Matches in SemOpenAlex for { <https://semopenalex.org/work/W2949676897> ?p ?o ?g. }
- W2949676897 endingPage "158" @default.
- W2949676897 startingPage "148" @default.
- W2949676897 abstract "Abstract The hexamethylbenzene ruthenium(II) dimer [{RuCl(μ‐Cl)(η 6 ‐C 6 Me 6 )}] 2 (5 mol%), tested among a series of ruthenium(II) and ruthenium(IV) complexes, represents an efficient precatalyst source for the dimerization of terminal arylalkynes ArCCH [Ar=C 6 H 5 , 3,4,5‐(OMe) 3 C 6 H 2 , 4‐MeOC 6 H 4 , 2‐MeOC 6 H 4 , 4‐MeC 6 H 4 , 2,4,5‐Me 3 C 6 H 2 , 4‐BrC 6 H 4 , 4‐ClC 6 H 4 , 4‐FC 6 H 4 , 4‐HC(O)C 6 H 4 , 4‐CH 2 CHC 6 H 4 , 3‐NCC 6 H 4 , 4‐O 2 NC 6 H 4 , 4‐EtO 2 C‐(CH 2 ) 3 OC 6 H 4 , 4‐HO(CH 2 CH 2 O) 3 C 6 H 4 , 3‐HO(CH 2 CH 2 O) 3 ‐C 6 H 4 ] in acetic acid/water mixture (1:1, v/v). The reactions proceed for 24 h at room temperature under heterogeneous conditions and afford the dimeric enyne derivatives ( E )‐ArCHCHCCAr in high yields and stereoselectivity. The preformed acetato complex [RuCl(η 6 ‐C 6 Me 6 )(κ 2 ‐OAc)] catalyzes the dimerization of phenylacetylene under analogous conditions, with rapid substrate conversion. The presence of cosolvents of acetic acid different from water reduces dramatically the efficiency and selectivity of the reaction. The aqueous medium facilitates the activation stage of the precatalyst by assisting the splitting of the ruthenium dimer. The addition or generation in situ of acetate salts results in shorter reactions times (0.5–3 h) and excellent yields, due to the rapid formation of active acetato complexes. Circumstantial evidence indicates that the π‐bound alkyne molecule is activated by intramolecular proton abstraction. This is currently the most efficient, E ‐selective and wide‐scope catalytic system for the alkyne dimerization reaction in protic aqueous media." @default.
- W2949676897 created "2019-06-27" @default.
- W2949676897 creator A5026483743 @default.
- W2949676897 creator A5062391907 @default.
- W2949676897 creator A5065851999 @default.
- W2949676897 creator A5085375950 @default.
- W2949676897 date "2012-01-01" @default.
- W2949676897 modified "2023-10-18" @default.
- W2949676897 title "Dimerization of Terminal Arylalkynes in Aqueous Medium by Ruthenium and Acid Promoted (RAP) Catalysis: Acetate‐ Assisted (<i>sp</i>)C(<i>sp</i><sup>2</sup>)C Bond Formation" @default.
- W2949676897 cites W1532684710 @default.
- W2949676897 cites W1565924116 @default.
- W2949676897 cites W1902438951 @default.
- W2949676897 cites W1964602959 @default.
- W2949676897 cites W1964828238 @default.
- W2949676897 cites W1967392210 @default.
- W2949676897 cites W1968018529 @default.
- W2949676897 cites W1968019447 @default.
- W2949676897 cites W1968523322 @default.
- W2949676897 cites W1969327905 @default.
- W2949676897 cites W1969356009 @default.
- W2949676897 cites W1969566025 @default.
- W2949676897 cites W1969598536 @default.
- W2949676897 cites W1969627594 @default.
- W2949676897 cites W1969962788 @default.
- W2949676897 cites W1973199094 @default.
- W2949676897 cites W1976603595 @default.
- W2949676897 cites W1979134597 @default.
- W2949676897 cites W1980680647 @default.
- W2949676897 cites W1982219674 @default.
- W2949676897 cites W1985597923 @default.
- W2949676897 cites W1985886459 @default.
- W2949676897 cites W1986188386 @default.
- W2949676897 cites W1989683953 @default.
- W2949676897 cites W1993959006 @default.
- W2949676897 cites W1995877281 @default.
- W2949676897 cites W1995940710 @default.
- W2949676897 cites W1998718476 @default.
- W2949676897 cites W2001110257 @default.
- W2949676897 cites W2010040570 @default.
- W2949676897 cites W2012669063 @default.
- W2949676897 cites W2012780101 @default.
- W2949676897 cites W2014095348 @default.
- W2949676897 cites W2014876392 @default.
- W2949676897 cites W2015274604 @default.
- W2949676897 cites W2020446333 @default.
- W2949676897 cites W2020618574 @default.
- W2949676897 cites W2021416828 @default.
- W2949676897 cites W2021448085 @default.
- W2949676897 cites W2022686443 @default.
- W2949676897 cites W2022890554 @default.
- W2949676897 cites W2023199178 @default.
- W2949676897 cites W2025070505 @default.
- W2949676897 cites W2027289980 @default.
- W2949676897 cites W2028824397 @default.
- W2949676897 cites W2031580869 @default.
- W2949676897 cites W2033365783 @default.
- W2949676897 cites W2034477724 @default.
- W2949676897 cites W2036930848 @default.
- W2949676897 cites W2037503876 @default.
- W2949676897 cites W2044542781 @default.
- W2949676897 cites W2045569018 @default.
- W2949676897 cites W2047445222 @default.
- W2949676897 cites W2047627084 @default.
- W2949676897 cites W2053236886 @default.
- W2949676897 cites W2055321335 @default.
- W2949676897 cites W2056349155 @default.
- W2949676897 cites W2058279586 @default.
- W2949676897 cites W2060108236 @default.
- W2949676897 cites W2060231246 @default.
- W2949676897 cites W2060953989 @default.
- W2949676897 cites W2060982534 @default.
- W2949676897 cites W2064276240 @default.
- W2949676897 cites W2065857235 @default.
- W2949676897 cites W2066669246 @default.
- W2949676897 cites W2068379856 @default.
- W2949676897 cites W2069394976 @default.
- W2949676897 cites W2072297544 @default.
- W2949676897 cites W2075909808 @default.
- W2949676897 cites W2079362689 @default.
- W2949676897 cites W2081282991 @default.
- W2949676897 cites W2081676541 @default.
- W2949676897 cites W2085441037 @default.
- W2949676897 cites W2088230223 @default.
- W2949676897 cites W2088246493 @default.
- W2949676897 cites W2088623222 @default.
- W2949676897 cites W2089602042 @default.
- W2949676897 cites W2089822872 @default.
- W2949676897 cites W2092255775 @default.
- W2949676897 cites W2105016835 @default.
- W2949676897 cites W2106508600 @default.
- W2949676897 cites W2109059520 @default.
- W2949676897 cites W2115697879 @default.
- W2949676897 cites W2116272579 @default.
- W2949676897 cites W2120876202 @default.
- W2949676897 cites W2125591426 @default.
- W2949676897 cites W2128501936 @default.
- W2949676897 cites W2137163376 @default.
- W2949676897 cites W2139409824 @default.