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1.
Vratislav Langer Shiming Li Knut Lundquist 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(3):o163-o165
Racemic erythro‐1,2‐diphenyl‐1,3‐propanediol, C15H16O2, is a model compound representative of erythro forms of structural elements of the 1,2‐diaryl‐1,3‐propanediol type in lignins. In the crystal structure, the torsion angle between the bulky phenyl groups is −62.26 (11)°. Strong hydrogen bonds take part in a directed co‐operative O—H⋯O—H⋯O—H⋯O—H pattern that is assumed to have a decisive influence on the conformation. This is supported by comparisons with the geometries of related compounds. 相似文献
2.
David D. Xu George T. Lee Xinglong Jiang Kapa Prasad Oljan Repic Thomas J. Blacklock 《Journal of heterocyclic chemistry》2005,42(1):131-135
A general synthesis of 1,3‐diaryl‐4‐pyrazoleacetic acid esters has been realized via the condensation of a γ‐carboxy ester hydrazone with the Vilsmeier reagent. 相似文献
3.
V. Sridharan S. Muthusubramanian S. Sivasubramanian 《Journal of heterocyclic chemistry》2005,42(7):1321-1330
A new synthetic route was developed for the synthesis of 4,6‐diaryl‐2‐methyl‐l,3‐benzoxazoles and their hydrogenated derivatives. The target compounds were obtained via the Neber rearrangement from 3,5‐diaryl‐2‐cyclohexen‐l‐ones. The formation of the isomers in the dihydro derivatives was explained by the [1,5] sigmatropic shift of hydrogen under thermal condition. DDQ was employed for the dehydrogenation of the dihydro benzoxazoles. 相似文献
4.
We investigated the generation and the reactivity of selected 1,2‐diaryl‐1,2‐disodioethanes employing cyclopentyl methyl ether and 2‐methyltetrahydrofuran as green solvent alternatives to tetrahydrofuran. Both solvents proved suitable for the generation of these vic‐diorganometals, as well as for their employment as single‐electron transfer reagents. On the other hand, 2‐methyltetrahydrofuran appears as the solvent of choice in reactions involving the employment of these diorganometals as nucleophiles or bases. Accordingly, our results disclose an environmentally more sustainable approach to the chemistry of these diorganometals and, in a wider sense, to reductive metalation reactions. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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Irradiation of triazole thiones in thin‐film reactor furnished the corresponding desulfurized triazoles in good yield. The required triazole thiones were synthesized from the respective acid hydrazide and isothiocyanate. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:269–272, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10140 相似文献
6.
Zilong Tang Weiwen Chen Zhonghua Zhu Hanwen Liu 《Journal of heterocyclic chemistry》2011,48(2):255-260
A series of novel 2,3‐diaryl‐3,4‐dihydro‐2H‐1,3‐benzoxazines have been prepared in high yields from o‐arylaminomethylphenols and aromatic aldehydes in the presence of SnCl4 for the first time, and their fungicidal activities were investigated too. Some of the products showed good fungicidal activities against Rhizoctonia solani justified by 100% activity of compound 1b. J. Heterocyclic Chem., (2010) 相似文献
7.
Hsiencheng Shih Renshuay J. Shih Dennis A. Carson 《Journal of heterocyclic chemistry》2011,48(6):1243-1250
2,3‐Diaryl‐substituted maleic anhydrides were prepared by a modified one‐pot synthesis of Perkin condensation using mixed sodium salts of arylglyoxylic acid and arylacetic acid with acetic anhydride in 1,4‐dioxane. The treatment of these anhydrides with ammonium bicarbonate, or methanolic hydrazine, offered the corresponding 2,3‐diaryl‐substituted maleimides and maleic hydrazides (4,5‐diaryl‐substituted 1,2‐dihydropyridazine‐3,6‐dione), respectively. Evidence obtained from NMR, UV, and mass spectra suggest that 2,3‐diaryl‐substituted maleic hydrazides do not exhibit monolactim forms. Ring contraction of the diaryl‐substituted maleic hydrazide by nitrosation led to the formation of the corresponding maleimide. Interconversion between the corresponding maleic hydrazide and maleimide was observed following equilibrium reaction. Our experiment proposes that the chemistry of 2,3‐diaryl‐substituted maleic hydrazides rarely involves the function of ethylene moiety and resembles that of succinic hydrazine. J. Heterocyclic Chem.,(2011). 相似文献
8.
Majid M. Heravi Samaheh Sadjadi Sodeh Sadjadi Hossein A. Oskooie Rahim Hekmat Shoar Fatemeh F. Bamoharram 《中国化学会会志》2009,56(2):246-250
Silica‐supported Preyssler nanoparticles (H14[NaP5W30O110])/SiO2 are used as a new and recyclable catalyst for the preparation of 1,3‐diaryl‐5‐spirohexahydropyrimidines via a one‐pot condensation of anilines, formaldehyde, and cyclohexanone. 相似文献
9.
Latifeh Navidpour Leila Karimi Mohsen Amini Mohssen Vosooghi Abbas Shafiee 《Journal of heterocyclic chemistry》2004,41(2):201-204
Arylation of the readily available 3‐alkythio‐5‐aryl‐1,2,4‐triazoles gave 5‐alkylthio‐1,3‐diaryl‐1,2,4‐triazoles in moderate yield. The structures of the latter were confirmed by NOE and 13C‐NMR. 相似文献
10.
