A new and efficient procedure for the synthesis of hexahydropyrimidine-fused 1,4-naphthoquinones

Título:

A new and efficient procedure for the synthesis of hexahydropyrimidine-fused 1,4-naphthoquinones

Autor:

Vinícius Rangel Campos

Ano:

2015

DOI:

10.3762/bjoc.11.137

Revista:

Beilstein Journal of Organic Chemistry

ISSN:

18605397

Home:

[http://www.beilstein-journals.org/bjoc/single/articleFullText.htm?publicId=1860-5397-11-137][doi:10.3762/bjoc.11.137]

Idioma:

Inglês

Buscar essa publicação no Google Acadêmico

Publicações com a mesma autoria

Synthesis of a new class of naphthoquinone glycoconjugates and evaluation of their potential as antitumoral agents

Synthesis and in vitro and in silico studies of 1H- and 2H-1,2,3-triazoles as antichagasic agents

Insight into and Computational Studies of the Selective Synthesis of 6 H -Dibenzo[ b , h ]xanthenes

Synthesis and Biological Evaluation of Benzo[f]indole-4,9-diones N-Linked to Carbohydrate Chains as New Type of Antitumor Agents

( )-3-(2,5-Difluorophenyl)-1-phenylprop-2-en-1-one

Selective AMPK activator leads to unfolded protein response downregulation and induces breast cancer cell death and autophagy

Synthesis, biological, and theoretical evaluations of new 1,2,3-triazoles against the hemolytic profile of the Lachesis muta snake venom

Synthesis and antimicrobial evaluation of promising 7-arylamino-5,8-dioxo-5,8-dihydroisoquinoline-4-carboxylates and their halogenated amino compounds for treating Gram-negative bacterial infections

Efficient access to β - vinylporphyrin derivatives via palladium cross coupling of β-bromoporphyrins with N -tosylhydrazones