One platform for all researcher needs
AI-powered academic writing assistant
Your #1 AI companion for literature search
AI tool for graphics, illustrations, and artwork
Unlock unlimited use of all AI tools with the Editage Plus membership.
Explore Editage Plus
Audio Papers
Ask R Discovery
Translation
Auto-sync
Collaboration
https://doi.org/10.1016/0040-4020(79)87008-8
Copy DOI
Export
Save
Share
Cite Journal: Tetrahedron |  Publication Date: Jan 1, 1979 |
 Citations: 13 |
Affiliation: Institut de Chimie des Substances Naturelles
Dye-sensitized photooxidation of the imino-ether 5, prepared from yohimbine 1a, led to the α-amino nitrile 9a when the reaction was performed in the presence of oxygen and KCN. Derivative 9a was hydrolyzed to the amide 9b, the transformation of which to carboxamido-5β-yohimbine 15 was studied.
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
