A novel and efficient amidation of 2-aminothiazole
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Choi, Minho | - |
dc.contributor.author | Won, Sun-Woo | - |
dc.contributor.author | Jo, Hyeju | - |
dc.contributor.author | Viji, Mayavan | - |
dc.contributor.author | Seo, Seung-Yong | - |
dc.contributor.author | Lee, Yeon-Ju | - |
dc.contributor.author | Lee, Hyi-Seung | - |
dc.contributor.author | Lee, Heesoon | - |
dc.contributor.author | Hong, Jin Tae | - |
dc.contributor.author | Kwak, Young-Shin | - |
dc.contributor.author | Jung, Jae-Kyung | - |
dc.date.accessioned | 2021-09-05T02:49:14Z | - |
dc.date.available | 2021-09-05T02:49:14Z | - |
dc.date.created | 2021-06-15 | - |
dc.date.issued | 2014-11-26 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/96736 | - |
dc.description.abstract | A facile and efficient method has been developed for the synthesis of novel thiazolyl carboxamide derivatives by direct reaction of the corresponding esters and 2-aminothiazole. Treatment of 2-aminothiozole with various carboxylic esters in the presence of t-butylmagnesium chloride provides the biologically significant thiazolyl carboxamide derivatives in good to excellent yields. (C) 2014 Elsevier Ltd. All rights reserved. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.subject | AMIDE BOND FORMATION | - |
dc.subject | CARBOXYLIC-ACIDS | - |
dc.subject | MANUFACTURE | - |
dc.subject | MELOXICAM | - |
dc.subject | AMINES | - |
dc.title | A novel and efficient amidation of 2-aminothiazole | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Kwak, Young-Shin | - |
dc.identifier.doi | 10.1016/j.tetlet.2014.10.031 | - |
dc.identifier.scopusid | 2-s2.0-84910107283 | - |
dc.identifier.wosid | 000345488900017 | - |
dc.identifier.bibliographicCitation | TETRAHEDRON LETTERS, v.55, no.48, pp.6582 - 6584 | - |
dc.relation.isPartOf | TETRAHEDRON LETTERS | - |
dc.citation.title | TETRAHEDRON LETTERS | - |
dc.citation.volume | 55 | - |
dc.citation.number | 48 | - |
dc.citation.startPage | 6582 | - |
dc.citation.endPage | 6584 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | AMIDE BOND FORMATION | - |
dc.subject.keywordPlus | CARBOXYLIC-ACIDS | - |
dc.subject.keywordPlus | MANUFACTURE | - |
dc.subject.keywordPlus | MELOXICAM | - |
dc.subject.keywordPlus | AMINES | - |
dc.subject.keywordAuthor | Amide | - |
dc.subject.keywordAuthor | 2-Aminothiazole | - |
dc.subject.keywordAuthor | Carboxamide | - |
dc.subject.keywordAuthor | Transamidation | - |
dc.subject.keywordAuthor | t-Butylmagnesium chloride | - |
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