Organic Disulfides and Related Substances. 43. Properties of a Mercaptoalkyl Sulfoxide, a Novel Class of Structure

DOI: 10.1021/jo00326a034

Source and publish data:

Journal of Organic Chemistry p. 2771 - 2775 (1981)

Update date:2022-08-05

Topics: Synthesis Properties Reaction Conditions HPLC Analysis Spectroscopic Analysis

Authors:

Field, Lamar

Bowman, Gary T.

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

Article abstract of DOI:10.1021/jo00326a034

3-Mercaptopropyl phenyl sulfoxide (4) was prepared by reaction of 3-chloropropyl phenyl sulfoxide (2) with sodium trithiocarbonate (3).The mercaptopropyl sulfoxide 4 could be obtained only in a maximum purity of 93percent (and yield of 75percent) because

Full text of DOI:10.1021/jo00326a034

Products guided by the article

Product name:3-Mercaptopropyl Phenyl Sulfoxide

Cas No:77400-50-1

R&D Labs maybe for 77400-50-1

Hangzhou GreenCo Science & Technology Co., Ltd.

Contact:86-571-88257303

Address:1713 Room,Jingui Building,Gudun Road,Xihu District,Hangzhou,China
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang
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.
Changsha Easchem Co.,Limited

website:http://www.easchem.com

Contact:+86-731-89722861 89722891

Address:2/F-4/Bld Colorful Palace, No.605 Changsha Ave, Yuhua Area Changsha Hunan China.
Jinan Jinguilin Chemical Co.,Ltd

Contact:+86-531-81188412

Address:3rd floor of Torch Building, Huanyuan Rd, City of Jinan

Relevant to this article

STRUCTURAL STUDIES ON PALYTOXIN, A POTENT COELENTERATE TOXIN

Doi:10.1016/0040-4039(80)80159-6
(1980)
Elimination-addition mechanism for nucleophilic substitution reaction of cyclohexenyl iodonium salts and regioselectivity of nucleophilic addition to the cyclohexyne intermediate

Doi:10.1021/ja0496672
(2004)
A novel trifunctional organocatalyst for the asymmetric aldol reaction: A facile enantioselective synthesis of β-hydroxyketones

Doi:10.1016/j.tetasy.2011.05.001
(2011)
Palladium-Catalyzed Reductive Coupling of Acid Chlorides with β-Stannyl Enones: Synthesis of 1,4-Diketones and Mechanistic Aspects

Doi:10.1021/jo00094a032
(1994)
Ring-Strain Effects in Base-Induced Sommelet–Hauser Rearrangement: Application to Successive Stereocontrolled Transformations

Doi:10.1002/ejoc.201600611
(2016)
A rapid synthesis of p-nitrophenyl 2-O-α-L-fucopyranosyl-β-D-galactopyranoside

Doi:10.1016/S0008-6215(00)85626-8
(1981)

Article Doi