Subscribe to RSS
DOI: 10.1055/s-0031-1289296
[2.2]Paracyclophane Derivatives: Synthesis and Application in Catalysis
Publication History
Publication Date:
19 October 2011 (online)
Abstract
Advances in the field of [2.2]paracyclophane chemistry are reviewed including syntheses, resolution of enantiomers and application in organic synthesis. Transition-metal catalyzed as well as organocatalytic transformations are presented focusing on the development of [2.2]paracyclophane derived ligands and catalysts.
1 Introduction
2 [2.2]Paracyclophane Syntheses
3 Ligand Design on the Basis of [2.2]Paracyclophane
4 Application in Asymmetric Catalysis
4.1 Addition of Organozinc Reagents to Carbonyl Compounds
4.2 Application of [2.2]Paracyclophane-Derived Phosphines
4.2.1 Hydrogenation Reactions
4.2.2 Transition-Metal-Catalyzed C-C and C-X Bond Formation Employing Planar-Chiral Phosphines
4.2.3 Planar-Chiral Carbenes
4.2.4 [2.2]Paracyclophanes in Organocatalysis
5 Summary
Key words
[2.2]paracyclophane - catalyst - asymmetric synthesis - phosphine - carbine - hydrogen bond - hydrogenation - cross-coupling
-
1a
Gleiter R.Hopf H. Modern Cyclophane Chemistry Wiley-VCH; Weinheim: 2004. -
1b
Vögtle F. Cyclophane Chemistry Wiley; New York: 1993. - 2
Hopf H. Angew. Chem. Int. Ed. 2008, 47: 9808 ; Angew. Chem. 2008, 120, 9954 - 3
Pye PJ.Rossen K.Reamer RA.Tsou NN.Volante RP.Reider PJ. J. Am. Chem. Soc. 1997, 119: 6207 - 4
Rozenberg V.Sergeeva E.Hopf H. In Modern Cyclophane ChemistryGleiter R.Hopf H. Wiley-VCH; Weinheim: 2004. p.435-462 - 5
Gibson SE.Knight JD. Org. Biomol. Chem. 2003, 1: 1256 -
6a
Hopf H. Org. Synth. 1981, 60: 41 -
6b
Winberg HE.Fawcett FS. Org. Synth., Coll. Vol. V Wiley and Sons; New York: 1973. p.883 -
6c
Winberg HE.Fawcett FS.Mochel WE.Theobald CW. J. Am. Chem. Soc. 1960, 82: 1428 - 7
Longone DT.Reetz MT. Chem. Commun. 1967, 46 - 8
Chow H.-F.Low K.-H.Wong KY. Synlett 2005, 2130 - 9
Dolbier WR.Xie P.Zhang L.Xu W.Chang Y.Abboud KA. J. Org. Chem. 2008, 73: 2469 - 10
Zhang L.Ogawa K.Ghiviriga I.Dolbier WR.
