Tetrahedron Asymmetry p. 609 - 624 (1995)
Update date:2022-08-02
Topics:
Anaya
Barton
Gero
Grande
Hernando
Laso
Different stereocontrolled syntheses of optically active 1,3,6-trisubstituted and 1,2,3,6-tetrasubstituted carbapenems are reported. D-glucosamine, as chiral auxiliary, trans-cinnamaldehyde and methoxyacetyl chloride were used as starting materials in the Staudinger ketene-imine monobactam formation. Radical cyclization and oxidation reactions led to the desired carbapenems.
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Doi:10.14233/ajchem.2014.15551
(2014)Doi:10.1021/acs.joc.1c00590
(2021)Doi:10.1021/ol501753b
(2014)Doi:10.1021/jo00111a007
(1995)Doi:10.1021/ja00986a025
(1967)Doi:10.1016/0040-4039(94)00020-Y
(1995)