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排序方式: 共有302条查询结果,搜索用时 15 毫秒
1.
Kaname SasakiHideyuki Nagai Shuichi MatsumuraKazunobu Toshima 《Tetrahedron letters》2003,44(30):5605-5608
The glycosidations of glucopyranosyl diethyl phosphite and alcohols using an ionic liquid, 1-n-hexyl-3-methylimidazolium trifluoromethanesulfonimidide (C6mim[NTf2]) containing a protic acid, trifluoromethanesulfonimide (HNTf2), as a novel solvent-catalyst system, effectively proceeded under mild conditions to give the corresponding glycosides in good to high yields. Furthermore, this acid-ionic liquid combination could be reused many times for the glycosidations without any loss in efficiency. 相似文献
2.
Zhi-En Lin 《Journal of solid state chemistry》2006,179(3):723-728
A new layered cobalt-zinc phosphite, Co(H2O)4Zn4(HPO3)6·C2N2H10 has been synthesized in the presence of ethylenediamine as the structure-directing agent. The compound crystallizes in the monoclinic system, space group Cc (No. 9), a=18.2090(8), b=9.9264(7), c=15.4080(7) Å, β=114.098(4)°, V=2542.3(2) Å3, Z=4, R=0.0323, wR=0.0846. The structure consists of ZnO4 tetrahedra, CoO6 octahedra and HPO3 pseudopyramids through their vertices forming bimetallic phosphite layers parallel to the ab plane. Organic cations, which reside between the inorganic layers, are mobile and can be exchanged by NH4+ cations without the collapse of the framework. 相似文献
3.
Two inorganic-organic hybrid solids, Zn2(phen)(HPO3)2 (1) and Zn(phen)(HPO3) (2), have been synthesized under solvothermal conditions in the presence of 1,10-phenanthroline (phen) ligands. Their structures were determined by single-crystal X-ray diffraction and further characterized by FTIR, elemental analysis, powder X-ray diffraction, thermogravimetric analysis and fluorescent spectra. Compound 1 crystallizes in the triclnic system, space group P-1, , , , α=75.609(1)°, β=79.145(2)°, γ=67.157(2)°, , Z=2. Compound 2 is monoclinic, C2/c, , , , β=94.175(4)°, , Z=8. Both structures consist of 1D chains constructed from strictly alternating ZnO4 and HPO3 polyhedra through sharing vertices. The chains are further decorated by Zn-centered complex architectures, [Zn(phen)]2+ for 1 and [Zn(phen)2]2+ for 2. The 2D and 3D supramolecular arrays for 1 and 2 are stably stacked via strong π-π interactions of the phen groups, respectively. 相似文献
4.
Mariappan Periasamy Neela Kishorebabu K. Natarajan Jayakumar 《Tetrahedron letters》2007,48(11):1955-1958
N,N-Dialkylarylamines react with trimethyl orthoformate and TiCl4 under ambient conditions to give the corresponding formyl derivatives in 75-89% yields, whereas the corresponding arylated products are obtained from benzyl ethers and acetals in 42-78% yields. 相似文献
5.
An operationally simple, inexpensive, efficient, and environmentally friendly esterification of various carboxylic acids, phosphonic acids, and phosphinic acids with triethyl orthoacetate or trimethyl orthoacetate under neutral conditions in a typical room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate, was successfully carried out to provide the corresponding ethyl esters or methyl esters in high yields. 相似文献
6.
Ga3(HPO3)4F4(H3DETA) is a new open-framework fluorinated gallium phosphite obtained by mild hydrothermal synthesis using diethylenetriamine as templated agent and characterized by single crystal X-ray diffraction, the powder X-ray diffraction, IR spectroscopy, TGA, ICP and elemental analyses. It crystallizes in the monoclinic space group C2/c, a=12.741(6) Å, b=12.068(6) Å, c=11.988(5) Å, β=94.902(8)o, V=1836.6(15) Å3, Z=4. The construction of 3D open-framework structure in the title compound may be viewed as the assembly of pentameric building units and HPO3 groups. The pentameric building unit is the first to be found, which lead to form the three types of channels along a-, b- and c-axes, respectively, in gallium phosphite. The triprotonated DETA cations are inserted within the 10-membered ring channels and interact with anions of the framework via hydrogen bonds. 相似文献
7.
