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卷 86, 编号 3 (2016)
- 年: 2016
- 文章: 47
- URL: https://journals.rcsi.science/1070-3632/issue/view/13333
Article
N-alkyl-2-halo- and 2,2-dihaloaldimines in the Pudovik reaction
摘要
The use of N-alkyl-2-haloaldimines in the imine version of the Pudovik reaction, namely, in the reaction of imines with acid esters of phosphorus acids, much extended the synthetic potential of this reaction due to the fact that the primary addition and protonation product, having quite a mobile single hylogen atom, can undergo both spontaneous transformations and transformations involving other reagents. The reduction of the С–Hlg bond in N-alkyl-2-halo- and -2,2-dihaloaldiminium salts with О,О-dialkyl phosphorodithioic acids was observed for the first time.
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Features of homolytic organophosphorus synthesis and its application
摘要
The features and selected applications of the homolytic organophosphorus synthesis based on the addition of phosphorous acid and its acid esters to unsaturated compounds, discovered by A.N. Pudovik in 1954.
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C-phosphorylation of unsaturated ketones with phosphorus pentachloride
摘要
C-Phosphorylation of a number of unsaturated ketones with phosphorus pentachloride has been studied. Structure of the obtained dienyltrichlorophosphonium hexachlorophosphorates was established by means of 1H, 13C, and 31P NMR spectroscopy.
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Phosphorylation of betti base with diethyl chlorophosphate
摘要
Phosphoric acid derivatives containing chiral Betti base fragment were synthesized by reacting racemic and enantiopure N-Boc-protected 1-(α-aminobenzyl)-2-naphthols with diethyl chlorophosphate followed by deprotection.
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Reactions of C-phosphorylated acetimidates and acetamidines, involving the CH-acid methylene group
摘要
Organophosphorus compounds are widely used in the synthesis of pharmaceuticals, fungicides, pesticides, and other biologically active compounds. The review presents the main methods of synthesis of C-phosphorylated acetimidates and acetamidines containing a CH-acid methylene group, as well as reactions involving this group.
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2-Ethoxy-2,3-dihydro[d][1,2]oxaphosphole 2-oxide in the synthesis of dialkyl(diaryl)(2-hydroxybenzyl)phosphine oxides
摘要
A facile method of synthesis of functionally substituted P(IV) derivatives―dialkyl(diaryl)(2-hydroxybenzyl) phosphine oxides―by the reaction of 2-ethoxy-2,3-dihydro[d][1,2]oxaphosphole 2-oxide with organomagnesium compounds, which allows wide variation of substituents on the phosphorus atom was developed.
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Cycloaddition and chlorotropic transformations in reactions of dichloromethylenetrifluoroacetamide with phosphites
摘要
Reactions of dichlormethylenetrifluoroacetamide with triphenyl phosphite, diethylchlorophosphite (o-phenylene)diethylamidophosphite, (o-phenylene)chlorphosphite, and 2-fluoro-3-isopropyl-5-tert-butyl-1,3,2-oxazaphospholine proceeded as cheletropic [4+1]-cycloaddition. The formed λ5-1,4,2-oxazaphospholines underwent 1,3-migration of the chlorine atom in C=N–C cyclic triad.
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1-chloroacetyloxindole(isatin) in reactions with some N-nucleophiles. Unexpetedly easy cleavage of chloroacetyl group
摘要
Reactions of 1-chloroacetyloxindole and 1-chloroacetylisatin with some secondary amines, Girard’s reagent T and thiourea were studied. All investigated reactions proceeded via cleavage of the acyl group to form 3-substituted isatin or oxindole derivatives.
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Phosphorylation of aminomethylated derivatives of 2,7-dihydroxynaphthalenes
摘要
Phosphorylation of 2,7-dihydroxynaphthalene derivatives, containing different amine components was performed by full amides of phosphorous acid. A substantial effect of the intramolecular hydrogen bond on the process of phosphorylation was shown. Cyclophosphorylation was performed and principal possibility of the synthesis of naphthophosphacrownaphanes having aminomethyl linkers was shown. Mannich aminomethylation of naphthophosphacyclophanes was found to be impossible.
