The stereochemistry of 2,4-disubstituted γ-butyrolactones and 2,4,6-trisubstituted-5,6-dihydro-4H-1, 3-oxazines

2,4-Disubstituted butyrolactones and 2,4,6-trisubstituted-5,6 dihydro-4H-1,3-oxazines show similar features in their ¹H and ¹³C- NMR spectra. Two geminal ring hydrogens of cis isomers give rise to a complex ABXY spectra when the substituent is alkyl or aryl. In spectra of trans isomers these patterns are degenerated. When R is OMe(in 4) or OCOMe (in 6) the difference in chemical shifts of geminal protons and vicinal coupling constants cannot be used for diagnosis. In ¹³C spectra ring carbons C-2 and C-3 in lactones and C-4 and C-5 in oxazine of trans isomers show a small but consistent shift to higher fields.     

Three new decarbonyl prenylphloroglucinols bearing unusual spirost subunits from Hypericum scabrum and their neuronal activities

Three novel polycyclic polyprenyled acylphloroglucinols,Hyperscabins A-C,were obtained from the aerial parts of Hypericum scabrum.They featured an unprecedented 5,5-spiro ketal subunit with the loss of C-2' carbonyl in the phloroglucinol ring.Their structures were characterized by extensive spectroscopic analyses,NMR calculations with DP4+analysis,calculated electronic circular dichroism(ECD) spectra and the application of modified Mosher's methods.In the assay of [3 H]-5-HT and [~3 H]-NE reuptake inhibition,compounds 1 and 2 showed good inhibito ry activity(81.8% and 83.2%) in 10 μmol/L.In addition,compound 1 significantly increased cell viability in the experiment of oxygen and glucose deprivation/deoxygenation.     

New compounds from the roots of Coriaria nepalensis

One new sesquiterpene lactone possessing novel variations in the structure, corialactone E (1), one new neolignan, coriarianeolignan A (2), together with three known apocarotenoids (3-5) and one known neolignan (6), have been isolated from a CHCl₃ extract of the roots of Coriaria nepalensis.     

Aufkl?rung der 1H- und 13C-NMR-spektren sowie der kristallstruktur unges?ttigter glycosylphosphonate und konformationsberechnungen an modellen1

By application of a modified LAOCN-3 program a complete elucidation of the ¹H NMR spectra of 2,3-unsaturated glycosyl phosphonates 1–5 could be achieved. The exactly determined ⁿJ(H, H) and novel ⁿJ(C, P) coupling constants are discussed, and permit a conclusive deduction of the conformations. The ¹³C NMR spectra of 1 to 6 can be fully interpreted. By a close inspection of chemical shifts as well as ¹J(C-H) and ⁿJ(C, P) coupling constants the conformational assignment is supported. For all the derivatives the correlations ¹J(C-1,H_e)>¹J(C-1, H_a) and ¹J(C-1, P_e) >¹J(C-1, P_a) can be used for the assignment of anomers. The crystal structure of 1 is in accordance with this assignment of anomers and displays an unexpected conformation. Calculations by MINDO-3 in resembling model compounds serve to elucidate such conformative effects.     

Chemie der pleuromutiline—II : Synthese des 12-desvinylpleuromutilins

Oxidation of the AB-trans-anellated Pleuromutilin-derivative 7¹ with Ozone followed by decarbonyl- ation gave the corresponding desvinyl-compound 10. A 1,5-hydride shift between C-3 and C-11 leads to the title compound 11. The 12-methyl group of10 was assigned the α-configuration on the basis of chemical and spectroscopic data.     

Artanomadimers A–F: six new dimeric guaianolides from Artemisia anomala

A novel dimeric guaianolide with an unprecedented skeleton, named artanomadimer A (1), and five new analogues, artanomadimers B–F (2–6), were isolated from the aerial parts of Artemisia anomala. Their structures and stereochemistry were elucidated by extensive spectroscopic methods, and the absolute stereochemistry of compound 4 was confirmed by X-ray crystallographic analysis. Artanomadimer A (1) is probably formed through a Diels–Alder reaction with the new carbon–carbon bond formation of C-11/C-2′ and C-13/C-5′ based on its structure. A cytotoxic evaluation showed that compounds 1 and 6 exhibited significant inhibitory effects against the cell growth of BGC-823 tumor cell lines with IC₅₀ values of 2.71 and 6.25 μM, respectively.     

