Rearrangements of N-acyl-2-aza-1,5-hexadienes: application to synthesis of traechelanthamidine and supinidine
β Scribed by David J. Hart; Teng-Kuei Yang
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 204 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Efficient syntheses of the pyrrolizidine bases traechelanthamldlne (4) and supinldine (2) via an N-acyllminlum ion rearrangement-cycllzatlon are described.
π SIMILAR VOLUMES
The N-acylating and N-alkoxycarbonylation ability of the N-substituted 1,2,3-triazolo[4,5-c]pyridines 1a-e have been investigated. The alkoxycarbonyl triazolopyridine derivatives (1c-e) were readily prepared in 81-96 % yield (the corresponding tetrafluoroborate > 95 %). Triazolo[4,5-c]pyridine (1) h
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