6,7,8,9-Tetrahydro-5H-pyrido[2,3-b]azepine-5,8-dione: a hydrogen-bonded dimer structure

In the title compound, C9H8N2O2, two crystallographically independent molecules form a dimer structure, in which two N-H center dot center dot center dot N hydrogen bonds generate an intermolecular R-2(2)( 8) ring.

New reductive addition of hard nucleophiles to 6,7-bis(methylsulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione

A new reaction mode of 6,7-bis(methylsulfanyl)-1,4-dihydro-1,4-methanonaphthalene-5,8-dione 1 with the hard nucleophiles sodium benzene- or methane-sulfinate and cyanide, in DMSO, at room temperature, leads to the unexpected hydroquinonoid products 3a-c. All the data are in agreement with a mechanistic pathway involving the initial attack of the hard nucleophile onto the hard carbonyl group, followed by a symbiotic re-attack of the oxygen on the incoming group. In the case of soft nucleophiles, reaction on the olefinic carbon of the enedione system is preferential.

Charge transfer complexes of crown ethers with neutral organic gyama-acceptor, 2-dicyanoethylene 1,3-indane dione

The interaction of benzo-15-crown-5, dibenzo-18-crown-6 and dibenzo-24-crown-8 with 2-dicyanoethylene 1,3-indane dione in CH2Cl2 has been described in terms of the formation of 1 : 1 molecular complexes. The magnitude of association constants and thermodynamic parameters indicate cooperative interactions of oxygens with the acceptors. The 1H and 13C NMR spectra of the complexes show that gyama-gyama interactions are a major source of ground state stabilization in these complexes.

Knoevenagel condensation of 2-carbethoxycyclohexanone and malononitrile: Synthesis of 4-cyano-3-ethoxy-1-hydroxy-5,6,7,8-tetrahydroisoquinoline, an isomer of the abnormal product

The structure of the abnormal product 1a formed in the Knoevenagel condensation of 2-carbethoxycyclohexanone and malononitrile has been further confirmed. Oxidation of the tetrahydroisoquinoline 3b using Na2Cr2O-AcOH-H2SO4 gave the keto isoquinoline 3d and the isoquinoline-1-carboxylic acid 5a. The acid chloride of 5a was condensed with diethyl ethoxymagnesiomalonate to afford after decarbethoxylation the methyl ketone 5d which on Baeyer-Villiger oxidation gave a mixture of the acetate 1g and the title compound 1b. The unambiguous synthesis of 1b confirms the structure assigned earlier to the title compound also formed during the partial hydrolysis of the diethoxy compound 1c. Condensation of 2-acetylcyclohexane-1,3-dione with malononitrile gave the quinoline derivative 4c which on ethylation yielded the ketoquinoline 4d. The present studies have confirmed that the quinoline compound 4a is also formed in the condensation of 2-acetylcyclohexanone and cyanoacetamide.

On the conformation of cyclohexane-1,4-dione and its derivatives—I : Infrared and raman spectra of cyclohexane 1,4-dione and infrared spectrum of its octadeutero analogue

Raman spectra of cyclohexane 1,4-dione (I), in chloroform, benzene and water solutions have been recorded. Temperature effect on the spectrum has been studied. The IR spectra of I and its octadeutero analogue in the solid state have also been studied. The spectra have been found on the basis of selection rules applicable for Raman and IR spectra, to be consistent with a single conformer of C2 symmetry. Plausible causes of conformational preference have been discussed.

Synthesis Of (+/-)-2-Isopropyl-5,6-Dimethylbicyclo[3.2.1]Oct-6-En-8-One

Methanolic hydrogen chloride cyclization of the triketone 8, prepared from the Mannich base 7 and 2-methylcyclopentane-1,3-dione, gives ketones 9 and 10. NaBH4 reduction of 9 followed by Grignard reaction with CH3MgI affords the diol 12. Catalytic hydrogenation of 12 followed by PCC oxidation yields the ketoalcohol 13. Dehydration of 13 with SOCl2/pyridine results in a 1:1 mixture of the endo-14 and exo-15 olefins, separated by chromatography.

Structure of pregna-4,16-diene-7[alpha],14[alpha]-diol-3,20-dione

7a,14a-Dihydroxypregna-4,16-diene-3,20- dione, C21H2804, M r = 344.45, orthorhombic, P212121, a = 7.136 (1), b = 12.342 (1), c = 20.049 (3)/k, V= 1765.7 (3)/k 3, Z = 4, Dx = 1.295 g cm -3, A(Cu Kte) = 1.5418/k, /z = 6.7 cm- a, F(000) = 744, T = 293 K, R = 0.048 for 1345 observations. The A ring may be described as in a l a,2flhalf- chair conformation or a l a-sofa conformation. The B and C rings adopt normal chair conformations and the D ring has a 14a-envelope conforma tion. The molecules are held together by a hydrogen bond [0(3)...0(7)= 2.767 A].

