BF3·OEt2-Catalyzed Unexpected Stereoselective Formation of 2,4-trans-Diallyl-2-methyl-6-aryltetrahydro-2H-pyrans with Quaternary Stereocenters | The Journal of Organic Chemistry
![Unique Synthetic Utility of BF3·OEt2 in the Highly Diastereoselective Reduction of Hydroxy Carbonyl and Dicarbonyl Substrates | Organic Letters Unique Synthetic Utility of BF3·OEt2 in the Highly Diastereoselective Reduction of Hydroxy Carbonyl and Dicarbonyl Substrates | Organic Letters](https://pubs.acs.org/cms/10.1021/ol000056y/asset/images/large/ol000056yn00001.jpeg)
Unique Synthetic Utility of BF3·OEt2 in the Highly Diastereoselective Reduction of Hydroxy Carbonyl and Dicarbonyl Substrates | Organic Letters
![Catalysts | Free Full-Text | BF3·Et2O-Promoted Decomposition of Cyclic α-Diazo-β-Hydroxy Ketones: Novel Insights into Mechanistic Aspects Catalysts | Free Full-Text | BF3·Et2O-Promoted Decomposition of Cyclic α-Diazo-β-Hydroxy Ketones: Novel Insights into Mechanistic Aspects](https://pub.mdpi-res.com/catalysts/catalysts-08-00600/article_deploy/html/images/catalysts-08-00600-ag-550.jpg?1570771183)