Gallium Chloride-Mediated Hydrolysis of Dithioacetals
- 1 May 1990
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 19 (5), 831-834
- https://doi.org/10.1246/cl.1990.831
Abstract
Acyclic dithioacetals of ketones are easily hydrolyzed with the action of gallium chloride in the presence of A) water or B) methanol with bubbling oxygen to give the parent carbonyl compounds in high yields.Keywords
This publication has 3 references indexed in Scilit:
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- Gallium‐induced Barbier coupling of carbonyl compounds with allyl iodideApplied Organometallic Chemistry, 1988
- Alkylmetal asymmetric reduction. XVI. Tris(-myrtanyl)gallium: An unusual organometallic compound as enantioselective reducing agent of ketonesTetrahedron Letters, 1985