A remarkable stabilization of complexes formed by 2,6-diaminopurine oligonucleotide N3′→P5′ phosphoramidates

DOI: 10.1080/15257770008045446

Source and publish data:

Nucleosides, nucleotides and nucleic acids p. 1553 - 1567 (2000)

Update date:2022-08-03

Topics:

Authors:

Matray Matray

Gamsey Gamsey

Pongracz

Gryaznov

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1080/15257770008045446

2′-Deoxyribo- and ribo-oligonucleotide N3′→P5′phosphoramidates containing 2,6-diaminopurine nucleosides were synthesized. Thermal denaturation experiments demonstrated a significant stabilization of the complexes formed by these compounds with DNA and RNA

Full text of DOI:10.1080/15257770008045446

Nucleosides, Nucleotides and Nucleic Acids

ISSN: 1525-7770 (Print) 1532-2335 (Online) Journal homepage: http://www.tandfonline.com/loi/lncn20

A Remarkable Stabilization of Complexes Formed

by 2,6-Diaminopurine Oligonucleotide N3′→P5′

Phosphoramidates

Tracy Matray , Soya Gamsey , Krisztina Pongracz & Sergei Gryaznov

To cite this article: Tracy Matray , Soya Gamsey , Krisztina Pongracz & Sergei Gryaznov (2000) A

Remarkable Stabilization of Complexes Formed by 2,6-Diaminopurine Oligonucleotide N3′→P5′

Phosphoramidates, Nucleosides, Nucleotides and Nucleic Acids, 19:10-12, 1553-1567, DOI:

10.1080/15257770008045446

To link to this article: http://dx.doi.org/10.1080/15257770008045446

Published online: 17 Apr 2008.

Submit your article to this journal

Article views: 32

View related articles

Citing articles: 6 View citing articles

Full Terms & Conditions of access and use can be found at

http://www.tandfonline.com/action/journalInformation?journalCode=lncn20

Download by: [University of Tasmania]

Date: 30 September 2015, At: 07:19

Products guided by the article

Product name:4-Methyl-benzoic acid (2S,3R,4R,5R)-4-acetoxy-3-azido-5-[2,6-bis-(2-phenoxy-acetylamino)-purin-9-yl]-tetrahydro-furan-2-ylmethyl ester

Cas No:256485-51-5

R&D Labs maybe for 256485-51-5

Qingdao Pana-Life Biochem Co.,Ltd.

Contact:86-532-87683902

Address:No.967 Dalao Road, Licang Zone, Qingdao City,Shandong, China 266021
Changsha Yonta Industry Co., Ltd.

Contact:+ 86-731-8535 2228

Address:Rm.1717, North Bldg., No.368, East 2nd Ring Road(2nd Section)
Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
Shanghai Kangxin Chemical Co., Ltd

Contact:+86 21 60717227

Address:118,Ganbai Village,Waigang Town,Jiading District,Shanghai
Shandong Yubin Chemical CO.,LTD

website:http://www.yukaichem.com/en.html

Contact:+86-536-8865336

Address:binhai economic development zone，262737 shangdong，china

Relevant to this article

Inductive Charge Dispersal in the Solvolyses of 4- and 5-Substituted 2-Norbonyl p-Toluenesulfonates

Doi:10.1002/hlca.19860690834
(1986)
A selective small molecule NOP (ORL-1 receptor) partial agonist for the treatment of anxiety

Doi:10.1016/j.bmcl.2014.12.015
(2015)
Synthesis of Readily Modifiable Cyclodextrin Analogues via Cyclodimerization of an Alkynyl-Azido Trisaccharide

Doi:10.1021/ja039374t
(2004)
Generation of (E)-Silylketene acetals in a Rhodium-DuPhos catalyzed two-step reductive aldol reaction

Doi:10.1021/ol016279l
(2001)
Doi:10.1016/S0040-4039(01)94511-3
(1978)
Total synthesis of thienamycin analogs. II. Synthesis of 2-alkyl and 2-aryl thienamycin nuclei

Doi:10.1016/S0040-4039(00)71473-0
(1980)

Article Doi