J. Org. Chem. 2009, 74: 6831 - 11
Friedmann CJ.Ay S.Bräse S. J. Org. Chem. 2010, 75: 4612 - 12
Rowlands GJ.Seacome RJ. Beilstein J. Org. Chem. 2009, No. 5 -
13a
Rowlands GJ. Org. Biomol. Chem. 2008, 6: 1527 -
13b
Hitchcock PB.Rowlands GJ.Seacome RJ. Org. Biomol. Chem. 2005, 3: 3873 - 14
Reich HJ.Yelm KE. J. Org. Chem. 1991, 56: 5672 -
15a
Quesnelle C.Iihama T.Aubert T.Perrier H.Snieckus V. Tetrahedron Lett. 1992, 33: 2625 -
15b
Snieckus V. Chem. Rev. 1990, 90: 879 -
16a
Knochel P.Melzig L.Rauhut CB.Naredi-Rainer N. Chem. Eur. J. 2011, 17: 5361 -
16b
Knochel P.Melzig L.Rauhut CB. Synthesis 2009, 1041 -
16c
Knochel P.Melzig L.Rauhut CB. Chem. Commun. 2009, 3536 -
16d
Knochel P.Rauhut CB.Melzig L. Org. Lett. 2008, 10: 3891 -
16e
Kopp F.Sklute G.Polborn K.Marek I.Knochel P. Org. Lett. 2005, 7: 3789 -
17a
Parmar R.Coles MP.Hitchcock PB.Rowlands GJ. Synthesis 2010, 4177 -
17b
Hitchcock PB.Rowlands GJ.Parmar R. Chem. Commun. 2005, 4219 - 18
Jiang B.Zhao X.-L. Tetrahedron: Asymmetry 2004, 15: 1141 - 19
Zhuravsky R.Starikova Z.Vorontsov E.Rozenberg V. Tetrahedron: Asymmetry 2008, 19: 216 - 20
Braddock DC.MacGilp ID.Perry BG. J. Org. Chem. 2002, 67: 8679 -
21a
Rozenberg V.Zhuravsky R.Sergeeva E. Chirality 2006, 18: 95 -
21b
Rozenberg VI.Antonov DY.Zhuravsky RP.Vorontsov EV.Starikova ZA. Tetrahedron Lett. 2003, 44: 3801 - 22
Kreis M.Nieger M.Bräse S. J. Organomet. Chem. 2006, 691: 2171 -
23a
Duthaler RO.Hafner A. Chem. Rev. 1992, 92: 807 -
23b
Soai K.Niwa S. Chem. Rev. 1992, 92: 833 -
23c
Rossiter BE.Swingle NM. Chem. Rev. 1992, 92: 771 -
24a
Maruoka K. Pure Appl. Chem. 2002, 74: 123 -
24b
Maruoka K.Ooi T.Miura T. Angew. Chem. Int. Ed. 1998, 37: 2347 ; Angew. Chem. 1998, 110, 2524 -
24c
Lewis Acid
Reagents: A Practical Approach
Yamamoto H. Oxford University Press; New York: 1999. - 25
Sergeeva EV.Rozenberg VI.Antonov DY.Vorontsov EV.Starikova ZA.Fedyanin IV.Hopf H. Chem. Eur. J. 2005, 11: 6944 -
26a
Atkinson RCJ.Gibson VC.Long NJ. Chem. Soc. Rev. 2004, 33: 313 -
26b
Colacot TJ. Chem. Rev. 2003, 103: 3101 -
27a
Togni A.Haltermann RL. Metallocenes Wiley-VCH; Weinheim: 1998. -
27b
Togni A. Angew. Chem. Int. Ed. 1996, 35: 1475 ; Angew. Chem. 1996, 108, 1581 -
27c
Togni A. Ferrocenes: Homogeneous Catalysis/Organic Synthesis/Materials Science Wiley-VCH; Weinheim: 1994. - 28
