Allylation with Pummerer-generated substituted vinylthionium ions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Alkylation of enol silyl ethers by Pummerer-generated vinylthionium ions: a novel masked Michael reaction
2. OXIDATIVE COUPLING OF KETENE DITHIOACETALS WITH SILYLATED CARBON NUCLEOPHILES BY THE USE OF TRITYL TETRAFLUOROBORATE
3. The Trityl Cation Mediated Michael Reaction of Ethylthioketene Dithioacetals with Silyl Enol Ethers
4. The Trityl Cation Catalyzed Michael Type Reaction of Stannylated Nucleophiles with Ethylthioketene Dithioacetals
5. Generation ofF-Alkyl-substituted Vinyl Thionium Ion Intermediates and Their Reaction with Silyl Enol Ethers. A New Route to δ-F-Alkyl-α,β;γ,δ-unsaturated Carbonyl Compounds
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1. ChemInform Abstract: Allylation with Pummerer Generated Substituted Vinylthionium Ions.;ChemInform;2010-08-18
2. Intramolecular [4+3] Cycloadditions. Towards a Synthesis of Widdrol;HETEROCYCLES;2004
3. Homologation of ketones into carboxylic acids;Tetrahedron;2004-01
4. Carbon−Carbon Bond Forming Reactions Mediated by Silicon Lewis Acids;Chemical Reviews;2003-02-05
5. Trimethylsilyl trifluoromethanesulfonate (TMSOTf) andN,N-di-iso-propyl ethyl amine (Hünig base): an effective reagent combination for selective silylation and elimination reactions;Journal für praktische Chemie;1999-05
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