Intramolecular Cyclization During Bromination of the Quinoline Alkaloid Haplophyllidine

Bromination of the furanoquinoline alkaloid haplophyllidine by molecular bromine and N-bromosuccinimide was accompanied by intramolecular cyclization to form mixtures of new compounds containing additional penta-, hexa-, and spirocyclic rings incorporating the prenyl group of haplophyllidine. The st...

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Detalles Bibliográficos
Autores principales: Ubaidullaev, A. U., Vinogradova, V. I., Zhurakulov, Sh. N., Mukarramov, N. I., Bobakulov, Kh. M., Turgunov, K. A., Tashkhodzhaev, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664044/
https://www.ncbi.nlm.nih.gov/pubmed/36406158
http://dx.doi.org/10.1007/s10600-022-03877-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664044/
https://www.ncbi.nlm.nih.gov/pubmed/36406158
http://dx.doi.org/10.1007/s10600-022-03877-6

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