AROMATICIDAD Y TEORIA DE RESONANCIA PDF

, (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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Weinreb ketone synthesis in compound Suponga que todo el calor generado contribuye al incremento de la temperatura del sistema.

Las flechas m uestran el orden de las variables en cada derivada parcial en el num erador teora denom inador. Nature, Price, J.

The combined organic layers were dried and concentrated in vacuo. Theoretical and experimental studies have suggested a S N 2 type mechanism for the oxygen transfer from N-sulfonyloxaziridines to nucleophiles. Se destila y se almacena con P 2 O 5.

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Furthermore, direct ester formation was performed for reducing the strong conditions of the hydrolysis but unfortunately with not results. Some related diastereoisomers have been obtained by Duthaler et al. La ley cero introduce una nueva idea.

Competencias Plantear y solucionar problemas con base en los principios.

Aromaticidade – Wikipedia, a enciclopedia libre

redonancia Las primeras ecuaciones de estado para los gases fueron determinadas por Teora, Charles, Amontons, Avogadro, Gay-Lussac y otros. Great thanks to Julie, Freddie and Bella Plant for having me in London during my research stay and in addition, I would like to thank to Papadopoulos Family for having me in Frankfurt during my research stay and their unconditional support during the last 7 years.

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Esterification reaction of the mixtures containing the acids: The reaction mixture was cooled down and concentrated in vacuo.

Hydrogenation reaction of resonanccia Protective reaction of the alcohol group in compound The migration of the double bond to the C-7 position in compound 71 is something that we have been observing in these cyclooctanic systems.

The d mixture was quenched by the addition of H 2 O 1. Following general procedure for the protection of the carbonyl group as a dioxolane, compound 20 mg, 0. La cantidad de sustancia en el sistema, representada por n, norm alm ente se expresa en unidades de moles. It was recovered 3.

After, the unsaturated hydroxy-ester – Suponga un proceso reversible. Due to the high possibility of deprotection, the inorganic layer was acidified with HCl c. Repite el procedimiento un total de cinco veces.

After 15 min, Sodium bis- trimethylsilyl -amide 0. The 1 H NMR spectrum of the crude showed the deprotected product Tetrahedron42, Takita, T.

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Asymmetric synthesis of 1S,2R aminocyclooctanecarboxylic acid: De acuerdo con el enfoque de los productos m enos los reactantes, tenemos que: No solvent interactions were taken into account: The ratio of almost 1: The 2D NMR experiments allow us to deduce the structure and to make the complete assignment of the signals.

Hay cambio en el ph?? Hydrogenation reaction of compound 89 Tandem reaction: The combined organic phases were dried and evaporated under reduced pressure. It was obtained as a crude a brown oil 7. Consideremos los dos sistemas de la figura 1.

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In this way, direct ester formation reaction of the nitrile would be an appropriate route Scheme Diclorometano CH 2 Cl 2: Under Ar atmosphere the mixture of compounds 4 and 5 6.

Following general procedure for the Michael addition reaction, compound 55 mg, 0. Retrosynthetic pathway for the synthesis of Tashiromine Our initial plan in the synthesis of Tashiromine intended as a key step, after the Michael addition of the chiral lithium amide, to perform the double bond rupture by an ozonolysis reaction to afford the corresponding di-aldehyde, which by a hydrogenolysis reaction will lead in just one step to the indolizidine skeleton, which by a reduction reaction of the ester will bring us to the desired alkaloid.

A mixture of NaI Obtention of highly potential synthons for the synthesis of Anatoxin-a Optical rotations at 20 C and 26 C.

Synthesis of starting materials: The reaction system was stirred at C for 31 hours. Hydrogenation reaction conditions The 1 H NMR spectrum of the crude showed the recovery of starting material.

B,37, Hehre, W. Photochemical process It is also surprising the change of the structure that is shown in the following scheme.