专利号:US-RE29882-E 优先权日:1973-04-27 标题 :Synthesis of oxindoles from anilines and intermediates therein 摘要:Preparing oxindoles and intermediates therefor by reacting an N-haloaniline with β-thio ester or β-thio amides to form an azasulfonium halide, reacting the azasulfonium halide with a base to form an ortho[thio-ether (hydrocarbonoxycarbonyl) alkyl]aniline, or a [thio-ether (aminocarbonyl) alkyl]aniline, reacting the ortho-substituted aniline with an acid to form a 3-thio-ether-2-oxindole, and then reducing the 3-thio-ether-2-oxindole with Raney Nickel to form the 2-oxindole.
专利号:US-3996264-A 优先权日:1973-04-27 标 题 :Synthesis of oxindoles from anilines and intermediates therein 发明人:GASSMAN PAUL G 权利人:UNIV OHIO STATE RES FOUND 摘要:Preparing oxindoles and intermediates therefor by reacting an N-haloaniline with β-thio esters or β-thio amides to form an azasulfonium halide, reacting the azasulfonium halide with a base to form an ortho-[thio-ether (hydrocarbonoxycarbonyl) alkyl]aniline, or a [thio-ether (aminocarbonyl) alkyl]aniline, reacting the ortho-substituted aniline with an acid to form a 3-thio-ether-2-oxindole, and then reducing the 3-thio-ether-2-oxindole with Raney Nickel to form the 2-oxindole.
专利号:US-3972894-A 优先权日:1973-04-27 标 题:Synthesis of oxindoles from anilines and β-thio carboxylic esters or amides 发明人:GASSMAN PAUL G 权利人:UNIV OHIO STATE RES FOUND 摘要:Preparing oxindoles and intermediates therefor by reacting an N-haloaniline with β-thio esters or β-thio amides to form an azasulfonium halide, reacting the azasulfonium halide with a base to form an ortho-[thio-ether (hydrocarbonoxycarbonyl) alkyl]aniline, or a [thio-ether (aminocarbonyl) alkyl]aniline, reacting the orthosubstituted aniline with an acid to form a 3-thio-ether-2-oxindole, and then reducing the 3-thio-ether-2-oxindole with Raney Nickel to form the 2-oxindole.
专利号:CA-1042447-A 优先权日:1973-04-27 标 题:Synthesis of oxindoles from anilines and intermediates therein
专利号:US-8466287-B2 优先权日:2005-06-09 标题 :Process for producing tricyclic ketone 发明人:NISHIYAMA HIROYUKI; SAWADA SEIGO 权利人:NISHIYAMA HIROYUKI; SAWADA SEIGO; YAKULT HONSHA KK 摘要:In order to efficiently supply CPT, which is a starting compound of irinotecan hydrochloride and a variety of camptothecin derivatives, by a practical total synthesis, the invention provides a means of efficiently preparing a tricyclic ketone that corresponds to a CDE ring moiety of a camptothecin (CPT) skeleton.
1: Gentle M, Speed J, Allen BL, Harris S, Haapakoski H, Bell K. The longevity of para-aminopropiophenone (PAPP) wild dog baits and the implications for effective and safe baiting campaigns. Environ Sci Pollut Res Int. 2017 May;24(13):12338-12346. doi: 10.1007/s11356-017-8668-3. Epub 2017 Mar 29. doi: 10.1016/j.bmcl.2013.10.046. Epub 2013 Oct 31. doi: 10.1111/j.1749-4877.2010.00183.x. Epub 2007 Jun 7. Epub 2007 Jun 9. Chinese. Chinese.
合成参考文献
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