RSS-Feed abonnieren
DOI: 10.1055/s-2007-967959
Sulfur-Containing Chiral Ferrocene Derivatives: Synthesis and Applications
Publikationsverlauf
Publikationsdatum:
07. Februar 2007 (online)

Abstract
This account describes the different synthetic approaches used for the preparation of sulfur-containing chiral ferrocenes in which a CFc-S bond is present and the strategies for introducing planar and central chirality. The advantages of using these compounds as ligands for soft metals like palladium and copper are highlighted for several catalytic reactions, including the palladium-catalyzed enantioselective allylic alkylation, epoxidation, and aza-Diels-Alder reactions.
-
1 Introduction
-
2 Synthesis of Planar Chiral Ferrocenes Containing Sulfur Functionalities
-
2.1 Diastereoselective ortho-Lithiation of Ferrocenyl Derivatives Bearing Carbon-Based Chiral Auxiliaries
-
2.2 Planar Chirality by Enantioinduction Using Alkyllithium/
(-)-Sparteine Reagent -
2.3 Diastereoselective ortho-Metalation of Ferrocenyl Derivatives Bearing Chiral Sulfur Directing Groups
-
2.3.1 Diastereoselective ortho-Lithiation of Chiral Ferrocenyl Sulfoxides
-
2.3.2 Other Chiral Sulfur ortho-Directing Groups
-
2.3.3 Ortho-Directed Metalation Involving Chiral Phosphorus Auxiliaries
-
2.4 Chiral Ferrocenyl Sulfoxides as Interchangeable Directing Groups
-
3 Thio-Substituted Ferrocenyl Derivatives as Ligands in Asymmetric Catalysis
-
3.1 S,S Ferrocenyl Ligands
-
3.2 S,P Ferrocenyl Ligands
-
3.3 S,N Ferrocenyl Ligands
-
3.4 S,Oxazoline Ferrocenyl Ligands
-
4 Thioferrocenyl-Based Pincer Ligands
-
5 Potentially Biologically Active Ferrocenyl Derivatives
-
5.1 Ferrocene-Containing β-Lactams
-
6 Conclusions and Outlook
Key words
metallocenes - sulfur - chirality - ligands - asymmetric catalysis
- 1
Keally TJ.Pauson PL. Nature 1951, 168: 1039 -
2a
Togni A.Hayashi T. Ferrocenes VCH; Weinheim: 1995. -
2b
Togni A.Halterman RL. Metallocenes Wiley-VCH; Weinheim: 1998. -
3a
Sharma V.Piwnica-Worms D. Chem. Rev. 1999, 99: 2545 -
3b
Hillard E.Vessières A.Thouin L.Jaoun G.Amatore C. Angew. Chem. Int. Ed. 2006, 45: 285 ; and references therein -
3c
Bjelosevic H.Spégel C.Sykfont Snygg Å.Gorton L.Elmroth SKC.Persson T. Tetrahedron 2006, 62: 4519 ; and references therein -
4a
Rebière F.Riant O.Ricard L.Kagan HB. Angew. Chem. Int. Ed. 1993, 32: 568 -
4b
Riant O.Argouarch G.Guillaneux D.Samuel O.Kagan HB. J. Org. Chem. 1998, 63: 3511 -
4c
Kagan HB.Diter P.Gref A.Guillaneux D.Masson-Szymezak A.Rebière F.Riant O.Samuel O.Taudien S. Pure Appl. Chem. 1996, 68: 29 - 5
Togni A.Hayashi T. Ferrocenes VCH; Weinheim: 1995. Chap. 4. p.173 -
6a For pioneering work, see:
Marquarding D.Klusacek H.Gokel G.Hoffman P.Ugi I. J. Am. Chem. Soc. 1970, 92: 5389 -
6b
Herrmann R.Hübener G.Ugi I. Tetrahedron 1985, 41: 941 - 7
Karlstom ASE.Huerta FF.Meuzelaar GJ.Bäckvall JE. Synlett 2001, 923 -
8a
