Process Safety Evaluation of a Tungsten-Catalyzed Hydrogen Peroxide Epoxidation Resulting In a Runaway Laboratory Reaction-Reference-Cited by-同舟云学术

Process Safety Evaluation of a Tungsten-Catalyzed Hydrogen Peroxide Epoxidation Resulting In a Runaway Laboratory Reaction

Published:2011-10-14 Issue:6 Volume:15 Page:1464-1469
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Shilcrat Susan¹

Affiliation:

1. Investigational Manufacturing Operations, GlaxoSmithKline Pharmaceutical R&D, 709 Swedeland Road, King of Prussia, Pennsylvania 19406, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op200133q

Reference24 articles.

1. Synthesis of Side-Chain Unsaturatedendo- andexo-Brevicomins. Representatives of Pheromone Analogs in the Dioxabicyclo[3.2.1]octane Series

2. Palladium-mediated vicinal cleavage of allyl epoxides with retention of stereochemistry: a cis hydroxylation equivalent

3. Practical and Environmentally Friendly Epoxidation of Olefins Using Oxone

4. Epoxidation of Allyl Chloride to Epichlorohydrin by a Reversible Supported Catalyst with H2O2 under Solvent-Free Conditions

5. Epoxidations with 30% hydrogen peroxide catalyzed by tungstic acid in buffered media

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