Iodine catalyzed C (sp(3))-H functionalization of tosylhydrazones with beta-enamino esters under visible light irradiation for the synthesis of trisubstituted pyrroles has been described. The present method is also applicable to a alpha-substituted tosylhydrazones to yield the tetra-substituted pyrroles.
Pd‐Catalyzed Tandem Coupling Reaction of 2‐
<i>gem</i>
‐Dibromovinylanilines and
<i>N</i>
‐Tosylhydrazones to Construct 2‐(1‐phenylvinyl)‐indoles
A novel palladium(0)‐catalyzed intermolecular coupling reaction of 2‐gem‐dibromovinylanilines and N‐tosylhydrazones was reported to construct 2‐(1‐phenylvinyl)‐indoles efficiently. The indole bearing 1, 1‐disubstituted alkenes were obtained in one step with short reaction time, in high yields and broad substrate scope. The formed indole derivates could be easily transformed into much more valuable
Pd-catalyzed oxidative cross-coupling of N-tosylhydrazones with arylboronic acids
作者:Xia Zhao、Jing Jing、Kui Lu、Yan Zhang、Jianbo Wang
DOI:10.1039/b925590g
日期:——
The Pd-catalyzed reaction of N-tosylhydrazones and arylboronic acids provides olefin derivatives. This oxidative cross-coupling is suggested to proceed through a migratory insertion process of a Pd carbene intermediate.