Stereospecific hydroxylation of chiral allylic β-hydroxysulfoxides: Applications to the asymmetric synthesis of optically active vicinal triols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxides
2. Reduction of .beta.-keto sulfoxides: a highly efficient asymmetric synthesis of both enantiomers of allylic alcohols
3. Highly diastereoselective reduction of chiral β-ketosulphoxides under chelation control: application to the synthesis of (R)-(+)-n-hexadecano-1,5-lactone
4. Osmium tetroxide catalyzed hydroxylation of hindered olefins
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1. A Non-Aldol Preparation of Enantiopure Propionate-Derived Motifs with the Assistance of Chiral Sulfoxides: Application to a Convergent Synthesis of the Lactone Core of Octalactins;European Journal of Organic Chemistry;2015-07-17
2. Osmium Tetroxide;Encyclopedia of Reagents for Organic Synthesis;2013-04-22
3. Novel Oxidation Reaction of Tertiary Amines with Osmium Tetroxide;Synlett;2009-08-07
4. Diisobutylaluminum Hydride;Encyclopedia of Reagents for Organic Synthesis;2008-09-15
5. References;Stereoselective Synthesis;2007-12-15
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