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81.
82.
Hamid Reza Shaterian Hassan Hadadzadeh 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5):1059-1071
A novel and simple method for the chemoselective deprotection of S,S- and S,O-acetals and ketals in the presence of their O,O-analogs with electrophilic halogens to their corresponding carbonyl compounds is described using N-bromosuccinimide, N-chlorosuccinimide, 2,4,4,6-tetrabromo-2,5-cyclohexen-1-one, trichlorocyanuric acid, or molecular bromine in aqueous acetonitrile. The use of these reagents in the presence of hydrated silica gel provide efficient, novel, and mild procedures for the deprotection of cyclic and acyclic O,O-, S,S-, and S,O-acetals and ketals in excellent yields in short reaction times. 相似文献
83.
Hamid Reza Shaterian Asghar Hosseinian Majid Ghashang 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):3136-3144
Herein, we describe a green procedure for the one-pot preparation of 1,8-dioxo-octahydroxanthene derivatives by condensation of dimedone and substituted benzaldehydes in the presence of FeCl 3 -SiO 2 as an efficient and heterogeneous catalyst under microwave irradiation and thermal conditions. This method has the advantages of high yields, cleaner reactions, efficient and cost-effective method, simple methodology, short reaction times, easy workup, and greener conditions. 相似文献
84.
Ali Ramazani Ali Morsali Bijan Ganjeie Ali Reza Kazemizadeh Ebrahim Ahmadi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2439-2442
Abstract Selenourea reacts with dialkyl acetylenedicarboxylates in acetone to form 1:1 adducts, which undergo a cyclization reaction to produce alkyl Z-2-(2-amino-4-oxo-1,3-selenazol-5(4H)-yliden) acetates in fairly good yields. The reaction is completely stereoselective. 相似文献
85.
Ali Ramazani Ali Reza Kazemizadeh Bijan Ganjeie Ebrahim Ahmadi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2569-2572
Tiourea reacts with dialkyl acetylenedicarboxylates in solventless conditions to form 1:1 adducts, which undergo a cyclization reaction to produce alkyl Z-2-(2-amino-4-oxo-1,3-thiazol-5(4H)-yliden)acetates in fairly good yields. The stereochemistry of the ethyl Z-2-(2-amino-4-oxo-1,3-thiazol-5(4H)-yliden)acetate was established by the use of X-ray single crystal structure analysis. The reaction is completely stereoselective. 相似文献
86.
Davood Nori-Shargh Hossein Aghabozorgh Karim Zare Mohammad Reza Talei Bavil Olyai Saeed Jameh-Bozorghi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):341-351
Molecular structures, metallotropic and prototropic shifts of cyclopentadienyl(trimethyl)silane ( 1 ), cyclopentadienyl(trimethyl)germane ( 2 ), and cyclopentadienyl(trimethyl)stannane ( 3 ) were investigated using ab initio molecular orbital and the Becke, Lee, Yang, and Parr density functional (B3LYP) methods. The results show that the most stable structure of compounds 1-3 has the (CH 3 ) 3 M fragment in the allylic position. The energy barrier of metallotropic shifts in compound 1 is higher than in 2 , and in compound 2 higher than in 3 , in good agreement with experimental data. The cyclopentadienyl rings in compounds 1-3 are found to be planar but this result contradicts the reported experimental data. 相似文献
87.
Frank Jordan Reza Fathi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-3):341-344
Abstract α-D-Ribofuranosyl-1,2-cyclic monophosphate and 5-phospho-α-D-ribofuranosy1-1, 2-cyclic monophosphate were synthesized in good yields. The five-membered ring cyclic phosphates have 31p chemical shifts similar to those found for such structures, presumably reflecting the smaller O-P-O bond angle, compared to that in six-membered ring phosphates. The rate of OH? catalyzed ring opening was similar to that reported for ethylene phosphate, indicating relief of ring strain during hydrolysis. α-D-Ribofuranosyl-1, 2-cyclic monophosphate was found to irreversibly inactivate purine nucleoside phosphorylase (EC 2.4.2.1) at its catalytic center. 相似文献
88.
Foad Kazemi Ali Reza Kiasat 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):1333-1337
Epoxids are efficiently converted to the corresponding thiiranes by ammonium thiocyanate (NH 4 SCN) in the presence of catalytic amounts of oxalic acid with excellent isolated yields under mild and nonaqueous reaction conditions. This conversion performed under both conventional heating and microwave conditions. Distinct rate enhancement is observed under microwave irradiation. 相似文献
89.
Abdolreza Iraj Mansouri Zahra Hassani Mohammad Reza Islami 《Phosphorus, sulfur, and silicon and the related elements》2013,188(8):1753-1758
2-Aminobenzoic acids or 4-aminobenzoic acid react with dimethyl acetylenedicarboxylate/triphenylphosphine in less than 20 min at 15–25°C to produce new organic phosphorus compounds in good to excellent yields. The conversion occurs with selective N- over O-alkylation of the amino group and isolation of the products is accomplished simply by filtration. 相似文献
90.
Hossein Reza Darabi Abbas Darestani Farahani Mohammad Hashemi Karouei Kioumars Aghapoor Rohoullah Firouzi Rainer Herges 《Supramolecular chemistry》2013,25(9):653-657
A new E,E-stilbenophane was synthesised and characterised. The crystal structure of this cyclophane shows that this molecule has a cup-shaped structure, which hosts a phenyl ring of neighbouring molecule as guest in its cavity with a π–π distance of about 3.7 Å. Moreover, the NMR spectra and theoretical analysis (gauge-independent atomic orbitals (GIAO) and quantum theory of atoms in molecules (QTAIM)) suggest that the silver recognition by E,E-stilbenophane host molecules is based on cation–π interactions in which the π-electrons of the double bonds play a major role. 相似文献