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Synlett 2000; 2000(6): 0805-0806
DOI: 10.1055/s-2000-6692
DOI: 10.1055/s-2000-6692
letter
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Zirconium Tetrachloride (ZrCl4) as an Efficient and Chemoselective Catalyst for Conversion of Carbonyl Compounds to 1,3-Oxathiolanes
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
![](https://www.thieme-connect.de/media/synlett/200006/lookinside/thumbnails/10.1055-s-2000-6692-1.jpg)
Different types of aldehydes and ketones can be efficiently converted into their corresponding 1,3-oxathiolanes using 2-mercaptoethanol (1.5 - 3.2 equiv.) in the presence of catalytic amount (0.04 - 0.15 equiv.) of ZrCl4 in CH2Cl2 as solvent at room temperature. Chemoselective monothioacetalization of aldehydes in the presence of ketones can also be achieved in high yield. The work-up is easy and removal of water is not necessary.
acetals - 1,3-oxathiolanes - protecting groups - zirconium tetrachloride - O,S-acetals