Iodine-mediated rearrangements of diallylsilanes
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. Stereocontrolled Synthesis of 1,3-Diols from Enones: Cooperative Lewis Base-Mediated Intramolecular Carbonyl Hydrosilylations
2. Direct Conversion of β-Hydroxyketones to Cyclic Disiloxanes
3. Noncatalyzed Stereoselective Allylation of Carbonyl Compounds with Allylsilacyclobutanes
4. Silicon-directed aldol reactions. Rate acceleration by small rings
5. Chemistry of Enoxysilacyclobutanes: Highly Selective Uncatalyzed Aldol Additions
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1. Synthesis of (+)-epicolidine C and the 6/6/6/5 tetracyclic core of spylidone;Tetrahedron Letters;2024-08
2. Regioselective Fluorohydrin Synthesis from Allylsilanes and Evidence for a Silicon–Fluorine Gauche Effect;The Journal of Organic Chemistry;2024-03-08
3. Sequential iodine-mediated diallylsilane rearrangement/asymmetric dihydroxylation: Synthesis and reactions of enantioenriched oxasilacycles;Tetrahedron Letters;2021-10
4. Revisiting applications of molecular iodine in organic synthesis;New Journal of Chemistry;2021
5. Chemoselective Carbonyl Allylations with Alkoxyallylsiletanes;The Journal of Organic Chemistry;2019-02-27
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