Subscribe to RSS
DOI: 10.1055/s-0030-1258465
Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes
Publication History
Publication Date:
14 March 2011 (online)
Abstract
Catalytic asymmetric gold-catalyzed reactions provide versatile routes to enantiomerically enriched carbo- and heterocycles. This review summarizes the recent work on the development of novel catalytic systems combining gold and a chiral ligand.
1 Introduction
2 Gold-Catalyzed Activation of Carbonyl and Imine-Type Bonds
3 Gold-Catalyzed Activation of Alkenes
3.1 Hydrogenation Reactions
3.2 Nucleophilic Additions to Alkenes
4 Gold-Catalyzed Activation of Allenes
4.1 In the Presence of a Chiral Gold Complex
4.1.1 Oxygen Nucleophiles
4.1.2 Nitrogen Nucleophiles
4.1.3 Carbon Nucleophiles
4.2 In the Presence of a Chiral Silver Salt
5 Gold-Catalyzed Activation of Alkynes
5.1 Rearrangement of Propargylic Esters
5.2 Desymmetrization Reactions
5.3 Cycloisomerization of Enynes
5.3.1 In the Absence of an External Nucleophile
5.3.2 In the Presence of a Nucleophile: Domino Processes
5.3.2.1 Oxygen and Nitrogen Nucleophiles
5.3.2.2 Carbon Nucleophiles
6 Conclusion
Key words
gold - asymmetric catalysis - cycloisomerization - alkenes - allenes - alkynes - domino processes
-
1a
Trost BM. Acc. Chem. Res. 2002, 35: 695 -
1b
Trost BM. Angew. Chem. 1995, 107: 285 -
1c
Trost BM. Science 1991, 254: 1471 -
2a
Anastas PT.Kirchhoff MM. Acc. Chem. Res. 2002, 35: 686 -
2b
Anastas PT.Warner JC. Green Chemistry: Theory and Practice Oxford University Press; Oxford: 1998. p.11 - For recent reviews on gold catalysis, see:
-
3a
Hashmi ASK. Angew. Chem. Int. Ed. 2010, 49: 5232 -
3b
Hashmi ASK.Bührle M. Aldrichimica Acta 2010, 43: 27 -
3c
Shapiro ND.Toste FD. Synlett 2010, 675 -
3d
Das A.Abu Sohel SM.Liu R.-S. Org. Biomol. Chem. 2010, 8: 860 -
3e
Abu Sohel SM.Liu R.-S. Chem. Soc. Rev. 2009, 38: 2269 -
3f
Fürstner A. Chem. Soc. Rev. 2009, 38: 3208 -
3g
Arcadi A. Chem. Rev. 2008, 108: 3266 -
3h
Patil NT.Yamamoto Y. Chem. Rev. 2008, 108: 3395 -
3i
Li Z.Brouwer C.He C. Chem. Rev. 2008, 108: 3239 -
3j
Shen HC. Tetrahedron 2008, 64: 3885 -
3k
Skouta R.Li C.-J. Tetrahedron 2008, 64: 4917 -
3l
Hashmi ASK.Rudolph M. Chem. Soc. Rev. 2008, 37: 1766 -
3m
Muzart J. Tetrahedron 2008, 64: 5815 -
3n
Gorin DJ.Sherry BD.Toste FD. Chem. Rev. 2008, 108: 3351 -
3o
Hashmi ASK. Chem. Rev. 2007, 107: 3180 -
3p
Fürstner A.Davies PW. Angew. Chem. Int. Ed. 2007, 46: 3410 -
3q
Gorin DJ.Toste FD. Nature 2007, 446: 395 -
3r
Hashmi ASK.Hutchings GJ. Angew. Chem. Int. Ed. 2006, 45: 7896 -
3s
Jimenez-Nunez E.Echavarren AM. Chem. Commun. 2007, 333 -
3t
Chianese AR.Lee SJ.Gagné MR. Angew. Chem. Int. Ed. 2007, 46: 4042 -
3u
Ma S.Yu S.Gu Z. Angew. Chem. Int. Ed. 2006, 45: 200 -
3v
Hashmi ASK. Angew. Chem. Int. Ed. 2005, 44: 6090 -
3w
Höffmann-Röder A.Krause N. Org. Biomol. Chem. 2005, 23: 387 -
3x
Haruta M. Gold Bull. 2004, 37: 27 -
3y
Bond G. C.Thompson D. T. Catal. Rev. 1999, 41: 319 - For recent reviews, see:
-
4a
