THE REACTION OF NITROACETAMIDES WITH THIONATION REAGENTS SYNTHESIS OF MONO- AND DITHIO- OXALIC ACID DIAMIDES

DOI: 10.1016/S0040-4039(00)99198-6

Source and publish data:

Tetrahedron Letters p. 3189 - 3192 (1989)

Update date:2022-09-26

Topics:

Authors:

Harris, Philip A.

Jackson, Arthur

Joule, John A.

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

Article abstract of DOI:10.1016/S0040-4039(00)99198-6

Nitroacetamides, R¹(R²)N.CO.CH₂NO₂, react with phosphorus sulphide (P₄S₁₀) or 2,4-bis(4-methoxyphenyl)-1,2-dithiadiphosphetane-2,4-disulphide, Lawesson's reagent, to give amidethioamides, R¹(R²)N.CO.CS.NH2.

Full text of DOI:10.1016/S0040-4039(00)99198-6

Products guided by the article

Product name:2-Amino-N-(4-chloro-phenyl)-2-thioxo-acetamide

Cas No:125244-76-0

R&D Labs maybe for 125244-76-0

Liaoyang Xinyou Chemical Products Co.,Ltd.

Contact:+86-419-5165433 13604191870

Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Shanghai Hanshare Industry Co.,Ltd.

Contact:86 21 20960688

Address:RM902-903,Building E, Wanda Plaza,No.26,Zhoukang Road, Pudong District, Shanghai, China
Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,China
Quhua Zhongxing Refrigeration Technology Co.,Ltd.

Contact:+86-5708886618

Address:318 Bulding 2, No.866 Quhua Rd.,Kecheng District
Synasia Inc

Contact:17316303296

Address:240 Amboy Ave

Relevant to this article

A New Route to +/-Quadrone

Doi:10.1039/c39890001090
(1989)
Doi:10.1007/BF02531790
(1969)
Syntheses, structure characterisation and X-ray structures of the complexes Ru₃(CO)₁₁L [L = Ph₂P(C₆H ₄Me-p), Ph₂PC₆F₅, P(C ₆H₄Cl-p)₃,

Doi:10.1016/j.poly.2010.06.013
(2010)
Asymmetric total synthesis of rugulactone, an α-pyrone from Cryptocarya rugulosa

Doi:10.1055/s-0029-1218836
(2010)
Scaled-up transition-metal-catalyzed cross-coupling reactions of thioether-substituted N-heterocycles with organozinc reagents

Doi:10.1055/s-0030-1258145
(2010)
A unique approach to the concise synthesis of highly optically active spirooxazolines and the discovery of a more potent oxindole-type phytoalexin analogue

Doi:10.1021/ja106349m
(2010)

Article Doi