Isolation of unique heterocycles formed from pyridine-thiocarboxamides as diiodine, iodide, or polyiodide salts-Reference-Cited by-同舟云学术

Isolation of unique heterocycles formed from pyridine-thiocarboxamides as diiodine, iodide, or polyiodide salts

Published:2022 Issue:35 Volume:24 Page:6251-6261
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Peloquin Andrew J.¹^ORCID,McMillen Colin D.¹^ORCID,Pennington William T.¹^ORCID

Affiliation:

1. Department of Chemistry, Clemson University, 219 Hunter Laboratories, Clemson, SC 29634-0973, USA

Abstract

The reaction of pyridine-thiocarboxamides with I2 provided a variety of novel heterocyclic products as iodide, triiodide, and/or pentaiodide salts. Bismuth triiodide was incorporated as a crystallization aid to access other structural types.

Funder

Air Force Institute of Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CE/D2CE00904H

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1. New and efficient approach for synthesis of novel bioactive [1,3,4]thiadiazoles incorporated with 1,3-thiazole moiety

2. Synthesis and anticancer activity of 5-(3-indolyl)-1,3,4-thiadiazoles

3. Synthesis and Anticancer Evaluation of 1,3,4-Oxadiazoles, 1,3,4-Thiadiazoles, 1,2,4-Triazoles and Mannich Bases

4. Synthesis of novel sulfonamide-1,2,4-triazoles, 1,3,4-thiadiazoles and 1,3,4-oxadiazoles, as potential antibacterial and antifungal agents. Biological evaluation and conformational analysis studies

5. Synthesis of Novel 2,5-Disubstituted-1,3,4-thiadiazoles Clubbed 1,2,4-Triazole, 1,3,4-Thiadiazole, 1,3,4-Oxadiazole and/or Schiff Base as Potential Antimicrobial and Antiproliferative Agents

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