Literature DB >> 19099417

Syntheses of heterocyclic ethenyl C-nucleosides for recognition of inverted base pairs within the DNA triple helix by stereoselective intramolecular cyclization and olefin metathesis.

Jeffrey H Rothman1.   

Abstract

Canonical recognition of gene sequences would allow precise means for specific genetic intervention. Unfortunately, specific recognition of two of the four possible base pairs by triplex-forming oligonucleotide (TFO) as X x T-A and Y x C-G within a triplex currently remains elusive. A series of C1-ethenyl nucleosides have been devised and evaluated extensively for stability and specificity by molecular dynamics simulation. A synthesis via olefin metathesis of the unprotected heterocycle and a conveniently prepared anomerically pure C1-vinyl 2-deoxyribofuranose is presented as a significant improvement over a previously reported strategy.

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Year:  2009        PMID: 19099417     DOI: 10.1021/jo801910u

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


  2 in total

1.  Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes.

Authors:  Ivan Šnajdr; Kamil Parkan; Filip Hessler; Martin Kotora
Journal:  Beilstein J Org Chem       Date:  2015-08-10       Impact factor: 2.883

2.  Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes.

Authors:  Sajal Kumar Maity; Tuomas A Lönnberg
Journal:  ACS Omega       Date:  2019-11-01
  2 in total

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