950609-01-5Relevant academic research and scientific papers
Palladium-catalyzed alkene carboamination reactions for the synthesis of substituted piperazines
Nakhla, Josephine S.,Schultz, Danielle M.,Wolfe, John P.
experimental part, p. 6549 - 6570 (2011/02/25)
A strategy for the stereoselective preparation of enantiomerically enriched cis-2,6-disubstituted piperazines from amino acid precursors is described. The target compounds are generated in 95-99% ee with good to excellent levels of diastereoselectivity (usually 14:1 to >20:1) using Pd-catalyzed carboamination reactions between aryl or alkenyl halides and substituted ethylenediamine derivatives to form the heterocyclic rings. The synthesis requires only 4-5 steps from commercially available amino acids, and allows for the modular construction of piperazines bearing different substituents at N1, N4, C2, and C6. The use of this strategy for the construction of 2,3-disubstituted piperazines, fused bicyclic piperazines, and tetrahydroquinoxalines is also reported. In addition, the mechanism of the key carboamination reactions is discussed, and new models that predict and explain the stereochemical outcome of these transformations are presented.
A concise asymmetric synthesis of cis-2,6-disubstituted N-aryl piperazines via Pd-catalyzed carboamination reactions
Nakhla, Josephine S.,Wolfe, John P.
, p. 3279 - 3282 (2008/02/12)
A concise, modular, asymmetric synthesis of cis-2,6-disubstituted piperazines from readily available amino acid precursors is described. The key step in the synthesis is a Pd-catalyzed carboamination of a N 1-aryl-N2-allyl-1,2-diamin
