Oligo-α-deoxyribonucleotides with a modified nucleic base and covalently linked to reactive agents

DOI: 10.1016/S0040-4020(01)87973-4

Source and publish data:

Tetrahedron p. 6975 - 6990 (1993)

Update date:2022-08-04

Topics:

Authors:

Kurfuerst, Robin

Roig, Victoria

Chassignol, Marcel

Asseline, Ulysse

Thuong, Nguyen T.

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

Article abstract of DOI:10.1016/S0040-4020(01)87973-4

Solid-phase preparation of oligo-α-deoxyribonucleotides attached to intercalator, chemically or photochemically reactive groups through either their 5′- or 3′-ends, including use of the 5-methyl-α-deoxycytidine.

Full text of DOI:10.1016/S0040-4020(01)87973-4

Products guided by the article

Product name:5'-O-dimethoxytrityl-3'-O-(tert-butyldimethylsilyl)-α-thymidine

Cas No:152581-54-9

R&D Labs maybe for 152581-54-9

Daqing E-shine Chemical Co.,LTD

Contact:0086-024-31285112

Address:Hongweiyuan area, Ranghulu district
Wuhan Konberd Biotech Co., Ltd.

Contact:+86-27-87205925

Address:NO.666, Gaoxin Road, Eastlake High-tech zone
Feiyang Biotechnology Co., Ltd.

Contact:+86-533-7866339

Address:Qilu Chemistry Park, 200m north of Management Community Building of Park
Engineering Research Center of Pesticide, Heilongjiang Province

Contact:+86-451-86609001

Address:No.74 of Xuefu Road, Nangang District,
Taizhou KEDE Chemical.Co.,Ltd.

Contact:86-576-84613060

Address:Jiangkou Chemical Zoon

Relevant to this article

Discovery of potent, reversible MetAP2 inhibitors via fragment based drug discovery and structure based drug design - Part 2

Doi:10.1016/j.bmcl.2016.04.072
(2016)
Efficient and benign one-pot conversion of n-tosyl-1,4,5,6- tetrahydropyrimidines to pyrimidines via tandem β-elimination and aromatization

Doi:10.1080/00397911.2013.764433
(2013)
Microbial enantioselective ester hydrolysis for the preparation of optically active 4,1-benzoxazepine-3-acetic acid derivatives as squalene synthase inhibitors

Doi:10.1248/cpb.50.59
(2002)
Asymmetric syn-Dihydroxylation of β-Substituted (2R)-N-(α,β-Enoyl)bornane-10,2-sultams

Doi:10.1002/hlca.19980810537
(1998)
Synthesis of anthranilic acid derivatives through iron-catalyzed ortho amination of aromatic carboxamides with N-chloroamines

Doi:10.1021/ja412521k
(2014)
Design and synthesis of novel N-acetylgalactosamine-terminated glycolipids for targeting of lipoproteins to the hepatic asialoglycoprotein receptor

Doi:10.1021/jm049481d
(2004)

Article Doi