全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
化学进展  2010 

超临界二氧化碳介质中的有机反应*

, PP. 1274-1285

Keywords: 超临界二氧化碳,绿色介质,催化

Full-Text   Cite this paper   Add to My Lib

Abstract:

本文主要介绍了超临界近5年来超临界二氧化碳中的有机反应研究的最新进展,包括加氢反应、氧化反应、羰基化反应、碳碳键形成反应、酯化反应和酶催化反应的研究现状;同时,还介绍了超临界二氧化碳作为反应底物用于合成碳酸酯和氨基甲酸酯的研究进展;并对未来的发展进行了展望。

References

[1]  [1 ] Jiang H. Curr. Org. Chem. ,2005,9: 289—297
[2]  47
[3]  [3 ] Matsuda T, Harada T, Nakamura K, et al. Tetrahedron:
[4]  Asymmetry,2005,16: 909—915
[5]  Chemistry) ,2007,19(9) :1267—1274
[6]  [6 ] 岳晓东(Yue X D) ,何良年( He L N) . 有机化学( Chinese
[7]  [8 ] Lyubimov S E,Davankov V A,Said-Galiev E E,et al. Catal.
[8]  [9 ] Lyubimov S E,Said-Galiev E E,Khokhlov A R,et al. J.
[9]  Supercrit. Fluids,2008,45: 70—73
[10]  2007,13: 2798—2804
[11]  Clark P,Poliakoff M,Wells A. Adv. Synth. Catal. ,2007,
[12]  349: 2655—2659
[13]  2009,351: 1912—1924
[14]  Hiyoshi N,Rode C V,Sato O,et al. J. Catal. ,2007,252:
[15]  Xi C,Cheng H,Hao J,et al. Molecular Catal. A: Chem. ,
[16]  Hiyoshi N,Osada M,Rode C V,et al. Appl. Catal. A: Gen. ,
[17]  2007,331: 1—7
[18]  Hiyoshi N,Yamaguchi A,Rode C V,et al. Catal. Commun. ,
[19]  2005,288: 43—47
[20]  Chatterjee M, Yokoyama T, Kawanami H, et al. Chem.
[21]  Commun. ,2009,701—703
[22]  Wang Q,Cheng H,Liu R,et al. Catal. Commun. ,2009,10:
[23]  Phys. ,2005,7: 278—285
[24]  Maayan G,Ganchegui B,Leitner W,et al. Chem. Commun. ,
[25]  2006,2230—2232
[26]  Kimmerle B,Grunwaldt J D,Baiker A. Topics Catal. ,2007,
[27]  Gen. ,2008,349: 86—90
[28]  Chem. ,2006,71: 1039—1042
[29]  Ciriminna R, Campestrinib S, Pagliaro M. Org. Biomol.
[30]  Chem. ,2006,4: 2637—2641
[31]  Olsen M H N,Salomo G C,Drago V,et al. Supercrit. Fluids,
[32]  Theyssen N,Hou Z,Leitner W. Chem. Eur. J. ,2006,12:
[33]  3401—3409
[34]  887
[35]  González-Núez M E, Mello R, Olmos A, et al. J. Org.
[36]  Patcas F,Maniut C,Ionescu C,et al. Appl. Catal. B,2007,
[37]  2008,10: 545—552
[38]  Lett. ,2006,107: 205—208
[39]  Giménez-Pedrós M,Aghmiz A,Ruiz N,et al. Eur. J. Inorg.Chem. ,2006,1067—1075
[40]  Chem. ,2007,268: 244—250
[41]  Estorach C T,Masdeu-Bultó A M. Catal. Lett. ,2008,122:
[42]  76—79
[43]  2006,310: 155—163
[44]  Amandi R,Licence P,Ross S K,et al. Org. Process Res.
[45]  Amandi R,Scovell K,Licence P,et al. Green Chem. ,2007,
[46]  Xing H,Wang T,Dai Y. J. Supercrit. Fluids,2009,49: 52—
[47]  58
[48]  Stevens J G,Bourne R A,Poliakoff M. Green Chem. ,2009,
[49]  11: 409—416
[50]  Ballini R,Noè M,Perosa A,et al. J. Org. Chem. ,2008,73:
[51]  8520—8528
[52]  Jiang H F,Tang J Y,Wang A Z,et al. Synthesis,2006,
[53]  1155—1161
[54]  Jiang H F,Wang A Z. Synthesis,2007,1649—1654
[55]  Zhou L,Zhang W D,Jiang H F. Sci. China Ser. B-Chem. ,
[56]  49: 377—384
[57]  Jiang H F,Huang X. J. Supercrit. Fluids,2007,43: 291—
[58]  294
[59]  Jiang H F,Shen Y X,Wang Z Y. Tetrahedron,2008,64(3) :
[60]  Zou B,Jiang H F. Sci. China Ser. B-Chem. ,2008,51 (5 ) :
[61]  447—451
[62]  Rodríguez L I,Rossell O, Seco M, et al. J. Organometal.
[63]  Ghaziaskar H S,Daneshfara A,Calvo L. Green Chem. ,2006,
[64]  Harada T,Kubota Y,Kamitanaka T,et al. Tetrahedron Lett. ,
[65]  Matsuda T,Marukado R,Mukouyama M,et al. Tetrahedron:
[66]  Asymmetry,2008,19: 2272—2275
[67]  Yasmin T,Jiang T,Han B,et al. J. Mol. Catal. B: Enzym. ,
[68]  Technol. ,2006,39: 621—625
[69]  Celebi N,Yildiz N,Demir A S,et al. J. Supercrit. Fluids,
[70]  Kayaki Y,Yamamoto M,Ikariya T. J. Org. Chem. ,2007,72:
[71]  647—649
[72]  8: 1019—1021
[73]  Qi C R,Jiang H F,Wang Z Y,et al. Synlett,2007,255—258
