Stereoselektive Synthese von γ‐Aminocarbonsäureestern
- 1 December 1989
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 101 (12) , 1732-1734
- https://doi.org/10.1002/ange.19891011231
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Enantioselective Synthesis of (R)‐N‐Boc‐1‐amino‐2‐arylcyclopropene‐1‐carboxylic Acid Methyl EsterAngewandte Chemie International Edition in English, 1988
- Enantioselektive Synthese von (R)‐N‐Boc‐1‐amino‐2‐arylcyclopropen‐1‐carbonsäuremethylesterAngewandte Chemie, 1988
- Asymmetric synthesis of α-amino acids by alkylation of -[ -bis-(methylthio)methyleneglycyl]-2,5-bis(methoxymethoxymethyl)pyrrolidine and enantioselective synthesis of protected (2 ,9 )-2-amino-8-oxo-9,10-epoxydecanoic acidTetrahedron, 1988
- Resolution and use in α-amino acid synthesis of imidazolidinone glycine derivativesTetrahedron, 1988
- Enantioselective systheses of α-amino acids from 10-sulfonamido-isobornyl esters and di-t-butyl azodicarboxylateTetrahedron, 1988
- Carbohydrates as chiral templates: asymmetric ugi-synthesis of alpha-amino acids using galactosylamines as the chiral matricesTetrahedron, 1988
- New syntheses of α-amino acids based on n-acylimino acetatesTetrahedron, 1988
- Stereoselective Synthesis of β‐Amino Alcohols from Optically Active α‐Amino AcidsAngewandte Chemie International Edition in English, 1987
- Stereoselektive Synthese von β‐Aminoalkoholen aus optisch aktiven α‐AminosäurenAngewandte Chemie, 1987
- Electrophilic glycinates: new and versatile templates for asymmetric amino acid synthesisJournal of the American Chemical Society, 1986