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化学进展  2010 

水相不对称转移氢化*

, PP. 1242-1253

Keywords: 手性二胺,过渡金属,水相,不对称转移氢化

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Abstract:

手性醇和胺是重要的精细化学品,不对称转移氢化是获得这类手性化合物有效、实用的途径之一。在众多的催化剂中,Noyori等发展的手性二胺与过渡金属钌TsDPEN-Ru(TsDPEN=1,2—二苯基乙二胺)络合物是最有效的催化剂。近年来,随着化学家对绿色化学的日益重视,水作为绿色溶剂被广泛地用作为不对称催化转移氢化的反应介质,具有很高的反应活性、对映选择性和化学选择性。本文综述近年来应用未经修饰和修饰的手性二胺配体与过渡金属钌[(cymene)RuCl2]2、铑[(Cp*)RhCl2]2和铱[(Cp*)IrCl2]2的络合物催化的水相中酮、亚胺和活化烯烃的不对称转移氢化的研究进展。

References

[1]  1308
[2]  [4 ] Wu X F,Xiao J L. Chem. Commun. ,2007,2449—2466
[3]  1750—1770
[4]  Am. Chem. Soc. ,1996,118: 2521—2522
[5]  Am. Chem. Soc. ,1996,118: 4916—4917
[6]  686—694
[7]  2173
[8]  Clark J H,Tavener S J. Org. Proc. Res. Dev. ,2007,11:
[9]  Sheldon R A. Green Chem. ,2007,9: 1273—1283
[10]  Muxworthy J P,Thorpea T,Williams J M J. Tetrahedron Lett. ,
[11]  2001,42: 4037—4039
[12]  Thorpe T,Blacker J,Brown S M,Bubert C,Crosby J,Fitzjohn
[13]  S,Muxworthy J P,Williams J M P. Tetrahedron Lett. ,2001,
[14]  Ma Y P,Liu H,Chen L,Cui X,Zhu J,Deng J G. Org. Lett. ,
[15]  Canivet J,Labat G,Evans H S,Fink G S. Eur. J. Inorg.
[16]  Chem. ,2005,4493—4500
[17]  Wu J S,Wang F,Ma Y P,Cui X,Cun L F,Zhu J,Deng J G,
[18]  Deng J G. Green Chem. ,2007,9: 23—25
[19]  Xue D,Chen Y C,Cui X,Wang Q W,Zhu J,Deng J G. J.
[20]  Tang Y F,Xiang J,Cun L F,Wang Y Q,Zhu J ,Liao J,Deng
[21]  J G. Tetrahedron: Asymmetry,2010,21: DOI: 10. 1016 / j.
[22]  Soltani O,Ariger M A,Carreira E M. Org. Lett. ,2009,11:
[23]  4196—4198
[24]  Wu X F,Vinci D,Ikariya T,Xiao J L. Chem. Commun. ,
[25]  2005,4447—4449
[26]  Matharu D S,Morris D J,Clarkson G J,Wills M. Chem.
[27]  Li X H,Blacker J,Houson I,Wu X F,Xiao J L. Synlett. ,
[28]  2006,1155—1160
[29]  Lin G Q,Xu M H,Zhong Y W,Sun X W. Acc. Chem. Res. ,
[30]  2008,41: 831—840
[31]  4715
[32]  Wang F,Liu H,Cun L F,Zhu J,Deng J G. Jiang Y Z. J.
[33]  Ahlford K,Lind J,Mler L,Adolfsson H. Green Chem. ,2008,
[34]  Ed. ,2004,43: 6731—6734
[35]  Chem. Int. Ed. ,2009,48: 6524—6528
[36]  Guan H,Iimura M,Magee M P,Norton J R,Zhu G. J. Am.
[37]  Noyori R. J. Am. Chem. Soc. ,2006,128: 8724—8725
[38]  Li C Q,Wang C,Marcos B V,Xiao J L. J. Am. Chem. Soc. ,
[39]  2008,130: 14450—14451
[40]  131: 6967—6969
[41]  Aberg J B,Samec J S M,Bckvall J E,Chem. Commun. 2006,
[42]  Fan Q H,Pan J,Gu L Q,Chan A S C. Angew. Chem. Int.
[43]  Samec J S M,Bckvall J E,Andersson P G,Brandt P. Chem.
[44]  Liu P L,Deng J G,Tu Y Q,Wang S H. Chem. Commun. ,
[45]  2004,2070—2071
