-
3
-
-
84865100409
-
-
C. Queffélec, M. Petit, P. Janvier, D. A. Knight, B. Bujoli, Chem. Rev. 2012, 112, 3777;
-
(2012)
Chem. Rev.
, vol.112
, pp. 3777
-
-
Queffélec, C.1
Petit, M.2
Janvier, P.3
Knight, D.A.4
Bujoli, B.5
-
4
-
-
84877130803
-
-
6ed, th ed, CRC Press, Taylor & Francis Group
-
D. E. C. Corbridge, Phosphorus: Chemistry, Biochemistry and Technology, 6edth edCRC Press, Taylor & Francis Group, 2013.
-
(2013)
Phosphorus: Chemistry, Biochemistry and Technology
-
-
Corbridge, D.E.C.1
-
7
-
-
0003795078
-
-
in, John Wiley & Sons, Chichester
-
K. B. Dillon, F. Mathey, J. F. Nixon, in Phosphorus: The Carbon Copy, John Wiley & Sons, Chichester, 1998.
-
(1998)
Phosphorus: The Carbon Copy
-
-
Dillon, K.B.1
Mathey, F.2
Nixon, J.F.3
-
8
-
-
14844320755
-
-
H. Onouchi, T. Miyagawa, A. Furuko, K. Maeda, E. Yashima, J. Am. Chem. Soc. 2005, 127, 2960;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2960
-
-
Onouchi, H.1
Miyagawa, T.2
Furuko, A.3
Maeda, K.4
Yashima, E.5
-
10
-
-
0345368045
-
-
M. Koziołkiewicz, A. Maciaszek, W. J. Stec, D. Semizarov, L. Victorova, A. Krayevsky, FEBS Lett. 1998, 434, 77.
-
(1998)
FEBS Lett.
, vol.434
, pp. 77
-
-
Koziołkiewicz, M.1
Maciaszek, A.2
Stec, W.J.3
Semizarov, D.4
Victorova, L.5
Krayevsky, A.6
-
12
-
-
0003544583
-
1
-
In, Ojima, I., Ed., Wiley-VCH, Weinheim, Germany, , Chapter
-
T. Ohkuma, M. Kitamura, R. Noyori, In Catalytic Asymmetric Synthesis Ojima, I., Ed., Wiley-VCH, Weinheim, Germany, 2000, Chapter 1.
-
(2000)
Catalytic Asymmetric Synthesis
-
-
Ohkuma, T.1
Kitamura, M.2
Noyori, R.3
-
14
-
-
33947597616
-
-
A. Grabulosa, J. Granell, G. Muller, Coord. Chem. Rev. 2007, 251, 25;
-
(2007)
Coord. Chem. Rev.
, vol.251
, pp. 25
-
-
Grabulosa, A.1
Granell, J.2
Muller, G.3
-
15
-
-
69949190011
-
-
V. S. Chan, M. Chiu, R. G. Bergman, F. D. Toste, J. Am. Chem. Soc. 2009, 131, 6021;
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 6021
-
-
Chan, V.S.1
Chiu, M.2
Bergman, R.G.3
Toste, F.D.4
-
16
-
-
33645816082
-
-
N. F. Blank, K. C. McBroom, D. S. Glueck, W. S. Kassel, A. L. Rheingold, Organometallics 2006, 25, 1742;
-
(2006)
Organometallics
, vol.25
, pp. 1742
-
-
Blank, N.F.1
McBroom, K.C.2
Glueck, D.S.3
Kassel, W.S.4
Rheingold, A.L.5
-
17
-
-
84897549017
-
-
Y. Huang, Y. Li, P.-H. Leung, T. Hayashi, J. Am. Chem. Soc. 2014, 136, 4865.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 4865
-
-
Huang, Y.1
Li, Y.2
Leung, P.-H.3
Hayashi, T.4
-
18
-
-
85043096184
-
-
For examples of transition-metal-catalyzed CH functionalizations, see
-
For examples of transition-metal-catalyzed CH functionalizations, see:
-
-
-
-
20
-
-
68949185025
-
-
O. Daugulis, H.-Q. Do, D. Shabashov, Acc. Chem. Res. 2009, 42, 1074;
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 1074
-
-
Daugulis, O.1
Do, H.-Q.2
Shabashov, D.3
-
22
-
-
74549178746
-
-
C.-L. Sun, B.-J. Li, Z.-J. Shi, Chem. Commun. 2010, 46, 677;
-
(2010)
Chem. Commun.
