Copper-catalyzed enantioselective Sonogashira-type oxidative cross-coupling of unactivated C(sp3)−H bonds with alkynes | Nature Communications
Synthesis and Use of Reactive Molecular Precursors for the Preparation of Carbon Nanomaterials
Homo-coupling of terminal alkynes on a noble metal surface | Nature Communications
Recent advances and applications of Glaser coupling employing greener protocols - RSC Advances (RSC Publishing) DOI:10.1039/C4RA02416H
Figure 2 from Preventing Alkyne-Alkyne (i.e., Glaser) Coupling Associated with the ATRP Synthesis of Alkyne-Functional Polymers/Macromonomers and for Alkynes under Click (i.e., CuAAC) Reaction Conditions. | Semantic Scholar
A merged copper(I/II) cluster isolated from Glaser coupling | Nature Communications
Chapter 11.6 Solutions | Green Organic Chemistry 1st Edition | Chegg.com
Hay Coupling - an overview | ScienceDirect Topics
3: The Glaser coupling (1869). | Download Scientific Diagram
The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library
Glaser Coupling | SpringerLink
Recent advances and applications of Glaser coupling employing greener protocols | Semantic Scholar
3: The Glaser coupling (1869). | Download Scientific Diagram
The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library
Glaser Coupling, Hay Coupling
Hay Coupling - an overview | ScienceDirect Topics
Chemistry lovers - The Cadiot–Chodkiewicz coupling The Cadiot–Chodkiewicz coupling in organic chemistry is a coupling reaction between a terminal alkyne and a haloalkyne catalyzed by a copper(I) salt such as copper(I) bromide
Glaser Coupling, Hay Coupling
Cadiot–Chodkiewicz coupling - Wikipedia
Glaser coupling - Wikipedia
Benzotriazole as an Efficient Ligand in Cu-Catalyzed Glaser Reaction. - Abstract - Europe PMC
Glaser Coupling | SpringerLink
