-
1
-
-
84859616806
-
High-valent organometallic copper and palladium in catalysis
-
Hickman, A. J. & Sanford, M. S. High-valent organometallic copper and palladium in catalysis. Nature 484, 177-185 (2012).
-
(2012)
Nature
, vol.484
, pp. 177-185
-
-
Hickman, A.J.1
Sanford, M.S.2
-
2
-
-
79957603696
-
Catalysis for fluorination and trifluoromethylation
-
Furuya, T., Kamlet, A. S. & Ritter, T. Catalysis for fluorination and trifluoromethylation. Nature 473, 470-477 (2011).
-
(2011)
Nature
, vol.473
, pp. 470-477
-
-
Furuya, T.1
Kamlet, A.S.2
Ritter, T.3
-
3
-
-
80555125102
-
A fluoride-derived electrophilic late-stage fluorination reagent for PET imaging
-
Lee, E. et al. A fluoride-derived electrophilic late-stage fluorination reagent for PET imaging. Science 334, 639-642 (2011).
-
(2011)
Science
, vol.334
, pp. 639-642
-
-
Lee, E.1
-
4
-
-
77949867611
-
Mechanism of C-F reductive elimination from palladium(IV) fluorides
-
Furuya, T. et al. Mechanism of C-F reductive elimination from palladium(IV) fluorides. J. Am. Chem. Soc. 132, 3793-3807 (2010).
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 3793-3807
-
-
Furuya, T.1
-
5
-
-
37049033864
-
Reactivity of Pd(II) complexes with electrophilic chlorinating reagents: Isolation of Pd(IV) products and observation of C2Cl bondforming reductive elimination
-
Whitfield, S. R. & Sanford, M. S. Reactivity of Pd(II) complexes with electrophilic chlorinating reagents: Isolation of Pd(IV) products and observation of C2Cl bondforming reductive elimination. J. Am. Chem. Soc. 129, 15142-15143 (2007).
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 15142-15143
-
-
Whitfield, S.R.1
Sanford, M.S.2
-
6
-
-
0001203082
-
Rigid five-and six-membered C,N,N9-bound aryl-, Benzyl-, And alkylorganopalladium complexes: Sp2 vs. Sp3 carbon-hydrogen activation during cyclopalladation and palladium(IV) intermediates in oxidative addition reactions with dihalogens and alkyl halides
-
Alsters, P. L. et al. Rigid five-and six-membered C,N,N9-bound aryl-, benzyl-, and alkylorganopalladium complexes: sp2 vs. sp3 carbon-hydrogen activation during cyclopalladation and palladium(IV) intermediates in oxidative addition reactions with dihalogens and alkyl halides. Organometallics 12, 1831-1844 (1993).
-
(1993)
Organometallics
, vol.12
, pp. 1831-1844
-
-
Alsters, P.L.1
-
7
-
-
84896513155
-
Development of catalysts and ligands for enantioselective gold catalysis
-
Wang, Y.-M., Lackner, A. D. & Toste, F. D. Development of catalysts and ligands for enantioselective gold catalysis. Acc. Chem. Res. 47, 889-901 (2014).
-
(2014)
Acc. Chem. Res.
, vol.47
, pp. 889-901
-
-
Wang, Y.-M.1
Lackner, A.D.2
Toste, F.D.3
-
8
-
-
79952686693
-
Gold-catalyzed nucleophilic cyclization of functionalized allenes: A powerful access to carbo-and heterocycles
-
Krause, N. & Winter, C. Gold-catalyzed nucleophilic cyclization of functionalized allenes: a powerful access to carbo-and heterocycles. Chem. Rev. 111, 1994-2009 (2011).
-
(2011)
Chem. Rev.
, vol.111
, pp. 1994-2009
-
-
Krause, N.1
Winter, C.2
-
9
-
-
79952677038
-
Gold-catalyzed carbon-heteroatom bond-forming reactions
-
Corma, A., Leyva-Pérez, A. & Sabater, M. J. Gold-catalyzed carbon-heteroatom bond-forming reactions. Chem. Rev. 111, 1657-1712 (2011).
-
(2011)
Chem. Rev.
, vol.111
, pp. 1657-1712
-
-
Corma, A.1
Leyva-Pérez, A.2
Sabater, M.J.3
-
10
-
-
34547567515
-
A powerful chiral counterion strategy for asymmetric transition metal catalysis
-
Hamilton, G. L., Kang, E. J., Mba, M. & Toste, F. D. A powerful chiral counterion strategy for asymmetric transition metal catalysis. Science 317, 496-499 (2007).
