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871.
A one-pot base-mediated reaction of azides and β- or α-vinyl bromides has been reported. The effects of bases and solvents have been investigated in the process. A variety of 1,5-disubstituted triazoles were prepared in low to good yields. Further studies reveal that the corresponding alkynes were produced as intermediates via elimination reaction. Under the same reaction conditions, the reactions of alkyl alkynes with phenyl azide would give 1,5-disubstituted 1,2,3-triazoles. 相似文献
872.
Jia Sun Peicheng Zhang Qi Wei Hang Xun Feng Tang Yongde Yue Li Li Xuefeng Guo Rong Zhang 《Tetrahedron letters》2014
Amarusine A (1), a new polyketide derivative possessing an unusual dioxaspiro[4.4]nonane derivative with a butyrolactone ring, was isolated from the leaves of Pleioblastus amarus. The structure and absolute stereochemistry of compound 1 were rigorously determined using UV, IR, HRESIMS, and 1D and 2D NMR techniques and by comparing experimental and calculated electronic circular dichroism (ECD) spectra. Amarusine A (1) exhibits a good antioxidant activity for scavenging the DPPH radical. A possible biosynthetic pathway was postulated. 相似文献
873.
Mingxia Zhao Liqin Xiong Shilei Li Jin Chang Hongyu Ning Chuanmin Qi 《无机化学与普通化学杂志》2014,640(1):159-167
Four complexes with supramolecular architectures, namely, MZCA · 3H2O ( 1 ), [Zn(H2O)6]2+ · [MZCA]2 · [H2O]6 ( 2 ), [Mn(MZCA)2(H2O)4] · 2H2O ( 3 ), and [Ni(MZCA)2(H2O)4] · 2H2O ( 4 ) [MZCA = 3‐(carboxymethyl)‐2, 7‐dimethyl‐3H‐benzo[d]imidazole‐5‐carboxylic acid], were synthesized and characterized by elemental analysis, IR spectroscopy, and single‐crystal X‐ray diffraction. Complexes 1 and 2 display a remarkable 3D network with 1D hydrophilic channels. Complexes 3 and 4 are isostructural and exhibit a 3D structure encapsulating 1D 24‐membered ring microporous channels. The UV/Vis and fluorescent spectra were measured to characterize complexes 1 – 4 . The thermal stability of complexes 2 – 4 were also examined. 相似文献
874.
Manganese‐Catalyzed Dehydrogenative [4+2] Annulation of N?H Imines and Alkynes by C?H/N?H Activation
Ruoyu He Zhi‐Tang Huang Qi‐Yu Zheng Congyang Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(19):5050-5053
Described herein is a manganese‐catalyzed dehydrogenative [4+2] annulation of N H imines and alkynes, a reaction providing highly atom‐economical access to diverse isoquinolines. This transformation represents the first example of manganese‐catalyzed C H activation of imines; the stoichiometric variant of the cyclomanganation was reported in 1971. The redox neutral reaction produces H2 as the major byproduct and eliminates the need for any oxidants, external ligands, or additives, thus standing out from known isoquinoline synthesis by transition‐metal‐catalyzed C H activation. Mechanistic studies revealed the five‐membered manganacycle and manganese hydride species as key reaction intermediates in the catalytic cycle. 相似文献
875.
Conghui Tang Ning Jiao 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(25):6646-6650
A novel copper‐catalyzed aerobic oxidative C(CO) C(alkyl) bond cleavage reaction of aryl alkyl ketones for C N bond formation is described. A series of acetophenone derivatives as well as more challenging aryl ketones with long‐chain alkyl substituents could be selectively cleaved and converted into the corresponding amides, which are frequently found in biologically active compounds and pharmaceuticals. 相似文献
876.
Xue‐Jun Wu Xiao Huang Xiaoying Qi Hai Li Bing Li Hua Zhang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(34):9075-9079
Two‐dimensional (2D) copper‐based ternary and quaternary semiconductors are promising building blocks for the construction of efficient solution‐processed photovoltaic devices at low cost. However, the facile synthesis of such 2D nanoplates with well‐defined shape and uniform size remains a challenge. Reported herein is a universal template‐mediated method for preparing copper‐based ternary and quaternary chalcogenide nanoplates, that is, CuInS2, CuInxGa1−xS2, and Cu2ZnSnS4, by using a pre‐synthesized CuS nanoplate as the starting template. The various synthesized nanoplates are monophasic with uniform thickness and lateral size. As a proof of concept, the Cu2ZnSnS4 nanoplates were immobilized on a Mo/glass substrate and used as semiconductor photoelectrode, thus showing stable photoelectrochemical response. The method is general and provides future opportunities for fabrication of cost‐effective photovoltaic devices based on 2D semiconductors. 相似文献
877.
Wu Jinming Zhu Xiting Chen Qi Ge Cunwang Dai Bin Jia Xueping Shen Aibao Chen Tingting 《Journal of solution chemistry》2014,43(8):1421-1435
Journal of Solution Chemistry - The binding interaction of 4β-(benzoyl-thioureido)-4-deoxypodophyllotoxin (HY-1) with human serum albumin (HSA) was investigated by fluorescence,... 相似文献
878.
A novel approach to prepare 4-anilinoquinazoline derivatives based on the transformation of indoline-2,3-dione to formamidine was developed. The processes with this approach are simple, efficient, and environmentally friendly. The efficiency of this approach was evaluated by synthesizing 17 4-anilinoquinazolines and comparing the obtained yields with those achievable through conventional synthetic methods. It was the first time that compounds 8d, 8e, 8h, and 13b–f were synthesized. The characteristics of the IR and the UV spectra of these compounds and the effects of their substituents on the spectra were observed. 相似文献
879.
A general and efficient P(V)–N activation method for the preparation of symmetrical and asymmetrical dinucleoside polyphosphates (NpnN′s, n=2–4) and P2,P3-CX2-dinucleoside tetraphosphates (X=H, F, and Cl) has been established. Twenty-two dinucleoside polyphosphates and their phosphonate analogs were synthesized from nucleoside 5′-phosphoropiperidates with 4,5-dicyanoimidazole as the activator in good to high yields. 相似文献
880.
Yuanpeng Liang Bin Xiang Chao Liu Xiangdong Zhou Dan Wang Shan Song Genghua Bai Qi An Quehong Huang Shujun Chen Xuefeng Wei 《Tetrahedron》2014
Novel fluorine-containing ultraviolet absorbers (FBPs) with low surface energy were successfully synthesized based on 2,4-dihydroxy benzophenone (BP-1), and their structures were characterized by 1H NMR, 13C NMR, FTIR, and HRMS. UV absorption of FBPs was studied in 10−4 M dichloromethane (CH2Cl2), which demonstrated the superior UV absorption capability of FBPs (ca. ?=1.7×104 to 2.2×104 at λmax) over the matrix (?=1.7×104 at λmax). Quantum chemistry calculation was performed to investigate the stable structure and UV electronic absorption bands of FBPs. The surface chemistry information of high-chlorinated polyethylene (HCPE) coating films embedded with ultraviolet absorbers (UVAs) was given by X-ray photoelectron spectroscopy (XPS) and contact angle measurement. The results show that the surface enrichment capability of FBPs is remarkably better than traditional UVAs (including BP-1, BP-3, BP-12) because of the low surface energy properties of FBPs. 相似文献