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Synthesis and antimalarial activity of N-benzylated (N-arylcarbamoyl)alkylphosphonic acid derivatives.

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Title: Synthesis and antimalarial activity of N-benzylated (N-arylcarbamoyl)alkylphosphonic acid derivatives.
Authors: Adeyemi CM; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa., Faridoon; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa., Isaacs M; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa., Mnkandhla D; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa., Hoppe HC; Department of Biochemistry and Microbiolgy, Rhodes University, Grahamstown 6140, South Africa; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa., Krause RW; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa., Kaye PT; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. Electronic address: P.Kaye@ru.ac.za.
Source: Bioorganic & medicinal chemistry [Bioorg Med Chem] 2016 Dec 01; Vol. 24 (23), pp. 6131-6138. Date of Electronic Publication: 2016 Apr 09.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Elsevier Science Country of Publication: England NLM ID: 9413298 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1464-3391 (Electronic) Linking ISSN: 09680896 NLM ISO Abbreviation: Bioorg Med Chem Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Synthesis and antimalarial activity of N-benzylated (N-arylcarbamoyl)alkylphosphonic acid derivatives.
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  Data: <searchLink fieldCode="AU" term="%22Adeyemi+CM%22">Adeyemi CM</searchLink>; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa.<br /><searchLink fieldCode="AU" term="%22Faridoon%22">Faridoon</searchLink>; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa.<br /><searchLink fieldCode="AU" term="%22Isaacs+M%22">Isaacs M</searchLink>; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa.<br /><searchLink fieldCode="AU" term="%22Mnkandhla+D%22">Mnkandhla D</searchLink>; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa.<br /><searchLink fieldCode="AU" term="%22Hoppe+HC%22">Hoppe HC</searchLink>; Department of Biochemistry and Microbiolgy, Rhodes University, Grahamstown 6140, South Africa; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa.<br /><searchLink fieldCode="AU" term="%22Krause+RW%22">Krause RW</searchLink>; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa.<br /><searchLink fieldCode="AU" term="%22Kaye+PT%22">Kaye PT</searchLink>; Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. Electronic address: P.Kaye@ru.ac.za.
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  Data: <searchLink fieldCode="JN" term="%229413298%22">Bioorganic & medicinal chemistry</searchLink> [Bioorg Med Chem] 2016 Dec 01; Vol. 24 (23), pp. 6131-6138. <i>Date of Electronic Publication: </i>2016 Apr 09.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Science%22">Elsevier Science </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9413298 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1464-3391 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209680896%22">09680896 </searchLink><i>NLM ISO Abbreviation: </i>Bioorg Med Chem <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.bmc.2016.04.021
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        Text: English
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              Text: 2016 Dec 01
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