Structures and ambiphilic reactivities of indolizines. 5. Acylation of 2-methylindolizine
β Scribed by S. I. Bobrovskii; D. E. Lushnikov; Yu. G. Bundel'
- Book ID
- 104781633
- Publisher
- Springer US
- Year
- 1989
- Tongue
- English
- Weight
- 445 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0009-3122
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β¦ Synopsis
The acylation and carbomethoxylation of 2-methylindolizine were studied. In most cases minor amounts of the 1-substituted isomers were isolated in addition to the "usual" products of substitution in the 3 position. The data from the PMR and mass spectra of the 2-methyl-3-and l-acylindolizines obtained are discussed.
π SIMILAR VOLUMES
## Abstract An efficient two step route has been developed to synthesize pyrrolo[2,1,5β__cd__]indolizine derivatives. The reaction sequence proceeds __via__ preparation of 3βacylβ5βmethylindolizines followed by an intramolecular condensation. The procedures were carried out under convenient conditi
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