The Role of Amino Acid Esters and the Amide Group in the Chiral Induction Process by a Novel Monoamide-Linked Monozinc Bisporphyrinate
Author:
Publisher
Wiley
Subject
Inorganic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/zaac.201400124/fullpdf
Reference29 articles.
1. Probing molecular chirality by CD-sensitive dimeric metalloporphyrin hosts
2. Chirality-Sensing Supramolecular Systems
3. Chiral memory: Induction, amplification, and switching in porphyrin assemblies
4. Zinc Porphyrin Tweezer in Host−Guest Complexation: Determination of Absolute Configurations of Diamines, Amino Acids, and Amino Alcohols by Circular Dichroism
5. Chiral Recognition by CD-Sensitive Dimeric Zinc Porphyrin Host. 2. Structural Studies of Host−Guest Complexes with Chiral Alcohol and Monoamine Conjugates
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1. Stoichiometry-controlled chirality inversion in the amide-linked zinc bisporphyrinates induced by amino acid esters;Journal of Porphyrins and Phthalocyanines;2023-05-12
2. Enantioselectivity of a tartaric acid amide linked zinc bisporphyrinate towards amino acid esters;Dyes and Pigments;2020-05
3. Crystallographic and Spectroscopic Studies of a Host–Guest Complex Consisting of a Novel Zinc Trisporphyrinate and a Chiral Monoamine;Inorganic Chemistry;2016-03-29
4. Discrimination between alkyl and aryl substituents of chiral monoamines by m-phthalic diamide-linked zinc bisporphyrinates;Dalton Transactions;2015
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