TY - JOUR
T1 - Self-assembled receptors for enantioselective recognition of chiral carboxylic acids in a highly cooperative manner
AU - Ishi-I, Tsutomu
AU - Crego-Calama, Mercedes
AU - Timmerman, Peter
AU - Reinhoudt, David N.
AU - Shinkai, Seiji
PY - 2002/6/3
Y1 - 2002/6/3
N2 - Stereospecific recognition of substrate molecules for certain chiral carboxylic acids is achieved by a noncovalent receptor system based on acid-base interactions of amino groups in the host system with the carboxylic acids. Enantioselectivity in the binding process is caused by secondary interactions with a chiral platform that preorganizes the amino functionalities (see scheme).
AB - Stereospecific recognition of substrate molecules for certain chiral carboxylic acids is achieved by a noncovalent receptor system based on acid-base interactions of amino groups in the host system with the carboxylic acids. Enantioselectivity in the binding process is caused by secondary interactions with a chiral platform that preorganizes the amino functionalities (see scheme).
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U2 - 10.1002/1521-3773(20020603)41:11<1924::AID-ANIE1924>3.0.CO;2-H
DO - 10.1002/1521-3773(20020603)41:11<1924::AID-ANIE1924>3.0.CO;2-H
M3 - Article
C2 - 19750635
AN - SCOPUS:0037014085
SN - 1433-7851
VL - 41
SP - 1924
EP - 1929
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 11
ER -