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Structure of the alleged diels-alder adduct from 2,3-dimethyl-quinoxaline and maleic anhydride

✍ Scribed by Edward C. Taylor; E. Smakula Hand


Publisher
Elsevier Science
Year
1962
Tongue
French
Weight
303 KB
Volume
3
Category
Article
ISSN
0040-4039

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✦ Synopsis


Frequentreferencelamade lnthe lIteraturea to the Mele-Alder reaatlon of 2,+kuethylquinoxallne (purportedly reacting in itr tautomeric ram I) vlth maleic anhydride to give the "edduct" 11s or IIb. This cm-lr re-ported= to ha= the elementary analyale C14HLpllnOe, not to mlt below 300Β°, to be yellow, rublimable, unrasctlre towswb dluomethane, ud to be I Ifa IIb recrystalUzable from acetic acid, eoluble In aqueoue loo/o rodlu hydroxide, and recoverable after refluxing for one hour In aqueoue ZOO/o rodlue hydroxide. Since the atability of the coapouud seemed at variance vlth itr aeeigned 1 Thie vork wa8 rtrpported by a grant (CY-2551) to


πŸ“œ SIMILAR VOLUMES


Synthetic application of the diels-alder
✍ K.T. Joseph; G.S. Krishna Rao πŸ“‚ Article πŸ“… 1967 πŸ› Elsevier Science 🌐 French βš– 414 KB

## Abstnw -By a series of reactions the Diels-Alder adduct N of maleic anhydride and &trans-Ckiine gave l-hydroxy-l,4-dimethyl-7-hydroxymcthybctahydroindane (XII). Its further synthetic elaboration furnished 1,4-dimethyl-7-(2-ethoxycarbonyl-l-propenyl)-A\*-octahydroindane of the valerenic acid ske