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Angelo C. Pinto

Researcher at Federal University of Rio de Janeiro

Publications -  307
Citations -  7329

Angelo C. Pinto is an academic researcher from Federal University of Rio de Janeiro. The author has contributed to research in topics: Isatin & Diterpene. The author has an hindex of 39, co-authored 307 publications receiving 6744 citations. Previous affiliations of Angelo C. Pinto include Oswaldo Cruz Foundation & University of Graz.

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Cromatografia de Troca-Iônica Aplicada ao Isolamento da Fração Ácida do Óleo de Copaíba (Copaifera multijuga) e da Sacaca (Croton cajucara)

TL;DR: Anionic macroporous resin in non-aqueous medium was used with success in this article for separation of the acid fraction of Copaifera multijuga (Copaiba oil), rich in labdanic diterpenes and for the methanolic extract of Croton cajucara (acetyl aleuritoric acid).
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Rapid cleavage of phosphate triesters by the oxime 2‐(hydroxyimino)‐N‐phenyl‐acetamide

TL;DR: In this article, the dephosphorylation reactions of the organophosphates diethyl 2,4-dinitrophenyl phosphate (DEDNPP) and dimethyl 4-nitrophenymethyl phosphate (methyl paraoxon) by oxime 2-(hydroxyimino)-N-phenyl-acetamide (Ox 1) were reported.
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Two monoisoprenylated flavonoids from Vellozia graminifolia

TL;DR: In this article, a mixture of two monoisoprenylated flavonols velloquercetin 3,3,4,4′-dimethyl ether (Vellozia graminifolia) was isolated and characterized from the hexane whole plant extract.
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Minor cleisthantane and tetranorfriedolabdane from Vellozia flavicans

TL;DR: In this paper, six diterpenes with the cleistanthane skeleton have been identified from Vellozia flavicans, three of which are reported as natural products.
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An investigation of a palladium catalysed biaryl synthesis of pyrrolophenanthridine derivatives. Extension of the Heck reaction

TL;DR: In this paper, N-Benzylisatin derivatives have been found to readily undergo cyclisation via hydrogen halide elimination in a biaryl synthesis reaction when using palladium catalysts, in the absence of phosphine ligands, to yield oxopyrrolo[3,2,1-de]phenanthridine derivatives.