共查询到20条相似文献,搜索用时 15 毫秒
1.
Ali Reza Kazemizadeh Nahid Shajari Reza Shapouri Neda Adibpour Reza Teimuri‐Mofrad Parisa Dinmohammadi 《应用有机金属化学》2016,30(3):148-153
A four‐component reaction between aromatic carboxylic acids, (N‐isocyanimino)triphenylphosphorane, ferrocenecarbaldehyde and dibenzylamine is reported. This approach is an efficient, simple and high‐yield procedure for the synthesis of 1,3,4‐oxadiazole derivatives containing a ferrocene unit. The antimicrobial activities of the products were investigated against Staphylococcus aureus and Pseudomonas aeruginosa in in vitro and in vivo assays. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
2.
A mild and facile Wittig reaction between N‐substituted maleimides and aldehydes has been developed. Various synthetically valuable alkylidenesuccinimides were obtained from this one‐pot reaction in high yields (up to 99%). The product was obtained by simple filtration and no extra purification was necessary. Ethanol, an environment‐benign solvent, was found to be a suitable reaction medium. 相似文献
3.
A chitosan‐based magnetic nanocomposite was synthesized by an eco‐friendly and simple procedure, and was characterized using scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray diffraction and Fourier transform infrared spectroscopy. It was then used for the efficient synthesis of tetrahydrobenzoxanthen‐11‐one derivatives via a one‐pot three‐component condensation of 2‐naphthol, various aldehydes and dimedone in ethanol. The catalyst was recovered easily and reused several times without significant loss of catalytic activity. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
4.
Masoumeh Zakeri Majid M. Heravi Mina Saeedi Narges Karimi Hossein A. Oskooie Niloofar Tavakoli‐Hoseini 《中国化学》2011,29(7):1441-1445
An efficient one‐pot condensation of β‐naphthol, aldehydes and cyclic 1,3‐dicarbonyl compound has been achieved with ionic liquids as catalyst, thus a variety of 8,9,10,12‐tetrahydrobenzo[a]xanthen‐11‐one derivatives were prepared in good yields. The present approach offers several advantages such as shorter reaction times, good yields and mild reaction conditions. 相似文献
5.
Silica‐supported ionic liquid Si–[SbSipim][PF6] as a catalyst was used first in the synthesis of polyhydroquinolines. The catalyst exhibits high catalytic activity in the reaction, and can be easily recovered and reused without significant loss of its activity for six runs. This green method offers several advantages, including high yield, short reaction time, simple work‐up procedure, ease of separation, and recyclability of the catalyst. 相似文献
6.
A tandem one‐pot synthesis of polysubstituted 1,3‐thiazines has been developed by reacting with cyanoacetamide and isothiocyanate derivatives to give rise to 2‐cyano‐3‐mercaptoacrylamides, which are trapped in situ by various aldehydes or diversely substituted ketones through intermolecular cyclization, providing polysubstituted 1,3‐thiazine derivatives in short reaction times with good to excellent yields. The salient features of this novel protocol are operational simplicity, accessing the desired products from the readily available starting materials and easy of product isolation and may find wide spread applications in medicinal chemistry. 相似文献
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8.
Hakan Durmaz Aydan Dag Alp Hizal Gurkan Hizal Umit Tunca 《Journal of polymer science. Part A, Polymer chemistry》2008,46(21):7091-7100
3‐Arm star‐block copolymers, (polystyrene‐b‐poly(methyl methacrylate))3, (PS‐b‐PMMA)3, and (polystyrene‐b‐poly(ethylene glycol))3, (PS‐b‐PEG)3, are prepared using double‐click reactions: Huisgen and Diels–Alder, with a one‐pot technique. PS and PMMA blocks with α‐anthracene‐ω‐azide‐ and α‐maleimide‐end‐groups, respectively, are achieved using suitable initiators in ATRP of styrene and MMA, respectively. However, PEG obtained from a commercial source is reacted with 3‐acetyl‐N‐(2‐hydroxyethyl)‐7‐oxabicyclo[2.2.1]hept‐5‐ene‐2‐carboxamide (7) to give furan‐protected maleimide‐end‐functionalized PEG. Finally, PS/PMMA and PS/PEG blocks are linked efficiently with trialkyne functional linking agent 1,1,1‐tris[4‐(2‐propynyloxy)phenyl]‐ethane 2 in the presence of CuBr/N,N,N′,N″,N″‐pentamethyldiethylenetriamine (PMDETA) at 120 °C for 48 h to give two samples of 3‐arm star‐block copolymers. The results of the peak splitting using a Gaussian deconvolution of the obtained GPC traces for (PS‐b‐PMMA)3 and (PS‐b‐PEG)3 displayed that the yields of target 3‐arm star‐block copolymers were found to be 88 and 82%, respectively. © Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7091–7100, 2008 相似文献
9.
