Preparation of 2-Substituted Vinylamino Acid Derivatives
- 1 September 1991
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 21 (17) , 1743-1754
- https://doi.org/10.1080/00397919108021572
Abstract
Solid-liquid phase transfer catalysis in the absence of any added solvent efficiently promotes Michael addition of glycine Schiff bases to phenylvinylsulfoxide. The vinyl group was formed by thermolysis of the phenylsulfinyl function.Keywords
This publication has 23 references indexed in Scilit:
- Synthesis, brain uptake, and pharmacological properties of a glyceryl lipid containing GABA and the GABA-T inhibitor .gamma.-vinyl-GABAJournal of Medicinal Chemistry, 1990
- Stereoselective synthesis of optically pure β,γ-unsaturated α-amino acids in both L and D configurationsTetrahedron Letters, 1989
- N-(Benzyloxycarbonyl)-L-vinylglycike Methyl Ester from L-Methionine Methyl Ester HydrochlorideSynthetic Communications, 1989
- ORGANIC REACTIONS WITHOUT SOLVENT: MICHAEL ADDITIONS ON AN UNSATURATED SULFONE AND SULFOXIDEPhosphorus and Sulfur and the Related Elements, 1988
- The use of semiempirical energy partitioning terms in the study of through space (homoaromatic) interactionsTetrahedron, 1988
- Synthesis of α-amino acids with β,γ-unsaturated side chainsTetrahedron, 1987
- The free radical chemistry of carboxylic esters of 2-selenopyridine--oxide: a convenient synthesis of (L)-vinylglycineTetrahedron, 1985
- Synthesis of β,γ-unsaturated amino acids as potential catalytic irreversible enzyme inhibitorsTetrahedron Letters, 1977
- Mechanisms of action of naturally occurring irreversible enzyme inhibitorsAccounts of Chemical Research, 1975
- A synthesis of trans-1-alkylthio-1-alkenesTetrahedron, 1966