-
1
-
-
52149114261
-
-
doi:10.1038/nature07369.PMID:18800130
-
Hartwig, J. F. Nature 2008, 455 (7211), 314. doi:10.1038/nature07369. PMID:18800130.;
-
(2008)
Nature
, vol.455
, Issue.7211
, pp. 314
-
-
Hartwig, J.F.1
-
3
-
-
57549097790
-
-
doi:10.1021/ar800098p. PMID:18681463
-
Hartwig, J. F. Acc. Chem. Res. 2008, 41 (11), 1534. doi:10.1021/ ar800098p. PMID:18681463.;
-
(2008)
Acc. Chem. Res.
, vol.41
, Issue.11
, pp. 1534
-
-
Hartwig, J.F.1
-
4
-
-
53549095407
-
-
doi:10.1021/cr0306788.PMID:18729420
-
Müller, T. E.; Hultzsch, K. C.; Yus, M.; Foubelo, F.; Tada, M. Chem. Rev. 2008, 108 (9), 3795. doi:10.1021/cr0306788. PMID:18729420.
-
(2008)
Chem. Rev.
, vol.108
, Issue.9
, pp. 3795
-
-
Müller, T.E.1
Hultzsch, K.C.2
Yus, M.3
Foubelo, F.4
Tada, M.5
-
5
-
-
34250014986
-
-
doi:10.1039/b706301f. PMID:17551648
-
Ackermann, L.; Kaspar, L. T.; Althammer, A. Org. Biomol. Chem. 2007, 5 (12), 1975. doi:10.1039/b706301f. PMID:17551648.;
-
(2007)
Org. Biomol. Chem.
, vol.5
, Issue.12
, pp. 1975
-
-
Ackermann, L.1
Kaspar, L.T.2
Althammer, A.3
-
6
-
-
0037007706
-
-
doi:10.1021/ol025659j. PMID:11975606
-
Schlummer, B.; Hartwig, J. F. Org. Lett. 2002, 4 (9), 1471. doi:10.1021/ol025659j. PMID:11975606.
-
(2002)
Org. Lett.
, vol.4
, Issue.9
, pp. 1471
-
-
Schlummer, B.1
Hartwig, J.F.2
-
7
-
-
65749115628
-
-
For some recent lead references, see :doi:10.1021/om9000023
-
For some recent lead references, see: Yuen, H. F.; Marks, T. J. Organometallics 2009, 28 (8), 2423. doi:10.1021/om9000023.;
-
(2009)
Organometallics
, vol.28
, Issue.8
, pp. 2423
-
-
Yuen, H.F.1
Marks, T.J.2
-
8
-
-
65349111264
-
-
doi:10.1021/om900040r
-
Lu, E.; Gan, W.; Chen, Y. Organometallics 2009, 28 (7), 2318. doi:10.1021/om900040r.;
-
(2009)
Organometallics
, vol.28
, Issue.7
, pp. 2318
-
-
Lu, E.1
Gan, W.2
Chen, Y.3
-
9
-
-
41749098446
-
-
doi:10.1002/chem.200701090
-
Aillaud, I.; Collin, J.; Duhayon, C.; Guillot, R.; Lyubov, D.; Schulz, E.; Trifonov, A. Chem. Eur. J. 2008, 14 (7), 2189. doi:10.1002/chem.200701090.
-
(2008)
Chem. Eur. J.
, vol.14
, Issue.7
, pp. 2189
-
-
Aillaud, I.1
Collin, J.2
Duhayon, C.3
Guillot, R.4
Lyubov, D.5
Schulz, E.6
Trifonov, A.7
-
10
-
-
55249091147
-
-
doi:10.1021/om8005382
-
Ge, S.; Meetsma, A.; Hessen, B. Organometallics 2008, 27 (20), 5339. doi:10.1021/om8005382.;
-
(2008)
Organometallics
, vol.27
, Issue.20
, pp. 5339
-
-
Ge, S.1
Meetsma, A.2
Hessen, B.3
-
11
-
-
34247098477
-
-
doi:10.1021/ja0665444. PMID:17371022
-
Stubbert, B. D.; Marks, T. J. J. Am. Chem. Soc. 2007, 129 (14), 4253. doi:10.1021/ja0665444. PMID:17371022.;
-
(2007)
