70975-29-0Relevant academic research and scientific papers
Asymmetric hydrogenation of alkynyl ketones with the η6- arene/TsDPEN-ruthenium(II) catalyst
Arai, Noriyoshi,Satoh, Hironori,Utsumi, Noriyuki,Murata, Kunihiko,Tsutsumi, Kunihiko,Ohkuma, Takeshi
supporting information, p. 3030 - 3033 (2013/07/26)
Enantioselective hydrogenation of alkynyl ketones catalyzed by Ru(OTf)(TsDPEN)(η6-p-cymene) (TsDPEN = N-(p-toluenesulfonyl)-1,2- diphenylethylenediamine) affords the propargylic alcohols in up to 97% ee. The alkynyl moieties are left intact in most cases. The reaction can be conducted with a substrate-to-catalyst molar ratio as high as 5000 under 10 atm of H 2. The mode of enantioselection is elucidated with the transition state models directed by the CH/π attractive interaction between the substrate and the catalytic species.
Enantiospecific synthesis of 1,3-disubstituted allenes by palladium-catalyzed coupling of propargylic compounds with arylboronic acids
Yoshida, Masahiro,Okada, Tatsuro,Shishido, Kozo
, p. 6996 - 7002 (2008/02/05)
An enantiospecific coupling of propargylic esters and carbonates with arylboronic acids has been developed using a palladium catalyst. Optically active 1,3-disubstituted allenes were synthesized with high enantiomeric excesses by carrying out the reaction
