-
1
-
-
84969535016
-
-
N. Schneider, D. M. Lowe, R. A. Sayle, M. A. Tarselli, G. A. Landrum, J. Med. Chem. 2016, 59, 4385.
-
(2016)
J. Med. Chem.
, vol.59
, pp. 4385
-
-
Schneider, N.1
Lowe, D.M.2
Sayle, R.A.3
Tarselli, M.A.4
Landrum, G.A.5
-
3
-
-
84959450281
-
-
J. Cornella, J. T. Edwards, S. Kawamura, J. Wang, C.-M. Pan, R. Gianatassio, M. Schmidt, M. D. Eastgate, P. S. Baran, J. Am. Chem. Soc. 2016, 138, 2174.
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 2174
-
-
Cornella, J.1
Edwards, J.T.2
Kawamura, S.3
Wang, J.4
Pan, C.-M.5
Gianatassio, R.6
Schmidt, M.7
Eastgate, M.D.8
Baran, P.S.9
-
4
-
-
84964558188
-
-
T. Qin, J. Cornella, C. Li, L. Malins, J. T. Edwards, S. Kawamura, B. D. Maxwell, M. D. Eastgate, P. S. Baran, Science 2016, 352, 801.
-
(2016)
Science
, vol.352
, pp. 801
-
-
Qin, T.1
Cornella, J.2
Li, C.3
Malins, L.4
Edwards, J.T.5
Kawamura, S.6
Maxwell, B.D.7
Eastgate, M.D.8
Baran, P.S.9
-
5
-
-
84966292281
-
-
Shortly after ref. [3] was published, D. J. Weix reported that NHPI esters could undergo reductive cross-coupling with aryl iodides using Zn, as the reducing agen
-
Shortly after ref. [3] was published, D. J. Weix reported that NHPI esters could undergo reductive cross-coupling with aryl iodides using Zn0as the reducing agent: K. M. M. Huihui, J. A. Caputo, Z. Melchor, A. M. Olivares, A. M. Spiewak, K. A. Jonhson, T. A. DiBenedetto, S. Kim, L. K. G. Ackerman, D. J. Weix, J. Am. Chem. Soc. 2016, 138, 5016.
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 5016
-
-
Huihui, K.M.M.1
Caputo, J.A.2
Melchor, Z.3
Olivares, A.M.4
Spiewak, A.M.5
Jonhson, K.A.6
DiBenedetto, T.A.7
Kim, S.8
Ackerman, L.K.G.9
Weix, D.J.10
-
6
-
-
85043129294
-
-
For the use of NHPI esters in photochemically initiated SET processes, se
-
For the use of NHPI esters in photochemically initiated SET processes, see:
-
-
-
-
8
-
-
84969435032
-
-
Angew. Chem. 2012, 124, 9714;
-
(2012)
Angew. Chem.
, vol.124
, pp. 9714
-
-
-
9
-
-
84934921868
-
-
G. Pratsch, G. L. Lackner, L. E. Overman, J. Org. Chem. 2015, 80, 6025;
-
(2015)
