-
1
-
-
0003779363
-
-
(Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim
-
a) Transition Metals for Organic Synthesis, Vol. 1 and 2 (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 1998;
-
(1998)
Transition Metals for Organic Synthesis, Vol. 1 and 2
, vol.1-2
-
-
-
2
-
-
0003445429
-
-
(Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin
-
b) Comprehensive Asymmetric Catalysis I-III (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999.
-
(1999)
Comprehensive Asymmetric Catalysis I-III
-
-
-
3
-
-
20444365340
-
-
For a review on iron-catalyzed cross-coupling, see: A. Fürstner, R. Martin, Chem. Lett. 2005, 34, 624.
-
(2005)
Chem. Lett.
, vol.34
, pp. 624
-
-
Fürstner, A.1
Martin, R.2
-
6
-
-
0000683254
-
-
a) Y. Morisaki, T. Kondo, T.-A. Misudo, Organometallics 1999, 18, 4742;
-
(1999)
Organometallics
, vol.18
, pp. 4742
-
-
Morisaki, Y.1
Kondo, T.2
Misudo, T.-A.3
-
12
-
-
0000952360
-
-
b) M. T. Didiuk, J. P. Morken, A. H. Hoveyda, J. Am. Chem. Soc. 1995, 117, 7273.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 7273
-
-
Didiuk, M.T.1
Morken, J.P.2
Hoveyda, A.H.3
-
17
-
-
84989509466
-
-
E. S. M. Persson, M. van Kaveren, D. M. Grove, J.-E. Bäckvall, G. van Koten, Chem. Eur. J. 1995, 1, 351.
-
(1995)
Chem. Eur. J.
, vol.1
, pp. 351
-
-
Persson, E.S.M.1
Van Kaveren, M.2
Grove, D.M.3
Bäckvall, J.-E.4
Van Koten, G.5
-
18
-
-
0001313668
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-
B. M. Trost, K. Dogra, I. Hachiya, T. Emura, D. L. Hughes, S. W. Krska, R. A. Reamer, M. Palucki, N. Yasuda, P. J. Reider, Angew. Chem. 2002, 114, 2009;
-
(2002)
Angew. Chem.
, vol.114
, pp. 2009
-
-
Trost, B.M.1
Dogra, K.2
Hachiya, I.3
Emura, T.4
Hughes, D.L.5
Krska, S.W.6
Reamer, R.A.7
Palucki, M.8
Yasuda, N.9
Reider, P.J.10
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20
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2542458288
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The use of ligands sometimes leads to a shift in the regioisomer ratio towards the branched products; for example, see: J. W. Fuller, J. C. Wilt, J. Parr, Org. Lett. 2004, 6, 1301.
-
(2004)
Org. Lett.
, vol.6
, pp. 1301
-
-
Fuller, J.W.1
Wilt, J.C.2
Parr, J.3
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21
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33746248112
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note
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The character of the metal influences the regiochemical course of allylic alkylations. Ruthenium, molybdenum, rhodium, tungsten, and iridium catalysts often lead to the formation of the branched product, regardless of the substitution pattern of the starting material.
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24
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2542504340
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B. L. Ashfeld, K. A. Miller, S. F. Martin, Org. Lett. 2004, 6, 1321.
-
(2004)
Org. Lett.
, vol.6
, pp. 1321
-
-
Ashfeld, B.L.1
Miller, K.A.2
Martin, S.F.3
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28
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33746232318
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For reviews on the chemistry of tricarbonyl iron complexes, see: a) M. Periasamy, C. Rameshkumar, U. Radhahrishnan, A. Devasagayaraj, Curr. Sci. 2002, 71, 1307;
-
(2002)
Curr. Sci.
, vol.71
, pp. 1307
-
-
Periasamy, M.1
Rameshkumar, C.2
Radhahrishnan, U.3
Devasagayaraj, A.4
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30
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0035889187
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For a comprehensive study on iron-mediated allylic alkylations, see: D. Enders, B. Jandeleit, S. von Berg, G. Raabe, J. Runsink, Organometallics 2001, 20, 4312.
-
(2001)
Organometallics
, vol.20
, pp. 4312
-
-
Enders, D.1
Jandeleit, B.2
Von Berg, S.3
Raabe, G.4
Runsink, J.5
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31
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10044237251
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For an interesting Fe-catalyzed allylic alkylation of allyl halides, see: R. Martin, A. Fürstner, Angew. Chem. 2004, 116, 4045;
-
(2004)
Angew. Chem.
, vol.116
, pp. 4045
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Martin, R.1
Fürstner, A.2
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33
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33746232314
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patent pending (102005040752.8)
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B. Plietker, patent pending (102005040752.8)
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Plietker, B.1
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34
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0039208016
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3 was previously reported: K. Itoh, S. Nakanishi, Y. Otsuji, Bull. Chem. Soc. Jpn. 1991, 64, 2965.
-
(1991)
Bull. Chem. Soc. Jpn.
, vol.64
, pp. 2965
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Itoh, K.1
Nakanishi, S.2
Otsuji, Y.3
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35
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33746204441
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note
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[21]
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36
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33746232319
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note
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[13a]
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37
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33746248108
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note
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The presented mechanism, including the molecular structures, represents a model. Detailed spectroscopic investigations on the structure of the active catalyst as well as on reactive intermediates are currently underway in our laboratories.
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