共查询到20条相似文献,搜索用时 31 毫秒
1.
Palakodety Radha Krishna Bonepally Karunakar Reddy Palabindela Srinivas 《Tetrahedron》2012,68(3):841-845
Total synthesis of 2-(2-hydroxyalkyl)-piperidine alkaloids, (?)-halosaline and (?)-8-epi-halosaline is reported from n-butyraldehyde using iterative asymmetric allylation, nucleophilic substitution with an azide and ring-closing metathesis as the key reactions. 相似文献
2.
Ahmed Kamal Saidi Reddy Vangala N.V. Subba Reddy V. Santhosh Reddy 《Tetrahedron: Asymmetry》2009,20(22):2589-2593
An asymmetric synthesis of the piperidine alkaloid (+)-β-conhydrine has been developed starting from (R)-protected glyceraldehyde as the chiral precursor using Barbier allylation, azide nucleophilic substitution, and ring-closing metathesis as the key steps. 相似文献
3.
Mirko ZajaStephen J Connon Aideen M DunneMichael Rivard Nicole BuschmannJan Jiricek Siegfried Blechert 《Tetrahedron》2003,59(34):6545-6558
A series of olefin metathesis catalysts with modified isopropoxybenzylidene ligands were synthesised, and the effects of ligands on the rate of metathesis investigated. Increased steric hinderance ortho to the isopropoxy group enhanced reaction rates. In the case of N-heterocyclic carbene complexes, decreasing electron density at both the chelating oxygen atom and the RuC bond accelerated reaction rates appreciably. Catalysts containing a tricyclohexylphosphane ligand, followed the same trend with regard to benzylidene electrophilicity, while higher electron density at oxygen enhanced reaction rates. 相似文献
4.
A concise synthesis of two diastereomers of (+)-castanospermine namely 1- and 8a-epi-castanospermine 1b and 1c, respectively, is reported from d-glucose. The methodology involves stereoselective cross metathesis of d-glucose derived alkene 2 with 4-bromo-1-butene followed by azide displacement and m-CPBA oxidation to afford diastereomeric γ,δ-epoxyazides 5a/5b. The Staudinger reaction of epoxyazide 5a followed by reaction with benzylchloroformate (CbzCl) unexpectedly furnished 1,3-oxazinan-2-one derivative 7 whose stereochemistry was establish by single crystal X-ray. This helps to assign the stereochemistry in the epoxidation reaction. The reduction of 5a/5b was then carried out by transfer hydrogenation to provide γ,δ-epoxyamine that concomitantly undergoes intramolecular 5-endo-tet cyclization to afford hydroxypyrrolidine ring skeleton with sugar framework-a precursor to castanospermine analogues 1b/1c. 相似文献
5.
The pentacyclic Melodinus alkaloid (±)-meloscine was synthesized in 19 chemical steps from 2-bromobenzaldehyde through a route featuring an allenyl azide cyclization cascade to deliver the core azabicyclo[3.3.0]octane substructure. Peripheral functionalization of this core included a Tollens-type aldol condensation to set the quaternary center at C(20) and a diastereoselective ring-closing metathesis to forge the tetrahydropyridine ring. 相似文献
6.
In aqueous solution containing azide ion as a nucleophile, electrochemical oxidation of hydroquinone and some dihydroxybenzoic acids have been studied using cyclic voltammetry and controlled-potential coulometry. The voltammetric data show that electrochemically generated para and ortho-benzoquinones participate in Michael addition reactions with azide ions to form the corresponding diazido or diaminobenzoquinones. In this work, we have proposed various mechanisms for the electrode process and we report an efficient and one-pot method for the synthesis of 2,5-diazido-1,4-benzoquinone, 2,5-diamino-1,4-benzoquinone, 4,5-diamino-1,2-benzoquinone, and 2,3-diamino-5,6-dioxocyclohexa-1,3-dienecarboxylic acid based on the Michael reaction of electrochemically generated ortho and para-benzoquinones with azide ion in an undivided cell using an environmentally friendly reagent-less method in ambient conditions. An estimation of the observed homogeneous rate constant (kobs) of the reaction of electrochemically generated para-benzoquinone with azide ion by the digital simulation method is also presented. 相似文献
7.
Sourav Maiti Pritam Biswas Jaydip Ghosh Michael G.B. Drew Chandrakanta Bandyopadhyay 《Tetrahedron》2014
Iodine/cuprous iodide-mediated intramolecular alkyne–carbonyl metathesis reaction has been developed using 2-(N-aryl-N-propargyl)aminochromone-3-carbaldehyde as the substrate. It led to the synthesis of hitherto unreported chromeno[2,3-b]azepine-3,6-dione. The special features of this methodology are mild reaction conditions, 100% atom economy and use of inexpensive reagents. This is the first example of I2/CuI-mediated alkyne–carbonyl metathesis reaction. 相似文献
8.
