Stereoselective Michael addition of the imines of .alpha.-amino esters in the presence of lithium bromide/1,8-diazabicyclo[5.4.0]undec-7-ene
- 1 July 1990
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 55 (14), 4411-4417
- https://doi.org/10.1021/jo00301a037
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Resolution and use in α-amino acid synthesis of imidazolidinone glycine derivativesTetrahedron, 1988
- Stereospecific alkylation of the Schiff base ester of alanine with 2-substituted-(E)- and -(Z)-vinyl bromides. An efficient synthesis of 2-methyl-(E)-3,4-didehydroglutamic acid, a potent substrate-induced irreversible inhibitor of L-glutamate-1-decarboxylaseThe Journal of Organic Chemistry, 1980
- .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