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3
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77950261392
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Ed.: B. List); Top. Curr. Chem. 291, Springer, Berlin, Germany
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Asymmetric Organocatalysis (Ed.: B. List); Top. Curr. Chem. 291, Springer, Berlin, Germany, 2010.
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Asymmetric Organocatalysis
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4
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84862728116
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Ed.: M. Waser); Prog. Ch. Org. Nat. Prod., 96, Springer, Berlin, Germany
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Asymmetric Organocatalysis in Natural Product Syntheses (Ed.: M. Waser); Prog. Ch. Org. Nat. Prod., 96, Springer, Berlin, Germany, 2012.
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(2012)
Asymmetric Organocatalysis in Natural Product Syntheses
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7
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79651474136
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A subjective selection of recent examples is presented. The interested reader is encouraged to consult the primary literature or the following comprehensive review on the general use of hypervalent iodine reagents for the α-functionalization of carbonyls compounds
-
A subjective selection of recent examples is presented. The interested reader is encouraged to consult the primary literature or the following comprehensive review on the general use of hypervalent iodine reagents for the α-functionalization of carbonyls compounds: E. A. Merritt, B. Olofsson, Synthesis 2011, 517-538.
-
(2011)
Synthesis
, pp. 517-538
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-
Merritt, E.A.1
Olofsson, B.2
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8
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84862735088
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For a few selected examples, see:
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For a few selected examples, see:
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10
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0001082990
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U. H. Hirt, B. Spingler, T. Wirth, J. Org. Chem. 1998, 63, 7674-7679;
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Hirt, U.H.1
Spingler, B.2
Wirth, T.3
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11
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0035048950
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U. H. Hirt, M. F. H. Schuster, A. N. French, O. G. Wiest, T. Wirth, Eur. J. Org. Chem. 2001, 1569-1579;
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(2001)
Eur. J. Org. Chem.
, pp. 1569-1579
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Hirt, U.H.1
Schuster, M.F.H.2
French, A.N.3
Wiest, O.G.4
Wirth, T.5
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12
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33947259792
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R. D. Richardson, T. K. Page, S. Altermann, S. M. Paradine, A. N. French, T. Wirth, Synlett 2007, 538-542;
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(2007)
Synlett
, pp. 538-542
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Richardson, R.D.1
Page, T.K.2
Altermann, S.3
Paradine, S.M.4
French, A.N.5
Wirth, T.6
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13
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55049084431
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S. M. Altermann, R. D. Richardson, T. K. Page, R. K. Schmidt, E. Holland, U. Mohammed, S. M. Paradine, A. N. French, C. Richter, A. M. Bahar, B. Witulski, T. Wirth, Eur. J. Org. Chem. 2008, 5315-5328;
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(2008)
Eur. J. Org. Chem.
, pp. 5315-5328
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Altermann, S.M.1
Richardson, R.D.2
Page, T.K.3
Schmidt, R.K.4
Holland, E.5
Mohammed, U.6
Paradine, S.M.7
French, A.N.8
Richter, C.9
Bahar, A.M.10
Witulski, B.11
Wirth, T.12
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14
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77749327716
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U. Farooq, S. Schafer, A. A. Shah, D. M. Freudendahl, T. Wirth, Synthesis 2010, 1023-1029;
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(2010)
Synthesis
, pp. 1023-1029
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Farooq, U.1
Schafer, S.2
Shah, A.A.3
Freudendahl, D.M.4
Wirth, T.5
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15
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0032830171
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M. Ochiai, Y. Kitagawa, N. Takayama, Y. Takaoka, M. Shiro, J. Am. Chem. Soc. 1999, 121, 9233-9234;
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Ochiai, M.1
Kitagawa, Y.2
Takayama, N.3
Takaoka, Y.4
Shiro, M.5
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16
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35848951629
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M. Fujita, S. Okuno, H. J. Lee, T. Sugimura, T. Okuyama, Tetrahedron Lett. 2007, 48, 8691-8694;
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Fujita, M.1
Okuno, S.2
Lee, H.J.3
Sugimura, T.4
Okuyama, T.5
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17
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84862776800
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For a review on the use of chiral hypervalent iodine reagents, see:
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J. Yu, J. Cui, X. S. Hou, S. S. Liu, W. C. Gao, S. Jiang, J. Tian, C. Zhang, Tetrahedron: Asymmetry 2011, 22, 2039-2055. For a review on the use of chiral hypervalent iodine reagents, see:
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(2011)
Tetrahedron: Asymmetry
, vol.22
, pp. 2039-2055
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Yu, J.1
Cui, J.2
Hou, X.S.3
Liu, S.S.4
Gao, W.C.5
Jiang, S.6
Tian, J.7
Zhang, C.8
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18
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83455208461
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For a review on the catalytic generation of hypervalent iodine reagents and hypoiodites, see:
-
H. Liang, M. A. Ciufolini, Angew. Chem. 2011, 123, 12051-12053; Angew. Chem. Int. Ed. 2011, 50, 11849-11851. For a review on the catalytic generation of hypervalent iodine reagents and hypoiodites, see:
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(2011)
Angew. Chem. 2011, 123, 12051-12053; Angew. Chem. Int. Ed.
