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

期刊

ADVANCED SYNTHESIS & CATALYSIS
卷 354, 期 6, 页码 1061-1068

出版社

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

关键词

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

资金

  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

向作者/读者索取更多资源

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.

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