavage from the support leading directly to the C-6 modified nucleoside analogues. To our knowledge, these are the first examples of the application of such technology for nucleoside modification. Where possible, results of reactions with the polymer-supported nucleosides are compared to those from solution chemistry, providing insight into the differences between the two techniques. These new polymer-supported nucleosides can be conveniently utilized for diversity-oriented synthesis.

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Year:  2008        PMID: 18429630     DOI: 10.1021/jo702558n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  17 in total

1.  Azide-tetrazole equilibrium of C-6 azidopurine nucleosides and their ligation reactions with alkynes.

Authors:  Mahesh K Lakshman; Manish K Singh; Damon Parrish; Raghavan Balachandran; Billy W Day
Journal:  J Org Chem       Date:  2010-04-16       Impact factor: 4.354

2.  Two-step, one-pot synthesis of inosine, guanosine, and 2'-deoxyguanosine O6-ethers via intermediate O6-(benzotriazol-1-yl) derivatives.

Authors:  Hari Prasad Kokatla; Mahesh K Lakshman
Journal:  Curr Protoc Nucleic Acid Chem       Date:  2012-06

3.  One-pot etherification of purine nucleosides and pyrimidines.

Authors:  Hari Prasad Kokatla; Mahesh K Lakshman
Journal:  Org Lett       Date:  2010-10-15       Impact factor: 6.005

4.  Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products.

Authors:  Hari K Akula; Hariprasad Kokatla; Graciela Andrei; Robert Snoeck; Dominique Schols; Jan Balzarini; Lijia Yang; Mahesh K Lakshman
Journal:  Org Biomol Chem       Date:  2017-02-01       Impact factor: 3.876

5.  Diarylmethanes through an Unprecedented Palladium-Catalyzed C-C Cross-Coupling of 1-(Aryl)methoxy-1 H-Benzotriazoles with Arylboronic Acids.

Authors:  Manish K Singh; Mahesh K Lakshman
Journal:  ChemCatChem       Date:  2015-11-04       Impact factor: 5.686

6.  Facile Modifications at the C4 Position of Pyrimidine Nucleosides via In Situ Amide Activation with 1H-Benzotriazol-1-yloxy-tris(dimethyl-amino)phosphonium Hexafluorophosphate.

Authors:  Hari K Akula; Mahesh K Lakshman
Journal:  Curr Protoc Nucleic Acid Chem       Date:  2019-01-28

7.  A simple method for C-6 modification of guanine nucleosides.

Authors:  Mahesh K Lakshman; Josh Frank
Journal:  Org Biomol Chem       Date:  2009-06-01       Impact factor: 3.876

8.  Synthesis of N6 ,N6-Dialkyl Adenine Nucleosides With In Situ Formed Hexaalkylphosphorus Triamides.

Authors:  Mahesh K Lakshman; Asad Choudhury; Suyeal Bae; Eliezer Rochttis; Padmanava Pradhan; Amit Kumar
Journal:  European J Org Chem       Date:  2009-01-01

9.  A novel bis(pinacolato)diboron-mediated N-O bond deoxygenative route to C6 benzotriazolyl purine nucleoside derivatives.

Authors:  Vikram Basava; Lijia Yang; Padmanava Pradhan; Mahesh K Lakshman
Journal:  Org Biomol Chem       Date:  2016-07-05       Impact factor: 3.876

10.  DNA interstrand cross-link formation by the 1,4-dioxobutane abasic lesion.

Authors:  Lirui Guan; Marc M Greenberg
Journal:  J Am Chem Soc       Date:  2009-10-28       Impact factor: 15.419

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