对烷氧基取代MeO-BIPHEP类手性双膦配体的合成与应用研究
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摘要
自1990年以来,不对称催化研究发展迅速,在基础研究和手性技术的开发与应用方面都获得了巨大的成功,成为不对称合成研究的热点。其中,手性膦配体的设计合成及其在不对称催化反应中的应用研究占有非常重要的地位。本文设计合成了一类新的长链烷氧基取代的手性双膦配体(S)-p-Alkoxy- MeO-BIPHEP((S)-165c~(S)-165f),并对其在(Z)-2-乙酰胺基肉桂酸酯和芳香酮的不对称催化加氢反应中的性能进行了研究。
     首先,利用改进的方法合成了MeO-BIPHEP及其长链烷氧基取代的衍生物((S)-165c~(S)-165f)。该方法适用于各种不同取代的MeO-BIPHEP类双膦配体的合成,同中时具有收率高、低成本和操作简便等特点。
     采用及时分出溴乙烷的新工艺和微波辅助合成两种方法,改进了传统无水氯化镍催化亚磷酸三乙脂和间溴茴香醚反应生成间甲氧基苯基磷酸二乙脂的反应,缩短了反应时间,提高了收率,适合于大量制备。
     以无水三氯化铁催化氧化偶联的“一锅煮”法,替代文献中常用的邻位锂化、碘代、Ullmann偶合反应法,制备了重要的合成中间体6, 6`-二甲氧基-1, 1`-联苯-2, 2`-二磷酸二乙酯(rac-162)。以廉价的无水三氯化铁代替昂贵的碘和活性铜粉,降低了试剂成本。同时,无水三氯化铁催化的“一锅煮”法具有操作简便、产物易纯化和后处理简单的优点,易于中间体的放大制备。通过对rac-162拆分条件的研究,成功地获得了光学纯的重要中间体(S)-162。
     偶联产物(S)-162经膦酰化反应,制备了光学纯的膦酰氯(S)-163,再与格氏试剂反应,以较高的收率制备了新的双膦氧化物(S)-164。其经还原得到了新
Asymmetric hydrogenation has become increasingly popular for producing enantiomerically pure compounds in pharmaceutical and other chemical industries. The demand for new ligands with unique structural features and physical properties continues to grow in order to meet the requirements of a wide range of reactions and substrates. In this paper, a series of new optically active MeO-BIPHEP-type ligands, (S)-6,6`-dimethoxy-2,2`-bis(di-p-alkoxyphenylphosphine)-1,1`-biphenyl ((S)-165c ~ (S)-165f) were prepared and applied in asymmetric hydrogenation.
     Starting from the commercially available triethyl phosphorite and m-bromoanisole, an optically active (S)-6,6`-dimethoxybiphenyl-2,2`-diyl-bis (phosphonic acid diester) was prepared by an improved method. First, (3-Methoxyphenyl)-phosphonic acid diethyl ester 161 was prepared by the reaction of m-bromoanisole with triethyl phosphorite in the presence of anhydrous NiCl2. Removing of the by-product or microwave assistant synthesis could effectively accelerate the reaction and enhance the yield of product 161. Instead of the the Schmid’s method, a new one-pot oxidative home-coupling of 161 catalyzed by anhydrous FeCl3 was used to form rac-6,6`-dimethoxybiphenyl-2,2`-diyl-bis (phosphonic acid diethyl ester) rac-162. The new approach could avoid the preparation and purification of iodide derived from 161 and was much easier to manipulate and more cost-effective. A suitable resolution of rac-162 was studied and
引文
1. Tang, W. J.; Zhang, X. M. New chiral phosphorus ligands for enantioselective hydrogenation. Chem. Rev. 2003, 103, 3029-3069.
    2. Noyori, R. (Nobel Lecture) . Asymmetric Catalysis: Science and Opportunities. Angew. Chem., Int. Ed. 2002, 41, 2008–2022
    3. Noyori, R.; Ohkuma, T.Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones Angew. Chem., Int. Ed. 2001, 40, 40–73
    4. Schmid, R.; Broger, E. A.; Cereghetti, M.; Crameri, Y.; Foricher, J.; Lalonde, M.; Muller, R. K.; Scalone, M.; Schoettel, G.; Zutter, U. New developments in enantioselective hydrogenation. Pure appl. Chem. 1996, 68, 131-138
    5. Antonio Z. G.; William H.; Michelle G.; Fred H. Ruthenium-Catalysed Asymmetric Reduction of Ketones. Platinum Metals Rev., 2005, 49, 158-165
    6. Han, Y.F.; Ying, D. Q.; Xu, F.; Dong, J.X.. Progress of Rhodium- Catalyzed Asymmetric Hydrogenation. Chemical Industry Times(in chinese), 2004, 11, 1-7 (韩英锋, 杨定乔, 徐峰, 董建霞. 铑催化不对称氢化反应的研究进展. 化工时刊, 2004, 11, 1-7)
    7. Li, K. Y.; Zhou, Z. H.;Tang, C. C.Progress of Chiral Phosphorus Ligands Catalysts in Asymmetric Synthesis ( Ⅰ ) .Chemical Research.(China). 2002,13, 58-64 (in chinese). (李康应,周正洪,唐除痴,不对称合成中手性磷配体催化剂的研究进展(1) (待续). 化学研究, 2002, 13,(1), 58.) Li, K.Y.; Zhou, Z. H.; Tang, C. C.Progress of Chiral Phosphorus Ligands Catalysts in Asymmetric Synthesis(2). Chemical Research.(China). 2002,13(2),49(in chinese). (李康应,周正洪,唐除痴,不对称合成中手性磷配体催化剂的研究进展(2) (续完).化学研究, 2002, 13,,49-58