Ongoing challenges in topological polymer chemistry are reviewed. In particular, we focus on recent developments in an “electrostatic self-assembly and covalent fixation (ESA–CF)” process in conjunction with effective linking/cleaving chemistry including a metathesis process and an alkyne–azide click reaction. A variety of novel cyclic polymers having specific functional groups and unprecedented multicyclic macromolecular topologies have been realized by combining intriguing synthetic protocols. 相似文献
9.
Juanjuan Wang Gengwen Tan Dongli An Dr. Hongping Zhu Dr. Ying Yang 《无机化学与普通化学杂志》2011,637(11):1597-1601
The N‐heterocyclic carbene‐stabilized chromium(II) alkyl, aryl, and alkynyl complexes (IPM)2CrR2 [R = Me ( 2 ), Ph ( 3 ), C≡CPh ( 3 ); IPM = 1,3‐diisopropyl‐4,5‐dimethylimidazole‐2‐ylidene] were prepared by metathesis reactions of (IPM)2CrCl2 ( 1 ) with the corresponding organolithium reagents. Further reaction of 3 with an organic azide, 1‐azidoadamantane, yielded an organonitridochromium(V) compound (IPM)2Ph2Cr≡N ( 5 ). Compounds 2 – 5 are fully characterized by 1H NMR and IR spectroscopy, X‐ray crystallography as well as by elemental analysis. The structural analysis shows that the metal atom adopts a nearly square‐planar arrangement in the respective 2 , 3 , and 4 and a square‐pyramidal one in 5 . The reaction of 3 with the organic azide to 5 appears a novel way to the organonitridochromium compound. 相似文献
10.
A. S. Medvedeva M. M. Demina T. L. H. Nguyen T. D. Vu D. A. Bulanov V. V. Novokshonov 《Russian Journal of Organic Chemistry》2013,49(8):1221-1225
A highly efficient method was developed for the synthesis of new polyfunctional 1H-1,2,3-triazoles by the reaction of γ-hydroxypropynals with trimethylsilyl azide in water at room temperature without catalyst. The addition of trimethylsilyl azide to γ-hydroxypropynals occurs regioselectively: Previously unknown hydroxyalkyl-1H-1,2,3-triazolecarbaldehydes have been isolated in 69-96% yields with the prevalence of 1,5-isomers and the content of minor 1,4-isomers equal 9-21%. In the reaction of γ-hydroxypropynals with sodium azide in DMSO the formation of 4-hydroxyalkyl-1H-1,2,3-triazole-5-carbaldehydes is accompanied by the dimerization of initial aldehydes into the corresponding 1,3-dioxolanes. 相似文献
11.
《Polyhedron》1986,5(6):1143-1147
The azide ligand substitution reaction in tetrahedral zinc bis(diethyldithiocarbamate) has been studied by extraction. The reaction has been shown to proceed by both solvent and azide ion interactions with k0 = 5.0 × 10−4 s−1 and k1 = 1.9 × 10−3 M−1 s−1. A general discussion of the reaction mechanism is provided. 相似文献
12.
We report on the synthesis of the II-IV-N2 semiconductors ZnSiN2, MnSiN2, and the Zn1–xMnxSiN2 solid solutions by a one-step solid-state metathesis reaction. The successful syntheses were carried out by reacting the corresponding metal halides with stoichiometric amounts of silicon nitride and lithium azide in sealed tantalum ampoules. After washing out the reaction byproduct LiCl, powder X-ray diffraction patterns were indexed with orthorhombic space group Pna21. Single phase products were obtained without applying external pressure and at a moderate reaction temperature of 700 °C. The resulting ZnSiN2 was found to consist of nano-sized grains and needle-shaped nano-crystals. With increasing manganese content in the Zn1–xMnxSiN2 solid solution, we found the reaction product to be increasingly crystalline. Both the cell parameters and the bandgap values across the different compositions of the solid solutions change linearly. The sample Zn0.95Mn0.05SiN2 synthesized by means of solid-state metathesis reaction is an intense red emitter with a broad emission maximum at λmax ≈ 619 nm when excited with ultraviolet light after annealing the sample at a pressure of 6 GPa and a temperature of 1200 °C. 相似文献
13.
