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Progress on Chiral NAD(P)H Model Compounds.

Authors :
Cui-Bing Bai
Nai-Xing Wang
Yalan Xing
Xing-Wang Lan
Source :
Synlett; 2017, Vol. 28 Issue 4, p402-414, 13p, 31 Diagrams, 2 Charts, 3 Graphs
Publication Year :
2017

Abstract

NAD(P)H and NAD<superscript>+</superscript> have a significant role in biochemistry, and many NAD(P)H models received particular attention. Research in NADH models mainly focuses on asymmetric reduction and life sciences. Over the past few decades, a particularly large number of new chiral NAD(P)H models have appeared, and there have been significant developments in this area. We summarized advanced research in chiral NAD(P)H models in this paper. These models not only show very good performance in asymmetric reduction, but also have excellent fluorescence features. In addition, we present a discussion about some recent studies on the asymmetric reduction of NAD(P)H-dependent dehydrogenase, and we open a new door on research into NAD(P)H models. At last, some advances focused on the fluorescence phenomenon of some chiral NAD(P)H models have also been summarized. 1 Introduction 2 NAD(P)H Models with Symmetric Structure 2.1 Chiral NAD(P)H Models with C <subscript>1</subscript> Symmetry 2.2 Chiral NAD(P)H Models with C <subscript>2</subscript> Symmetry 2.3 Chiral NAD(P)H Models with C <subscript>3</subscript> Symmetry 3 Symmetric Reduction 3.1 Effect of the Substituents of Dihydronicotinamide 3.2 Effect of the C-4 Substituent of Dihydropyridine 3.3 Special Structures 3.4 Applying Dehydrogenase to Biocatalytic Asymmetric Reductions with NADPH 4 Fluorescence Properties 5 Conclusion. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09365214
Volume :
28
Issue :
4
Database :
Complementary Index
Journal :
Synlett
Publication Type :
Academic Journal
Accession number :
121374184
Full Text :
https://doi.org/10.1055/s-0036-1588665