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Preparation and crystal structure of 1,1-tetramethylethylenedioxy-3,4-diphenyl-6-trichloromethyl-2,5,7,1-trioxaphosphabicyclo[2.2.11,4]heptane and 2-(1-hydroxy-2,2,2-trichloroethoxy)-4,4,5,5-tetramethyl- 2-oxo-1,3,2-dioxaphospholane
摘要
The state of the art of chloral applications in the chemistry of tricoordinate phosphorus derivatives has been analyzed. The highly stereoselective reaction of 4,4,5,5-tetramethyl-2-(2-oxo-1,2-diphenylethoxy)-1,3,2-dioxaphospholane with chloral has been shown to afford a caged phosphorane with the phosphorus–carbon bond, 1,1-tetramethylethylenedioxy-3,4-diphenyl-6-trichloromethyl-2,5,7,1-trioxaphosphabicyclo- [2.2.11,4]heptane. Structure of the phosphorane and its hydrolysis product, 2-(1-hydroxy-2,2,2-trichloroethoxy)- 4,4,5,5-tetramethyl-2-oxo-1,3,2-dioxaphospholane, has been elucidated by X-ray diffraction analysis.
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Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol
摘要
Carvacrol trimethylsilyl ether when reacting with P4S10 forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimethylsilyl ether yield the S-trimethylsilyl esters of the corresponding dithiophosphoric acids.
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Application of the Todd–Atherton synthetic approach for chemical modification of tetraene macrolide antibiotic lucensomycin
摘要
Lucensomycin, tetraene macrolide antibiotic, has been chemically modified with dialkyl(diaryl) phosphites under conditions of the Todd–Atherton reaction. The reaction has yielded the corresponding dialkyl-(diaryl) amidophosphate derivatives of the antibiotic. Physico-chemical properties of the prepared derivatives as well as their toxicity and antifungal activity towards a series of pathogenic Candida yeast-like fungi have been studied. The automated decision-making information system for selection of highly efficient antibiotics has been described.
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Synthesis of aminobismethylenephosphonic acids on a platform of p-tert-Butylthiacalix[4]arene in 1,3-alternate configuration
摘要
Aminobismethylenephosphonic acids on a platform of p-tert-butylthiacalix[4]arene were obtained by reacting macrocyclic amines with phosphorous acid and formaldehyde under acid catalysis. Free phenol hydroxy groups on the lower rim of p-tert-butylthiacalix[4]arene were found to inhibit the interaction with the amino moieties of the macrocycle. In the case of amino derivatives of thiacalix[4]arene containing no hydroxy groups the reaction led to the formation of target compounds in good yields.
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Structure and dynamics of eight-membered P,N-heterocycles in solution
摘要
Conformational analysis of eight-membered P,N-heterocycles (P2NR2R') in the solution has been performed by means of NMR spectroscopy and quantum chemical calculations. The equilibrium of the С2-symmetrical (crown, major) and Сs-symmetrical (chair-boat, minor) forms of the compounds has been revealed, the transition barriers being of about 12 kcal/mol. The presence of an aromatic substituent at the nitrogen atom significantly shifts the equilibrium towards the dominating form.
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Synthesis and conformational analysis of phosphine selenides
摘要
Methods of preparation of complex phosphine selenide via the original Trofimov–Gusarova reaction are described. The results of the products conformational analysis by means of a set of physical methods (IR spectroscopy, dipole moments, and quantum chemical calculation) are presented.
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Synthesis and antioxidant activity of modified sterically hindered phenols
摘要
Salicylaldehyde derivatives containing sterically hindered phenol fragments were synthesized. The compounds obtained are capable to offer protection against UV radiation.
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Pyridoxal reactions with amines and aliphatic diamines
摘要
Interaction of pyridoxal (3-hydroxy-5-hydroxymethyl-2-methylisonicotinaldehyde) with amines, mono- and disubstituted diamines led to the formation of compounds having in their structure imine, imidazolidine, and pyrimidine moieties. Structure of the obtained compounds was proved by IR data, 1H NMR spectroscopy, mass spectrometry, and X-ray diffraction analysis.
