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dc.contributor.authorSlavchev, Ivaylo
dc.contributor.authorWard, Jas. S.
dc.contributor.authorRissanen, Kari
dc.contributor.authorDobrikov, Georgi M.
dc.contributor.authorSimeonov, Svilen
dc.date.accessioned2022-08-11T11:50:31Z
dc.date.available2022-08-11T11:50:31Z
dc.date.issued2022
dc.identifier.citationSlavchev, 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.otherCONVID_150865022
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/82476
dc.description.abstractThe 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.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.ispartofseriesRSC Advances
dc.rightsCC BY 3.0
dc.subject.otheramidointi
dc.subject.otheramidation
dc.titleBase-promoted direct amidation of esters : beyond the current scope and practical applications
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202208114022
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange20555-20562
dc.relation.issn2046-2069
dc.relation.numberinseries32
dc.relation.volume12
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 The Author(s)
dc.rights.accesslevelopenAccessfi
dc.subject.ysoorgaaninen kemia
dc.subject.ysoorgaaniset yhdisteet
dc.subject.ysoemäkset
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p11902
jyx.subject.urihttp://www.yso.fi/onto/yso/p3841
jyx.subject.urihttp://www.yso.fi/onto/yso/p697
dc.rights.urlhttps://creativecommons.org/licenses/by/3.0/
dc.relation.doi10.1039/d2ra03524c
jyx.fundinginformationThe 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.okmA1


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