✦ LIBER ✦

Electrochemical oxidation of organosilicon compounds I. Oxidative cleavage of carbon-silicon bond in allylsilanes and benzylsilanes

✍ Scribed by Jun-ichi Yoshida; Toshiki Murata; Sachihiko Isoe

Publisher: Elsevier Science
Year: 1986
Tongue: French
Weight: 221 KB
Volume: 27
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)84799-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Carbon—Silicon Bond Cleavage of Orga

The Carbon—Silicon Bond Cleavage of Organosilicon Compounds in Supercritical Water.

✍ Kenichiro Itami; Koji Terakawa; Jun-ichi Yoshida; Okitsugu Kajimoto 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 23 KB

Electrochemical oxidation of organosilic

Electrochemical oxidation of organosilicon compounds: V. Electrochemical oxidation of α-silyethers. remarkable effect of silicon on oxidation potentials and reaction pathways

✍ Jun-ichi Yoshida; Toshiki Murata; Sachihiko Isoe 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 302 KB

Silafunctional compounds in organic synt

Silafunctional compounds in organic synthesis: XVIII. Oxidative cleavage of the silicon-carbon bond in alkenylfluorosilanes to carbonyl compounds: Synthetic and mechanistic aspects

✍ Kohei Tamao; Munetaka Akita; Makoto Kumada 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 627 KB

ChemInform Abstract: Oxidative Cleavage

ChemInform Abstract: Oxidative Cleavage of the Silicon-Carbon Bond: Development, Mechanism, Scope, and Limitations

✍ K. TAMAO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

ChemInform Abstract: Electrochemical Cle

ChemInform Abstract: Electrochemical Cleavage of the Carbon—Halogen Bond in Aromatic Compounds

✍ M. Borsari; C. Fontanesi; G. Gavioli 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

Carbon silicon bond cleavage in the oxid

Carbon silicon bond cleavage in the oxidation of benzylic silanes by cerium(IV) ammonium nitrate

✍ Enrico Baciocchi; Tiziana Del Giacco; Cesare Rol; Giovanni Vittorio Sebastiani 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 234 KB

Benzyltrirrethylsilanes react with cerium(IV) ammonium nitrate in AcOH to give products -of C-Si cleavage (benzyl nitrate and acetate), under very mild conditions and in quantitative yields. The reaction rate is very sensitive to the nature of the ring substituents (y= -5.4), which clearly suggests