Conformational Preferences of trans-1,2- and cis-1,3-Cyclohexanedicarboxylic Acids in Water and Dimethyl Sulfoxide as a Function of the Ionization State As Determined from NMR Spectroscopy and Density Functional Theory Quantum Mechanical Calculations-Reference-Cited by-同舟云学术

Conformational Preferences of trans-1,2- and cis-1,3-Cyclohexanedicarboxylic Acids in Water and Dimethyl Sulfoxide as a Function of the Ionization State As Determined from NMR Spectroscopy and Density Functional Theory Quantum Mechanical Calculations

Published:2012-08-28 Issue:36 Volume:134 Page:14772-14780
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Garza Alejandro J.¹,Nag Mrinmoy¹,Carroll William R.¹,Goddard William A.¹,Roberts John D.¹

Affiliation:

1. Crellin Laboratory of Chemistry and ‡Materials and Process Simulation Center, California Institute of Technology, Pasadena, California 91125, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja302133s

Reference40 articles.

1. Physical Organic Chemistry: Quantitative Conformational Analysis; Calculation Methods

2. Cyclohexane-Based Conformationally Controlled Crowns and Podands

3. Trans-1,2-Cyclohexanedicarboxylic acid derivatives as pH-trigger for conformationally controlled crowns

4. Axial/equatorial proportions for 2-substituted cyclohexanones

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