๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Isolation and Decomposition of the Intermediate of an ElcB Elimination

โœ Scribed by Dr. A. Berndt

Publisher
John Wiley and Sons
Year
1969
Tongue
English
Weight
224 KB
Volume
8
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Kinetic studies on the chemiluminescent
Kinetic studies on the chemiluminescent decomposition of an isolated intermediate in the peroxyoxalate reaction
โœ Cassius V. Stevani; Wilhelm J. Baader ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 104 KB ๐Ÿ‘ 2 views

The peroxyoxalate system undergoes one of the most efficient chemiluminescence reactions and is the only one considered to involve an intermolecular chemically initiated electron exchange luminescence mechanism, with proven high efficiency. Several reactive intermediates have been proposed, which, u

Thwarting ฮฒ-Hydride Elimination: Capture
Thwarting ฮฒ-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction
โœ Martin Oestreich; Philip R. Dennison; Jeremy J. Kodanko; Larry E. Overman ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 102 KB

In spite of containing three conformationally accessible ฮฒ-H atoms, palladacycle 1โ€‰a is an isolable intermediate in the asymmetric Heck cyclization of 2โ€‰a. Although 1โ€‰a is stable in the presence of the hydrotriflate salt of 1,2,2,6,6-pentamethylpiperidine, it is converted into the oxindole Heck prod