Epoxidation of Olefinic Compounds with Combined Use of Molecular Oxygen and Propionaldehyde Diethyl Acetal Catalyzed by Cobalt(II) Complex. Efficient Method for the Preparation of Acid-sensitive Epoxides
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/22/9/22_9_1579/_pdf
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1. Recent advances in the preparation and synthetic applications of oxiranes
2. The mechanism of epoxidation of olefins by peracids
3. Epoxidation reaction with m-chloroperoxybenzoic acid in water
4. High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxide
5. Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesol
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1. Cobalt(II) acetylacetonate;Fieser and Fieser's Reagents for Organic Synthesis;2013-04-26
2. Cobalt( II ) acetylacetonate;Fieser and Fieser's Reagents for Organic Synthesis;2013-04-26
3. Cobalt(II) acetylacetonate;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15
4. ChemInform Abstract: Epoxidation of Olefinic Compounds with Combined Use of Molecular Oxygen and Propionaldehyde Diethyl Acetal Catalyzed by a Cobalt(II) Complex. Efficient Method for the Preparation of Acid-Sensitive Epoxides;ChemInform;2010-08-19
5. Cobalt(II) acetylacetonate;Fieser and Fieser's Reagents for Organic Synthesis;2010-02-16
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