The maleic anhydride adducts of tropolone and 2-methoxytropone
✍ Scribed by Shô Itô; Hitoshi Takeshita; Yoshikazu Shoji; Yasuo Toyooka; Tetsuo Nozoe
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 214 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The Diels-Alder reaction of troponoid compounds has been studied using symmetric dienophiles in the cases of tropone (1,2), 2-halotropones (J), 4-methoxytropone (4).
2-methoxytropone (5),
tropolone and its homologues (6,7) and halotropolones (8,s).
Although crystalline adducts were obtained from all of these troponoids, only those from the first four were investigated in sufficient detail to permit reliable structures to be proposed. In light of our present knowledge on structures of three adduots (1 2 3 4 9 9 9 , 5), the ff-diketone structures proposed by Sebe and Osako (7) for the adduots from hinoki-
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## Abstract Two 2:1 maleic anhydride–α‐methylstyrene adducts and two naphthalene derivatives were isolated as low molecular weight by‐products of thermal copolymerizations of maleic anhydride and α‐methylstyrene under different conditions. Their structures were deduced by means of ^1^H^1^H and ^1^
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 300°, to be yellow, r