Rozenberg VI.Danilova TI.Sergeeva EV.Shouklov IA.Starikova ZA.Hopf H.Kuhlein K. Eur. J. Org. Chem. 2003, 432 - 29
Enders D.Noll S.Raabe G.Runsink J. Synthesis 2008, 1288 - 30
Enders D.Noll S.Bats JW. Synlett 2005, 2679 - 31
Enders D.Job A.Janeck CF.Bettray W.Peters R. Tetrahedron 2002, 58: 2253 - 32
Bosnich B.Gavrilova AL. Chem. Rev. 2004, 104: 349 -
33a
Gladiali S.Mroczek A.Erre G.Taras R. Tetrahedron: Asymmetry 2010, 21: 1921 -
33b
Stoccoro S.Soro B.Minghetti G.Zucca A.Cinellu MA.Manassero M.Gladiali S. Inorg. Chim. Acta 2006, 359: 1879 -
33c
Chelucci G.Murineddu G.Pinna GA. Tetrahedron: Asymmetry 2004, 15: 1373 -
33d
von Zelewsky A.Mamula O. Coord. Chem. Rev. 2003, 242: 87 -
33e
Chelucci G.Gladiali S.Sanna MG.Brunner H. Tetrahedron: Asymmetry 2000, 11: 3419 -
33f
Bark T.Von Zelewsky A. Chimia 2000, 54: 589 -
33g
Bolm C.Schlingloff G.Harms K. Chem. Ber. 1992, 125: 1191 -
33h
Bolm C. Tetrahedron: Asymmetry 1991, 2: 701 - 34
Fu GC. Acc. Chem. Res. 2006, 39: 853 -
35a
Wörsdörfer U.Vögtle F.Glorius F.Pfaltz A. J. Prakt. Chem. 1999, 341: 445 -
35b
Wörsdörfer U.Vögtle F.Nieger M.Waletzke M.Grimme S.Glorius F.Pfaltz A. Synthesis 1999, 597 - 36
Hopf H.Aly AA.Swaminathan VN.Ernst L.Dix I.Jones PG. Eur. J. Org. Chem. 2004, 68 - 37
Ricci G.Ruzziconi R.Giorgio E. J. Org. Chem. 2005, 70: 1011 - 38
Falk H.Reichroh P.Schlögl K. Tetrahedron 1970, 26: 511 - 39
Pu L.Yu HB. Chem. Rev. 2001, 101: 757 -
40a
Kozlowski MC.Fennie MW.DiMauro EF.O’brien EM.Annamalai V. Tetrahedron 2005, 61: 6249 -
40b
Dahmen S.Bräse S. Chem. Commun. 2002, 26 -
40c
Carreira EM.Frantz DE.Fassler R. J. Am. Chem. Soc. 2000, 122: 1806 -
40d
Ye MC.Logaraj S.Jackman LM.Hillegass K.Hirsh KA.Bollinger AM.Grosz AL.Mani V. Tetrahedron 1994, 50: 6109 -
41a
Rozenberg V.Danilova T.Sergeeva E.Vorontsov E.Starikova Z.Korlyukov A.Hopf H. Eur. J. Org. Chem. 2002, 468 -
41b
Hopf H.Barrett DG. Liebigs Ann. 1995, 449 -
41c
Antonov DY.Belokon YN.Ikonnikov NS.Orlova SA.Pisarevsky AP.Raevski NI.Rozenberg VI.Sergeeva EV.Struchkov YT.Tararov VI.Vorontsov EV. J. Chem. Soc., Perkin Trans. 1 1995, 1873 -
41d
Rozenberg V.Kharitonov V.Antonov D.Sergeeva E.Aleshkin A.Ikonnikov N.Orlova S.Belokon Y. Angew. Chem. Int. Ed. 1994, 33: 91 ; Angew. Chem. 1994, 106, 106 -
42a
Dahmen S. Org. Lett. 2004, 6: 2113 -
42b
Dahmen S.Bräse S. Org. Lett. 2001, 3: 4119 - 43
