3526-43-0Relevant articles and documents
N1[P(OPH)3]4 catalyzed transfer hydrogenation using HCOONH4
Iyer, Suresh,Sattar, Aruna K.
, p. 1721 - 1725 (1998)
Ni[P(OPh)3]4 was found to catalyze the transfer hydrogenation of various organic functional groups using HCOONH4.
An Insight into Transfer Hydrogenation Reactions Catalysed by Iridium(III) Bis-N-heterocyclic Carbenes
García, Nestor,Jaseer,Munarriz, Julen,Sanz Miguel, Pablo J.,Polo, Victor,Iglesias, Manuel,Oro, Luis A.
, p. 4388 - 4395 (2015)
A variety of [M(L)2(L′)2{κC,C′-bis(NHC)}]BF4 complexes (M = Rh or Ir; L = CH3CN or wingtip group; L′ = I- or CF3COO-; NHC=N-heterocyclic carbene) have been tested as pre-catalyst
Design, synthesis and evaluation of novel bis-substituted aromatic amide dithiocarbamate derivatives as colchicine site tubulin polymerization inhibitors with potent anticancer activities
Sun, Ya-Xin,Song, Jian,Kong, Li-Jun,Sha, Bei-Bei,Tian, Xin-Yi,Liu, Xiu-Juan,Hu, Tao,Chen, Ping,Zhang, Sai-Yang
supporting information, (2021/12/31)
As the continuation of our work on the development of tubulin inhibitors with potential anticancer activities, novel bis-substituted aromatic amide dithiocarbamate derivatives were designed by contacting bis-substituted aryl scaffolds (potential anti-tubulin fragments) with N-containing heterocycles (potential anti-tubulin fragments) in one hybrid using the anticancer dithioformate unit as the linker. The antiproliferative activity against three digestive tract tumor cells was evaluated and preliminary structure activity relationships were summarized. Among these compounds, compound 20q exhibited most potent antiproliferative activity against MGC-803, HCT-116, Kyse30 and Kyse450 cells with IC50 values of 0.084, 0.227, 0.069 and 0.078 μM, respectively. In further studies, compound 20q was identified as a novel tubulin inhibitor targeting the colchicine binding site. Compound 20q could inhibit the microtubule assembly and disrupt cytoskeleton in Kyse30 and Kyse450 cells. The results of molecular docking suggested that compound 20q could tightly bind into the colchicine binding site of tubulin by hydrogen bonds and hydrophobic interactions. Compound 20q dose-dependently inhibited the cell growth and colony formation, effectively arrested cells at the G2/M phase and induce mitochondrial apoptosis in Kyse30 and Kyse450 cells. In addition, Compound 20q could regulate the expression of G2/M phase and mitochondrial apoptosis related proteins. Collectively, compound 20q was here reported as a novel tubulin inhibitor with potential anticancer activities.
Hydroboration and reductive amination of ketones and aldehydes with HBpin by a bench stable Pd(ii)-catalyst
Biswas, Bhaskar,Devadkar, Ajitrao Kisan,Gupta, Puneet,Joshi, Mayank,Mahato, Shreya,Panda, Tarun K.,Rawal, Parveen,Roy Choudhury, Angshuman
supporting information, p. 1103 - 1111 (2022/02/11)
A palladium(ii) complex [(κ4-{1,2-C6H4(NCH-C6H4O)2}Pd] (1) supported by a dianionic salen ligand [1,2-C6H4(NCH-C6H4O)2]2- (L) was synthesised and used as a molecular pre-catalyst in the hydroboration of aldehydes and ketones. The molecular structure of Pd(ii) complex 1 was established by single-crystal X-ray diffraction analysis. Complex 1 was tested as a competent pre-catalyst in the hydroboration of aldehydes and ketones with pinacolborane (HBpin) to produce corresponding boronate esters in excellent yields at ambient temperature under solvent-free conditions. Further, the complex 1 proved to be a competent catalyst in the reductive amination of aldehydes with HBpin and primary amines under mild and solvent-free conditions to afford a high yield (up to 97%) of corresponding secondary amines. Both protocols provided high conversion, superior selectivity and broad substrate scope, from electron-withdrawing to electron-donating and heterocyclic substitutions. A computational study based on density functional theory (DFT) revealed a reaction mechanism for Pd-catalysed hydroboration of carbonyl species in the presence of HBpin. The protocols also uncovered the dual role of HBpin in achieving the hydroboration reaction.