Fundamental chemistry of iodine. The reaction of di-iodine towards thiourea and its methyl-derivative: formation of aminothiazoles and aminothiadiazoles through dicationic disulfides-Reference-Cited by-同舟云学术

Fundamental chemistry of iodine. The reaction of di-iodine towards thiourea and its methyl-derivative: formation of aminothiazoles and aminothiadiazoles through dicationic disulfides

Published:2014 Issue:12 Volume:43 Page:4790-4806
ISSN:1477-9226
Container-title:Dalton Trans.
language:en
Short-container-title:Dalton Trans.

Author:

Biesiada M.¹²³⁴²,Kourkoumelis N.⁵⁶³⁷,Kubicki M.²⁸⁹,Owczarzak A. M.²⁸⁹,Balas V.¹²³⁴,Hadjikakou S. K.¹²³⁴

Affiliation:

1. Section of Inorganic and Analytical Chemistry

2. Department of Chemistry

3. University of Ioannina

4. , Greece

5. Medical Physics Laboratory

6. Medical School

7. Greece

8. A. Mickiewicz University

9. 61-614 Poznań, Poland

Abstract

The reactivity of di-iodine towards thiourea (TU) and its derivative methylthiourea (MeTU) is studied. A diversity of products was obtained from these reactions.

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/DT/C3DT53302F

Reference87 articles.

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4. Synthesis, Spectroscopic and Structural Characterization of Novel Diiodine Adducts with the Heterocyclic Thioamides, Thiazolidine-2-thione (tzdtH), Benzothiazole-2-thione (bztzdtH) and Benzimidazole-2-thione (bzimtH)

5. Synthesis and Characterization of (PTU)I 2 (PTU = 6‐ n ‐propyl‐2‐thiouracil) and (CMBZT)I 2 (CMBZT = 5‐chloro‐2‐mercaptobenzothiazole) and Possible Implications for the Mechanism of Action of Anti‐Thyroid Drugs

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