Resolution and use in α-amino acid synthesis of imidazolidinone glycine derivatives
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (17), 5277-5292
- https://doi.org/10.1016/s0040-4020(01)86036-1
Abstract
No abstract availableThis publication has 53 references indexed in Scilit:
- Methionin als Vorläufer zur enantioselektiven Synthese α‐verzweigter Vinylglycine und anderer AminosäurenHelvetica Chimica Acta, 1986
- Enantioselektive α‐Alkylierung von Asparagin‐ und Glutaminsäure über die Dilithium‐enolatocarboxylate von 2‐[3‐Benzoyl‐2‐(tert‐butyl)‐1‐methyl‐5‐oxoimidazolidin‐4‐yl]essigsäure und 3‐[3‐Benzoyl‐2‐(tert‐butyl)‐1‐methyl‐5‐oxoimidazolidin‐4‐yl]propionsäureHelvetica Chimica Acta, 1985
- Alkylierung in der 2‐Stellung von (2S, 4R)‐ 4‐Hydroxyprolin unter RetentionHelvetica Chimica Acta, 1985
- Hydroxyalkylierungen von Cystein über das Enolat von (2R,5R)‐2(tert‐Butyl)‐1‐aza‐3‐oxa‐7‐thiabicyclo[3.3.0]octan‐4‐on und unter Selbstreproduktion des CiralitätszentrumsHelvetica Chimica Acta, 1984
- (S)-(–)-1-Amino-2-(siloxymethyl)pyrrolidines: novel and efficient reagents for chromatographic resolution of α-substituted aldehydesJournal of the Chemical Society, Chemical Communications, 1984
- Crystal and molecular structure of 1-lithio-3,6-diethoxy-2,5-dimethyl-1,2-dihydropyrazine, the lithiated bis-lactim ether of the diketopiperazine from alanineJournal of the Chemical Society, Chemical Communications, 1984
- Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from α‐Heterosubstituted Carboxylic Acids. Preliminary CommunicationHelvetica Chimica Acta, 1981
- Amino acids and peptides. XXIX. A new efficient asymmetric synthesis of .ALPHA.-amino acid derivatives with recycle of a chiral reagent - asymmetric alkylation of a chiral Schiff base from glycine.CHEMICAL & PHARMACEUTICAL BULLETIN, 1978
- Herstellung von ar‐Pentafluor‐L‐phenylalaninHelvetica Chimica Acta, 1971
- The Use of N-Formylamino Acids in Peptide SynthesisJournal of the American Chemical Society, 1958