Remarkable generality in scope of DATs/Cu catalysts for enantioselective nitroaldol reaction is described; excellent levels of stereoinduction are recorded for a range of aldehydes (ee 81-99%, 17 examples) and the possibility to employ the present catalytic system as the key step for the preparation of highly functionalized tetrahydro-isoquinolines is demonstrated

Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes

PICCINELLI, FABIO;
2007-01-01

Abstract

Remarkable generality in scope of DATs/Cu catalysts for enantioselective nitroaldol reaction is described; excellent levels of stereoinduction are recorded for a range of aldehydes (ee 81-99%, 17 examples) and the possibility to employ the present catalytic system as the key step for the preparation of highly functionalized tetrahydro-isoquinolines is demonstrated
2007
nitroaldol reaction; chiral copper complexes; asymmetric catalisys
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/342604
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