Bongers N.Krause N. Angew. Chem. Int. Ed. 2008, 47: 2178 ; and references cited therein -
4b
Widenhoefer RA. Chem. Eur. J. 2008, 5382 -
4c
Sengupta S.Shi X. ChemCatChem 2010, 2: 609 - 5
Ito Y.Sawamura M.Hayashi T. J. Am. Chem. Soc. 1986, 108: 6405 - 6
Togni A.Pastor SD. J. Org. Chem. 1990, 55: 1649 - 7
Sawamura M.Nakayama Y.Kato T.Ito Y. J. Org. Chem. 1995, 60: 1727 - 8
Melhado AD.Luparia M.Toste FD. J. Am. Chem. Soc. 2007, 129: 12638 - 9
Gonzales-Arellano C.Corma A.Iglesias M.Sanchez F. Chem. Commun. 2005, 3451 - 10
Debono N.Iglesias M.Sanchez F. Adv. Synth. Catal. 2007, 349: 2470 - 11
Arnanz A.Gonzales-Arellano C.Juan A.Villaverde G.Corma A.Iglesias M.Sanchez F. Chem. Commun. 2010, 46: 3001 - 12
Corma A.Dominguez I.Doménech A.Fornés V.Gomez-Garcia CJ.Rodenas T.Sabater MJ. J. Catal. 2009, 265: 238 - 13
Zhang Z.Lee SD.Windehoefer RA. J. Am. Chem. Soc. 2009, 131: 5372 - 14
Bandini M.Eichholzer A. Angew. Chem. Int. Ed. 2004, 43: 2402 - For reviews on metal-catalyzed allene activation, see:
-
15a
Lopez F.Mascarenas JL. Chem. Eur. J. 2010, 418 -
15b
Hashmi ASK. Angew. Chem. Int. Ed. 2000, 39: 3590 - 16
Zhang Z.Widenhoefer RA. Angew. Chem. Int. Ed. 2007, 46: 283 - 17
Lalonde RL.Sherry BD.Kang EJ.Toste FD. J. Am. Chem. Soc. 2007, 129: 2452 - 18
Zhang Z.Bender CF.Widenhoefer RA. Org. Lett. 2007, 9: 2887 - 19
Lalonde RL.Wang ZJ.Mba M.Lackner AD.Toste FD. Angew. Chem. Int. Ed. 2010, 49: 598 - 20
Liu C.Widenhoefer RA. Org. Lett. 2007, 9: 1935 - 21
Tarselli MA.Chianese AR.Lee SJ.Gagné MR. Angew. Chem. Int. Ed. 2007, 46: 6670 - 22
Luzung MR.Mauleon P.Toste FD. J. Am. Chem. Soc. 2007, 129: 12402 - 23
Teller H.Flügge S.Goddard R.Fürstner A. Angew. Chem. Int. Ed. 2010, 49: 1949 - 24
Alonso I.Trillo B.López F.Montserrat F.Ujaque G.Castedo L.Lledós A.Mascareñas JL. J. Am. Chem. Soc. 2009, 131: 13020 - 25
González AZ.Toste FD. Org. Lett. 2010, 12: 200 - 26
Kleinbeck F.Toste FD. J. Am. Chem. Soc. 2009, 131: 9178 - 27
Hamilton GL.Kang EJ.Mba M.Toste FD. Nature 2007, 317: 496 -
28a
Aikawa K.Kojima M.Mikami K. Adv. Synth. Catal. 2010, 352: 3131 -
28b
Aikawa K.Kojima M.Mikami K. Angew. Chem. Int. Ed. 2009, 48: 6073 - 29
Johansson MJ.Gorin DJ.Staben ST.Toste FD. J. Am. Chem. Soc. 2005, 127: 18002 - 30
Watson IDG.Ritter S.Toste FD. J. Am. Chem. Soc. 2009, 131: 2056 - 31
Uemura M.Watson IDG.Katsukawa M.Toste FD. J. Am. Chem. Soc. 2009, 131: 3464 - 32
Wilckens K.Uhlemann M.Czekelius C. Chem. Eur. J. 2009, 15: 13323 - 33
Hashmi ASK.Hamzié M.Rominger F.Bats JW. Chem. Eur. J. 2009, 15: 13318 - 34
Murai M.Uenishi J.Uemura M. Org. Lett. 2010, 12: 4788 - For recent reviews on cycloisomerization reactions of enynes, see:
-
35a
Belmont P.Parker E. Eur. J. Org. Chem. 2009, 35: 6075 -
35b
Le SI.Chatani N. Chem. Commun. 2009, 371 -
35c
Jiménez-Nùñez E.Echavarren AM. Chem. Rev. 2008, 108: 3326 -
35d
Michelet V.Toullec PY.Genêt J.-P. Angew. Chem. Int. Ed. 2008, 47: 7427 -
35e
Zhang L.Sun J.Kozmin S. Adv. Synth. Catal. 2006, 348: 2271 -
35f
Fairlamb IJS. Angew. Chem. Int. Ed. 2004, 43: 1048 -
35g