In this article a rapid and facile method for synthesis of acyl azide is described. The cross-linked poly(N-methyl-4-vinylpyridinium) azide ion, [P4-VP]N3 is prepared and used as an efficient polymeric reagent for synthesis of acyl azides from acyl halides at room temperature under heterogeneous conditions. Various benzoyl halides, with electron-withdrawing groups as well as electron-donating groups, were transformed into the corresponding benzoyl azides in high to excellent yields in short reaction times. The acyl azide products were characterized by FT-IR, and some of them were also characterized by 1H-and/or 13C-NMR spectroscopy, and physical properties were compared to literature values of known compounds. The spent polymeric reagents can be regenerated and reused for several times without losing their activity. Relative to the reported methods, the present method has the advantages of operational simplicity, mild reaction conditions, fast reaction rates, simple reaction work-up and lower hazardous and potentially explosive nature. Also the present method is the first procedure for the synthesis of acyl azides from acyl halides by using a polymer-supported azide ion under heterogeneous conditions. 相似文献
14.
William R. Peterson Barry Arkles Stephen S. Washburne 《Journal of organometallic chemistry》1976,121(3):285-291
Bridged bicyclic olefins were found to undergo facile 1,3-cycloaddition reaction with trimethylsilyl azide. Norbornene produced cis,exo-1-trimethylsilyl-4,7-methano-3a,4,5,6,7,7a-hexahydrobenzotriazole, while norbornadiene formed a diadduct with cis,exo-stereochemistry, together with 2-trimethylsilyl-1,2,3-triazole produced by a retro-Diels—Alder reaction of an intermediate mono-adduct. Dicyclopentadiene reacted only at the norbornene position while α-pinene did not react with trimethylsilyl azide. In contrast to aryl- and sulfonyl-azide adducts of norbornene derivatives, which decompose upon heating the present adducts were recovered unchanged after prolonged treatment at 205°C. 相似文献
15.
Enantioselective imidation of alkyl aryl sulfides with N-alkoxycarbonyl azide as a nitrene precursor was effected by using (OC)Ru(salen) complex 1 as catalyst. The steric and electronic nature of the N-alkoxycarbonyl group was found to strongly affect the enantioselectivity and the reaction rate, and high enantioselectivity (up to 99% ee) and good chemical yields were achieved by using 2,2,2-trichloro-1,1-dimethylethoxycarbonyl azide as the nitrene precursor at room temperature. 相似文献
16.
Gowravaram Sabitha Narjis Fatima E. Venkata Reddy J.S. Yadav 《Tetrahedron letters》2008,49(42):6087-6089
The total syntheses of (6R)-6-[(2R)-2-hydroxyhexyl]tetrahydro-2H-2-pyranone and 7-hydroxy-5-dodecanolide are described utilizing a Prins reaction and ring closing metathesis reaction sequence. 相似文献
17.
S. A. Konovalova A. P. Avdeenko V. M. Vasil’eva S. A. Goncharova 《Russian Journal of Organic Chemistry》2014,50(3):351-354
N-Phenyl(benzylidene, phenoxy)acetyl-1,4-benzoquinone imines reacted with sodium azide to give the corresponding 1,4-addition products, N-(4-hydroxyphenyl) carboxamides. Quantum chemical calculations showed that the initial step in the examined reaction is addition of azide ion to neutral quinone imine molecule. 相似文献
18.
DRAB David M. SHAMSHINA Julia L. SMIGLAK Marcin COJOCARU O. Andreea KELLEY Steven P. ROGERS Robin D. 《中国科学:化学(英文版)》2012,55(8):1620-1626
Zinc halide-complexed alkyl-bridged bi-heterocycles were obtained as zwitterions from the Click reaction of a series of N-cyanoalkyl-N-alkylimidazolium halide ionic liquids with sodium azide. Reaction optimization showed fast reaction times and milder conditions compared to conventional Click syntheses from neutral nitriles. 相似文献
19.
S. A. Konovalova A. P. Avdeenko A. G. Sergeeva I. L. Marchenko 《Russian Journal of Organic Chemistry》2014,50(3):346-350
N-Arylcarbamoyl-1,4-benzoquinone imines reacted with sodium azide in completely regioselective fashion according to the 1,4-addition pattern with formation of 1-(3-azido-4-hydroxyphenyl)-3-arylureas. The reaction of N-arylcarbamoyl-2,6-dichloro-3,5-dimethyl-1,4-benzoquinone imines with sodium azide afforded N-arylcarbamoyl-2,6-diazido-3,5-dimethyl-1,4-benzoquinone imines as a result of nucleophilic substitution of the chlorine atoms. 相似文献
20.
Ring opening of protected 3-aminoalkyl-substituted azetidin-2-ones with O-, N- or S-nucleophiles led to β,β′-diaminocarboxylic esters, amides and thioesters, respectively. The reaction outcome is improved by the addition of catalytic amounts of sodium azide. Utilization of a glycine derivative with unprotected amino function as nucleophile was possible. When bulkier amino acid esters were used, the intermediate acid azide underwent a Curtius rearrangement. The isocynates formed were trapped as the corresponding urea derivatives. Reduction of β-lactam's amide moiety led to diaminoalcohols. 相似文献