One-electron oxidation of N-benzylphenothiazine by nitric acid in the presence of β-cyclodextrin

DOI: 10.1246/cl.1998.449

Source and publish data:

Chemistry Letters p. 449 - 450 (1998)

Update date:2022-08-11

Topics:

Authors:

Zhang, Hai-Ming

Ruan, Xiu-Qin

Guo, Qing-Xiang

Liu, You-Cheng

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

Article abstract of DOI:10.1246/cl.1998.449

Oxidation of N-benzylphenothiazine with nitric acid in aqueous solution was investigated in the presence of β-cyclodextrin by means of UV-vis and ESR spectroscopy. The N-benzylphenothiazine radical cation generated in β-cyclodextrin cavity is much more st

Full text of DOI:10.1246/cl.1998.449

Products guided by the article

Product name:N-benzylphenothiazine radical cation

Cas No:56301-51-0

R&D Labs maybe for 56301-51-0

Geen Chemical Technology Co., Ltd

Contact:86-769-21660847

Address:1408, Yingfeng Commercial Center, Nancheng District
Laizhou City Laiyu Chemical CO.,Ltd

Contact:+86-535-2719337/2719339

Address:Chenggang road zhuyou laizhou City Shangdong China
Shenzhen Feiming Science and Technology Co,. Ltd

Contact:+86-755-85232577

Address:#B2309, Fenglin International Center ,Jixiang Road, Longcheng street, LongGang District, Shenzhen city, Guangdong province, China.
Suzhou Lixin Pharmaceutical Co., Ltd.

Contact:86-512-88169812

Address:21 Tangxi Road, Suzhou New District, Suzhou 215151
Jining tiansheng chemical co.,ltd.

Contact:+86-537-5158722

Address:ROOM 1011, BLOCK B, CUIDU INTERNATIOAL BUSINESS CENTER, JINING CITY, CHINA

Relevant to this article

Organoselenium-Catalyzed Regioselective C?H Pyridination of 1,3-Dienes and Alkenes

Doi:10.1002/anie.201610657
(2017)
Electrochemical Carboxylation of Ketones RCOCH2R' Coupled with CO2 Reduction by ²⁺

Doi:10.1246/cl.1988.2033
(1988)
Transition state for alkyl group hydrogenation on Pt(111)

Doi:10.1021/ja075292j
(2008)
2,5′-disubstituted adenosine derivatives: Evaluation of selectivity and efficacy for the adenosine A₁, A_2A, and A₃ receptor

Doi:10.1021/jm010952v
(2002)
New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 3: 7β-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2- ethoxyiminoacetamido] cephalosporins beari

Doi:10.1016/j.bmc.2004.05.021
(2004)
Two-component supramolecular hydrogel for controlled drug release

Doi:10.1039/d0cc03962d
(2020)

Article Doi