Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 85, Issue 7, Pages 5109-5113Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c00284
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- JSPS KAKENNHI [C 17K08220]
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The addition of methanesulfonic acid to N-(2,6-dimethylpyridin-4-yl)-N-methyl-2-iso-propylaniline led to the selective protonation of the pyridine nitrogen atom, resulting in a significant deceleration of the rotation rates around both N-pyridyl and N-(i-Pr)phenyl bonds through a relayed brake mechanism.
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