    8. Dai, H. C.; Chen, H. L.; Zhen, Z.; Zhang, X. F.; Progress in New Chiral Phosphine Ligands and Their Application of in Asymmetric Catalysis. .Journal of Molecular Catalysis(China). 2000, 6, 426-439 (戴慧聪, 陈惠麟, 郑卓, 张遂之, 张秀峰. 新型手性膦配体的合成及其在不对称催化中应用的新进展.分子催化. 2000, 6, 426-439)
    9. Xu, L. W.; Sun,W.; Li, F. W. Progress in Preparation and Application of Chiral Phosphine Ligands in Asymmetric Catalysis. Chinese Journal of Organic Chemistry. 2003, 23, 919-932 (in chinese). (徐立文,孙伟,李福伟,手性膦配体的合成及其在不对称催化反应中的应用研究进展. 有机化学,2003, 23,919-932)
    10. Xu, X. H.; Lv, S. J.; Fu, H. X. Progress in Chiral Phosphine Ligands and Their Application of in Asymmetric Catalysishiral. Journal of Molecular Catalysis(China). 1996,10 (5),391-399 (in chinese). (徐小红,吕士杰,傅宏祥,手性膦配体及其不对称催化的研究进展. 分子催化, 1996, 10,391-399)
    11. Zhang, T. Z.; Xu, L. J.; Sun,W. H.Syntheses of Phosphine Ligands via Palladium-Catalyzed P2C Coupling ReactionsProgress in Chemistry(China).2004,16,90-98(in chinese). (张天柱,徐立进,孙文华,Pd 催化 P2C 偶联合成膦配体的进展. 化学进展, 2004, 16,90-98
    12. Miyashita, A.; Yasuda, A.; Takaya, H.; Toriumi, K.; Souchi, T.; Noyori, R. Syntheisis of 2,2`-Bis(diarylphosphino)-1,1`-binaphthyl(BINAP), an atropisomeric chiral Bis(triaryl) phosphine, and it use in Rhodium-catalyzed asymmetric hydrogenation of a-(acylamino)acrylic acids. J. Am. Chem. Soc. 1980, 102, 7932-7934
    13. Takaya, H.; Mashima, K.; Koyano, K.; Yagi, M.; Kumobayashi, H.; Taketomi, T.; Akutagawa, S.; Noyori, R.; Practical synthesis of (R)-or (S)-2,2`-Bis(diarylphosphino)- 1,1`-binaphthyls(BINAPs) . J. Org. Chem.. 1986, 51, 629-635. Noyori, R.; Ohkuma, T.; Kitamura, M.; Takaya, H.; Syyo, N.; Kumobayashi, H.; Akutagawa, S. Asymmetric hydrogenation of B-keto Carboxylic Esters. A practical, Purely chemical access to B-hydroxy Esters in high enantiomeric Purity. J. Am. Chem. Soc. 1987, 109, 5856-5858.
    14. Schmid,R. Gereghetti, M.; Heiser, B.; Schonholzer, P.; Hansen, H. J. Axially dissymmetric Bis(triaryl)phosphines in the Biphenyl Series: synthesis of (6,6`-dimethylbiphenyl-2,21-diyl) bis(diphenylphosphine) (BIPHEMP) and analogues, and their use in Rh-catalyzed asymmetric Isomerizations of N,N-diethylnerylamine. Helv. Chem.Acta, 1988, 71, 897
    15. Frejd, T.; Klingstedt, T. Acta Chem. Scand. 1989, 43, 670
    16. Miyashita, A.; Nagano, T.; Ojima, T.; Nohira, H.; Takaya, H.; Noyori, R. 51th Annual Meeting of the Chemical Society of Japan, Kyoto, April, 1986, pp1267
    17. Yamamoto, N.; Murata, M.; Motimoto, T.; Achiwa, K. Chem. Pharm. Bull. 1991, 39, 1085
    18. Yoshikawa, K.; Yamamoto, N.; Murata, M.; Awano, K.; Motimoto, T.; Achiwa, K. Tetrahedron Asymmetry. 1992, 3, 13-
    19. Cereghetti, M.; Arnold, W.; Broger, E. A.; Rageot, A.; (R)- and (S)-6,6`-dimethyl and 6,6`-dimethoxy- 2,2`--diiodo-1,1`-biphenyls: versatile intermediates foe the synthesis of atropisomeric diphosphine ligands. Tetrahedron Lett. 1996, 30, 5347–5350
    20. Henschke, J. P.; Burk, M. J.; Malan, C. G.;. Herzberg, D; Peterson, J. A, . Wildsmith, A. J.; Cobley, C. J.; Casy, G..Synthesis and Applications of HexaPHEMP, a Novel Biaryl Diphosphine Ligand. Adv. Synth. Catal. 2003, 345, 300-307
    21. Henschke, J.P.; Antonio, Z. G.; Moran, P., Harrison, P.; Mullen,B.; Gasy, G.; Lennon, I. C.A concise synthesis of a new xylyl-biaryl diphosphine ligand for asymmetric hydrogenation of ketones Tetrahedron Letters.2003,44,4379.
