Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review

Nowadays, organic chemists are interested in the field of heterocyclic chemistry due to its use in the synthesis of a great variety of biologically active compounds. Heterocyclic compounds are widely found in nature and are essential for life. Among these, some natural nitrogen containing heterocycl...

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Autores principales: Efrén V. García-Báez, Itzia I. Padilla-Martínez, Feliciano Tamay-Cach, Alejandro Cruz
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:addaac14af8641b387c7ea8a332c21f12021-11-11T18:30:39ZBenzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review10.3390/molecules262165181420-3049https://doaj.org/article/addaac14af8641b387c7ea8a332c21f12021-10-01T00:00:00Zhttps://www.mdpi.com/1420-3049/26/21/6518https://doaj.org/toc/1420-3049Nowadays, organic chemists are interested in the field of heterocyclic chemistry due to its use in the synthesis of a great variety of biologically active compounds. Heterocyclic compounds are widely found in nature and are essential for life. Among these, some natural nitrogen containing heterocyclic compounds have been used as chemotherapeutic agents. Their attachment to sugar molecules either as thioglycosides or as nucleosides analogues plays an important role in vital biological processes as well as in synthetic organic chemistry. Molecules containing benzothiazole (BT) nuclei are of this interesting class of compounds because some of them have been found to have a wide variety of biological activities. In this sense, we selected this topic to review and to then summarize the procedures related to the condensation reactions of <i>o</i>-aminothiophenoles (ATPs) as well as their disulfides with carboxylic acids, esters, orthoesters, acyl chlorides, amides, and nitriles. The condensation reactions with carbon dioxide (CO<sub>2</sub>) are included. Conventional methods with the use of acid and metal catalysts as well as recent green techniques, such as microwave irradiation, the use of ionic liquids, and ultrasound (US) chemistry, which have proven to have many advantages, were found in the review.Efrén V. García-BáezItzia I. Padilla-MartínezFeliciano Tamay-CachAlejandro CruzMDPI AGarticle<i>o</i>-aminothiophenolcarboxylic acid and derivatives2-substitutedbenzothiazolesacid catalysismicrowave assistedcondensation reactionOrganic chemistryQD241-441ENMolecules, Vol 26, Iss 6518, p 6518 (2021)
institution DOAJ
collection DOAJ
language EN
topic <i>o</i>-aminothiophenol
carboxylic acid and derivatives
2-substitutedbenzothiazoles
acid catalysis
microwave assisted
condensation reaction
Organic chemistry
QD241-441
spellingShingle <i>o</i>-aminothiophenol
carboxylic acid and derivatives
2-substitutedbenzothiazoles
acid catalysis
microwave assisted
condensation reaction
Organic chemistry
QD241-441
Efrén V. García-Báez
Itzia I. Padilla-Martínez
Feliciano Tamay-Cach
Alejandro Cruz
Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
description Nowadays, organic chemists are interested in the field of heterocyclic chemistry due to its use in the synthesis of a great variety of biologically active compounds. Heterocyclic compounds are widely found in nature and are essential for life. Among these, some natural nitrogen containing heterocyclic compounds have been used as chemotherapeutic agents. Their attachment to sugar molecules either as thioglycosides or as nucleosides analogues plays an important role in vital biological processes as well as in synthetic organic chemistry. Molecules containing benzothiazole (BT) nuclei are of this interesting class of compounds because some of them have been found to have a wide variety of biological activities. In this sense, we selected this topic to review and to then summarize the procedures related to the condensation reactions of <i>o</i>-aminothiophenoles (ATPs) as well as their disulfides with carboxylic acids, esters, orthoesters, acyl chlorides, amides, and nitriles. The condensation reactions with carbon dioxide (CO<sub>2</sub>) are included. Conventional methods with the use of acid and metal catalysts as well as recent green techniques, such as microwave irradiation, the use of ionic liquids, and ultrasound (US) chemistry, which have proven to have many advantages, were found in the review.
format article
author Efrén V. García-Báez
Itzia I. Padilla-Martínez
Feliciano Tamay-Cach
Alejandro Cruz
author_facet Efrén V. García-Báez
Itzia I. Padilla-Martínez
Feliciano Tamay-Cach
Alejandro Cruz
author_sort Efrén V. García-Báez
title Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
title_short Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
title_full Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
title_fullStr Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
title_full_unstemmed Benzothiazoles from Condensation of <i>o</i>-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
title_sort benzothiazoles from condensation of <i>o</i>-aminothiophenoles with carboxylic acids and their derivatives: a review
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/addaac14af8641b387c7ea8a332c21f1
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