peri-Dimethylamino substituent effects on proton transfer at carbon in α-naphthylacetateesters: a model for mandelate racemase-Reference-Cited by-同舟云学术

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peri-Dimethylamino substituent effects on proton transfer at carbon in α-naphthylacetateesters: a model for mandelate racemase

Published:2012 Issue:3 Volume:10 Page:590-596
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Delley Richard J.,Bandyopadhyay Subhajit,Fox Mark A.,Schliehe Constanze,Hodgson David R. W.,Hollfelder Florian,Kirby Anthony J.,O'Donoghue AnnMarie C.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C1OB06525D

Reference30 articles.

1. Primary kinetic hydrogen isotope effects in deprotonations of a nitroalkane by intramolecular phenolate groups

2. Efficiency of Proton Transfer Catalysis in Models and Enzymes

3. Primary kinetic hydrogen isotope effects in deprotonations of carbon acids

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1. Evaluation of the Catalytic Contribution from a Positioned General Base in Ketosteroid Isomerase;Journal of the American Chemical Society;2016-07-27

2. Proton transfer reactions ofN-aryl triazolium salts: unusualortho-substituent effects;Journal of Physical Organic Chemistry;2014-12-07

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