𝔖 Bobbio Scriptorium
✦   LIBER   ✦

First intramolecular benzyne diels-alder reaction with an acyclic diene. Unusual effect of diene geometry on the course of the reaction

✍ Scribed by Keith R. Buszek


Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
231 KB
Volume
36
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Intramolecular diels-alder reactions of
✍ Daniel D. Sternbach; Debby M. Rossana πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 262 KB

An internal Diels-Alder reaction, using furan as the diene component, formed a highly functionalized 5-membered carbocycllc ring in excellent yield. Solvent and substituent effects of this reaction were examined. In connection with a proJect devoted to the synthesis of some natural products contai

An efficient cobalt catalyst for the neu
✍ Gerhard Hilt; Tobias J Korn πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 58 KB

The efficiently cobalt(I)-catalysed neutral Diels-Alder type reactions of internal alkynes with substituted 1,3-dienes is described. The regiochemistry for the dihydroaromatic products of reactions of isoprene with unsymmetrical reaction partners (2-alkynes and 1-trimethylsilyl-1-hexyne) is investig

The effect of side chain substituents on
✍ Christine Rogers; Brian A. Keay πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 296 KB

The effect of side chain substituents on the Intramolecular Diels-Alder reaction of the Furan diene (IMDAF) is reported in which the side chain connecting the furan diene to the dienophile contain four carbon atoms. The synthesis of 1,4epoxycadinane