Electrophilic 5-endo-trig cyclisations of 2-silyl-3-alkenols. A stereoselective route to polysubstituted tetrahydrofurans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference55 articles.
1. Rules for ring closure
2. Stereoselection in iodolactonisations of 3-silyloxy-5-alkenoic acids
3. Iodine-induced cyclisations of (E)- and (Z)-3-hydroxy-5-alkenoates: Stereoselective approaches to trisubstituted tetrahydrofurans
4. Iodoetherification of homoallylic alcohols : A stereoselective approach to tetrahydrofurans
5. A stereoselective route to trans-2,5-disubstituted tetrahydrofurans
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