J. Org. Chem.
, vol.80
, pp. 6025
-
-
Pratsch, G.1
Lackner, G.L.2
Overman, L.E.3
-
10
-
-
0001112346
-
-
K. Okada, K. Okamoto, M. Oda, J. Am. Chem. Soc. 1988, 110, 8736;
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 8736
-
-
Okada, K.1
Okamoto, K.2
Oda, M.3
-
11
-
-
0001476677
-
-
K. Okada, K. Okamoto, N. Morita, K. Okubo, M. Oda, J. Am. Chem. Soc. 1991, 113, 9401.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 9401
-
-
Okada, K.1
Okamoto, K.2
Morita, N.3
Okubo, K.4
Oda, M.5
-
12
-
-
85043102530
-
-
As mentioned in ref. [3], redox-active esters are analogous to alkyl halides, a mechanistic parallel can be directly drawn to pioneering work in the area of Ni-catalyzed single-electron transfer cross-coupling of those species, se
-
As mentioned in ref. [3], redox-active esters are analogous to alkyl halides. Thus, a mechanistic parallel can be directly drawn to pioneering work in the area of Ni-catalyzed single-electron transfer cross-coupling of those species, see:
-
-
-
-
13
-
-
3042734823
-
-
T. J. Anderson, G. D. Jones, D. A. Vicic, J. Am. Chem. Soc. 2004, 126, 8100;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8100
-
-
Anderson, T.J.1
Jones, G.D.2
Vicic, D.A.3
-
14
-
-
33749519198
-
-
G. D. Jones, J. L. Martin, C. McFarland, O. R. Allen, R. E. Hall, A. D. Haley, R. J. Brandon, T. Konovalova, P. J. Desrochers, P. Pulay, D. A. Vicic, J. Am. Chem. Soc. 2006, 128, 13175;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13175
-
-
Jones, G.D.1
Martin, J.L.2
McFarland, C.3
Allen, O.R.4
Hall, R.E.5
Haley, A.D.6
Brandon, R.J.7
Konovalova, T.8
Desrochers, P.J.9
Pulay, P.10
Vicic, D.A.11
-
16
-
-
36749022699
-
-
V. B. Phapale, E. Buñuel, M. García-Iglesias, D. J. Cárdenas, Angew. Chem. Int. Ed. 2007, 46, 8790–8795;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 8790-8795
-
-
Phapale, V.B.1
Buñuel, E.2
García-Iglesias, M.3
Cárdenas, D.J.4
-
17
-
-
63449111326
-
-
Angew. Chem. 2007, 119, 8946–8951;
-
(2007)
Angew. Chem.
, vol.119
, pp. 8946-8951
-
-
-
18
-
-
84928492420
-
-
O. Gutierrez, J. C. Tellis, D. N. Primer, G. A. Molander, J. Am. Chem. Soc. 2015, 137, 4896;
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 4896
-
-
Gutierrez, O.1
Tellis, J.C.2
Primer, D.N.3
Molander, G.A.4
-
20
-
-
84899720423
-
-
B. Zheng, F. Tang, J. Luo, J. W. Schultz, N. P. Rath, L. M. Mirica, J. Am. Chem. Soc. 2014, 136, 6499;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 6499
-
-
Zheng, B.1
Tang, F.2
Luo, J.3
Schultz, J.W.4
Rath, N.P.5
Mirica, L.M.6
-
21
-
-
84882289438
-
-
J. Breitenfeld, J. Ruiz, M. D. Wodrich, X. Hu, J. Am. Chem. Soc. 2013, 135, 12004;
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 12004
-
-
Breitenfeld, J.1
Ruiz, J.2
Wodrich, M.D.3
Hu, X.4
-
23
-
-
85043133473
-
-
For selected examples of Ni-catalyzed alkyl- -aryl Suzuki–Miyaura cross-couplings, se
-
For selected examples of Ni-catalyzed alkyl- -aryl Suzuki–Miyaura cross-couplings, see:
-
-
-
-
27
-
-
84859355289
-
-
A. Wilsily, F. Tramutola, N. A. Owston, G. C. Fu, J. Am. Chem. Soc. 2012, 134, 5794;
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 5794
-
-
Wilsily, A.1
Tramutola, F.2
Owston, N.A.3
Fu, G.C.4
-
29
-
-
79952656192
-
-
R. Jana, T. P. Pathak, M. S. Sigman, Chem. Rev. 2011, 111, 1417.
-
(2011)
Chem. Rev.
, vol.111
, pp. 1417
-
-
Jana, R.1
Pathak, T.P.2
Sigman, M.S.3
-
30
-
-
85043132237
-
-
See Supporting Information for details
-
See Supporting Information for details.