J. Am. Chem. Soc.
, vol.129
, Issue.14
, pp. 4253
-
-
Stubbert, B.D.1
Marks, T.J.2
-
12
-
-
34249082758
-
-
doi:10.1021/ja0675898. PMID:17441716
-
Stubbert, B. D.; Marks, T. J. J. Am. Chem. Soc. 2007, 129 (19), 6149. doi:10.1021/ja0675898. PMID:17441716.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, Issue.19
, pp. 6149
-
-
Stubbert, B.D.1
Marks, T.J.2
-
13
-
-
62049085521
-
-
For some recent lead references, see: doi:10.1016/j.tet.2008.09.045
-
For some recent lead references, see: Zhang, W.; Werness, J. B.; Tang, W. Tetrahedron 2009, 65 (16), 3090.doi:10.1016/j.tet.2008.09.045.
-
(2009)
Tetrahedron
, vol.65
, Issue.16
, pp. 3090
-
-
Zhang, W.1
Werness, J.B.2
Tang, W.3
-
14
-
-
67650482921
-
-
doi:10.1021/ja9003377. PMID:19552442
-
Crimmin, M. R.; Arrowsmith, M.; Barrett, A. G. M.; Casely, I. J.; Hill, M. S.; Procopiou, P. A. J. Am. Chem. Soc. 2009, 131 (28), 9670.doi:10.1021/ ja9003377. PMID:19552442.;
-
(2009)
J. Am. Chem. Soc.
, vol.131
, Issue.28
, pp. 9670
-
-
Crimmin, M.R.1
Arrowsmith, M.2
Barrett, A.G.M.3
Casely, I.J.4
Hill, M.S.5
Procopiou, P.A.6
-
15
-
-
41749117743
-
-
doi:10.1021/om701014d
-
Datta, S.; Gamer, M. T.; Roesky, P. W. Organometallics 2008, 27 (6), 1207. doi:10.1021/om701014d.;
-
(2008)
Organometallics
, vol.27
, Issue.6
, pp. 1207
-
-
Datta, S.1
Gamer, M.T.2
Roesky, P.W.3
-
17
-
-
63849238245
-
-
For some recent lead references, see: doi:10.1055/s-00281083279
-
For some recent lead references, see: Lee, A. V.; Sajitz, M.; Schafer, L. L. Synthesis 2009, 97. doi:10.1055/s-0028- 1083279.;
-
(2009)
Synthesis
, vol.97
-
-
Lee, A.V.1
Sajitz, M.2
Schafer, L.L.3
-
18
-
-
58249124537
-
-
doi:10.1002/ejic.200800977
-
Lian, B.; Spaniol, T. P.; Horrillo-Martinez, P.; Hultzsch, K. C.; Okuda, J. Eur. J. Inorg. Chem. 2009, 2009 (3), 429. doi:10.1002/ejic.200800977.
-
(2009)
Eur. J. Inorg. Chem.
, vol.2009
, Issue.3
, pp. 429
-
-
Lian, B.1
Spaniol, T.P.2
Horrillo-Martinez, P.3
Hultzsch, K.C.4
Okuda, J.5
-
19
-
-
41749102664
-
-
doi:10.1021/om700883a
-
Majumder, S.; Odom, A. L. Organometallics 2008, 27 (6), 1174. doi:10.1021/om700883a.;
-
(2008)
Organometallics
, vol.27
, Issue.6
, pp. 1174
-
-
Majumder, S.1
Odom, A.L.2
-
20
-
-
33846422708
-
-
doi:10.1002/anie.200603017
-
Wood, M. C.; Leitch, D. C.; Yeung, C. S.; Kozak, J. A.; Schafer, L. L. Angew. Chem. Int. Ed. 2007, 46 (3), 354. doi:10.1002/anie.200603017.;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, Issue.3
, pp. 354
-
-
Wood, M.C.1
Leitch, D.C.2
Yeung, C.S.3
Kozak, J.A.4
Schafer, L.L.5
-
21
-
-
34347398902
-
-
refs. cited therein doi:10.1002/ejic.200700036
-
Lee, A. V.; Schafer, L. L. Eur. J. Inorg. Chem. 2007, 2245, and refs. cited therein. doi:10.1002/ejic.200700036.
-
(2007)
Eur. J. Inorg. Chem.
