An α-alkylation/reduction of ketones via radical cyclizations of β-chloroethylsilyl enol ethers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Silylmethyl radical cyclization: new stereoselective method for 1,3-diol synthesis from allylic alcohols
2. Control of ring junction stereochemistry via radical cyclization
3. Stereospecific reductive methylation via a radical cyclization desilylation process
4. Methylation and hydroxymethylation involving free radicals. An application to stereoselective construction of 20(S) sterol side-chain
5. 1-Silylvinyl radical cyclization: silicon-mediated regio- and stereoselective hydroacylation and hydrovinylation of allyl alcohols
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1. Unique Diastereoselectivity Trends in Aminyl Radical Cyclizations onto Silyl Enol Ethers;The Journal of Organic Chemistry;2009-12-31
2. Preparation of Alcohols;Compendium of Organic Synthetic Methods;2006-11-22
3. The First Radical Method for the Introduction of an Ethynyl Group Using a Silicon Tether and Its Application to the Synthesis of 2‘-Deoxy-2‘-C-ethynylnucleosides1;The Journal of Organic Chemistry;2003-04-09
4. An Efficient Method for the Preparation of 1′α-Branched-Chain Sugar Pyrimidine Ribonucleosides from Uridine: The First Conversion of a Natural Nucleoside into 1′-Substituted Ribonucleosides;Chemistry;2001-06-01
5. Synthesis of Pyrimidine 2‘-Deoxy Ribonucleosides Branched at the 2‘-Position via Radical Atom-Transfer Cyclization Reaction with a Vinylsilyl Group as a Radical-Acceptor Tether1;The Journal of Organic Chemistry;2000-12-01
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