(Q104664502)

English

Bulbine-Knipholone, a New, Axially Chiral Phenylanthraquinone fromBulbine abyssinica (Asphodelaceae): Isolation, Structural Elucidation, Synthesis, and Antiplasmodial Activity

scientific article published on 25 August 2002

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scholarly article

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Bulbine-Knipholone, a New, Axially Chiral Phenylanthraquinone fromBulbine abyssinica (Asphodelaceae): Isolation, Structural Elucidation, Synthesis, and Antiplasmodial Activity (English)

1 reference

http://api.crossref.org/works/10/c94mmr

Bulbine abyssinica

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Bulbine-knipholone

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4-(3-acetyl-2,6-dihydroxy-4-methoxy-phenyl)-1,8-dihydroxy-3-methyl-10H-anthracen-9-one

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1 reference

1-(3-Acetyl-2,4,6-trihydroxyphenyl)-4,5-dihydroxy-2-methylanthra-9,10-quinone

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object named as

Asphodelaceae

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based on heuristic

inferred from title

author name string

Gerhard Bringmann

1

1 reference

http://api.crossref.org/works/10/c94mmr

Dirk Menche

2

1 reference

http://api.crossref.org/works/10/c94mmr

Reto Brun

3

1 reference

http://api.crossref.org/works/10/c94mmr

Thomas Msuta

4

1 reference

http://api.crossref.org/works/10/c94mmr

Berhanu Abegaz

5

1 reference

http://api.crossref.org/works/10/c94mmr

publication date

March 2002

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16 September 2022

European Journal of Organic Chemistry

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http://api.crossref.org/works/10/c94mmr

2002

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http://api.crossref.org/works/10/c94mmr

6

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http://api.crossref.org/works/10/c94mmr

1107-1111

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http://api.crossref.org/works/10/c94mmr

Antiplasmodial and antioxidant isofuranonaphthoquinones from the roots of Bulbine capitata.

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

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Intercalating agents with covalent bond forming capability. A novel type of potential anticancer agents. 2. Derivatives of chrysophanol and emodin

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Novel anthraquinone inhibitors of human leukocyte elastase and cathepsin G

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Antiplasmodial activity of knipholone and related natural phenylanthraquinones.

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Knipholone: a unique anthraquinone derivative from Kniphofia foliosa

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Knipholone from Bulbine latifolia and Bulbine frutescens

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Isofuranonaphthoquinones and phenolic and knipholone derivatives from the roots of Bulbine capitata

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

2′,6′-Dihydroxy-4′-methoxyacetophenone, a phytoalexin from the roots of Sanguisorba minor

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Knipholone anthrone from Kniphofia foliosa

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

4′-Demethylknipholone from aerial parts of bulbine capitata

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

An anthrone, an anthraquinone and two oxanthrones from Kniphofia foliosa

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

First, Atropo-Enantioselective Total Synthesis of the Axially Chiral Phenylanthraquinone Natural Products Knipholone and 6'-O-Methylknipholone Novel Concepts in Directed Biaryl Synthesis, Part 93. This work was supported by the Deutsche Forschungsge

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Stereoselective total synthesis of axially chiral natural products via biaryl lactones

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Gardenamide A fromRothmannia urcelliformis (Rubiaceae) − Isolation, Absolute Stereostructure, and Biomimetic Synthesis from Genipine

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique

1 reference

https://api.crossref.org/works/10.1002%2F1099-0690%28200203%292002%3A6%3C1107%3A%3AAID-EJOC1107%3E3.0.CO%3B2-4

21 January 2018

4-aminoquinoline analogs of chloroquine with shortened side chains retain activity against chloroquine-resistant Plasmodium falciparum

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In vitro and in vivo activities of trybizine hydrochloride against various pathogenic trypanosome species

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Identifiers

10.1002/1099-0690(200203)2002:6<1107::AID-EJOC1107>3.0.CO;2-4

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