The first thermally stable half-sandwich titanium zwitterionic complex

Thermally stable zwitterionic complex [(η⁵-C₅Me₅)Ti(Ot-Bu)₂]^(δ+)[(μ-Me)B(C₆F₅)₃]^(δ−) (5) was formed by mixing equimolar quantities of [(η⁵-C₅Me₅)TiMe(Ot-Bu)₂] and [B(C₆F₅)₃]. The compound was recrystallized from hot toluene and has been stable so far for 1 year at ambient temperature in the solid state and in toluene solution. The ¹H, ¹⁹F and 1D NOESY NMR spectra in C₆D₆ solution proved the inner sphere ion pair structure of 5. The X-ray crystal structure of 5 revealed that the bridging methyl group is σ-bonded to boron, and all its C-H bonds fulfil criteria for agostic bonding interaction with the titanium atom. In contrast to the stable solution in C₆D₆ compound 5 decomposed in CD₂Cl₂ solvent within hours at room temperature.     

Didemnaketals D and E,bioactive terpenoids from a Red Sea ascidian Didemnum species

Two new spiroketals, didemnaketals D (1) and E (2) were isolated from a marine ascidian species belonging to the genus Didemnum. The structures of the compounds were elucidated by extensive 1D (¹H, ¹³C, and DEPT) and 2D (COSY, TOCSY, HSQC, HMBC, NOESY, and ROESY) NMR studies and high-resolution mass spectroscopic data. The new didemnaketals differ from the reported ones in which that they lack the methyl functionality at C-6 and the hydroxy moiety at C-21. Instead, they possess an ester moiety at C-6 in addition to new oxygen functionality at C-20 of the didemnaketals. Compounds 1 and 2 were evaluated for their protein kinase inhibitory activity against different kinases (CDK5, CK1, DyrK1A, and GSK3) at 10 μg/mL. Compounds 1 and 2 showed moderate activity against these kinases. In addition, the compounds displayed moderate antimicrobial activity against Staphylococcus aureus and Bacillus subtilis, respectively.     

Antifungal diastereomeric furanones from Mutisia friesiana: structural determination and conformational analysis

Two diastereomeric furanones, (4S,5S)-5-(4′-methyl-3′-pentenyl)-4-hydroxy-5-methyldihydrofuran-2-one 1 and (4S,5R)-5-(4′-methyl-3′-pentenyl)-4-hydroxy-5-methyldihydrofuran-2-one 2 were isolated for the first time from the shrub Mutisia friesiana. The relative stereochemistries of 1 and 2 were ascertained from NOESY NMR data and confirmed by a combination of molecular modeling (molecular mechanics and ab initio molecular orbital calculations) and NMR data. Comparison between experimental and calculated ¹H–¹H vicinal coupling constants revealed that both furanones exist in an equilibrium of two stable conformers of the five-membered ring. Application of Mosher's method suggests that both diastereomeric furanones have the same (S)-configuration at C-(4) and are epimers at C-(5). Furanones 1 and 2 showed antifungal activity against the pathogenic fungus Cladosporium cucumerinum.     

A study of the reaction of 2-thiazolin-4-ones with some electrophiles under microwave irradiation versus conventional condition

Coupling of 5-dimethylaminomethylene-3-methyl-2-(pyridine-2-ylimino)-thiazolidin-4-one (3) with diazotized methyl anthranilate afforded the 3-methyl-5-(2-methoxycarbonylphenylhydrazono)-2-pyridine-2-ylimino)thiazolidin-4-one (5). Reaction of 2-(arylamino)thiazol-4-ones 1a,b with arylidenemalononitriles under microwave irradiation gave 2-substituted amino-5-arylidenethiazolin-4-ones 9a–f. Alternatively, compound 9 could also be obtained by reacting compound 1 with aromatic aldehydes. Treatment of compound 9 with acetic acid yielded the corresponding thiazolin-2,4-diones 10. However, the reaction of 1 with cyanoacetic acid yielded the corresponding 4-cyanoacetyl derivative 12, in good yield. The ¹H, ¹³C NMR spectra of some representative products and X-ray crystal structure determination are discussed.     

A taxane with a novel 9α,13α-oxygen bridge from Taxus cuspidata needles

A novel taxane with an unprecedented hemiacetal ring between C-13 and C-9 was isolated from the needles of Taxus cuspidata. The structure was characterized as (12αH)-2α,10β-diacetoxy-5α-cinnamoyloxy-9α,13α-epoxytax-4(20)-ene-11β,13β-diol (1). This is the first example of a natural taxane with a C-13 and C-9 oxygen bridge to form an unusual 6/8/6/6-membered ring system.     

On the relative stereochemistry of atomaric acid and related compounds

The stereochemistry at C-3 of the known compounds atomaric acid 2a, 5′a-desmethyl-5′-acetylatomaric acid 4a, and stypoquinonic acid 5a is revised to 2, 4, and 5 on the basis of a careful study of 2D NOESY experiments and also from comparison of their ¹H and ¹³C chemical shifts with those of the related metabolites 6 and 7 isolated from Stypopodium zonale. Compound 7 is a novel unusually functionalized 1-keto-5′a-desmethyl atomaric acid derivative whose structure and stereochemistry were determined by spectroscopic means.     

