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利多卡因的合成-資料下載頁

2025-06-24 22:29本頁面
  

【正文】 學(xué)實(shí)驗(yàn)手冊[M],西安:陜西師范大學(xué), 2015[4] 周楨堂,錢國軍等. 14C標(biāo)記利多卡因的合成[J].核技術(shù),2002,25(1),5456[5] 朱曉亮,[J],南方醫(yī)科大學(xué)學(xué)報(bào),2010,30(3): 451455[6] 屠世忠,[J],China Academic Journal Electronic Publishing House,1998, 14(3):1819[7] Yilu G, Peiyi W.FTIR spectroscopic study of the acrylamide states in AOT reversed micelles.Journal of Molecular Structure,2008,883,30:3137.[8] Klyuev, . Influence of various factors on lidocaine synthesis by reductive acylation in the presence of palladium catalysts[J],Izvestiya Vysshikh Uchebnykh Zavedenii, Khimiya Khimicheskaya Tekhnologiya,2009,52(1), 2327 [9] Simon K. Shannon, Mandy J. Peacock, Steven A. Kates. BaranySolidPhase Synthesis of Lidocaine and Procainamide Analogues Using Backbone Amide Linker (BAL) Anchoring[J],Comb. Chem. 2003, 5, 8608685
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