[ 1 ] Zhan B Z, Thompson A. Tetrahedron , 2004 , 60 : 2917 —2935
[ 2 ] Ten Brink G J , Arends I W C E , Sheldon R A. Science , 2000 ,287 : 1636 —1639
[ 3 ] Guan B T, Xing D , Shi Z J , et al . J . Am. Chem. Soc. , 2005 ,127 : 18004 —18005
[ 4 ] Sheldon R A , Arends I W C E , Dijksman A. Catalysis Today ,2000 , 57 : 157 —166
[ 5 ] Mallat T, Baiker A. Chem. Rev. , 2004 , 104 : 3037 —3058
[ 6 ] Enache D I , Edwards J K, Hutchings GJ , et al . Science , 2006 ,311 : 362 —364
[ 7 ] Son Y C , Makwana V D , Suib S L , et al . Angew. Chem. Int .Ed. , 2001 , 40 : 4280 —4083
[ 8 ] Musawir M, Davey P N , Kozhevnikov I V , et al . Chem.Commun. , 2003 , 1414 —1415
[ 9 ] Krishnaveni N S , Surendra K, Rao K R. Adv. Synth. Catal . ,2004 , 346 : 346 —350
[10] Edegger K, Mang H , Kroutil W, et al , J . Mol . Catal . A:Chem. , 2006 , 251 : 66 —70
[11] Csjernyik G, *ll A H , Báckvall J E , et al . J . Org. Chem. ,2002 , 67 : 1657 —1662
[12] Adam W, Saha-Mê ller C R , Ganeshpure P A. Chem. Rev. ,2001 , 101 : 3499 —3548
[13] De Nooy A EJ , Besemer A C , van Bekkum H. Synthesis , 1996 ,1153 —1176
[14] Sheldon R A , Arends I W C E. Adv. Synth. Catal . , 2004 , 346 :1051 —1071
[15] Sheldon R A , Arends I W C E. J . Mol . Catal . A: Chem. ,2006 , 251 : 200 —214
[16] Sheldon R A , Arends I W C E , Brink GJ T. Acc. Chem. Res. ,2002 , 35 : 774 —781
[17] Calderon F. Synlett , 2006 , 657 —658
[18] Minisci F , Punta C , Recupero F. J . Mol . Catal . A: Chem. ,2006 , 251 : 129 —149
[19] Minisci F , Recupero F , Pedulli G F , et al . J . Mol . Catal . A:Chem. , 2003 , 204P205 : 63 —90
[20] Caron S , Dugger R W, Ripin D H B , et al . Chem. Rev. , 2006 ,106 : 2943 —2989
[21] Bjärsvik H R , Liguori L , Minisci F , et al . Org. Proc. Res.Dev. , 2002 , 6 : 197 —200
[22] Fritz-Langhals E. Org. Proc. Res. Develop. , 2005 , 9 : 577 —582
[23] Bragd P L , van Bekkum H , Besemer A C. Topics Catal . , 2004 ,27 : 49 —66
[24] Mahoney L R , Mendenhall G D , Ingold K U. J . Am. Chem.Soc. , 1973 , 95 : 8610 —8614
[25] Ganiev I M, Timerghazin Q K, Khalizov A F , et al . J . Phys.Org. Chem. , 2001 , 14 : 38 —42
[26] Minisci F , Recupero F , Cecchetto A , et al . Eur. J . Org.Chem. , 2004 , 109 —119
[27] Ma Z K, Bobbitt J M. J . Org. Chem. , 1991 , 56 : 6110 —6114
[28] Golubev V A , Rozantsev E G, Neiman M B. Bull . Acad. Sci .USSR , Chem. Ser. , 1965 , 14 : 1898
[29] Rychovsky S D , Vaidyanathan R. J . Org. Chem. , 1999 , 64 :310 —312
[30] Bolm C , Magnus A S , Hildebrand J P. Org. Lett . , 2000 , 2 :1173 —1175
[31] Hunter D H , Barton D H R , Motherwell WJ . Tetrahedron Lett . ,1984 , 25 : 603 —606
[32] Kim S S , Nehru K. Synlett , 2002 , 616 —618
