Oxidation of Primary Amines by Dimethyldioxirane

DOI: 10.1021/jo00285a027

Source and publish data:

Journal of Organic Chemistry p. 5783 - 5788 (1989)

Update date:2022-08-10

Topics:

Authors:

Murray, Robert W.

Rajadhyaksha, Shirish N.

Mohan, Lily

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

Article abstract of DOI:10.1021/jo00285a027

Dimethyldioxirane oxidizes primary amines rapidly, and generally in high yield, to the corresponding nitro compounds.The method can also be used to syntesize polynitro compounds.

Full text of DOI:10.1021/jo00285a027

Products guided by the article

Product name:4-Chloronitrobenzene

Cas No:100-00-5

R&D Labs maybe for 100-00-5

Changsha Goomoo Chemical Technology Co.Ltd

Contact:+86-731-82197655

Address:No.649,Chezhan Rd.(N),Changsha,Hunan,China
WUXI HONOR SHINE CHEMICAL CO.,LTD

Contact:+86-510-83593312

Address:No.1699 Huishan avenue,Huishan district,Wuxi ,Jiangsu,China,214177.(Wuxi Huishan Ecomonic Develop Zone )
Allicon Pharmaceuticals,Inc.

Contact:+86-519-86339586，13584329896

Address:Changzhou Scientific and Education Park
Tianjin Jiuri New Materials Co., Ltd.

Contact:+86-22-58889220

Address:C-5/6, Vison Hill, No.1 Gonghua Road, Huayuan Hi-tech Park, Tianjin, China.
Xi’an Gaoyuan Bio-Chem Co.,Ltd.

Contact:+86-29-65692259

Address:R11702, Block B, Greenland Soho, 1st Zhangba Rd, Xi'an Hi-tech Zone, Xi'an, Shaanxi, China. 710065

Relevant to this article

Acrylates via Metathesis of Crotonates

Doi:10.1021/op5003006
(2015)
Ring-Opening Copolymerization of Maleic Anhydride with Functional Epoxides: Poly(propylene fumarate) Analogues Capable of Post-Polymerization Modification

Doi:10.1002/anie.201807419
(2018)
Enhanced yields of furfural and other products by simultaneous solvent extraction during thermochemical treatment of cellulosic biomass

Doi:10.1039/c3ra41857j
(2013)
A highly effective and practical biaryl synthesis with triallyl(aryl) silanes and aryl chlorides

Doi:10.1246/cl.2004.632
(2004)
Less symmetrical dicopper(II) complexes as catechol oxidase models - An adjacent thioether group increases catecholase activity

Doi:10.1002/chem.200400768
(2005)
Stereoselective Yang cyclizations of α-amido ketones

Doi:10.1039/a901723b
(1999)

Article Doi