Riant O.Samuel O.Kagan HB. J. Am. Chem. Soc. 1993, 115: 5835 -
8b
Riant O.Samuel O.Flessner T.Taudien S.Kagan HB. J. Org. Chem. 1997, 62: 6733 -
9a
Bernardi L.Bonini BF.Capitò E.Dessole G.Femoni C.Fochi M.Comes-Franchini M.Mincio A.Ricci A. ARKIVOC 2004, (ii): 72 -
9b
Bernardi L.Bonini BF.Comes-Franchini M.Dessole G.Fochi M.Ricci A. Phosphorus, Sulfur Silicon Relat. Elem. 2005, 180: 1273 - 10
Bernardi L.Bonini BF.Comes-Franchini M.Femoni C.Fochi M.Ricci A. Tetrahedron: Asymmetry 2004, 15: 1133 - 11
Bernardi L.Bonini BF.Capitò E.Comes-Franchini M.Dessole G.Fini F.Fochi M.Herrera RP.Ricci A. Eur. J. Org. Chem. 2006, 207 -
12a
Richards CJ.Damalidis T.Hibbs DE.Hursthouse MB. Synlett 1995, 74 -
12b
Sammakia T.Latham HA.Schaad DR. J. Org. Chem. 1995, 60: 10 -
12c
Nishibayashi Y.Uemura S. Synlett 1995, 79 -
12d
Sammakia T.Latham HA. J. Org. Chem. 1995, 60: 6002 -
12e
Zhang W.Adachi Y.Hirao T.Ikeda I. Tetrahedron: Asymmetry 1996, 7: 451 -
12f
Nishibayashi Y.Segawa K.Arikawa Y.Ohe K.Hidai M.Uemura S. J. Organomet. Chem. 1997, 545-546: 381 - 13 For a recent review in this field, see:
Sutcliffe OB.Bryce MR. Tetrahedron: Asymmetry 2003, 14: 2297 -
14a
You S.-L.Zhou Y.-G.Hou X.-L.Dai L.-X. Chem. Commun. 1998, 2765 -
14b
You S.-L.Hou X.-L.Dai L.-X.Yu Y.-H.Xia W. J. Org. Chem. 2002, 67: 4684 -
15a
Enders D.Peters R.Lochtman R.Runsink J. Synlett 1997, 1462 -
15b
Enders D.Peters R.Lochtman R.Raabe G. Angew. Chem. Int. Ed. 1999, 38: 2421 -
15c
Enders D.Peters R.Lochtman R.Raabe G.Runsink J.Bats JW. Eur. J. Org. Chem. 2000, 3399 -
16a
Widhalm M.Mereiter K.Bourghida M. Tetrahedron: Asymmetry 1998, 9: 2983 -
16b
Widhalm M.Nettekoven U.Mereiter K. Tetrahedron: Asymmetry 1999, 10: 4369 - 17
Ganter C.Wagner T. Chem. Ber. 1995, 128: 1157 - 18
Xiao L.Kitzler R.Weissensteiner W. J. Org. Chem. 2001, 66: 8912 - 19
Lotz M.Ireland T.Tappe K.Knokel P. Chirality 2000, 12: 389 - 20
Peters R.Fischer DF. Org. Lett. 2005, 7: 4137 -
21a
Tsukazaki M.Tinkl M.Roglans A.Chapell BJ.Taylor NJ.Snieckus V. J. Am. Chem. Soc. 1996, 118: 685 -
21b
Laufer RS.Veith U.Taylor NJ.Snieckus V. Org. Lett. 2000, 2: 629 -
22a
Bonini BF.Comes-Franchini M.Fochi M.Mazzanti G.Ricci A.Alberti A.Macciantelli D.Marcaccio M.Roffia S. Eur. J. Org. Chem. 2002, 543 -
22b
Alberti A.Benaglia M.Bonini BF.Fochi M.Macciantelli D.Marcaccio M.Paolucci F.Roffia S. J. Phys. Org. Chem. 2004, 17: 1084 -
23a
Hua DH.Lagneau NM.Chen Y.Robben PM.Clapham G.Robinson PD. J. Org. Chem. 1996, 61: 4508 -
23b
Lagneau NM.Chen Y.Robben PM.Sin HS.Takasu K.Chen JS.Robinson PD.Hua DH. Tetrahedron 1998, 54: 7301 - 24
Patti A.Lambusta D.Piattelli M.Nicolosi G.McArdle P.Cunningham D.Walsh M. Tetrahedron 1997, 53: 1361 - 25
Cotton HK.Huerta FF.Bäckvall J.-E. Eur. J. Org. Chem. 2003, 2756 - 26
Fernandez I.Valdivia V.Gori B.Alcudia F.Alvarez E.Khiar N. Org. Lett. 2005, 7: 1307 - 27
