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Structure of a novel bisindole derivative

Acta Crystallographica Section C Crystal Structure Communications, 1991
(3aR-[3a alpha,4 beta,5a beta,9[1R,3R(2S),5R,7aS,-12aS],10bR,13a alpha])-Methyl-4-(acetyloxy)-3a-ethyl-3a,4,5,5a,6,11,12,13a-oct ahy dro-9- [1,2,3,4,6,7,7a,- 12-octahydro-3-(2-hydroxy-2-hydroxymethylbutyl)- 1-(methoxycarbonyl)indolizino[1,2-b]indol-7a-yl]-5- hydroxy-8-methoxy-6-methyl-1H-indolizino[8,1-c,d]- carbazole-5-carboxylate methanol hydrate ...
V M, Lynch   +3 more
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Catalytic repertoire of bacterial bisindole formation

Current Opinion in Chemical Biology, 2016
Bacterial bisindole alkaloids that derive from the oxidative dimerization of l-tryptophan possess diversified biological activities and unique molecular structures. In recent years, the number of bisindoles and their gene clusters has greatly expanded, revealing a large genetic toolbox for the generation of unique structural modifications.
Yi-Ling, Du, Katherine S, Ryan
openaire   +2 more sources

Enantioselective Synthesis of N−N Bisindole Atropisomers

Angewandte Chemie, 2022
AbstractN−N Atropisomers are a common motif in natural products and represent a significant dimension for exploration in modern pharmaceutical and medicinal chemistry. However, the catalytic atroposelective synthesis of such molecules remains challenging, hampering meaningful development.
Peng Zhang   +6 more
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Bisindole alkaloids from Tabernaemontana corymbosa

Phytochemistry, 2018
Continued study in bioactive monoterpenoid alkaloids led to the isolation of nine undescribed alkaloids, taberyunines A-I, together with 32 known ones from the aerial parts of Tabernaemontana corymbosa Roxb. ex Wall (Apocynaceae). Among the undescribed alkaloids, taberyunines A-G and H-I were assigned to Aspidosperma-Aspidosperma and Vobasinyl-Ibogan ...
Bing-Jie, Zhang   +6 more
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New Synthetic Protocol for the Preparation of Unsymmetrical Bisindoles.

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Hanns Martin, Kaiser   +5 more
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Synthesis of a novel series of cytotoxic bisindole alkaloids

Bioorganic & Medicinal Chemistry Letters, 2001
Original cytotoxic bisindole alkaloids with a 1,2,3,4-tetrahydroquinoline bridge were synthesized by reductive amination with various anilines. The most cytotoxic compounds display a high and dose-dependent cell cycle effect with accumulation in the G1 phase.
M, Raoul   +6 more
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Bisindole alkaloids.

The Alkaloids. Chemistry and biology, 2007
This chapter provides an overview on bisindole alkaloids. The indole–indole and tryptamine–tryptamine type, and related alkaloids are discussed. Tryptamine–tryptamine type with an additional monoterpene unit and related alkaloids are briefly discussed.
Kam, Toh Seok, Choo, Yeun Mun
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Synthesis of Marine Sponge Bisindole Alkaloids Dihydrohamacanthins

Organic Letters, 2002
[structure: see text] A convergent synthesis of the marine sponge bisindole alkaloids dihydrohamacanthins is described. The synthesis centers on the construction of 3,5- and 3,6-linked pyrazinones and their reduction to the requisite piperazinones with sodium cyanoborohydride.
Fumiko Y, Miyake   +2 more
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ChemInform Abstract: Bisindole Alkaloids

ChemInform, 2009
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Toh‐Seok Kam, Yeun‐Mun Choo
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Bisindoles. 30. Acid condensation of bisindoles with aromatic aldehydes and the synthesis of new endole-containing polyamines

Chemistry of Heterocyclic Compounds, 1993
Reaction of 2,2′-diethoxycarbonyl-bis(5-indolyl)sulfone with benzaldehyde gave an active dibromide — 2,2′diethoxycarbonyl-3,3′-di(bromobenzyl)bis(5-indolyl)sulfone; derivatives of di(bisindolyl)phenylmethane have been prepared by condensation of 2,2′-diethoxycarbonyl-bis (N-methyl-5-indolyl)sulfone with benzaldehyde and p-methoxybenzaldhyde.
N. N. Ovsyannikova   +3 more
openaire   +1 more source

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