245663-89-2Relevant academic research and scientific papers
Traceless linking of pyrroles: General methology and solid phase supported functionalizations
Bergauer, Markus,Gmeiner, Peter
, p. 274 - 278 (2002)
Transacetalization reaction of the diethoxymethyl (DEM) protected pyrroles 2a-f with the diol functionalized resin 3 resulted in the formation of the immobilized pyrroles 4a-f. Regioselective transformations including Pd-catalyzed coupling reactions and reductive aminations on solid phase were demonstrated.
New types of bi- and tri-dentate pyrrole-piperazine ligands and related zinc compounds: Synthesis, characterization, reaction study, and ring-opening polymerization of ε-caprolactone
Wu, Ming-Chun,Hu, Ting-Chia,Lo, Ya-Chun,Lee, Ting-Yu,Lin, Chia-Her,Lu, Wei-Yi,Lin, Chu-Chieh,Datta, Amitabha,Huang, Jui-Hsien
, p. 141 - 147 (2015)
Reactions of one or two equivalents of formaldehyde and phenylpiperazine with pyrrole in methanol or ethanol generated substituted pyrrole ligands C4H3NH-[2-CH2N(CH2CH2)2NPh] (1) and C
2,2-Dicyanovinyl as a nonaromatic aryl bioisostere: Synthesis, binding experiments and SAR studies of highly selective dopamine D4 receptor ligands
Haubmann, Christian,Huebner, Harald,Gmeiner, Peter
, p. 1969 - 1972 (2007/10/03)
The phenylpiperazinylmethyl substituted pyrrolylmethylenemalononitriles of type 3 and 4 were synthesized and evaluated as strong and selective dopamine D4 receptor ligands.