-
(2007)
Science
, vol.317
, pp. 496-499
-
-
Hamilton, G.L.1
Kang, E.J.2
Mba, M.3
Toste, F.D.4
-
11
-
-
33947578482
-
Relativistic effects in homogeneous gold catalysis
-
Gorin, D. J. & Toste, F. D. Relativistic effects in homogeneous gold catalysis. Nature 446, 395-403 (2007).
-
(2007)
Nature
, vol.446
, pp. 395-403
-
-
Gorin, D.J.1
Toste, F.D.2
-
12
-
-
84864089050
-
Gold(III) compounds for homogeneous catalysis: Preparation, reaction conditions, and scope of application
-
Schmidbaur, H. & Schier, A. Gold(III) compounds for homogeneous catalysis: preparation, reaction conditions, and scope of application. Arabian J. Sci. Eng. 37, 1187-1225 (2012).
-
(2012)
Arabian J. Sci. Eng.
, vol.37
, pp. 1187-1225
-
-
Schmidbaur, H.1
Schier, A.2
-
13
-
-
84871036371
-
Small gold clusters formed in solution give reaction turnover numbers of 107 at room temperature
-
Oliver-Meseguer, J. et al. Small gold clusters formed in solution give reaction turnover numbers of 107 at room temperature. Science 338, 1452-1455 (2012).
-
(2012)
Science
, vol.338
, pp. 1452-1455
-
-
Oliver-Meseguer, J.1
-
14
-
-
84855609485
-
Similarities and differences between the relativistic triad gold, platinum, and mercury in catalysis
-
Leyva-Pérez, A. & Corma, A. Similarities and differences between the "relativistic" triad gold, platinum, and mercury in catalysis. Angew. Chem. Int. Ed. 51, 614-635 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 614-635
-
-
Leyva-Pérez, A.1
Corma, A.2
-
15
-
-
74549129371
-
Synthetic and structural studies of [AuCl3(NHC)] complexes
-
Gaillard, S. et al. Synthetic and structural studies of [AuCl3(NHC)] complexes. Organometallics 29, 394-402 (2010).
-
(2010)
Organometallics
, vol.29
, pp. 394-402
-
-
Gaillard, S.1
-
16
-
-
33947700898
-
Synthesis characterization and reactivity of N-heterocyclic carbene gold(III) complexes
-
de Frémont, P., Singh, R., Stevens, E. D., Petersen, J. L. & Nolan, S. P. Synthesis, characterization and reactivity of N-heterocyclic carbene gold(III) complexes. Organometallics 26, 1376-1385 (2007).
-
(2007)
Organometallics
, vol.26
, pp. 1376-1385
-
-
De Frémont, P.1
Singh, R.2
Stevens, E.D.3
Petersen, J.L.4
Nolan, S.P.5
-
17
-
-
33645059154
-
Gold catalysis: Evidence for the in situ reduction of gold(III)Duringthe cyclizationof allenyl carbinols
-
Hashmi, A. S. K., Blanco, M. C., Fischer, D. & Bats, J. W. Gold catalysis: evidence for the in situ reduction of gold(III)Duringthe cyclizationof allenyl carbinols. Eur. J. Org. Chem. 1387-1389 (2006).
-
(2006)
Eur. J. Org. Chem.
, pp. 1387-1389
-
-
Hashmi, A.S.K.1
Blanco, M.C.2
Fischer, D.3
Bats, J.W.4
-
18
-
-
84893011475
-
Exceptionally fast carbon-carbon bond reductive elimination from gold(III)
-
Wolf, W. J., Winston, M. S. & Toste, F. D. Exceptionally fast carbon-carbon bond reductive elimination from gold(III). Nature Chem. 6, 159-164 (2013).
-
(2013)
Nature Chem.
, vol.6
, pp. 159-164
-
-
Wolf, W.J.1
Winston, M.S.2
Toste, F.D.3
-
19
-
-
0000966832
-
Synthesis and reactivity of somenitroaryl complexes ofHgII andAuIII-synthesis of a substituted biphenyl by C-C coupling-crystal structure of [Hg(C6H4NO2-3,OnBu-6)2]
-
Vicente, J., Bermúdez, M.-D., Carrió n, F.-J. & Jones, P. G. Synthesis and reactivity of somenitroaryl complexes ofHgII andAuIII-synthesis of a substituted biphenyl by C-C coupling-crystal structure of [Hg(C6H4NO2-3,OnBu-6)2]. Chem. Ber. 129, 1395-1399 (1996).
-
(1996)
Chem. Ber.
