Synthesis of chiral NADH model compounds in the pyrrolo[3,2-b]pyridine series : models with a chiral group on the pyrrole nitrogen or on the carboxamide side chain
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Reduction by a model of NAD(P)H. 25. A chiral model which induces high asymmetry
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3. Efficient chirality transfer between a chiral 4-methyl-1,4-dihydropyridine and benzoylformic ester. An example of a pure intermolecular self-immolative process
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1. ChemInform Abstract: Synthesis of Chiral NADH Model Compounds in the Pyrrole (3,2-b) pyridine Series: Models with a Chiral Group on the Pyrrole Nitrogen or on the Carboxamide Side Chain.;ChemInform;2010-08-20
2. α-Hydroxylation of Enolates and Silyl Enol Ethers;Organic Reactions;2003-07-22
3. Multidrug resistance reversal activity of key ningalin analogues;Bioorganic & Medicinal Chemistry Letters;2003-05
4. Synthesis of 2,3-Difunctionalized 4-Nitropyrroles;The Journal of Organic Chemistry;2001-09-25
5. NAD(P)+−NAD(P)H Models. 90. Stereoselection Controlled by Electronic Effect of a Carbonyl Group in Oxidation of NAD(P)H Analog;The Journal of Organic Chemistry;2000-09-13
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