| Literature DB >> 24280974 |
Zhiqian Wang1, Brandon J Reinus, Guangbin Dong.
Abstract
A unique strategy to synthesize β-alkenylated α-enamino-ketones via catalytic C-H/alkyne coupling is described. The slow addition of alkyne substrates and the use of NaI as an additive play key roles in controlling the alkyne insertion. Replacement of the pyridyl group with carbamates was also developed. This method allows for rapid synthesis of highly functionalized vinyl-substituted enamino-ketones.Entities:
Year: 2013 PMID: 24280974 DOI: 10.1039/c3cc47556e
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222