𝔖 Bobbio Scriptorium
✦   LIBER   ✦

AN EFFICIENT PREPARATION OF 1,2-DIHYDROCYCLOBUTA[a]NAPHTHALENE

✍ Scribed by Hunt, David A.

Book ID
126033690
Publisher
Taylor and Francis Group
Year
1989
Tongue
English
Weight
259 KB
Volume
21
Category
Article
ISSN
0030-4948

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Reactions of the dimethyl cyclobutane-1,
Reactions of the dimethyl cyclobutane-1,2-dicarboxylate dianion. A simple synthesis of 1,2-dihydrocyclobuta [b] naphthalene-3, 8-dione
✍ Peter J. Garratt; Robert Zahler πŸ“‚ Article πŸ“… 1979 πŸ› Elsevier Science 🌐 French βš– 148 KB

Vicinal diester dianions have considerable potential as synthetic intermediates, have recently described the formation and basicities of the dimethyl cyclobutane-l,Z-. dicarboxylate dianion (1) and the dimethyl cyclobut-3-ene-1,2-dicarboxylate dianion.\* and we We now report some reactions of dianio

A very efficient preparation of 1,2-dike
A very efficient preparation of 1,2-diketones
✍ M.C. Carre; P. Caubere πŸ“‚ Article πŸ“… 1985 πŸ› Elsevier Science 🌐 French βš– 190 KB

Summahy : 1teaAmen.t 04 a-AiomethtrLktstnneci with CL&.+CuO in aqueous actione addoh& do\_ cowrtienaondin\_a J,Z-o!icutbonqL compouvd. We have previously shown1 that condensation of benzyne on 1,2-diketone monoketal enolates led to the formation of benzocyclobutenols in good to excellent yields. The