95116-31-7Relevant academic research and scientific papers
New pyrrole inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity
La Regina, Giuseppe,Silvestri, Romano,Artico, Marino,Lavecchia, Antonio,Novellino, Ettore,Befani, Olivia,Turini, Paola,Agostinelli, Enzo
, p. 922 - 931 (2007/10/03)
A series of new pyrrole derivatives have been synthesized and evaluated for their monoamine oxidase (MAO) A and B inhibitory activity and selectivity. N-Methyl,N-(benzyl),N-(pyrrol-2-ylmethyl)amine (7) and N-(2-benzyl),N-(1- methylpyrrol-2-ylmethyl)amine
Highly enantioselective synthesis of tetrahydro-β-carbolines and tetrahydro-γ-carbolines via Pd-catalyzed intramolecular allylic alkylation
Bandini, Marco,Melloni, Alfonso,Piccinelli, Fabio,Sinisi, Riccardo,Tommasi, Simona,Umani-Ronchi, Achille
, p. 1424 - 1425 (2007/10/03)
A novel Pd-catalyzed intramolecular allylic alkylation of indoles allows THBCs and THGCs to be effectively synthesized in high yields and excellent enantiomeric excesses (ee up to 97%). Copyright
Diversity in complexation of [Rh(I)(cod)]+ and [Ir(I)(cod)]+ by pyridine-amine-pyrrole ligands
De Bruin, Bas,Kicken, Reinout J. N. A. M.,Suos, Nicolaas F. A.,Donners, Maurice P. J.,Den Reijer, Carolien J.,Sandee, Albertus J.,De Gelder, Rene,Smits, Jan M. M.,Gal, Anton W.,Spek, Anton L.
, p. 1581 - 1592 (2007/10/03)
Complexation of [Rh(I)(cod)]+ and [Ir(I)(cod)]+ by the new pyridine- amine-pyrrole ligands Py-CH2-N(R)-CH2-Pyr-H (HL(R); R = H, Bzl, Bu) and the corresponding pyridine-amine-pyrrolate ligands [Py-CH2-
