A novel synthesis of bis(benzoxazole) derivatives via tandem Claisen rearrangement
β Scribed by Emiko Koyama; Gang Yang; Kazuhisa Hiratani
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 82 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Novel bis(benzoxazole) derivatives were easily synthesized from isobutenyl bis(amide-ether)s by tandem Claisen rearrangement and subsequent intramolecular cyclization of the amide-phenol intermediates. The yields of the bis(benzoxazole)s depended on whether the reaction was carried out with or witho
We wish to report a facile thermal rearrangement of an N-aryl propynylamine oxide to an indole. The present study, to our knowledge, is the first report of such a rearrangement. Compound 1 (89.5%; m.p. 76-77)\* was prepared by the condensation of l-(4-chlorophenoxy)-4chloro-2-butyne3 with two moles
## Abstract Novel macrocyclic bis(phenylbenzoxazole) derivatives were easily synthesized from macrocyclic isobutenyl bis(amideβether)s by tandem Claisen rearrangement and subsequent intramolecular cyclization of the amideβphenol intermediates. The position of substitution of the oligoethylene glyco