Konstantin N. Gavrilov Pavel V. Petrovskii AntonS. Safronov Vadim A. Davankov 《Tetrahedron》2005,61(44):10514-10520
Novel P-monodentate aryl phosphite ligands have been synthesised in one step from (R)-BINOL, (R)-H8-BINOL and (R)-H8-3,3′-dibromo-BINOL. With the new aryl phosphites, up to 86% ee was observed in the asymmetric Pd-catalysed amination of 1,3-diphenyl-2-propenyl acetate with sodium diformylamide. In the enantioselective alkylation of 1,3-diphenyl-2-propenyl acetate with dimethyl malonate, up to 97% enantioselectivity was achieved. 相似文献
8.
Synthesis and properties of novel poly(amide-imide)s containing pendent diphenylamino groups 总被引:1,自引:0,他引:1
A new dicarboxylic acid, 2,4-bis(N-trimellitoyl)triphenylamine, bearing two preformed imide rings was synthesized from the condensation of 2,4-diaminotriphenylamine and trimellitic anhydride at 1:2 molar ratio. A series of poly(amide-imide)s (PAIs) with inherent viscosities of 0.38-0.66 dl/g were prepared by triphenyl phosphite-activated polycondensation from the diimide-dicarboxylic acid with various aromatic diamines. All the resulting PAIs were readily soluble in a variety of organic solvents and formed strong and tough films via solution casting. These PAIs have useful levels of thermal stability associated with moderately high glass-transition temperatures (259-314 °C) and 10% weight loss temperatures in excess of 530 °C in nitrogen or in air. 相似文献
9.
Richard J CohenDaniel L Fox Jarrod F EubankRalph Nicholas Salvatore 《Tetrahedron letters》2003,44(47):8617-8621
A mild and convenient synthesis for phosphonates using cesium carbonate (Cs2CO3), tetrabutylammonium iodide (TBAI) and DMF was developed at room temperature. Numerous dialkyl phosphites were screened using a diverse array of alkyl halides and these reaction conditions were found to be highly efficient producing various phosphonates exclusively in moderate to high yields. 相似文献
10.
F. Preuss M. Steidel M. Vogel G. Overhoff G. Hornung W. Towae W. Frank G. Reiß S. Müller-Becker 《无机化学与普通化学杂志》1997,623(8):1220-1228
Phosphane, Phosphite, Phosphido, Complexes of Vanadium(V) Complex formation of tert-butylimidovanadium(V)trichloride ( 1 ) with phosphanes und phosphites has been studied. Syntheses of phosphidovanadium(V) compounds tC4H9N?VCp(NHtC4H9)[P(SiMe3)2] and tC4H9N?VCp(NiProp2)(PR2) (R?SiMe3, Ph) are described starting from the corresponding chlorovanadium(V) complexes. The reaction of 1 with silver hexafluorophosphate yields a bis(fluoro)phosphidovanadium(IV complex [(μ-PF2)2V2Cl2)(NtC4H9)2]; as primary intermediate product of the unknown redox reaction a cationic vanadium(V) complex [tC4H9N?VCl2 · PPh3]+PF6? has been isolated. 1 reacts with an excess of diisopropylamine forming tC4H9N?V(NiProp2)Cl2 ( 16 ); in addition the following diisopropylamido-tert-butylimidovanadium(V) compounds tC4H9N?VCp(NiProp2)Cl ( 3 ) and tC4H9N?V(NiProp2)X2 (X?CH2CMe3, OtC4H9, CH3COO) has been prepared. All compounds obtained are characterized by 1H, 51V, 31P NMR spectroscopy. The X-ray diffraction analysis of 16 and 3 indicate a planar coordination sphere of the amido nitrogen atom. 相似文献