219581-98-3Relevant academic research and scientific papers
Asymmetric synthesis of 3-phenyl-2,3-methanophenylalanine developed by panning catalysts in a library format
Moye-Sherman, Destardi,Welch, Mike B.,Reibenspies, Joe,Burgess, Kevin
, p. 2377 - 2378 (1998)
Optimal catalysts for the key cyclopropanation step in a synthesis of the title compound were identified by screening libraries of metal complex-ligand combinations; the synthesis was completed, and a derivative of the final product was crystallized to es
Composite polymer/oxide hollow fiber contactors: Versatile and scalable flow reactors for heterogeneous catalytic reactions in organic synthesis
Moschetta, Eric G.,Negretti, Solymar,Chepiga, Kathryn M.,Brunelli, Nicholas A.,Labreche, Ying,Feng, Yan,Rezaei, Fateme,Lively, Ryan P.,Koros, William J.,Davies, Huw M. L.,Jones, Christopher W.
supporting information, p. 6470 - 6474 (2015/06/02)
Flexible composite polymer/oxide hollow fibers are used as flow reactors for heterogeneously catalyzed reactions in organic synthesis. The fiber synthesis allows for a variety of supported catalysts to be embedded in the walls of the fibers, thus leading
Novel dirhodium tetraprolinate catalysts containing bridging prolinate ligands for asymmetric carbenoid reactions
Davies, Huw M.L.,Panaro, Stephen A.
, p. 5287 - 5290 (2007/10/03)
The D2-symmetric dirhodium prolinate complex 3 is an effective catalyst for asymmetric vinylcarbenoid and phenylcarbenoid cyclopropanations.
Cyclopropane amino acids that mimic two χ1-conformations of phenylalanine
Moye-Sherman, Destardi,Jin, Song,Li, Shiming,Welch, Michael B.,Reibenspies, Joe,Burgess, Kevin
, p. 2730 - 2739 (2007/10/03)
A highly constrained analogue of phenylalanine was prepared in optically pure form. This disubstituted cyclopropane amino acid, DiFi, realises two χ1 values of the phenylalanine side chain. Unlike monosubstituted analogues, amino acids of this
