Functionalized 2-azabicyclo[3.3.1]nonanes. III.1 reductive rearrangement of an hexahydro-2-oxopyrano[3,2-b]pyridine
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (12), 1297-1298
- https://doi.org/10.1016/s0040-4039(00)87087-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Application of metalated enamines to alkaloid synthesis. An expedient approach to the synthesis of morphine-based analgesicsJournal of the American Chemical Society, 1980
- Synthesis of 2-Azabicyclo[3.3.1]nonanesHETEROCYCLES, 1980
- Stereoselective synthesis of (.+-.)-gymnomitrolJournal of the American Chemical Society, 1979
- Stereoselective total syntheses of (+-)-longicyclene, (+-)-longicamphor, and (+-)-longiborneolThe Journal of Organic Chemistry, 1974
- Synthesis of 1, 2, 3, 4, 5, 6-Hexahydro-1, 5-methano-2-methylpyrido [2, 3-c] azocineCHEMICAL & PHARMACEUTICAL BULLETIN, 1974
- Total synthesis of (±)-trichoderminJournal of the Chemical Society, Perkin Transactions 1, 1973
- Reaction of enol lactone with lithium aluminum hydrideTetrahedron Letters, 1965
- 48. Bridged ring systems. Part III. Homoallylic alcohols of the bicyclo[3,3,1]nonane seriesJournal of the Chemical Society, 1964