The ω, φ, and ψ Space of N-Hydroxy-N-methylacetamide and N-Acetyl-N ‘-hydroxy-N ‘-methylamide of Alanine and Their Boron Isosteres
Author:
Affiliation:
1. Department of Pharmaceutical Chemistry, Bombay College of Pharmacy, Kalina, Santacruz (E), Mumbai 400 098, India
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry,Computer Science Applications
Link
https://pubs.acs.org/doi/pdf/10.1021/ct050242v
Reference39 articles.
1. Experimental and theoretical studies of the barrier to rotation about the N-C.alpha. and C.alpha.-C' bonds (.vphi. and .psi.) in amides and peptides
2. Designing peptide receptor agonists and antagonists
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2. Integrating the intrinsic conformational preferences of noncoded α-amino acids modified at the peptide bond into the noncoded amino acids database;Proteins: Structure, Function, and Bioinformatics;2011-04-12
3. Isosteres of peptides: boron analogs as dipolar forms of α-amino acids – a theoretical study;Journal of Physical Organic Chemistry;2007
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