Alan R. Katritzky Boris V. Rogovoy Christophe Chassaing Vladimir Vvedensky Behrouz Forood Brenton Flatt Hisao Nakai 《Journal of heterocyclic chemistry》2000,37(6):1655-1658
The condensation of α,β‐unsaturated ketones with substituted o‐aminothiophenols, obtained by reductive cleavage of the corresponding disulfides in the presence of triphenylphosphine, is an effective method for the synthesis of 2,4‐diaryl‐2,3‐dihydro‐1,5‐benzothiazepines under neutral conditions. 相似文献
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(R)‐2,3‐Cyclohexylideneglyceraldehyde,a Chiral Pool Synthon for the Synthesis of 2‐Azido‐1,3‐diols 下载免费PDF全文
Abdul Rouf Mushtaq A. Aga Brijesh Kumar Subhash C. Taneja 《Helvetica chimica acta》2015,98(6):823-833
A new approach was proposed for the synthesis of 2‐azido‐1,3‐diols from easily available and inexpensive chiral pool synthon (R)‐2,3‐O‐cyclohexylidene‐D ‐glyceraldehyde, through Mitsunobu azidation of 1,2‐diols. Both C(2) and C(1) azides in variable ratios were obtained in alkyl substituted diols with C(2) as the major one. 相似文献
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14.
Synthesis of 1‐Amino‐5,6‐diaryl‐3‐cyano‐1H‐pyridin‐2‐ones and 6,7‐Diaryl‐4‐cyano‐3‐hydroxy‐1H‐[1,2]diazepines from Isoflavones 下载免费PDF全文
Mu‐Lin Zhu Zun‐Ting Zhang Dong Xue Hui‐Liang Hua Yong Liang Stanislaw F. Wnuk 《Helvetica chimica acta》2014,97(4):561-568
The one‐step cyclocondensation of substituted isoflavones (=3‐phenyl‐4H‐1‐benzopyran‐4‐ones) with cyanoacetohydrazide in the presence of KOH afforded a mixture of 1‐amino‐5,6‐diaryl‐3‐cyano‐1H‐2‐pyridin‐2‐ones and 6,7‐diaryl‐4‐cyano‐3‐hydroxy‐1H‐[1,2]diazepines. 相似文献
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Masood Parvez Kaleem M. Khosa Muhammad Mazhar Saqib Ali Manzar Sohail 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(1):m51-m54
The crystal structures of 3,3‐dimethyl‐3‐(trichlorogermyl)propionic acid, [Ge(C5H9O2)Cl3], 3,3‐dimethyl‐3‐(triphenylgermyl)propionic acid, [Ge(C6H5)3(C5H9O2)], and 3,3‐dimethyl‐3‐(tri‐p‐tolylgermyl)propionic acid, [Ge(C7H7)3(C5H9O2)], have slightly distorted tetrahedral geometries about the Ge atoms. All the structures form dimers via strong O—H·O hydrogen bonds, resulting in eight‐membered rings that can be best described in terms of graph‐set notation (8). 相似文献
17.
The synthesis of chiral (2R) 2,5‐diaryl‐2,3‐dihydropyrano[2,3‐b]quinolin‐4‐ones, was achieved, at ambient temperature, by the reaction of 3‐acetyl‐4‐aryl‐carbostyril and an aldehyde, in the presence of bismuth triflate–L(?)‐proline complex, formed in situ. The products were obtained in 62–78% yield with high enantioselectivity (72–96% ee). J. Heterocyclic Chem., (2011). 相似文献
18.
Johny Wehbe Valrie Rolland Jean Martinez Marc Rolland 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(8):o473-o475
The crystal and molecular structure of 1‐tert‐butyl 4‐ethyl (2′R,3′R,5′R,2S,3S)‐3‐bromomethyl‐3‐hydroxy‐2‐[(2′‐hydroxy‐2′,6′,6′‐trimethylbicyclo[3.1.1]hept‐3′‐ylidene)amino]succinate, C21H34BrNO6, is presented. This compound is an intermediate in the new synthetic route to β‐substituted β‐hydroxyaspartates, which are blockers of glutamate transport. 相似文献
19.
Maria B. García Isabel A. Perillo Liliana R. Orelli 《Journal of heterocyclic chemistry》2001,38(5):1209-1211
In the present communication we describe two examples of a new kind of configurationally stable non‐biaryl atropisomers in which the Ar‐N bond is the chiral axis, namely 1‐(o‐nitrophenyl)‐2‐aryl‐3‐methyl‐1,4,5,6‐tetrahydropyrimidinium iodides 1. Stereochemical features of such compounds are analyzed on the basis of their 1H and 13C one‐ and two‐dimensional nmr spectra. A comparison is made with the corresponding amidines 2 . 相似文献
20.
Lionel Salmon Pierre Thury Michel Ephritikhine 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(6):m246-m248
The title complex, bis(acetylacetonato‐κ2O,O′)[N,N′‐bis(3‐hydroxy‐2‐oxidobenzaldimino)‐2‐methyl‐1,2‐propanediamine‐κ4N,O,O′,N′]uranium(IV) tetrahydrofuran solvate, [U(C18H18N2O4)(C5H7O2)2]·C4H8O, is a rare example of a uranium(IV) complex with a compartmental Schiff base. The U atom is located in the N2O2 inner site of the hexadentate N,N′‐bis(3‐hydroxy‐2‐oxidobenzaldimino)‐2‐methyl‐1,2‐propanediamine group and is bound also to the two O atoms of both acetylacetonate moieties, which results in a dodecahedral coordination environment. Centrosymmetric dimers are formed through intermolecular hydrogen bonds that link the terminal uncoordinated hydroxy groups to one another and to the O atoms of the acetylacetonate ligands. 相似文献