1,2‐Carbonyl Transposition of a Protected Rubanone: Stereoselective synthesis of bicyclic and tricyclic lactams derived from quinidine
- 1 January 1998
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 81 (5-8), 1429-1438
- https://doi.org/10.1002/hlca.19980810551
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- From Quinidine to new Enantiopure Materials–Tricyclic AllylicN,O-Acetals and a Stereospecific, Onepot Conversion of 1,2-Secondary, Tertiary Diols into SpiroepoxidesChemistry – A European Journal, 1996
- Face‐Selective and endo‐Selective Cycloadditions with Enantiomerically Pure CyclopentadienesEuropean Journal of Inorganic Chemistry, 1994
- Access to naturally occurring cyclooctanoids by two-carbon intercalation. Total synthesis of (+)-ceroplastol IJournal of the American Chemical Society, 1993
- Facial selectivity of the intramolecular SN2' cyclization: stereocontrolled total synthesis of brevianamide BJournal of the American Chemical Society, 1988
- Total synthesis of (.+-.)-chaenorhineJournal of the American Chemical Society, 1983
- Carbonyl group transpositionsChemical Society Reviews, 1982
- The brevianamides: a new class of fungal alkaloidJournal of the Chemical Society D: Chemical Communications, 1969
- The conversion of hecogenin acetate into 11-oxotigogenin acetateJournal of the Chemical Society, 1954
- Über Steroide. 118. Mitteilung. Ein neues Verfahren zur Herstellung von Steroiden mit 11β‐Hydroxylgruppe. I. Versuche an Verbindungen der SpirostanreiheHelvetica Chimica Acta, 1952
- Über Steroide und Sexualhormone. (95. Mitteilung). Herstellung von 2‐Keto‐, 2 α‐Oxy‐ und 2 β‐Oxy‐cholestanHelvetica Chimica Acta, 1944