Arabinose as a chiral auxiliary for the asymmetric α-hydroxyallylation of aldehydes to syn-1,2-diols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. [(Z)-.gamma.-[(Diisopropylidene-.alpha.-D-mannopyranosyl)oxy]allyl]tributylstannane: A New Chiral Reagent for the Asymmetric .alpha.-Hydroxyallylation of Aldehydes
2. Asymmetric synthesis of syn 1,2-diols via the reaction of aldehydes with chiral .gamma.-(tetrahydropyranyloxy)allylstannanes
3. Selective asymmetric dihydroxylation (AD) of dienes
4. Chiral synthesis via organoboranes. 13. A highly diastereoselective and enantioselective addition of [(Z)-.gamma.-alkoxyallyl]diisopinocampheylboranes to aldehydes
5. Asymmetric synthesis of (–)-exo-brevicomin. Chirality transfer from a chiral (tetrahy-dropyranyloxyallyl)boronate in the condensation with aldehydes
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1. Enantioselective syn- and anti-Alkoxyallylation of Aldehydes via Brønsted Acid Catalysis;Organic Letters;2018-09-26
2. Addition To C=O Bonds I;Key Chiral Auxiliary Applications;2014
3. ChemInform Abstract: Arabinose as a Chiral Auxiliary for the Asymmetric α-Hydroxyallylation of Aldehydes to syn-1,2-Diols.;ChemInform;2010-06-22
4. Diastereo- and Enantioselective anti-Alkoxyallylation Employing Allylic gem-Dicarboxylates as Allyl Donors via Iridium-Catalyzed Transfer Hydrogenation;Journal of the American Chemical Society;2010-01-25
5. Nucleophilic Cyclopropanation Reaction with Bis(iodozincio)methane by 1,4-Addition to α,β-Unsaturated Carbonyl Compounds;Chemistry - An Asian Journal;2009-08-03
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