A concise enantioselective route to (+)- and (-)-allokainic acid from D- and L- serine has been established by enantio- and diastereoselective tandem Michael reaction methodology for the construction of three chiral centers in a single stage.
Enantioselective synthesis of (+)- and (-)-α-allokainic acid
BENETTI, Simonetta;
1990
Abstract
A concise enantioselective route to (+)- and (-)-allokainic acid from D- and L- serine has been established by enantio- and diastereoselective tandem Michael reaction methodology for the construction of three chiral centers in a single stage.File in questo prodotto:
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