-
2
-
-
84876828644
-
C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
-
Wencel-Delord, J. & Glorius, F. C-H bond activation enables the rapid construction and late-stage diversification of functional molecules. Nature Chem. 5, 369-375 (2013).
-
(2013)
Nature Chem.
, vol.5
, pp. 369-375
-
-
Wencel-Delord, J.1
Glorius, F.2
-
3
-
-
84865497366
-
Beyond directing groups: Transition-metal-catalyzed C-H activation of simple arenes
-
Kuhl, N., Hopkinson, M. N., Wencel-Delord, J. & Glorius, F. Beyond directing groups: transition-metal-catalyzed C-H activation of simple arenes. Angew. Chem. Int. Ed. 51, 10236-10254 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 10236-10254
-
-
Kuhl, N.1
Hopkinson, M.N.2
Wencel-Delord, J.3
Glorius, F.4
-
4
-
-
84863446276
-
Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions
-
Engle, K. M., Mei, T.-S., Wasa, M. & Yu, J.-Q. Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions. Acc. Chem. Res. 45, 788-802 (2011).
-
(2011)
Acc. Chem. Res.
, vol.45
, pp. 788-802
-
-
Engle, K.M.1
Mei, T.-S.2
Wasa, M.3
Yu, J.-Q.4
-
5
-
-
77949381429
-
Palladium-catalyzed ligand-directed C-H functionalization reactions
-
Lyons, T. W. & Sanford, M. S. Palladium-catalyzed ligand-directed C-H functionalization reactions. Chem. Rev. 110, 1147-1169 (2010).
-
(2010)
Chem. Rev.
, vol.110
, pp. 1147-1169
-
-
Lyons, T.W.1
Sanford, M.S.2
-
6
-
-
84862977089
-
Activation of remote meta-C-H bonds assisted by an end-on template
-
Leow, D., Li, G., Mei, T.-S. & Yu, J.-Q. Activation of remote meta-C-H bonds assisted by an end-on template. Nature 486, 518-522 (2012).
-
(2012)
Nature
, vol.486
, pp. 518-522
-
-
Leow, D.1
Li, G.2
Mei, T.-S.3
Yu, J.-Q.4
-
7
-
-
84894283977
-
Rhodium-catalyzed intermolecular C-H silylation of arenes with high steric regiocontrol
-
Cheng, C. & Hartwig, J. F. Rhodium-catalyzed intermolecular C-H silylation of arenes with high steric regiocontrol. Science 343, 853-857 (2014).
-
(2014)
Science
, vol.343
, pp. 853-857
-
-
Cheng, C.1
Hartwig, J.F.2
-
8
-
-
77349125577
-
C-H activation for the construction of C-B bonds
-
Mkhalid, I. A. I., Barnard, J. H., Marder, T. B., Murphy, J. M. & Hartwig, J. F. C-H activation for the construction of C-B bonds. Chem. Rev. 110, 890-931 (2009).
-
(2009)
Chem. Rev.
, vol.110
, pp. 890-931
-
-
Mkhalid, I.A.I.1
Barnard, J.H.2
Marder, T.B.3
Murphy, J.M.4
Hartwig, J.F.5
-
9
-
-
84928501363
-
Para-C-H borylation of benzene derivatives by a bulky iridium catalyst
-
Saito, Y., Segawa, Y. & Itami, K. para-C-H borylation of benzene derivatives by a bulky iridium catalyst. J. Am. Chem. Soc. 137, 5193-5198 (2015).
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 5193-5198
-
-
Saito, Y.1
Segawa, Y.2
Itami, K.3
-
10
-
-
84942902491
-
Site-selective arene C-H amination via photoredox catalysis
-
Romero, N. A., Margrey, K. A., Tay, N. E. & Nicewicz, D. A. Site-selective arene C-H amination via photoredox catalysis. Science 349, 1326-1330 (2015).
