Stereoselective synthesis of enantiopure cyclopropane didehydroamino acid derivatives: (−)-(Z)-2-Benzyloxycarbonylamino-4,5-cyclopropane-2-hexenodioic acid dimethyl ester
- 30 September 1994
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 5 (9) , 1657-1660
- https://doi.org/10.1016/0957-4166(94)80074-x
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Asymmetric 1,3-dipolar cycloadditions to 5-(R)-menthyloxy-2(5H)-furanoneTetrahedron: Asymmetry, 1994
- Opportunities in asymmetric synthesis: An industrial prospectTetrahedron, 1994
- The Stereoselective Photochemical Addition of Alcohols to 5-Substituted Furan-2(5H)-onesSynlett, 1992
- D-3,4-‘cyclopropylglutamate’ isomers as nmda receptor ligands: Synthesis and enantioselective activity.Tetrahedron Letters, 1990
- Cyclopropane amino acidsTetrahedron, 1990
- A new stereoselective synthesis of a γ-azetidinylgb-hydroxy-α-amino acid moiety of mugineic acid — a formal synthesis of mugineic acidTetrahedron Letters, 1990
- Diels-alder cycloadditions of chiral butenolides with butadiene and isoprene:diastereofacial selectivity and regioselectivityTetrahedron, 1988
- Didehydroamino Acids (DDAA) and Didehydropeptides (DDP)Synthesis, 1988
- Synthesis of the enantiomers of umbelactoneTetrahedron, 1987
- Stereochemical control of nature's biosynthetic pathways:A general strategy for the synthesis 0f polypropionate-derived structural units from a single chiral progenitorTetrahedron, 1987