90145-22-5Relevant academic research and scientific papers
Novel generation of azomethine imines from α-silylnitrosamines by 1,4- silatropic shift and their cycloaddition
Washizuka, Ken-Ichi,Nagai, Keiko,Minakata, Satoshi,Ryu, Ilhyong,Komatsu, Mitsuo
, p. 8849 - 8853 (2007/10/03)
Novel and facile generation of azomethine imines from α- silylnitrosamines and subsequent cycloaddition with dipolarophiles leading to a variety of pyrazole derivatives have been developed. The key to the reaction is a 1,4-silatropic shift caused by stron
1,3-Dipolar Cycloadditions, 91. The Chemistry of N-Methyl-C-phenylnitrilimine
Fliege, Werner,Grashey, Rudolf,Huisgen, Rolf
, p. 1194 - 1214 (2007/10/02)
The treatment of N'--N-methylhydrazinium bromide, accessible by bromination of benzaldehyde-N-methylhydrazone, with triethylamine furnishes the title compound; this method is superior to the thermolysis and photolysis of 2-methyl-5-phe
Studies on Organic Fluorine Compounds. XLII. Synthesis and Reactions of Phenyltrifluoromethylacetylenes
Kobayashi, Yoshiro,Yamashita, Toshinori,Takahashi, Katsuhiro,Kuroda, Hisashi,Kumadaki, Itsumaro
, p. 4402 - 4409 (2007/10/02)
Phenyltrifluoromethylacetylene (4a) was synthesized by the pyrolysis of triphenylphosphonium α-(trifluoroacetyl)benzylide (3a), which was easily derived from benzyl halide (1a).This method can be used for the synthesis of 4-substituted-phenyltrifluoromethylacetylenes (4).The 1,3-dipolar reaction of 4 with diazomethane and phenyl azide proceeds readily to give trifluoromethylated pyrazoles and triazoles.Keywords - trifluoromethyl; acetylene; 1,3-dipolar reaction; intramolecular Wittig reaction; trifluoroacetylphosphonium ylide; pyrazole; diazomethane; phenyl azide
