109270-63-5Relevant academic research and scientific papers
Structural Characterization of N-Alkylated Twisted Amides: Consequences for Amide Bond Resonance and N-C Cleavage
Hu, Feng,Lalancette, Roger,Szostak, Michal
, p. 5062 - 5066 (2016)
Herein, we describe the first structural characterization of N-alkylated twisted amides prepared directly by N-alkylation of the corresponding non-planar lactams. This study provides the first experimental evidence that N-alkylation results in a dramatic
σ N-C Bond Difunctionalization in Bridged Twisted Amides: Sew-and-Cut Activation Approach to Functionalized Isoquinolines
Hu, Feng,Nareddy, Pradeep,Lalancette, Roger,Jordan, Frank,Szostak, Michal
, p. 2386 - 2389 (2017)
A rare example of highly selective σ N-C bond difunctionalization in bridged twisted lactams through N-C cleavage has been achieved. In combination with the intramolecular Heck cyclization, this method affords a two-step bond reorganization event (“sew-an
Synthesis and use of water-soluble sulfonated dibenzofuran-based phosphine ligands
Sollewijn Gelpke, Arjan E.,Veerman, Johan J.N.,Goedheijt, Marcel Schreuder,Kamer, Paul C.J.,Van Leeuwen, Piet W.N.M.,Hiemstra, Henk
, p. 6657 - 6670 (2007/10/03)
The syntheses of three triphenylphosphine analogues with one, two or three phenyl groups replaced by 2-dibenzofuranyl groups, respectively, and one enantiopure analogue of the atropisomeric diphosphine MeO-BIPHEP with all four phenyl groups replaced by 2-dibenzofuranyl are reported. Sulfonation of these compounds with sulfuric acid at rt proceeded with complete regioselectivity at the 8-position in the dibenzofuran moieties. These results proved the usefulness of dibenzofuran as a structural moiety in the synthesis of water-soluble phosphine ligands. The dibenzofuran-based, water- soluble triphenylphosphine analogues were used as ligands in palladium- catalysed aqueous phase Heck and Suzuki reactions and in the rhodium- catalysed two-phase hydroformylation of propene.
The synthesis of bridged-ring carbo- and hetero-cycles via palladium catalysed regiospecific cyclisation reactions
Grigg,Santhakumar,Sridharan,Stevenson,Teasdale,Thornton-Pett,Worakun
, p. 9703 - 9720 (2007/10/02)
A catalyst system comprising 10 mol % (Pd(OAc)) and 20 mol % PPh3 effects the cyclisation of aryl halides onto proximate alkenes via 5-, 6-, and 7-exo-trig, and 7-endo-trig processes giving a variety of bridged-ring carbo- and hetero-cycles in
