Marc Anteunis
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Partial synthesis of five new analogues of the peptido-lactone Virginiamycine Si, modified in the fifth and/or sixth position ([Xxx^J-VSi with Xxx=Ala, Asp, Asn and Lys and [Ala5,Gly6]-VSi).
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CYCLO(L-PROLYL-L-N-METHYLPHENYLALANYL) - CONFORMATION IN SOLUTION AND IN THE CRYSTAL.
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New compounds isolated from the pyrolysis of cellulose
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Structure, conformation and stereoelectronics of 9,10-annelated-1,4,5,8-tetraoxadecalines : a multidisciplinary probe
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A serendipitous synthesis of bis(α-cyano-4-nitrostyrene-β-yl) ether
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The active ester α-cyano-4-nitrostyrene-β-yl acetate is also the captodative olefin 2-acetoxy-1-cyano-1-(4-nitrophenyl)ethene : synthesis of 2,4-bis(4-nitrophenyl)pent-2-enedinitrille
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A search for phenolic protection in virginiamycin S
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Cyclization of a linear precursor of virginiamycin S1 (VS1) mediated by Woodward's reagent K
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The synthesis of Nγ-phthalyl-Nα-methyl-α, γ-diaminobutyryl congener of virginiamycin S1
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Enantiomeric quantifications of amino acids through their Na-acyl amides by gas chromatography