Stereoselective reactions of lithium enolates derived from N-BOC protected pyroglutamic esters
- 1 September 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (38) , 8665-8678
- https://doi.org/10.1016/s0040-4020(01)96272-6
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Stereocontrolled Access to all-transα,β,γ-Substituted Pyrrolidinones and Pyrrolidines of High Optical Purity from D-Pyroglutamic AcidSynlett, 1990
- Synthesis of (2S,4S)- and (2S,4R)-4-Substituted Glutamic Acid Analogues for Neuroexcitatory Activity StudiesHETEROCYCLES, 1990
- Synthesis of (+)-1-Deoxynojirimycin from (S)-Pyroglutamic AcidHETEROCYCLES, 1989
- Synthesis of (2R,3S)-2-Hydroxymethyl-3-hydroxypyrrolidine and the Geissman-Waiss Lactone from (S)-Pyroglutamic AcidHETEROCYCLES, 1988
- A new approach for the total synthesis of L-.GAMMA.-carboxyglutamic acid : Utility of ruthenium tetroxide oxidation.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- A novel synthesis of L-pyroglutamic acid derivatives from L-proline : Utility of N-protecting groups for ruthenium tetroxide oxidation of cyclic .ALPHA.-amino acids.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- Enantioselective synthesis and absolute configuration of (-)-.alpha.-kainic acidJournal of the American Chemical Society, 1982
- Total synthesis of (-)-domoic acid. A revision of the original structureJournal of the American Chemical Society, 1982
- Total synthesis of pretyrosine (arogenate)Journal of the American Chemical Society, 1981
- Sulfenylation and selenenylation of lactamsThe Journal of Organic Chemistry, 1976