𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Radical Intermediates in the Jacobsen – Katsuki Epoxidation

✍ Scribed by Luigi Cavallo; Heiko Jacobsen

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
102 KB
Volume
39
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Jacobsen–Katsuki Epoxidation and Its
The Jacobsen–Katsuki Epoxidation and Its Controversial Mechanism
✍ Priv.-Doz. Dr. Torsten Linker 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB

Epoxidation reactions have been established as an important method for the formation of carbon-oxygen bonds. In 1980 Sharpless and Katsuki developed an enantioselective variant for allylic alcohols which is still one of the most elegant methods in asymmetric synthesis. ['] Over the last few years un

Selectivity Enhancement for the Jacobsen
Selectivity Enhancement for the Jacobsen–Katsuki Epoxidation in Fluorinated Solvents
✍ Nizam Havare; Dietmar A. Plattner 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 German ⚖ 169 KB

## Abstract magnified image In 1,1,1,2,3,4,4,5,5,5‐Decafluoropentane using 2‐phenylpyridine __N‐__oxide as donor ligand, the enantioselectivity of the __Jacobsen–Katsuki__ epoxidation is improved up to 10% ee as compared to established protocols.

ChemInform Abstract: Selectivity Enhance
ChemInform Abstract: Selectivity Enhancement for the Jacobsen—Katsuki Epoxidation in Fluorinated Solvents.
✍ Nizam Havare; Dietmar A. Plattner 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 22 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v