69225-38-3Relevant articles and documents
Cyclotrimerization of phenylacetylene catalyzed by a cobalt half-sandwich complex embedded in an engineered variant of transmembrane protein FhuA
Thiel,Sauer,Mertens,Polen,Chen,Schwaneberg,Okuda
, p. 5452 - 5456 (2018)
An (η5-cyclopentadienyl)cobalt(i) complex was covalently incorporated into an engineered variant of the transmembrane protein ferric hydroxamate uptake protein component: A, FhuA ΔCVFtev, using a thiol-ene reaction. A CD spectrum shows the structural integrity of the biohybrid catalyst. MALDI-TOF of the segment containing the anchoring site for the cobalt complex Cys545 confirmed successful conjugation. This biohybrid catalyst catalyzed the cyclotrimerization of phenylacetylene to give a mixture of regioisomeric 1,2,4- and 1,3,5-triphenylbenzene in aqueous medium.
Efficient and regioselective nickel-catalyzed [2 + 2 + 2] cyclotrimerization of ynoates and related alkynes
Rodrigo, Sanjeewa K.,Powell, Israel V.,Coleman, Michael G.,Krause, Jeanette A.,Guan, Hairong
supporting information, p. 7653 - 7657 (2013/11/06)
A nickel-based catalytic system has been developed for [2 + 2 + 2] cyclotrimerization of various alkynes, especially ynoates. This catalytic system enables facile construction of substituted aromatic compounds in excellent yields with high regioselectivity. The Royal Society of Chemistry 2013.
Diazadienes as Controlling Ligands in Homogeneous Catalysis, IX. Catalytic Cyclotetramerization of Propynoic Esters
Diercks, Rainer,Dieck, Heindirk tom
, p. 428 - 435 (2007/10/02)
Propynoic esters HCC-CO2R 2 react at low temperature in cyclohexane in the presence of precatalysts of the type diazadiene-nickel(0) complexes 3 and 4 or diazadiene-nickel-(η2-alkyne) complexes such as 5b to give exclusively or preponderantly c