[33] De Luca L , Giacomelli G, Masala S , Porcheddu A. J . Org.Chem. , 2003 , 68 : 4999 —5001
[34] De Luca L , Giacomelli G, Porcheddu A. Org. Lett . , 2001 , 3 :3041 —3043
[35] Semmelhack M F , Chou C S , Cortes D A. J . Am. Chem. Soc. ,1983 , 105 : 4492 —4494
[36] Palmisano G, Ciriminna R , Pagliaro M. Adv. Synth. Catal . ,2006 , 348 : 2033 —2037
[37] Anelli P L , Biffi C , Montanari F , Quici S. J . Org. Chem. ,1987 , 52 : 2559 —2562
[38] Anelli P L , Banfi S , Montanari F , Quici S. J . Org. Chem. ,1989 , 54 : 2970 —2972
[39] Anelli P L , Montanari F , Quici S. Org. Synth. , 1990 , 69 :212 —219
[40] Lin F , Peng W, Yu B , et al . Carbohydr. Res. , 2004 , 339 :1409 —1409
[41] Zhao M Z, Li J , Mano E , Reider P J , et al . J . Org. Chem. ,1999 , 64 : 2564 —2566
[42] Melvin F , McNeill A , Herbert R B , et al . Tetrahedron Lett . ,1999 , 40 : 1201 —1202
[43] Semmelhack M F , Schmid C R , Cortés D A , et al . J . Am.Chem. Soc. , 1984 , 106 : 3374 —3376
[44] Betzemeier B , Cavazzini M, Knochel P , et al . Tetrahedron Lett . ,2000 , 41 : 4343 —4346
[45] Ragagnin G, Betzemeier B , Knochel P , et al . Tetrahedron ,2002 , 58 : 3985 —3991
[46] Gamez P , Arends I W C E , Sheldon R A , et al . Chem.Commun. , 2003 , 2414 —2415
[47] Gamez P , Arends I W C E , Sheldon R A , et al . Adv. Synth.Catal . , 2004 , 346 : 805 —811
[48] Striegler S. Tetrahedron , 2006 , 62 : 9109 —9114
[49] Jiang N , Ragauskas A J . J . Org. Chem. , 2006 , 71 : 7087 —7090
[50] Jiang N , Ragauskas A J . Org. Lett . , 2005 , 7 : 3689 —3692
[51] Velusamy S , Srinivasan A , Punniyamurthy T. Tetrahedron Lett . ,2006 , 47 : 923 —926
[52] Boudreau J , Doucette M, Ajjou A N. Tetrahedron Lett . , 2006 ,47 : 1695 —1698
[53] Velusamy S , Punniyamurthy T. Eur. J . Org. Chem. , 2003 ,3913 —3915
[54] Cecchetto A , Fontana F , Miniscia F , et al . Tetrahedron Lett . ,2001 , 42 : 6651 —6653
[55] Dijksman A , Arends I W C E , Sheldon R A. Chem. Commun. ,1999 , 1591 —1592
[56] Dijksman A , Arends I W C E , Sheldon R A , et al . J . Am.Chem. Soc. , 2001 , 123 : 6826 —6833
[57] Kim S S , Jung H C. Synthesis , 2003 , 2135 —2137
[58] Wang N W, Liu R H , Liang X M, et al . Chem. Commun. ,2005 , 5322 —5324
[59] Yang G Y, Ma J P , Wang W, et al . Catal . Lett . , 2006 , 112 :83 —87
[60] Lenoir D. Angew. Chem. Int . Ed. , 2006 , 45 : 3206 —3210
[61] Liu R H , Liang X M, Hu X Q , et al . J . Am. Chem. Soc. ,2004 , 126 : 4112 —4113
[62] Liu R H , Liang X M, Hu X Q , et al . J . Org. Chem. , 2005 ,70 : 729 —731
[63] Xie Y, Mo W M, Hu X Q , et al . J . Org. Chem. , 2007 , 72 :4288 —4291
[64] Miller R A , Hoerrner R S. Org. Lett . , 2003 , 5 : 285 —287
[65] Lei M, Hu R J , Wang Y G. Tetrahedron , 2006 , 62 : 8928 —8932
