Regioselective nucleophilic attack on N-BOC-pyroglutamate ethyl ester
- 15 September 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (38), 5589-5590
- https://doi.org/10.1016/s0040-4039(00)61153-x
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Enantioselective syntheses of Monomorium minutum ant venom alkaloids : (5R)-2-(5-Hexenyl)-5-nonyl-3,4-dihydro-2H-pyrrole and (2R,5R)-2-(5-hexenyl)-5-nonylpyrrolidine from (s)-pyroglutamic acid.Tetrahedron Letters, 1991
- Asymmetric synthesis from α-amino acids; some reactions of (S)-pyroglutamateTetrahedron Letters, 1991
- Convenient Preparation of Dissymmetrical Diesters of N-Boc Glutamic AcidSynthetic Communications, 1990
- Synthesis of (+)-1-Deoxynojirimycin from (S)-Pyroglutamic AcidHETEROCYCLES, 1989
- Regioselective mono-addition of lithium enolates to N-carbamoyl-L-pyroglutamatesTetrahedron Letters, 1988
- Direct Chain Elongation of N-Carbamoylpyroglutamate. An Efficient Synthesis of (−)-Pyrrolidine-2,5-Dicarboxylic AcidChemistry Letters, 1987
- Assignment of quaternary carbons via two‐bond heteronuclear selective NOE difference, a useful structure elucidation aidMagnetic Resonance in Chemistry, 1985
- A mild two-step method for the hydrolysis of lactams and secondary amidesThe Journal of Organic Chemistry, 1983
- 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