-
(2015)
Science
, vol.349
, pp. 1326-1330
-
-
Romero, N.A.1
Margrey, K.A.2
Tay, N.E.3
Nicewicz, D.A.4
-
11
-
-
70350662846
-
Mechanism of N-fluorobenzenesulfonimide promoted diamination and carboamination reactions: Divergent reactivity of a Pd(IV) species
-
Sibbald, P. A., Rosewall, C. F., Swartz, R. D. & Michael, F. E. Mechanism of N-fluorobenzenesulfonimide promoted diamination and carboamination reactions: divergent reactivity of a Pd(IV) species. J. Am. Chem. Soc. 131, 15945-15951 (2009).
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 15945-15951
-
-
Sibbald, P.A.1
Rosewall, C.F.2
Swartz, R.D.3
Michael, F.E.4
-
12
-
-
80052318722
-
Pd(II)-catalyzed para-selective C-H arylation of monosubstituted arenes
-
Wang, X., Leow, D. & Yu, J.-Q. Pd(II)-catalyzed para-selective C-H arylation of monosubstituted arenes. J. Am. Chem. Soc. 133, 13864-13867 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13864-13867
-
-
Wang, X.1
Leow, D.2
Yu, J.-Q.3
-
14
-
-
84884179823
-
Pd-catalyzed aryl C-H imidation with arene as the limiting reagent
-
Boursalian, G. B., Ngai, M.-Y., Hojczyk, K. N. & Ritter, T. Pd-catalyzed aryl C-H imidation with arene as the limiting reagent. J. Am. Chem. Soc. 135, 13278-13281 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 13278-13281
-
-
Boursalian, G.B.1
Ngai, M.-Y.2
Hojczyk, K.N.3
Ritter, T.4
-
15
-
-
0035901673
-
Factors controlling the addition of carbon-centered radicals to alkenes-an experimental and theoretical perspective
-
Fischer, H. & Radom, L. Factors controlling the addition of carbon-centered radicals to alkenes-an experimental and theoretical perspective. Angew. Chem. Int. Ed. 40, 1340-1371 (2001).
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 1340-1371
-
-
Fischer, H.1
Radom, L.2
-
16
-
-
0001051921
-
Comparison of the addition of CH3• CH2OH•, and CH2CN•radicals to substituted alkenes: A theoretical study of the reaction mechanism
-
Wong, M. W., Pross, A. & Radom, L. Comparison of the addition of CH3•, CH2OH•, and CH2CN• radicals to substituted alkenes: a theoretical study of the reaction mechanism. J. Am. Chem. Soc. 116, 6284-6292 (1994).
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 6284-6292
-
-
Wong, M.W.1
Pross, A.2
Radom, L.3
-
17
-
-
0041059705
-
Addition of tert-butyl radical to substituted alkenes: A theoretical study of the reaction mechanism
-
Wong, M.W., Pross, A. & Radom, L. Addition of tert-butyl radical to substituted alkenes: a theoretical study of the reaction mechanism. J. Am. Chem. Soc. 116, 11938-11943 (1994).
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 11938-11943
-
-
Wong, M.W.1
Pross, A.2
Radom, L.3
-
18
-
-
0042534101
-
Density functional approach to the frontier-electron theory of chemical reactivity
-
Parr, R. G. & Yang, W. Density functional approach to the frontier-electron theory of chemical reactivity. J. Am. Chem. Soc. 106, 4049-4050 (1984).
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 4049-4050
-
-
Parr, R.G.1
Yang, W.2
-
20
-
-
0034423181
-
Perspective on Density functional approach to the frontier-electron theory of chemical reactivity
-
Ayers, P. W. & Levy, M. Perspective on Density functional approach to the frontier-electron theory of chemical reactivity. Theor. Chem. Acc. 103, 353-360 (2000).
-
(2000)
Theor. Chem. Acc.
, vol.103
, pp. 353-360
-
-
Ayers, P.W.1
Levy, M.2
-
21
-
-
0000219286
-
Ipso substitution in free-radical aromatic substitution reactions
-
Traynham, J. G. Ipso substitution in free-radical aromatic substitution reactions. Chem. Rev. 79, 323-330 (1979).
-
(1979)
Chem. Rev.
