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 |
|