We have located links that may give you full text access.
Journal Article
Research Support, Non-U.S. Gov't
Synthesis of the Cyclohepta[e]hydrindane Core of the Marine Homoverrucosane Diterpenoid Gagunin E.
Organic Letters 2017 Februrary 18
The synthesis of the A-B-cis B-C-trans annulated cyclohepta[e]hydrindane core of gagunin E with a fully elaborated B-C ring segment has been achieved. Using an adaptable A ring building block, the B ring was annulated by (4 + 2)-cycloaddition and the C ring by ring-closing metathesis. The angular methyl groups were attached by electrophilic cyclopropanation-ring opening.
Full text links
Related Resources
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app