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Reactions of terpene alcohols and diols with chlorine dioxide in dimethylformamide
摘要
The system chlorine dioxide–dimethylformamide in combination with or without a catalytic amount of MoCl5, CeCl3, ZrOCl2, or VO(acac)2 induces oxidative chlorination of a number of bicyclic terpene alcohols and vicinal diols. 2α-Chloropinan-3-one, 3α-chloro-10β-pinan-4-one, 5α-chloro-3α-hydroxycaran-4-one, 5β-chloro-3β-hydroxycaran-4-one, and 4α-chloro-2α-hydroxypinan-3-one were thus synthesized in good preparative yields.
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Synthesis of new bicyclic compounds containing fused sulfolane and pyrazolidine rings
摘要
3-Aryl-6а-methyl-6-nitro-1-carbamoylhexahydrothieno[2,3-d]pyrazole-4,4-dioxides, novel original bicyclic species consisting of fused pyrazolidine and sulfolane rings, and 1,4-adducts were obtained by reacting 2-benzylidene-3-methyl-4-nitro-3-thiolene-1,1-dioxide and its derivatives with semicarbazide.
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α- and β-diphenylphosphorylated secondary alkanols: I. general method of synthesis and extraction properties towards f-elements
摘要
A simple and effective general method of synthesis of α- and β-diphenylphosphorylated secondary alkanols by the reduction of the corresponding phosphorylalkanones with NaBH4 was developed. The extraction properties of the resulting phosphorylalkanols Ph2P(O)(CR2)nCH2CH(OH)Me (n = 0, 1; R = H, Me) were studied in the recovery of f-elements (LaIII, NdIII, HoIII, YbIII, UVI, ThIV) from nitric acid solutions into chloroform and compared with those of both related phosphorylketones and known extractants (n-BuO)3PO, (n-C8H17)3PO, and Ph2P(O)CH2C(O)N(n-Bu)2.
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NMR study of 1,7-diamino-4-oxyheptane-1,1,7,7-tetraphosphonic acid interaction with samarium(III) cation
摘要
1,7-Diamino-4-oxypentane-1,1,7,7-tetraphosphonic acid has been synthesized while searching for potential components for 153Sm radiopharmaceuticals. Its interaction with samarium(III) cation has been studied by 13C and 31P NMR spectroscopy in comparison with 1,5-diamino-3-oxypentane-N,N'-tetra-(methylenephosphonic acid) which is the ligand component of the osteotropic drug Samarium 153Sm oxabifore. NMR spectroscopy provides a simple, convenient, and informative method for studying interactions between the ligand and prospective radionuclide cation.
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Synthesis and hydrophosphorylation of π-complexes of dibenzylideneacetone and cyclic conjugated dienones with homocarbonyl and carbonylcyclopentadienyl molybdenum compounds
摘要
Reactions of dibenzylideneacetone and cyclic cross-conjugated dienones with hexacarbonylmolybdenum(0) and bis[tricarbonyl(cyclopentadienyl)molybdenum(0)] afforded the corresponding complexes with η2-(C=C),η2-(C=O) coordination of the diketone to metal center, regardless of the ligand structure and initial molybdenum compound. The reactivity of the multidentate ligands may change as a result of coordination.
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Self-assembling catalytic systems based on new amphiphile containing purine fragment, exhibiting substrate specificity in hydrolysis of phosphorus acids esters
摘要
Micellar catalytic systems based on new purine-containing amphiphile for hydrolytic decomposition of organophosphorus toxicants have been prepared. The aggregation threshold of the system has been estimated by means of tensiometry, conductometry, spectrophotometry, and dynamic light scattering. The solubilizing action of the amphiphile towards the hydrophobic dye has been demonstrated. Kinetic studies of hydrolysis of phosphonates differing in the hydrophobicity have disclosed the substrate specificity of the micellar catalysts; inhibition instead of catalysis has been observed in the case of the less hydrophobic substrate.
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Colloidal stability and photophysical characteristics of luminesent silica nanoparticles modified with various nitrogen/oxygen-containing trialkoxysilanes
摘要
Surface modification of the luminescent silica nanoparticles doped with Tb(III)–p-sulfonatothiacalix[ 4]arene complex was carried out using a series of nitrogen/oxygen-containing trialkoxysilanes. It was found that groups capable of nonspecific interactions on the surface of the nanoparticles cause a significant decrease in their colloidal stability. The chromophore moieties in the modifiers were found to quench the luminescence of the nanoparticles. The surface modification of the nanoparticles is responsible for the change in the mechanism of luminescence quenching in the presence of copper(II) ions due to decreased accessibility of luminophores to the quencher.
