Enantioselective systheses of α-amino acids from 10-sulfonamido-isobornyl esters and di-t-butyl azodicarboxylate
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (17) , 5541-5552
- https://doi.org/10.1016/s0040-4020(01)86059-2
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Enantioselective synthesis of nonproteinogenic amino acidsPublished by Springer Nature ,2005
- Asymmetric halogenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure α-amino acids.Tetrahedron Letters, 1987
- Asymmetric syntheses of α-amino acids from α-halogenated 10-sulfonamido-isobornyl esters.Tetrahedron Letters, 1986
- Asymmetric synthesis of α-amino acids by alkylation of a glycine amide derivative bearing chiral 2,5-disubstituted pyrrolidine as an amine componentTetrahedron Letters, 1986
- Electrophilic glycinates: new and versatile templates for asymmetric amino acid synthesisJournal of the American Chemical Society, 1986
- The Chiral Glycine Enolate Derivative from 1‐Benzoyl‐2‐(tert‐butyl)‐3‐methyl‐1,3‐imidazolidin‐4‐one is Alkylated in the 5‐Position with Relative Topicitylk. Preliminary CommunicationHelvetica Chimica Acta, 1985
- Enantio- and diastereo-selective synthesis of amino acids via the reaction of allylic boron compounds with α-imino-estersJournal of the Chemical Society, Chemical Communications, 1985
- Neue natürliche AminosäurenAngewandte Chemie, 1983
- Asymmetric hydrogenationAccounts of Chemical Research, 1983
- Wittig‐Umlagerung von AllylethernNachrichten aus Chemie, Technik und Laboratorium, 1982