Literature DB >> 15987191

Synthesis of a soluble ureido-naphthyridine oligomer that self-associates via eight contiguous hydrogen bonds.

Michael F Mayer1, Shoji Nakashima, Steven C Zimmerman.   

Abstract

[structure; see text] An iterative synthetic route to organic-soluble ureido-naphthyridine oligomers has been developed. Use of this protocol allowed synthesis of a short ureido-naphthyridine oligomer, which presents a self-complementary DDAADDAA hydrogen bonding array (D = hydrogen bond donor, A = hydrogen bond acceptor). Strong self-association via eight hydrogen bonds was observed in organic solution.

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Year:  2005        PMID: 15987191     DOI: 10.1021/ol050987f

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Bifacial nucleoside as a surrogate for both T and A in duplex DNA.

Authors:  Dongwon Shin; Yitzhak Tor
Journal:  J Am Chem Soc       Date:  2011-04-15       Impact factor: 15.419

2.  Proton transfer reaction and intermolecular interactions in associates of 2,5-dihydroxy-1,8-naphthyridine.

Authors:  Borys Ośmiałowski
Journal:  J Mol Model       Date:  2011-07-30       Impact factor: 1.810

3.  Synthesis of 1,8-naphthyridines and their application in the development of anionic fluorogenic chemosensors.

Authors:  Celso R Nicoleti; Diogo N Garcia; Luiz E da Silva; Iêda M Begnini; Ricardo A Rebelo; Antonio C Joussef; Vanderlei G Machado
Journal:  J Fluoresc       Date:  2012-03-27       Impact factor: 2.217

  3 in total

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