, vol.2245
-
-
Lee, A.V.1
Schafer, L.L.2
-
22
-
-
40949123181
-
-
For examples involving the late metal-mediated addition of secondary amides, carbamates, or ureas to unactivated olefins, see: doi:10.1021/ja0734997. PMID:18254623
-
For examples involving the late metal-mediated addition of secondary amides, carbamates, or ureas to unactivated olefins, see: Cochran, B. M.; Michael, F. E. J. Am. Chem. Soc. 2008, 130 (9), 2786. doi:10.1021/ja0734997. PMID:18254623.;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, Issue.9
, pp. 2786
-
-
Cochran, B.M.1
Michael, F.E.2
-
23
-
-
38749153968
-
-
doi:10.1021/ol702891p. PMID:18154298
-
Cochran, B. M.; Michael, F. E. Org. Lett. 2008, 10 (2), 329. doi:10.1021/ol702891p. PMID:18154298.;
-
(2008)
Org. Lett.
, vol.10
, Issue.2
, pp. 329
-
-
Cochran, B.M.1
Michael, F.E.2
-
24
-
-
33746216342
-
-
doi:10.1002/anie.200503789
-
Komeyama, K.; Morimoto, T.; Takaki, K. Angew. Chem. Int. Ed. 2006, 45 (18), 2938. doi:10.1002/anie.200503789.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, Issue.18
, pp. 2938
-
-
Komeyama, K.1
Morimoto, T.2
Takaki, K.3
-
25
-
-
33645463109
-
-
doi:10.1021/ja060126h. PMID:16568997
-
Michael, F. E.; Cochran, B. M. J. Am. Chem. Soc. 2006, 128 (13), 4246. doi:10.1021/ja060126h. PMID:16568997.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, Issue.13
, pp. 4246
-
-
Michael, F.E.1
Cochran, B.M.2
-
27
-
-
33845263000
-
-
doi:10.1021/ol062107i. PMID:17078703
-
Bender, C. F.; Widenhoefer, R. A. Org. Lett. 2006, 8 (23), 5303. doi:10.1021/ol062107i. PMID:17078703.;
-
(2006)
Org. Lett.
, vol.8
, Issue.23
, pp. 5303
-
-
Bender, C.F.1
Widenhoefer, R.A.2
-
28
-
-
33244465401
-
-
doi:10.1021/ja053864z. PMID:16464072
-
Zhang, J.; Yang, C.-G.; He, C. J. Am. Chem. Soc. 2006, 128 (6), 1798. doi:10.1021/ja053864z. PMID:16464072.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, Issue.6
, pp. 1798
-
-
Zhang, J.1
Yang, C.-G.2
He, C.3
-
29
-
-
33746110458
-
-
doi:10.1021/ol060719x. PMID:16774237
-
Liu, X.-Y.; Li, C.-H.; Che, C.-M. Org. Lett. 2006, 8 (13), 2707. doi:10.1021/ol060719x. PMID:16774237.;
-
(2006)
Org. Lett.
, vol.8
, Issue.13
, pp. 2707
-
-
Liu, X.-Y.1
Li, C.-H.2
Che, C.-M.3
-
31
-
-
64349107462
-
-
The late metal-mediated addition of secondary alkyl- or aryl-amines to unactivated olefins is limited to the following reports: doi:10.1021/ol900174f. PMID:19231849
-
The late metal-mediated addition of secondary alkyl- or aryl-amines to unactivated olefins is limited to the following reports: Hesp, K. D.; Stradiotto, M. Org. Lett. 2009, 11 (6), 1449. doi:10.1021/ol900174f. PMID:19231849.
-
(2009)
Org. Lett.
, vol.11
, Issue.6
, pp. 1449
-
-
Hesp, K.D.1
Stradiotto, M.2
-
32
-
-
66149085671
-
-
doi:10.1021/ol9007712. PMID:9379007
-
Ohmiya, H.; Moriya, T.; Sawamura, M. Org. Lett. 2009, 11 (10), 2145. doi:10.1021/ol9007712. PMID:19379007.;
-
(2009)
Org. Lett.
