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Regio- and Stereoselective 1,3-dipolar Cycloaddition of Azomethine Ylides Based on Isatins and (thia)proline to 3-nitro-2-(trifluoro(trichloro)methyl)-2H-chromenes: Synthesis and Cytotoxic Activity of 6-(trihalomethyl)-spiro[chromeno(thia)pyrrolizidine-11,3'-indolin]-2'-ones

Igor B. Kutyashev, Maria V. Ulitko, Alexey Yu. Barkov, Nikolay S. Zimnitskiy, Vladislav Yu. Korotaev, Vyacheslav Ya. Sosnovskikh

2021Chemistry of Heterocyclic Compounds10 citationsDOI

Topics & Concepts

ChemistryHeLaStereoselectivityProlineNitroCycloadditionCytotoxic T cell1,3-Dipolar cycloadditionStereochemistryMedicinal chemistryOrganic chemistryAmino acidCatalysisBiochemistryIn vitroAlkylFluorine in Organic ChemistrySynthesis and Catalytic ReactionsBioactive Compounds and Antitumor Agents
Regio- and Stereoselective 1,3-dipolar Cycloaddition of Azomethine Ylides Based on Isatins and (thia)proline to 3-nitro-2-(trifluoro(trichloro)methyl)-2H-chromenes: Synthesis and Cytotoxic Activity of 6-(trihalomethyl)-spiro[chromeno(thia)pyrrolizidine-11,3'-indolin]-2'-ones | Litcius