, vol.79
, pp. 323-330
-
-
Traynham, J.G.1
-
22
-
-
84867533187
-
A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination
-
Bloom, S. et al. A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination. Angew. Chem. Int. Ed. 51, 10580-10583 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 10580-10583
-
-
Bloom, S.1
-
23
-
-
84904015912
-
Direct, catalytic monofluorination of sp3 C-H bonds: A radicalbased mechanism with ionic selectivity
-
Pitts, C. R. et al. Direct, catalytic monofluorination of sp3 C-H bonds: a radicalbased mechanism with ionic selectivity. J. Am. Chem. Soc. 136, 9780-9791 (2014).
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 9780-9791
-
-
Pitts, C.R.1
-
24
-
-
84856714142
-
Intermolecular Ritter-type C-H amination of unactivated sp3 carbons
-
Michaudel, Q., Thevenet, D. & Baran, P. S. Intermolecular Ritter-type C-H amination of unactivated sp3 carbons. J. Am. Chem. Soc. 134, 2547-2550 (2012).
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 2547-2550
-
-
Michaudel, Q.1
Thevenet, D.2
Baran, P.S.3
-
25
-
-
84879224625
-
Visible-light photoredox in homolytic aromatic substitution: Direct arylation of arenes with aryl halides
-
Cheng, Y., Gu, X. & Li, P. Visible-light photoredox in homolytic aromatic substitution: direct arylation of arenes with aryl halides. Org. Lett. 15, 2664-2667 (2013).
-
(2013)
Org. Lett.
, vol.15
, pp. 2664-2667
-
-
Cheng, Y.1
Gu, X.2
Li, P.3
-
26
-
-
84899029820
-
N-Acyloxyphthalimides as nitrogen radical precursors in the visible light photocatalyzed room temperature C-H amination of arenes and heteroarenes
-
Allen, L. J., Cabrera, P. J., Lee, M. & Sanford, M. S. N-Acyloxyphthalimides as nitrogen radical precursors in the visible light photocatalyzed room temperature C-H amination of arenes and heteroarenes. J. Am. Chem. Soc. 136, 5607-5610 (2014).
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 5607-5610
-
-
Allen, L.J.1
Cabrera, P.J.2
Lee, M.3
Sanford, M.S.4
-
27
-
-
0001127820
-
Polar effects in free radical reactions. Homolytic aromatic amination by the amino radical cation,•+ NH3: Reactivity and selectivity
-
Citterio, A. et al. Polar effects in free radical reactions. Homolytic aromatic amination by the amino radical cation,•+NH3: reactivity and selectivity. J. Org. Chem. 49, 4479-4482 (1984).
-
(1984)
J. Org. Chem.
, vol.49
, pp. 4479-4482
-
-
Citterio, A.1
-
28
-
-
84959947882
-
Novel applications of free-radical reactions in preparative organic chemistry
-
Minisci, F. Novel applications of free-radical reactions in preparative organic chemistry. Synthesis 1-24 (1973).
-
(1973)
Synthesis
, pp. 1-24
-
-
Minisci, F.1
-
29
-
-
84918269940
-
Nuovi processi per introdurre lazoto inmolecole organiche con reazioni radicaliche: Azidazione e amminazione
-
Minisci, F. Nuovi processi per introdurre lazoto inmolecole organiche con reazioni radicaliche: azidazione e amminazione. Chim. Ind. (Milano) 49, 705-719 (1967).
-
(1967)
Chim. Ind. (Milano)
, vol.49
, pp. 705-719
-
-
Minisci, F.1
-
30
-
-
84898721607
-
Rings in drugs
-
Taylor, R. D., MacCoss, M. & Lawson, A. D. G. Rings in drugs. J. Med. Chem. 57, 5845-5859 (2014).
-
(2014)
J. Med. Chem.
, vol.57
, pp. 5845-5859
-
-
Taylor, R.D.1
MacCoss, M.2
Lawson, A.D.G.3
-
31
-
-
78751554725
-
Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds
-
Fischer C. & Koenig, B. Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds. Beilstein J. Org. Chem. 7. 59-74 (2011).
-
(2011)
Beilstein J. Org. Chem.
, vol.7
, pp. 59-74
-
-
Fischer, C.1
Koenig, B.2
|