Chain-Walking Strategy for Organic Synthesis: Catalytic Cycloisomerization of 1,n-Dienes
摘要:
The catalytic construction of carbon-carbon bonds in small organic molecules via chain walking is described. Catalytic cycloisomerization of 1,n-dienes via chain walking was achieved using a palladium-1,10-phenanthroline catalyst to form five-membered-ring products. By means of a cycloisomerization/hydrogenation protocol, 1,7- to 1,14-dienes were selectively converted to bicyclo[4.3.0]nonane derivatives. The use of chain walking provides a new method in organic synthesis to functionalize unreactive carbon-hydrogen bonds by letting the catalyst look for preferable bond-forming sites by moving around on the substrate.
Chain-walking Cycloisomerization of 1,<i>n</i>-Dienes Catalyzed by Pyridine–Oxazoline Palladium Catalysts and Its Application to Asymmetric Synthesis
作者:Taro Hamasaki、Fumitoshi Kakiuchi、Takuya Kochi
DOI:10.1246/cl.151138
日期:2016.3.5
Palladium catalysts possessing pyridine–oxazoline ligands were found to catalyze the chain-walking cycloisomerization of 1,n-dienes to form five-membered rings and were particularly effective for t...