dc.contributor.author | Slavchev, Ivaylo | |
dc.contributor.author | Ward, Jas. S. | |
dc.contributor.author | Rissanen, Kari | |
dc.contributor.author | Dobrikov, Georgi M. | |
dc.contributor.author | Simeonov, Svilen | |
dc.date.accessioned | 2022-08-11T11:50:31Z | |
dc.date.available | 2022-08-11T11:50:31Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Slavchev, I., Ward, J. S., Rissanen, K., Dobrikov, G. M., & Simeonov, S. (2022). Base-promoted direct amidation of esters : beyond the current scope and practical applications. <i>RSC Advances</i>, <i>12</i>(32), 20555-20562. <a href="https://doi.org/10.1039/d2ra03524c" target="_blank">https://doi.org/10.1039/d2ra03524c</a> | |
dc.identifier.other | CONVID_150865022 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/82476 | |
dc.description.abstract | The base-promoted direct amidation of unactivated esters is among the most useful reactions for amide bond formation in contemporary organic chemistry. The intensive research in this area has led to the development of a number of new methods to achive this transformation. However, to date, the existing literature is more methodological and in many instances lacks practical directions. Therefore, the full potential of this transformation is yet to be revealed by broadening the substrate scope. In a search for new practical applications of the amidation reaction, herein we present a comprehensive study of a number of base-promoted direct amidations that encompass a wide range of amines and esters. Furthermore, we applied our findings in the synthesis of phosphoramidates and several industrially relevant products. | en |
dc.format.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Royal Society of Chemistry (RSC) | |
dc.relation.ispartofseries | RSC Advances | |
dc.rights | CC BY 3.0 | |
dc.subject.other | amidointi | |
dc.subject.other | amidation | |
dc.title | Base-promoted direct amidation of esters : beyond the current scope and practical applications | |
dc.type | research article | |
dc.identifier.urn | URN:NBN:fi:jyu-202208114022 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Orgaaninen kemia | fi |
dc.contributor.oppiaine | Organic Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 20555-20562 | |
dc.relation.issn | 2046-2069 | |
dc.relation.numberinseries | 32 | |
dc.relation.volume | 12 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2022 The Author(s) | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.subject.yso | orgaaninen kemia | |
dc.subject.yso | orgaaniset yhdisteet | |
dc.subject.yso | emäkset | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p11902 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p3841 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p697 | |
dc.rights.url | https://creativecommons.org/licenses/by/3.0/ | |
dc.relation.doi | 10.1039/d2ra03524c | |
jyx.fundinginformation | The authors acknowledge the financial support from National Scientific Program “VIHREN” (grant KP-06-DV-1). The project leading to this application has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 951996. | |
dc.type.okm | A1 | |