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10.1021/acs.orglett.5c04718 http://scihub22266oqcxt.onion/10.1021/acs.orglett.5c04718 41391011!?!41391011       Org+Lett 2025 ; ? (?): ? Nephropedia Template TP {{tp|p=41391011|t=2025. Copper-Catalyzed Stereoselective Synthesis of Fluorinated 1,3-Dienes via Sequential Iodine-Fluorine Elimination |pdf=|usr=}}{{41391011}} gab.com Text Copper-Catalyzed Stereoselective Synthesis of Fluorinated 1,3-Dienes via Sequential Iodine-Fluorine Elimination JO: Org Lett http://www.kidney.de/pget.php?&tw=1&pmid=41391011 #FOAvip We report a copper-catalyzed stereoselective synthesis of fluorinated 1,3-dienes from unactivated alkenes via base-promoted sequential iodine-fluorine elimination. This protocol leverages commercially available polyfluoroalkyl iodides and beta,gamma-unsaturated amides to deliver structurally diverse fluoro-dienes with excellent selectivity and broad functional group tolerance, including complex natural product derivatives. This method provides efficient access to previously challenging fluorinated conjugated systems, offering a versatile platform for fluorine-containing molecular design in pharmaceuticals and materials. Twit Text FOAVip Copper-Catalyzed Stereoselective Synthesis of Fluorinated 1,3-Dienes via Sequential Iodine-Fluorine Elimination ????Org Lett http://www.kidney.de/pget.php?&tw=1&pmid=41391011 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=41391011 #FOAvip English Wikipedia <ref>{{Cite pmid|41391011}}</ref> Copper-Catalyzed Stereoselective Synthesis of Fluorinated 1,3-Dienes via Sequential Iodine-Fluorine Elimination #MMPMID41391011 Zhao L; Liu C; Zhang J; Li J; Li C; Zeng X Org Lett 2025[Dec]; ? (?): ? PMID41391011show ga We report a copper-catalyzed stereoselective synthesis of fluorinated 1,3-dienes from unactivated alkenes via base-promoted sequential iodine-fluorine elimination. This protocol leverages commercially available polyfluoroalkyl iodides and beta,gamma-unsaturated amides to deliver structurally diverse fluoro-dienes with excellent selectivity and broad functional group tolerance, including complex natural product derivatives. This method provides efficient access to previously challenging fluorinated conjugated systems, offering a versatile platform for fluorine-containing molecular design in pharmaceuticals and materials. ?Copper-Catalyzed Stereoselective Synthesis of Fluorinated 1,3-Dienes v(epmc).pdf DeepDyve Pubget Overpricing