dc.contributor.author |
Spindler B. |
|
dc.contributor.author |
Kataeva O. |
|
dc.contributor.author |
Knölker H. |
|
dc.date.accessioned |
2019-01-22T20:33:09Z |
|
dc.date.available |
2019-01-22T20:33:09Z |
|
dc.date.issued |
2018 |
|
dc.identifier.issn |
0022-3263 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/147677 |
|
dc.description.abstract |
© Copyright 2018 American Chemical Society. We describe the first enantioselective total synthesis and the assignment of the absolute configuration of the furo[3,2-a]carbazole alkaloid furoclausine-B. As key steps for our approach we used a palladium(II)-catalyzed double C-H-bond activation for the construction of the carbazole framework, a Shi epoxidation, and an intramolecular opening of the epoxide for annulation of the dihydrofuran moiety. |
|
dc.relation.ispartofseries |
Journal of Organic Chemistry |
|
dc.title |
Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2- a]carbazole Alkaloid Furoclausine-B |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
24 |
|
dc.relation.ispartofseries-volume |
83 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
15136 |
|
dc.source.id |
SCOPUS00223263-2018-83-24-SID85058567783 |
|