107939-57-1Relevant articles and documents
Hydrostannylation-cross-coupling strategy for the stereoselective synthesis of alkylidenemalonates and related α,β-unsaturated esters
Fujiwara, Shinichi,Cadou, Romain,Yamaoka, Yousuke,Takasu, Kiyosei,Yamada, Ken-Ichi
, p. 1264 - 1272 (2015/03/04)
A method for the stereoselective synthesis of alkylidenemalonates and related α,β-unsaturated esters by a hydrostannylation-cross-coupling process has been developed. Pd-catalyzed and radical hydrostannylation of propiolate derivatives stereoselectively provided α-alkoxycarbonyl (E)- and (Z)-vinylstannanes, respectively, which were then converted into alkylidenemalonates by the Stille coupling reaction. A one-pot process was also realizable for the Pd-catalyzed reactions.
Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes
Cox, Russell J.,Ritson, Dougal J.,Dane, Thomas A.,Berge, John,Charmant, Jonathan P. H.,Kantacha, Anob
, p. 1037 - 1039 (2007/10/03)
Conditions are reported for the facile, high-yielding coupling of acyl chlorides with terminal alkynes in a reaction involving palladium and copper iodide; the reaction is tolerant of a wide variety of acyl chlorides and terminal alkynes and provides a co