    22. Malan, C. G. Antonio, Z. G.; Henschke, J. P. preparation of aryl diphosphine chiral ligands and their ruthenium complexes for asymmetric catalysis. WO 2003/048137. 2003 (Chem. Abatr. 2003, 139, 36635)
    23. Trabesinger, G.; Albinati, A.; Feiken, N.; Kunz, R.; Pregosin, P. S.; schoerner, M. J. Am. Chem. Soc. 1997, 119, 6315
    24. Selvakumar, K.; Valentini, M.; Pregosin, P. S.; Albinati, A.; Eisentra¨ger, F. Organometallics 2000, 19, 1299
    25. Dotta, P.; Kumar, P. G.; Pregosin, P. S. 3,5-Dialkyl Effect on Enantioselectivity in Pd Chemistry: Applications Involving Both Bidentate and Monodentate Auxiliaries. Organometallics 2004, 23, 2295-2304
    26. Wu, J.; Chen, H.; Kwok, W.; Guo, R.; Zhou, Z.; Yeung, C.; Chan, A. S. C A new chairal dipyriddylphosphine ligands Xyl-P-Phos and its application in Ru-catalyzed asymmetric hydrogenation of β-ketoesters. J. Org. Chem. 2002, 67, 7908
    27. Shibata, T.; Tsuruta, H.; Danjo, H.; Imamoto, T. Preparation of an optically active bis(diethylphosphino)biphenyl ligand designed for highly reactive catalytic processes. J. of Mol. Cata. A: Chemical. 2003, 196, 117
    28. Schmid, R.; Foricher, J.; Cereghetti, M.; Schonholzer, P. Axially dissymmetric diphosphines in biphenyl series: synthesis of (6, 6`-dimethoxybiphenyl-2, 2`-diyl) bis (diphenylphosphine) (“MeO-BIPHEP”) and analogues via an ortho-lithiation/Iodination Ullmann-reaction approach. Helv. Chim. Acta. 1991, 74, 370-381.
    29. Foricher,J.;Schmid,R.Process for the manufacture of bis(phosphine oxide)- and bis (phosphonate)-compounds. EP 926152.1997. (Chem. Abatr. 1998, 131, P44958)
    30. Lalonde, M.; Schmid, R. Tetrasulfonated diphosphine compounds and metal complexes thereof for asymmetric catalytic reactions.US 5, 536,858, 1996; Chem. Abstr. 1996, 124, P8995c
    31. Cereghetti, M.; Foricher, J.; Heiser, B.; Chiral phosphorus compounds. Schmid, R. US 5,488,172, 1996
    32. Foricher,J.;Schmid,R. phosphorus compounds US 5457219.1993. (Chem. Abatr. 1994, 119, P271399k)
    33. Foricher, J.; Heiser, B.; Schmid, R. Chiral phosphines. US 5,302,738, 1994; (Chem. Abstr. 1993, 118, P147774u)
    34. Broger, E. A.; Foricher, J.; Heiser, B.; Schmid, R. Chiral phosphines. US5,274,125, 1993; (Chem. Abstr. 1993, 118, P59878a)
    35. Gelpke, A. E. S.; Veerman, J. J. N.; Goedheijt, M.S.; Kamer, P. C. J.; Hiemstra, H. Synthesis and use of water-soluble sulfonated dibenzofuran-based phosphine ligands. Tetrahedron. 1999, 55, 6657-6670
    36. Gelpke, A. E. S.; Kooijman, H.; Spek, A. L.; Hiemstra, H. Synthesis of Dibenzofuran-Based Diphosphine ligands BIFAP and it water-soluble derivative BIFAPS and Their Use in Ruthenium-Catalyzed Asymmetric Hydrogenation. Chem. Eur. J. 1999, 5,2472-2482
    37. Tang, W.; Chi, Y.; Zhang, X. M. An ortho-substitited BIPHEP ligand and it application in Rh-catalyzed hydrogenation of cyclic enamides. Org. Lett. 2002, 10, 1695-1698
    38. Wu, S.L.; He, M. S.; Zhang, X. M. Synthesis of ortho-phenyl substituted MeO-BIPHEP ligand and its application in Rh-catalyzed asymmetric hydrogenation. Tetrahedron Asymmetry. 2004, 15, 2177-2180
    39. Pohl, T.; Prinze, T.; Giffels, G.; Sirges, W.; Process for preparation of enantiomerically pure (5,5'-Dichloro-6,6'-dimethoxy-biphenyl-2,2'-diyl)-bis(diphenylphosphine oxide). US 2002/0058814. 2002 (Chem. Abatr. 2002, 136, 369840)
    40. Birgit, D. H.; ;Joachim, K.; Friederike, A.; Christian, S.; Hu, C. H. Preaparation diphosphines as cocatalyst for asymmetric reaction. US 2002/055653. 2002 (Chem. Abatr. 2002, 136, 232396)
    41. Driben-Holscher, B.; Kralik, J.; Agel, F.; Steffens, C.; Hu, C. H. New Route to Biaryl Phosphanes with Axial Chirality as Ligands for Enantioselective Hydrogenations. Adv. Synth. Catal. 2004, 346, 979-982