[74]  Jiang H F,Ye J W,Qi C R. Huang L B,Tetrahedron Lett. ,
[75]  2010,51: 928—932
[76]  Jiang H F,Zhao J W,Wang A Z. Synthesis,2008,763—769
[77]  [2 ] Campestrini S,Tonellato U. Curr. Org. Chem. ,2005,9: 31—
[78]  [4 ] Beckman E J. J. Supercrit. Fluids,2004,28: 121—191
[79]  [5 ] 胡玉(Hu Y) ,侯震山( Hou Z S ) . 化学进展( Progress in
[80]  Journal of Organic Chemistry) ,2006,26(5) : 610—617
[81]  [7 ] Stephenson P, Kondor B, Licence P, et al. Adv. Synth.
[82]  Catal. ,2006,348: 1605—1610
[83]  Commun. ,2008,9: 1851—1852
[84]  Burgemeister K,Franciò G,Gego V H,et al. Chem. Eur. J. ,
[85]  Chatterjee M,Kawanami H,Sato M,et al. Adv. Synth. Catal. ,
[86]  57—68
[87]  Hiyoshi N,Bando K K,Sato O,et al. Catal. Commun. ,2009,
[88]  10: 1702—1705
[89]  Liu H Z, Jiang T,Han B X, et al. Science,2009,326:
[90]  1250—1252
[91]  Ichikawa S,Tada M, Iwasawa Y, et al. Chem. Commun. ,
[92]  2005,924—926
[93]  2008,282: 80—84
[94]  2009,10: 1681—1684
[95]  Hiyoshi N,Rode C V,Sato O,et al. Appl. Catal. A: Gen. ,
[96]  Altinel H,Avsar G,Guzel B. Transition Met. Chem. ,2009,
[97]  34: 331—335
[98]  592—595
[99]  Caravati M,Grunwaldt J D,Baiker A. Phys. Chem. Chem.
[100]  44: 285—292
[101]  Wang X,Kawanami H,Dapurkar S E,et al. Appl. Catal. A:
[102]  González-Núez M E, Mello R, Olmos A, et al. J. Org.
[103]  Hou Z,Theyssen N,Brinkmann A,et al. Angew. Chem. Int.
[104]  Ed. ,2005,44: 1346—1349
[105]  2005,34: 119—124
[106]  Yu K M K,Abutaki A,Zhou Y,et al. Catal. Lett. ,2007,
[107]  113: 115—119
[108]  Dapurkar S E, Kawanami H, Yokoyama T, et al. New J.
[109]  Chem. ,2009,33: 538—544
[110]  Wang X, Venkatarmanan N S, Kawanami H, et al. Green
[111]  Chem. ,2007,9: 1352—1355
[112]  Wang J,Cai F,Wang E,et al. Green Chem. ,2007,9: 882—
[113]  Wang Z,Jiang H,Qi C,et al. Green Chem. ,2005,7: 582—
[114]  585
[115]  Chem. ,2006,71: 6432—6436
[116]  Koeken A C J,van Vliet M C A,van de Broeke L J P,et al.
[117]  Adv. Synth. Catal. ,2006,348: 1553—1559
[118]  70: 630—636
[119]  Estorach C T,Orejón A,Masdeu-Bultó A M. Green Chem. ,
[120]  Pedrósa M G,Masdeu-Bultó A M,Bayardon J,et al. Catal.
[121]  Fujita S,Akihara S,Fujisawa S,et al. J. Mol. Catal. A:
[122]  Tortosa-Estorach C, Ruiz N, Masdeu-Bultó A M. Chem.
[123]  Commun. ,2006,2789—2791
[124]  Kamalakar G,Komura K, Sugi Y. Appl. Catal. A: Gen. ,
[125]  Kamalakar G,Komura K,Sugi Y. Ind. Eng. Chem. Res. ,
[126]  2006,45: 6118—6126
[127]  Dev. ,2005,9: 451—456
[128]  9: 797—801
[129]  Hagiwara H,Hamaya J,Hoshib T,et al. Tetrahedron Lett. ,
[130]  2005,46: 393—395
[131]  Seki T,Grunwaldt J,van Vegten N,et al. Adv. Synth. Catal. ,
[132]  2008,350: 691—705
[133]  2008,51: 241—247
[134]  Jiang H F,Xu Q X,Wang A Z. J. Supercritical Fluid,2009,
[135]  Leeke G A,Santos R C D,Al-Duri B,et al. Org. Process Res.
[136]  Dev. ,2007,11: 144—148
[137]  508—514
[138]  Chem. ,2008,693: 1857—1860
[139]  8: 576—581
[140]  Rezayat M,Ghaziaskar H S. Green Chem. ,2009,11: 710—
[141]  715
[142]  Sakthivel A,Komura K, Sugi Y. Ind. Eng. Chem. Res. ,
[143]  2008,47: 2538—2544
[144]  2009,50: 4934—4936
[145]  2006,41: 27—31
[146]  Olsen T, Kerton F, Marriott R, et al. Enzym. Microb.
[147]  2007,41: 386—390
[148]  Palocci C,Falconi M,Chronopoulou L,et al. J. Supercrit.
[149]  Fluids,2008,45: 88—93
[150]  Jiang H F,Wang A Z,Liu H L,et al. Eur. J. Org. Chem. ,
[151]  2008,2309—2312
[152]  Kayaki Y,Yamamoto M,Suzuki T,et al. Green Chem. ,2006,
[153]  Jiang H F,Zhao J W. Tetrahedron Lett. ,2009,50: 60—62
[154]  Qi C R,Jiang H F. Green Chem. ,2007,9: 1284—1286

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133