z-logo
Premium
Hydrosilylation of Internal Alkynes Catalyzed by Tris‐ Imidazolium Salt‐Stabilized Palladium Nanoparticles
Author(s) -
Planellas Marc,
Guo Wusheng,
Alonso Francisco,
Yus Miguel,
Shafir Alexandr,
Pleixats Roser,
Parella Teodor
Publication year - 2014
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201300641
Subject(s) - chemistry , hydrosilylation , palladium , catalysis , tris , salt (chemistry) , nanoparticle , inert gas , stereoselectivity , inert , polymer chemistry , organic chemistry , chemical engineering , biochemistry , engineering
Palladium nanoparticles stabilized with tris‐imidazolium tetrafluoroborates catalyze the stereoselective hydrosilylation of internal alkynes in a dry inert atmosphere to give ( E )‐vinylsilanes in excellent yields. In the presence of controlled amounts of water a transfer hydrogenation reaction takes place with the formation of ( Z ) ‐ alkenes or the corresponding alkanes.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here