H8-BINOL chiral imidodiphosphoric acids catalyzed cyclization reactions of β,γ-unsaturated α-ketoesters, arylamines and 1,3-dicarbonyl compounds: enantioselective synthesis of 1,4-dihydropyridines-Reference-Cited by-同舟云学术

H8-BINOL chiral imidodiphosphoric acids catalyzed cyclization reactions of β,γ-unsaturated α-ketoesters, arylamines and 1,3-dicarbonyl compounds: enantioselective synthesis of 1,4-dihydropyridines

Published:2015-09 Issue:17 Volume:26 Page:897-906
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

An Dong,Zhu Ziqian,Zhang Guangliang,Gao Yang,Gao Jigang,Han Xu,Zheng Liangyu,Zhang Suoqin

Funder

National Natural Science Foundation of China

Jilin Provincial Science and Technology Sustentation Program

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference45 articles.

1. Hantzsch-type dihydropyridine hypotensive agents

2. 1,4-dihydropyridine calcium channel ligands: Selectivity of action. The roles of pharmacokinetics, state-dependent interactions, channel isoforms, and other factors

3. Fused 1,4-Dihydropyridines as Potential Calcium Modulatory Compounds

4. Dihydropyridines: evaluation of their current and future pharmacological applications

5. Synthesis and biological evaluation of 2-amino-7,7-dimethyl 4-substituted-5-oxo-1-(3,4,5-trimethoxy)-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile derivatives as potential cytotoxic agents

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