Conformationally restricted amino acids: Diastereoselective substitution at the β-position of L-tryptophan
- 1 October 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (42) , 6251-6254
- https://doi.org/10.1016/s0040-4039(00)60945-0
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- The Stereocontrolled Synthesis of (2S,3R)-3-Alkyl-L-aspartic Acids Using a 2-Azetidinone Framework as a Chiral TemplateSynlett, 1992
- Asymmetric syntheses of 1-aminocyclopropane-1-carboxylic acid derivatives.Journal of the American Chemical Society, 1991
- Benzyl (R)- and (S)-2-tert-butyl-5-oxo-oxazolidine-3-carboxylate for convenient preparation ofD- andL-threonine analogs from aldehydesEuropean Journal of Organic Chemistry, 1991
- Stereoselective synthesis of 3-alkylated glutamic acids: application to the synthesis of secokainic acidThe Journal of Organic Chemistry, 1991
- Stereoselektive Umsetzungen von rac‐, (R), oder (S)‐5‐Alkyliden‐2‐t‐butyl‐3‐methyl‐4‐oxo‐1‐imidazolidincarbonsäure‐t‐butylestern (chirale 2,3‐Dehydroaminosäure‐Derivate) und Herstellung einiger nichtproteinogener AminosäurenEuropean Journal of Organic Chemistry, 1991
- Diastereoselective synthesis of (2S,3R) 2-carboxy-3-pyrrolidine acetic acid, a simple kainic acid analogueTetrahedron Letters, 1991
- ()-pyroglutamic acid as a chiral starting material for asymmetric synthesisTetrahedron Letters, 1991
- Cooxidation reaction in the singlet oxygenation of cyclic and benzylic sulfides: S-hydroperoxysulfonium ylide intermediate as a new epoxidizing speciesJournal of the American Chemical Society, 1991
- Asymmetric intramolecular amidation of N-(tert-butoxycarbonyl)-3-hydroxy-4-pentenylamine. A new entry to chiral building blocks for the synthesis of biologically active nitrogen-containing compoundsThe Journal of Organic Chemistry, 1991
- Synthesis of homochiral hydroxy-α-amino acid derivativesTetrahedron Letters, 1990