𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Oxidation of furans II. Use of furans as masked dienophiles in the intramolecular diels-alder reaction

✍ Scribed by Peter D. Williams; Eugene LeGoff

Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
214 KB
Volume
26
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Stereochemical studies on the intramolec
Stereochemical studies on the intramolecular diels alder reaction of furans with doubly activated dienophiles.
✍ Laurence M. Harwood; Geraint Jones; John Pickard; Royston M. Thomas; David Watki πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 338 KB

The stereochemical outcome of intramolecular Diels-Alder reactions of furans with Z-and E-2-ene-1,4-dione units attached by a bridging chain to C-2 of the furan results from modification of the steric demands of the bridging chain by the preference of the external activating group to adopt an endost

The high pressure mediated intramolecula
The high pressure mediated intramolecular diels-alder reaction of furans: Factors controlling cycloaddition with monoactivated dienophiles.
✍ Laurence M. Harwood; Sarah A. Leeming; Neil S. Isaacs; Geraint Jones; John Picka πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 313 KB

The Intramolecular Diels-Alder reactions of furans possessing a 2-alkyl substituent with a terminal @unsaturated ketone have been surveyed. The consequences of varying the degree of substitution of the furan, the bridging chain length, and position of the activating group on the dienophile upon the

High pressure intramolecular Diels-Alder
High pressure intramolecular Diels-Alder reactions of the furan diene
✍ Brian A. Keay; Peter W. Dibble πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 147 KB

A variety of substituted furans a-6J undergo the intramolecular Die&Alder reaction at high pressure (12.5 kbar) to provide oxatricyclo adducts Q-12) within 24 hours at room temperature.