    42. Gorobets, E.; Sun, G. R.; Wheatley, B. M.; Parvez, M.; Keay, B. A.Synthesis, resolution and applications of 3,3-bis(RO)-MeOBIPHEP derivatives. Tetrahedron Letters, 2004, 45, 3597–3601
    43. Gorobets, E.; Wheatley, B. M.; Hopkins, J. M.; McDonaldb, R.; Keaya, B. A. Avoiding the classical resolution during the synthesis of MeO-BIPHEP and 3,3-disubstituted derivatives. Tetrahedron Letters, 2005, 46, 3843–3846
    44. Zhang, X.; Mashima, K.; Koyano, K.; K.; Sayo, n.; Kumobayashi, H.; Akutagawa, S.; Takaya, H. Tetrahedron Lett. 1991, 32, 7283
    45. Zhang, X.; Mashima, K.; Koyano, K.; K.; Sayo, n.; Kumobayashi, H.; Akutagawa, S.; Takaya, H. J. Chem. Soc., Perkin Trans. 1 1994, 2309
    46. Guo, R. W.; Wu, J.; Michael C. K. Albert S.C. Chan. Modified BINAPO ligands for Rh-catalysed enantioselective hydrogenation of acetamidoacrylic acids and esters. Tetrahedron Asymmetry. 2002, 13, 2519-2522
    47. Zhang, Z, G.; Qian, H.; Longmire, J.; Zhang, X. M. Synthesis of Chiral Bisphosphines with Tunable Bite Angles and Their Applications in Asymmetric Hydrogenation of a-Ketoesters. J. Org. Chem. 2000, 65, 6223-6226
    48. Saito,T.; Yokozawa, T.; Ishizaki, T.; Moroi, T.; Sayo,N.; Miura, T.; Kumobayashi, H. New Chiral Diphosphine Ligands Designed to Have a Narrow Dihedral Angle in the Biaryl Backbone. Adv.Synth.Catal.2001.3, 343, 264
    49. Qiu, L.Q.; Qi, J.Y.; Pai, C.C.; Chan, S.S.; Zhou, Z.Y.; Choi, M.C.K.; Albert, S.C. Chan. Synthesis of Novel Diastereomeric Diphosphine Ligands and Their Applications in Assymmetric Hydrogenation Reaction.Org. Lett. 2002, 26, 4599-4602
    50. Pai C. C.; Li, Y. M.; Zhou, Z. Y.; Chan, A. S. C. Synthesis of new chiral diphosphine ligand (BisbenzodioxanPhos) and its application in asymmetric catalytic hydrogenation. Tetrahedron Lett. 2002, 43, 2789-2792
    51. Sebastien, D. P.; Jeulin, S.; Virginie, R. V.; Genet, J. P.; Champion, N.; Dellis, P. Synthesis and Molecular Modeling Studies of SYNPHOS, a New, Efficient Diphosphane Ligands for Ruthenium-Catalyzed Asymmetric Hydrogenation. Eur. J. Org. Chem. 2003,1931-1941
    52. Sebastien, D. P.; Jeulin, S.; Virginie, R. V.; Genet, J. P.; Champion, N.; Dellis, P. SYNPHOS?, a new chiral diphosphine ligand: synthesis, molecular modeling and application in asymmetric hydrogenation. Tetrahedron Letters.2003,44,823
    53. Jeulin, S.; Sebastien D. P.; Ratovelomanana, V.; Genet, J. P.;Champion, N.; Dellis, P.Chiral biphenyl diphosphines for asymmetric catalysis: Stereoelectronic design and industrial perspectives. Proceedings of the National Academy of Sciences of the United States of America. 2004, 101(16), 5799-5804
    54. Jeulin, S. Sebastien, D. P.;Ratovelomanana, V.; Genet, J. P.; Champion, N.; Dellis, P. Difluorphos, an Electron-Poor Diphosphane: A Good Match Between Electronic and Steric Features. Angew. Chem. Int. Ed. 2004, 43, 320 –325
    55. Qiu, L. Q.; Wu, J.; Chan, S. S.; Terry, T, Y.; Ji, J. X.; Guo, R. W.; Pai, C. C.; Zhou, Z. Y.; Li, X. S.; Fan, Q. H; Albert S. C. Chan. Remarkably diastereoselective synthesis of a chiral biphenyl diphosphine ligand and its application in asymmetric hydrogenation. Proceedings of the National Academy of Sciences of the United States of America. 2004, 101(16), 5799-5804.
    56. Albert, S. C. Chan; Qiu, L. Q.Preparation of biphenyldiphosphine compounds useful in asymmetric reactions.US 2005014633, 2005 (Chem. Abstr.2005,.142:137081)
    57. Wan, X. B.; Sun, Y. H; Luo, Y. F; Zhang, Z. G. Process for preparation of chiral phosphine ligands.CN 1563020, 2005(Chem. Abatr. 2005, 143, 367395) ( in Chinese). 万小兵, 孙延晖, 罗云飞, 张兆国. 膦配体、合成及其在不对称催化反应中的应用.CN156320, 2005
    58. Murata, M.; Morimoto, T.; Achiwa, K. Synllett. 1991,827
    59. Aikawa, K.; Mikami, K. Atropos but achiral tris(phosphanyl)biphenyl ligands for Ru-catalyzed asymmetric hydrogenation. Angew. Chem. Int. Ed. 2003, 42, 5455-5458
