![Ruthenium-Catalyzed Propargylic Reduction of Propargylic Alcohols with Hantzsch Ester,Organometallics - X-MOL Ruthenium-Catalyzed Propargylic Reduction of Propargylic Alcohols with Hantzsch Ester,Organometallics - X-MOL](https://xpic.x-mol.com/20200609%2F10.1021_acs.organomet.0c00187.gif)
Ruthenium-Catalyzed Propargylic Reduction of Propargylic Alcohols with Hantzsch Ester,Organometallics - X-MOL
![Molecules | Free Full-Text | A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst | HTML Molecules | Free Full-Text | A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst | HTML](https://www.mdpi.com/molecules/molecules-21-01000/article_deploy/html/images/molecules-21-01000-sch010.png)
Molecules | Free Full-Text | A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst | HTML
Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis - Organic & Biomolecular Chemistry (RSC Publishing)
![Proposed mechanism for the oxidation of Hantzsch dihydropyridines by... | Download Scientific Diagram Proposed mechanism for the oxidation of Hantzsch dihydropyridines by... | Download Scientific Diagram](https://www.researchgate.net/profile/Ja-Squella/publication/8631799/figure/fig6/AS:277893633593355@1443266413581/Proposed-mechanism-for-the-oxidation-of-Hantzsch-dihydropyridines-by-electrogenerated.png)
Proposed mechanism for the oxidation of Hantzsch dihydropyridines by... | Download Scientific Diagram
![Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15268H Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15268H](https://pubs.rsc.org/image/article/2012/CS/c1cs15268h/c1cs15268h-s51.gif)
Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15268H
![Mechanism of the highly selective transfer hydrogenation using Hantzsch... | Download Scientific Diagram Mechanism of the highly selective transfer hydrogenation using Hantzsch... | Download Scientific Diagram](https://www.researchgate.net/profile/Robert-Comito/publication/317703442/figure/fig20/AS:507456615665668@1497998493838/Mechanism-of-the-highly-selective-transfer-hydrogenation-using-Hantzsch-ester-hydride_Q640.jpg)
Mechanism of the highly selective transfer hydrogenation using Hantzsch... | Download Scientific Diagram
![Reaction design and mechanistic proposal. One chiral rhodium catalyst... | Download Scientific Diagram Reaction design and mechanistic proposal. One chiral rhodium catalyst... | Download Scientific Diagram](https://www.researchgate.net/publication/319420954/figure/fig1/AS:613947036151841@1523387788469/Reaction-design-and-mechanistic-proposal-One-chiral-rhodium-catalyst-for-both.png)
Reaction design and mechanistic proposal. One chiral rhodium catalyst... | Download Scientific Diagram
Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing)
![Substituted Hantzsch Esters as Versatile Radical Reservoirs in Photoredox Reactions - Gu - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library Substituted Hantzsch Esters as Versatile Radical Reservoirs in Photoredox Reactions - Gu - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d2c2d603-5693-41ed-bc2a-27d46f58eb18/adsc201701348-fig-5009-m.jpg)
Substituted Hantzsch Esters as Versatile Radical Reservoirs in Photoredox Reactions - Gu - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
![Molecules | Free Full-Text | A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst | HTML Molecules | Free Full-Text | A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst | HTML](https://www.mdpi.com/molecules/molecules-21-01000/article_deploy/html/images/molecules-21-01000-sch002.png)
Molecules | Free Full-Text | A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst | HTML
![Electron paramagnetic resonance spectroscopic studies of the electron transfer reaction of Hantzsch ester and a pyrylium salt - RSC Advances (RSC Publishing) DOI:10.1039/C8RA05693E Electron paramagnetic resonance spectroscopic studies of the electron transfer reaction of Hantzsch ester and a pyrylium salt - RSC Advances (RSC Publishing) DOI:10.1039/C8RA05693E](https://pubs.rsc.org/image/article/2018/RA/c8ra05693e/c8ra05693e-s2_hi-res.gif)
Electron paramagnetic resonance spectroscopic studies of the electron transfer reaction of Hantzsch ester and a pyrylium salt - RSC Advances (RSC Publishing) DOI:10.1039/C8RA05693E
![Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB01289C Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB01289C](https://pubs.rsc.org/image/article/2019/OB/c9ob01289c/c9ob01289c-s27_hi-res.gif)