Results 171 to 180 of about 3,343 (218)
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Total Synthesis of (−)-Lycorine and (−)-2-epi-Lycorine by Asymmetric Conjugate Addition Cascade
Organic Letters, 2009Total syntheses of (-)-lycorine and (-)-2-epi-lycorine were accomplished using chiral ligand-controlled asymmetric cascade conjugate addition methodology, which enables the formation of two C-C bonds and three stereogenic centers in one pot to give synthetically useful chiral cyclohexane derivatives.
Ken-Ichi, Yamada +4 more
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Lycorine: Studies in synthesis
Tetrahedron, 1973Abstract Several unsuccessful attempts are described at the synthesis of the carbon-nitrogen skeleton of lycorine, utilising 1,2-dihydroisoquinoline intermediates.
S.F. Dyke, M. Sainsbury, J.R. Evans
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Multiple biological functions and pharmacological effects of lycorine [PDF]
Lycorine is the major active component from the amaryllidaceae family plant Lycoris radiate, a represent traditional Chinese medicinal herb, and is one of the typical alkaloids with pyrrolophenanthridine nucleus core. Lycorine has drawn great interest in medicinal field due to its divergent chemical structures and multiple biological functions, as well
Zhifei Cao
exaly +3 more sources
ChemInform Abstract: SYNTHESIS OF LYCORINE‐TYPE ALKALOIDS. II. SYNTHESIS OF D,L‐LYCORINE
Chemischer Informationsdienst, 1978AbstractDie Darstellung der für die Titelverbindung (XI) bedeutenden Zwischenverbindung (VIIIa) wird verbessert.
O. MOELLER +2 more
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Synthesis and antiplasmodial activity of lycorine derivatives
Bioorganic & Medicinal Chemistry, 2010Twenty seven lycorine derivatives were prepared and evaluated for their in vitro antimalarial activity against chloroquine-sensitive strains of Plasmodium falciparum. The best antiplasmodial activities were achieved with lycorine derivatives that present free hydroxyl groups at C-1 and C-2 or esterified as acetates or isobutyrates.
Juan C, Cedrón +4 more
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ChemInform Abstract: LYCORIN, SYNTH.‐UNTERSUCHUNGEN
Chemischer Informationsdienst, 1973AbstractVersuche zur Darstellung der für die Synthese der Titelverbindung (I) benötigten Vorstufe (IIa) bzw. der Modellverbindung (IIb) werden beschrieben.
S. F. DYKE, M. SAINSBURY, J. R. EVANS
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Chemistry – A European Journal, 2014
AbstractWe report the first catalytic asymmetric approach to octahydroindolones and a divergent enantioselective synthesis of perhydroindole alkaloids, as exemplified by lycorine‐type Amaryllidaceae alkaloids (+)‐α‐lycorane and (+)‐lycorine, from a common intermediate by using a highly concise route.
Zhongwen, Sun +6 more
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AbstractWe report the first catalytic asymmetric approach to octahydroindolones and a divergent enantioselective synthesis of perhydroindole alkaloids, as exemplified by lycorine‐type Amaryllidaceae alkaloids (+)‐α‐lycorane and (+)‐lycorine, from a common intermediate by using a highly concise route.
Zhongwen, Sun +6 more
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Lycorine and its Derivatives for Anticancer Drug Design
Mini-Reviews in Medicinal Chemistry, 2010Amaryllidaceae alkaloids are extensively studied for their biological activities in several pharmaceutical areas, including, for example, Alzheimer's disease for which galanthamine has already reached the market. Among this chemical family, lycorine displays very promising anti-tumor properties.
Lamoral-Theys, Delphine +7 more
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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.
Ken‐ichi Yamada +4 more
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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.
Ken‐ichi Yamada +4 more
openaire +1 more source
Bioorganic and Medicinal Chemistry, 2008
A new lycorine derivative LT1 (4) was isolated from the aerial part and bulbs of Lycoris traubii Hayward (Amaryllidaceae). Its structure including absolute configuration was established by spectroscopic analysis and semi-synthesis to be 1-O-(3'S)-hydroxybutanoyllycorine.
Yosuke, Toriizuka +8 more
exaly +3 more sources
A new lycorine derivative LT1 (4) was isolated from the aerial part and bulbs of Lycoris traubii Hayward (Amaryllidaceae). Its structure including absolute configuration was established by spectroscopic analysis and semi-synthesis to be 1-O-(3'S)-hydroxybutanoyllycorine.
Yosuke, Toriizuka +8 more
exaly +3 more sources

