"2"^^ . "I, P(GAP207/12/0072)" . . . . . "https://www.beilstein-journals.org/bjoc/single/articleFullText.htm?vt=f&publicId=1860-5397-9-43&tpn=1&bpn=singleVolume&vn=9" . "RIV/61388963:_____/13:00391782!RIV14-GA0-61388963" . . "Beier, Petr" . . "10.3762/bjoc.9.43" . "109554" . "9" . . "Synthesis of SF5-containing benzisoxazoles, quinolines, and quinazolines by the Davis reaction of nitro-(pentafluorosulfanyl)benzenes" . . . . "Feb 21" . "Meta- or para-nitro-(pentafluorosulfonyl)benzenes underwent the Davis reaction with arylacetonitriles to provide the SF5-containing benzisoxazoles. Good yields were obtained with arylacetonitriles containing the electron-neutral or electron-donor group, while those with the electron-acceptor group were found to be unreactive. Reductions of the benzisoxazoles gave ortho-aminobenzophenones in high yields. Their synthetic utility was demonstrated by condensation reactions with carbonyl compounds or amines to provide SF5-containing quinolines and quinazolines, respectively."@en . . . "Past\u00FD\u0159\u00EDkov\u00E1, Tereza" . "1860-5397" . "Synthesis of SF5-containing benzisoxazoles, quinolines, and quinazolines by the Davis reaction of nitro-(pentafluorosulfanyl)benzenes"@en . . "RIV/61388963:_____/13:00391782" . . "[F289FAB9F473]" . "Synthesis of SF5-containing benzisoxazoles, quinolines, and quinazolines by the Davis reaction of nitro-(pentafluorosulfanyl)benzenes"@en . . . . "Synthesis of SF5-containing benzisoxazoles, quinolines, and quinazolines by the Davis reaction of nitro-(pentafluorosulfanyl)benzenes" . "000315411800001" . "6"^^ . "DE - Spolkov\u00E1 republika N\u011Bmecko" . "Beilstein Journal of Organic Chemistry" . "benzisoxazoles; pentafluorosulfanyl group; quinazolines; quinolines; sulfurpentafluorides"@en . . "Meta- or para-nitro-(pentafluorosulfonyl)benzenes underwent the Davis reaction with arylacetonitriles to provide the SF5-containing benzisoxazoles. Good yields were obtained with arylacetonitriles containing the electron-neutral or electron-donor group, while those with the electron-acceptor group were found to be unreactive. Reductions of the benzisoxazoles gave ortho-aminobenzophenones in high yields. Their synthetic utility was demonstrated by condensation reactions with carbonyl compounds or amines to provide SF5-containing quinolines and quinazolines, respectively." . . "2"^^ . .