Literature DB >> 16639768

A general synthesis of C6-azolyl purine nucleosides.

Pallavi Lagisetty1, Larry M Russon, Mahesh K Lakshman.   

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Year:  2006        PMID： 16639768     DOI： 10.1002/anie.200504565

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  5 in total

1.  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

2.  Palladium-catalyzed synthesis of nucleoside adducts from bay- and fjord-region diol epoxides.

Authors:  Elise Champeil; Padmanava Pradhan; Mahesh K Lakshman
Journal:  J Org Chem       Date:  2007-06-09       Impact factor: 4.354

3.  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

4.  Palladium-Catalyzed Aryl Amination Reactions of 6-Bromo- and 6-Chloropurine Nucleosides.

Authors:  Paul F Thomson; Pallavi Lagisetty; Jan Balzarini; Erik De Clercq; Mahesh K Lakshman
Journal:  Adv Synth Catal       Date:  2010-07-05       Impact factor: 5.837

5.  1,2,3-Triazoles as leaving groups: SNAr reactions of 2,6-bistriazolylpurines with O- and C-nucleophiles.

Authors:  Dace Cīrule; Irina Novosjolova; Ērika Bizdēna; Māris Turks
Journal:  Beilstein J Org Chem       Date:  2021-02-11       Impact factor: 2.883
  5 in total

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