Structural and mechanistic study of monoalkyl diazenes. Synthesis, characterization, and reactivity of 1,6-didehydro[10]annulene

Methodology for the preparation of allenes from propargylic hydrazine precursors under mild conditions is described. Oxidation of the propargylic hydrazines, which can be readily prepared from propargylic alcohols, with either of two azo oxidants, diethyl azodicarboxylate (DEAD) or 4-methyl 1,2-triazoline-3,5-dione (MTAD), effects conversion to the allenes, presumably via sigmatropic rearrangement of a monoalkyl diazene intermediate. This rearrangement is demonstrated to proceed with essentially complete stereospecificity. The application of this methodology to the preparation of other allenes, including two that are notable for their reactivity and thermal instability, is also described.

The structural and mechanistic study of a monoalkyl diazene intermediate in the oxidative transformation of propargylic hydrazines to allenes is described. The use of long-range heteronuclear NMR coupling constants for assigning monoalkyl diazene stereochemistry (E vs Z) is also discussed. Evidence is presented that all known monoalkyl diazenes are the E isomers, and the erroneous assignment of stereochemistry in the previous report of the preparation of (Z)-phenyldiazene is discussed.

The synthesis, characterization, and reactivity of 1,6-didehydro[10]annulene are described. This molecule has been recognized as an interesting synthetic target for over 40 years and represents the intersection of two sets of extensively studied molecules: nonbenzenoid aromatic compounds and molecules containing sterically compressed π-systems.The formation of 1,5-dehydronaphthalene from 1 ,6-didehydro[10]annulene is believed to be the prototype for cycloaromatizations that produce 1,4-dehydroaromatic species with the radical centers disposed anti about the newly formed single bond. The aromaticity of this annulene and the facility of its cycloaromatization are also analyzed.

Syntheses, structures and near-IR luminescent studies on ternary lanthanide (Er-III, Ho-III, Yb-III, Nd-III) complexes containing 4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dionate

The ligand Hhfth [4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dione], which contains a heptafluoropropyl group, has been used to synthesize several new ternary lanthanide complexes (Ln = Er, Ho, Yb, Nd) in which the synergistic ligand is 1,10-phenanthroline (phen) or 2,2'-bipyridine (bipy). The two series of complexes are [Ln(hfth)(3)phen] [abbreviated as (Ln)1, where Ln = Er, Ho, Yb] and [Ln(hfth)(3)bipy] [abbreviated as (Ln)2, where Ln = Er, Ho, Yb, Nd]. Members of the two series have been structurally characterized. The growth morphology, diffuse reflectance (DR) spectra, thermogravimetric analyses, and photophysical studies of these complexes are described in detail. After ligand-mediated excitation of the complexes, they all show the characteristic near-infrared (NIR) luminescence of the corresponding Ln(3+) ions (Ln = Er, Ho, Yb, Nd). This is attributed to efficient energy transfer from the ligands to the central Ln(3+) ions, i.e. an antenna effect. The heptafluorinated substituent in the main hfth sensitizer serves to reduce the degree of vibrational quenching. With these NIR-luminescent lanthanide complexes, the luminescent spectral region from 1300 to 1600 nm, which is of particular interest for telecommunication applications, can be covered completely.

Achiral, selective CCK2 receptor antagonists based on a 1,3,5-benzotriazepine-2,4-dione template

Novel, achiral 1H-1,3,5-benzotriazepine-2,4(3H,5H)-diones have been prepared and structurally characterized. These compounds are potent CCK2 receptor antagonists that display a high degree of selectivity over CCK1 receptors.

Vibrational properties, crystal X-ray diffraction structure and quantum chemical calculations on a divalent sulfur substituted phthalimide: 1H-Isoindole-1,3(2H)-dione, 2-[(methoxycarbonyl)thio]

Structural and conformational properties of 1H-Isoindole-1,3(2H)-dione, 2-[(methoxycarbonyl)thio] (S-phthalimido O-methyl thiocarbonate) are analyzed using a combined approach including X-ray diffraction, vibrational spectra and theoretical calculation methods. The vibrational properties have been studied by infrared and Raman spectroscopies along with quantum chemical calculations (B3LYP and B3PW91 functional in connection with the 6-311++G** and aug-cc-pVDZ basis sets). The crystal structure was determined by X-ray diffraction methods. The substance crystallizes in the monoclinic P2(1)/c space group with a = 6.795(1), b = 5.109(1), c = 30.011(3) angstrom, beta = 90.310(3)degrees and Z = 4 molecules per unit cell. The conformation adopted by the N-S-C=O group is syn (C=O double bond in synperiplanar orientation with respect to the N-S single bond). The experimental molecular structure is well reproduced by the MP2/aug-cc-pVDZ method. (C) 2010 Elsevier B.V. All rights reserved.