[66] Vatele J M. Synlett , 2006 , 2055 —2058
[67] Schulze A , Giannis A. Synthesis , 2006 , 257 —260
[68] De Mico A , Margarita R , Piancatelli G, et al . J . Org. Chem. ,1997 , 62 : 6974 —6977
[69] Vatèle J M. Tetrahedron Lett . , 2006 , 47 : 715 —718
[70] Tashino Y, Togo H. Synlett , 2004 , 2010 —2012
[71] Sakuratani K, Togo H. Synthesis , 2003 , 21 —23
[72] Herrerías C I , Zhang T Y, Li CJ . Tetrahedron Lett . , 2006 , 47 :13 —17
[73] Fabbrini M, Galli C , Macchitella D , et al . Tetrahedron Lett . ,2001 , 42 : 7551 —7553
[74] Baiocco P , Barreca A M, Galli C , et al . Org. Biomol . Chem. ,2003 , 1 : 191 —197
[75] Galli C , Gentili P. J . Phys. Org. Chem. , 2004 , 17 : 973 —977
[76] Fabbrini M, Galli C , Gentili P J . Mol . Catal . B : Enz. , 2002 ,16 : 231 —240
[77] Arends I W C E , Li Y X, Sheldon R A , et al . Tetrahedron ,2006 , 62 : 6659 —6665
[78] Kulys J , Vidziunaite R. J . Mol . Catal . B : Enz. , 2005 , 37 :79 —83
[79] Ciriminna R , Bolm C , Pagliaro M, et al . Adv. Synth. Catal . ,2002 , 344 : 159 —163
[80] Bolm C , Fey T. Chem. Commun. , 1999 , 1795 —1796
[81] Testa M L , Ciriminna R , Pagliaro M, et al . Adv. Synth. Catal . ,2004 , 346 : 655 —660
[82] Ciriminna R , Pagliaro M. Adv. Synth. Catal . , 2003 , 345 :383 —388
[83] Ciriminna R , Blum J , Avnir D , Pagliaro M. Chem. Commun. ,2000 , 1441 —1442
[84] Brunel D , Fajula F , Nagy J B , et al . Appl . Catal . A: Gen. ,2001 , 213 : 73 —82
[85] Brunel D , Lentz P , Sutra P , et al . Stud. Surf . Sci . Catal . ,1999 , 125 : 237 —244
[86] Dijksman A , Arends I W C E , Sheldon R A. Chem. Commun. ,2000 , 271 —272
[87] Dijksman A , Arends I W C E , Sheldon R A. Synlett , 2001 ,102 —104
[88] Minisci F , Recupero F , Rodino M, et al . Org. Process Res.Dev. , 2003 , 7 : 794 —798
[89] Ferreira P , Hayes W, Tsang S C , et al . Green Chem. , 2004 , 6 :310 —312
[90] Benaglia M, Puglisi A , Pozzi G, et al . Tetrahedron , 2005 , 61 : 12058 —12064
[91] Pozzi G, Cavazzini M, Quici S , et al . Org. Lett . , 2004 , 6 :441 —443
[92] Cozzi F. Adv. Synth. Catal . , 2006 , 348 : 1367 —1390
[93] Gilhespy M, Lok M, Baucherel X. Catal . Today , 2006 , 117 :114 —119
[94] Gilhespy M, Lok M, Baucherel X. Chem. Commun. , 2005 ,1085 —1086
[95] Tanyeli C , Gümüä A. Tetrahedron Lett . , 2003 , 44 : 1639 —1642
[96] Kashiwagi Y, Ikezoe H , Ono T. Synlett , 2006 , 69 —72
[97] Wu X E , Ma L , Gao L X, et al . Synlett , 2005 , 607 —610
[98] Holczknecht O , Cavazzini M, Pozzi G, et al . Adv. Synth.Catal . , 2005 , 347 : 677 —688
[99] Pozzi G, Cavazzini M, Holczknecht O , et al . Tetrahedron Lett . ,2004 , 45 : 4249 —4251
[100] Gheorghe A , Cuevas2Yanez E , Reiser O , et al . Synlett , 2006 ,2767 —2770 |