Liquid-assisted grinding and ion pairing regulates percentage conversion and diastereoselectivity of the Wittig reaction under mechanochemical conditions
Open Access
- 23 March 2018
- journal article
- research article
- Published by Beilstein Institut in Beilstein Journal of Organic Chemistry
- Vol. 14 (1) , 688-696
Abstract
Mechanochemistry is maturing as a discipline and continuing to grow, so it is important to continue understanding the rules governing the system. In a mechanochemical reaction, the reactants are added into a vessel along with one or more grinding balls and the vessel is shaken at high speeds to facilitate a chemical reaction. The dielectric constant of the solvent used in liquid-assisted grinding (LAG) and properly chosen counter-ion pairing increases the percentage conversion of stilbenes in a mechanochemical Wittig reaction. Utilizing stepwise addition/evaporation of ethanol in liquid-assisted grinding also allows for the tuning of the diastereoselectivity in the Wittig reaction.Keywords
This publication has 30 references indexed in Scilit:
- Recent advances in mechanochemical C–H functionalization reactionsTetrahedron Letters, 2018
- 1,1′-Carbonyldiimidazole and Mechanochemistry: A Shining Green CombinationACS Sustainable Chemistry & Engineering, 2017
- Mechanochemical synthesis of small organic moleculesBeilstein Journal of Organic Chemistry, 2017
- Mechanochemical synthesis of thioureas, ureas and guanidinesBeilstein Journal of Organic Chemistry, 2017
- Chemistry 2.0: Developing a New, Solvent-Free System of Chemical Synthesis Based on MechanochemistrySynlett, 2017
- Mechanochemistry: A Force of SynthesisACS Central Science, 2016
- Mechanochemistry of inorganic and organic systems: what is similar, what is different?Chemical Society Reviews, 2013
- Mechanochemical organic synthesisChemical Society Reviews, 2013
- The historical development of mechanochemistryChemical Society Reviews, 2013
- Mechanochemistry: opportunities for new and cleaner synthesisChemical Society Reviews, 2011