Ionic Liquid Supported Organotin Reagents: Green Tools for Stille Cross‐Coupling Reactions with Brominated Substrates | Zendy

Louaisil Nicolas | Zendy; Pham Phuoc Dien | Zendy; Boeda Fabien | Zendy; Faye Djibril | Zendy; Castanet AnneSophie | Zendy; Legoupy Stéphanie | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Ionic Liquid Supported Organotin Reagents: Green Tools for Stille Cross‐Coupling Reactions with Brominated Substrates

Author(s) -

Louaisil Nicolas,

Pham Phuoc Dien,

Boeda Fabien,

Faye Djibril,

Castanet AnneSophie,

Legoupy Stéphanie

Publication year - 2011

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201001195

Subject(s) - stille reaction , chemistry , reagent , ionic liquid , aryl , tin , solvent , coupling reaction , catalysis , organic chemistry , green chemistry , combinatorial chemistry , ligand (biochemistry) , ionic bonding , ion , alkyl , biochemistry , receptor

Efficiency of ionic liquid supported organotin reagents in Stille cross‐coupling reactions involving aryl bromides has been investigated. In a general manner, products were isolated with good yields by using a very simple catalytic system without the need of solvent, ligand, or additives. The organotin compounds were recycled without loss of activity and the contamination by tin was limited and controlled ([Sn] < 3 ppm).

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research