The addition of Organolithiums to Ketenethioacetals: a new cyclopentannulation sequence leading to indanes.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference31 articles.
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1. Regio- and Stereoselective Synthesis of 1,2,3-Trisubstituted Indanes from Diarylmethanols and Allylamides through Iron(III) Chloride Hexahydrate;Advanced Synthesis & Catalysis;2016-06-16
2. ChemInform Abstract: The Addition of Organolithiums to Ketene Thioacetals: A New Cyclopentannulation Sequence Leading to Indanes.;ChemInform;2010-08-21
3. Intramolecular Carbolithiation Reactions for the Synthesis of 2,4-Disubstituted Tetrahydro-quinolines: Evaluation of TMEDA and (−)-Sparteine as Ligands in the Stereoselectivity † Dedicated to Prof. Josep Font on the occasion of his 70th birthday.;Organic Letters;2009-02-17
4. Synthesis of Pyrrolo[1,2-b]isoquinolines through Mesityllithium-Mediated Intramolecular Carbolithiation;Synlett;2008-11-26
5. Stereoselective synthesis of thiaerythrinanes based on an α-amidoalkylation/RCM approach;Tetrahedron;2008-02
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