    60. Saluzzo, C.; Lamouille, T.; Lemaire, M.; Halle, R. T.Water soluble charily diphosphine..US 2004/0102649A1.2004.
    61. Arlet, D.; Meseguer, B, Chiral phosphanes for use in asymmetric syntheses. US 2005/0085377, 2005 (Chem. Abatr. 2005, 142, 316957)
    62. Michaud, G.; Bulliaed, M.; Ricard, L.; Genet, J. P.; Maeinetti, A.A Strategy for the Stereoselective Synthesis of Unsymmetric Atropisomeric Ligands: Preparation of NAPhePHOS, a New Biaryl Diphosphine Chem. Eur. J. 2002, 15, 3327
    63. Madec, J.; Michaud, G.; Genet, J. P.; Marinetti, A. New developments in the synthesis of heterotopic atropisomeric diphosphines via diastereoselective aryl coupling reactions. Tetrahedron Asymmetry. 2004, 15, 2253-2261
    64. Steiner, I.; Aufdenblattrn, R.; Togni, A.; Blaser, H. U.; Pugin, B. Novel silica gel supported chiral biaryl-diphosphine ligands for enantioselective hydrogenation. Tetrahedron Asymmetry. 2004, 15, 2307-2311.
    65. Miyashita,A.;Karino,H.;Shimamura,J.; Chiba, T.; Nagano, H.; Nohira, H.; Takaya, H. Chem.Lett.1989,1849
    66. Fujie, N.; Matsui, M; Achiwa K. Chem. Pharm. Bull. 1999, 47, 436-439
    67. Terry, T. L.; Au, Y.; Albert S.C. Chan. Biheteroaromatic diphosphines and their transition metal complexes: synthesis, characterisation and applications in asymmetric catalysis. Coordination Chemistry Reviews. 2004, 248, 2151–2164
    68. Chiba, T, Miyashita, A.; Nohira, H.; Takaya, H. synthesis of chiral Rh-BIChep complexes, highy efficient catalysts for asymmetric hydrogenations. Tetrahedron Lett. 1991, 20, 4745-4748
    69. Walsh, J. C.; Padgett, H. C. Method for making fluorine-labeled L-dopa. US 2005137421 2005 (Chem. Abstr.2005,.143:60250)
    70. V. Fehring., R. Selke., Angew. Chem. Int.Eng.,1998,37,1827
    71. T. Ohkuma, H. Ooka, , T.Ikariya, R. Noyori, J. Am. Chem. Soc., 1995, 117, 2675
    72. D. Pini, A. IuIiano, C. Rosini, P. Salvadori, Synthesis, 1990,1023
    73. J. H. Xie, L. X. Wang, Q. L. Zhou, J Am Chem. Soc, 2003,125, 4404
    74. L. Karame, M. Jahjah, A. Messaoudi, M. L. Tommasino, M. Lemaire, Tetrahedron: Asymmetry, 2004,15, 1569
    75. H.J. Shine, J.C. Trisler, J Am Chem. Soc. 1960, 83,4054
    76. Li, X. G.; Chen, W. P.; Hems, W.; King, F.; Xiao, J. L. Asymmetric Hydrogenation of Ketones with Polymer-Supported Chiral 1,2-Diphenylethylenediamine Org. Lett. 2003, 24, 4559-4561
    77. Lipshutz, B. H.; Noson, K.; Chrisman, W.; Lower, A. Asymmetric Hydrosilylation of Aryl Ketones Catalyzed by Copper Hydride Complexed by Nonracemic Biphenyl Bis-phosphine Ligands. J. Am. Chem. Soc. 2003, 125, 8779-8789
    78. Geldbach, T. J.; Pregosin, P. S. A Facile Synthesis of a Wide Variety of Cationic Ruthenium Hydrido-Arene Complexes of binap ( 1,1 -Binaphthalene-2,2 -diylbis(diphenylphosphane)) and MeO biphep ( 6,6 -Dimethoxybiphenyl-2,2 –diylbis (diphenylphosphane)). Helvetica Chem. Acta. 2002, 85, 3937-3948
    79. Rajanbabu, T. V.; Ayers, T. A.; Casalnuovo, A. L. J. Am. Chem. Soc. 1994, 116, 4101
    80. calone, M.; Waldmeier, P. Efficient Enantioselective Synthesis of the NMDA 2B Receptor Antagonist Ro 67-8867. Organic Process Research & Development. 2003, 7, 418-425
    81. Dominique, M. (Lonza A.-G., Switz.). Preparation of enantiomerically pure 1-substituted- 3-amino alcohols. EP 1566383 2005 (Chem. Abstr.2005, 143:248273)
    82. Dominique, M. (Lonza A.-G., Switz.). Process for the asymmetric hydrogenation of -amino ketones using transition metal complexes of chiral bidentate phosphines as catalysts. EP 1510517 2003 (Chem. Abstr.2005, 142:280046)
    83. Dominique, M.; Hanspeter, M.; John, M. (Lonza A.-G., Switz.).Process for the preparation of enantiomerically pure 1-substituted-3-aminoalcohols. WO 2005080370 2005 (Chem. Abstr.2005, 143:266590)
    84. Genet, J. P.; Pinel, C. V.; Ratovelomanana, V.; Mallart, S. Pfister, X.; Bischoff, L. Andrsde, M. C.; Darses, S.; Galopin, C. Laffitte, J. A. enantionselective hydrogenation reactions with fullset of preformed and prepared in situ chiral diphosphine-ruthenium catalysis. Tetrahedron Asymmetry, 1994, 4, 675–690
