A reductive coupling strategy towards ripostatin A
Synthetic studies on the antibiotic natural product ripostatin A have been carried out with the aim to construct the C9−C10 bond by a nickel(0)-catalyzed coupling reaction of an enyne and an epoxide, followed by rearrangement of the resulting dienylcyclopropane intermediate to afford the skipped 1,4...
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Article |
| Language: | en_US |
| Published: |
Beilstein-Institut
2013
|
| Online Access: | http://hdl.handle.net/1721.1/82124 https://orcid.org/0000-0002-8601-7799 |