Publication | Closed Access
A Convenient General Access to α-Sulfenylated Acetophenones and Alkanones
12
Citations
10
References
1989
Year
Abstract Friedel-crafts AcylationEngineeringNatural SciencesDiversity-oriented SynthesisReady AccessOrganic Chemistryα-Sulfenylated AlkanonesChemistryConvenient General AccessHeterocycle ChemistrySynthetic ChemistryBiomolecular Engineering
Abstract Friedel-Crafts acylation of arenes with methylthio- (1) or phenylthio-acetyl chloride (2) provides ready access to α-methylthio- or α-phenylthio-substituted acetophenones. The acyl chlorides 1 and 2 reacted also with organoaluminum reagents to give α-sulfenylated alkanones.
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