Results 151 to 160 of about 48,569 (170)
Some of the next articles are maybe not open access.
A partial synthesis of the Alstonia bisindole alkaloid villalstonine
Tetrahedron Letters, 1994Abstract 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 +2 more
openaire +1 more source
Biomimetic synthesis and structure of the bisindole alkaloid alstonisidine
Journal of the Chemical Society, Chemical Communications, 1972Alstonisidine, 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 +2 more
openaire +1 more source
Vincazalidine A, a unique bisindole alkaloid from Catharanthus roseus
Journal of Natural MedicinesA 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 +7 more
openaire +2 more sources
Partial synthesis of the antiamoebic bisindole alkaloid (−)-macrocarpamine
Tetrahedron Letters, 1996Abstract 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
openaire +1 more source
New Bisindole Alkaloids from Tabernaemontana corymbosa
Journal of Natural Products, 2002Ten 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 +2 more
openaire +2 more sources
Aspidospermatan–aspidospermatan and eburnane-sarpagine bisindole alkaloids from Leuconotis
Phytochemistry, 2010Leucofoline and leuconoline, representing the first members of the aspidospermatan-aspidospermatan and eburnane-sarpagine subclasses of the bisindole alkaloids, respectively, were isolated from the Malayan Leuconotis griffithii. The structures of these bisindole alkaloids were established using NMR and MS analysis, and in the case of leuconoline ...
Gan, Chew Yan +4 more
openaire +3 more sources
Syntheses of the Bisindole Alkaloids of the Genera Borreria and Flindersia
2014Abstract 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
openaire +1 more source
The bisindole alkaloid catharine
Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1976J. Guilhem +3 more
openaire +1 more source
Novel Bisindole Derivatives Of Catharanthus Alkaloids With Potential Cytotoxic Properties
2003Pantropical plant Catharanthus roseus (L) G. Don is known as a source of valuable bisindole alkaloids: vinblastine (VBL) and vincristine (VCR), oncolytics widely used as sulfates in therapy of malignant diseases. They are biosynthesized in the plant from monoindolic vindoline and catharanthine, both derived from L-tryptophan and loganine units.
Joanna, Ruszkowska +3 more
openaire +2 more sources
Bisindole Alkaloids of Pandaca caducifolia
Journal of Natural Products, 1982Monique Zeches +3 more
openaire +1 more source

