Abstract
The significance of
site selective functionalization stands upon the superior selectivity, easy
synthesis and diverse product utility. In this work we demonstrate the para-selective
introduction of versatile nitrile moiety, enabled by detachable and reusable
H-bonded auxiliary. The methodology holds its efficiency irrespective of
substrate electronic bias. The conspicuous shift in the step energetics was
probed by both experimental and computational mechanistic tools heralds the
inception of para-deuteration. The synthetic impact of the methodology
was highlighted with reusability of directing group and post synthetic
modifications
Supplementary materials
Title
para cyanation SI D. Maiti
Description
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