1228660-88-5Relevant articles and documents
Electrochemical synthesis of copper(i) acetylides: Via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
Seavill, Peter W.,Holt, Katherine B.,Wilden, Jonathan D.
, p. 29300 - 29304 (2019)
We report an efficient and sustainable electrochemical synthesis of copper(i) acetylides using simultaneous copper oxidation and Hofmann elimination of quaternary ammonium salts. The electrochemically-generated base was also regenerated electrochemically,
Access to difluoromethylated alkynes through the castro-stephens reaction
Besset, Tatiana,Poisson, Thomas,Pannecoucke, Xavier
, p. 7220 - 7225 (2015/02/02)
An efficient synthesis of difluoromethylated alkynes is described. A panel of readily available CuI acetylides undergo direct difluoromethylation by using BrCF2CO2Et, which is an inexpensive, easy to handle, commercially available fluorinated reagent. The reaction, which is based on a Castro-Stephens transformation, proceeds smoothly under mild conditions offering a new synthetic route for the direct introduction of the difluoromethylated group into alkynes that does not involve ozone-depleting reagents. The resulting products were obtained with good yields by using CsOPiv and Cu(OAc)2 as additives.