RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2011(17): 2796-2802
DOI: 10.1055/s-0030-1260129
DOI: 10.1055/s-0030-1260129
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Electronically Deficient Atropisomeric Bisphosphine Ligands and Their Application in Asymmetric Hydrogenation of Quinolines
Weitere Informationen
Received
9 May 2011
Publikationsdatum:
21. Juli 2011 (online)
Publikationsverlauf
Publikationsdatum:
21. Juli 2011 (online)
Abstract
A series of electronically deficient atropisomeric bisphosphine ligands have been synthesized from (S)-MeO-BiPhep. The introduction of electron-withdrawing groups in the ligands had a dramatic influence on both the enantioselectivity and the activity of catalyst. The iridium complex of the MeO-BiPhep-based ligand bearing a trifluoromethanesulfonyl group was successfully applied in the asymmetric hydrogenation of quinolines with ee values of up to 95% and turnover numbers (TON) of up to 14,600.
Key words
iridium - asymmetric hydrogenation - electron-deficient ligands - quinolines
- Supporting Information for this article is available online:
- Supporting Information
-
1a
Keay JG. In Comprehensive Organic Synthesis Vol. 8: Pergamon; Oxford: 1991. p.579 -
1b
Katrizky AR.Rachwal S.Bachwal B. Tetrahedron 1996, 52: 15031 -
1c
Barton DH.Nakanishi K.Meth-Cohn O. In Comprehensive Natural Products Chemistry Vol. 1-9: Elsevier; Oxford: 1999. - 2
Wang W.-B.Lu S.-M.Yang P.-Y.Han X.-W.Zhou Y.-G. J. Am. Chem. Soc. 2003, 125: 10536 - For recent reviews on hydrogenation of heteroaromatic compounds, see:
-
3a
Dyson PJ. Dalton Trans. 2003, 2964 -
3b
Glorius F. Org. Biomol. Chem. 2005, 3: 4171 -
3c
Lu S.-M.Han X.-W.Zhou Y.-G. Chin. J. Org. Chem. 2005, 25: 634 -
3d
Zhou Y.-G. Acc. Chem. Res. 2007, 40: 1357 -
3e
Kuwano R. Heterocycles 2008, 76: 909 - For our group’s work on the asymmetric hydrogenation of quinolines, see:
-
4a
Lu S.-M.Han X.-W.Zhou Y.-G. Adv. Synth. Catal. 2004, 346: 909 -
4b
Yang P.-Y.Zhou Y.-G. Tetrahedron: Asymmetry 2004, 15: 1145 -
4c
Zhao Y.-J.Wang Y.-Q.Zhou Y.-G. Chin. J. Catal. 2005, 26: 737 -
4d
Lu S.-M.Wang Y.-Q.Han X.-W.Zhou Y.-G. Angew. Chem. Int. Ed. 2006, 45: 2260 -
4e
Wang D.-W.Zeng W.Zhou Y.-G. Tetrahedron: Asymmetry 2007, 18: 1103 -
4f
Wang X.-B.Zhou Y.-G. J. Org. Chem. 2008, 73: 5640 -
4g
Wang D.-W.Wang X.-B.Wang D.-S.Lu S.-M.Zhou Y.-G.Li Y.-X. J. Org. Chem. 2009, 74: 2780 -
4h
Wang D.-W.Wang D.-S.Chen Q.-A.Zhou Y.-G. Chem. Eur. J. 2010, 16: 1133 -
4i
Wang D.-S.Zhou Y.-G. Tetrahedron Lett. 2010, 51: 3014 - For other groups’ work on metal-catalyzed asymmetric hydrogenation of quinolines, see:
-
5a
Fache F. Synlett 2004, 2827 -
5b
Fujita K.-I.Kitatsuji C.Furukawa S.Yamaguchi R. Tetrahedron Lett. 2004, 45: 3215 -
5c
Xu L.-J.Lam K.-H.Ji J.-X.Wu J.Fan Q.-H.Lo W.-H.Chan ASC. Chem. Commun. 2005, 1390 -
5d
Lam K.-H.Xu L.-J.Feng L.-C.Fan Q.-H.Lam F.-L.Lo W.-H.Chan ASC. Adv. Synth. Catal. 2005, 347: 1755 -
5e
Wu J.Chan ASC. Acc. Chem. Res. 2006, 39: 711 -
5f
Reetz MT.Li X.-G. Chem. Commun. 2006, 2159 -
5g
Qiu L.Kwong FY.Wu J.Lam WH.Chan S.Yu W.-Y.Li Y.-M.Guo R.Zhou Z.Chan ASC. J. Am. Chem. Soc. 2006, 128: 5955 -
5h
Yamagata T.Tadaoka H.Nagata M.Hirao T.Kataoka Y.Ratovelomanana-Vidal V.Genet JP.Mashima K. Organometallics 2006, 25: 2505 -
5i
Chan S.-H.Lam K.-H.Li Y.-M.Xu L.-J.Tang W.-J.Lam F.-L.Lo W.-H.Yu W.-Y.Fan Q.-H.Chan ASC. Tetrahedron: Asymmetry 2007, 18: 2625 -
5j
Deport C.Buchotte M.Abecassis K.Tadaoka H.Ayad T.Ohshima T.Genet J.-P.Mashima K.Ratovelomanana-Vidal V. Synlett 2007, 2743 -
