Model studies for damage to nucleic acids mediated by thiyl radicals

DOI: 10.1016/S0040-4020(01)88306-X

Source and publish data:

Tetrahedron p. 5543 - 5556 (1992)

Update date:2022-08-04

Topics:

Authors:

Griffiths

Murphy Murphy

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

Article abstract of DOI:10.1016/S0040-4020(01)88306-X

The ability of phenylthiovinyl radicals to abstract hydrogen from appropriately substituted carbon atoms has been studied as a model for the reactions of the deoxyribose units of DNA with similar radicals in two.

Full text of DOI:10.1016/S0040-4020(01)88306-X

Products guided by the article

Product name:Benzene, [1-[(2-methoxyethoxy)methyl]-2-(phenylthio)ethenyl]-, (Z)-

Cas No:144252-31-3

R&D Labs maybe for 144252-31-3

SPRING CHEMICAL INDUSTRY CO.,LTD

Contact:86-187-66672125

Address:linchi industry park.zouping
Laohekou Jinghong Chemical Co.,Ltd

Contact:+86-0710-3702747

Address:163.East，Huagong Road，Laohekou
Chengdu Cogon Bio-tech Co., Ltd.

Contact:86-28-85171192

Address:NO.52.YongFeng Rd. Chengdu,610041,P.R.China.
ANGCHEN BRIGHTCHEM CO., LTD

website:http://www.angchenchem.com

Contact:+86-510-88302099 82327577

Address:Rm. 404/405, Floor 4th, No. 983 FengXiang Road, Wuxi, China
Shantou Baokang Pharmaceutical Co., Ltd.

Contact:+86-754-88873487

Address:5/F B Block Huangshan Bldg Huangshan Rd Shantou

Relevant to this article

Pd-catalyzed asymmetric allylic alkylation of pyrazol-5-ones with allylic alcohols: The role of the chiral phosphoric acid in C-O bond cleavage and stereocontrol

Doi:10.1021/ja402740q
(2013)
Metal-free decarboxylative three-component coupling reaction for the synthesis of propargylamines

Doi:10.1021/ol401358t
(2013)
FeCl₃-mediated cyclization of [60]fullerene with N-benzhydryl sulfonamides under high-speed vibration milling conditions

Doi:10.1021/ol4014602
(2013)
Dimerization of Substituted 1,3-Diarylallenes

Doi:10.1021/jo00052a063
(1992)
Synthesis of N-(5-amino-2-pyrimidyl)-N′-[4-(p-fluorophenyl)-4-oxobutyl]piperazine, a useful intermediate to antipsychotic agents

Doi:10.1080/00304949909355731
(1999)
Highly Enantioselective Allylation of Ketones: An Efficient Approach to All Stereoisomers of Tertiary Homoallylic Alcohols

Doi:10.1002/chem.201701740
(2017)

Article Doi