Cited 3 time in
A Green Chemical Approach for Iodination of Pyrimidine Derivatives by Mechanical Grinding under Solvent-Free Conditions
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Balasubramaniyam, Thananjeyan | - |
| dc.contributor.author | Kim, Byeong-Seon | - |
| dc.contributor.author | Pallavi, Badvel | - |
| dc.contributor.author | Jin, Ho-Seong | - |
| dc.contributor.author | Kim, Sung Kuk | - |
| dc.contributor.author | Lee, Joon-Hwa | - |
| dc.date.accessioned | 2023-01-03T06:00:04Z | - |
| dc.date.available | 2023-01-03T06:00:04Z | - |
| dc.date.issued | 2022-10 | - |
| dc.identifier.issn | 1420-3049 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/29861 | - |
| dc.description.abstract | The iodination of pyrimidines is usually carried out by using toxic reagents under acidic conditions, such as with sulfuric acid and nitric acid. To avoid toxic reagents, we developed a simple and eco-friendly approach for the iodination of pyrimidine derivatives under solvent-free conditions using solid iodine and AgNO3 as an electrophilic iodinating reagent. The advantages of this method are the relatively short reaction time (20-30 min), simple set-up procedure, high yields (70-98%), and environmentally friendly reaction conditions. Our novel approach for the iodination of pyrimidines, as well as a variety of their derivatives, will contribute to the development of nucleobase-related drug candidates. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | - |
| dc.title | A Green Chemical Approach for Iodination of Pyrimidine Derivatives by Mechanical Grinding under Solvent-Free Conditions | - |
| dc.type | Article | - |
| dc.publisher.location | 스위스 | - |
| dc.identifier.doi | 10.3390/molecules27196386 | - |
| dc.identifier.scopusid | 2-s2.0-85139794148 | - |
| dc.identifier.wosid | 000867986100001 | - |
| dc.identifier.bibliographicCitation | Molecules, v.27, no.19 | - |
| dc.citation.title | Molecules | - |
| dc.citation.volume | 27 | - |
| dc.citation.number | 19 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.subject.keywordPlus | N-IODOSUCCINIMIDE | - |
| dc.subject.keywordPlus | NUCLEOSIDES | - |
| dc.subject.keywordPlus | IODINE | - |
| dc.subject.keywordPlus | ARENES | - |
| dc.subject.keywordPlus | ARYLATION | - |
| dc.subject.keywordPlus | NITRATE | - |
| dc.subject.keywordPlus | MILD | - |
| dc.subject.keywordAuthor | green synthesis | - |
| dc.subject.keywordAuthor | mechanochemistry | - |
| dc.subject.keywordAuthor | nitrate salts | - |
| dc.subject.keywordAuthor | pyrimidine derivatives | - |
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