Summary
The purpose of this study was to examine the conditions of sulfenylation reactions of chiralα-amino esters Schiff bases to protect the chirality in theα-position.
Similar content being viewed by others
References
El Achqar A, Roumestant ML, Viallefont P (1988) Reactions of Schiff base anions with electrophiles: role of the initial stereochemistry. Tetrahedron Lett 29: 2441–2444
El Marini A, Roumestant ML, Pappalardo L, Viallefont P (1989) Utilisation des organocuprates dans la synthèse desα-aminoacides hétérocycliques. Bull Soc Chim Fr 4: 554–558
Horner L, Doms G (1978) Studien zum Vorgang der Wasserstoffübertragung 51 Raneynickel als Reagenz zur hydrierenden Abspaltung des Chalkogenatoms aus Schwefel-Selen-und Tellur-Verbindungen. Phosphorus Sulfur 4: 259–265
Newman MS, Walborsky HM (1950) Reduction ofα- andβ-ketoesters. JA Chem Soc 72: 4295–4297
Oguri T, Kawai N, Shioiri T, Yamada S (1978) Aminoacids and peptides. XXIX. A new efficient derivatives with recycling of a chiral reagent, asymmetric alkylation of achiral Schiff base from glycine. Chem Pharm Bull 26: 803–808
Schmidt H (1960) Spatial isomerism in the pinane series.VI. Hydroxypinocamphone and the two diastereoisomericα-pinene glycols. Chem Ber 93: 2485–2490
Tabcheh M, El Achqar A, Pappalardo L, Roumestant ML, Viallefont P (1991) Alkylation and protonation of chiral Schiff bases: diastereoselectivity as a function of the nature of reactants. Tetrahedron 47: 4611–4618
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Bentama, A., Hoarau, S., Pappalardo, L. et al. Sulfenylation of chiral Schiff bases. Amino Acids 7, 105–108 (1994). https://doi.org/10.1007/BF00808452
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00808452