Synthesis of trans and cis-α-(car☐ycyclopropyl)glycines. Novel neuroinhibitory amino acids as L-glutamate analogue
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (10) , 1181-1184
- https://doi.org/10.1016/s0040-4039(00)86682-4
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Acromelic acid, a novel excitatory amino acid from a poisonous mushroom: effects on the crayfish neuromuscular junctionBrain Research, 1986
- Selective transformation of N--butoxycarbonyl group into n-alkoxy-carbonyl group n-carboxylate ion equivalentTetrahedron Letters, 1985
- The palladium(II)-assisted syntheses of (±)α-(methylenecyclopropyl)glycine and (±)trans-α-(carboxycyclopropyl) glycine, two bioactive amino acids.Tetrahedron Letters, 1985
- Effects of glutamic acid analogues on identifiable giant neurones, sensitive to β‐hydroxy‐L‐glutamic acid, of an African giant snail (Achatina fulica Férussac)British Journal of Pharmacology, 1985
- Synthesis of the serine equivalent, (2) and (2)-amino-3-butenol derivatives. Synthetic approaches to the metal chelating poly-amino acid, “aspergillomarasmine A”Tetrahedron Letters, 1984
- Total synthesis of (-)-domoic acid. A revision of the original structureJournal of the American Chemical Society, 1982
- STRUCTURE‐ACTIVITY STUDIES ON AN EXCITATORY RECEPTOR FOR GLUTAMATE ON LEECH RETZIUS NEURONESBritish Journal of Pharmacology, 1980
- Cyclopropane amino acids from Aesculus and BlighiaPhytochemistry, 1969