Enantio- and diastereodivergent synthesis of all four diastereomers of the 2,6-disubstituted 3-piperidinol chiral building block
- 22 May 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (21) , 3715-3718
- https://doi.org/10.1016/0040-4039(95)00661-u
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Construction of Hydroxylated Alkaloids (.+-.)-Mannonolactam, (.+-.)-Deoxymannojirimycin, and (.+-.)-Prosopinine through Aza-AnnulationThe Journal of Organic Chemistry, 1994
- Aza-annulation as a route to hydroxylated alkaloid lipids. The synthesis of (±)-prosopinineTetrahedron Letters, 1994
- Azetidine, pyrrole, pyrrolidine, piperidine, and pyridine alkaloidsNatural Product Reports, 1992
- Pyrrole, pyrrolidine, piperidine, pyridine, and azepine alkaloidsNatural Product Reports, 1992
- Pyrrolidine, piperidine, and pyridine alkaloidsNatural Product Reports, 1990
- Total synthesis of (±)-isoprosopinine B and (±)-desoxoprosopinineJournal of the Chemical Society, Chemical Communications, 1985
- Application of the Oxygenative Nucleophile Introduction Reaction to 1-Alkoxycarbonyl-2-alkynyl-1,2-dihydropyridines. A Facile Synthesis of (±)-SedacryptineHETEROCYCLES, 1983
- Total Synthesis of ProsophyllineHETEROCYCLES, 1981
- Stereoselective Synthesis of dl-Carpamic Acid and dl-Azimic AcidHETEROCYCLES, 1980
- Stereoselective Synthesis of dl-Prosafrinine and dl-Pseudocarpamic AcidHETEROCYCLES, 1980