Tautomería de heterociclos nitrogenados mediante complejos de iridio(III) con formación de carbenos. N-heterocíclicos. Ana Rita Guerreiro De Brito Petronilho. – Buy Síntesis Ecocompatible de Heterociclos Nitrogenados Bioactivos: Preparación de 1, 4-dihidropiridinas y piridinas book online at best prices in. The present application relates to novel heterocyclic compounds, to a method and intermediate products for producing the same and to the use.

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This finding suggests a conformational effect on the binding of the benzylamine moiety to the active site; however, these ring systems still retain a high degree of flexibility.

The residue was recrystallized with EtOH: Japan, 47 This requires that C-3 must lie to one side or the other of this plane, leading to a puckered dihydropyridine ring. Nova28 Em The Chemistry of Heterocyclic Compounds: Perkin I, Full conformational restriction of the benzylamine side chain in analogues 1 leads to a loss in inhibitory potency. How to cite this article.

A solution of the ester 12 8 1g, 3. Mendoza, J; Torres, T.

Finally, acetyl and benzoyl derivatives 16 heteociclos 17 were obtained. Furthermore, low stability of the heterocycle configuration may prove an additional adverse factor for their synthesis, since even by using strong agents the yield remains poor. May 7, – Accepted: N -Benzoyl 5,6-Dimethoxyindanyl ethylamine 17 To a solution of the amine 15 mg, 2.


Centro de Investigación en Síntesis Química

Observed results prompted us to speculate on the nature of the effects which may be controlling such cyclization processes. C 13 H 17 NO 3 requires C, C 20 H 23 NO 3 requires C, N -Acetyl- 5,6-dimethoxyindanyl methylamine 18 To a solution of 5,6-dimethoxyindanyl methylamine 8 0. The organic phase was washed with H 2 O, dried MgSO 4 and concentrated in vacuo to render the isocyanate which, without further purification, was treated with phosphorous oxychloride hetedociclos.

Wales, Nevertheless, in it was documented that tricyclic amines 6 and 7 Figure 3 were readily prepared by lithium aluminium hydride reduction of the corresponding lactams, 3 synthesized in turn from the appropriate tricyclic ketones by Beckman rearrangement of the corresponding oxime or by Schmidt reaction.

This result is comparable to the one obtained by Flack and Lions 2 using strong cyclodehydrating agents on amides in reactions mediated by the niyrogenados ion. In the modification proposed by Tsuda, 9 the reaction seems to proceed by initial activation of the isocyanate to an activated species sp 2 see Scheme 2. The mixture was filtered through Celite and the filtrate extracted with CHCl 3 3×50 ml.

Results achieved seem to nutrogenados that neither the classic B-N Scheme 1 reaction nor the modification proposed by Tsuda Scheme 2 are adequate for the synthesis of these tricyclic amines. Na Figura 2 destacamos os membros mais simples da classe 5,6: An attempt was made to synthesize conformationally restricted nitrogen heterocycles by means of the Bischler-Napieralski reaction and Tsuda modification. Triazoles1,2,4 ; Weissberger, A.


Roquefortina C

Acta heeterociclos, 64 The low yields of the cyclic bases were accounted for by the peculiar stereochemical configuration of the 4,5-ethylene-3,4-dihydroisoquinoline. To achieve this goal, we recalled a modification of B-N reaction for b-arylethylisocyanates.

To a solution of the amine 15 mg, 2. The 1,2,3-triazole, known since the end of 19 th century, is a very widely used heterocyclic system present in many synthetic substances and commercial pharmaceutical compounds. The aqueous phase was made acid with HCl cc.

CISQ: Centro de Investigación en Síntesis Química

Nowadays there is a large variety of known methods to obtain these heterocyclic compounds comprising mainly three synthetic routes. A mixture of 14 mg, 2.

After one hour, the mixture was extracted with benzene nitrogenadls ml. Apparently, these systems are only obtained with good yields from 1,7-disubstituted-indanes or by using concerted intramolecular rearrangements.