![The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/98ccb751-df92-487e-a7dc-74cce885fe35/mscheme6.jpg)
The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library
![Toward a mechanistic understanding of oxidative homocoupling: the Glaser–Hay reaction - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C4CY00322E Toward a mechanistic understanding of oxidative homocoupling: the Glaser–Hay reaction - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C4CY00322E](https://pubs.rsc.org/image/article/2014/CY/c4cy00322e/c4cy00322e-s3_hi-res.gif)
Toward a mechanistic understanding of oxidative homocoupling: the Glaser–Hay reaction - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C4CY00322E
![The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/99cf6598-9b51-43bb-b22d-bbe35b72eb54/mscheme2.jpg)
The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library
![Cu(I)-azidopyrrolo[3,2-d]pyrimidine Catalyzed Glaser–Hay Reaction under Mild Conditions | ACS Organic & Inorganic Au Cu(I)-azidopyrrolo[3,2-d]pyrimidine Catalyzed Glaser–Hay Reaction under Mild Conditions | ACS Organic & Inorganic Au](https://pubs.acs.org/cms/10.1021/acsorginorgau.1c00015/asset/images/large/gg1c00015_0001.jpeg)
Cu(I)-azidopyrrolo[3,2-d]pyrimidine Catalyzed Glaser–Hay Reaction under Mild Conditions | ACS Organic & Inorganic Au
![The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/30c9e44e-a17f-4732-8059-13e34a95d951/mfig000.jpg)
The Glaser–Hay Reaction: Optimization and Scope Based on 13C NMR Kinetics Experiments - Vilhelmsen - 2013 - European Journal of Organic Chemistry - Wiley Online Library
Glaser–Hay hetero-coupling in a bimetallic regime: a Ni(ii)/Ag(i) assisted base, ligand and additive free route to selective unsymmetrical 1,3-diynes - Chemical Communications (RSC Publishing)
![Glaser-Hay hetero-coupling in a bimetallic regime: a Ni(ii)/Ag(i) assisted base, ligand and additive free route to selective unsymmetrical 1,3-diynes. | Semantic Scholar Glaser-Hay hetero-coupling in a bimetallic regime: a Ni(ii)/Ag(i) assisted base, ligand and additive free route to selective unsymmetrical 1,3-diynes. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/2cc61f3091202e81610e7f63d25133455fdb384b/3-Figure1-1.png)