Absolute Configurations of N,N-Dialkyl α-Amino Acids and β-Amino Alcohols from Exciton-Coupled Circular Dichroism Spectra of Cu(II) Complexes
Author:
Affiliation:
1. Department of Chemistry, New York University, New York, New York 10003
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol990715a
Reference20 articles.
1. Determination of the Absolute Configuration of Optically Active Compounds by Means of X-Rays
2. Optically Active Amines. 41.1 Application of the Benzene Chirality Rule to Chiral Ring-Substituted Benzylcarbinamines and Benzylcarbinamine Salts
3. Asymmetric substituent effect on the reaction of (R)- and (S)-indan-1-carboxylic acids with (S)-α-phenylethylamine derivatives
4. Chirality Assignment of Amines and Amino Alcohols Based on Circular Dichroism Induced by Helix Formation of a Stereoregular Poly((4-carboxyphenyl)acetylene) through Acid−Base Complexation
5. Nakanishi, K.; Berova, N. InCircular Dichroism: Principles and Applications; Nakanishi, K., Berova, N., Woody, R. W., Eds.; VCH Publishers: New York, 1994; p 361.
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