Asymmetric Synthesis of α-Quaternary γ-Lactams through Palladium-Catalyzed Asymmetric Allylic Alkylation-Reference-Cited by-同舟云学术

Asymmetric Synthesis of α-Quaternary γ-Lactams through Palladium-Catalyzed Asymmetric Allylic Alkylation

Published:2019-01-15 Issue:3 Volume:21 Page:603-607
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Song Tao¹,Arseniyadis Stellios¹²^ORCID,Cossy Janine¹^ORCID

Affiliation:

1. Laboratoire de Chimie Organique, Institute of Chemistry, Biology and Innovation (CBI), ESPCI Paris/CNRS/PSL Research University, 10 rue Vauquelin, 75231 Paris Cedex 05, France

2. Queen Mary University of London, School of Biological and Chemical Sciences, Mile End Road, London, E1 4NS, U.K.

Funder

China Scholarship Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b03613

Reference71 articles.

1. Biologically active γ-lactams: synthesis and natural sources

2. Pramanicin, a novel antimicrobial agent from a fungal fermentation

3. Fleming−Tamao Oxidation and Masked Hydroxyl Functionality: Total Synthesis of (+)-Pramanicin and Structural Elucidation of the Antifungal Natural Product (−)-Pramanicin

4. Asymmetric Total Synthesis of (−)-Azaspirene, a Novel Angiogenesis Inhibitor

5. Azaspirene: A Novel Angiogenesis Inhibitor Containing a 1-Oxa-7-azaspiro[4.4]non-2-ene-4,6-dione Skeleton Produced by the Fungus Neosartorya sp.

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