, vol.46
, pp. 677
-
-
Sun, C.-L.1
Li, B.-J.2
Shi, Z.-J.3
-
23
-
-
80054728269
-
-
S. H. Cho, J. Y. Kim, J. Kwak, S. Chang, Chem. Soc. Rev. 2011, 40, 5068;
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 5068
-
-
Cho, S.H.1
Kim, J.Y.2
Kwak, J.3
Chang, S.4
-
24
-
-
80054105790
-
-
J. Wencel-Delord, T. Drcge, F. Liu, F. Glorius, Chem. Soc. Rev. 2011, 40, 4740;
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4740
-
-
Wencel-Delord, J.1
Drcge, T.2
Liu, F.3
Glorius, F.4
-
28
-
-
79958848824
-
-
L. McMurray, F. O. Hara, M. J. Gaunt, Chem. Soc. Rev. 2011, 40, 1885;
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 1885
-
-
McMurray, L.1
Hara, F.O.2
Gaunt, M.J.3
-
30
-
-
84857325043
-
-
M. C. White, Science 2012, 335, 807;
-
(2012)
Science
, vol.335
, pp. 807
-
-
White, M.C.1
-
31
-
-
84863446276
-
-
K. M. Engle, T.-S. Mei, M. Wasa, J.-Q. Yu, Acc. Chem. Res. 2012, 45, 788;
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 788
-
-
Engle, K.M.1
Mei, T.-S.2
Wasa, M.3
Yu, J.-Q.4
-
32
-
-
84871962677
-
-
J. Yamaguchi, A. D. Yamaguchi, K. Itami, Angew. Chem. 2012, 124, 9092;
-
(2012)
Angew. Chem.
, vol.124
, pp. 9092
-
-
Yamaguchi, J.1
Yamaguchi, A.D.2
Itami, K.3
-
35
-
-
36849030278
-
-
E. M. Beccalli, G. Broggini, M. Martinelli, S. Sottocornola, Chem. Rev. 2007, 107, 5318;
-
(2007)
Chem. Rev.
, vol.107
, pp. 5318
-
-
Beccalli, E.M.1
Broggini, G.2
Martinelli, M.3
Sottocornola, S.4
-
36
-
-
84896265403
-
-
R.-Y. Tang, G. Li, J.-Q. Yu, Nature 2014, 507, 215.
-
(2014)
Nature
, vol.507
, pp. 215
-
-
Tang, R.-Y.1
Li, G.2
Yu, J.-Q.3
-
37
-
-
85043141807
-
-
For examples of enantioselective CH functionalizations, see
-
For examples of enantioselective CH functionalizations, see:
-
-
-
-
39
-
-
70350494926
-
-
R. Giri, B.-F. Shi, K. M. Engle, N. Maugel, J.-Q. Yu, Chem. Soc. Rev. 2009, 38, 3242;
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 3242
-
-
Giri, R.1
Shi, B.-F.2
Engle, K.M.3
Maugel, N.4
Yu, J.-Q.5
-
42
-
-
84867768045
-
-
T. K. Hyster, L. Knörr, T. R. Ward, T. Rovis, Science 2012, 338, 500.
-
(2012)
Science
, vol.338
, pp. 500
-
-
Hyster, T.K.1
Knörr, L.2
Ward, T.R.3
Rovis, T.4
-
43
-
-
85043118453
-
-
For our previous studies on the Ir-catalyzed CH amidation procedures, see
-
For our previous studies on the Ir-catalyzed CH amidation procedures, see:
-
-
-
-
44
-
-
84883301466
-
-
J. Ryu, J. Kwak, K. Shin, D. Lee, S. Chang, J. Am. Chem. Soc. 2013, 135, 12861;
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 12861
-
-
Ryu, J.1
Kwak, J.2
Shin, K.3
Lee, D.4
Chang, S.5
-
45
-
-
84887036529
-
-
D. Lee, Y. Kim, S. Chang, J. Org. Chem. 2013, 78, 11102;
-
(2013)
J. Org. Chem.
, vol.78
, pp. 11102
-
-
Lee, D.1
Kim, Y.2
Chang, S.3
-
48
-
-
84896496785
-
-
T. Kang, Y. Kim, D. Lee, Z. Wang, S. Chang, J. Am. Chem. Soc. 2014, 136, 4141.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 4141
-
-
Kang, T.1
Kim, Y.2
Lee, D.3
Wang, Z.4
Chang, S.5
-
49
-
-
85043096234
-
-
For previous examples of acid effects in CH activation, see
-
For previous examples of acid effects in CH activation, see:
-
-
-
-
50
-
-
84893331462
-
-
D. Zhao, Z. Shi, F. Glorius, Angew. Chem. 2013, 125, 12652;
-
(2013)
Angew. Chem.
