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A Functionalized, Deep Cavitand Catalyzes the Aminolysis of a Choline Derivative
Author(s) -
Arnaud Gissot,
Julius Rebek
Publication year - 2004
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja049074r
Subject(s) - aminolysis , chemistry , cavitand , derivative (finance) , substrate (aquarium) , stereochemistry , catalysis , organic chemistry , molecule , supramolecular chemistry , oceanography , financial economics , economics , geology
The aminolysis of choline p-nitrophenyl carbonate is catalyzed with turnover by a deep cavitand bearing an introverted pyridone function. The synergy of action between the recognition of the guest in the binding pocket and the catalytic activity brought to bear by the pyridone is responsible for the high substrate specificity observed.

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