Electrophilic 5-endo-trig Cyclizations of 2-Silyl-3-alkenols. A Stereoselective Route to Polysubstituted Tetrahydrofurans. -The scope and limitations of the 5-endo-trig-like cyclization of 9 2-silyl-3-alkenols, e.g. (I), to give tetrahydrofurans, e.g. (III), is investigated. The regioselectivity see
✦ LIBER ✦
Stereoselective synthesis of substituted tetrahydrofurans via selenoetherification of 2-silyl-3-alkenols. A study of allylic stereocontrol
✍ Scribed by Yannick Landais; Denis Planchenault; Valéry Weber
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 254 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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