Di- and Trisubstituted γ-Lactams via Rh(II)-carbenoid Reaction of N-Cα-Branched, N-Bis(trimethylsilyl)methyl α-Diazoamides. Synthesis of (±)-α-Allokainic Acid-Reference-Cited by-同舟云学术

Di- and Trisubstituted γ-Lactams via Rh(II)-carbenoid Reaction of N-Cα-Branched, N-Bis(trimethylsilyl)methyl α-Diazoamides. Synthesis of (±)-α-Allokainic Acid

Published:2010-11-10 Issue:23 Volume:12 Page:5386-5389
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Bao¹,Wee Andrew G. H.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Regina, Regina, Saskatchewan, Canada S4S 0A2

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol1021564

Reference34 articles.

1. Catalytic Carbene Insertion into C−H Bonds

2. Rhodium(II)-Catalyzed Reaction of Diazocompounds in the Service of Organic Synthesis of Natural and Non-Natural Products

3. Stereo‐ and Regiocontrol in the Formation of Lactams by Rhodium‐Carbenoid C−H Insertion of α‐Diazoacetamides

4. Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion

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