Metal-Mediated Diastereoselective Allylation Reaction of Chiral α,β-Epoxy Aldehyde. Part 1.
✍ Scribed by Su Ho Park; Hee Kyoon Yoon; Hyo Won Lee
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 23 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Allylindium reagents, prepared from excess allylic halide (Br or I) and indium metal, react with α,β-unsaturated ketones and aldehydes to give, after aerobic acidic workup, homoallyl-substituted vinylcyclopropanes. This process was explored and developed after a chance discovery arising from a side
## 1999 hydroxycarboxylic acids hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters P 0280 ## 26 -081 Regio-and Diastereoselective Boron-Mediated Aldol Reactions of Chiral α,β,γ,δ-Unsaturated N-Acyloxazolidinones. -The established boron-mediated stereoselective aldol