Automated chemical synthesis of long oligoribonucleotides using 2'-O-silylated ribonucleoside 3'-O-phosphoramidites on a controlled-pore glass support: Synthesis of a 43-nucleotide sequence similar to the 3'-half molecule of an Escherichia coli formylmeth

DOI: 10.1021/ja00259a037

Source and publish data:

Journal of the American Chemical Society p. 7845 - 7854 (1987)

Update date:2022-07-30

Topics:

Authors:

Usman Usman

Ogilvie Ogilvie

Jiang Jiang

Cedergren

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

Article abstract of DOI:10.1021/ja00259a037

Full text of DOI:10.1021/ja00259a037

Products guided by the article

Product name:Adenosine, N-benzoyl-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-5'-O-[(4-methoxyphenyl )diphenylmethyl]-, 3'-[methyl bis(1-methylethyl)phosphoramidite]

Cas No:101904-21-6

R&D Labs maybe for 101904-21-6

xujianqiang

Contact:86-21-57725962

Address:shanghai
Hubei Xinjing New Material Co.,Ltd

Contact:+86-27-83313147

Address:Room402.#Bthe 7th,Headquarter of Huifeng Corporation Qiaokou District,Wuhan China
Shanghai birch chemical technology co.,ltd

Contact:+86-21-54096810

Address:No.2588,Jungong Road,Shanghai,China
Changyi Xinxing Technology Development Co., Ltd.

Contact:0086-510-86651065(Time Zone:8),86651656

Address:94 Yingbinxilu WestRoad, Huangtu Town, Jiangyin City, Jiangsu, China
Hebei Kangtai Pharmaceutical Co.,Ltd

Contact:+86-0317-3512963

Address:Wugang Road,Mengcun of Cangzhou City,Hebei Province ,China

Relevant to this article

Synthesis and activity of novel 5-substituted pyrrolo[2,3-d]pyrimidine analogues as pp60c-Src tyrosine kinase inhibitors

Doi:10.1002/ardp.200700141
(2008)
Doi:10.1021/jo01064a032
(1961)
Chemical stability of the peroxide bond enables diversified synthesis of potent tetraoxane antimalarials

Doi:10.1021/jm701417a
(2008)
An unexpected cyclization discovered during the synthesis of 8-substituted purines from a 4,5-diaminopyrimidine

Doi:10.1016/j.tetlet.2008.01.095
(2008)
Redox-Neutral α-Arylation of Alkyl Nitriles with Aryl Sulfoxides: A Rapid Electrophilic Rearrangement

Doi:10.1021/jacs.7b00969
(2017)
Doi:10.1021/jo01091a014
(1959)

Article Doi