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Ze-Qi Xu

Researcher at University of Illinois at Chicago

Publications -  33
Citations -  648

Ze-Qi Xu is an academic researcher from University of Illinois at Chicago. The author has contributed to research in topics: Phosphonate & Calanolide A. The author has an hindex of 12, co-authored 33 publications receiving 616 citations. Previous affiliations of Ze-Qi Xu include Southern Research Institute.

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Synthesis, chromatographic resolution, and anti-human immunodeficiency virus activity of (±)-calanolide A and its enantiomers

TL;DR: The anti-HIV agent (+/-)-calanolide A (1) has been synthesized in a five-step approach starting with phloroglucinol, which includes Pechmann reaction, Friedel-Crafts acylation, chromenylation with 4,4-dimethoxy- 2-methylbutan-2-ol, cyclization, and Luche reduction.
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Anti-HIV natural product (+)-calanolide A is active against both drug-susceptible and drug-resistant strains of Mycobacterium tuberculosis

TL;DR: In this article, the anti-HIV-1 agent (+)-calanolide A was found to be active against all of the strains of Mycobacterium tuberculosis tested, including those resistant to the standard antitubercular drugs.
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Structural analogues of the calanolide anti-HIV agents. Modification of the trans-10,11-dimethyldihydropyran-12-ol ring (ring C).

TL;DR: (+)-Calanolide A is a potent inhibitor of reverse transcriptase from human immunodeficiency virus type 1 (HIV-1), which was isolated from an extract of Calophyllum lanigerum, along with seven related compounds, which were confirmed to be inhibitors of HIV-1reverse transcriptase.
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Novel approach for synthesis of (±)-calanolide a and its anti-HIV activity

TL;DR: The key intermediate, chromene 5, was synthesized by the sequence of Pechmann reaction, acylation and chromenylation by 4,4-dimethoxy-2-methylbutan- 2-ol.
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Synthesis of (+)-calanolide A, an anti-HIV agent, Via enzyme-catalyzed resolution of the aldol products

TL;DR: The synthesis of (+)-calanolide A, an anti-HIV-1 agent, is described, which was resolved by a lipase-catalyzed acylation reaction of compound 2 stereoselectively produced the desired syn diastereomer.