Selectfluor-Triggered Tandem Cyclization of o-Hydroxyarylenaminones To Access Difluorinated 2-Amino-Substituted Chromanones-Reference-Cited by-同舟云学术

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Selectfluor-Triggered Tandem Cyclization of o-Hydroxyarylenaminones To Access Difluorinated 2-Amino-Substituted Chromanones

Published:2017-08-25 Issue:18 Volume:82 Page:9837-9843
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhao Qinglan¹,Xiang Haoyue¹^ORCID,Xiao Jun-An¹,Xia Peng-Ju¹,Wang Jun-Jie¹,Chen Xiaoqing¹,Yang Hua¹^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, PR China

Funder

Central South University

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b01339

Reference50 articles.

1. Binding Model Construction of Antifungal 2-Aryl-4-chromanones Using CoMFA, CoMSIA, and QSAR Analyses

2. Synthesis, Structure–Activity Relationship Studies, and Antibacterial Evaluation of 4-Chromanones and Chalcones, as Well as Olympicin A and Derivatives

3. Chromanones: selective and reversible monoamine oxidase B inhibitors with nanomolar potency

4. Synthesis of 2-substituted chromones, chromanones, and their thio analogues using organocopper reagents

5. Asymmetric synthesis of substituted chromanones via C–H insertion reactions of α-diazoketones catalysed by homochiral rhodium(II) carboxylates

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3. An efficient synthesis of 3-fluoro chromones from the tandem cyclization of enaminones by using N-Fluoro benzenesulfonimide;Synthetic Communications;2023-07-17

4. Synthesis and crystal structure (E)-1-(4-bromo-2-hydroxyphenyl)-3-(dimethylamino)prop-2-en-1-one, C₁₁H₁₂BrNO₂;Zeitschrift für Kristallographie - New Crystal Structures;2023-05-16

5. Nickel‐Catalyzed Tandem Ring Contraction of TEMPO and C−N Bond Transamination of Enaminones toward Amino Diversity of Enaminones;European Journal of Organic Chemistry;2022-07-11

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