An Expedient Procedure for the Oxidative Cleavage of Olefinic Bonds with PhI(OAc)2, NMO, and Catalytic OsO4-Reference-Cited by-同舟云学术

An Expedient Procedure for the Oxidative Cleavage of Olefinic Bonds with PhI(OAc)2, NMO, and Catalytic OsO4

Published:2010-02-25 Issue:7 Volume:12 Page:1552-1555
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Nicolaou K. C.¹,Adsool Vikrant A.¹,Hale Christopher R. H.¹

Affiliation:

1. Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, and the Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol100290a

Reference24 articles.

1. Notes - Osmium Tetroxide-Catalyzed Periodate Oxidation of Olefinic Bonds

2. Use of the Composite Material RuO2/BaTi4O9 as an Environmentally Benign Solid Catalyst for the Oxidative Cleavage of Olefins

3. Heterogeneously catalysed cleavage of carbon–carbon double bonds with hydrogen peroxide using calcined heteropolyacids on oxide supports

4. Efficient Oxidative Cleavage of Olefins to Carboxylic Acids with Hydrogen Peroxide Catalyzed by Methyltrioctylammonium Tetrakis(oxodiperoxotungsto)phosphate(3−) under Two-Phase Conditions. Synthetic Aspects and Investigation of the Reaction Course

5. A "Green" Route to Adipic Acid: Direct Oxidation of Cyclohexenes with 30 Percent Hydrogen Peroxide

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