Hantzsch Ester as a Visible‐Light Photoredox Catalyst for Transition‐Metal‐Free Coupling of Arylhalides and Arylsulfinates - Zhu - 2020 - Chemistry – A European Journal - Wiley Online Library
Transfer Hydrogenation with Hantzsch Ester | Chem-Station Int. Ed.
Transfer Hydrogenation with Hantzsch Ester | Chem-Station Int. Ed.
Hantzsch Ester Hydrogenation
Hantzsch ester triggered metal-free cascade approach to isoindolinones - ScienceDirect
Mechanism of the highly selective transfer hydrogenation using Hantzsch... | Download Scientific Diagram
Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15268H
Hantzsch Ester, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
Transfer hydrogenation with Hantzsch esters and related organic hydride donors. | Semantic Scholar
Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB01289C
Hantzsch Dihydropyridine (Pyridine) Synthesis
Hantzsch pyridine synthesis - overview
Transfer Hydrogenation with Hantzsch Ester | Chem-Station Int. Ed.
Hantzsch Ester, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
![Fesipmim]Cl as highly efficient and reusable catalyst for solventless synthesis of dihydropyridine derivatives through Hantzsch reaction | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12039-020-01770-9/MediaObjects/12039_2020_1770_Figa_HTML.png "Fesipmim]Cl as highly efficient and reusable catalyst for solventless synthesis of dihydropyridine derivatives through Hantzsch reaction | SpringerLink")
Fesipmim]Cl as highly efficient and reusable catalyst for solventless synthesis of dihydropyridine derivatives through Hantzsch reaction | SpringerLink
Hantzsch ester - Wikipedia
B(C 6 F 5 ) 3 -catalyzed transfer hydrogenations of imines with Hantzsch esters - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB00023A
Hantzsch Ester Hydrogenation
Recent Developments in Asymmetric Transfer Hydrogenation with Hantzsch Esters: A Biomimetic Approach - You - 2007 - Chemistry – An Asian Journal - Wiley Online Library
Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15268H
Hantzsch Ester as a Visible‐Light Photoredox Catalyst for Transition‐Metal‐Free Coupling of Arylhalides and Arylsulfinates - Zhu - 2020 - Chemistry – A European Journal - Wiley Online Library
On-water” reduction of α-keto amide by Hantzsch ester: A chemoselective catalyst- and additive-free way to α-hydroxy amide - ScienceDirect
Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB01289C
