Diastereoselection in the reactions of thioallylic anions with benzaldehyde
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. C-alkylation of allyl, dithiocarbamates followed by allylicrearrangement
2. Lithiated S-(2-methoxyallyl) N,N-dimethyldithiocarbamate, a new, versatile reagent for the introduction of the acetonyl functional group into organic substrates
3. Metalated allylic ethers as homoenolate anion equivalents
4. Das Magnesium-Derivat des Thioacrolein-Dianions. Ein einfacher Zugang zu Vinyl- und Divinyloxiranen
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1. A new method for the synthesis of dithiocarbamates by CuI-catalyzed coupling reaction;Tetrahedron Letters;2007-07
2. By Proton-Metal Exchange with Acidic C-H Bonds1-5;Inorganic Reactions and Methods;2007-05-29
3. Diastereogene Addition von Crotyl-Metall-Verbindungen an Aldehyde;Angewandte Chemie;2006-01-16
4. The Synthesis and Configurational Stability of Enantioenriched α-Thioallyllithium Compounds and the Stereochemical Course of Their Electrophilic Substitution;European Journal of Organic Chemistry;2002-09
5. Hypervalent Iodine in Synthesis XXXV: A Simple and Convenient Stereospecific Synthesis of Vinyl Esters of Dithiocarbamic Acids;Synthetic Communications;1999-08
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