Design and Syntheses of Novel Calix[4](aza)crowns: Neutral Receptors for α‐Amino Acids
Author:
Affiliation:
1. a College of Chemistry and Materials Science, Fujian Normal University , Fuzhou, China
2. b State Key Laboratory of Structural Chemistry , Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou, China
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910600978150
Reference11 articles.
1. Calixarenes, Macrocycles with(Almost) Unlimited Possibilities
2. A xanthone-based neutral receptor for zwitterionic amino acids
3. Dominant factors affecting extraction behavior of amino compounds by a calix[6]arene carboxylic acid derivative
4. Liquid membrane transport of amino acids by a calix[6]arene carboxylic acid derivative
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1. Synthesis of hydrazones containing sterically hindered phenol groups and tetrathiacalix[4]arene fragment;Russian Journal of Organic Chemistry;2012-10
2. Synthesis and coordination ability of tartrate-derived N-alkyl dicarbohydrazides towards Cu2+ ions;Arkivoc;2012-09-06
3. An expedient synthesis and conformational features of acylhydrazone macrocycles derived from tartaric acid: evidence of water and π aromatic hydrogen bond interactions;Tetrahedron: Asymmetry;2012-02
4. Syntheses of Novel Chiral Calix[4]crown: Lariat Calix[4]-1,3-aza-crowns with Chiral Amino Acid Groups as Branched Chains;Synthetic Communications;2011-08-04
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