, vol.11
, Issue.10
, pp. 2145
-
-
Ohmiya, H.1
Moriya, T.2
Sawamura, M.3
-
33
-
-
44649159029
-
-
doi:10.1021/om8000982
-
Bender, C. F.; Hudson, W. B.; Widenhoefer, R. A. Organometallics 2008, 27 (10), 2356. doi:10.1021/om8000982.;
-
(2008)
Organometallics
, vol.27
, Issue.10
, pp. 2356
-
-
Bender, C.F.1
Hudson, W.B.2
Widenhoefer, R.A.3
-
34
-
-
38949090658
-
-
doi:10.1021/ja710126x. PMID:18183986
-
Liu, Z.; Hartwig, J. F. J. Am. Chem. Soc. 2008, 130 (5), 1570.doi:10.1021/ja710126x. PMID:18183986.;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, Issue.5
, pp. 1570
-
-
Liu, Z.1
Hartwig, J.F.2
-
35
-
-
50849141450
-
-
doi:10.1021/ol8000766. PMID:18293992
-
Bauer, E. B.; Andavan, G. T. S.; Hollis, T. K.; Rubio, R. J.; Cho, J.; Kuchenbeiser, G. R.; Helgert, T. R.; Letko, C. S.; Tham, F. S. Org. Lett. 2008, 10 (6), 1175. doi:10.1021/ol8000766. PMID:18293992.;
-
(2008)
Org. Lett.
, vol.10
, Issue.6
, pp. 1175
-
-
Bauer, E.B.1
Andavan, G.T.S.2
Hollis, T.K.3
Rubio, R.J.4
Cho, J.5
Kuchenbeiser, G.R.6
Helgert, T.R.7
Letko, C.S.8
Tham, F.S.9
-
36
-
-
13644249121
-
-
doi:10.1021/ja043278q .PMID:15669824
-
Bender, C. F.; Widenhoefer, R. A. J. Am. Chem. Soc. 2005, 127 (4), 1070.doi:10.1021/ja043278q. PMID:15669824.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, Issue.4
, pp. 1070
-
-
Bender, C.F.1
Widenhoefer, R.A.2
-
37
-
-
84891301272
-
-
For a review documenting the use of Ir complexes as catalysts for the hydroamination of activated alkenes as well as aminoalkynes, see: Oro, L. A., Claver, C., Eds.; Wiley-VCH: Weinheim, Germany
-
For a review documenting the use of Ir complexes as catalysts for the hydroamination of activated alkenes as well as aminoalkynes, see:
-
(2009)
Iridium Complexes in Organic Synthesis
, pp. 145-172
-
-
Dorta, R.1
-
38
-
-
35748950704
-
-
doi:10.1021/om7006437
-
Hesp, K. D.; Wechsler, D.; Cipot, J.; Myers, A.; McDonald, R.; Ferguson, M. J.; Schatte, G.; Stradiotto, M. Organometallics 2007, 26 (22), 5430.doi:10.1021/om7006437.
-
(2007)
Organometallics
, vol.26
, Issue.22
, pp. 5430
-
-
Hesp, K.D.1
Wechsler, D.2
Cipot, J.3
Myers, A.4
McDonald, R.5
Ferguson, M.J.6
Schatte, G.7
Stradiotto, M.8
-
39
-
-
74549174245
-
-
Note added in proof: Following the acceptance of this manuscript, the enantioselective cyclohydroamination of unactivated alkenes in good yields with excellent enantioselectivites was reported, see: doi:10.1002/ anie.200905402
-
Note added in proof: Following the acceptance of this manuscript, the enantioselective cyclohydroamination of unactivated alkenes in good yields with excellent enantioselectivites was reported, see: Shen, X.; Buchwald, S. L. Angew. Chem. Int. Ed. 2010, 49, 564. doi:10.1002/ anie.200905402.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 564
-
-
Shen, X.1
Buchwald, S.L.2
-
41
-
-
0030838312
-
-
doi:10.1021/ja972594k
-
Dorta, R.; Egli, P.; Zürcher, F.; Togni, A. J. Am. Chem. Soc. 1997, 119 (44), 10857. doi:10.1021/ja972594k.;
-
(1997)
J. Am. Chem. Soc.
, vol.119
, Issue.44
, pp. 10857
-
-
Dorta, R.1
Egli, P.2
Zürcher, F.3
Togni, A.4
-
42
-
-
51949104311
-
-
doi:10.1021/ja803523z. PMID:18715004
-
Zhou, J. S.; Hartwig, J. F. J. Am. Chem. Soc. 2008, 130 (37), 12220.doi:10.1021/ja803523z. PMID:18715004.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, Issue.37
, pp. 12220
-
-
Zhou, J.S.1
Hartwig, J.F.2
-
43
-
-
0033610498
-
-
doi:10.1021/ja992493h, 1-Aryl-2,5-dialkylphospholane chiral fragments are established motifs in asymmetric catalysis, see:
-
1-Aryl-2,5-dialkylphospholane chiral fragments are established motifs in asymmetric catalysis, see: Nandi, M.; Jin, J.; RajanBabu, T. V. J. Am. Chem. Soc. 1999, 121 (42), 9899. doi:10.1021/ja992493h.;
-
(1999)
