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

HANGZHOU PANYU CHEMICAL CO.,LIMITED

Contact:+86-571-86578491

Address:Rm 605, NO.1870 Binsheng Road,Binjiang Dist, Hangzhou, China
Esuccess Material Limited

Contact:852-29282288

Address:HONGKONG
Suzhou Time-chem Technologies Co., Ltd.

Contact:0512-63983931/68086856

Address:No. 1326 of Binhe Road, New District, Suzhou, Jiangsu, P. R. China
Shanghai Bosman Industrial Co., Ltd

Contact:86-21-63065878-8006

Address:Rm907, No.1611, North Sichuan Road, Hongkou District, Shanghai, 200080 China
Shijiazhuang Frontierchem Co., Ltd.

Contact:+86-311-89271196

Address:4-4-202 No.15 Biandian Street,Shijiazhuang

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