Iron/acetic acid-mediated carbon degradation: a facile route for the synthesis of quinoline derivatives-Reference-Cited by-同舟云学术

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Iron/acetic acid-mediated carbon degradation: a facile route for the synthesis of quinoline derivatives

Published:2010-10 Issue:40 Volume:51 Page:5234-5237
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ramesh Chintakunta,Kavala Veerababurao,Kuo Chun-Wei,Yao Ching-Fa

Funder

National Taiwan Normal University

National Science Council

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference63 articles.

1. New synthetic reactions. Oxidative decarboxylation of .alpha.-methylthiocarboxylic acids, new approach to acyl anion and ketene synthons

2. Allergenic α-methylene-γ-butyrolactones. A one-carbon degradation of isoalantolactone via Pummerer rearrangement of sulfoxides

3. Synthesis of 24-nor-5 beta-cholan-23-oic acid derivatives: a convenient and efficient one-carbon degradation of the side chain of natural bile acids

4. 1-Amino-2-oxo-3-oxabicyclo[3.1.0]hexane (2,3-methanohomoserine lactone), a conformationally constrained amino acid

5. Synthesis of the trioxadecalin-part of mycalamide B

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1. Study on 6-Bromo-2-methylquinoline in Ten Monosolvents and Four Binary Blends at 278.15–323.15 K: Solubility, Correlation, and Solvent Effect;Journal of Chemical & Engineering Data;2023-04-11

2. Mild and efficient copper-catalyzed oxidative cyclization of oximes with 2-aminobenzyl alcohols at room temperature: synthesis of polysubstituted quinolines;Organic & Biomolecular Chemistry;2021

3. Effective and Sustainable Access to Quinolines and Acridines: A Heterogeneous Imidazolium Salt Mediates C-C and C-N Bond Formation;European Journal of Organic Chemistry;2019-08-02

4. Quinolines synthesis by reacting 1,3-butanediol with anilines in the presence of iron catalysts;Russian Journal of General Chemistry;2016-07

5. Brønsted acid-promoted synthesis of common heterocycles and related bio-active and functional molecules;RSC Adv.;2016

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