Palladium-Catalyzed Heteroannulation of Salicylamides with Propargyl Carbonates: Synthesis of 1,4-Benzoxazepin-5-ones-Reference-Cited by-同舟云学术

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Palladium-Catalyzed Heteroannulation of Salicylamides with Propargyl Carbonates: Synthesis of 1,4-Benzoxazepin-5-ones

Published:2024-07-01 Issue:14 Volume:89 Page:10037-10046
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Abe Masahiro¹^ORCID,Kawamoto Megumu¹,Mizukami Akiho¹,Kimachi Tetsutaro¹,Inamoto Kiyofumi¹

Affiliation:

1. School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women’s University, 11-68, 9-Bancho, Koshien, Nishinomiya, Hyogo 663-8179, Japan

Funder

Japan Society for the Promotion of Science

Promotion and Mutual Aid Corporation for Private Schools of Japan

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00898

Reference19 articles.

1. Discovery of 3,4-Dihydrobenzo[f][1,4]oxazepin-5(2H)-one Derivatives as a New Class of Selective TNIK Inhibitors and Evaluation of Their Anti-Colorectal Cancer Effects

2. Synthesis, SAR studies, and evaluation of 1,4-benzoxazepine derivatives as selective 5-HT1A receptor agonists with neuroprotective effect: Discovery of Piclozotan

3. A Selective Prostaglandin E2 Receptor Subtype 2 (EP2) Antagonist Increases the Macrophage-Mediated Clearance of Amyloid-Beta Plaques

4. The Application of the Schmidt Reaction and Beckmann Rearrangement to the Synthesis of Bicyclic Lactams: Some Mechanistic Considerations

5. Azido-Schmidt reaction for the formation of amides, imides and lactams from ketones in the presence of FeCl3

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