碳酸二乙酯置于sodium Hydride体系中,用 N,N-二甲基甲酰胺 用作溶剂,化学反应 6.5H,以90%的收率获得3-(4-甲氧苯基)-3-氧代丙酸乙酯 参考文献: Novel Pyrimidine Compounds,Process For Their Preparation And Compositions Containing Them[fr] Nouveaux Composes De Pyrimidine,Leur Procede De Preparation,Et Compositions Les Contenant 标题: Novel Pyrimidine Compounds,Process For Their Preparation And Compositions Containing Them[fr] Nouveaux Composes De Pyrimidine,Leur Procede De Preparation,Et Compositions Les Contenant
专利号:CN-107876092-A 优先权日:2017-11-24 标 题 :High Stability Titanium Catalyst for the Synthesis of Benzyl Carbonate and Diphenyl Carbonate by Transesterification
专利号:US-8883763-B2 优先权日:2010-03-01 标题 :Use of isoquinolones for preparing drugs, novel isoquinolones and method for synthesising same 发明人:POPOV ANDREI; JUHEM AURÉLIE; FLORENT JEAN-CLAUDE; N GUYEN CHI-HUNG 权利人:POPOV ANDREI; JUHEM AURÉLIE; FLORENT JEAN-CLAUDE; N GUYEN CHI-HUNG; UNIV JOSEPH FOURIER; CENTRE NAT RECH SCIENT; INST CURIE 摘要:The use of isoquinolones for preparing drugs, including novel isoquinolones as well as their synthesis method. In particular, isoquinolone derivatives used in the treatment of pathological angiogenesis, and more particularly of cancer.
专利号:WO-2024254278-A9 优先权日:2023-06-08 标题 :Ophthalmic films 发明人:BANERJEE AMRITA; MITRAGOTRI SAMIR; LEVINSON DOUGLAS 权利人:FOUNT BIO INC 摘要:The present application describes the synthesis, formulation and uses of systems comprising conjugates or materials prepared therefrom, capable of retaining systems on the ocular surface.
专利号:EA-032434-B1 优先权日:2010-03-01 标题 :APPLICATION OF IZHOCHINOLONES FOR THE PREPARATION OF MEDICINES, IZHOCHOLONES AND METHOD OF THEIR SYNTHESIS
参考标题:Glutamate As An Efficient Amine Donor For The Synthesis Of Chiral β‐ And γ‐amino Acids Using Transaminase 作者:Geon‐hee Kim,Hyunwoo Jeon,Taresh P. Khobragade,Mahesh D. Patil,Sihyong Sung,Sanghan Yoon,Yumi Won,Sharad Sarak,Hyungdon Yun |发布日期:2019.3.6 摘要:A Recyclable Glutamate Amine Donor System Employing Transaminase (Ta), Glutamate Dehydrogenase (Gludh) And Mutant Formate Dehydrogenase (Fdhm) Was Developed, Wherein Amine Donor Glu Was Regenerated Using Gludh And Thereby Circumvented The Inhibition Of Ta By α‐ketoglutarate. Various Enantiopure β‐, γ‐amino Acids, And Amines Were Successfully Synthesized With High Conversions And Excellent Enantiomeric
合成参考文献
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