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9
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70349527578
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For remarkable recent advance, see: 2009 Science 2008 321 1188; and references cited therein
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For remarkable recent advance, see:, Watson D A., Su M, Teverovskiy G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald S L., Science 2009 325 1661, Douvris C, Ozerov O V., Science 2008 321 1188; and references cited therein
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Science
, vol.325
, pp. 1661
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Watson, D.A.1
Su, M.2
Teverovskiy, G.3
Zhang, Y.4
García-Fortanet, J.5
Kinzel, T.6
Buchwald, S.L.7
Douvris, C.8
Ozerov, O.V.9
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10
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61349130720
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For recent representative studies on catalyzed functionali-zations of C-F bonds with metals other than nickel, see: 2009 J.Am. Chem. Soc. 2009 131 11203 J. Am. Chem. Soc. 2009 131 1847 Angew. Chem. Int. Ed. 2009 48 1546 Organometallics 2009 28 2356 J. Am. Chem. Soc. 2008 130 15499 J. Am. Chem. Soc. 2008 130 15490 Synthesis 2008 2645 Org. Lett. 2007 9 5629 Synthesis 2006 5347; and references cited therein
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For recent representative studies on catalyzed functionali-zations of C-F bonds with metals other than nickel, see:, Braun T, Salomon M A., Altenhoner K, Teltewskoi M, Hinze S, Angew. Chem. Int. Ed. 2009 48 1818, Gu W, Haneline M R., Douvris C, Ozerov O V., J.Am. Chem. Soc. 2009 131 11203, Reade S P., Mahon M F., Whittlesey M K., J. Am. Chem. Soc. 2009 131 1847, Meier G, Braun T, Angew. Chem. Int. Ed. 2009 48 1546, Buckley H L., Wang T, Tran O, Love J A., Organometallics 2009 28 2356, Nova A, Erhardt S, Jasim N A., Perutz R N., Macgregor S A., McGrady J E., Whitwood A C., J. Am. Chem. Soc. 2008 130 15499, Erhardt S, Macgregor S A., J. Am. Chem. Soc. 2008 130 15490, Manabe K, Ishikawa S, Synthesis 2008 2645, Wang T, Alfonso B J., Love [nl]J A., Org. Lett. 2007 9 5629, Korn T J., Schade M A., Cheemala M N., Wirth S, Guevara S A., Cahiez G, Knochel P, Synthesis 2006 5347; and references cited therein
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Angew. Chem. Int. Ed.
, vol.48
, pp. 1818
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Braun, T.1
Salomon, M.A.2
Altenhoner, K.3
Teltewskoi, M.4
Hinze, S.5
Gu, W.6
Haneline, M.R.7
Douvris, C.8
Ozerov, O.V.9
Reade, S.P.10
Mahon, M.F.11
Whittlesey, M.K.12
Meier, G.13
Braun, T.14
Buckley, H.L.15
Wang, T.16
Tran, O.17
Love, J.A.18
Nova, A.19
Erhardt, S.20
Jasim, N.A.21
Perutz, R.N.22
MacGregor, S.A.23
McGrady, J.E.24
Whitwood, A.C.25
Erhardt, S.26
MacGregor, S.A.27
Manabe, K.28
Ishikawa, S.29
Wang, T.30
Alfonso, B.J.31
Love, J.A.32
Korn, T.J.33
Schade, M.A.34
Cheemala, M.N.35
Wirth, S.36
Guevara, S.A.37
Cahiez, G.38
Knochel, P.39
more..
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14
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33845585240
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For examples of nickel-catalyzed cross-coupling reactions between aryl fluorides and boronic acids, see: 2006 See also: J. Am. Chem. Soc. 2008 130 9304
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For examples of nickel-catalyzed cross-coupling reactions between aryl fluorides and boronic acids, see:, Schaub T, Backes M, Radius U, J. Am. Chem. Soc. 2006 128 15964 See also:, Schaub T, Fischer P, Steffen A, Braun T, Radius U, Mix A, J. Am. Chem. Soc. 2008 130 9304
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J. Am. Chem. Soc.
