3-Haloquinolines by Friedländer Reaction of α-Haloketones-Reference-Cited by-同舟云学术

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3-Haloquinolines by Friedländer Reaction of α-Haloketones

Published:2011-06-15 Issue:14 Volume:76 Page:5774-5781
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ryabukhin Sergey V.¹²,Naumchik Vasiliy S.¹³,Plaskon Andrey S.¹³,Grygorenko Oleksandr O.¹³,Tolmachev Andrey A.¹³

Affiliation:

1. Kyiv National Taras Shevchenko University, 64 Volodymyrska str., Kyiv 01601, Ukraine

2. The Institute of High Technologies, Kyiv National Taras Shevchenko University, 4 Glushkov str., Kyiv 03187, Ukraine

3. Enamine Ltd., 23 A. Matrosova str., Kyiv 01103, Ukraine

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo2008252

Reference45 articles.

1. Privileged scaffolds for library design and drug discovery

2. Quinoline, quinazoline and acridone alkaloids (July 1999 to June 2000)

3. Practical Route to a New Class of LTD4 Receptor Antagonists

4. Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives

5. 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities

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1. NBS-mediated bromination and dehydrogenation of tetrahydro-quinoline in one pot: scope and mechanistic study;RSC Advances;2023

2. Photoinduced Three‐Component Cyclization of Arylamines, Enaminones and Difluorobromoacetates to 2,3‐Difunctionalized Quinolines;Advanced Synthesis & Catalysis;2022-09

3. Synthesis of multiple quinoline derivatives using novel ionic liquid-based nano-magnetic catalyst (MNPs@SiO2-Pr-AP-tribromide);Research on Chemical Intermediates;2022-02-07

4. Synthesis of Multibromo-Substituted Quinolines by NBS-Mediated Cascade Electrophilic Bromination/Cyclization of N-(3-Phenylprop-2-ynyl)anilines;Synthesis;2021-02-22

5. Recent advances in the chemistry of thieno[2,3-b]pyridines 1. Methods of synthesis of thieno[2,3-b]pyridines;Russian Chemical Bulletin;2020-10

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