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The use of esters of dichloromaleic acid in intramolecular diels alder reactions

✍ Scribed by Mark J. Batchelor; John M. Mellor


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

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✦ Synopsis


Intramolecular cyclisation of acyclic triene esters derived from dichloromaleic anhydride affords bicyclic lactones, which by dechlorodecarboxylation, dechlorination or dehydrochlorination are readily elaborated to give novel unsaturated lactones.


πŸ“œ SIMILAR VOLUMES


Intramolecular diels-alder reaction of i
✍ Yoshinao Tamaru; Osamu Ishige; Shin-ichi Kawamura; Zen-ichi Yoshida πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 247 KB

Diels-Alder reaction of dienyl ff-methacrylthioimidates has been investigated under thermal or Lewis acid or protonic acid catalyzed conditions. The utility of the reaction is shown by desulfurative ring contraction of bicycle L4.4.0 1 to bicycle [ 4.3.0 I system.