Sequential iodine-mediated diallylsilane rearrangement/asymmetric dihydroxylation: Synthesis and reactions of enantioenriched oxasilacycles-Reference-Cited by-同舟云学术

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Sequential iodine-mediated diallylsilane rearrangement/asymmetric dihydroxylation: Synthesis and reactions of enantioenriched oxasilacycles

Published:2021-10 Issue: Volume:82 Page:153392
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Myers Christopher R.,Spaltenstein Paul,Baker Lauren K.,Schwans Cody L.,Clark Timothy B.,O'Neil Gregory W.

Funder

National Institutes of Health

American Chemical Society Petroleum Research Fund

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Iodine-mediated rearrangements of diallylsilanes

2. Lewis acid mediated domino allylation of diallylsilane to α,β-unsaturated ketones

3. Unusual product of the Si-C bond cleavage in diallyldiphenylsilane

4. Transformations of diallylsilanes under the action of electrophilic reagents

5. The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Regiodivergent Medium-Ring Oxasilacycle Synthesis from Diallylsilanes;HETEROCYCLES;2022

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