Synthesis of 1,3,4-Thiadiazoles: Review

Abstract Molecules with 1,3,4-thiadiazole ring structures have potential biological relevance. These organic molecules have potentially reported for their medicinal importance. In this review, different strategies for the synthesis of biologically important molecules of 1,3,4-thiadiazole ring are briefly summarized and an attempt has been made with recent research findings on this nucleus, to review the structural modifications on different thiadiazole derivatives. Its covers advances made in the last two decades and a brief account of various alterations done on the thiadiazoles nucleus. Keywords: 1,3,4-Thiadiazole, isomers, isosterism, thiosemicarbazides, 1,2,5-thiadiazole, thiophene, thiazole.

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Journal
INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT
Published
2025-05-27
DOI
https://doi.org/10.55041/ijsrem48848
Primary Topic
Synthesis and biological activity
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article
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article

Synthesis of 1,3,4-Thiadiazoles: Review

Ram Dulare
INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT
Synthesis and biological activity
article

Synthesis of 1,3,4-Thiadiazoles: Review

Ram Dulare
article en

Abstract

Abstract Molecules with 1,3,4-thiadiazole ring structures have potential biological relevance. These organic molecules have potentially reported for their medicinal importance. In this review, different strategies for the synthesis of biologically important molecules of 1,3,4-thiadiazole ring are briefly summarized and an attempt has been made with recent research findings on this nucleus, to review the structural modifications on different thiadiazole derivatives. Its covers advances made in the last two decades and a brief account of various alterations done on the thiadiazoles nucleus. Keywords: 1,3,4-Thiadiazole, isomers, isosterism, thiosemicarbazides, 1,2,5-thiadiazole, thiophene, thiazole.

INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENTVol. 09(05)
Post Graduate Medical Institute (PK)
Openalex Percentile: Top 91%
Synthesis and biological activity
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