Alkylation of silyl enol ethers with pummerer generated vinyl thionium ions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. The indole 2-3-quinodimethane strategy for the synthesis of indole alkaloids
2. Mild reaction of pummerer rearrangement products with aromatic compounds in the presence of lewis acids. Application to the preparation of arylmethylene ketones, arylacetoesters, and arylacetonitriles.
3. Alkylation of aromatic compounds with pummerer rearrangement intermediates. Application to the preparation of methyl-aryl compounds
4. The methoxycarbonylalkylation and methoxycarbonylalkylidenation of silyl enol ethers
5. Synthetic transformations using trimethylsilyl iodide: The generation of vinyl sulfides from sulfoxides
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1. Sulfoxide synthesis from sulfinate esters under Pummerer-like conditions;Chemical Communications;2020
2. Catalytic Generation of Vinylthionium Ions. (4 + 3)-Cycloadditions and Friedel–Crafts Alkylations;Organic Letters;2014-08-11
3. Pummerer-type reactions in the (2-methylsulfanyl-2-phosphonyl) thiopyran 1-oxide series;Tetrahedron Letters;2008-07
4. Modern Pummerer-type reactions;Tetrahedron;2006-05
5. Intramolecular [4+3] Cycloadditions. Towards a Synthesis of Widdrol;HETEROCYCLES;2004
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