, vol.50
, pp. 11849-11851
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Liang, H.1
Ciufolini, M.A.2
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20
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14644408766
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M. Engqvist, J. Casas, H. Sundén, I. Ibrahem, A. Córdova, Tetrahedron Lett. 2005, 46, 2053-2057.
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(2005)
Tetrahedron Lett.
, vol.46
, pp. 2053-2057
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Engqvist, M.1
Casas, J.2
Sundén, H.3
Ibrahem, I.4
Córdova, A.5
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21
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3242814515
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A. Córdova, H. Sundén, M. Engqvist, I. Ibrahem, J. Casas, J. Am. Chem. Soc. 2004, 126, 8914-8915;
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J. Am. Chem. Soc.
, vol.126
, pp. 8914-8915
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Córdova, A.1
Sundén, H.2
Engqvist, M.3
Ibrahem, I.4
Casas, J.5
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22
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11144326714
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H. Sundén, M. Engqvist, J. Casas, I. Ibrahem, A. Córdova, Angew. Chem. 2004, 116, 6694-6697; Angew. Chem. Int. Ed. 2004, 43, 6532-6535.
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Angew. Chem. 2004, 116, 6694-6697; Angew. Chem. Int. Ed.
, vol.43
, pp. 6532-6535
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Sundén, H.1
Engqvist, M.2
Casas, J.3
Ibrahem, I.4
Córdova, A.5
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24
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40149104139
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N. T. Vo, R. D. M. Pace, F. O′Hara, M. J. Gaunt, J. Am. Chem. Soc. 2007, 130, 404-405.
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Vo, N.T.1
Pace, R.D.M.2
O'Hara, F.3
Gaunt, M.J.4
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26
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68249144236
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D. A. Nagib, M. E. Scott, D. W. C. MacMillan, J. Am. Chem. Soc. 2009, 131, 10875-10876.
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, vol.131
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Nagib, D.A.1
Scott, M.E.2
MacMillan, D.W.C.3
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28
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84862728121
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For a few selected examples, see:
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For a few selected examples, see:
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29
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15744377645
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M. Bella, S. Kobbelgaard, K. A. Jorgensen, J. Am. Chem. Soc. 2005, 127, 3670-3671;
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, pp. 3670-3671
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Bella, M.1
Kobbelgaard, S.2
Jorgensen, K.A.3
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30
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34547178180
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J. Alemán, S. Cabrera, E. Maerten, J. Overgaard, K. A. Jorgensen, Angew. Chem. 2007, 119, 5616-5619; Angew. Chem. Int. Ed. 2007, 46, 5520-5523;
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(2007)
Angew. Chem. 2007, 119, 5616-5619; Angew. Chem. Int. Ed.
, vol.46
, pp. 5520-5523
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Alemán, J.1
Cabrera, S.2
Maerten, E.3
Overgaard, J.4
Jorgensen, K.A.5
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31
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34547184381
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J. Alemán, B. Richter, K. A. Jorgensen, Angew. Chem. 2007, 119, 5611-5615; Angew. Chem. Int. Ed. 2007, 46, 5515-5519;
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(2007)
Angew. Chem. 2007, 119, 5611-5615; Angew. Chem. Int. Ed.
, vol.46
, pp. 5515-5519
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Alemán, J.1
Richter, B.2
Jorgensen, K.A.3
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73349084638
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K. L. Jensen, P. T. Franke, L. T. Nielsen, K. Daasbjerg, K. A. Jorgensen, Angew. Chem. 2010, 122, 133-137; Angew. Chem. Int. Ed. 2010, 49, 129-133.
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(2010)
Angew. Chem. 2010, 122, 133-137; Angew. Chem. Int. Ed.
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, pp. 129-133
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Jensen, K.L.1
Franke, P.T.2
Nielsen, L.T.3
Daasbjerg, K.4
Jorgensen, K.A.5
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77955825507
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D. FernándezGonzález, J. P. Brand, J. Waser, Chem. Eur. J. 2010, 16, 9457-9461;
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FernándezGonzález, D.1
Brand, J.P.2
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P.-O. Norrby, T. B. Petersen, M. Bielawski, B. Olofsson, Chem. Eur. J. 2010, 16, 8251-8254.
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Norrby, P.-O.1
Petersen, T.B.2
Bielawski, M.3
Olofsson, B.4
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35
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84862729851
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On-going investigations in our group have shown that optimisation of the catalyst and ester structures can lead to a substantial increase in the enantioselectivity of the reaction (up to 79%ee): D. Fernández González, J. Waser, unpublished results.
-
On-going investigations in our group have shown that optimisation of the catalyst and ester structures can lead to a substantial increase in the enantioselectivity of the reaction (up to 79%ee): D. Fernández González, J. Waser, unpublished results.
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36
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33846220324
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T. B. Poulsen, L. Bernardi, J. Aleman, J. Overgaard, K. A. Jorgensen, J. Am. Chem. Soc. 2007, 129, 441-449.
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Poulsen, T.B.1
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Jorgensen, K.A.5
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