, vol.128
, pp. 15964
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Schaub, T.1
Backes, M.2
Radius, U.3
Schaub, T.4
Fischer, P.5
Steffen, A.6
Braun, T.7
Radius, U.8
Mix, A.9
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15
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69049084551
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For representative examples, see: 2009 J. Am. Chem. Soc. 2009 131 9590 Synlett 2005 1771 J. Am. Chem. Soc. 2005 127 17978 J. Organomet. Chem. 2005 690 932 Angew. Chem. Int. Ed. 2001 40 3387 Bull. Chem. Soc. Jpn. 1976 49 1958 J. Organomet. Chem. 1973 50 C12; and references cited therein
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For representative examples, see:, Hatekeyama T, Hashimoto S, Ishizuka K, Nakamura M, J. Am. Chem. Soc. 2009 131 11949, Yoshikai N, Matsuda H, Nakamura E, J. Am. Chem. Soc. 2009 131 9590, Saeki T, Takashima Y, Tamao K, Synlett 2005 1771, Yoshikai N, Mashima H, Nakamura E, J. Am. Chem. Soc. 2005 127 17978, Dankwardt J W., J. Organomet. Chem. 2005 690 932, Böhm V P. W., Gstöttmayr [nl]C W. K., Weskamp T, Herrmann W A., Angew. Chem. Int. Ed. 2001 40 3387, Tamao K, Sumitani K, Kiso Y, Zembayashi M, Fujioka A, Kodama S, Nakajama I, Minato A, Kumada M, Bull. Chem. Soc. Jpn. 1976 49 1958, Kiso Y, Tamao K, Kumada M, J. Organomet. Chem. 1973 50 C12; and references cited therein
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J. Am. Chem. Soc.
, vol.131
, pp. 11949
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Hatekeyama, T.1
Hashimoto, S.2
Ishizuka, K.3
Nakamura, M.4
Yoshikai, N.5
Matsuda, H.6
Nakamura, E.7
Saeki, T.8
Takashima, Y.9
Tamao, K.10
Yoshikai, N.11
Mashima, H.12
Nakamura, E.13
Dankwardt, J.W.14
Böhm, V.P.W.15
Gstöttmayr, C.W.K.16
Weskamp, T.17
Herrmann, W.A.18
Tamao, K.19
Sumitani, K.20
Kiso, Y.21
Zembayashi, M.22
Fujioka, A.23
Kodama, S.24
Nakajama, I.25
Minato, A.26
Kumada, M.27
Kiso, Y.28
Tamao, K.29
Kumada, M.30
more..
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19
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74549139701
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Representative examples of HASPO preligands in catalyzed cross-coupling chemistry from our laboratories: 2009 Synlett 2009 808 Org. Lett. 2008 5043 Angew. Chem. Int. Ed. 2006 45 2619 Angew. Chem. Int. Ed. 2006 45 7627 Chem. Commun. 2006 1419 Org. Lett. 2006 8 3457 Org. Lett. 2005 7 3123
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Representative examples of HASPO preligands in catalyzed cross-coupling chemistry from our laboratories:, Ackermann L, Potukuchi H K., Synlett 2009 2852, Ackermann L, Barfüßer S, Synlett 2009 808, Ackermann L, Mulzer M, Org. Lett. 2008 10 5043, Ackermann L, Althammer A, Born R, Angew. Chem. Int. Ed. 2006 45 2619, Ackermann L, Spatz J H., Gschrei C J., Born R, Althammer A, Angew. Chem. Int. Ed. 2006 45 7627, Ackermann L, Gschrei C J., Althammer A, Riederer M, Chem. Commun. 2006 1419, Ackermann L, Althammer A, Org. Lett. 2006 8 3457, Ackermann L, Org. Lett. 2005 7 3123
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Synlett
, vol.10
, pp. 2852
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Ackermann, L.1
Potukuchi, H.K.2
Ackermann, L.3
Barfüßer, S.4
Ackermann, L.5
Mulzer, M.6
Ackermann, L.7
Althammer, A.8
Born, R.9
Ackermann, L.10
Spatz, J.H.11
Gschrei, C.J.12
Born, R.13
Althammer, A.14
Ackermann, L.15
Gschrei, C.J.16
Althammer, A.17
Riederer, M.18
Ackermann, L.19
Althammer, A.20
Ackermann, L.21
more..
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27844437252
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2005
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Ackermann L, Born R, Spatz J H., Meyer D, Angew. Chem. Int. Ed. 2005 44 7216
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Angew. Chem. Int. Ed.
, vol.44
, pp. 7216
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Ackermann, L.1
Born, R.2
Spatz, J.H.3
Meyer, D.4
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22
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33644543729
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2006
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Ackermann L, Born R, Spatz J H., Althammer A, Gschrei C J., Pure Appl. Chem. 2006 78 209
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Pure Appl. Chem.
, vol.78
, pp. 209
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Ackermann, L.1
Born, R.2
Spatz, J.H.3
Althammer, A.4
Gschrei, C.J.5
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23
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0000276628
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For an example of a secondary phosphine sulfide preligand in a cross-coupling of aryl chlorides, see: 2002
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For an example of a secondary phosphine sulfide preligand in a cross-coupling of aryl chlorides, see:, Li G W., Marshall W J., Organometallics 2002 21 590
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Organometallics
, vol.21
, pp. 590
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Li, G.W.1
Marshall, W.J.2
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