Enantioselective synthesis of α-hydroxyketones using the ditox asymmetric building block
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Ruthenium-catalyzed oxidative transformation of alkenes to .alpha.-ketols with peracetic acid. Simple synthesis of cortisone acetate
2. Concise asymmetric synthesis of (5S, 6S)- aeginetolide and (5S)- dihydroactinidiolide
3. Total synthesis of (±)-sterpuric acid
4. Stereoselective reduction of α-hydroxy ketones
5. cited by Maycock,6 ref 3
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1. Diarylpentanol constituents from the aerial part of Stelleropsis tianschanica;Journal of Asian Natural Products Research;2016-05-12
2. Diarylpentanoids from Diplomorpha canescens and Diplomorpha ganpi;Phytochemistry Letters;2012-06
3. Lead(IV) acetate mediated cleavage of β-hydroxy ethers: enantioselective synthesis of α-acetoxy carbonyl compounds;Tetrahedron;2011-11
4. Lead(IV) acetate oxidative ring-opening of 2,3-epoxy primary alcohols: a new entry to optically active α-hydroxy carbonyl compounds;Tetrahedron Letters;2011-08
5. ChemInform Abstract: Enantioselective Synthesis of α-Hydroxyketones Using the DiTOX Asymmetric Building Block.;ChemInform;2010-08-04
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