Stereoselective reduction of C=X by a chiral 1,4-dihydropyridine (NADH-MIMIC) in a self-immolative process
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Efficient chirality transfer between a chiral 4-methyl-1,4-dihydropyridine and benzoylformic ester. An example of a pure intermolecular self-immolative process
2. The first nonenzymic stereospecific intramolecular reduction by an NADH-mimic containing a covalently bound carbonyl moiety
3. Marcus theory of hydride transfer from an anionic reduced deazaflavin to NAD+ analogs
4. Free-radical reduction reactions of chiral dihydronicotinamides. Enantioselective hydrogen atom transfer and electron-transfer processes during the reduction of ketones
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