## Abstract For Abstract see ChemInform Abstract in Full Text.
Lewis Acid Mediated endo-Cyclization of Trimethylsilylmethylenecyclopropyl Imines — A Stereoselective Route to Indolizidines.
✍ Scribed by Suvi Rajamaki; Jeremy D. Kilburn
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 19 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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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