Enantioselective copper catalysed intramolecular C–H insertion reactions of α-diazo-β-keto sulfones, α-diazo-β-keto phosphine oxides and 2-diazo-1,3-diketones; the influence of the carbene substituent
Author:
Affiliation:
1. Department of Chemistry
2. Analytical and Biological Chemistry Research Facility
3. University College Cork
4. Cork
5. Ireland
6. Department of Chemistry and School of Pharmacy
7. Synthesis and Solid State Pharmaceutical Centre
Abstract
Enantioselective C–H insertion reactions are described.
Funder
Irish Research Council
Irish Research Council for Science, Engineering and Technology
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00214A
Reference35 articles.
1. Modern Organic Synthesis with α-Diazocarbonyl Compounds
2. Catalytic asymmetric C–H insertion reactions of α-diazocarbonyl compounds
3. M. P. Doyle , M. A.McKervey and T.Ye , Modern Catalytic Methods for Organic Synthesis with Diazo Compounds: From Cyclopropanes to Ylides , Wiley , New York , 1998
4. Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion
5. Catalytic Carbene Insertion into C−H Bonds
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