Conformational Analysis and Intramolecular Interactions of l-Proline Methyl Ester and Its N-Acetylated Derivative through Spectroscopic and Theoretical Studies-Reference-Cited by-同舟云学术

Conformational Analysis and Intramolecular Interactions of l-Proline Methyl Ester and Its N-Acetylated Derivative through Spectroscopic and Theoretical Studies

Published:2014-02-21 Issue:9 Volume:118 Page:1748-1758
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Braga Carolyne B.¹,Ducati Lucas C.²,Tormena Cláudio F.¹,Rittner Roberto¹

Affiliation:

1. Physical Organic Chemistry Laboratory, Chemistry Institute, University of Campinas, 13083-970 Campinas, SP, Brazil

2. Chemistry Institute, University of Sao Paulo, 05513-970 São Paulo, SP, Brazil

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp5007632

Reference41 articles.

1. Ab Initio Studies of Amino Acid Conformations. 1. The Conformers of Alanine, Serine, and Cysteine

2. The Structure of Neutral Proline

3. Lowest-Lying Conformers of Alanine: Pushing Theory to Ascertain Precise Energetics and Semiexperimental Re Structures

4. Proline Zwitterion Dynamics in Solution, Glass, and Crystalline State

5. Zwitterion vs Neutral Structures of Amino Acids Stabilized by a Negatively Charged Site: Infrared Photodissociation and Computations of Proline–Chloride Anion

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