采用Pd(Oac)2/[mmim]I催化体系,在不同反应条件下可以将烷基胺、芳香胺及氨基醇(酚)一步转化为氨基甲酸酯、脲和 2-口恶唑啉酮. N-苯基氨基甲酸甲酯、二苯基脲及苯并-2-口恶唑酮的催化转化频率分别为 12 417, 17 638 和 4 114 h-1.
参考文献
[1] | Mounetou E;Legault J;Lacroix J;Gaudreault R C .[J].Journal of Medicinal Chemistry,2003,46(23):5055. |
[2] | Reddy P V G;Reddy C S;Venugopal M .[J].Heteroatom Chemistry,2003,14(06):509. |
[3] | Baraldi P G;Bovero A;Fruttarolo F;Romagnoli R Tabrizi M A Preti D Varani K Borea P A Moorman A R .[J].Bioorganic and Medicinal Chemistry Letters,2003,11(19):4161. |
[4] | Kumar M;Hosur M V .[J].European Journal of Biochemistry,2003,270(06):1231. |
[5] | Yoshida H;Shirakawa E;Honda Y;Hiyama T .[J].Angewandte Chemie International Edition,2002,41(17):3247. |
[6] | Humphrey JM.;Liao YS.;Ali A.;Rein T.;Wong YL.;Chen HJ.;Courtney AK. Martin SF. .Enantioselective total syntheses of manzamine A and related alkaloids[J].Journal of the American Chemical Society,2002(29):8584-8592. |
[7] | Hegarty A F;Drennan L J;Katritzky A R;Meth-Cohn O,Rees C W.Comprehensive Organic Functional Group Transformations[M].Oxford:pergamon Press,1995:499. |
[8] | Crego M;Marugan J J;Raposo C;Sanz M J Alcazar V Caballero M C Moran J R .[J].Tetrahedron Letters,1991,32(33):4185. |
[9] | Tingoli M.;Temperini A.;Tiecco M.;Testaferri L. .INTRAMOLECULAR NUCLEOPHILIC DESELENENYLATION REACTIONS PROMOTED BY BENZENESELENENYL TRIFLATE - STEREOSPECIFIC SYNTHESIS OF VICINAL AMINO ALCOHOL PRECURSORS[J].The Journal of Organic Chemistry,1996(20):7085-7091. |
[10] | Bacchi A;Chiusoli G P;Costa M;Gabriele B Righi C Salerno G.[J].Chemical Communications,1997(13):1209. |
[11] | Inesi A.;Rossi L.;Mucciante V. .A convenient method for the synthesis of carbamate esters from amines and tetraethylammonium hydrogen carbonate[J].The Journal of Organic Chemistry,1998(4):1337-1338. |
[12] | Vani P S N;Chida A S;Srinivasan R;Chandrasekharam M Singh A K .[J].Synthetic Communications,2001,31(13):2043. |
[13] | Ono Y .[J].Catalysis Today,1997,35(1-2):15. |
[14] | Delledonne D;Rivetti F;Romano U .[J].Applied Catalysis A:General,2001,221(1-2):241. |
[15] | Bhanage B M;Fujita S I;Ikushima Y;Arai M .[J].Green Chemistry,2003,5(03):340. |
[16] | Abla M;Choi J C;Sakakura T .[J].Green Chemistry,2004,6(05):524. |
[17] | Shi F;Deng Y Q;Sima T L;Peng J J,Gu Y L,Qiao B T .[J].Angewandte Chemie International Edition,2003,42(28):3257. |
[18] | Bigi F;Maggi R;Sartori G .[J].Green Chemistry,2000,2(04):140. |
[19] | Chiarotto I.;Feroci M. .Selective and environmentally friendly methodologies based on the use of electrochemistry for fine chemical preparation: An efficient synthesis of N,N '-disubstituted ureas[J].The Journal of Organic Chemistry,2003(18):7137-7139. |
[20] | 石峰,司马天龙,邓友全.一种胺氧化羰化制氨基甲酸酯新催化剂体系[J].高等学校化学学报,2000(10):1566-1568. |
[21] | Gabriele B;Salerno G;Mancuso R;Costa M .[J].Journal of Organic Chemistry,2004,69(14):4741. |
[22] | 杨瑛,陆世维.硒催化的乙二胺、乙醇胺和环胺的氧化羰基化反应[J].催化学报,2000(04):355-358. |
[23] | Gabriele B;Mancuso R;Salerno G;Costa M.[J].Chemical Communications,2003(04):486. |
[24] | Kim H S;Kim Y J;Lee H;Lee S D Chin C S .[J].Journal of Catalysis,1999,184(02):526. |
[25] | Li F;Xia C .[J].Journal of Catalysis,2004,227(02):542. |
[26] | 张庆华,石峰,邓友全.硅胶担载离子液体催化剂的制备及其在由胺制二取代脲反应中的应用[J].催化学报,2004(08):607-610. |
[27] | Peng XG;Li FW;Xia CG .A highly efficient sulfur-catalyzed oxidative carbonylation of primary amines and beta-amino alcohols[J].Synlett,2006(8):1161-1164. |
[28] | 薛燕,陆世维.硒催化法合成2-吡啶脲的研究[J].催化学报,2001(04):387-389. |
[29] | 杨瑛,陆世维.硒催化硝基苯的还原羰基化生成苯氨基甲酸酯[J].催化学报,1999(03):224-226. |
[30] | Tafesh A M;Weiguny J .[J].Chemical Reviews,1996,96(06):2035. |
[31] | Bonhote P.;Papageorgiou N.;Kalyanasundaram K.;Gratzel M.;Dias AP. .HYDROPHOBIC, HIGHLY CONDUCTIVE AMBIENT-TEMPERATURE MOLTEN SALTS[J].Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics,1996(5):1168-1178. |
[32] | Pri-Bar I;Alper H .[J].Canadian Journal of Chemistry,1990,68(09):1544. |
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