-
-
-
-
31
-
-
84969776862
-
-
E. J. Horn, B. R. Rosen, Y. Chen, J. Tang, K. Chen, M. D. Eastgate, P. S. Baran, Nature 2016, 533, 77.
-
(2016)
Nature
, vol.533
, pp. 77
-
-
Horn, E.J.1
Rosen, B.R.2
Chen, Y.3
Tang, J.4
Chen, K.5
Eastgate, M.D.6
Baran, P.S.7
-
32
-
-
84935142468
-
-
For an older route involving Friedel–Crafts of benzene with cyclohexene followed by bromination, se
-
K. Ueda, H. Umihara, S. Yokoshima, T. Fukuyama, Org. Lett. 2015, 17, 3191; For an older route involving Friedel–Crafts of benzene with cyclohexene followed by bromination, see:
-
(2015)
Org. Lett.
, vol.17
, pp. 3191
-
-
Ueda, K.1
Umihara, H.2
Yokoshima, S.3
Fukuyama, T.4
-
34
-
-
84931269941
-
-
I. Papanastasiou, S. Riganas, G. B. Foscolos, A. Tsotinis, S. A. Akhtar, M. A. Khan, K. M. Rahman, D. E. Thurston, Lett. Org. Chem. 2015, 12, 319;
-
(2015)
Lett. Org. Chem.
, vol.12
, pp. 319
-
-
Papanastasiou, I.1
Riganas, S.2
Foscolos, G.B.3
Tsotinis, A.4
Akhtar, S.A.5
Khan, M.A.6
Rahman, K.M.7
Thurston, D.E.8
-
35
-
-
84891674765
-
-
D. M. Allwood, D. C. Blakemore, A. D. Brown, S. V. Ley, J. Org. Chem. 2014, 79, 328.
-
(2014)
J. Org. Chem.
, vol.79
, pp. 328
-
-
Allwood, D.M.1
Blakemore, D.C.2
Brown, A.D.3
Ley, S.V.4
-
37
-
-
33748595300
-
-
R. F. W. Jackson, J. L. Frase, N. Wishart, B. Porter, M. J. Wythes, J. Chem. Soc. Perkin Trans. 1 1998, 1903.
-
(1998)
J. Chem. Soc. Perkin Trans. 1
, pp. 1903
-
-
Jackson, R.F.W.1
Frase, J.L.2
Wishart, N.3
Porter, B.4
Wythes, M.J.5
-
38
-
-
84963522319
-
-
Recently, the formation of hydroxy-bridged species between a boronate and the metal center have disclosed as key step for transmetalation in Suzuki cross-couplings with P
-
Recently, the formation of hydroxy-bridged species between a boronate and the metal center have disclosed as key step for transmetalation in Suzuki cross-couplings with Pd: A. A. Thomas, S. E. Denmark, Science 2016, 352, 329.
-
(2016)
Science
, vol.352
, pp. 329
-
-
Thomas, A.A.1
Denmark, S.E.2
-
39
-
-
84904797499
-
-
The capture of similar radicals was also invoked during the decarboxylative coupling of α-heteroatom stabilized acids with aryl halide
-
The capture of similar radicals was also invoked during the decarboxylative coupling of α-heteroatom stabilized acids with aryl halides: Z. Zuo, D. T. Ahneman, L. Chu, J. A. Terrett, A. G. Doyle, D. W. C. MacMillan, Science 2014, 345, 437.
-
(2014)
Science
, vol.345
, pp. 437
-
-
Zuo, Z.1
Ahneman, D.T.2
Chu, L.3
Terrett, J.A.4
Doyle, A.G.5
MacMillan, D.W.C.6
-
40
-
-
85043100115
-
-
This reaction is currently being enlisted at Bristol-Myers Squibb in several ongoing programs, including one involving the co-authors (B, V. and S.A.S.)
-
This reaction is currently being enlisted at Bristol-Myers Squibb in several ongoing programs, including one involving the co-authors (B.V. and S.A.S.).
-
-
-
-
41
-
-
85043103849
-
-
X-ray information for compound 17 can be obtained free of charge from The, Crystallographic Data center with number CCDC 1477360
-
X-ray information for compound 17 can be obtained free of charge from The Cambridge Crystallographic Data center with number CCDC 1477360.
-
-
-
|