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1.
《Arabian Journal of Chemistry》2014,7(5):623-629
The multi-component reaction of 1-benzothiopyran-4-ones with heterocyclic amines and dimethylformamide-dimethylacetal (DMFDMA) in DMF at 150 °C under controlled microwave heating afforded novel poly-heterocyclic ring systems. Also, reaction of 3-dimethylaminomethylene-1-benzothiopyran-4-one with activemethylene derivatives was investigated. The structure of all products was established on the bases of spectral data and elemental analyses and alternative synthesis if possible. The prepared compounds were screened for their antitumor activity against HCT-116 “colon” cancer cell line and some derivatives showed promising activity. 相似文献
2.
《Arabian Journal of Chemistry》2022,15(3):103640
Complexes of transition metals [Co(II), Cd(II) and Mo(0)] with a new enaminone (PA) 3-chloro-4-((4-methoxyphenyl)amino)pent-3-en-2-one were synthesized and afterwards characterized by 1H NMR, 13C NMR, FAB-MS, UV–Vis, ICP-OES, TGA and FTIR. The spectroscopic and conductance data suggested that the ligand (PA) is attached to the metal ions in bidentate, neutral form through the nitrogen atom of amino group and the oxygen of carbonyl group. Metal complexes displayed octahedral geometries. In vitro urease inhibition and cytotoxic activities of all the compounds were evaluated. Results revealed that Co(II) complex (PA-Co) was even more significant than the reference drug thiourea. Analysis of the cytotoxicity indicated that, the Co(II) complex has more cytotoxic effect than enaminone ligand and other complexes when assessed on the human cancer cell lines MCF-7.Molecular docking simulation was also performed to find out the putative binding mode within the target protein. 相似文献
3.
Ze-Hun Cao Yu-Hao Wang Dr. Subarna Jyoti Kalita Dr. Uwe Schneider Prof. Dr. Yi-Yong Huang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(5):1900-1906
Unprecedented phosphine-catalyzed [4+1] cycloadditions of allenyl imides have been discovered using various N-based substrates including methyl ketimines, enamines, and a primary amine. These transformations provide a one-pot access to cyclopentenoyl enamines and imines, or (chiral) γ-lactams through two geminal C−C bond or two C−N bond formations, respectively. Several P-based key intermediates including a 1,4-(bis)electrophilic α,β-unsaturated ketenyl phosphonium species have been detected by 31P NMR and HRMS analyses, which shed light on the postulated catalytic cycle. The synthetic utility of this new chemistry has been demonstrated through a gram-scaling up of the catalytic reaction as well as regioselective hydrogenation and double condensation to form cyclopentanoyl enamines and fused pyrazole building blocks, respectively. 相似文献
4.
Drissa Sissouma Geoffroy DequirezSylvain Collet André Guingant 《Tetrahedron letters》2011,52(18):2336-2339
We have developed an efficient synthesis of both enantiomers of a key azadiene for the preparation of 5-aza analogues of angucyclinones through a hetero Diels-Alder reaction. These dienes were efficiently prepared via a 4-step procedure from known and readily available chiral diketoesters. 相似文献
5.
Sarangthem Joychandra Singh 《Tetrahedron letters》2008,49(25):3991-3994
Regioselective allylation of enaminones using CuCl2 as the catalyst to give C-allylated products is reported for the first time. The C-allylated products undergo hydrolysis followed by a rearrangement yielding β-keto allyl enamides in excellent yields. 相似文献
6.
An improved methodology for the synthesis of substituted pyrido[2,3-d]pyrimidinediones from 6-aminouracils and the corresponding enaminone has been developed which provides high yields via an operationally simple process. The method has been extended to encompass a range of electron-rich enaminones, a substrate class that does not perform well under the standard conditions. 相似文献
7.
Heshmatollah Alinezhad Mahmood Tajbakhsh Mahboobeh Zare 《Journal of fluorine chemistry》2011,132(11):995-1000
A simple, efficient and three component one-pot synthesis of 1,4,5-trisubstituted pyrazoles by condensation of β-dicarbonyls, N,N-dimethylformamide dimethyl acetal (DMFDMA) and hydrazine derivatives in 2,2,2-trifluoroethanol without using any catalyst and activation, is described. 相似文献
8.
Reactions of ferrocenoylacetone with 2-(aminomethyl)pyridine and N-(2-hydroxyethyl)-1,2-diaminoethane afford the multidentate enaminones HL1 and H3L2, respectively. Reactions of copper acetate with the two enaminones generate the corresponding mixed-ligand complexes I and II, which are formulated as [CuL1(OAc)] and [Cu(H2L2)(OAc)], respectively. The structures of HL1, I and II have been determined by single-crystal X-ray crystallography. In complex I, HL1 acts as a monoanionic tridentate donor via the carbonyl oxygen, deprotonated enamine nitrogen and pyridyl nitrogen atoms, the acetate anion is monodentate and the coordination geometry of the central metal is square planar. In complex II, H3L2 is a monoanionic tetradentate ligand via the carbonyl oxygen, deprotonated enamine nitrogen, secondary amine nitrogen and hydroxy oxygen atoms, the acetate anion is monodentate and the coordination geometry of the central metal is a distorted trigonal bipyramid. 相似文献
9.
LI Ming WANG Shu-wen WEN Li-rong KE Zi-qin 《高等学校化学研究》2005,21(6):663-667
Ethyl 7-aryl-2-benzyhhiopyrazolo [ 1,5-a ] pyrimidine-3-carboxylates (3a-3f) were conveniently synthesized through the reactions of enaminones with 5-amino-3-benzyhhio4-ethoxycarbonyl-1 H-pyrazole in good yields and high regioselectivity. The structures of the new compounds were fully characterized by spectroscopic measurmehts, elemental analysis and X-ray diffraction analysis. A plausible reaction mechanism for the formation of the title compounds was also presented. 相似文献
10.
Sandip Balasaheb Wakade Dipak Kumar Tiwari Mandalaparthi Phanindrudu Dharmendra Kumar Tiwari 《Tetrahedron》2019,75(30):4024-4030
An efficient and transition metal-free approach for the synthesis of functionalized 3-ketoquinolines from readily available anilines, enaminones and DMSO in the presence of K2S2O8 has been conducted. This one pot tandem reaction proceeds through [3+2+1] cycloaddition reaction involving DMSO, enaminones and amines. In this environmental benign approach, DMSO acts as both a one carbon source and the solvent. A broad range of variously substituted amines and enaminones are successfully employed in this one pot tandem process to access a broad range of substituted 3-ketoquinolines. 相似文献