2'-O-propargyl oligoribonucleotides: Synthesis and hybridisation

DOI: 10.1016/S0040-4020(98)00271-3

Source and publish data:

Tetrahedron p. 5899 - 5914 (1998)

Update date:2022-07-30

Topics:

Authors:

Grotli, Morten

Douglas, Mark

Eritja, Ramon

Sproat, Brian S.

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

Article abstract of DOI:10.1016/S0040-4020(98)00271-3

Fully modified oligonucleotide sequences containing 2'-O- propargylribonucleotides were synthesised on automated DNA-synthesisers using the phosphoramidite approach. A highly selective alkylation procedure was used to introduce the propargyl functionality

Full text of DOI:10.1016/S0040-4020(98)00271-3

Products guided by the article

Product name:6-(2,6-Dichloro-phenoxy)-9-((2R,3R,3aR,9aR)-5,5,7,7-tetraisopropyl-3-prop-2-ynyloxy-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-9H-purine

Cas No:210096-42-7

R&D Labs maybe for 210096-42-7

Refine Chemicals Science & Technology Technology Developing Co., Ltd.

Contact:+86-22-87899130

Address:No.12,west keyan road,Tianjin City
Allicon Pharmaceuticals,Inc.

Contact:+86-519-86339586，13584329896

Address:Changzhou Scientific and Education Park
Okeanos Tech.Co.,LTD

Contact:+86-10-62651721

Address:29 Yongxing Road, Daxing District,Beijing China
Anhui Gusheng Import&Export CO.,LTD

Contact:86-551-63662296

Address:Jinzhai Road NO.162 ,hefei, china
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park

Relevant to this article

The first and convenient synthesis of acyclic dienediynes related to neocarzinostatin chromophore

Doi:10.1016/S0040-4039(98)00693-5
(1998)
Identification of a dihydropyridine as a potent α(1a) adrenoceptor- selective antagonist that inhibits phenylephrine-induced contraction of the human prostate

Doi:10.1021/jm980077m
(1998)
Metal-mediated generation, stabilization, and controlled release of a biologically relevant, simple para quinone methide: BHT-QM [10]

Doi:10.1021/ja9809612
(1998)
Sulfoxides as stereochemical controllers in intermolecular Heck reactions

Doi:10.1002/1521-3765(20010917)7:18<3890::AID-CHEM3890>3.0.CO;2-Y
(2001)
Preparation of modified glycosyl glycerol derivatives by glycal rearrangement

Doi:10.1016/S0008-6215(98)00038-X
(1998)
Ansa macrolides as molecular workbenches: Stereocontrolled syn additions to E olefins

Doi:10.1002/(SICI)1521-3773(19980619)37:11<1566::AID-ANIE1566>3.0.CO;2-U
(1998)

Article Doi