Synthesis and crystal structure analysis of 2-(4-fluorobenzyl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazole and its chlorophenyl derivative

Preparations of 2-(4-fluorobenzyl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazole (3a) and its chlorophenyl derivative (3b) are described. Preliminary analysis was done spectroscopically by means of ¹H NMR, ¹³C NMR spectra, mass spectra and elemental analyses. Further the structures were confirmed by X-ray crystal structure analyses. The compound (3a) has crystallized in a triclinic P-1 space group with three independent molecules in the asymmetric unit, while the compound (3b) belongs to P2₁/c space group with one molecule in the asymmetric unit. The molecule (3b) differs from molecule (3a) by the presence of chlorine substituent. Additionally, the imidazo-thiadiazole entity is as usual planar. Intramolecular C–H⋯N hydrogen bonding between the imidazole and the phenyl ring of the molecule can be observed in (3a) & (3b). The molecules of (3a) are linked into two dimensional supramolecular hexagonal hydrogen bonded network sustained by C–H⋯F interaction, while those of (3b) are linked by bifurcated C–H⋯N interactions. Further, the molecular packing of both the compounds is stabilized by π–π stacking interactions between the benzene and imidazo-thiadiazole ring systems.     

Theoretical Study and Experimental Analysis on 2-(1-Ethyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)-2-oxoacetic Acid (<Emphasis Type="Bold">3</Emphasis>) Using the DFT Approach

Riley oxidation of 3-acetyl-4-hydroxyquinolin-2(1H)-one (1) with selenium dioxide furnished the unexpected product 2-(1-ethyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)-2-oxoacetic acid (3). The expected product 2-(1-ethyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)-2-oxoacetaldehyde (2) was excluded based on the spectral data. The elemental analysis and spectral data (IR, and ¹H NMR) was used to deduce the structure of compound 3. Density functional theory (DFT) and time-dependent density functional theory (TD-DFT) calculations of the electronic structure at the B3LYP/6-311G (d,p) level of theory have been employed for compound 3 to investigated its geometry, linear polarizability 〈Δα〉, first-order hyperpolarizability 〈β〉, natural bonding orbital (NBO), molecular electrostatic potential contours (MEP and ESP), electrophilicity, and UV–Vis spectra in both ethanol and dioxane solvents. The geometrical and energetic parameters have been extensively investigated to reveal the reason behind the selective formation of compound 3, rather than the expected product 2. FT-IR spectra in the solid phase were recorded for compound 3. The thermo-chemical parameters, harmonic vibration frequencies, and the equilibrium geometries have been calculated at the DFT/B3LYP/6-311G (d,p) level. Time-dependent density functional theory (TD-DFT) was used to calculate the excited states of compound 3. Changes in the solvent cause changes in the band intensities and in the positions of the band maxima (λ_max). The excited state was identified and contributes to the electronic configurations, and it was characterized in terms of the relevant MOs. The theoretical spectra were computed using the Coulomb-attenuating method (CAM-B3LYP), using the basis set 6-311G (d,p) in the gas phase, and the polarizable continuum model (PCM) in dioxane and ethanol. The results indicate good agreement with the observed spectra.     

Design and synthesis of self-included pillar[5]arene-based bis-[1]rotaxanes

Two strategies for the design of new pillar[5]arene-based mechanically self-interlocked molecules (MSMs) are reported here. The first strategy is based on the construction of an intermediate pseudo[1]rotaxane followed by the desired bis-[1]rotaxane. The other one is based on the construction of the desired bis-[1]-rotaxane directly via a condensation reaction through host-guest interactions between a mono-functionalized pillar[5]arene and the axle. This compound has interesting self-assembly properties in methanol and some extended applications of this compound will be reported in the near future.     

Synthesis,spectral and computational studies of some N-acyl-t(3)-isopropyl-r(2),c(6)-bis-2′-furylpiperidin-4-one oximes

Four N-acyl-t(3)-isopropyl-r(2),c(6)-bis-2′-furylpiperidin-4-one oximes 1–4 were synthesized and the high resolution ¹H and ¹³C NMR spectra have been recorded at various temperatures and analyzed. The spectra reveal the presence of two rotameric forms (syn and anti) in solution. ¹H-¹H COSY and ¹H-¹³C COSY spectra have been recorded to assist the assignment of the signals for the syn and anti isomers of 1–4. Coupling constants predict an equilibrium mixture of boat form B₁ and alternate chair form CA for 1–4. The effect of varying the substituents at nitrogen and at C(4) on the ¹H and ¹³C chemical shifts has been analyzed in detail. The molecular structures of the N-acyl derivatives 1–4 were also determined using AM1 Hamiltonian and the results have been compared to the results derived from spectral studies. Mass spectra have also been recorded for 1–4.     

