Rearrangement of 1,2-dihydro-2-(3-indolyl)-1-[2-(1-pyrrolinyl)]quinolines to 9-(3-indolylvinyl)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolines
β Scribed by Ryan, R. P.; Hamby, R. A.; Combs, C. M.; Wu, Yao Hua
- Book ID
- 127054158
- Publisher
- American Chemical Society
- Year
- 1975
- Tongue
- English
- Weight
- 462 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
The 1:1 intermediate generated by the addition of quinoline to dialkyl acetylenedicarboxylates is trapped by 1,3-indanedione to yield dialkyl 3-spiroindanedione-1,2,3,3a-tetrahydropyrrolo[1,2-a]quinoline-1,2-dicarboxylates in good yields. The structures of these products were confirmed by NMR and si
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