𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Participation of substituents at the ortho position of aryl groups in the rearrangements of 5-chloro-3-aryl-2,1-benzisoxazoles

✍ Scribed by Vladimir Yu. Orlov; Aleksandr D. Kotov; Valentin V. Ganzha; Vitaliy G. Sokolov


Book ID
119768131
Publisher
Royal Society of Chemistry
Year
2004
Tongue
English
Weight
49 KB
Volume
14
Category
Article
ISSN
0959-9436

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mucochloric Acid: A Useful Synthon for t
✍ Fabio Bellina; Chiara Anselmi; Francesca Martina; Renzo Rossi πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 224 KB πŸ‘ 1 views

## Abstract 3,4‐Dichloro‐2(5__H__)‐furanone, which has been prepared efficiently from mucochloric acid, has been transformed selectively into 4‐aryl‐3‐chloro‐2(5__H__)‐furanones either by Suzuki‐ or Stille‐type reactions. These monochloro derivatives have been used as precursors either to (__Z__)‐4

Primary dependence of 7-aryl-2,5-di-t-bu
✍ Ken'ichi Takeuchi; Hiroshi Fujimoto; Kunio Okamoto πŸ“‚ Article πŸ“… 1981 πŸ› Elsevier Science 🌐 French βš– 245 KB

l3 C NMR studies showed that the population of the norcaradiene form of the title systems containing p-CH30, H, and p-CF3 on the 7-aryl group increases in this order. The result is consistent with the prediction from the n-acceptor strength of the aryl group estimated by INDO calculations.