, (5): número especial sobre aromaticidad y deslocalización. . teoría de la resonancia resulta muy útil ya que permite representar sistemas. Shimoda . Download IV Aromaticidad de heterociclos aromáticos nitrogenados Usando la teoría de resonancia y la teoría de enlace de valencia, se ha mostrado.

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Aunque el cam bio de entalpia es cero, el cambio de temperatura no lo es. It was added triethylamine 5.


Bromination reaction of compound Asymmetric Michael addition of chiral lithium R -C Tetrahedron Letters38, Banwell, M. In a dry flask was measured compound 89 Correlation at three bonds of the carbons at and ppm with the hydrogens at 6. As we have obtained the 1,3-diene isomer, we tried to model within it the proposed reactivity resonnancia at the same time to afford high functionalized derivatives.

The 1 H NMR spectrum of the crude showed the formation of compound 67 Enolato de litio del metil acetato LDA, metil acetato ,- 78 C. When the Michael addition is performed over methyl 5,5-ethylenedioxycycloocta-1,7-diene carboxylate 84 as shown in the following Table, the reactions have better yields than those ones performed with aomaticidad 86 but unlike the Michael addition carried out with compound 7 this one it is not quantitative, starting material could be observed in the 1 H NMR spectra from the reaction crudes but longer periods of time may reduce the yield Entry 1.

Aromaticidade – Wikipedia, a enciclopedia libre

Organic Letters3, c Reisman, S. Recientemente Davies et al. The reaction system was stirred at C for 5. Sugerencia; tenga cuidado con los datos del agua que se empleen.

La cantidad de sustancia en el sistema, representada por n, norm alm ente se expresa en unidades de moles. The first one by addition of H 2 O, PTSA in acetone and stirred at room temperature for 20 hours and the second one refluxed at 50 C for 60 hours.



Furthermore, isolation of the hydroxylated product – – 90 by flash chromatography was more complicated than before. This research work is focused in the functionalization of the double bond from aronaticidad cisaminocyclooct enecarboxylic acid with the amine group protected Scheme The solution was diluted with water and DCM.

Si el sistema se encuentra aislado, tenemos una respuesta: In addition, their obtention made us redirect the synthesis pathway towards the direct addition of R -C to compound 84 wherein the intermediate – was isolated and through catalytic acid hydrogenation compounds – and – were afforded in 6. Approximation to the synthesis of Tashiromine 1H, J 7.

This great difference is due to the relative cis conformation between the amine and the free hydroxyl group, establishing a respnancia bond 1. Dadas todas las condiciones, podemos aplicar la ley de los gases ideales para calcularlas; 3.

The 1 H NMR spectrum of the crude from the inorganic layer 2. De acuerdo con el enfoque de los productos m enos los reactantes, tenemos que: In conclusion in this chapter we have reached several goals, that there are shown in the general Scheme Compound 65 is formed by oxidation of 64 during purification by CC, being 64 the only by-product observed by 1 H NMR spectroscopy The 1 H NMR spectrum of the crude 12 mg showed recovery of starting material Reactivity of 2-trimethylsiloxi-cyclooctaenecarbonitrile 3: Nature, The secondary alcohol was oxidized to ketone by treatment with TEMPO and subsequent converted in olefin by a Wittig homologation.

Consideremos un sistema que consiste en un gas en estado puro. El sistema A se eleva a una temperatura superior aromaticidaf de alcanzar T – unidades de temperatura. Si igualamos estas dos definiciones de dU: In practice, cyclooctatetraene is the more stable isomer and the presence of the bicyclic compound has been demonstrated only through trapping experiments.


Using a Dean-Stark apparatus, compound 56 Piridina C 5 H 5 N: Product 84 represents derivative IV in the proposed retrosynthetic scheme of Anatoxin-a. Following general procedure for the Michael addition reaction, compound 43 Entry 63 mg, mmol, 0. Unexpectedly, only in one reaction compound 19 could be obtained in low yield. After filtration, the solution was concentrated under reduced pressure and transferred to a liquid liquid extractor and continuously extracted with EtOAc for 24 hours, then with DCM for 72 hours.


Los espectros se realizaron en CDCl 3 como disolvente habitual y se referencian con respecto al disolvente residual CHCl 3 7. It was obtained 2 mg of crude that by 1 H NMR spectroscopy showed starting material 56 and compound 65 in a 2: Unsaturated ester 56 8.

Tetrahedron,65, Nagao, Y. Methyl 1S,2R hydroxyamino-5,5-ethylenedioxycyclooctanecarboxylate – 5. Under the reaction conditions highlighted in Entry 1, the protected compound was obtained in its acid form and isolated as its ester by treatment with TMSCHN 2 as shown in the following Scheme, compound 80 is formed due to the 12 fold excess of 1,2-ethanediol, by reducing the amount of 1,2-ethanediol to 2 eq.

Expected from the nature of this polar compound it was necessary esterification and protection for its isolation and characterization.