Enantioselective recognition of an inherently chiral calix[4]arene crown-6 carboxylic acid cone conformer towards chiral aminoalcohols-Reference-Cited by-同舟云学术

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Enantioselective recognition of an inherently chiral calix[4]arene crown-6 carboxylic acid cone conformer towards chiral aminoalcohols

Published:2014 Issue:13 Volume:4 Page:6517
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Yang Ke,Li Si-Zhe,Wang Yin-Hu,Zhang Wen-Zhen,Xu Zhan-Hui,Zhou Xiang-Yong,Zhu Rong-Xiu,Luo Jun,Wan Qian

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C3RA46723F

Reference55 articles.

1. Inherently chiral calixarenes

2. Stereochemical control of calixarenes useful as rigid and conformationally diversiform platforms for molecular design

3. Phosphorus-Containing Chiral Macrocycles

4. A brief review ofCn-symmetric calixarenes and resorcinarenes

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1. Enantiospecific Analysis of Carboxylic Acids Using Cinchona Alkaloid Dimers as Chiral Solvating Agents;Analytical Chemistry;2024-05-02

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3. Synthesis and Optical Resolution of Inherently Chiral Fluorescent Calix[4]arenes and Their Application in Chiral Recognition;Synthesis;2023-05-24

4. Chiral Analysis of Pharmaceuticals Using NMR Spectroscopy: A Review;Asian Journal of Organic Chemistry;2022-11-24

5. Chiral Recognition of Hydantoin Derivatives Enabled by Tetraaza Macrocyclic Chiral Solvating Agents Using ¹H NMR Spectroscopy;The Journal of Organic Chemistry;2022-06-08

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