NAD(P)+-NAD(P)H model. 38. Reduction of aldehyde by 1,4-dihydroquinolin derivative
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Reduction by a model of NAD(P)H. 29. Kinetics and isotope effects for the reduction of substituted trifluoroacetophenone
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1. A strong hydride donating, acid stable and reusable 1,4-dihydropyridine for selective aldimine and aldehyde reductions;Organic & Biomolecular Chemistry;2022
2. Mechanistic insight into the catalytic hydrogenation of nonactivated aldehydes with a Hantzsch ester in the presence of a series of organoboranes: NMR and DFT studies;RSC Advances;2019
3. Organoborane-Catalyzed Hydrogenation of Unactivated Aldehydes with a Hantzsch Ester as a Synthetic NAD(P)H Analogue;Synlett;2015-06-23
4. Atropisomeric Transition State Analogs;European Journal of Organic Chemistry;2000-04
5. An efficient synthesis of 3-cyanoquinoline derivatives;Tetrahedron Letters;1998-06
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