, vol.125
, pp. 12652
-
-
Zhao, D.1
Shi, Z.2
Glorius, F.3
-
52
-
-
79959904644
-
-
E. F. Flegeau, C. Bruneau, P. H. Dixneuf, A. Justand, J. Am. Chem. Soc. 2011, 133, 10161.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10161
-
-
Flegeau, E.F.1
Bruneau, C.2
Dixneuf, P.H.3
Justand, A.4
-
53
-
-
20944450464
-
-
S. L. Cockroft, C. A. Hunter, K. R. Lawson, J. Perkins, C. J. Urch, J. Am. Chem. Soc. 2005, 127, 8594;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 8594
-
-
Cockroft, S.L.1
Hunter, C.A.2
Lawson, K.R.3
Perkins, J.4
Urch, C.J.5
-
54
-
-
17044429438
-
-
F. Hof, D. M. Scofield, W. B. Schweizer, F. Diederich, Angew. Chem. 2004, 116, 5166;
-
(2004)
Angew. Chem.
, vol.116
, pp. 5166
-
-
Hof, F.1
Scofield, D.M.2
Schweizer, W.B.3
Diederich, F.4
-
58
-
-
0035929793
-
-
T. Katagiri, S. Yamaji, M. Handa, M. Irie, K. Uneyama, Chem. Commun. 2001, 2054.
-
(2001)
Chem. Commun.
, pp. 2054
-
-
Katagiri, T.1
Yamaji, S.2
Handa, M.3
Irie, M.4
Uneyama, K.5
-
59
-
-
84894184671
-
-
S. H. Park, J. Kwak, K. Shin, J. Ryu, Y. Park, S. Chang, J. Am. Chem. Soc. 2014, 136, 2492;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 2492
-
-
Park, S.H.1
Kwak, J.2
Shin, K.3
Ryu, J.4
Park, Y.5
Chang, S.6
-
60
-
-
84899563578
-
-
L.-L. Zhang, L.-H. Li, Y.-Q. Wang, Y.-F. Yang, X.-Y. Liu, Y.-M. Liang, Organometallics 2014, 33, 1905.
-
(2014)
Organometallics
, vol.33
, pp. 1905
-
-
Zhang, L.-L.1
Li, L.-H.2
Wang, Y.-Q.3
Yang, Y.-F.4
Liu, X.-Y.5
Liang, Y.-M.6
-
61
-
-
85043109222
-
-
For examples of transition-metal-catalyzed CH functionalizations of phosphine oxides, see
-
For examples of transition-metal-catalyzed CH functionalizations of phosphine oxides, see:
-
-
-
-
63
-
-
84879214838
-
-
B. C. Chary, S. Kim, Y. Park, J. Kim, P. H. Lee, Org. Lett. 2013, 15, 2692;
-
(2013)
Org. Lett.
, vol.15
, pp. 2692
-
-
Chary, B.C.1
Kim, S.2
Park, Y.3
Kim, J.4
Lee, P.H.5
-
64
-
-
84880004626
-
-
Y. Unoh, Y. Hashimoto, D. Takeda, K. Hirano, T. Satoh, M. Miura, Org. Lett. 2013, 15, 3258;
-
(2013)
Org. Lett.
, vol.15
, pp. 3258
-
-
Unoh, Y.1
Hashimoto, Y.2
Takeda, D.3
Hirano, K.4
Satoh, T.5
Miura, M.6
-
65
-
-
84883810736
-
-
D. Zhao, C. Nimphius, M. Lindale, F. Glorius, Org. Lett. 2013, 15, 4504.
-
(2013)
Org. Lett.
, vol.15
, pp. 4504
-
-
Zhao, D.1
Nimphius, C.2
Lindale, M.3
Glorius, F.4
-
66
-
-
85099670984
-
-
Deoxygenation of 2 was carried out efficiently by using HSiCl, to afford the corresponding amidated phosphine in 89 % yielddetailed experimental procedures are presented in the Supporting Information
-
3 to afford the corresponding amidated phosphine in 89 % yield, and detailed experimental procedures are presented in the Supporting Information.
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