25976-83-4Relevant articles and documents
Photocyclization reaction of some 2-methyl-4-phenyl- substituted aldehyde thiosemicarbazones. Mechanistic aspects
Buscemi, Silvestre,Gruttadauria, Michelangelo
, p. 999 - 1004 (2007/10/03)
Irradiation of 2-methyl-4-phenyl- substituted benzaldehyde thiosemicarbazones led with good yields to the corresponding ?21,2,4- triazoline-5-thione derivatives through the formation of stable 1,2,4- triazolidine-5-thione intermediates. The relative quantum yields of photocyclization at 313 nm were analysed by means of the Hammett equation and p values determined: We interpreted the results in terms of the mechanism of photocyclization of 2-methyl-4-phenyl-substituted benzaldehyde thiosemicarbazones. (C) 2000 Elsevier Science Ltd.
Photochemical Cyclization of Some Aldehyde Thiosemicarbazones
Gruttadauria, Michelangelo,Buccheri, Francesco,Buscemi, Silvestre,Cusmano, Giuseppe,Noto, Renato,Werber, Giuseppe
, p. 233 - 236 (2007/10/02)
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 remaining thiosemicarbazones 1g-j gave 1,2,4-triazoline 4-derivatives.
Oxidative cyclisation of ketone thiosemicarbazones. II. Derivatives of phenoxyacetone.
Landquist
, p. 323 - 324 (2007/10/04)
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