Bonini BF.Comes-Franchini M.Fochi M.Mazzanti G.Ricci A.Tomasulo M.Varchi G. J. Organomet. Chem. 2001, 637-639: 407 - 28
Bonini BF.Fochi M. Rev. Heteroat. Chem. 1997, 16: 47 - 29
Bonini BF.Comes-Franchini M.Fochi M.Mazzanti G.Ricci A.Varchi G. Tetrahedron Lett. 1999, 40: 6473 - 30
Bonini BF.Fochi M.Comes-Franchini M.Ricci A.Thijs L.Zwanenburg B. Tetrahedron: Asymmetry 2003, 14: 3321 - 31
Costa M.Snieckus V. Org. Lett. 2002, 4: 1935 - 32
Bonini BF.Femoni C.Fochi M.Gulea M.Masson S.Ricci A. Tetrahedron: Asymmetry 2005, 16: 3003 -
33a
Bolm C.Muñiz K.Aguilar N.Kesselgruber M.Raabe G. Synthesis 1999, 1251 -
33b
Bolm C.Kesselgruber M.Muñiz K.Raabe G. Organometallics 2000, 19: 1648 - 34
Nettekoven U.Widhalm M.Kamer PCJ.van Leeuwen PWNM.Mereiter K.Lutz M.Spek AL. Organometallics 2000, 19: 2299 - 35
Vinci D.Mateus N.Wu X.Hancock F.Steiner A.Xiao J. Org. Lett. 2006, 8: 215 - 36
Xiao L.Mereiter K.Spindler F.Weissensteiner W. Tetrahedron: Asymmetry 2001, 12: 1105 -
37a
Jensen JF.Sotofte I.Sørensen HO.Johannsen M. J. Org. Chem. 2003, 68: 1258 -
37b
Jensen JF.Johannsen M. Org. Lett. 2003, 5: 3025 - 38
Seitzberg JG.Dissing C.Søtofte I.Norrby P.-O.Johannsen M. J. Org. Chem. 2005, 70: 8332 - 39
D’Antona N.Lambusta D.Morrone R.Nicolosi G.Secundo F. Tetrahedron: Asymmetry 2004, 15: 3835 - 40
Togni A. Angew. Chem. Int. Ed. 1996, 35: 1475 - 41
Wang C.-H.Brubaker CH. J. Mol. Catal. 1992, 75: 221 - 42
Gibson VC.Long NJ.Williams CK.Fontani M.Zanello P. Dalton Trans. 2003, 3599 - 43
Routaboul L.Vincendeau S.Daran J.-C.Manoury E. Tetrahedron: Asymmetry 2003, 16: 2685 - 44
Enders D.Peters R.Runsink J.Bats JW. Org. Lett. 1999, 1: 1863 -
45a
Priego J.García Mancheño O.Cabrera S.Gómez Arrayás R.Llamas T.Carretero JC. Chem. Commun. 2002, 2512 -
45b
García Mancheño O.Priego J.Cabrera S.Gómez Arrayás R.Llamas T.Carretero JC. J. Org. Chem. 2003, 68: 3679 ; and references therein - 46
Tu T.Zhou Y.-G.Hou X.-L.Dai L.-X.Dong X.-C.Yu Y.-H.Sun J. Organometallics 2003, 22: 1255 - 47
García Mancheño O.Gómez Arrayás R.Carretero JC. J. Am. Chem. Soc. 2004, 126: 456 - 48
Cabrera S.Gómez Arrayás R.Carretero JC. J. Am. Chem. Soc. 2005, 127: 16394 - 49
García Mancheño O.Gómez Arrayás R.Carretero JC. Organometallics 2005, 24: 557 - 50
Koning B.Hulst R.Kellogg RM. Recl. Trav. Chim. Pays-Bas 1996, 115: 49 - 51
Adams H.Anderson JC.Cubbon R.James DS.Mathias JP. J. Org. Chem. 1999, 64: 8256 - 52
Bernardi L.Bonini BF.Comes-Franchini M.Fochi M.Mazzanti G.Ricci A.Varchi G. Eur. J. Org. Chem. 2002, 2776 - 53
Hu X.Bai C.Dai H.Chen H.Zheng Z. J. Mol. Catal. A: Chem. 2004, 218: 107 - 54
Miniére S.Reboul V.Metzner P.Fochi M.Bonini BF. Tetrahedron: Asymmetry 2004, 15: 3275 - 55
Muñiz K.Bolm C. Chem. Eur. J. 2000, 6: 2309 - 56
Gèrard S.Pressel Y.Riant O. Tetrahedron: Asymmetry 2005, 16: 1889 ; and references therein - 57
Allen JV.Coote SJ.Dawson GJ.Frost CG.Martin CJ.Williams JMJ. J. Chem. Soc., Perkin Trans. 1 1994, 2065 - 58
