Oxidative coupling of tetraalkynyltin with aldehydes leading to alkynyl ketones
Author:
Affiliation:
1. Department of Organic Chemistry & Technologies, Kuban State University
2. 350040 Krasnodar
3. Russian Federation
4. Department of Chemistry
5. North Caucasus Federal University
6. 355009 Stavropol
7. Peoples Friendship University Russia
Abstract
A small library of acetylenic ketones was synthesized by the reaction of tetraalkynyltin reagents with aldehydes.
Funder
Ministry of Education and Science of the Russian Federation
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C7NJ01376K
Reference43 articles.
1. Facile one-pot synthesis of 5-substituted isoxazoles and pyrazoles through microwave-promoted intramolecular cyclization of γ-hydroxyalkynal oximes and hydrazones
2. Preparation of 3,5-Disubstituted Pyrazoles and Isoxazoles from Terminal Alkynes, Aldehydes, Hydrazines, and Hydroxylamine
3. A concise total synthesis of biologically active frutinones via tributylphosphine-catalyzed tandem acyl transfer-cyclization
4. Sequential [3+2] Cycloaddition/Air Oxidation Reactions: Triazoloyl Ion Assisted Oxidative Cleavage of Alkynes
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