𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Bishomoaromatic interaction in the disrotatory ring opening of cyclopropyl carbenoids

✍ Scribed by Loozen, Hubert J. J.; Castenmiller, Wim A.; Buter, Els J. M.; Buck, Henk M.


Book ID
125953070
Publisher
American Chemical Society
Year
1976
Tongue
English
Weight
420 KB
Volume
41
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Ring opening in the reaction of diphenyl
✍ Gernot Boche; Michael Marsch πŸ“‚ Article πŸ“… 1983 πŸ› Elsevier Science 🌐 French βš– 238 KB

The reaction of cyclopropanes like 2,3,4-triphenyl-endo-tricyclo[3.2.1.02'0]octane (la) with base is initiated by proton and not by ele$trov transfer. The facile disrotatory cyclopropyl anion ring opening reaction of 2JR2=CN, M =Ll ) at -75Β°C does not occur synchronously. 2,3,4-Triphenyl-endo-tricyc

ChemInform Abstract: Cyclopropyl Buildin
✍ M. BRANDL; S. I. KOZHUSHKOV; S. BRAESE; A. DE MEIJERE πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views

Cyclopropyl Building Blocks for Organic Synthesis. Part 43. Ring Opening of Methylenecyclopropane Moieties in the Palladium-Catalyzed Cross-Coupling of Methylenecyclopropyl Bromides with Metalated CH-Acidic Compounds. -The title reactions are found to proceed with opening of the three-membered ring