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Unusual indole alkaloid-pyrrole, -pyrone, and -carbamic acid adducts from Alstonia angustifolia.

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TLDR
In this paper, three unusual natural products, viz., alstopirocine, a macroline alkaloid incorporating a substituted pyrrole moiety, pleiomaltinine, an alkaloidepyrone adduct, and pleiomalicine (pyrrole substituted with pleiocarpamine), were isolated from the Malayan Alstonia angustifolia.
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This article is published in Tetrahedron.The article was published on 2010-09-25. It has received 38 citations till now. The article focuses on the topics: Alstonia angustifolia & Carbamic acid.

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Living on pyrrolic foundations – Advances in natural and artificial bioactive pyrrole derivatives

TL;DR: A summary and checklist of the most recent developments, indicating the classes of compounds, which have attracted the most significant research attention are contributed.
Journal ArticleDOI

Thiourea-Catalyzed Enantioselective Addition of Indoles to Pyrones: Alkaloid Cores with Quaternary Carbons

TL;DR: Arylpyrrolidino-derived thioureas catalyze the addition of indoles to pyrone-derived electrophiles with high stereoselectivity in the presence of catalytic quantities of an achiral Brønsted acid.
Journal ArticleDOI

Oxidized derivatives of macroline, sarpagine, and pleiocarpamine alkaloids from Alstonia angustifolia.

TL;DR: A total of 20 new indole alkaloid comprising mainly oxidized derivatives of macroline- (including alstofonidine, a macroline indole incorporating a butyrolactone ring-F), pleiocarpamine-, and sarpagine-type alkaloids were isolated from the bark and leaf extracts of Alstonia angustifolia.
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Angustilobine and andranginine type indole alkaloids and an uleine-secovallesamine bisindole alkaloid from Alstonia angustiloba.

TL;DR: A total of 20 alkaloids were isolated from the leaf and stem-bark extracts of Alstonia angustiloba, of which two are hitherto unknown, and a bisindole alkaloid angustiphylline, derived from the union of uleine and secovallesamine moieties was established.
References
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BookDOI

Alkaloids : chemical and biological perspectives

TL;DR: In this paper, the total synthesis of amaryllidaceae alkaloids has been studied using radical cyclization reactions in total syntheses of naturally occurring indole alkaloid.
Journal ArticleDOI

Antiplasmodial activity of extracts and alkaloids of three Alstonia species from Thailand.

TL;DR: It has been found that the active alkaloids, in contrast to chloroquine, have significantly higher affinity to the K1 strain than to the T9-96 strain of Plasmodium falciparum.
Journal ArticleDOI

Synthesis of 8-heteroatom-substituted 4,4-difluoro-4-bora-3a, 4a-diaza-s-indacene dyes (BODIPY)

TL;DR: In this paper, the structures of the thioethers 6a-6c and compound 10a were determined by X-ray diffraction and they were better described by structure 10 than 7.
Journal ArticleDOI

Coumarins and γ-pyrone derivatives from Prangos pabularia: antibacterial activity and inhibition of cytokine release

TL;DR: The n-hexane and ethyl acetate extracts of the stems and the ethyl ethanol extracts of roots from Prangos pabularia afforded an gamma-pyrone derivative and furanocoumarin derivatives with three glucose and gamma- pyrone (pabularin A, B and C), along with 26 previously known compounds.
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