Are Carboxyl Groups the Most Acidic Sites in Amino Acids? Gas-Phase Acidity, H/D Exchange Experiments, and Computations on Cysteine and Its Conjugate Base-Reference-Cited by-同舟云学术

Are Carboxyl Groups the Most Acidic Sites in Amino Acids? Gas-Phase Acidity, H/D Exchange Experiments, and Computations on Cysteine and Its Conjugate Base

Published:2007-04-10 Issue:17 Volume:129 Page:5403-5407
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Tian Zhixin¹,Pawlow Anna¹,Poutsma John C.¹,Kass Steven R.¹

Affiliation:

1. Contribution from the Department of Chemistry, The College of William and Mary, Williamsburg, Virginia 23187, and Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0666194

Reference34 articles.

1. The kinetic method of making thermochemical determinations

2. Additional data on valine, isoleucine, leucine, and methionine were cited in ref 1 and can be found in: Locke, M. J. Ph.D. Thesis, University of California, Irvine, CA, 1981.

3. Regio- and stereoselectivity of chiral binaphthyl reductive aminoalkylation. Rotational conformation and electron distribution of alkali-metal biarylides

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