Lloyd-Jones G. Org. Biomol. Chem. 2003, 1: 215 -
35h
Buisine O.Aubert C.Malacria M. Chem. Rev. 2002, 102: 813 -
36a
Blum J.Beer-Kraft H.Badrieh Y. J. Org. Chem. 1995, 60: 5567 -
36b
Fürstner A.Szillat H.Stelzer F. J. Am. Chem. Soc. 2000, 122: 6785 -
36c
Fürstner A.Stelzer F.Szillat H. J. Am. Chem. Soc. 2001, 123: 11863 -
36d
Nieto-Oberhuber C.Muñoz MP.Buñuel E.Nevado C.Càrdenas DJ.Echavarren AM. Angew. Chem. Int. Ed. 2004, 43: 2402 -
36e
Shibata T.Kobayashi Y.Maekawa S.Toshida N.Takagi K. Tetrahedron 2005, 61: 9018 -
36f
Brissy D.Skander M.Jullien H.Retailleau P.Marinetti A. Org. Lett. 2009, 11: 2137 -
36g
Nishimura T.Kawamoto T.Nagaosa M.Kumamoto H.Hayashi T. Angew. Chem. Int. Ed. 2010, 49: 1638 - 37
Chao C.-M.Beltrami D.Toullec PY.Michelet V. Chem. Commun. 2009, 6988 - 38
Martínez A.García-García P.Fernández-Rodríguez MA.Rodríguez F.Sanz R. Angew. Chem. Int. Ed. 2010, 49: 4633 - For selected examples on gold-catalyzed alkoxycyclization reactions of 1,n-enynes, see:
-
39a
Méndez M.Muñoz MP.Echavarren AM. J. Am. Chem. Soc. 2000, 122: 11549 -
39b
Méndez M.Muñoz MP.Nevado C.Càrdenas DJ.Echavarren AM. J. Am. Chem. Soc. 2001, 123: 10511 -
39c
Nevado C.Càrdenas DJ.Echavarren AM. Chem. Eur. J. 2003, 9: 2627 -
39d
Muñoz MP.Méndez M.Nevado C.Càrdenas DJ.Echavarren AM. Synthesis 2003, 2898 -
39e
Nevado C.Charuault L.Michelet V.Nieto-Oberhuber C.Muñoz MP.Méndez M.Rager M.-N.Genêt J.-P.Echavarren AM. Eur. J. Org. Chem. 2003, 706 -
39f
Nieto-Oberhuber C.Muñoz MP.Buñuel E.Nevado C.Càrdenas DJ.Echavarren AM. Angew. Chem. Int. Ed. 2005, 44: 6146 -
39g
Zhang L.Kozmin SA. J. Am. Chem. Soc. 2005, 127: 6962 -
39h
Mezailles N.Ricard L.Gagosz F. Org. Lett. 2005, 7: 4133 -
39i
Sherry BD.Maus L.Laforzeta BN.Toste FD. J. Am. Chem. Soc. 2006, 128: 8132 -
39j
Genin E.Leseurre L.Toullec PY.Genêt J.-P.Michelet V. Synlett 2007, 1780 -
39k
Buzas AK.Istrate FM.Gagosz F. Angew. Chem. Int. Ed. 2007, 46: 1141 -
39l
Chao C.-M.Toullec PY.Michelet V. Tetrahedron Lett. 2009, 50: 3719 -
39m
Li G.Liu Y. J. Org. Chem. 2010, 75: 2903 - 40
Muñoz MP.Adrio J.Carretero JC.Echavarren AM. Organometallics 2005, 24: 1293 - 41
Chao C.-M.Genin E.Toullec PY.Genêt J.-P.Michelet V. J. Organomet. Chem. 2009, 694: 538 - 42
Matsumoto Y.Selim KB.Nakanishi H.Yamada K.-I.Yamamoto Y.Tomioka K. Tetrahedron Lett. 2010, 51: 404 - 43
Liu F.Yu Y.Zhang J. Angew. Chem. Int. Ed. 2009, 48: 5505 - 44
Liu F.Qian D.Li L.Zhao X.Zhang J. Angew. Chem. Int. Ed. 2010, 49: 6669 - 45
Sethofer SG.Meyer T.Toste FD. J. Am. Chem. Soc. 2010, 132: 8276 - 46
Toullec PY.Blarre T.Michelet V. Org. Lett. 2009, 11: 2888 - 47
Fürstner A.Morency L. Angew. Chem. Int. Ed. 2008, 47: 5030 -
48a
Leseurre L.Toullec PY.Genêt J.-P.Michelet V. Org. Lett. 2007, 9: 4049 -
48b
Böhringer S.Gagosz F. Adv. Synth. Catal. 2008, 350: 2617 -
49a
Chao C.-M.Vitale MR.Toullec PY.Genêt J.-P.Michelet V. Chem. Eur. J. 2009, 15: 1319 -
49b For the racemic version,
see:
Toullec PY.Genin E.Leseurre L.Genêt J.-P.Michelet V. Angew. Chem. Int. Ed. 2006, 45: 7427