CAS: 170141-63-6; 3'-(Trifluoromethoxy)Acetophenone

相似化合物

347194-02-9 101975-23-9 1821840-58-7

上下游产品

3-(三氟甲氧基)苯甲醛 3-(Trifluoromethoxy)Benzaldehyde 52771-21-8
3-(三氟甲氧基)苯甲酸 3-(Trifluoromethoxy)Benzoic Acid 1014-81-9
3-羟基苯乙酮 3-Hydroxyacetophenone 121-71-1

3-(三氟甲氧基)苯甲醛置于哌啶,吡啶,Iron(II) Chloride体系中,用 乙醇 用作溶剂,化学反应 25.0H,反应生成3-(三氟甲氧基)苯乙酮
参考文献:Iron-Catalyzed Domino Decarboxylation-Oxidation Of α,β-Unsaturated Carboxylic Acids Enabled Aldehyde C-h Methylation
标题:Iron-Catalyzed Domino Decarboxylation-Oxidation Of α,β-Unsaturated Carboxylic Acids Enabled Aldehyde C-h Methylation
摘要:铁催化的α,β-不饱和羧酸的串联脱羧氧化反应,实现了醛的c-H甲基化,用于制备多样化的甲基酮,并可应用于复杂小分子的晚期修饰.
Doi:10.1039/d1Cc01536B

专利信息

专利号:WO-9925385-A1
优先权日:1997-11-17
标 题:A method of increasing nucleic acid synthesis with ultrasound
发明人：UNGER EVAN C; MCCREERY THOMAS; SADEWASSER DAVID
权利人:IMARX PHARMACEUTICAL CORP
摘要:The present invention is directed to a method of increasing nucleic acid synthesis in a cell comprising administering to the cell a therapeutically effective amount of ultrasound for a therapeutically effective time such that said administration of said ultrasound results in said increased nucleic acid synthesis. The nucleic acid sequence may comprise an endogenous sequence or an exogenous sequence.

专利号:US-6005103-A
优先权日:1993-11-19
标题 :Pyrone derivatives as protease inhibitors and antiviral agents
发明人：DOMAGALA JOHN MICHAEL; LUNNEY ELIZABETH; PARA KIMBERLY SUZANNE; PRASAD JOSYULA VENKATA NAGENDR; TAIT BRADLEY DEAN
权利人:WARNER LAMBERT CO
摘要:The present invention relates to novel tri- and tetrasubstituted pyrones and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The pyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized pyrones and of related structures.

专利号:EP-0729465-B1
优先权日:1993-11-19
标 题:Pyrone derivatives as protease inhibitors and antiviral agents
发明人：DOMAGALA JOHN MICHAEL; LUNNEY ELIZABETH; PARA KIMBERLY SUZANNE; PRASAD JOSYULA VENKATA NAGENDR; TAIT BRADLEY DEAN
权利人:PARKE DAVIS & CO
摘要:The present invention relates to novel tri- and tetrasubstituted pyrones and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The pyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized pyrones and of related structures.