Synthesis of Tri-Substituted Olefin Derivatives from 1-Alkene-1,2-Diboronic Esters via Sequential Suzuki-Suzuki Coupling Reaction and Their Biological Activity
“…24 We also demonstrated regioselective azidations 25 and synthesis of trisubstituted olefin derivatives from 1-alkene-1,2-diboronic esters. 26 Here we describe a simple method using a palladium catalyst to form E -enynes and Z -enediynes via Suzuki–Miyaura cross-coupling reactions between bis-boronic esters and alkynyl halides (Scheme 1e).…”
Herein, we present an efficient stereo-controlled synthesis of enyne and enediyne derivatives, via sequential Suzuki–Miyaura coupling reactions from easily prepared 1-alkene-1,2-diboronic esters.
“…24 We also demonstrated regioselective azidations 25 and synthesis of trisubstituted olefin derivatives from 1-alkene-1,2-diboronic esters. 26 Here we describe a simple method using a palladium catalyst to form E -enynes and Z -enediynes via Suzuki–Miyaura cross-coupling reactions between bis-boronic esters and alkynyl halides (Scheme 1e).…”
Herein, we present an efficient stereo-controlled synthesis of enyne and enediyne derivatives, via sequential Suzuki–Miyaura coupling reactions from easily prepared 1-alkene-1,2-diboronic esters.
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