Shujiang Tu Jinpeng Zhang Xiaotong Zhu Yan Zhang Qian Wang Jianing Xu Bo Jiang Runhong Jia Junyong Zhang Feng Shi 《Journal of heterocyclic chemistry》2006,43(4):985-988
Four‐component cyclocondensation of aromatic aldehydes, malononitrile, dimedone and ammonium acetate proceeds under microwave irradiation in solvent free conditions to give highly functionalized hexahydroquinolines in excellent yields. 相似文献
10.
A One‐Pot O‐Phosphinative Passerini/Pudovik Reaction: Efficient Synthesis of Highly Functionalized α‐(Phosphinyloxy)amide Derivatives 下载免费PDF全文
Dr. Takahiro Soeta Syunsuke Matsuzaki Prof. Dr. Yutaka Ukaji 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(17):5007-5012
A one‐pot O‐phosphinative Passerini/Pudovik reaction has been developed, based on reacting aldehydes, isocyanides, and phosphinic acids followed by the addition of second aldehydes to form the corresponding α‐(phosphinyloxy)amide derivatives. This is the first reported instance of a Passerini‐type, isocyanide‐based multicomponent reaction using a phosphinic acid instead of a carboxylic acid. The nucleophilicity of the phosphinate group allows a subsequent catalytic Pudovik‐type reaction, affording the highly functionalized α‐(phosphinyloxy)amide derivative in high yield. A wide range of aldehydes and isocyanides are applicable to this reaction. 相似文献
11.
A sulfonated magnetic cellulose‐based nanocomposite was prepared and characterized using scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray diffraction and Fourier transform infrared spectroscopy. Then, it was used as a green nanocatalyst for the synthesis of α‐aminonitriles by a one‐pot three‐component condensation reaction of aldehydes or ketones, amines and trimethylsilylcyanide in ethanol at room temperature. The reaction procedure is simple, yields are very high, reaction time is very short and the catalyst can be easily separated from the reaction mixture and reused in subsequent reactions without significant loss of catalytic activity. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
12.
NIS‐Assisted Aza‐Friedel–Crafts Reaction with α‐Carbamoysulfides as Precursors of N‐Carbamoylimines 下载免费PDF全文
Dr. Nicolas George Mathieu Bekkaye Dr. Aurélien Alix Prof. Dr. Jieping Zhu Dr. Géraldine Masson 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(13):3621-3625
A general and practical N‐iodosuccinimide (NIS)‐promoted aza‐Friedel–Crafts reaction of various aromatic nucleophiles with N‐acylimines generated in situ from α‐amidosulfides to give a rapid access to highly functionalized amines is described. The newly developed methodology is very mild, fast, efficient, and complementary. 相似文献
13.
Wei Shu Guochen Jia Prof. Dr. Shengming Ma Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(15):2788-2791
A bicycle built for two : The title reaction affords cis‐fused bicyclo[4.3.0]nonenes from readily available 1,5‐bisallenes with structurally diverse propargylic carbonates and arylboronic acids (see scheme; X=NTs, C(E1)2 with E1=CO2Bn, SO2Ph, dba=trans,trans‐dibenzylidenacetone). The reaction may involve a sequential oxidative addition, two different types of three carbopalladations, and a Suzuki‐type coupling.
14.
《应用有机金属化学》2017,31(5)
A simple, efficient and environmentally benign route was developed for the preparation of spiro(indoline‐3,4‐pyrano[2,3‐c ]pyrazole) derivatives with good yields from condensation of isatins, malononitrile (or ethyl cyanoacetate), hydrazine hydrate and ethyl acetoacetate catalysed by PFu@Fe3O4 nanocomposite. The use of easily available catalyst, shorter reaction times, better yields, simplicity of reaction, heterogeneous system and easy work‐up are the advantages of the method presented. Characterization of the catalyst was performed using Fourier transform infrared spectroscopy, X‐ray diffraction and transmission electron microscopy. 相似文献
15.