Implicações ecológicas das plantas hospedeiras e da agregação larval sobre Dione juno juno (Cramer, 1779) (Lepidoptera : Nymphalidae)

As larvas de Dione juno juno (Cramer, 1779) (Lepidoptera: Nymphalidae) alimentam-se de plantas da família Passifloraceae e apresentam hábito gregário, características que interferem na sua performance. O significado ecológico deste hábito parece centrar-se na defesa contra predação, na termorregulação e na facilitação alimentar. Neste trabalho, dez espécies de passifloráceas ocorrentes no Rio Grande do Sul foram avaliadas em relação à preferência alimentar e performance larval de D. juno juno: Passifora alata Dryander, 1781; P. amethystina Mikan, 1820; P. caerulea Linnaeus, 1753; P. capsularis Linnaeus, 1753; P. edulis Sims, 1818; P. elegans Masters, 1872; P. misera Humbold, Bonpland et Kunth, 1817; P. suberosa Linnaeus, 1753; P. tenuifila Killip, 1927 e P. warmingii Masters, 1872. O efeito da densidade larval na performance foi também testado em P. edulis: grupos de uma, duas, quatro, oito, dezesseis, trinta e duas, e sessenta e quatro larvas. A preferência alimentar das larvas foi avaliada com base em testes utilizando-se discos foliares, com e sem chance de escolha. O efeito da densidade larval na performance foi testado em P. edulis: grupos de uma, duas, quatro, oito, dezesseis, trinta e duas e sessenta e quatro larvas Avaliou-se o efeito da agregação larval na termorregulação e/ou na termoconformação, e na facilitação alimentar. Em laboratório (fotofase de 14 horas, 75 + 5% UR), estimou-se suas exigências térmicas e, em campo, investigou-se a variação sazonal e o grau de desfolha das plantas. O efeito da agregação larval na termorregulação e na termoconformação foi avaliado criando-se larvas em P. edulis. Foram testadas três densidades: grupos de uma, cinco e dez larvas, que foram mantidas em quatro temperaturas (15, 20, 25 e 30ºC) em câmaras climatizadas. A temperatura do corpo das larvas agregadas e isoladas foi medida com um termômetro digital em duas situações: expostas ao sol e mantidas na sombra, em diferentes temperaturas do ambiente. O papel da agregação larval na facilitação alimentar foi investigado com ênfase na caracterização e análise de suas mandíbulas, sua forma de alimentação, bem como seu efeito na taxa de consumo. Comparou-se a área foliar de P. edulis consumida per capita entre os grupos de uma, três, cinco, sete, nove, dez e onze larvas. Investigou-se o desgaste das mandíbulas, bem como o tipo de dano causado às folhas Comparou-se, também, o número de larvas que se alimentaram em grupos de uma, cinco e dez larvas. Em campo, foram realizados levantamentos quinzenais, anotando-se o número de imaturos e o grau de desfolha da planta hospedeira, durante trinta meses. Em relação às plantas hospedeiras, concluiu-se que nem sempre a que lhe confere melhor performance é a escolhida pelas larvas. Ocorreu grande mortalidade no primeiro ínstar em todas as plantas testadas. A sobrevivência aumentou consideravelmente, a partir de oito larvas por grupo. As larvas deste inseto têm capacidade de efetuar tanto termorregulação quanto termoconformação. Não foi observado desgaste das mandíbulas, ao longo da ontogênese. Observou-se um maior número de larvas em atividade de alimentação e um maior consumo per capita quando criadas em grupo. Os resultados demonstraram que o forrageio em grupos acentua a eficiência alimentar das larvas. A viabilidade dos ovos e a sobrevivência larva-pupa foram maiores a 20 e 25ºC. O período de incubação e o tempo de desenvolvimento larval e pupal decresceram com o aumento de temperatura, quando as larvas foram criadas em grupos de dez. As temperaturas bases estimadas foram de 5,3ºC para a fase ovo, 8,4 ºC para larva e 9ºC para a pupa. As constantes térmicas foram de 126,6 graus dias para a fase ovo, 312,5 graus dias para larva e 141 graus dias para pupa. D. juno juno esteve presente em baixos níveis populacionais em quase todos os meses do ano com picos em novembro/dezembro de 2001/2 e janeiro de 2003. O índice de desfolha foi baixo em todas as ocasiões, exceto nos meses de maior densidade larval.

Dynamics of Enceladus and Dione inside the 2:1 mean-motion resonance under tidal dissipation

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)