Höfener S.Lauterwasser F.Bräse S. Adv. Synth. Catal. 2004, 346: 755 -
44a
Kagan HB.Girard C. Angew. Chem. Int. Ed. 1998, 37: 2923 ; Angew. Chem. 1998, 110, 3088 -
44b
Kitamura M.Okada S.Suga S.Noyori R. J. Am. Chem. Soc. 1989, 111: 4028 - 45
Lauterwasser F.Vanderheiden S.Bräse S. Adv. Synth. Catal. 2006, 348: 443 -
46a
Podlech J.Gehring T. Angew. Chem. Int. Ed. 2005, 44: 5776 ; Angew. Chem. 2005, 117, 5922 -
46b
Bolm C.Bienewald F.Seger A. Angew. Chem. Int. Ed. 1996, 35: 1657 ; Angew. Chem. 1994, 108, 1767 -
46c
Soai K.Hori H.Kawahara M. J. Chem. Soc., Chem. Commun. 1992, 106 -
46d
Soai K.Niwa S.Hori H. J. Chem. Soc., Chem. Commun. 1990, 982 - 47
Antonov DY.Rozenberg VI.Danilova TI.Starikova ZA.Hopf H. Eur. J. Org. Chem. 2008, 1038 - 48
Rozenberg VI.Antonov DY.Sergeeva EV.Vorontsov EV.Starikova ZA.Fedyanin IV.Schulz C.Hopf H. Eur. J. Org. Chem. 2003, 2056 - 49
Bolm C.Whelligan DK. Adv. Synth. Catal. 2006, 348: 2093 - 50
Xin DY.Ma YD.He FY. Tetrahedron: Asymmetry 2010, 21: 333 - 51
Danilova TI.Rozenberg VI.Sergeeva EV.Starikova ZA.Bräse S. Tetrahedron: Asymmetry 2003, 14: 2013 - 52
Belokon Y.Moscalenko M.Ikonnikov N.Yashkina L.Antonov D.Vorontsov E.Rozenberg V. Tetrahedron: Asymmetry 1997, 8: 3245 -
53a
Garcia H.Baleizao C. Chem. Rev. 2006, 106: 3987 -
53b
Gilheany DG.McGarrigle EM. Chem. Rev. 2005, 105: 1563 - 54
Hosoya N.Hatayama A.Irie R.Sasaki H.Katsuki T. Tetrahedron 1994, 50: 4311 - 55
Shi M.Wang CJ. Tetrahedron: Asymmetry 2002, 13: 2161 - 56
Sawamura M.Sasaki H.Nakata T.Ito Y. Bull. Chem. Soc. Jpn. 1993, 66: 2725 -
57a
Danilova TI.Rozenberg VI.Starikova ZA.Bräse S. Tetrahedron: Asymmetry 2004, 15: 223 -
57b
Danilova TI.Rozenberg VI.Vorontsov EV.Starikova ZA.Hopf H. Tetrahedron: Asymmetry 2003, 14: 1375 -
58a
Kelly BG.Gilheany DG. Tetrahedron Lett. 2002, 43: 887 -
58b
Krause N.Hoffmann-Roder A. Synthesis 2001, 171 - 59
Knochel P.Perea JJA.Jones P. Tetrahedron 1998, 54: 8275 -
60a
Sprout CM.Seto CT. J. Org. Chem. 2003, 68: 7788 -
60b
Nugent WA. Org. Lett. 2002, 4: 2133 -
60c
Long J.Ding KL. Angew. Chem. Int. Ed. 2001, 40: 544 ; Angew. Chem. 2001, 113, 562 -
61a
Ay S.Ziegert RE.Zhang H.Nieger M.Rissanen K.Fink K.Kubas A.Gschwind RM.Bräse S. J. Am. Chem. Soc. 2010, 132: 12899 -
61b
Ay S.Nieger M.Bräse S. Chem. Eur. J. 2008, 14: 11539 -
61c
