108240-32-0Relevant articles and documents
Mechanism of the Alkylation of Indoles with Nitrostyrenes Catalyzed by Chiral-at-Metal Complexes
Carmona, María,Rodríguez, Ricardo,Passarelli, Vincenzo,Carmona, Daniel
, p. 988 - 995 (2019)
Chiral-at-metal rhodium(III) complexes of the formula [Rh(4C,N,N,P-L)A(Solv)][SbF6]n (Solv = A = MeCN, n = 2 (1); Solv = H2O, A = MeCN, n = 2 (2); Solv = MeCN, A = Cl, n = 1 (3); Solv = H2O, A = Cl, n
Half-sandwich complexes of osmium containing guanidine-derived ligands
Parker, Amie,Lamata, Pilar,Viguri, Fernando,Rodríguez, Ricardo,López, José A.,Lahoz, Fernando J.,García-Ordu?a, Pilar,Carmona, Daniel
, p. 13601 - 13617 (2020)
Pyridinyl- and phosphano-guanidino complexes of formula [(η6-p-cymene)OsCl(H2L)][SbF6] (cymene = MeC6H4iPr; H2L = N,N′-bis(p-Tolyl)-N′′-(2-pyridinylmethyl)guanidine, H2L1 (1) and N,N′-bis(p-Tolyl)-N′′-(2-diphenylphosphanoethyl)guanidine, H2L2 (2)) have be
Bottom-Up Assembly of a Highly Efficient Metal-Organic Framework for Cooperative Catalysis
Li, Changda,Tang, Haitong,Fang, Yu,Xiao, Zhifeng,Wang, Kunyu,Wu, Xiang,Niu, Helin,Zhu, Chengfeng,Zhou, Hong-Cai
supporting information, p. 13912 - 13919 (2018/10/20)
In this study, we demonstrate a bottom-up assembly of a monomeric copper complex and a two-dimensional (2-D) heterometallic metal-organic framework (MOF) from a carboxylate-functionalized tridentate Schiff base ligand and metal ions. The obtained 2-D MOF
Quantification of Catalytic Activity for Electrostatically Enhanced Thioureas via Reaction Kinetics and UV-vis Spectroscopic Measurement
Fan, Yang,Payne, Curtis,Kass, Steven R.
, p. 10855 - 10863 (2018/07/30)
Charged thiourea derivatives containing one and two methylated or octylated pyridinium ion centers and a tetraarylborate or triflate counteranion are reported. These novel catalysts are much more active in the Friedel-Crafts reactions of trans-β-nitroalke
A combination of water and microwave irradiation promotes the catalyst-free addition of pyrroles and indoles to nitroalkenes
De Rosa, Margherita,Soriente, Annunziata
experimental part, p. 2981 - 2986 (2010/06/16)
A combination of water and microwave irradiation was used for the first time to perform a catalyst-free nitro-Michael addition of pyrroles and indoles. Under superheated conditions, the water trends to ionize by changing its chemical and physical properti
A practical indium tribromide catalysed addition of indoles to nitroalkenes in aqueous media
Bandini, Marco,Melchiorre, Paolo,Melloni, Alfonso,Umani-Ronchi, Achille
, p. 1110 - 1114 (2007/10/03)
The 1,4-conjugate addition of indoles to nitroalkenes was efficiently carried out in aqueous media using a catalytic amount of indium tribromide (5 mol%). The reusability of the indium tribromide was tested by performing consecutive cycles with the same c