Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Giuseppe Cusmano"'
Autor:
Giuseppe Cusmano, Giuseppe Werber, Renato Noto, Francesco Buccheri, Michelangelo Gruttadauria
Publikováno v:
Scopus-Elsevier
The reactions beetwen 2,4-disubstituted thiosemicarbazides and orthoesters in refluxing xylene led to the formation of the 1,2,4-triazoline-5-thione ring and to the 1,2,4-triazolium-5-thiolate ring. The formation of the mesoionic componds is due to r
Autor:
Paolo Lo Meo, Francesco Buccheri, Giuseppe Werber, Michelangelo Gruttadauria, Renato Noto, Giuseppe Cusmano
Publikováno v:
Journal of Heterocyclic Chemistry. 30:765-770
The oxidative cyclization of some aldehyde semicarbazones 10 with four different oxidizing agents has been effected. The structure of the semicarbazones and the nature of cyclizing agent affected the rate and yield of cyclization but they did not sho
Autor:
Girolamo Cirrincione, Gabriella Macaluso, Anna Maria Almerico, Patrizia Diana, Giuseppe Cusmano
Publikováno v:
ChemInform. 23
Autor:
Francesco Buccheri, Michelangelo Gruttadauria, Giuseppe Cusmano, Giuseppe Werber, Renato Noto
Publikováno v:
ChemInform. 23
The reactivity of aldehyde thiosemicarbazones 1 with ferric chloride solutions was examined. When compounds 1 are not substituted on the N-2 nitrogen atom formation of 1,3,4-thiadiazole 3 heterocyclic ring was observed. In contrast 1,2,4-triazoline 4
Autor:
Michelangelo Gruttadauria, Francesco Buccheri, Giuseppe Cusmano, Silvestre Buscemi, Giuseppe Werber, Renato Noto
Publikováno v:
ChemInform. 23
The photochemical behaviour of some substituted aldehyde thiosemicarbazones 1a-k has been investigated in methanol at 254 nm. Thiosemicarbazones of glyoxil methyl ester 1a-f cyclized to furnish the 3-thioxo- 1,2,4-triazin-5-one 2 ring system. The rem
ChemInform Abstract: Oxidative Cyclization of Some Aldehyde Semicarbazones Induced by Metallic Salts
Autor:
Renato Noto, Paolo Lo Meo, Giuseppe Werber, Francesco Buccheri, Michelangelo Gruttadauria, Giuseppe Cusmano
Publikováno v:
ChemInform. 24
The oxidative cyclization of some aldehyde semicarbazones 10 with four different oxidizing agents has been effected. The structure of the semicarbazones and the nature of cyclizing agent affected the rate and yield of cyclization but they did not sho
Publikováno v:
ChemInform. 24
The rearrangement reaction of 1,2,5-oxadiazole derivatives bearing quinoline and pyridine heterocycles in a N-C-N side chain sequence was investigated. Triazolo[1,5-a]quinoline and triazolo[1,5-a]pyridine oximes were obtained in good yield
Publikováno v:
ChemInform. 24
Autor:
Francesco Buccheri, Michelangelo Gruttadauria, Giuseppe Werber, Renato Noto, Giuseppe Cusmano
Publikováno v:
ChemInform. 29
Autor:
Giuseppe Werber, Michelangelo Gruttadauria, Silvestre Buscemi, Giuseppe Cusmano, Renato Noto, Francesco Buccheri
Publikováno v:
Journal of Heterocyclic Chemistry. 29:233-236
The photochemical behaviour of some substituted aldehyde thiosemicarbazones 1a-k has been investigated in methanol at 254 nm. Thiosemicarbazones of glyoxil methyl ester 1a-f cyclized to furnish the 3-thioxo- 1,2,4-triazin-5-one 2 ring system. The rem