[46]  Chem. ,2009,298: 31—35
[47]  Li X G,Wu X F,Chen W P,Hancock F E,King F,Xiao J L.
[48]  Liu J T, Zhou Y G, Wu Y N, Li X S, Chan A S C.
[49]  Huang L,Liu J T,Shan W J,Liu B,Shi A D,Li X S.
[50]  Chirality,2010,22: 206—211
[51]  Jiang L,Wu T F,Chen Y C,Zhu J,Deng J G. Org. Biomol.
[52]  Arakawa Y,Haraguchi N,Itsuno S. Tetrahedron Lett. ,2006,
[53]  Haraguchi N,Tsuru K,Arakawa Y,Itsuno S. Org. Biomol.
[54]  Catal. ,2008,350: 2295—2304
[55]  Ed. ,2008,47: 1400—1404
[56]  497—500
[57]  Soc. ,2003,125: 4149—4154
[58]  Wu X F,Liu J K,Tommaso D D,Iggo J A,Catlow C R A,
[59]  Bacsa J,Xiao J L. Chem. Eur. J. ,2008,14: 7699—7715
[60]  Rhyoo H Y,Park H J,Suh W H,Chung Y K. Tetrahedron
[61]  Lett. ,2002,43: 269—272
[62]  Mao J C,Wan B,Wu F,Lu S W. Tetrahedron Lett. ,2005,
[63]  Lett. ,2006,47: 4501—4503
[64]  Cortez N A,Apodaca R R,Aguirre G,Hake M P,Cole T,
[65]  Somanathan R. Tetrahedron Lett. ,2006,47: 8515—8518
[66]  Chem. ,2006,256: 85—89
[67]  Wu X F,Li X H,McConville M,Saidi O,Xiao J L. J. Mol.
[68]  Cat. A: Chem. ,2006,247: 153—158
[69]  Xu Z,Mao J C,Zhang Y W,Guo J,Zhu J L. Cat. Commun. ,
[70]  2008,9: 618—623
[71]  Zeror S,Collin J,Fiaud J C,Zouioueche L A. Adv. Synth.
[72]  Catal. ,2008,350: 197—204
[73]  [1 ] Noyori R,Hashiguchi S. Acc. Chem. Res. ,1997,30: 97—
[74]  102
[75]  [2 ] Palmer M J,Wills M. Tetrahedron: Asymmetry,1999,10:
[76]  2045—2061
[77]  [3 ] Ikariya T,Blacker A J. Acc. Chem. Res. ,2007,40: 1300—
[78]  [5 ] Wang C,Wu X F,Xiao J L. Chem. Asian J. ,2008,3:
[79]  [6 ] Wu X F,Wang C,Xiao J L. Platinum Metals Rev. ,2010,54:
[80]  3—19
[81]  [7 ] Hashiguchi S,Fujii A,Takehara J,Ikariya T,Noyori R. J.
[82]  Am. Chem. Soc. ,1995,117: 7562—7563
[83]  [8 ] Fujii A,Hashiguchi S,Uematsu N,Ikariya T,Noyori R. J.
[84]  [9 ] Uematsu N,Fujii A,Hashiguchi S,Ikariya T,Noyori,R. J.
[85]  Anastas P T,Warner J. Green Chemistry Theory and Practice.
[86]  New York: Oxford Univ. Press,1998
[87]  Anastas P T,Kirchhoff M M. Acc. Chem. Res. ,2002,35:
[88]  Poliakoff M, Fitzpatrick J M, Farren T R, Anastas P T.
[89]  Science,2002,297: 807—810
[90]  Horváth I T,Anastas P T. Chem. Rev. ,2007,107: 2169—
[91]  149—155
[92]  Lindstrm U M. Chem. Rev. ,2002,102: 2751—2772
[93]  Li C J,Chen L. Chem. Soc. Rev. ,2006,35: 68—82
[94]  Shaughnessy K H. Chem. Rev. ,2009,109: 643—710
[95]  Bubert C, Blacker J, Brown S M, Crosby J. Fitzjohn S,
[96]  42: 4041—4043
[97]  2003,5: 2103—2106
[98]  Yu B L. Chem. Commun. ,2006,1766—1768
[99]  Li L,Wu J S,Wang F,Liao J,Zhang H,Lian C X,Zhu J,
