Synthesis of highly enantiomerically enriched N-Boc-α-amino ketones from pseudoephedrine N-Boc-α-amino acid amides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. A one-step synthesis of pseudoephedrine glycinamide, a versatile precursor for the synthesis of α-amino acids
2. Practical method for the synthesis of D- or L-.alpha.-amino acids by the alkylation of (+)- or (-)-pseudoephedrine glycinamide.
3. .alpha.-Amino acids as chiral educts for asymmetric products. Amino acylation with N-acylamino acids
4. .alpha.-Amino acids as chiral educts for asymmetric products. Aminoacylation of metallo alkyls and alkenyls
5. Asymmetric synthesis of optically active threo- and erythro-pyrrolidinylbenzyl alcohol by the highly stereospecific arylation of (S)-proline and the subsequent highly diastereoselective reduction of the α-amino ketone
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