Stereoselective Hydrohalogenation of Alkynoic Acids and Their Esters in Ionic Liquids
Author:
Affiliation:
1. Departamento de Química, Universidad Simón Bolívar, Valle de Sartenejas, Baruta, Caracas 1080-A, Apartado 89000, Venezuela
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823407X200038
Reference26 articles.
1. Asymmetric Synthesis of the C3α Fragment of 5,6-Dihydro-α-pyrone Nonpeptidic HIV-1 Protease Inhibitors
2. Stereoselective syntheses of di-, tri-, and tetrasubstituted enediynes from enynyl iodides via Pd-catalyzed coupling reactions
3. Efficient Synthesis of Conjugated (2E)- or (2Z)-En-4-ynoic Acids and (2E,4E)- or (2Z,4E)-Dienoic Acids via Palladium-Catalysed Cross Coupling
4. A convenient synthesis of amides and nitriles with a branched and conjugated dienyne structure
5. An efficient stereoselective approach to silylated polyunsaturated γ-alkylidene butenolides
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1. Hydrohalogenation of Electron-Deficient Alkyne in Aqueous Solution;Hans Journal of Chemical Engineering and Technology;2024
2. Ionic Liquid, Surrogate Hydrogen Bromide Reagent for Ring Opening of Cyclopropyl Ketones;The Journal of Organic Chemistry;2008-04-05
3. Stereoselective Hydrohalogenation of Alkynoic Acids and Their Esters in Ionic Liquids.;ChemInform;2007-09-11
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