Oxidation of β-Ketoamides: The Synthesis of Vicinal Tricarbonyl Amides-Reference-Cited by-同舟云学术

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Oxidation of β-Ketoamides: The Synthesis of Vicinal Tricarbonyl Amides

Published:2017-03-07 Issue:7 Volume:82 Page:3901-3907
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Yueyang¹,Zhang Zhiguo¹^ORCID,Wan Yameng¹,Zhang Guisheng¹,Li Zhonglian¹,Bi Jingjing¹,Ma Nana¹,Liu Tongxin¹,Liu Qingfeng¹

Affiliation:

1. Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Henna Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, P. R. China

Funder

Henan Normal University

National Natural Science Foundation of China

Henan Educational Committee

Henan Province

Young Backbone Teachers Fund of Henan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b03062

Reference54 articles.

1. The Chemistry of Vicinal Tricarbonyls: Total Syntheses of Elastase Inhibitors YM-47141 and YM-47142

2. Oxidizing Morita–Baylis–Hillman adducts towards vicinal tricarbonyl compounds

3. A Unified Total Synthesis of the Immunomodulators (−)-Rapamycin and (−)-27-Demethoxyrapamycin: Assembly of the Common C(1−20) Perimeter and Final Elaboration

4. Facile synthesis of the “tricarbonyl” subunit in the immunosuppressant rapamycin

5. Total Synthesis of Cladoniamide G

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