    85. Ratovelomanana, V.; Girard, C.; Touati, R.; Tranchier, J. P.; Hassine, B.; Genet, J. P.; Enantioselective Hydrogenation of -Keto Esters using Chiral Diphosphine-Ruthenium Complexes: Optimization for Academic and Industrial Purposes and Synthetic Applications. Adv. Synth. Catal. 2003, 345, 261 -274
    86. Labeeuw, O.; Phansavath, P.;Genet. A short total synthesis of sulfobacin A. Tetrahedron Letters.2003, 44, 6383–6386
    87. Labeeuw, O.; Blanc, B.; Phansavath, P.; Ratovelomanana, V.;Genet, J. P.An Efficient Ruthenium-Catalyzed Formal Synthesis of ( )-Isoavenaciolide. Eur. J. Org. Chem. 2004, 2352- 2358
    88. Desroy, N.; Roux, R. L.; Phansavath, P.; Chiummiento, L.; Bonini, C.; Genet, J.P. Stereoselective synthesis of C15 C24 and C25 C30 fragments of dolabelides. Tetrahedron Letters.2003, 44, 1763–1766
    89. Mordant, C.; Reymond, S.; Ratovelomanana, V.; Genet, J.P.Synthesis of both syn and anti diastereoisomers of Boc-dolaproine from (S)-proline through DKR using ruthenium-catalyzed hydrogenation: a dramatic role of N-protecting groups. Tetrahedron, 2004, 60, 9715–9723
    90. Labeeuw, O.; Phansavath, P.;Genet, J. P. Total synthesis of sulfobacin A through dynamic kinetic resolution of a racemic b-keto-a-amino ester hydrochloride.Tetrahedron Asymmetry, 2004, 15, 1899–1908
    91. Makino, K.; Hiroki, Y.; Hamada, Y.Dynamic Kinetic Resolution Catalyzed by Ir Axially Chiral Phosphine Catalyst: Asymmetric Synthesis of anti Aromatic a-Hydroxy-r-amino Acid Esters. J. Am. Chem. Soc. 2005, 127, 5784-5785
    92. Cederbaum, F.; Lamberth, C.; Malan, C.; Naud, F.; Spindler, F.; Studer, M.; Blaserb, H. U. Synthesis of Substituted Mandelic Acid Derivatives via Enantioselective Hydrogenation: Homogeneous versus Heterogeneous Catalysis. Adv. Synth. Catal. 2004, 346, 842- 848
    93. Maligres, P. E.; Krska, S. W.; Humphrey, G. R. Enantioselective Hydrogenation of r-Aryloxy r,a-Unsaturated Acids. Asymmetric Synthesis of r-Aryloxycarboxylic Acids. Org. Lett., 2004,18, 3147-3150
    94. Houpis, I. N.; Patterson, L. E.; Charles A. A.; Rizzo, J.R.; Zhang, T. Y.; Haurez; M.Synthesis of PPAR Agonist via Asymmetric Hydrogenation of a Cinnamic Acid Derivative and Stereospecific Displacement of (S)-2-Chloropropionic Acid. Org. Lett. 2005, 10, 1947-1950
    95. Kurt, P; Michelangelo, S. Process for the production of chiral propionic acid derivatives. US 2005070714 , 2005 (Chem. Abstr.2005,142:355259)
    96. Wang, W. B.; Lu, S. M.; Yang, P. Y.; Han, X. W.; Zhou, Y. G. Highly Enantioselective Iridium-Catalyzed Hydrogenation of Heteroaromatic Compounds, Quinolines. J. Am. Chem. Soc. 2003, 125, 10536-10537
    97. Zhou, Y. G.; Lu, S. m.; Yang, P. Y.; Wang, W. B.Ir-catalyzed enantioselective hydrogenation of substituted aromatic pyridine and pyrazine rings. CN 1468852 2004 (Chem. Abatr. 2005, 142, 316861) (周永贵, 卢胜梅, 杨鹏宇, 王文波. 对映选择性铱催化氢化取代芳香吡啶环和吡嗪环的方法. CN 1468852 2004)
    98. Yang, P. Y.; Zhou, Y. G. The enantioselective total synthesis of alkaloid ())-galipeine. Tetrahedron Asymmetry, 2004, 15, 1145–1149
    99. Kurt, P.; Michelangelo, S.; Wang, S. N. process for asymmetric hydrogenation of hexahydroisoquinolinium salts. WO2003078399, 2003 (Chem. Abstr.2003,.139:261167)
    100. Cobley, C. J.; Henschke, J. P. Enantioselective Hydrogenation of Imines Using a Diverse Library of Ruthenium Dichloride(diphosphine)(diamine) Precatalysts. Adv. Synth. Catal. 2003, 345, 195 -201
    101. lipshutz, B. H.; Servesko, J. M.; Petersen, T. B.; Papa, P.; Andrew A. L. Asymmetric 1,4-Reductions of Hindered a-Substituted Cycloalkenones Using Catalytic SEGPHOS -Ligated CuH. Org. Lett. 2004, 8, 1273-1275
    102. Lipshutz, B.H.; Frieman, B. A.; Unger, J.B.; Nihan, D. M. Thermally accelerated asymmetric hydrosilylations using ligated copper hydride. Canadian Journal of Chemistry. 2005, 83, 606-614.
