Ruthenium(III) Chloride-Catalyzed Thioacetalization of Carbonyl Compounds: Scope, Selectivity, and Limitations

A variety of carbonyl compounds can be easily and rapidly converted to the corresponding cyclic and acylic dithioacetals in the presence of a catalytic amount of ruthenium chloride in acetonitrile at room temperature. Some of the major advantages of this protocol are high chemoselectivity, operation...

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Veröffentlicht in:	Advanced synthesis & catalysis 2005-04, Vol.347 (5), p.673-676
1. Verfasser:	De, Surya Kanta
Format:	Artikel
Sprache:	eng
Schlagworte:	aldehydes chemoselectivity dithioacetals ketones protecting groups ruthenium chloride
Online-Zugang:	Volltext
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