Bräse S.Hoefener S. Angew. Chem. Int. Ed. 2005, 44: 7879 ; Angew. Chem. 2005, 117, 8091 - 62
Bräse S.Hermanns N.Dahmen S.Bolm C. Angew. Chem. Int. Ed. 2002, 41: 3692 ; Angew. Chem. 2002, 114, 3844 - 63
Pietrusiewicz KM.Zablocka M. Chem. Rev. 1994, 94: 1375 - 64
Knowles WS.Noyori R. Acc. Chem. Res. 2007, 40: 1238 - 65
Noyori R.Takaya H. Acc. Chem. Res. 1990, 23: 345 -
66a
Wu J.Chen H.Kwok W.Guo RW.Zhou ZY.Yeung C.Chan ASC. J. Org. Chem. 2002, 67: 7908 -
66b
Ohkuma T.Koizumi M.Yoshida M.Noyori R. Org. Lett. 2000, 2: 1749 -
66c
Noyori R.Ohkuma T. Pure Appl. Chem. 1999, 71: 1493 -
66d
Mikami K.Korenaga T.Terada M.Ohkuma T.Pham T.Noyori R. Angew. Chem. Int. Ed. 1999, 38: 495 ; Angew. Chem. 1999, 111, 517 -
66e
Cao P.Zhang XM. J. Org. Chem. 1999, 64: 2127 -
66f
Noyori R.Doucet H.Ohkuma T.Murata K.Yokozawa T.Kozawa M.Katayama E.England AF.Ikariya T. Angew. Chem. Int. Ed. 1998, 37: 1703 ; Angew. Chem. 1995, 110, 1792 -
66g
Noyori R.Ohkuma T.Koizumi M.Doucet H.Pham T.Kozawa M.Murata K.Katayama E.Yokozawa T.Ikariya T. J. Am. Chem. Soc. 1998, 120: 13529 -
66h
Ohkuma T.Ooka H.Hashiguchi S.Ikariya T.Noyori R. J. Am. Chem. Soc. 1995, 117: 2675 -
66i
Ohkuma T.Ooka H.Ikariya T.Noyori R. J. Am. Chem. Soc. 1995, 117: 10417 - 67
Cheemala MN.Gayral M.Brown JM.Rossen K.Knochel P. Synthesis 2007, 3877 - 68
Dominguez B.Zanotti-Gerosa A.Hems W. Org. Lett. 2004, 6: 1927 - 69
Messerle BA.Field LD.Vuong KQ.Turner P. Organometallics 2005, 24: 4241 -
70a
Focken T.Raabe G.Bolm C. Tetrahedron: Asymmetry 2004, 15: 1693 -
70b
Bolm C.Focken T.Raabe G. Tetrahedron: Asymmetry 2003, 14: 1733 -
71a
Trost BM.Fandrick DR. Aldrichimica Acta 2007, 40: 59 -
71b
Trost BM. Acc. Chem. Res. 2006, 39: 747 -
71c
Trost BM. J. Org. Chem. 2004, 69: 5813 -
71d
Trost BM.Crawley ML. Chem. Rev. 2003, 103: 2921 -
71e
Trost BM.VanVranken DL. Chem. Rev. 1996, 96: 395 -
71f
Trost BM. Acc. Chem. Res. 1996, 29: 355 -
72a
Whelligan DK.Bolm C. J. Org. Chem. 2006, 71: 4609 -
72b
Wu XW.Yuan K.Sun W.Zhang MJ.Hou XL. Tetrahedron: Asymmetry 2003, 14: 107 - 73
Jiang B.Lei Y.Zhao X.-L. J. Org. Chem. 2008, 73: 7833 - 74
Lyubimov SE.Zhuravskii RP.Rozenberg VI.Safronov AS.Petrovskii PV.Davankov VA. Russ. Chem. Bull. 2008, 57: 137 -
75a
Surry DS.Buchwald SL. Chem. Sci. 2011, 2: 57 -
75b
Surry DS.Buchwald SL. Chem. Sci. 2011, 2: 27 -
75c