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The copper-catalyzed cross-coupling reactions of aryl diazonium salts and isocyanides
摘要
The copper-catalyzed cross-coupling reaction of aryl diazonium salts and isocyanides has been performed. This is a successful example of preparation of arylcarboxyamides with moderate to good yield under mild conditions.
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Synthesis of novel substituted pyridines from 1-(3-aminophenyl)-3-(1H-indol-3-yl)prop-2-en-1-one and their anticancer activity
摘要
A series of novel substituted pyridine derivatives have been synthesized via the reaction of 3-indole carboxaldehyde with 3-aminoacetophenone. The products structures have been elucidated from elemental analysis as well as IR, 1H NMR, 13C NMR, and MS spectroscopy data. All the synthesized compounds have shown anticancer activity against HEPG2 and MCF-7 in vitro; some of them have exhibited the in vivo activity.
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Synthesis and anticancer activity evaluation of (E)-3-{[5-(aryl)-1,3,4-oxadiazol-2-yl]methyl}-5-(3,4,5-trimethoxybenzylidene)thiazolidine-2,4-diones
摘要
A series of new substituted (E)-3-{[5-(aryl)-1,3,4-oxadiazol-2-yl]methyl}-5-(3,4,5-trimethoxy-benzylidene) thiazolidine-2,4-diones have been synthesized. The products have been characterized by their IR, 1H NMR, 13C NMR, and mass spectral properties and evaluated for anticancer activity against four human cancer cell lines: A549, A375, MCF-7, and HT-29.
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One-dimensional heterobimetallic cyanide-bridged Fe(III)–Mn(II) complex: Synthesis, crystal structure, and magnetic properties
摘要
A new cyanide-bridged heterobimetallic Fe(III)–Mn(II) complex {[MnL][FebpdBrb]} [FebpdBrb]n· 2nH2O has been synthesized by using pyridinecarboxamide trans-dicyanideiron as the building block. The X-ray diffraction analysis has revealed the one-dimensional infinite structure of the complex consisting of the alternating [Mn(L)]2+ and [Fe(bpdBrb)(CN)2]– units forming a cyanide-bridged cationic polymeric chain, with [Fe(bpdBrb)(CN)2]– as the free anions. The antiferromagnetic coupling between the neighboring Fe(III) and Mn(II) ions through the bridging cyanide group has been revealed. The magnetic coupling constant has been determined as of J =–3.17 cm–1.
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Preparation and adsorption properties of magnetic Co0.5Ni0.5Fe2O4–chitosan nanoparticles
摘要
Magnetic chitosan microspheres were prepared by the emulsification cross-linking technique in the presence of glutaraldehyde as cross-linking agent, liquid paraffin as dispersant, and Span-80 as emulsifier. The optimal cross-linking time and Co0.5Ni0.5Fe2O4: chitosan ratio were determined. The morphology of particles was studied by different techniques. The adsorption characteristics were studied and the effect exerted by the initial concentration of methyl orange, the time of cross-linking, and the amount of the adsorbent was determined. It is found that the product obtained at the Co0.5Ni0.5Fe2O4: chitosan ratio 1: 4 and the crosslinking time 5 h has the uniform morphology. At room temperature, the Co0.5Ni0.5Fe2O4–chitosan magnetic composite has maximal adsorption for methyl orange at the dosage 20 mg.
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Silica-supported perchloric acid (HClO4/SiO2) as efficient catalyst for the synthesis of tetraazamacrocyclic complexes of transition metals
摘要
Silica-supported perchloric acid (HClO4/SiO2) was used to catalyze the synthesis of tetraazamacrocyclic complexes of Co(II), Ni(II), Cu(II), and Zn(II) from the corresponding metal chlorides, nitrates, or acetates, isatin, and benzene-1,2-diamine in ethanol. The use of HClO4/SiO2 as catalyst allowed the reaction to be performed under stirring at room temperature instead of traditional reflux and completed in two hours. The synthesized complexes were characterized by molar conductance and magnetic susceptibility measurements, IR, electronic, 1H NMR, and mass spectra, and thermogravimetric and X-ray powder analyses. On the basis of these data, six-coordinate octahedral geometry was proposed for all complexes. The synthesized complexes were also tested for antimicrobial activity.
