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1.
J Org Chem ; 82(4): 1961-1968, 2017 02 17.
Artigo em Inglês | MEDLINE | ID: mdl-28177250

RESUMO

A concise route for the synthesis of indenoisoquinoline derivatives from 2-iodobenzamide and 1,3-indanedione derivatives in the presence of copper(II) chloride and cesium carbonate in acetonitrile solvent is reported. A wide variety of 2-iodobenzamide derivatives and indandiones could be used to synthesize indenoisoquinoline derivatives and other fused indenoisoquinoline in moderate to good yields. This methodology was adapted for the one-step synthesis of a series of clinically active topoisomerase I inhibitors such as NSC 314622, LMP-400, LMP-776.


Assuntos
Cobre/química , Indenos/síntese química , Isoquinolinas/síntese química , Catálise , Cristalografia por Raios X , Indenos/química , Isoquinolinas/química , Modelos Moleculares , Estrutura Molecular
2.
Molecules ; 20(6): 10910-27, 2015 Jun 12.
Artigo em Inglês | MEDLINE | ID: mdl-26076111

RESUMO

An efficient and straight forward procedure for the syntheses of bicyclic isoxazole/isoxazoline derivatives from the corresponding dimethyl-2-(2-nitro-1-aryl/alkyl)-2-(prop-2-yn-1yl)malonates or dimethyl 2-allyl-2-(2-nitro-1-aryl/alkyl ethyl)malonate is described. High yields and simple operations are important features of this methodology.


Assuntos
Reação de Cicloadição , Isoxazóis/síntese química , Óxido Nítrico/química
3.
Chem Commun (Camb) ; 53(10): 1676-1679, 2017 Feb 04.
Artigo em Inglês | MEDLINE | ID: mdl-28101546

RESUMO

A metal-free protocol for accessing both α and δ-carboline derivatives, starting from a common indolylchalcone oxime ester precursor is reported. The reaction involves mild conditions and uses a regiodivergent approach. DDQ is used as a switching agent in selectively generating α and δ-carboline derivatives in good to moderate yields.

4.
Chem Commun (Camb) ; 52(50): 7870-3, 2016 Jun 14.
Artigo em Inglês | MEDLINE | ID: mdl-27250103

RESUMO

The dual character of benzoquinone is exploited for the synthesis of benzo[a]carbazole derivatives starting from 3-ethylindole derivatives. A diene is generated in situ from the 3-ethylindole derivative with the help of benzoquinone, where it acts as an oxidizing agent. Later it serves as a dienophile and participates in a Diels-Alder reaction with the diene to afford benzo[a]carbazole derivatives.

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