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dc.contributor.authorKim, JM-
dc.contributor.authorWilson, TE-
dc.contributor.authorNorman, TC-
dc.contributor.authorSchultz, PG-
dc.date.accessioned2024-01-21T19:32:03Z-
dc.date.available2024-01-21T19:32:03Z-
dc.date.created2021-09-01-
dc.date.issued1996-07-22-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144382-
dc.description.abstractA cyclic urea trimer was synthesized from readily available amino acid derivatives using a simple, iterative approach. A selective amide reduction using borane (BH3-THF) and a triphosgens-mediated cyclization are the key features in a synthesis of the cyclic urea trimer 2. Copyright (C) 1996 Elsevier Science Ltd-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectPEPTIDE COMBINATORIAL LIBRARIES-
dc.subjectVINYLOGOUS SULFONYL PEPTIDES-
dc.subjectSOLID-PHASE SYNTHESIS-
dc.subjectUNNATURAL BIOPOLYMERS-
dc.subjectDRUG DISCOVERY-
dc.titleSynthesis of a cyclic urea as a nonnatural biopolymer scaffold-
dc.typeArticle-
dc.identifier.doi10.1016/0040-4039(96)01101-X-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.37, no.30, pp.5309 - 5312-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume37-
dc.citation.number30-
dc.citation.startPage5309-
dc.citation.endPage5312-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996UZ67400024-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusPEPTIDE COMBINATORIAL LIBRARIES-
dc.subject.keywordPlusVINYLOGOUS SULFONYL PEPTIDES-
dc.subject.keywordPlusSOLID-PHASE SYNTHESIS-
dc.subject.keywordPlusUNNATURAL BIOPOLYMERS-
dc.subject.keywordPlusDRUG DISCOVERY-
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