153648-98-7Relevant articles and documents
Reactions of 2-(methoxyimino)benzen-1-ones with α-alkylethoxycarbonylmethylene(triphenyl)phosphoranes
Nicolaides, Demetrios N,Gautam, Daman R,Litinas, Konstantinos E,Manouras, Christos,Fylaktakidou, Konstantina C
, p. 9469 - 9474 (2001)
The title 2-(methoxyimino)benzen-1-ones react with α-alkylethoxycarbonylmethylene(triphenyl)phosphoranes to give 2H-[b][1,4]benzoxazine derivatives along with benzoxazole and indole derivatives. Reaction mechanisms to explain the formation of products obt
Reactions of 7-(Methoxyimino)-4-methyl-2H-chromene-2,8(7H)-dione with Phosphorus Ylides. Synthesis of 2-Substituted 6-Methyl-8H-benzopyranooxazol-8-ones
Bezergiannidou-Balouctsi, Catherine,Litinas, Konstantinos E.,Malamidou-Xenikaki, Elizabeth,Nicolaides, Demetrios N.
, p. 1175 - 1178 (2007/10/02)
7-(Methoxyimino)-4-methyl-2H-chromene-2,8(7H)-dione (3) reacts with phosphonium salts 1a-c, 8a, b under phase-transfer catalysis conditions to afford the title 2-substituted 6-methylbenzopyranooxazol-8-ones 5a-c, 10a, b, respectively, along with compound 6, instead of the expected Wittig reaction products.However, the reaction of 3 with the stable phosphorus ylides 11a-c in addition to the corresponding benzopyranooxazoles 12a-c and compound 6 affords in the last case compound 16 as well according to a sequence involving an initial Wittig reaction between 11c and 3. - Key Words: Oxazolocoumarins / Phosphorus ylides / 2H-Chromene-2,8(7H)-dione, 7-(methoxyimino)-4-methyl- / Wittig reaction / Benzopyranooxazol-8-ones