    103. Rainka, M.P.; Milne,J.E.; Buchwald,S.L. Dynamic Kinetic Resolution of a,b-UnsaturatedLactones through Asymmetric Copper-Catalyzed Conjugate Reduction: Application to the Total Synthesis of Eupomatilone-3. Angew. Chem. Int. Ed. 2005, 44, 6177 –6180
    104. Oestreich,M; Fernando, S.C.;Machotta,A.B. Catalytic Desymmetrizing Intramolecular Heck Reaction: Evidence for an Unusual Hydroxy-Directed Migratory Insertion. Angew. Chem Int.Ed. 2005, 44,149~152
    105. Bercot, E. A.; Rovis; T. A Palladium-Catalyzed Enantioselective Alkylative Desymmetrization of meso-Succinic Anhydrides. J. Am.. Chem. Soc. 2004, 126, 10248-10249
    106. Sinou, D.; Rabeyrin, C.; Nguefack, C. Catalytic Asymmetric Alkylation in Water in the Presence of Surfactants. Adv. Synth. Catal. 2003, 345, 357 -363
    107. Labrosse, J. P.; Lhoste, P.; Sinou, D.; Asymmetric Palladium-Catalyzed Annulation of Benzene-1,2-diols and Propargylic Carbonates. Eur. J. Org. Chem. 2002, 1966 1971
    108. Koh, J. H.; Larsen, A. O.; White, P. S.; Gagne, M. R. Disparate Roles of Chiral Ligands and Molecularly Imprinted Cavitied in Asymmetric Catalysis And Chiral Poisoning. Organometallices. 2002, 21, 7-9
    109. Jang, H. Y.; Hughes, F. W.; Gong, H.; Zhang, J.; Brodbelt, J. S.; Krische, M. J. Enantioselective reductive cyclization of 1,6-enynes via rhodium-catalyzed asymmetric hydrogenation: C-C bond formation precedes hydrogen activation. J. Am. Chem. Soc. 2005, 127, 6174-6175.
    110. Doherty, S.; Knight, J. G.; Rakesh, K. R.; William C.; Harrington, R. W.; Newman, C. R.; Campbell, R.; Amin H.Ruthenium Complexes of Six-Electron-Donor NUPHOS-Type Diphosphines: Highly Selective Catalysts for the Hydrocarboxylation of Terminal Alkynes. Organometallics 2005, 24, 2633-2644
    111. Maerten, E.; Delerue, H.; Queste, M.; Nowicki, A.; Suisse, I.;Agbossou, N.F. Catalytic asymmetric carbonylative silylcarbocyclization of enynes. Tetrahedron: Asymmetry, 2004, 15, 3019–3022
    112. Huddleston, R. R.; Jang, H. Y.; Krische, M. J.First Catalytic Reductive Coupling of 1,3-Diynes to Carbonyl Partners: A New Regio- and Enantioselective C-C Bond Forming Hydrogenation. J. Am. Chem. Soc. 2003, 125, 11488-11489
    113. Wadamoto, M; Yamamoto, H. Silver-Catalyzed Asymmetric Sakurai-Hosomi Allylation of Ketones. J. Am. Chem. Soc. 2005, 127, 14556-14557
    114. Lam, H. W.; Joensuu, P. M.Cu(I)-Catalyzed Reductive Aldol Cyclizations: Diastereo- and Enantioselective Synthesis of a-Hydroxylactones.Org. Lett. 2005, 19, 4225-4228
    115. Yamamoto, Y.; Yamamoto, H. Catalytic asymmetric hetero Diels-Alder reaction of a heteroaromatic C-nitroso dienophile: a novel method for synthesis of chiral non-racemic amino alcohols. WO 2005068457,2005 (Chem. Abstr.2005,.143:172883)
    116. Suto, Y.; Tsuji, R.; Kanai, M.; Shibasaki. M. Cu(I)-Catalyzed Direct Enantioselective Cross Aldol-Type Reaction of Acetonitrile.Org. Lett.2005, 17, 3757-3760
    117. Berkowitz, D. B.; Maiti, G. Following an ISES Lead: The First Examples of Asymmetric Ni(0)-Mediated Allylic Amination. Org. Lett. 2004, 16, 2661-2664
    118. Lambert, J. B.; Jeung, H. S. Phosphonium ions rather than phosphenium ions from the reaction of secondary phosphine with trityl cation. J. Org. Chem. 1991, 56,5960-5962
    119. Rajanbabu, T. V.; Ayers, T. A.; Gary, A. H.; Kimberly, K. Y.; Joseph, C. Carbohydrate phosphintes as practical ligands in asymmetric catalysis: electronic effect and dependence of backbone chirality in Rh-catalyzed asymmetric hydrogenations. J. Org. Chem. 1997, 62,6012-6028
