Chiral mono and diamide derivatives of calix[4]arene for enantiomeric recognition of chiral amines-Reference-Cited by-同舟云学术

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Chiral mono and diamide derivatives of calix[4]arene for enantiomeric recognition of chiral amines

Published:2007 Issue:1 Volume:20 Page:26-34
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Kocabas Erdal,Durmaz Mustafa,Alpaydin Sabri,Sirit Abdulkadir,Yilmaz Mustafa

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference59 articles.

1. Chiral recognition of (18-crown-6)-tetracarboxylic acid as a chiral selector determined by NMR spectroscopy

2. A practical approach to chiral separations by liquid chromatography. editor. New York: VCH; 1994.

3. Molecular Recognition between 2,4,6-Triaminopyrimidine Lipid Monolayers and Complementary Barbituric Molecules at the Air/Water Interface: Effects of Hydrophilic Spacer, Ionic Strength, and pH

4. Molecular Recognition-Induced Function and Competitive Replacement by Hydrogen-Bonding Interactions: Amphiphilic Barbituric Acid Derivatives, 2,4,6-Triaminopyrimidine, and Related Structures at the Air−Water Interface

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3. Enantiodiscrimination of carboxylic acids using the diphenylprolinol NMR chiral solvating agents;Organic Chemistry Frontiers;2016

4. New Technologies Powered by Protein-Binding Calixarenes;Calixarenes and Beyond;2016

5. Chiral Cups (Calixarenes) via Dötz Benzannulation;Synthesis;2014-05-28

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