𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reaction of norbornenes with phenylpalladium chloride

✍ Scribed by Hiroshi Horino; Mannosuke Arai; Naoto Inoue

Publisher
Elsevier Science
Year
1974
Tongue
French
Weight
208 KB
Volume
15
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

The chromyl chloride oxidation of norbor
The chromyl chloride oxidation of norbornenes
✍ F.W. Bachelor; U.O. Cheriyan πŸ“‚ Article πŸ“… 1973 πŸ› Elsevier Science 🌐 French βš– 165 KB

The oxidation of norbornene (la) by chromyl chloride has recently been carried out by Freeman et al. as part of a kinetic study of the mechanism of oxidation by this reagent (1). Unfortunately no product analysis was made. We have repeated this reaction and the products

The Reaction of Phenyl(trichloromethyl)m
The Reaction of Phenyl(trichloromethyl)mercury with Substituted Norbornenes
✍ C. W. Jefford; D. T. Hill; J. GorΓ©; B. Waegell πŸ“‚ Article πŸ“… 1972 πŸ› John Wiley and Sons 🌐 German βš– 605 KB

## Abstract The addition of phenyl(trichloromethyl)mercury to five substituted norbornenes is described, and the results compared with those obtained with bicyclo[2.2.2]oct‐2‐ene and 3,3,5,5‐tetramethylcyclopentene. The reaction proves to be useful for synthetic purposes, in that it leads usually t

Stereospecific phenylation of alkenylsil
Stereospecific phenylation of alkenylsilanes with phenylpalladium acetate
✍ Kiyoshi Kikukawa; Kazutoshi Ikenaga; Fumio Wada; Tsutomu Matsuda πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 224 KB

El-and (Z)-RCH=CHSiMe3(R=Ph, n-C6H13, CH30CH2) reacted stereospecifically with Ph-Pd-OAc to give RCH=C(Ph)SiMe3 and R(Ph)C=CHSiMe3 with inversion of the starting geometry with respect to R and Me3Si groups. Alkenylsilanes are known to react regio-and stereospecifically with a wide range of electroph