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Facile Synthesis of N-(9-Fluorenylmethyloxycarbonyl)-3-amino-3-(4,5-dimethoxy-2-nitrophenyl)propionic Acid as a Photocleavable Linker for Solid-Phase Peptide Synthesis

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dc.contributor.authorKim, Jaehi-
dc.contributor.authorKyeong, San-
dc.contributor.authorShin, Dong-Sik-
dc.contributor.authorYeo, Sewon-
dc.contributor.authorYim, Joonhyuk-
dc.contributor.authorLee, Yoon-Sik-
dc.date.accessioned2022-04-19T10:10:26Z-
dc.date.available2022-04-19T10:10:26Z-
dc.date.issued2013-04-
dc.identifier.issn0936-5214-
dc.identifier.issn1437-2096-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/147468-
dc.description.abstractA photocleavable linker, N-(9-fluorenylmethyloxycarbonyl)-3-amino-3-(4,5-dimethoxy-2-nitrophenyl) propionic acid was synthesized from veratraldehyde, with simple reaction and separation steps. This linker was stable under the normal solid-phase peptide synthesis conditions and rearranged to a labile form when irradiated with UV light (lambda = 365 nm). A model peptide sequence (YGGFL) was synthesized and released from solid supports with high efficiency by UV irradiation.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherGEORG THIEME VERLAG KG-
dc.titleFacile Synthesis of N-(9-Fluorenylmethyloxycarbonyl)-3-amino-3-(4,5-dimethoxy-2-nitrophenyl)propionic Acid as a Photocleavable Linker for Solid-Phase Peptide Synthesis-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1055/s-0032-1318314-
dc.identifier.scopusid2-s2.0-84874397105-
dc.identifier.wosid000317956600012-
dc.identifier.bibliographicCitationSYNLETT, v.24, no.6, pp 733 - 736-
dc.citation.titleSYNLETT-
dc.citation.volume24-
dc.citation.number6-
dc.citation.startPage733-
dc.citation.endPage736-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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