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21.
V. M. Timoshenko Ya. V. Nikolin A. N. Chernega E. B. Rusanov Yu. G. Shermolovich 《Chemistry of Heterocyclic Compounds》2001,37(4):470-476
The reaction of 1,1-dihydropolyfluoroalkyl benzyl sulfones with sodium azide or trimethylsilyl azide in the presence of tertiary amines gives ammonium salts of 4-benzylsulfonyl-5-polyfluoroalkyl--triazoles. The proposed reaction scheme includes the participation of catalytic amounts of azide ion in the cyclization of the formed intermediate vinyl azides to triazoles. X-ray analysis of 1,4-diazabicyclo[2.2.2]octane salt of 4-benzylsulfonyl-5-(-H-hexafluoropropyl)--triazole has been carried out. 相似文献
22.
相转移催化芳基亚磺酸盐S-烷基化合成砜的研究 总被引:1,自引:0,他引:1
相转移催化芳基亚磺酸盐S-烷基化合成砜的研究李毅群(暨南大学化学系广州510632关键词相转移催化剂S-烷基化砜合成中图分类号O623.83砜基作为活化官能团能在温和条件下引入和除去,因此砜作为有机合成中间体越来越受到重视[1]。砜可以从硫醚氧化得到... 相似文献
23.
Der-Jang Liaw 《Journal of polymer science. Part A, Polymer chemistry》1995,33(4):605-613
Several sulfone-containing polyesters having inherent viscosities 0.43-0.19 dL g?1 were prepared by direct polycondensation of 4,4′-dicarboxydiphenyl sulfone (DCDPS) with various aromatic and aliphatic diols, by p-toluenesulfonyl chloride and N,N′-dimethylformamide in pyridine solution. The polyesters were examined by elementary analysis, IR spectra, inherent viscosity, x-ray diffraction, solubility, DSC, and TGA. The diffraction diagram showed that all polyesters were crystalline except that obtained from bisphenol-A. All polymers were soluble in sulfonic acid (18M), phenol and p-chlorophenol, but not in acetone and toluene. These polymers obtained from aromatic bisphenols lost no mass below 325°C, but 10% loss of mass was recorded above 396°C in nitrogen. DCDPS copolymerized with isophthalic acid (IPA) and bisphenol-A had inherent viscosity up to 0.49 dL g?1, with relatively narrow distribution of molar mass . © 1995 John Wiley & Sons, Inc. 相似文献
24.
采用毛细管气相色谱法对间接电氧化法合成的二甲砜及反应物二甲亚砜进行了分离分析。研究了分离二甲砜、二甲亚砜的最佳条件,内标法定量。两种化合物的线性范围在2-30μg,且有较好的精密度。 相似文献
25.
Yunsong Yang 《European Polymer Journal》2004,40(3):531-541
A series of α,ω-dihydroxy polyarylene sulfones (PAES) were synthesized comprising bisphenol A (PAES1, Mn=1800, 4900, and 9500 daltons), 4,4′-biphenol (PAES2, Mn=4100 daltons), and hexafluorobisphenol A (PAES3, Mn=3300 daltons). These were reacted with α,ω-dibromo poly(vinylidene fluoride) (PVDF, Mn=1200 daltons) prepared by telomerization, to yield block copolymers possessing rigid and flexible segments. Block copolymers were characterized by FTIR, NMR, GPC, DSC, TGA and TEM. In several cases the block copolymers exhibited distinct thermal transitions, i.e. Tm and Tg for PVDF and PAES segments, respectively. Where observable, Tg of PAES domains in the block copolymers occurred at a temperature lower than the corresponding PAES homopolymer due to the flexible nature of the surrounding PVDF domains. Block copolymers exhibited a similar thermal stability to the corresponding PAES homopolymers but higher stability than the PVDF homopolymer, and much higher still than α,ω-dibromo PVDF. TEM analyses indicate that phase separation of PAES and PVDF domains occurs on the nanometer scale. 相似文献
26.
Carmen R. Alonso-Cruz Francisco J. Ortiz-López Ernesto Suárez 《Tetrahedron letters》2005,46(32):5265-5268
The reaction of derivatives of 3-acetyl-d-glucal, 3-acetyl-l-rhamnal, 3-acetyl-d-galactal, and 3-acetyl-d-lactal with sodium benzenesulfinate in acid medium catalyzed by HgSO4 afforded diastereoisomeric mixtures of the corresponding 2,3-dideoxy-3-(phenylsulfonyl)-hexopyranoses through a Ferrier rearrangement. The anomeric alkoxyl radical fragmentation of these γ-hydroxy sulfones using the system (diacetoxyiodo)benzene and iodine gave vinyl sulfones with structures of 1,2-dideoxy-4-O-formyl-2-(phenylsulfonyl)-pent-1-enitol and configurations d-erythro, l-erythro, and d-threo at the two stereogenic centers. 相似文献
27.
Yoshiyuki Oishi Shoichi Nakata Masa-Aki Kakimoto Yoshio Imai 《Journal of polymer science. Part A, Polymer chemistry》1992,30(10):2217-2221
New segmented aromatic poly(ether sulfone)-amide and poly(ether sulfone)-imide copolymers were synthesized by the chain extension of α,w-diamine-terminated poly(ether sulfone) oligomer with both aromatic dicarboxylic acid chlorides and tetracarboxylic dianhydrides, respectively. Crystallization of the poly(ether sulfone)unit was suppressed by the introduction of amide or imide linkage along the polymer backbone, giving amorphous copolymers that were +eadily soluble in various organic solvents. The copolymers had somewhat higher glass transition temperatures than the parent poly(ether sulfone). They afforded transparent and tough films by solution casting. © 1992 John Wiley & Sons, Inc. 相似文献
28.
Convenient selective methods of synthesis of the title compounds, based on oxidation of di(propen-1-yl)sulfide with 30% H2O2, have been developed.Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, 664033 Irkutsk. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 3, pp. 675–679, March, 1992. 相似文献
29.
The reaction scope of trifluoromethanesulfonyl azide in diazo transfer reactions was extended to include the preparation of α-cyano-α-diazo-carbonyls, phenyl sulfonyl diazoacetophenone and diethyl diazomalonate in high yields. The effect of the bases used in the diazo transfer reactions were found to have a dramatic influence on the success of the reaction with pyridine being the base of choice. 相似文献
30.
Biswanath Das Kongara Damodar Darshanala Saritha Nikhil Chowdhury Martha Krishnaiah 《Tetrahedron letters》2007,48(45):7930-7933
The Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane in the presence of a catalytic amount of indium(III) chloride at room temperature produces the corresponding protected homoallylic amines in high yields. 相似文献