Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Inácio, Luduvico"'
Autor:
Rosemeire B. Alves, Leandro José dos Santos, Rossimiriam Pereira de Freitas, Inácio Luduvico, Guilherme Rocha Pereira
Publikováno v:
Tetrahedron Letters. 51:1022-1025
A bis-malonate C60 derivative bearing terminal alkyne groups prepared by the Bingel reaction has been used as a building block under copper-catalyzed azide–alkyne cycloaddition conditions to produce a series of new fullerene glycoconjugate derivati
Autor:
Mara R. C. Couri, Leandro José dos Santos, Rosemeire B. Alves, Inácio Luduvico, Maria Auxiliadora Fontes Prado, Rossimiriam Pereira de Freitas Gil
Publikováno v:
Carbohydrate Research. 343:536-540
Several novel N-1, N-2, and S -5 tetrazole and 1,3,4-oxadiazole derivatives of α,α-trehalose disubstituted at C-6,6′, with potential synthetic and pharmacological interest were prepared from commercial tetrazoles and 1,3,4-oxadiazoles in reaction
Autor:
Leandro José dos Santos, Inácio Luduvico, Mara R. C. Couri, Rossimiriam Pereira de Freitas Gil, Maria Auxiliadora Fontes Prado, Rosemeire B. Alves
Publikováno v:
Synthetic Communications. 37:3059-3066
Five new nitrogen heterocycles, mono‐and disubstituted tetrazoles with potential synthetic and pharmacological interest, were synthesized from α, α‐trehalose via the alkylation of commercial tetrazoles. This method appears to have broad scope w
Autor:
Inácio, Luduvico, Mara R C, Couri, Leandro J, dos Santos, Maria A F, Prado, Rossimiriam P Freitas, Gil, Rosemeire B, Alves
Publikováno v:
Carbohydrate research. 343(3)
Several novel N-1, N-2, and S-5 tetrazole and 1,3,4-oxadiazole derivatives of alpha,alpha-trehalose disubstituted at C-6,6', with potential synthetic and pharmacological interest were prepared from commercial tetrazoles and 1,3,4-oxadiazoles in react
Autor:
Leandro de Arruda Santos, Mara R. C. Couri, Maria Auxiliadora Fontes Prado, Rossimiriam Pereira de Freitas Gil, Inácio Luduvico, Rosemeire B. Alves
Publikováno v:
Carbohydrate research. 342(8)
A series of novel N-1, N-2 and S-5 saccharide substituted tetrazole derivatives linked at anomeric and nonanomeric positions were obtained from commercial tetrazoles under microwave irradiation. Yields are compared with conventional methodologies.