Tetrahedron Letters p. 4917 - 4920 (1990)
Update date:2022-08-02
Topics:
Barco
Benetti
Casolari
Pollini
Spalluto
A concise enantioselective route to (+)- and (-)-α-allokainic acid from D- and L-serine respectively has been established by enantio- and diastereo-selective tandem Michael reaction methodology for the construction of three chiral centers in a single stage.
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(1977)