Tuanjie Meng Lantao Liu Huiyi Jia Lifeng Ren Cuilan Feng Xiaojuan Wang Wenxian Zhao 《应用有机金属化学》2016,30(1):47-50
An efficient method for the synthesis 3,4‐dihydropyridin‐2‐ones has been developed via tandem one‐pot Michael‐type addition and cyclization of the Blaise reaction intermediate and acrylic ester. A series of readily available nitriles, bromoacetic esters and acrylic esters have been employed to examine the scope of substrates for this method. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
16.
A picolinaldehyde–melamine copper complex was loaded on a magnetic Fe3O4 core, so that it contained 0.33 mmol of Cu per gram, and was used as an efficient catalyst. The as‐synthesized catalyst was characterized using various techniques, including Fourier transform infrared spectroscopy, X‐ray diffraction, energy‐dispersive X‐ray spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometry and thermogravimetric analysis. The catalyst was used to activate the raw materials in the synthesis of hexahydroquinoline derivatives in one‐pot four‐component reactions. Low reaction time (minutes versus half an hour), solvent‐free condition and magnetically separable catalyst are some salient features of the developed catalyst. Also, the optimum amount of catalyst and temperature were determined as 0.07 g and 87.6 °C, respectively, which were obtained using response surface methodology and optimization techniques. 相似文献
17.
Jian Li Wenxian Lv Danfeng Huang Ke‐Hu Wang Teng Niu Yingpeng Su Yulai Hu 《应用有机金属化学》2014,28(4):286-289
A convenient and facile method for the synthesis of homoallylic amines was disclosed. The one‐pot reaction of aldehydes, aromatic amines and allylic bromide with tin powder at room temperature could afford the homoallylic amines in good to excellent yield without any promoter or additive. The method is highly efficient and environmentally benign with low cost and concise manipulation. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
18.
Zinatossadat Hossaini Faramarz Rostami‐Charatib Rahimeh Hajinasiria Hojatollah Jafaryanc Mehdi Shahrakid 《Journal of heterocyclic chemistry》2012,49(2):402-404
A novel, convenient, and an efficient approach to the synthesis of 2H‐pyrans has been reported based on the multicomponent reaction. Solvent‐free condition for the reaction of dithiocarbamates, alkyl propiolates and isocyanides lead to the formation of 2H‐pyrans in good yields. In these reactions, synthesis of 2H‐pyrans is possible based on the one‐pot reaction and without using any catalyst. The mild reaction conditions and high yields of the products exhibit the good synthetic advantage of these methods. J. Heterocyclic Chem., lpar;2011). 相似文献
19.
A series of new carbazole‐based N‐heterocyclic carbene (NHC) ligands have been synthesized in a simple and facile synthetic route and subsequently used in a Pd/carbazole‐based NHC catalytic system, which was found to be effective in catalyzing Heck reactions to provide substituted stilbene derivatives in good yields. Several bioactive stilbenes, including pterostilbene, pinosylvin, trimethoxy resveratrol, and resveratrol, were synthesized in good yields, and a 10 mmol scale‐up was also performed for trimethoxy resveratrol. The synthetic application was also extended by performing a double‐tandem chemoselective Heck reaction followed by Miyaura borylation in a one‐pot procedure to give single‐step access to synthetically useful stilbenyl boronate esters. Similarly, a unique triple‐tandem protocol of a chemoselective Heck reaction/Miyaura borylation/Suzuki–Miyaura coupling reaction sequence was performed for the one‐pot modification of biologically relevant molecules. 相似文献
20.
Assembly of homoallylamine derivatives through iron‐catalyzed three‐component sulfonamidoallylation reaction 下载免费PDF全文
Xiaohui Fan Hong‐Bo Zhu Hao Lv Kun Guo Yong‐Hong Guan Xiao‐Meng Cui Bin An Yan‐Ling Pu 《应用有机金属化学》2015,29(9):588-592
An efficient FeCl3‐catalyzed three‐component reaction between aldehydes, sulfonamides and allylsilanes has been achieved, which provides a convenient, atom‐economic and green way to construct homoallylamine derivatives. In addition, this reaction exhibits excellent syn stereoselectivity with γ‐substituted allylsilanes. 相似文献