Literature DB >> 15043159

Nucleosides. IX. Synthesis of purine N(3),5'-cyclonucleosides and N(3),5'-cyclo-2',3'-seconucleosides via Mitsunobu reaction as TIBO-like derivatives.

Grace Shiahuy Chen1, Chien-Shu Chen, Tun-Cheng Chien, Jun-Yen Yeh, Chia-Chi Kuo, Rahul Subhash Talekar, Ji-Wang Chern.   

Abstract

The Mitsunobu reaction was applied to prepare, in one step, purine N(3),5'-cyclonucleosides 10a-d. A subsequent ring opening in the ribose moiety of the resultant N(3),5'-nucleosides by sodium periodate led to the corresponding N(3),5'-cyclo-2',3'-seconucleosides. These products consist of 5-, 6-, and 7-membered tricyclic system which is the basic skeleton of TIBO derivatives, known antiviral agents.

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Year:  2004        PMID: 15043159     DOI: 10.1081/ncn-120027904

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  2 in total

Review 1.  Marine Alkylpurines: A Promising Group of Bioactive Marine Natural Products.

Authors:  Pablo A García; Elena Valles; David Díez; María-Ángeles Castro
Journal:  Mar Drugs       Date:  2018-01-01       Impact factor: 5.118

2.  Further investigation of the Mediterranean sponge Axinella polypoides: isolation of a new cyclonucleoside and a new betaine.

Authors:  Marialuisa Menna; Anna Aiello; Filomena D'Aniello; Ernesto Fattorusso; Concetta Imperatore; Paolo Luciano; Rocco Vitalone
Journal:  Mar Drugs       Date:  2012-11-09       Impact factor: 5.118

  2 in total

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