Albrecht M.van Koten G. Angew. Chem. Int. Ed. 2001, 40: 3750 -
59a
van der Boom ME.Milstein D. Chem. Rev. 2003, 103: 1759 -
59b
Singleton JT. Tetrahedron 2003, 59: 1837 ; and references therein -
60a
Farrington EJ.Viviente EM.William BS.van Koten G.Brown JM. Chem. Commun. 2002, 308 -
60b
Koridze AA.Kuklin SA.Sheloumov AM.Dolgushin FM.Lagunova VYu.Petukhova II.Ezernitskaya MG.Peregudov AS.Petrovskii PV.Vorontsov EV.Baya M.Poli R. Organometallics 2004, 23: 4585 - 61
Bonini BF.Capitò E.Comes-Franchini M.Fochi M.Ricci A. ARKIVOC 2006, (vi): 85 - 62
Pichon C.Odell B.Brown JM. Chem. Commun. 2004, 598 - 63
Dombrowski KE.Baldwin W.Sheats JE. J. Organomet. Chem. 1986, 302: 281 - 64
Yamada H.Matsue T.Uchida I. Biochem. Biophys. Res. Commun. 1991, 180: 1330 -
65a
Top S.Tang J.Vessieres A.Carrez D.Provot C.Jaouen G. J. Chem. Soc., Chem. Commun. 1990, 955 -
65b
Top S.Dauer B.Vaissermann J.Jaouen G. J. Organomet. Chem. 1997, 541: 355 -
66a
Biot C.Glorian G.Maciejewski L.Brocard J.Domarle O.Blampain G.Millet P.Georges AJ.Abessolo H.Dive D.Lebibi J. J. Med. Chem. 1997, 40: 3715 -
66b
Biot C.Delhaes L.N’Diaye CM.Maciejewski LA.Camus D.Dive D.Brocard JS. Bioorg. Med. Chem. 1999, 7: 2843 - For reviews on this subject, see:
-
67a
Southgate R. Contemp. Org. Synth. 1994, 1: 417 -
67b
Southgate R.Branch C.Coulton S.Hunt E. In Recent Progress in the Chemical Synthesis of Antibiotics and Related Microbial Products Vol. 2:Lukacs G. Springer; Berlin: 1993. p.621 -
67c
Ojima I. In The Organic Chemistry of β-LactamsGeorg GI. VCH; New York: 1993. p.621 -
68a
Palomo C.Aizpurua JM.Garcia JM.Iturburu M.Odriozola JM. J. Org. Chem. 1994, 59: 5184 -
68b
Ojima I. Acc. Chem. Res. 1995, 28: 383 -
68c
Palomo C.Aizpurua JM.Ganboa I.Odriozola B.Urchegui R.Görls H. Chem. Commun. 1996, 1269 -
68d
Ojima I.Delaloge F. Chem. Soc. Rev. 1997, 26: 377 ; and references therein -
68e
Palomo C.Oiarbide M.Esnal A.Landa A.Miranda JI.Linden A. J. Org. Chem. 1998, 63: 5838 -
69a
Edwards EI.Epton R.Marr G. J. Organomet. Chem. 1975, 85: C23 -
69b
Edwards EI.Epton R.Marr G. J. Organomet. Chem. 1976, 107: 351 -
69c
Scutaru D.Mazilu I.Vata M.Tataru L.Vlase A.Lixandru T.Simionescu C. J. Organomet. Chem. 1991, 401: 87 -
69d
Simionescu C.Lixandru T.Tataru L.Mazilu I.Vata M.Luca S. J. Organomet. Chem. 1983, 252: C43 -
70a
Abbady MA.Hassan KM.El-Maghraby MA. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1978, 16: 499 -
70b
Hassan KM. Z. Naturforsch., B: Chem. Sci. 1978, 33: 1508 -
70c
Hassan KM.El-Ezbawy SR.Abdel-Wahab AA. J. Indian Chem. Soc. 1979, 56: 290 - 71
Ghatak A.Becker FF.Banik BK. Heterocycles 2000, 53: 2769 - 72
Bonini BF.Femoni C.Comes-Franchini M.Fochi M.Mazzanti G.Ricci A.Varchi G. Synlett 2001, 1092 - 73
Sierra MA.Mancheno MJ.Vicente R.Gomez-Gallego M. J. Org. Chem. 2001, 66: 8920 - 74
Bernardi L.Bonini BF.Comes-Franchini M.Dessole G.Fochi M.Ricci A. Eur. J. Org. Chem. 2005, 3326