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

Antaeus Bio-technology Co., LTD(expird)

Contact:021-31252569

Address:shanghai pudong
Hangzhou Haichem Co.,Ltd.

Contact:+86-571-86025531 / 86024803

Address:1218-24 Guangyin Mansion,42 Fengqi East Road
Hangzhou yi lu biont technology Co., LTD

Contact:+86-571-88152630

Address:Hangzhoushi HuafengRoad Yicheng3Building1001room.
Antimex Chemical Limied

website:http://www.antimex.com

Contact:0086-21-50563169

Address:Room1027,No.Jinyu Road,Pudong
Puyang Huicheng Electronic Material Co., Ltd

website:http://huichengchem.weba.testwebsite.cn/index_en.html

Contact:+86-393-8910800

Address:West Section Shengli Road, Puyang457000, China

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