AuBr3-Catalyzed Thiooxime-to-Carbonyl Conversion: From Chiral Aliphatic Nitro Compounds to Ketones without Racemization-Reference-Cited by-同舟云学术

AuBr3-Catalyzed Thiooxime-to-Carbonyl Conversion: From Chiral Aliphatic Nitro Compounds to Ketones without Racemization

Published:2009-09-04 Issue:19 Volume:11 Page:4414-4417
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Burés Jordi¹,Isart Carles¹,Vilarrasa Jaume¹

Affiliation:

1. Departament de Química Orgànica, Facultat de Química, Universitat de Barcelona, Diagonal 647, 08028 Barcelona, Catalonia, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9017722

Reference35 articles.

1. Among dozens of reviews on the uses of gold in organic chemistry (the new “gold rush”, mainly involving interactions of Au(I) with multiple C−C bonds in the key steps), see the following general summaries:

2. Supported gold nanoparticles as catalysts for organic reactions

3. Gold catalysis in total synthesis

4. Alternative Synthetic Methods through New Developments in Catalysis by Gold

5. Gold-Catalyzed Organic Transformations

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