[100]  Org. Chem. ,2005,70: 3584—3591
[101]  tetasy. 2010. 05. 046
[102]  Wu X F,Li X G,Hems W,King F,Xiao J L. Org. Biomol.
[103]  Chem. ,2004,2: 1818—1821
[104]  Commun. ,2006,3232—3234
[105]  Zhang B,Xu M H,Lin G Q. Org. Lett. ,2009,11: 4712—
[106]  Zhou H F,Fan Q H,Huang Y Y,Wu L,He Y M,Tang W J,Gu L H,Chan A S C. J. Mol. Catal. A: Chem. ,2007,275:
[107]  47—53
[108]  Org. Chem. ,2005,70: 9424—9429
[109]  10: 832—835
[110]  Schlatter A,Kundu M K,Woggon W D. Angew. Chem. Int.
[111]  Schlatter A,Woggon W D. Adv. Synth. Catal. ,2008,350:
[112]  995—1000
[113]  Wang C,Li C Q,Wu X F,Pettman A,Xiao J L. Angew.
[114]  Chem. Soc. ,2005,127: 7805—7814
[115]  Ohkuma T,Utsumi N,Tsutsumi K,Murata K,Sandoval C,
[116]  Li C Q,Marcos B V,Xiao J L. J. Am. Chem. Soc. ,2009,
[117]  2771—2773
[118]  Zhou H F,Li Z W,Wang Z J,Wang T L,Xu L J,He Y M,
[119]  Ed. ,2008,47: 8464—8467
[120]  Soc. Rev. ,2006,35: 237—248
[121]  Liu P N,Gu P M,Deng J G,Tu Y Q,Ma Y P. Eur. J. Org.
[122]  Chem. ,2005,3221—3227
[123]  Li J,Zhang Y M,Han D F,Gao Q,Li C. J. Mol. Catal. A:
[124]  Org. Lett. ,2004,6: 3321—3324
[125]  Tetrahedron: Asymmetry,2008,19: 832—837
[126]  Chem. ,2006,4: 3319—3324
[127]  47: 3239—3243
[128]  Chem. ,2009,7: 69—75
[129]  Arakawa Y,Chiba A,Haraguchi N,Itsuno S. Adv. Synth.
[130]  Letondor C,Humbert N,Ward T R. Proc. Natl. Acad. Sci. ,
[131]  2005,102: 4683—4687
[132]  Letondor C,Pordea A,Humbert N,Ivanova A,Mazurek S,
[133]  Novic M,Ward T R. J. Am. Chem. Soc. ,2006,128: 8320—
[134]  8328
[135]  Creus M,Pordea A,Rossel T,Sardo A,Letondor C,Ivanova
[136]  A,LeTrong I,Stenkamp R E,Ward T R. Angew. Chem. Int.
[137]  Wu X F,Li X G,King F,Xiao J L. Angew. Chem. Int. Ed. ,
[138]  2005,44: 3407—3411
[139]  Makihara N,Ogo S,Watanabe Y. Organometallics,2001,20:
[140]  Abura T,Ogo S,Watanabe Y,Fukuzumi S. J. Am. Chem.
[141]  Wu X F,Li X H,Gerosa A Z,Pettman A,Liu J K,Mills A J,
[142]  Xiao J L. Chem. Eur. J. ,2008,14: 2209—2222
[143]  Rhyoo H Y,Park H J,Chung Y K. Chem. Commun. ,2001,
[144]  2064—2065
[145]  46: 7341—7344
[146]  Himeda Y,Komatsuzaki N O,Sugihara H,Arakawa H,Kasuga
[147]  K. J. Mol. Cat. A: Chem. ,2003,195: 95—100
[148]  Xing Y,Chen J S,Dong Z R,Li Y Y,Gao J X. Tetrahedron
[149]  Zeror S,Collin J,Fiaud J C,Zouioueche L A. J. Mol. Cat. A:
[150]  Li B Z,Chen J S,Dong Z R,Li Y Y,Li Q B,Gao J X. J.
[151]  Mol. Cat. A: Chem. ,2006,258: 113—117
[152]  Canivet J,Fink G S. Green Chem. ,2007,9: 391—397

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