REDUCTION OFN-METHYLACRIDINIUM ION BY 3-AMINOCARBONYL-N-BENZYL-1,4-DIHYDROQUINOLINE: SUPPORTING EVIDENCE FOR THE MULTI-STEP MECHANISM OF THE NADH MODEL REDUCTION-Reference-Cited by-同舟云学术

REDUCTION OFN-METHYLACRIDINIUM ION BY 3-AMINOCARBONYL-N-BENZYL-1,4-DIHYDROQUINOLINE: SUPPORTING EVIDENCE FOR THE MULTI-STEP MECHANISM OF THE NADH MODEL REDUCTION

Published:1981-09-05 Issue:9 Volume:10 Page:1203-1206
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Shinkai Seiji,Tsuno Takaharu,Manabe Osamu

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference12 articles.

1. Reactions of dihydronicotinamides. I. Evidence for an intermediate in the reduction of trifluoroacetophenone by 1-substituted dihydronicotinamides

2. Model dehydrogenase reactions. Reduction of N-methylacridinium by reduced nicotinamide adenine dinucleotide and its derivatives

3. Model dehydrogenase reactions. Zinc ion catalyzed reduction of chelating aldehydes by N-propyl-1,4-dihydronicotinamides and borohydride

4. Model dehydrogenase reactions. Direct observation of a charge-transfer complex in a dihydronicotinamide reduction

5. Models for NADH coenzymes. Reactions of 2-carboxyl-substituted pyridines with N-alkyl-1,4-dihydronicotinamides

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