Regioselective opening of ring E in spirostan sapogenins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. STEROLS. LXXXI. CONVERSION OF SARSASA-POGENIN TO PREGNANEDIOL-3(α),20(α)
2. Sterols. LXXXVIII. Pregnanediols from Sarsasapogenin
3. Degradation of Steroidal Sapogenins to 16-Dehydropregnan-20-ones
4. Catalytic Isomerization of Spirostans to Furostenols1
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1. First synthesis of furostans bearing a 1, 3-dioxane ring at C-26. XRD, Hirshfeld surfaces analysis, DFT studies;Journal of Molecular Structure;2022-01
2. Stereospecific synthesis and rearrangement of 22S-23-acetylsapogenins;Steroids;2020-08
3. Regioselective Spirostan E-Ring Opening for the Synthesis of Dihydropyran Steroidal Frameworks;Organic Letters;2016-03-24
4. Regio- and stereoselective cleavage of steroidal 22-oxo-23-spiroketals catalyzed by BF3·Et2O;Steroids;2015-08
5. Regioselective cleavage of 22-oxo-23-spiroketals. Novel cholestanic frameworks with pyranone and cyclopentenone E rings on the side chain;Steroids;2012-04
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