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Arci Dirceu Wastowski

Researcher at Universidade Federal de Santa Maria

Publications -  56
Citations -  547

Arci Dirceu Wastowski is an academic researcher from Universidade Federal de Santa Maria. The author has contributed to research in topics: Aryl & Alkyl. The author has an hindex of 14, co-authored 54 publications receiving 499 citations.

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Haloacetylated enol ethers: 12 [18]. Regiospecific synthesis and structural determination of stable 5-hydroxy-1H-pyrazolines

TL;DR: In this article, a series of twelve 3-aryl[alkyl]-5-hydroxy-5-trichloromethyl-4, 5-dihydro-1H-pyrazole-1-carboxyamides and analogous 1-thiocarboxy-amides is reported.
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Haloacetylated enol ethers 10. Condensation of β-alkoxyvinyl trifluoromethyl ketones with thiosemicarbazide. Synthesis of new trifluoromethyl 4,5-dihydro-1H-1-pyrazolethiocarboxyamides

TL;DR: In this paper, the synthesis of 3-aryl[alkyl]-5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H-1-pyrazolethiocarboxyamides (2a−g) from the direct cyclocondensation reaction of b-alkoxyvinyl trifluorsyl ketones with thiosemicarbazide in methanol, under mild conditions, is reported.
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A convenient method for the synthesis of 2-trichloromethyl-4-p-substituted-phenyl-3h-1,5-benzodiazepines

TL;DR: In this article, a method to obtain a new series of 2-trichloromethyl-4-aryl-3H-1,5-benzodiazepines from the reaction of β-methoxyvinyl trichlormethyl ketones derived from acetals and o-phenylenediamine is reported.
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Cyclocondensation reaction of 4-aryl-4-methoxy-1,1,1-trifluoro-3-buten-2-ones with urea Synthesis of novel 6-aryl(5-methyl)-4-trifluoromethyl-2(1H)-pyrimidinones

TL;DR: In this article, the synthesis of a series of 6-aryl(5-methyl)-4-trifluoromethyl-2(1H)-pyrimidinones from the reaction of 4-aryl-4-methoxy-1, 1,1,1-, trifluoro-3-buten-2-ones with urea in the presence of hydrochloric acid was reported.
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Dissimilaridade genética e análise de trilha de cultivares de soja avaliada por meio de descritores quantitativos

TL;DR: Alem das avaliacoes entre genotipos, a utilizacao de tecnicas multivariadas possibilita restringirem-se os erros, principalmente quanto a diversidade genetica, podendo-se, assim, prever combinacoes com maior efeito heterotico.