Diastereoselective intramolecular diels-alder reaction of N-alkoxycarbonyl -1-aza-1,3-butadienes and a total synthesis of the piperidine alkaloid, (±)-sedridine.
- 31 December 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (34) , 4371-4374
- https://doi.org/10.1016/s0040-4039(00)92173-7
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A new method for generation and intramolecular diels-alder reaction of N-acyl and N-alkoxycarbonyl-1-aza-1,3-butadibnes. A one-pot synthesis of 1,7,8,8a-tetrahydro-3(2H)-indolizinones and 1,2,3,8,9,9a-hexahydro-4(4h)-quinolinones from α,β-unsaturated aldehydesTetrahedron Letters, 1990
- New reagents. X. Reagents for functionalization. Triphosgene: a crystalline substitute for phosgene.Journal of Synthetic Organic Chemistry, Japan, 1990
- The Diels-Alder reaction of 1-azadienes. The effect of an α-cyano substituentTetrahedron Letters, 1989
- Carbonochloridic Acid(Trichloro Methyl Ester)Journal of Synthetic Organic Chemistry, Japan, 1989
- Diels-Alder reaction of 1-azadienes. A total synthesis of deoxynupharidineThe Journal of Organic Chemistry, 1985
- The IntramolecularDiels–Alder ReactionPublished by Wiley ,1984
- Diels-Alder reactions of 1-azadienesJournal of the American Chemical Society, 1983
- Diels-Alder reaction of 1-azadienesJournal of the American Chemical Society, 1981
- The stereochemistry of nitrone cycloadditions. d1-allosedamine and d1-sedridine.Tetrahedron Letters, 1978
- The complete configuration of sedridine and of pelletierineRecueil des Travaux Chimiques des Pays-Bas, 1965