✦ LIBER ✦

The cyclopropanation of cycloalkenone silyl enol ethers. The oriented α- or α′-monomethylation of cycloalkenones.

✍ Scribed by C. Girard; J.M. Conia

Publisher: Elsevier Science
Year: 1974
Tongue: French
Weight: 169 KB
Volume: 15
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)91898-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The cyclopropanation of silyl enol ether

The cyclopropanation of silyl enol ethers of cisoid or labile α-ethylenic ketones. A general and rapid route to cyclobutanones and cyclopentanones.

✍ C. Girard; P. Amice; J.P. Barnier; J.M. Conia 📂 Article 📅 1974 🏛 Elsevier Science 🌐 French ⚖ 241 KB

The 1,3 O→C silyl rearrangement of silyl

The 1,3 O→C silyl rearrangement of silyl enol ether anions - synthesis of α-silyl ketones

✍ E.J. Corey; Christoph Rücker 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 206 KB

Synthesis of α-silyloxyhydroperoxides fr

Synthesis of α-silyloxyhydroperoxides from the reaction of silyl enol ethers and hydrogen peroxide

✍ Isao Saito; Ryu Nagata; Kazuaki Yuba; Teruo Matsuura 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 194 KB

## ButyldimethylsilyL enol ethers derived from a wide range of ketones react with hydrogen peroxide in the presence of acid to give remarkably stable a-si 2.y Zoxyhydroperoxides.

The Copper(I) Chloride-Catalyzed Reactio

The Copper(I) Chloride-Catalyzed Reaction of Ketene Silyl Acetals or Silyl Enol Ethers with α-Halogen Substituted Allylsilanes to Form Carbonyl Compounds Bearing Vinylsilane Functionality.

✍ Michiharu Mitani; Masayuki Masuda 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

Reversal of the facial diastereoselectiv

Reversal of the facial diastereoselectivity in the Paternò-Büchi reaction of silyl enol ethers carrying a chiral substituent in α-position

✍ Thorsten Bach; Kai Jödicke; Birgit Wibbeling 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 981 KB

Pd(OH)2/C-Mediated Selective Oxidation o

Pd(OH)2/C-Mediated Selective Oxidation of Silyl Enol Ethers by tert-Butylhydroperoxide, a Useful Method for the Conversion of Ketones to α,β-Enones or β-Silyloxy-α,β-enones.

✍ Jin-Quan Yu; Hai-Chen Wu; E. J. Corey 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views