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Solid-phase total synthesis of (-)-Phenylhistine and (-)-Aurantiamine. Synthesis of a diverse dehydro-2,5-diketopiperazine library. Part II

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dc.contributor.author Couladouros, EA en
dc.contributor.author Magos, AD en
dc.date.accessioned 2014-06-06T06:46:39Z
dc.date.available 2014-06-06T06:46:39Z
dc.date.issued 2005 en
dc.identifier.issn 13811991 en
dc.identifier.uri http://dx.doi.org/10.1007/s11030-005-1295-9 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/3120
dc.subject 2,5-diketopiperazines en
dc.subject Amino acids en
dc.subject Combinatorial chemistry en
dc.subject Horner-Emmons reaction en
dc.subject Library en
dc.subject Natural products en
dc.subject Solid-phase synthesis en
dc.subject.other amine en
dc.subject.other amino acid en
dc.subject.other aurantiamine en
dc.subject.other benzene derivative en
dc.subject.other dehydro 2,5 diketopiperazine en
dc.subject.other glycine derivative en
dc.subject.other glycine phosphonate en
dc.subject.other imidazole derivative en
dc.subject.other indole derivative en
dc.subject.other phenylhistine en
dc.subject.other phosphonic acid derivative en
dc.subject.other piperazine derivative en
dc.subject.other pyridine derivative en
dc.subject.other thiazole en
dc.subject.other unclassified drug en
dc.subject.other article en
dc.subject.other combinatorial chemistry en
dc.subject.other drug structure en
dc.subject.other drug synthesis en
dc.subject.other priority journal en
dc.subject.other solid en
dc.subject.other Indicators and Reagents en
dc.subject.other Models, Molecular en
dc.subject.other Molecular Conformation en
dc.subject.other Piperazines en
dc.subject.other Spectroscopy, Fourier Transform Infrared en
dc.title Solid-phase total synthesis of (-)-Phenylhistine and (-)-Aurantiamine. Synthesis of a diverse dehydro-2,5-diketopiperazine library. Part II en
heal.type journalArticle en
heal.identifier.primary 10.1007/s11030-005-1295-9 en
heal.publicationDate 2005 en
heal.abstract The preparation of solid supported glycine phosphonate and its utilization for the total synthesis of two natural products is presented. The proposed protocol combines diversity with accessibility and speed, which makes this scaffold suitable for automated parallel synthesis and combinatorial chemistry. The preparation of a small library of dehydro-2,5-diketopiperazines, combining several natural amino acids with diverse heterocycles (including thiazoles, pyridines, indoles and imidazoles), is also demonstrated. © Springer 2005. en
heal.journalName Molecular Diversity en
dc.identifier.issue 1-3 en
dc.identifier.volume 9 en
dc.identifier.doi 10.1007/s11030-005-1295-9 en
dc.identifier.spage 111 en
dc.identifier.epage 121 en


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