J. Am. Chem. Soc.
, vol.121
, Issue.42
, pp. 9899
-
-
Nandi, M.1
Jin, J.2
RajanBabu, T.V.3
-
44
-
-
0000740766
-
-
doi:10.1021/ja00075a031
-
Burk, M. J.; Feaster, J. E.; Nugent, W. A.; Harlow, R. L. J. Am. Chem. Soc. 1993, 115 (22), 10125. doi:10.1021/ja00075a031.;
-
(1993)
Am. Chem. Soc.
, vol.115
, Issue.22
, pp. 10125
-
-
Burk, M.J.1
Feaster, J.E.2
Nugent, W.A.3
Harlow, R.L.J.4
-
45
-
-
3843089758
-
-
doi:10.1016/j.tetasy.2004.06.025
-
Clark, T. P.; Landis, C. R. Tetrahedron Asymmetry 2004, 15 (14), 2123. doi:10.1016/j.tetasy.2004.06.025.
-
(2004)
Tetrahedron Asymmetry
, vol.15
, Issue.14
, pp. 2123
-
-
Clark, T.P.1
Landis, C.R.2
-
46
-
-
0000395434
-
-
doi:10.1002/(SICI)1098-1071(1998)9:2<183::AID-HC14>3.0.CO;2-N
-
Heinicke, J.; He, M.; Kadyrov, R.; Jones, P. G. Heteroat. Chem. 1998, 9 (2), 183. doi:10.1002/(SICI)1098-1071(1998)9:2<183::AID-HC14>3.0.CO;2-N
-
(1998)
Heteroat. Chem.
, vol.9
, Issue.2
, pp. 183
-
-
Heinicke, J.1
He, M.2
Kadyrov, R.3
Jones, P.G.4
-
47
-
-
33646405458
-
-
doi:10.1002/ejoc. 200500937
-
Berens, U.; Englert, U.; Geyser, S.; Runsink, J.; Salzer, A. Eur. J. Org. Chem. 2006, 2006 (9), 2100.doi:10.1002/ejoc. 200500937.
-
(2006)
Eur. J. Org. Chem.
, vol.2006
, Issue.9
, pp. 2100
-
-
Berens, U.1
Englert, U.2
Geyser, S.3
Runsink, J.4
Salzer, A.5
-
48
-
-
33746903975
-
-
doi:10.1039/b607597e PMID:16896476
-
Dochnahl, M.; Pissarek, J.-W.; Blechert, S.; Löhnwitz, K.; Roesky, P. W. Chem. Commun. (Camb.) 2006, 3405. doi:10.1039/b607597e. PMID:16896476.
-
(2006)
Chem. Commun. (Camb.)
, vol.3405
-
-
Dochnahl, M.1
Pissarek, J.-W.2
Blechert, S.3
Löhnwitz, K.4
Roesky, P.W.5
-
49
-
-
0034474897
-
-
The Flack absolute structure parameter will refine to a value near zero if the structure is in the correct configuration and will refine to a value near one for the inverted configuration, see: doi:10.1107/S0021889800007184
-
The Flack absolute structure parameter will refine to a value near zero if the structure is in the correct configuration and will refine to a value near one for the inverted configuration, see: Flack, H. D.; Bernardinelli, G. J. Appl. Cryst. 2000, 33 (4), 1143. doi:10.1107/S0021889800007184.
-
(2000)
J. Appl. Cryst.
, vol.33
, Issue.4
, pp. 1143
-
-
Flack, H.D.1
Bernardinelli, G.2
-
50
-
-
33646767009
-
-
ORTEP-3 for Windows, version 1.074: doi:10.1107/S0021889897003117
-
ORTEP-3 for Windows, version 1.074: Farrugia, L. J. J. Appl. Cryst. 1997, 30 (5), 565. doi:10.1107/S0021889897003117
-
(1997)
J. Appl. Cryst.
, vol.30
, Issue.5
, pp. 565
-
-
Farrugia, L.J.1
|