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dc.contributor.author | Yamamoto T. | |
dc.contributor.author | Chang T.C. | |
dc.contributor.author | Tanaka K. | |
dc.date.accessioned | 2022-02-09T20:46:42Z | |
dc.date.available | 2022-02-09T20:46:42Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 2041-6520 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/170217 | |
dc.description.abstract | This study presents the novel concept of a transformable protecting group, which changes its properties through structural transformation. Based on this concept, we developed a 2-(2-ethynylphenyl)-2-(5-methylfuran-2-yl)-ethoxycarbonyl (Epoc) group. The Epoc group was transformed into an Fmoc-like structure with gold(iii)-catalyzed fluorene formation and was removable under Fmoc-like mild basic conditions post-transformation even though it was originally stable under strongly basic conditions. As an application for organic synthesis, the Epoc group provides the novel orthogonality of gold(iii)-labile protecting groups in solid-phase peptide synthesis. In addition, the high turnover number of fluorene formation in aqueous media is suggestive of the applicability of the Epoc group to biological systems. This journal is | |
dc.relation.ispartofseries | Chemical Science | |
dc.title | Epoc group: Transformable protecting group with gold(iii)-catalyzed fluorene formation | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 32 | |
dc.relation.ispartofseries-volume | 12 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 10703 | |
dc.source.id | SCOPUS20416520-2021-12-32-SID85113209086 |