SYNTHESIS AND REACTIONS OF 3-AMINOTHIAZOLIDINE-2-THION-4-ONE DERIVATIVES. 1. CONVERSION OF 3-AMINOTHIAZOLIDINE-2-THION-4-ONE DERIVATIVES TO SUBSTITUTED MERCAPTO-1,3,4-THIADIAZOLES

DOI: 10.1007/BF00507088

Source and publish data:

Chemistry of Heterocyclic Compounds p. 40 - 42 (1981)

Update date:2022-08-04

Topics:

Authors:

Mikitenko, E. K.

Romanov, N. N.

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

Article abstract of DOI:10.1007/BF00507088

The corresponding carboxymethylthiothiadiazoles are formed by the action of formic acid on 3-aminorhodanine and 3-(3-phenylthioureido)rhodanine, and the action of rhodanineaniline on 3-(3-phenylthioureido)rhodanine leads to 2-anilino-5-carboxymethylthioth

Full text of DOI:10.1007/BF00507088

Products guided by the article

Product name:3-formamido-5-(p-dimethylamino)benzylidenethiazolidine-2-thion-4-one

Cas No:76330-27-3

R&D Labs maybe for 76330-27-3

H&Y International Group Ltd

Contact:+86-571-86491666

Address:SHI XIANG ROAD
Tianjin Tongde Biological Technology Co., Ltd.

Contact:86-22-23309138

Address:Room 402, bulidingE3 Detection certification park, XiQingDistrict, Tianjin City
Chongqing Rong＆Quan Pharmaceutical Technology Co. , Ltd.

Contact:86-023-65268721

Address:No. 7, Manshanhong Village, Pingdingshan, Shapingba District, Chongqing Province, China
ZIBO GREEN TRADE CO., LTD

Contact:0543-3317184

Address:No.1401, Unit 1, Global building, Binzhou city, shandong PRC.
Wuxi Forest Biological Co.,Ltd

Contact:+86-510-81602300

Address:Room 317,Building D, No.159 middle Chengjiang Road,Jiangyin Wuxi city.

Relevant to this article

Studies of ruthenium(II) porphyrins containing tertiary diphosphine ligands, including the crystal structure of (5,10,15,20-tetraphenylporphinato)bis(bis(diphenylphosphino)methane) ruthenium(II)-dichloromethane

Doi:10.1021/ic50219a044
(1981)
Highly efficient KF/Al₂O₃-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds

Doi:10.1016/j.tetlet.2005.03.112
(2005)
Doi:10.1021/jm00324a006
(1966)
Doi:10.1021/ja00394a057
(1981)
A biocatalytic route to enantioenriched, sulfanyl aldol products

Doi:10.1016/j.tet.2004.06.033
(2004)
Purines. XXXVII. Synthesis and reduction of 3,9-dialkyladenine salts deuterated at the 2-position: Their use in the proton nuclear magnetic resonance study of isotopically unmodified species

Doi:10.1248/cpb.38.99
(1990)

Article Doi