5k
Li Z.-W.Wang T.-L.He Y.-M.Wang Z.-J.Fan Q.-H.Pan J.Xu L.-J. Org. Lett. 2008, 10: 5265 -
5l
Zhou H.-F.Li Z.-W.Wang Z.-J.Wang T.-L.Xu L.-J.He Y.-M.Fan Q.-H.Pan J.Gu L.-Q.Chan ASC. Angew. Chem. Int. Ed. 2008, 47: 8464 -
5m
Lu S.-M.Bolm C. Adv. Synth. Catal. 2008, 350: 1101 -
5n
Mršić N.Lefort L.Boogers JAF.Minnaard AJ.Feringa BL.de Vries JG. Adv. Synth. Catal. 2008, 350: 1081 -
5o
Eggenstein M.Thomas A.Theuerkauf J.Franciò G.Leitner W. Adv. Synth. Catal. 2009, 351: 725 -
5p
Wang C.Li C.-Q.Wu X.-F.Pettman A.Xiao J.-L. Angew. Chem. Int. Ed. 2009, 48: 6524 -
5q
Tadaoka H.Cartigny D.Nagano T.Gosavi T.Ayad T.Genet J.-P.Ohshima T.Ratovelomanana-Vidal V.Mashima K. Chem. Eur. J. 2009, 15: 9990 -
5r
Wang Z.-J.Zhou H.-F.Wang T.-L.He Y.-M.Fan Q.-H. Green Chem. 2009, 11: 767 -
5s
Parekh V.Ramsden JA.Wills M. Tetrahedron: Asymmetry 2010, 21: 1549 -
5t
Gou F.-R.Li W.Zhang XM.Liang Y.-M. Adv. Synth. Catal. 2010, 352: 2441 - For the work on organocatalytic asymmetric hydrogenation of quinolines, see:
-
6a
Rueping M.Antonchick AP.Theissmann T. Angew. Chem. Int. Ed. 2006, 45: 3683 -
6b
Rueping M.Theissmann T.Raja S.Bats JWP. Adv. Synth. Catal. 2008, 350: 1001 -
6c
Guo Q.-S.Du D.-M.Xu J. Angew. Chem. Int. Ed. 2008, 47: 759 - For selected examples on asymmetric hydrogenation of other heteroaromatic compounds, see, for quinoxalines:
-
7a
Cobley CJ.Henschke JP. Adv. Synth. Catal. 2003, 345: 195 -
7b
Mršić N.Jerphagnon T.Minnaard AJ.Feringa BL.de Vries JG. Adv. Synth. Catal. 2009, 351: 2549 -
7c
Tang W.-J.Xu L.-J.Fan Q.-H.Wang J.Fan B.-M.Zhou Z.-Y.Lam K.-H.Chan ASC. Angew. Chem. Int. Ed. 2009, 48: 9135 -
7d
Cartigny D.Nagano T.Ayad T.Genet JP.Ohshima T.Mashima K.Ratovelomanana-Vidal V. Adv. Synth. Catal. 2010, 352: 1886 - For furans, see:
-
7e
Ohta T.Miyake T.Seido N.Kumobayashi H.Takaya H. J. Org. Chem. 1995, 60: 357 -
7f
Kaiser S.Smidt SP.Pfaltz A. Angew. Chem. Int. Ed. 2006, 45: 5194 -
7g
Feiertag P.Albert M.Nettekoven U.Spindler F. Org. Lett. 2006, 8: 4133 - For pyridines, see:
-
7h
Raynor SA.Thomas JM.Raja R.Johnson BFG.Belle RG.Mantle MD. Chem. Commun. 2000, 1925 -
7i
Glorius F.Spielkamp N.Holle S.Goddard R.Lehmann CW. Angew. Chem. Int. Ed. 2004, 43: 2850 -
7j
Legault CY.Charette AB. J. Am. Chem. Soc. 2005, 127: 8966 -
7k
Wang X.-B.Zeng W.Zhou Y.-G. Tetrahedron Lett. 2008, 49: 4922 - For indoles, see:
-
7l
Kuwano R.Sato K.Kurokawa T.Karube D.Ito Y. J. Am. Chem. Soc. 2000, 122: 7614 -
7m
Kuwano R.Kaneda K.Ito T.Sato K.Kurokawa T.Ito Y. Org. Lett. 2004, 6: 2213 -
7n
Kuwano R.Kashiwabara M. Org. Lett. 2006, 8: 2653 -
7o
Baeza A.Pfaltz A. Chem. Eur. J. 2010, 16: 2036 -
7p
Wang D.-S.Chen Q.-A.Li W.Yu C.-B.Zhou Y.-G.Zhang XM. J. Am. Chem. Soc. 2010, 132: 8909 - For pyrroles, see:
-
7q
Kuwano R.Kashiwabara M.Ohsumi M.Kusano H. J. Am. Chem. Soc. 2008, 130: 808 - 8
Wang Z.-J.Deng G.-J.Li Y.He Y.-M.Tang W.-J.Fan Q.-H. Org. Lett. 2007, 9: 1243 - 9
Wang D.-S.Zhou J.Wang D.-W.Guo Y.-L.Zhou Y.-G. Tetrahedron Lett. 2010, 51: 525 - 10
Jahjah M.Alame M.Pellet-Rostaing S.Lemaire M. Tetrahedron: Asymmetry 2007, 18: 2305 -
11a
Tang W.-J.Tan J.Xu L.-J.Lam K.-H.Fan Q.-H.Chan ASC. Adv. Synth. Catal. 2010, 352: 1055 -
11b
Tang W.-J.Sun Y.-W.Xu L.-J.Wang T.-L.Fan Q.-H.Lam K.-H.Chan ASC. Org. Biomol. Chem. 2010, 8: 3464 -
12a
Mamat C.Flemming A.Köckerling M.Steinbach J.Wuest FR. Synthesis 2009, 3311 -
12b
Ishikawa S.Manabe K. Tetrahedron 2010, 66: 297 - 13
Michel B,Blandine L, andSonia R. inventors; PCT Int. Appl. WO 2002012253.