Nucleophilic addition of secondary nitro compounds to acetylene
Abstract
The products of C-vinylation were prepared in 52–65% yield by the reaction of secondary nitroalkanes with acetylene in DMSO–KOH.
Please wait while we load your content...
Article information
- Article type
- Paper
Mendeleev Commun., 2002,12, 63-64
Permissions
Nucleophilic addition of secondary nitro compounds to acetylene
B. F. Kukharev, V. K. Stankevich and G. R. Klimenko, Mendeleev Commun., 2002, 12, 63 DOI: 10.1070/MC2002v012n02ABEH001541
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.