𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Effects of para-Phenyl Group on the Reactivities of Sterically Congested Triplet Diphenylcarbene.

✍ Scribed by Katsuyuki Hirai; Takashi Iikubo; Hideo Tomioka


Publisher
John Wiley and Sons
Year
2003
Weight
107 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


πŸ“œ SIMILAR VOLUMES


Effects of Phenyl Substitution on the Fr
✍ Gano, James E.; Sekher, Padmanabhan; Weber, Lisa; Lenoir, Dieter πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 286 KB πŸ‘ 2 views

The characteristic mass spectrometric fragmentation patterns of sterically congested stilbenes, phenyl-substituted 2,2,5,5-tetramethyl-3,4-diphenylhex-3-enes, are described. In contrast to stilbene, these sterically congested stilbenes show facile loss of tert-butyl and/or isobutene and phenyl, ulti

On the Conformation of a Sterically Cong
✍ Andreas MΓΌhlebach; Gian Paolo Lorenzi; Volker Gramlich πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 German βš– 386 KB

The conformation in the crystdine state and in solution of the sterically congested tetramethylpiperidinederived arnidc group of the symmetric diamide I formed from 2,2,6,6-tetramethylpiperidine (b) and 1,2,5-thiadiarole-3,4-dicarbonyl dichloride (c), and of the mixed diamide 11 derived from b, c, a