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 s...

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Veröffentlicht in:	Chemistry of natural compounds 2022-11, Vol.58 (6), p.1101-1107
Hauptverfasser:	Ubaidullaev, A. U., Vinogradova, V. I., Zhurakulov, Sh. N., Mukarramov, N. I., Bobakulov, Kh. M., Turgunov, K. A., Tashkhodzhaev, B.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alkaloids Bromination Bromine Chemistry Chemistry and Materials Science Chemistry/Food Science Crystal structure NMR Nuclear magnetic resonance Organic Chemistry Plant Sciences Quinoline
Online-Zugang:	Volltext
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