. "Bure\u0161, Filip" . "11" . "Simple, straightforward and optimized procedures for preparing extended \u03C0-conjugated linkers are described. Either unsubstituted or 4-donor substituted \u03C0-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl \u03C0-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki-Miyaura or Sonogashira coupling reactions." . "3"^^ . . "Convenient methods for preparing \u03C0-conjugated linkers as building blocks for modular chemistry"@en . . . . "Convenient methods for preparing \u03C0-conjugated linkers as building blocks for modular chemistry" . "1860-5397" . "boronic acid; donor/acceptor; linker; Sonogashira reaction; property tuning; push- pull; Suzuki-Miyaura reaction"@en . . "Ludwig, Miroslav" . "3"^^ . "Beilstein Journal of Organic Chemistry" . "Convenient methods for preparing \u03C0-conjugated linkers as building blocks for modular chemistry" . . . . "308293" . . "25310" . . "Convenient methods for preparing \u03C0-conjugated linkers as building blocks for modular chemistry"@en . "[A4AD0CE9277A]" . . . "P(LA09041), Z(MSM0021627501)" . . . "Simple, straightforward and optimized procedures for preparing extended \u03C0-conjugated linkers are described. Either unsubstituted or 4-donor substituted \u03C0-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl \u03C0-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki-Miyaura or Sonogashira coupling reactions."@en . "DE - Spolkov\u00E1 republika N\u011Bmecko" . . "6"^^ . . . "RIV/00216275:25310/09:00008258" . . "Kulh\u00E1nek, Ji\u0159\u00ED" . . "RIV/00216275:25310/09:00008258!RIV10-MSM-25310___" . . "5" . . .