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Synthesis, characterization, and antibacterial activity of some thiazoles derived from allyl thioureas
摘要
Synthesis of thiazoles was carried out from allyl thioureas using different cyclizing agents such as hydrogen chloride gas and bromine. Synthesized compounds were characterized by IR, 1H and 13C NMR, mass spectrometry, and elemental analysis. The synthesized thiazoles were evaluated for their antibacterial activity against Gram postitive (Lactobacillus bulgaris and Streptococcus mitis) and Gram negative (Yersinia) as well as antifungal activity against Aspergillus niger fungi.
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Synthesis, spectroscopic, and antimicrobial study of Ca(II), Fe(III), Pd(II), and Au(III) complexes of amoxicillin antibiotic drug
摘要
Synthesis, spectroscopic characterization, theoretical and antimicrobial studies of Ca(II), Fe(III), Pd(II), and Au(III) complexes of amoxicillin (amox) antibiotic drug are presented in the current paper. Structure of 1: 1 (metal: amox) complexes were elucidated on the basis of elemental analyses, and IR, Raman, 1H NMR, and electronic spectral data. According to molar conductance measurements the complexes had electrolyte nature. Amoxicillin reacted with metal ions as a tridentate ligand coordinated with metal ions via–NH2,–NH, and β-lactam carbonyl groups. The complexes were formulated as [Ca(amox-Na)(H2O)]·Cl2·4H2O (1), [Fe(amox-Na)(H2O)3]·Cl3·3H2O (2), [Pd(amox-Na)(H2O)]·Cl2 (3), and [Au(amox-Na)(H2O)]·Cl3 (4). Kinetic thermodynamic parameters (E*, ΔS*, ΔH*, and ΔG*) were calculated based on the Coats–Redfern and Horowitz–Metzger methods using thermo gravimetric curves of TG and DTG. Nanosize particles of amoxicillin complexes have been studied by XRD, SEM, and TEM methods. Theoretical studies of the synthesized complexes have been performed.
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DNA binding, DNA cleavage, and cellular imaging of a copper(II) complex based on curcumin
摘要
Binding property between CT-DNA and a Cu(II) complex, namely CuL2, where HL = 1,7-bis(4-butoxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione, was determined by UV–Vis absorption, fluorescence spectroscopy, and viscosity measurements. The results showed that the binding of the complex with CT-DNA was through the intercalative mode and the binding constant (Kb) value was found to be 3.82 × 104 M. DNA cleavage studies showed that CuL2 exhibited effective cleavage activity on pBR322 plasmid DNA in absence of external agents. Additionally, cellular imaging studies also indicated that CuL2 has a higher toxicity to MCF-7 cell lines compared with its corresponding ligand HL.
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Letters to the Editor
Reaction of diethylpropa-1,2-dienylphosphonate with 2-aminobenzothiazole
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Reactions of novel acetal-containing α-aminophosphonates with 2-methylresorcinol
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Synthesis of dialkyl [(5-amino-1,3,4-thiadiazol-2-yl)methyl]phosphonates
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Steric control of regiodirectivity of reductive N-vinylation–C-phosphorylation of pyridines with the system alkyl propiolate–secondary phosphine oxide
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Synthesis of phosphonomethylornithine
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Preparation of new synthons for designing polyfunctional chelating agents
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Amidation of hydroxybenzoic acids with imidazole
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Reactions of Diphenylchlorothiophosphinate with Pyridoxalimines
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1,3-benzoxazines and some of their reactions
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Covalent assembly of tris-pillar[5]arene
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First examples of isatin acylhydrazones with ammonium fragment
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Interaction of α-aminoacetals with phenol. synthesis of new polyphenols
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Synthesis of new polyphenols containing sym-triazine fragment
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Azo coupling of 2-hydroxymethyl-4-tert-butylphenol with sulfamoylbenzenediazonium chloride
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