Total Synthesis of (-)-Owerreine and (-)-Anhydrovobtusine. [PDF]
Myeong IS, Pinto T, Movassaghi M.
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Synthesis and antiplasmodial activity of 6<i>H</i>,13<i>H</i>-pyrazino[1,2-<i>a</i>;4,5-<i>a</i>']diindole analogues substituted with basic side chains. [PDF]
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New spirooxindole pyrrolidine/pyrrolizidine analogs: design, synthesis, and evaluation as an anticancer agent. [PDF]
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Pathway economy in cyclization of 1<i>,n</i>-enynes. [PDF]
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Synthesis, Biological Evaluation, and Molecular Docking Studies of Novel Coumarin-Triazole-Isatin Hybrids as Selective Butyrylcholinesterase Inhibitors. [PDF]
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Shifting Merocyanine-Imine Exchange with Visible Light. [PDF]
Drichel A, Hecht S.
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Unveiling the correlations between benzoic acid content, key microbial genera, and metabolites during the storage and transportation of raw yak milk based on multi-omics analysis. [PDF]
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Silodosin as a Novel Inhibitor of Acetylcholinesterase, Butyrylcholinesterase, and BETA-Secretase 1: In Vitro and In Silico Studies. [PDF]
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In the presence of hexamethylphosphorous triamide, the reaction of isatin with arylidene pivaloylacetonitriles in dry methylene dichloride afforded functionalized spiro[cyclopropane-1,3′-indolines] in good yields and with high diastereoselectivity.
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N-(Cyanothioformyl)indoline; a new indoline ring forming reaction
Journal of the Chemical Society, Perkin Transactions 1, 1998Conversion of 2-hydroxymethyl- and 2-hydroxyethylaniline with Appel salt 1 into the arylimines 3 and 4 is accompanied by formation of the chloromethyl and chloroethyl derivatives 8 and 9. Triphenylphosphine converts compound 8 into the benzothiazine 6 but the chloroethyl compound 9 gives N-(cyanothioformyl)indoline 10 (55%) rather than the analogous ...
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