Search results for: Jose M. Jimenez
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Enantioselective Total Syntheses of (-)-allo-Coronamic Acid, (-)-(Z)-2,3-Methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe
Tetrahedron: Asymmetry > 1995 > 6 > 8 > 1849-1852
The title amino acids have been synthesized in 45, 47, and 63% overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as common key intermediate compounds.
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