We have located links that may give you full text access.
Diastereoselective [3 + 2] cycloaddition of 3-ylideneoxindoles with in situ generated CF 2 HCHN 2 : syntheses of CF 2 H-containing spirooxindoles.
Organic & Biomolecular Chemistry 2017 July 6
An efficient [3 + 2] cycloaddition of 3-ylideneoxindoles with in situ generated CF2 HCHN2 for the syntheses of spirooxindoles has been developed. This methodology gives access to a range of relatively complex spirooxindoles featuring a CF2 H group and three contiguous stereogenic centers in up to 84% yield and 99 : 1 trans/cis.
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