Palladium-Catalyzed Oxidative Silylation of Simple Olefins To Give Allylsilanes Using Hexamethyldisilane and Molecular Oxygen as the Sole Oxidant-Reference-Cited by-同舟云学术

Palladium-Catalyzed Oxidative Silylation of Simple Olefins To Give Allylsilanes Using Hexamethyldisilane and Molecular Oxygen as the Sole Oxidant

Published:2015-07-01 Issue:14 Volume:80 Page:7317-7320
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nakai Syunji¹,Matsui Masaki¹,Shimizu Yosuke¹,Adachi Yurina¹,Obora Yasushi¹

Affiliation:

1. Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan

Funder

New Energy and Industrial Technology Development Organization

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01216

Reference66 articles.

1. Silylallyl Anions in Organic Synthesis: A Study in Regio- and Stereoselectivity

2. Diastereoselective Reactions of Chiral Allyl and Allenyl Silanes with Activated C:X .pi.-Bonds

3. Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride

4. Reactions of allylsilanes with quinones. Synthesis of allyl-substituted hydroquinones

5. Observations on various silyl-cuprate reagents

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