On-water” reduction of α-keto amide by Hantzsch ester: A chemoselective catalyst- and additive-free way to α-hydroxy amide - ScienceDirect
Iodoimidazolinium-Catalyzed Reduction of Quinoline by Hantzsch Ester: Halogen Bond or Brønsted Acid Catalysis | The Journal of Organic Chemistry
出版物
Hantzsch Ester, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
Hantzsch Ester Hydrogenation
Hantzsch Ester‐Mediated Synthesis of Phenanthridines under Visible‐Light Irradiation - Nagode - 2020 - Chemistry – An Asian Journal - Wiley Online Library
Silver‐Catalyzed Biomimetic Transfer Hydrogenation of N‐Heteroaromatics with Hantzsch Esters as NADH Analogues - Pi - 2017 - ChemistrySelect - Wiley Online Library
Hantzsch Ester, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
Recent Developments in Asymmetric Transfer Hydrogenation with Hantzsch Esters: A Biomimetic Approach - You - 2007 - Chemistry – An Asian Journal - Wiley Online Library
4-Substituted Hantzsch Esters as Alkylation Reagents in Organic Synthesis
Hantzsch Ester Hydrogenation
Hantzsch ester - Wikipedia
Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15268H
Transfer Hydrogenation with Hantzsch Ester | Chem-Station Int. Ed.
Hantzsch Ester, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
Hantzsch Ester, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
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
Mechanism of the highly selective transfer hydrogenation using Hantzsch... | Download Scientific Diagram
Reaction design and mechanistic proposal. One chiral rhodium catalyst... | Download Scientific Diagram
Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis - Organic & Biomolecular Chemistry (RSC Publishing)
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
Reducing Alkenes Like Nature Does
Transfer hydrogenation with Hantzsch esters and related organic hydride donors - Chemical Society Reviews (RSC Publishing)
B(C 6 F 5 ) 3 -catalyzed transfer hydrogenations of imines with Hantzsch esters - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB00023A
