Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

José M. Jiménez, Joan Rifé, Rosa M. Ortuño

Research output: Contribution to journalArticleResearchpeer-review

18 Citations (Scopus)


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. © 1995.
Original languageEnglish
Pages (from-to)1849-1852
JournalTetrahedron: asymmetry
Issue number8
Publication statusPublished - 1 Jan 1995


Dive into the research topics of 'Enantioselective total syntheses of (-)-allo-coronamic acid, (-)-(Z)-2,3-methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe'. Together they form a unique fingerprint.

Cite this