Surry DS.Buchwald SL. Angew. Chem. Int. Ed. 2008, 47: 6338 ; Angew. Chem. 2008, 120, 6438 -
76a
Beller M.Schulz T.Torborg C.Schaffner B.Huang J.Zapf A.Kadyrov R.Borner A. Angew. Chem. Int. Ed. 2009, 48: 918 ; Angew. Chem. 2009, 121, 936 -
76b
Beller M.Schulz T.Torborg C.Enthaler S.Schaffner B.Dumrath A.Spannenberg A.Neumann H.Borner A. Chem. Eur. J. 2009, 15: 4528 -
76c
Sergeev AG.Schulz T.Torborg C.Spannenberg A.Neumann H.Beller M. Angew. Chem. Int. Ed. 2009, 48: 9391 ; Angew. Chem. 2009, 121, 7731 -
76d
Harkal S.Rataboul F.Zapf A.Fuhrmann C.Riermeier T.Monsees A.Beller M. Adv. Synth. Catal. 2004, 346: 1742 - 77
Seacome RJ.Coles MP.Glover JE.Hitchcock PB.Rowlands GJ. Dalton Trans. 2010, 39: 3687 - 78
Ruan JW.Shearer L.Mo J.Bacsa J.Zanotti-Gerosa A.Hancock F.Wu XF.Xiao JL. Org. Biomol. Chem. 2009, 7: 3236 - 79
Hartwig JF. Inorg. Chem. 2007, 46: 1936 -
80a
Ikawa T.Barder TE.Biscoe MR.Buchwald SL. J. Am. Chem. Soc. 2007, 129: 13001 -
80b
Fujita K.Yamashita M.Puschmann F.Alvarez-Falcon MM.Incarvito CD.Hartwig JF. J. Am. Chem. Soc. 2006, 128: 9044 - 81
Clarke ML.Konrad TM.Fuentes JA.Slawin AMZ. Angew. Chem. Int. Ed. 2010, 49: 9197 ; Angew. Chem. 2010, 122, 9383 - 82
Hii KK.Smith AMR.Rzepa HS.White AJP.Billen D. J. Org. Chem. 2010, 75: 3085 - 83
Falk F.Fröhlich R.Paradies J. Chem. Commun. 2011, in press; DOI: 10.1039/C1CC14844C. -
84a
Enders D.Niemeier O.Henseler A. Chem. Rev. 2007, 107: 5606 -
84b
Enders D.Niemeier O.Balensiefer T. Angew. Chem. Int. Ed. 2006, 45: 1463 ; Angew. Chem. 2006, 118, 1491 -
84c
Diez-Gonzalez S.Marion N.Nolan IP. Angew. Chem. Int. Ed. 2007, 46: 2988 ; Angew. Chem. 2007, 119, 3046 -
84d
Glorius F.Altenhoff G.Goddard R.Lehmann C. Chem. Commun. 2002, 2704 -
84e
Glorius F.Altenhoff G.Goddard R.Lehmann CW. Angew. Chem. Int. Ed. 2003, 42: 3690 ; Angew. Chem. 2003, 115, 3818 -
84f
Glorius F.Altenhoff G.Goddard R.Lehmann CW. J. Am. Chem. Soc. 2004, 126: 15195 - 85
Nolan SP.Diez-Gonzalez S.Marion N. Chem. Rev. 2009, 109: 3612 -
86a
Hoveyda AH.Lee KS.Brown MK.Hird AW. J. Am. Chem. Soc. 2006, 128: 7182 -
86b
Tomioka K.Matsumoto Y. Tetrahedron Lett. 2006, 47: 5843 -
86c
Grubbs RH.Seiders TJ.Ward DW. Org. Lett. 2001, 3: 3225 - 87
Focken T.Rudolph J.Bolm C. Synthesis 2005, 429 -
88a
Ma Q.Ma Y.Liu X.Duan W.Qu B.Song C. Tetrahedron: Asymmetry 2010, 21: 292 -
88b
Duan WZ.Ma YD.Xia HQ.Liu XY.Ma QS.Sun JS.
