Results 141 to 150 of about 954 (177)

New Bisindole Alkaloids from Petchia Ceylanica

HETEROCYCLES, 1988
Two new bisindole alkaloids, ceylanine and ceylanicine, habe been isolated from Petchia ceylanica and their structures have been established on the basis of spectroscopic ...
_ Atta-ur-Rahman, Azra Pervin, Anjun Muzaffar, Kuruneruge Tuley Dayanada de Silva, Wellage Susil Jayalath Silva   +4 more
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Crooksiine, a bisindole alkaloid from Haplophyton crooksii

Phytochemistry, 1991
Abstract Crooksiine, a new bisindole alkaloid with antiacetylcholinesterase activity was isolated from Haplophyton crooksii . Its structure was established utilizing spectrometric methods.
Mohamad Mroue, Maktoob Alam
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A partial synthesis of the Alstonia bisindole alkaloid villalstonine

Tetrahedron Letters, 1994
Abstract The partial synthesis of villalstonine 1 has been completed by coupling the macroline equivalent 2a with plant-derived (+)-pleiocarpamine 3 in 0.2N aq. hydrochloric acid in the presence of fluoride ion.
Yingzhi Bi, James M. Cook, Philip W. LeQuesne   +2 more
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Biomimetic synthesis and structure of the bisindole alkaloid alstonisidine

Journal of the Chemical Society, Chemical Communications, 1972
Alstonisidine, a bisindole alkaloid from Alstonia muelleriana, is assigned the revised structure (II) on the basis of its biomimetic synthesis from quebrachidine (III) and macroline (IV).
David E. Burke, James M. Cook, P. W. Le Quesne   +2 more
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Vincazalidine A, a unique bisindole alkaloid from Catharanthus roseus

Journal of Natural Medicines
A new dimeric indole alkaloid, vincazalidine A consisting of an aspidosperma type and a modified iboga type with 1-azatricyclo ring system consisting of one azepane and two piperidine rings coupled with an oxazolidine ring was isolated from Catharanthus roseus, and the structure including absolute stereochemistry was elucidated on the basis of ...
Yusuke, Hirasawa, Ayaka, Kase, Akie, Okamoto, Keigo, Suzuki, Mizuki, Hiroki, Toshio, Kaneda, Nahoko, Uchiyama, Hiroshi, Morita   +7 more
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Partial synthesis of the antiamoebic bisindole alkaloid (−)-macrocarpamine

Tetrahedron Letters, 1996
Abstract The partial synthesis of the antiamoebic bisindole alkaloid (−)-macrocarpamine 1 has been completed by coupling (−)-anhydromacrosalhine-methine 2 with plant-derived (+)-pleiocarpamine 3 in anhydrous 0.2 N HCl in THF in 75% yield.
Tong Gan, James M. Cook
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New Bisindole Alkaloids from Tabernaemontana corymbosa

Journal of Natural Products, 2002
Ten new bisindole alkaloids of the vobasinyl-ibogan type, viz., conodiparines A-F (1-6), conodutarines A and B (7, 8), and cononitarines A and B (9, 10), were obtained from the leaf extract of the Malayan species Tabernaemontana corymbosa. The structures were determined using NMR and MS analysis.
Toh-Seok, Kam, Kooi-Mow, Sim, Huey-Shen, Pang   +2 more
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Synthesis and Assignment of the Absolute Configuration of Indenotryptoline Bisindole Alkaloid BE-54017

Organic Letters, 2012
Synthesis of the indenotryptoline bisindole alkaloid, BE-54017, was accomplished using osmium-promoted cis-dihydroxylation of maleimide as a key step. After optical resolution, the absolute configuration of this molecule was determined by comparing its optical rotation and HPLC profile to those obtained for BE-54017 derived from enantiopure ...
Tomoyuki, Kimura, Shuhei, Kanagaki, Yusuke, Matsui, Masaya, Imoto, Takumi, Watanabe, Masakatsu, Shibasaki   +5 more
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Insecticidal bisindole alkaloids from leaves of Tabernaemontana divaricata 'Dwaft'

Phytochemistry
Six undescribed bisindole alkaloids, namely taberdisines A-F (1-6), were isolated from the leaves of Tabernaemontana divaricata 'Dwaft'. Among them, alkaloids 1 and 2 were the first examples of strychnos-iboga type alkaloid with both C-C linkage patterns. Alkaloid 3, a new type of aspidosperma-iboga with a furan-ring, as well as other three undescribed
Xiang-Hai Cai
exaly   +3 more sources

Syntheses of the Bisindole Alkaloids of the Genera Borreria and Flindersia

2014
Abstract The flinderoles and their structural isomers, the borreverines, have intriguing chemical structures and promising biological activity. These indole alkaloids each contain multiple stereocenters that challenge synthetic chemists to develop new reaction methods. Proven antimalarial activity further established the synthesis of these targets as
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