Alkylation of amino acids without loss of the optical activity: preparation of .alpha.-substituted proline derivatives. A case of self-reproduction of chirality
- 1 August 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 105 (16) , 5390-5398
- https://doi.org/10.1021/ja00354a034
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Substitution of HMPT by the cyclic urea DMPU as a cosolvent for highly reactive nucleophiles and basesHelvetica Chimica Acta, 1982
- Stereospezifische Synthese von (+)‐(3R, 4R)‐4‐Methyl‐3‐heptanol, das Enantiomere eines Pheromons des kleinen Ulmensplintkäfers (Scolytus multistriatus)Helvetica Chimica Acta, 1979
- Direct synthesis of .alpha.-halogenomethyl-.alpha.-amino acids from the parent .alpha.-amino acidsThe Journal of Organic Chemistry, 1979
- .alpha.-Alkylation and Michael addition of amino acids - a practical methodThe Journal of Organic Chemistry, 1977
- Alkylation and Michael additions of glycine ethyl ester. Use in .alpha.-amino acid synthesis and as acyl carbanion equivalentThe Journal of Organic Chemistry, 1976