4.7 Article

Ligand-Free Buchwald-Hartwig Aromatic Aminations of Aryl Halides Catalyzed by Low-Leaching and Highly Recyclable Sulfur-Modified Gold-Supported Palladium Material

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 354, Issue 6, Pages 1061-1068

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201100761

Keywords

amination; cross-coupling; gold; ligand effects; palladium; supported catalysts

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT)
  2. Japan Science and Technology Agency (JST)
  3. Noguchi Institute, Japan
  4. Grants-in-Aid for Scientific Research [24390023, 23246013, 11J03163, 23659049] Funding Source: KAKEN

Ask authors/readers for more resources

A stable heterogeneous catalyst precursor, sulfur-modified gold-supported palladium material (SAPd), has proved to be an excellent source of leached, ligand-free, Pd for the amination of aryl bromides and chlorides. The reaction-enabling catalyst is provided in situ as leached Pd in low catalyst loading (0.21 +/- 0.02 mol%). This allows the precatalyst (SAPd) to be filtered off and used for a minimum of ten reaction cycles without loss of catalytic activity. SAPd released only trace amounts, less than 0.6 ppm, of highly active Pd during the reaction without any aggregation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available