BEMP-Promoted C(4)-Alkylation of 4-Alkyloxazol-5(4H)-ones: A Rapid and Efficient Route to alpha,alpha-Dialkyl-alpha-amino Acids SCIE SCOPUS

DC Field Value Language
dc.contributor.author Lee, Yeon-Ju -
dc.contributor.author Seo, Jeyoung -
dc.contributor.author Kim, Dong-Guk -
dc.contributor.author Park, Hyeung-geun -
dc.contributor.author Jeong, Byeong-Seon -
dc.date.accessioned 2020-04-20T05:52:08Z -
dc.date.available 2020-04-20T05:52:08Z -
dc.date.created 2020-01-28 -
dc.date.issued 2013-04 -
dc.identifier.issn 0936-5214 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/3205 -
dc.description.abstract Rapid and efficient C(4)-alkylation of 4-alkyloxazol-5(4H)-ones has been achieved by the utilization of BEMP as base. 4,4-Dialkyloxazol-5(4H)-ones, which can easily be hydrolyzed into free alpha,alpha-dialkyl-alpha-amino acids, were obtained in high yields (up to 99%) within a few minutes (1-18 min). BEMP, a sterically hindered strong base with low nucleophilicity facilitated the desired reaction, while decreasing the rate of side reactions such as O-alkylation, C(2)-alkylation and the breakage of oxazolone. -
dc.description.uri 1 -
dc.language English -
dc.publisher GEORG THIEME VERLAG KG -
dc.subject ALPHA-AMINO-ACIDS -
dc.subject ASYMMETRIC-SYNTHESIS -
dc.subject STEREOSELECTIVE-SYNTHESIS -
dc.subject AZLACTONES -
dc.subject ALKYLATION -
dc.subject CONFORMATION -
dc.subject CATALYST -
dc.subject DESIGN -
dc.subject OXAZOL-5-(4H)-ONES -
dc.subject ORGANOCATALYSTS -
dc.title BEMP-Promoted C(4)-Alkylation of 4-Alkyloxazol-5(4H)-ones: A Rapid and Efficient Route to alpha,alpha-Dialkyl-alpha-amino Acids -
dc.type Article -
dc.citation.endPage 704 -
dc.citation.startPage 701 -
dc.citation.title SYNLETT -
dc.citation.volume 24 -
dc.citation.number 6 -
dc.contributor.alternativeName 이연주 -
dc.identifier.bibliographicCitation SYNLETT, v.24, no.6, pp.701 - 704 -
dc.identifier.doi 10.1055/s-0032-1317801 -
dc.identifier.scopusid 2-s2.0-84874608430 -
dc.identifier.wosid 000317956600005 -
dc.type.docType Article -
dc.description.journalClass 1 -
dc.subject.keywordPlus ALPHA-AMINO-ACIDS -
dc.subject.keywordPlus ASYMMETRIC-SYNTHESIS -
dc.subject.keywordPlus STEREOSELECTIVE-SYNTHESIS -
dc.subject.keywordPlus AZLACTONES -
dc.subject.keywordPlus ALKYLATION -
dc.subject.keywordPlus CONFORMATION -
dc.subject.keywordPlus CATALYST -
dc.subject.keywordPlus DESIGN -
dc.subject.keywordPlus OXAZOL-5-(4H)-ONES -
dc.subject.keywordPlus ORGANOCATALYSTS -
dc.subject.keywordAuthor alpha,alpha-dialkyl-alpha-amino acid -
dc.subject.keywordAuthor oxazol-5(4H)-one -
dc.subject.keywordAuthor C(4)-alkylation -
dc.subject.keywordAuthor BEMP -
dc.subject.keywordAuthor protecting group -
dc.subject.keywordAuthor chemoselectivity -
dc.relation.journalWebOfScienceCategory Chemistry, Organic -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Chemistry -
Appears in Collections:
Marine Resources & Environment Research Division > Marine Biotechnology &Bioresource Research Department > 1. Journal Articles
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