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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Doi:10.1016/j.bmc.2003.08.020
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(1999)Doi:10.1021/ic50202a058
(1979)Doi:10.1016/S0022-328X(98)00865-1
(1998)Doi:10.1246/bcsj.50.1097
(1977)Doi:10.1016/S0040-4039(01)83757-6
(1977)
