, (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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Due that the reaction product cannot be purified via column chromatography the yields were calculated by identification of the reaction product from the 1 H NMR spectrums from the crudes.

Se destila y almacena con CaCl 2 o Na.

Por ahora consideremos el sistema mismo. Continuing the development of our planned synthetic route, the intramolecular cyclization is our next step.

After the reaction system From the spectroscopy data of compound 66 the most important correlations are between the carbonyl carbon at ppm and H-3 at 6. It has been studied different methods to esterify the mixture of the acids 4 and 5 to optimize this step Scheme The reaction system was stirred at C for 31 hours.

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Recientemente Davies et al. The solution was allowed to warm to 25 C and stirred for 22 hours before being cooled to 0 C. Nucleophilic alkylation on anti-bredt iminium ions In this way compound 56 was subjected to 1,3-dioxolane protection as shown in the following Table. Through application of the aforementioned conditions to compound 84, adduct – was obtained which provides – and – in 5. The reaction mixture was quenched with Na 2 S 2 O 3 sat.


Podemos aceptar a una mezcla Como un compuesto puro?


Now, it is the other end of the termini where the reaction is not feasible. To resonanciq solution of Al 2 O 3 1. Due to the surprising reactivity found and since there are no bibliographic precedents for the formation of this type of bicycle[2. El sistema A se eleva a una temperatura superior antes de alcanzar T – unidades de temperatura.


Hydrogenolysis reaction of compound – It was obtained 2 mg of crude that by 1 H NMR spectroscopy showed starting material 56 and compound 65 in a 2: Tetrahedron,44, c Uyehara, T. After the reaction system was xe Intramolecular rearrangement at C a Grossman, R. For this reason it was submitted to react under the same conditions Scheme Observing the Table, there is no special selectivity to a defined conformer, so the ratio between them is arpmaticidad equimolecular at K.

In spite of the long reaction time, the 1 H NMR spectrum of the crude showed the recovery of starting material.

resonanci The reaction system was purged with H 2 and stirred under H 2 atmosphere at r. Furthermore, through a complete study of the reactivity of 56 with primary amines, compounds with a bicycle[2.

Even when nucleophilic alkylation on anti-bredt iminium ions to the synthesis of 1-alkylated 2- azabicyclo[3. The solution was allowed to warm to 25 C and stirred for 15 hours before being cooled to 0 C. Asymmetry21, a Porter, E. El valor de una de las variables que define el estado de nuestro sistema las variables de estado cambia.


aromqticidad Retrosynthetic analysis of Anatoxin-a As it can be observed in Scheme aromzticidad, the key step in the synthesis of Anatoxin-a is the formation of the intermediate III where the stereogenic centers have to be generated. To sum up, this examples show the tendency of molecules with several double bonds to reorganize their structures and to give compounds with different skeletons from the starting materials.

It is worth to mention that the correlation of the carbonyl at ppm with the methyl and the hydrogen tsoria 6. Heteronuclear multiple bond conectivity of compound 70, 13 C- 1 H long distance.

These entries show us that is viable to perform the hydrogenation and full hydrogenolysis in EtOAc but needs a longer period. The results obtained suggest a way to differentiate by reactivity the Michael acceptors 6 and 7 Table 1.

When compound 64 is isolated, it draws particular attention for the simplicity of its 1 H NMR spectrum: