✦ LIBER ✦

A novel allylic hydroxylation of sterically hindered olefins by Fe-porphyrin-catalyzed mCPBA oxidation

✍ Scribed by Toshiro Konoike; Yoshitaka Araki; Yasuhiko Kanda

Book ID: 104262219
Publisher: Elsevier Science
Year: 1999
Tongue: French
Weight: 231 KB
Volume: 40
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(99)01437-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Novel Allylic Hyd

ChemInform Abstract: A Novel Allylic Hydroxylation of Sterically Hindered Olefins by Fe—Porphyrin-Catalyzed mCPBA Oxidation.

✍ Toshiro Konoike; Yoshitaka Araki; Yasuhiko Kanda 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

A Novel Allylic Hydroxylation of Sterically Hindered Olefins by Fe-Porphyrin-Catalyzed mCPBA Oxidation. -Triterpenes such as (I) bearing a sterically hindered olefin readily undergo a novel allylic hydroxylation by MCPBA in the presence of iron(III) tetrakis(pentafluorophenyl)porphyrin chloride as

Transition state geometry in epoxidation

Transition state geometry in epoxidation by iron-oxo porphyrin at the compound I oxidation level. Epoxidation of alkenes catalyzed by a sterically hindered meso-tetrakis(2,6-dibromophenyl)porphinato iron(III) chloride

✍ Ostovic, Drazen.; Bruice, Thomas C. 📂 Article 📅 1988 🏛 American Chemical Society 🌐 English ⚖ 931 KB