Mechanistic Investigations into the Photochemical Oxidation of Thioketones

DOI: 10.1039/c39810000112

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 112 - 114 (1981)

Update date:2022-08-02

Topics:

Authors:

Ramnath, N.

Ramesh, V.

Ramamurthy, V.

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

Article abstract of DOI:10.1039/c39810000112

Singlet-oxygen reaction with dialkyl, aryl alkyl, and diaryl thioketones is found to give the corresponding sulphines and ketones in proportions depending on the nature of the thioketone.

Full text of DOI:10.1039/c39810000112

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:(Z)-1-phenyl-2,2-dimethylpropane-1-thione S-oxide

Cas No:78132-53-3

R&D Labs maybe for 78132-53-3

Shanghai Micro-mega Industry Co., Ltd.

Contact:0086-21-34628682;57153848

Address:Rm413,No.413,West Meilong Road, Minhang District,Shanghai P R China
QINGDAO DEVELOP chemistry Co.,Limited

Contact:+86-532-85807910

Address:98#Nanjing Road, Qingdao, China 266071
Linyi Shengxin Pharmaceutical R&D Co., Ltd

Contact:+86-18653953873

Address:West First of Yufeng Road, Yishui County
Wuxi Innopal International Trade CO.,LTD

Contact:+86-510-80711901-8003

Address:Room 402,Building 5,Longze Garden,No.17,South huanjiu Road,Yixing City, Jiangsu,China
Improve Medical Technology(Nanxiong) Co., Ltd

Contact:86-751-3836997

Address:No.33, Pingan First Road, Fine Chemical Industry Base, Nanxiong City, Shaoguan, Guangdong, China

Relevant to this article

Synthesis of oxytocin, arginine-vasopressin and its deamino-analogue using 2,4,6-trimethylbenzyl group for protection of the cysteine sulfur

Doi:10.1135/cccc19810286
(1981)
Spectroscopic characterization of tetradentate macrocyclic ligand: It's transition metal complexes

Doi:10.1016/j.saa.2004.01.015
(2004)
Synthesis, physicochemical and biochemical studies of 1′,2′- oxetane constrained adenosine and guanosine modified oligonucleotides, and their comparison with those of the corresponding cytidine and thymidine analogues

Doi:10.1021/ja048417i
(2004)
Effect of Substituents in the 5' and 7' Positions on the Spectra of Merocyanines of 1,3,3-Trimethyl-6'-nitroindoline-2-spiro-2'-<2H>-chromenes

Doi:10.1007/BF00503335
(1981)
Reaction of Olivanic Acids with Hypobromous Acid: The Preparation and Use of a Versatile Intermediate, the C-3 Thiol

Doi:10.1039/c39810000803
(1981)
Novel chemical modifications at the 4-position of chromones. Synthesis and reactivity of 4H-chromene-4-spiro-5′-isoxazolines and related compounds

Doi:10.1016/j.tetlet.2004.07.158
(2004)

Article Doi