6502-37-0Relevant articles and documents
Synthesis, characterization, DFT and molecular docking studies for novel 1,5-diphenylpenta-1,4-dien-3-one O-benzyl oximes
Erdogan, Taner
, p. 2243 - 2255 (2019/06/13)
The main objectives of this study are: (a) to synthesize novel 1,5-diphenylpenta-1,4-dien-3-one O-benzyl oximes in an efficient way, (b) to investigate the synthesized molecules computationally via DFT calculations, (c) to compare computationally obtained data with experimental results and (d) to perform molecular docking calculations for the newly synthesized compounds and heat shock protein HSP90A N-terminal domain to determine the binding affinities of the investigated molecules and to reveal possible receptor–ligand interactions. In the first part of the study, syntheses and characterizations of the investigated compounds have been carried out. In this part, the target compounds have been synthesized and characterized successively. In the synthesis of target compounds from corresponding oximes, ultrasound has been used alternatively and results showed that the usage of ultrasound considerably increases the reaction rate and the efficiency. In the second part, detailed density functional theory calculations have been performed on the investigated compounds with the use of Becke, three-parameter, Lee–Yang–Parr hybrid functional and various basis sets. In this part, geometry optimizations, frequency analyses, NMR spectral analyses, frontier molecular orbital calculations, and molecular electrostatic potential map calculations have been performed. In NMR spectral analyses, both continuous set of gauge transformations (CSGT) and gauge-independent atomic orbital (GIAO) methods have been used and the obtained results with the use of various basis sets have been compared. Results showed that in NMR calculations, GIAO method is more successful than CSGT method and can provide satisfactory results even with small basis sets. In the third part of the study, molecular docking calculations have been performed on the investigated compounds and HSP90A N-terminal domain. Results showed that investigated molecules show a good binding affinity for HSP90A N-terminal domain. The binding affinities were found to be in the range of ? 8.7 to ? 10.1?kcal/mol.
Rhodium(III)-catalyzed synthesis of pyridines from α,β- unsaturated ketoximes and internal alkynes
Too, Pei Chui,Noji, Toshiharu,Lim, Ying Jie,Li, Xingwei,Chiba, Shunsuke
supporting information; experimental part, p. 2789 - 2794 (2012/01/11)
A method for the synthesis of highly substituted pyri-dines from ,-unsaturated oximes and internal alkynes has been developed using [Cp*RhCl2]2-CsOPiv as the catalyst system. The present transformation is carried out by a redox-neutral sequence of vinylic C-H rhodation, alkyne insertion, and C-N bond formation of the putative vinyl rhodium intermediate with the oxime nitrogen, where the N-O bond of oxime derivatives could work as an internal oxidant to maintain the catalytic cycle. Georg Thieme Verlag Stuttgart · New York.
Pyridine synthesis from oximes and alkynes via rhodium(iii) catalysis: Cp* and Cpt provide complementary selectivity
Hyster, Todd K.,Rovis, Tomislav
supporting information; experimental part, p. 11846 - 11848 (2011/12/02)
The synthesis of pyridines from readily available α,β- unsaturated oximes and alkynes under mild conditions and low temperatures using Rh(iii) catalysis has been developed. It was found that the use of sterically different ligands allows for complementary selectivities to be achieved.
An efficient synthesis of l,5-diaryl-l,4-pentadien-3-one oxime in the presence of anhydrous sodium sulfate
Li, Ji-Tai,Zhai, Xin-Li,Bai, Bo,Liang, Yan-Hua
experimental part, p. 323 - 326 (2011/07/08)
A series of 1,5-diaryl-1,4-pentadien-3-one oximes were synthesized via the reaction of 1,5-diaryl-1,4- pentadien-3-one with hydroxylamine hydrochloride in the presence of anhydrous sodium sulfate at refluxing EtOH to give good yields. This method provided
A simple, modular synthesis of substituted pyridines
Liu, Songbai,Liebeskind, Lanny S.
, p. 6918 - 6919 (2008/09/21)
A simple, modular method to prepare highly substituted pyridines is disclosed. The method employs a cascade reaction comprising (1) a novel N-iminative, Cu-catalyzed cross-coupling of alkenylboronic acids at the N-O bond of α,β-unsaturated ketoxime O-pentafluorobenzoates, (2) electrocyclization of the resulting 3-azatriene, and (3) air oxidation affording highly substituted pyridines in moderate to excellent isolated yields (43-91%). Starting materials are readily available, and functional group tolerance is very good. Copyright
Extractive spectrophotometric determination of trace amounts of copper(II) using 1,5-diphenyl-1,4-pentadien-3-oxime
Sreedhar,Jyothi
, p. 1038 - 1040 (2007/10/03)
1,5-Diphenyl-1,4-pentadien-3-oxime (DPPDO) has been identified as a sensitive and selective analytical reagent for the extractive spectrophotometric determination of copper(II). This reagent reacts with copper(II) in the pH range of 2.0-12.0 to form a yel