    120. Brown, K. J.; Berry, M. S.; Waterman, K. C.; Lingenfelter D.; Murdoch, J. R. J. Am. Chem. Soc. 1984, 106, 4717.
    121. Fang, C. M.; Ma, M. L.; Zheng, X.. L.; Guo, Y.; Peng, Z. H.; Chen, H.; Li, X. J. Improvement on the Synthesis of Chiral Biphenyl Diphosphine Ligands. Chinese Journal of Organic Chemistry. 2006, 26, 252-255(in Chinese) 方春梅, 马梦林, 郑学丽, 郭 妤, 彭宗海, 陈 华, 李贤均. 有机化学, 2006, 26, 252-255
    122. Grabiak, R. C.; Miles, J. A.; Schwenzer, G. M. Phosphorus and Sulfur and the Related Elements. 1980, 9, 197.
    123. Toshikazu, H.; Toshio, M.; Yoshikiki, O.; Toshi, A. A novel synthesis of dialkyl arenephosphonates. Synthesis communication .1981, 56-57
    124. Abdelkader, B.; Elie, A. J.; Noel, C. A remarkable accelerating effect of iodide ions in the photostimulated phosphonylation of bromoaromatic compounds. J. Orgnometallic Chem.1992, 440, 297-301
    125. Atsuhiro, O.; Nobuko, O.; Yoshiki, Y.; Hitomi, S. Synthesis of arenephosphonates by copper iodidepromoted arylation of phosphate anions. Synthesis communication .1983, 69-70
    126. Maatschappij, N. V. Aryl and vinylphosphonates. Fr 1604652, 1972; (Chem. Abstr.1972, 77, 152351).
    127. David, W. A.; Barrie, G. H.; Malcolm, T. J. the chemistry of heteroarylphosphorus compound. Aryl-phosphonate ester. J. Chem. Soc., Perkin Trans. 1 1977, 789
    128. Sentenov, V. V.; Krasilnikova, E. A.; Berdnik, I. V. Mechanism of catalysis of Arbuzov reaction with transition-mete complexes. Effect of aryl halides on the course of Arbuzov reaction catalyzed by metal complexs. Zh. Obshch. Khim. 1989, 59, 3692; (Chem. Abstr. 1990, 112, 217085)
    129. Angel, G.; Ricardo, A.; Eduardo, D. synthesis of Aryl-phosphonate ester by reaction of Grignard reagents with diethyl cyanophosphonate. Synthesis communication .1999, 29, 3021-3024
    130. WANG, J.; IANG, F. C. Recent Development of Microwave Induced Organic Reaction. Chinese Journal of Organic Chemistry. 2002, 22, 212-219 (in chinese). (王静, 姜凤超.微波有机合成反应的新进展. 有机化学, 2003, 23,919-932)
    131. Abdelkader, B.; Elie, A. J.; Noel, C. Side-chain metallation of diethyl phosphonotoluenes. J. Orgnometallic Chem. 1994, 466, 89-94
    132. Maier, L. A convenient, one-step synthesis of alkyl- and arylphsophonyl dichlorides. Phosphorus, Sulfur, and sillcon. 1990, 47, 465-470
    133. 邓红霞, 孔小林.二苯甲酰-D-酒石酸及其一水盐的合成. 浙江化工, 2003, 16
    134. Bogdal, D.; Pielichowski, J.; Boron, A. New synthetic method of aromatic ethers under microwave irradiation in dry media. Synthetic Communications 1998, 16, 3029-3039
    135. Cenini, S.; Porta, F.; Pizzotti, M. J. Mol. Catal. 1982, 15, 297.
    136. Kamaluddin, A. R..; Lough, A.J. Morris, R. H. Orgnanometallics. 2001, 20, 1047.
    137. Kamaluddin, A. R..; M. Faatz, A. J Alan, R. H. Morris, J. Am. Chem. Soc. 2001,123,7473
    138. Genet, J. P.; Pinel, C.; Ratovelomanana, V. V.; Mallart, S.; Pfister, X.; Deandrade, M. C.; Laffitte, J. A. Tetrahedron: Asymmetry, 1994, 5, 665.
    139. Akotsi, O. M.; Metera, K.; Reid, R. D.; Macdonald, R.; Bergens, S. H. Chirality. 2000, 12, 514
    140. Doucet, H.; Okhuma, T.; Murata, K.; Yokozawa, T.; Kozawa, M.; Katayama, E.; England, A. F.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. 1998, 37, 1703–1707.
    141. Xiong, W.; Lin, Q.; Ma, H. X..; Hong, Y. Y.; Chen, H.; Li, X. J. Asymmetric Hydrogenation of Aromatic Ketones in Ionic-Liquid Media Catalyzed By Ru-TPPTS-(1S, 2S)-DPENDS Complexes. Tetrahedron Asymmetry. 2005, 16, 1959
    142. Sandoval. C. A, Ohkuma. L, Munlz. K, Noyori. R. J. Am. Chem. Soc. 2003, 125,:13490
    143. Rashid. K. A, Faatz. M, Lough. A. J, Morris. R. H. J. Am. Chem. Soc. 2001,123, 7473
    144. Synthes is of new types of chiral α-acetylamino-β-aryl acrylic acid compounds Huaxue Shiji, 2002, 24 , 365-366(in Chinese) (陈晓彬, 几种手性 α-乙酰氨基-β-芳基丙烯酸类化合物的合成. 化学试剂, 2002, 24, 365-366)
    145. Synthes is of new types of chiral (Z)-2-acetylamino-3-aryl acrylic acid compounds J. Hubei univwrsity (Nature science edition). 2002, 24 , 256-258(in Chinese) (陈晓彬, 几种手性(Z)-2-乙酰氨基-3-芳基丙烯酸类化合物的合成. 湖北大学学报(自然科学版), 2002, 24, 256-258)

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