The effect of polyether ligands on the solution structure of [Li]-α-(phenylthio)benzyllithium in tetrahydrofuran: A H,Li-HOESY NMR study

[⁶Li]-α-(phenylthio)benzyllithium 1-⁶Li was studied in THF/[D₈]THF solution (1:1) in the presence of several acyclic and cyclic polyether ligands by ¹H,⁶Li-HOESY, ¹H and ¹³C NMR spectroscopy. The question whether these ligands are bonded to lithium or not is important for physical–organic investigations as well as for studies of the ground state of (stereoselective) reactions of organolithium compounds in the presence of such ligands. Dimethoxyethane is not bonded to lithium under these conditions. The acyclic ethers diglyme and triglyme coordinate only weakly to the organolithium compound and form contact ion pairs (CIPs) at 25°C. At −80°C, CIPs are in equilibrium with separated ion pairs (SIPs). Very stable complexes of 1-⁶Li are obtained with crown ether ligands. Addition of 12-crown-4 and 15-crown-5, respectively, results in the exclusive formation of SIPs at 25°C and −80°C. With 18-crown-6, a CIP–SIP equilibrium is observed at 25°C which is shifted entirely to the SIP side at −80°C. Graphical analyses of the ¹H and ¹³C NMR spectra of the polyether complexes of 1-⁶Li revealed correlations between the chemical shifts of the para phenyl carbon C-5, the para phenyl proton H-5, the benzylic carbon C-1, and the proton–carbon coupling constant J(C-1,H-1) of 1-Li, which are useful probes for the charge distribution within the carbanionic moiety of 1-⁶Li in the respective complexes, and thus for the ion pair character as a function of the polyether complexation of lithium.     

Synthesis,properties and structural characterization of 4-(2-ammonioethyl)piperazin-1-ium tetrasulfidotungstate hemihydrate and 1-ethylpiperazinediium tetrasulfidotungstate

The reaction of ammonium tetrasulfidotungstate with 2-piperazin-1-ylethanamine or 1-ethylpiperazine results in the formation of 4-(2-ammonioethyl)piperazin-1-ium tetrasulfidotungstate hemihydrate (C₆H₁₇N₃)[WS₄]·½H₂O 1 or 1-ethylpiperazinediium tetrasulfidotungstate (C₆H₁₆N₂)[WS₄] 2. The hemihydrate 1 can be dehydrated to the anhydrous compound (C₆H₁₇N₃)[WS₄] 1a, which can be rehydrated to 1. Both 1 and 2 decompose to amorphous carbon containing tungsten disulphide. Compound 1 crystallizes in the centrosymmetric monoclinic space group C2/c, while compound 2 crystallizes in the centrosymmetric orthorhombic space group Pbca. The structures of 1 and 2 consist of a slightly distorted tetrahedral [WS₄]^2? anion and 4-(2-ammonioethyl)piperazin-1-ium (1) or 1-ethylpiperazinediium dication (2) and additionally a lattice water in 1. In the crystal structure of 1 and 2 the organic cation and the [WS₄]^2? anion are linked to each other via several weak N–H?S and C–H?S bonding interactions. The lattice water serves as a link between pairs of cations and pairs of anions with the aid of O–H?S and N–H?O interactions in compound 1.     

Structure of lilidine

The new alkaloid lilidine, isolated for the first time from the epigeal part ofLilium martagon has been studied by special methods. It has the composition B₅H₆NO₂, mp 118–110°C, [α]_D-26.3°. The¹H and¹³C NMR spectra were studied in detail. The values of the direct and long-range spin-spin coupling constants between the¹³C carbon nuclei and the¹H nuclei of the alkaloid molecule were measured with the aid of¹³C-[{su1}H] selective heteronuclear double resonance. The structure of 5-hydroxy-3-methyl-3-pyrrolin-2-one is suggested for lilidine.     

Chelating properties of permethylated 6A,6D-dideoxy-6A,6D-bis(1-imidazolyl)cyclodextrins towards Pt(II) and Ru(III)

Two imidazole-coordinating groups have been successfully grafted onto the C-6^A and C-6^D positions of permethylated α- and β-cyclodextrin scaffolds. Both water-soluble ligands L1 and L2 turned out to behave as good chelators when reacted with K₂PtCl₄. In the resulting diamagnetic cis-chelate complexes, the metal cation is pending above the cavity entrance. Paramagnetic ruthenium(III) chelate complexes have also been successfully synthesised from L1 and L2. In these more sterically demanding octahedral complexes, the imidazole groups coordinate the metal centre in a trans-fashion.