共查询到19条相似文献,搜索用时 187 毫秒
1.
2.
3.
以2-巯基-5-(3,4,5-三甲氧基苯基)-1,3,4-噻二唑为原料,经醚化、酰肼化、闭环、硫醚化四步反应合成了10个2-(3,4,5-三甲氧基苯基)-5-[(5-烷硫基-1,3,4-噁二唑-2-基)硫甲基]- 1,3,4-噻二唑类衍生物。通过元素分析、IR、MS、1H NMR和 13C NMR对目标化合物进行了表征。采用In(OTf)3催化下40 oC水相合成目标化合物,具有反应条件温和、合成收率高、催化剂可循环使用等特点。 相似文献
4.
5.
6.
麦芽酚及麦芽酚-3-O-β-D-葡萄糖甙的合成 总被引:1,自引:0,他引:1
以乙酰丙酮(1)为原料,经溴代、酯化反应得到3-苯甲酰氧基-2,4-戊二酮(2),2与甲酸乙酯缩合、脱水闭环、酯水解得麦芽酚(3),总收率50.4%。3与a一溴代四乙酰化葡萄糖(4)经糖甙化、脱乙酰基得麦芽酚-3-O-β-D-葡萄糖甙(5),收率60.8%,IR,^1H NMR和^13C NMR确证5的葡萄糖为β-构型。中间产物2无须纯化,可实现“一锅”反应合成3。 相似文献
7.
8.
9.
10.
11.
A series of novel N2-[2-chloro-4(3,4,5-trimethoxy phenyl azetidin-1-yl]-N4-(substituted aryl)-1,3-thiazole-2,4-diamine (4a–g) were synthesized starting from 3,4,5-trimethoxy benzaldehyde thiosemicarbazone (1). The compound (1) was obtained by condensing 3,4,5-trimethoxy benzaldehyde with thiosemicarbazide in methanol. 3,4,5-Trimethoxy benzaldehyde thiosemicarbazone (1) on treatment with chloracetyl chloride afforded 4-chloro-[2-(3,4,5-trimethoxy benzylidine) hydrazinyl]-1,3-thiazole (2). Compound (2) was reacted with chloracetyl chloride and triethylamine to obtain the corresponding 4-chloro-N-[2-chloro-4(3,4,5-trimethoxy phenyl) azetidin-1-yl]-1,3-thiazole-2-amine (3). Various substitutions on compound 3 with secondary amines yielded series of compounds (4a–g). The newly synthesized compounds were characterized by IR, 1H NMR, elemental analysis and mass spectral studies. All the compounds were screened for their in vitro antioxidant properties. The IC50 values of compounds 3 and 4a–g revealed that some of the synthesized compounds were showing potent antioxidant activity. 相似文献
12.
We developed a procedure to synthesize pinacolyl boronate containing stilbene derivatives and used this procedure to synthesize boron-containing combretastatin analogues. The key step involves the Wittig reaction of the ylide 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboratophenyl)-methyl triphenylphosphonium bromide 11 with 3,4,5-trimethoxy benzaldehyde in the presence of tBuONa in DMF, providing 88% yield. We are now in a position to evaluate the biological activity of these derivatives as modulators of TGF-beta signaling pathways. 相似文献
13.
Vikas Srivastava Arvind Singh Negi P. V. Ajayakumar Shamshad A. Khan Suchitra Banerjee 《Applied biochemistry and biotechnology》2012,166(6):1401-1408
The biotransformation potential of a selected Atropa belladonna hairy root clone (AB-09) had been evaluated with regard to three different aromatic carbonyl compounds, i.e., 3,4,5-trimethoxybenzaldehyde
(1), 3,4,5-trimethoxyacetophenone (2), and 3,4,5-trimethoxy benzoic acid (3). The results demonstrated for the first time the untapped potentials of the selected hairy root clone to perform simultaneous
oxidation (34.49%) and reduction (32.68%) of 3,4,5-trimethoxy benzaldehyde (1) into 3,4,5-trimethoxy benzoic acid (3), and 3,4,5-trimethoxy benzyl alcohol (4), respectively, without any intermediate separation or addition of reagents. The same hairy root clone also demonstrated
reduction (<5%) of a 3,4,5-trimethoxyacetophenone (2) into a secondary alcohol, i.e., 1-(3,4,5-trimethoxyphenyl) ethanol (5), while in the case of aromatic carboxylic acid substrate (3), no biotransformation could be obtained under the similar conditions. The current observations revealed oxidation and reduction
of the formyl group of the aromatic ring, and only reduction of the carbonyl group of acetophenone through the specific hairy
root clone. The concurrent oxidation and reduction reactions by the selected hairy root clone highlight the importance of
this study, which, as per our observations, is the first of its kind relating the hairy root culture of A. belladonna. 相似文献
14.
15.
16.
17.
Idebenone was synthesized directly by free-radical alkylation of 2,3-dimethyl-1,4-benzoquinone (Coenzyme Q0) with commercially available 11-hydroxyundecanoic acid in the presence of potassium peroxodisulfate and silver nitrate in a mixed solvent (CH3CN–H2O, 1:1) under mild condition in good yields (65%, based on Coenzyme Q0). The reaction is operationally simple and could be used in the preparation of other biologically Coenzyme Q analogues. 相似文献
18.
Tiffany N. Thompson Susan Ramos-Hunter Jasmine Robertson Natalie Y. Arnett 《Tetrahedron letters》2013
The effect of solvent purity on the synthesis and yield of bisphenol A tetrachlorocyclotriphosphazene (BATCCP) has not been described in the literature. The purpose of this research was to synthesize BATCCP hybrid monomers and to evaluate the effect of solvent purity on the BATCCP production. BATCCP monomers were prepared by an interfacial procedure in a water/toluene system as a function of time with the assistance of a phase transfer catalyst, tetraoctylammonium bromide. 1H and 31P NMR confirmed the production of BATCCP monomer by the appearance of chemical shifts at 7.18 and 5.35 ppm in the 1H NMR and 23.4 and 13.9 ppm in the 31P NMR, respectively. Distillation of the toluene, not suggested in previous reports of HCCP hybrid synthesis, resulted in an improvement of actual % yield to 40% and stability of the product throughout the 1440 min reaction as confirmed by MALDI, compared with an 11% actual yield at 15 min, decaying to 2% over a 1440 min reaction when the synthesis was performed with ‘anhydrous toluene’ as provided commercially without further distillation. 相似文献
19.
V. V. Sharutin O. K. Sharutina E. V. Bondar' A. P. Pakusina N. Yu. Adonin V. F. Starichenko 《Russian Journal of General Chemistry》2002,72(3):390-391
Pentaarylantimonies Ar5Sb (Ar = Ph, p-Tol) was reacted with triarylantimony bis(perfluorobenzoate) and bis(3,4,5-trifluorobenzoate) in toluene at elevated temperature to obtain tetraarylantimony fluorobenzoates in 90% yield. Triarylantimony bis(fluorobenzoates) were prepared in an yield of up to 98% from triarylstibine and fluorobenzoic acid by oxidative addition in ether in the presence of hydrogen peroxide. 相似文献