Diastereoselective Synthesis of 3,4-Dihydropyran-3-carboxamides with in Vitro Anti-inflammatory Activity-Reference-Cited by-同舟云学术

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Diastereoselective Synthesis of 3,4-Dihydropyran-3-carboxamides with in Vitro Anti-inflammatory Activity

Published:2019-08-21 Issue:10 Volume:21 Page:656-665
ISSN:2156-8952
Container-title:ACS Combinatorial Science
language:en
Short-container-title:ACS Comb. Sci.

Author:

Zeng Li-Yan¹,Xi Baomin¹,Huang Kaiqi¹,Bi Jingjie¹,Wei Lan¹,Cai Chun²^ORCID,Liu Shuwen¹³^ORCID

Affiliation:

1. Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China

2. Chemical Engineering College, Nanjing University of Science and Technology, Nanjing 210094, China

3. State Key Laboratory of Organ Failure Research, Guangdong Provincial Institute of Nephrology, Southern Medical University, Guangzhou 510515, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acscombsci.9b00050

Reference33 articles.

1. In vitro antioxidant and anti-inflammatory activities of Angelica decursiva

2. Synthesis and in vivo influenza virus-inhibitory effect of ester prodrug of 4-guanidino-7-O-methyl-Neu5Ac2en

3. Synthesis of Spiro[chroman/tetrahydrothiophene-3,3′-oxindole] ScaffoldsviaHeteroatom-Michael-Michael Reactions: Easily Controlled EnantioselectivityviaBifunctional Catalysts

4. Organocatalytic oxa/aza-Michael–Michael Cascade Strategy for the Construction of Spiro [Chroman/Tetrahydroquinoline-3,3′-oxindole] Scaffolds

5. Expeditious Synthesis of Benzopyrans via Lewis Acid-Catalyzed C−H Functionalization: Remarkable Enhancement of Reactivity by an Ortho Substituent

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