J. Org. Chem. 2008, 73: 4330 - 89
Andrus MB.Ma YD.Song C.Ma CQ.Sun ZJ.Chai Q. Angew. Chem. Int. Ed. 2003, 42: 5871 ; Angew. Chem. 2003, 115, 6051 - 90
Fürstner A.Alcarazo M.Krause H.Lehmann CW. J. Am. Chem. Soc. 2007, 129: 12676 - 91
Fürstner A.Alcarazo M.Stork T.Anoop A.Thiel W. Angew. Chem. Int. Ed. 2010, 49: 2542 ; Angew. Chem. 2010, 122, 2596 -
92a
Krische MJ.Park H.Cho CW. J. Org. Chem. 2006, 71: 7892 -
92b
Krische MJ.Cho CW.Kong JR. Org. Lett. 2004, 6: 1337 -
92c
Krische MJ.Cho CW. Angew. Chem. Int. Ed. 2004, 43: 6689 ; Angew. Chem. 2004, 116, 6857 - 93
Zhang T.-Z.Dai L.-X.Hou X.-L. Tetrahedron: Asymmetry 2007, 18: 1990 -
94a
Vedejs E.Duffey TA.Shaw SA. J. Am. Chem. Soc. 2009, 131: 14 -
94b
Wurz RP. Chem. Rev. 2007, 107: 5570 -
94c
Vedejs E.Shaw SA.Aleman P.Christy J.Kampf JW.Va P. J. Am. Chem. Soc. 2006, 128: 925 -
94d
Spivey AC.Arseniyadis S. Angew. Chem. Int. Ed. 2004, 43: 5436 ; Angew. Chem. 2004, 116, 5552 -
94e
Fu GC. Acc. Chem. Res. 2004, 37: 542 -
94f
Lectka T.France S.Guerin DJ.Miller SJ. Chem. Rev. 2003, 103: 2985 - 95
De R N.Marrot J.Couty F.David ORP. Eur. J. Org. Chem. 2011, 1980 -
96a
Malkova AV.Westwater MM.Gutnov A.Ramirez-Lopez P.Friscourt F.Kadlcikova A.Hodacova J.Rankovic Z.Kotora M.Kocovsky P. Tetrahedron 2008, 64: 11335 -
96b
Kwong HL.Yeung HL.Yeung CT.Lee WS.Lee CS.Wong WL. Coord. Chem. Rev. 2007, 251: 2188 - 97
Fulton JR.Glover JE.Kamara L.Rowlands GJ. Chem. Commun. 2011, 47: 433 - 98
Andrus MB.Chai Q.Song C.Sun ZJ.Ma YD.Ma CQ.Dai Y. Tetrahedron Lett. 2006, 47: 8611 -
99a
Pihko PM. Hydrogen Bonding in Organic Synthesis Wiley-VCH; Weinheim: 2009. -
99b
Schreiner PR. Chem. Soc. Rev. 2003, 32: 289 - 100
Wenzel AG.Jacobsen EN. J. Am. Chem. Soc. 2002, 124: 12964 - 101
Negru M.Schollmeyer D.Kunz H. Angew. Chem. Int. Ed. 2007, 46: 9339 ; Angew. Chem. 2007, 119, 9500 -
102a
Braddock DC.MacGilp ID.Perry BG. Adv. Synth. Catal. 2004, 346: 1117 -
102b
Braddock DC.MacGilp ID.Perry BG. Synlett 2003, 1121 - 103
Hine J.Linden SM.Kanagasabapathy VM. J. Org. Chem. 1985, 50: 5096 -
104a
Zhang ZG.Schreiner PR. Chem. Soc. Rev. 2009, 38: 1187 -
104b
Connon SJ. Synlett 2009, 354 -
104c
Connon SJ. Chem. Eur. J. 2006, 12: 5418 -
104d
Taylor MS.Jacobsen EN. Angew. Chem. Int. Ed. 2006, 45: 1520 ; Angew. Chem. 2006, 116, 1550 -
105a
Schneider JF.Fröhlich R.Paradies J. Synthesis 2010, 3486 -
105b
Schneider JF.Falk FC.Fröhlich R.Paradies J. Eur. J. Org. Chem. 2010, 12: 2265 - 106
Herrera RP.Sgarzani V.Bernardi L.Ricci A. Angew. Chem. Int. Ed. 2005, 44: 6576 ; Angew. Chem. 2008, 117, 6734 -
107a
Martin NJA.Cheng X.List B. J. Am. Chem. Soc. 2008, 130: 13862 -
107b
Martin NJA.Ozores L.List B. J. Am. Chem. Soc. 2007, 129: 8976