, vol.129
, pp. 1395-1399
-
-
Vicente, J.1
Bermúdez, M.-D.2
Carrión, F.-J.3
Jones, P.G.4
-
20
-
-
84867555036
-
Thermally stable gold(III) hydride: Synthesis, reactivity, and reductive condensation as a route to gold(II) complexes
-
Roşca, D.-A.,Smith, D. A., Hughes, D. L.& Bochmann, M. A thermally stable gold(III) hydride: synthesis, reactivity, and reductive condensation as a route to gold(II) complexes. Angew. Chem. Int. Ed. 51, 10643-10646 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 10643-10646
-
-
Roşca, D.-A.1
Smith, D.A.2
Hughes, D.L.3
Bochmann, M.A.4
-
21
-
-
84871969794
-
Fire and ice: A gold(III) monohydride
-
Hashmi, A. S. K. Fire and ice: a gold(III) monohydride. Angew. Chem. Int. Ed. 51, 12935-12936 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 12935-12936
-
-
Hashmi, A.S.K.1
-
22
-
-
85020934109
-
Synthesis and reactivity of dibenzometallole complexes of gold(III) and platinum(II)
-
Usó n, R., Vicente, J., Cirac, J. A. & Chicote, M. T. Synthesis and reactivity of dibenzometallole complexes of gold(III) and platinum(II). J. Organomet. Chem. 198, 105-112 (1980).
-
(1980)
J. Organomet. Chem.
, vol.198
, pp. 105-112
-
-
Usón, R.1
Vicente, J.2
Cirac, J.A.3
Chicote, M.T.4
-
23
-
-
33750591339
-
Comparative theoretical study of N-heterocyclic carbenes and other ligands bound to AuI
-
Pyykkö , P. & Runeberg, N. Comparative theoretical study of N-heterocyclic carbenes and other ligands bound to AuI. Chem. Asian J. 1, 623-628 (2006).
-
(2006)
Chem. Asian J.
, vol.1
, pp. 623-628
-
-
Pyykkö, P.1
Runeberg, N.2
-
24
-
-
84927738678
-
Mechanistic studies of transition metal-mediated C-C bond activation
-
Jones, W. D. Mechanistic studies of transition metal-mediated C-C bond activation. Top. Curr. Chem. 346, 1-31 (2013).
-
(2013)
Top. Curr. Chem.
, vol.346
, pp. 1-31
-
-
Jones, W.D.1
-
25
-
-
0037121126
-
Cleavage of the carbon-carbon bond in biphenylene using transition metals
-
Perthuisot, C. et al. Cleavage of the carbon-carbon bond in biphenylene using transition metals. J. Mol. Catal. Chem. 189, 157-168 (2002).
-
(2002)
J. Mol. Catal. Chem.
, vol.189
, pp. 157-168
-
-
Perthuisot, C.1
-
26
-
-
84867520736
-
Oxidative addition of carbon-carbon bonds with a redox-active bis(imino)pyridine iron complex
-
Darmon, J. M. et al. Oxidative addition of carbon-carbon bonds with a redox-active bis(imino)pyridine iron complex. J. Am. Chem. Soc. 134, 17125-17137 (2012).
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 17125-17137
-
-
Darmon, J.M.1
-
27
-
-
84902201841
-
Gold-catalyzed allylation of aryl boronic acids: Accessing cross-coupling reactivity with gold
-
Levin, L. D. & Toste, F. D. Gold-catalyzed allylation of aryl boronic acids: accessing cross-coupling reactivity with gold. Angew. Chem. Int. Ed. 53, 6211-6215 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 6211-6215
-
-
Levin, L.D.1
Toste, F.D.2
-
28
-
-
0001909785
-
Metal-metal bond formation in the oxidative addition to dinuclear gold(I) species, Implications from dinuclear and trinuclear gold chemistry for the oxidative addition process generally
-
Fackler, J. P. Jr. Metal-metal bond formation in the oxidative addition to dinuclear gold(I) species. Implications from dinuclear and trinuclear gold chemistry for the oxidative addition process generally. Polyhedron 16, 1-17 (1997).
-
(1997)
Polyhedron
, vol.16
, pp. 1-17
-
-
Fackler, J.P.1
-
29
-
-
84893741108
-
Activation of aryl halides at gold(I): Practical synthesis of (P,C) cyclometalated gold(III) complexes
-
Guenther, J. et al. Activation of aryl halides at gold(I): practical synthesis of (P,C) cyclometalated gold(III) complexes. J. Am. Chem. Soc. 136, 1778-1781 (2014).
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 1778-1781
-
-
Guenther, J.1
-
30
-
-
84908433260
-
Facile oxidative addition of aryl iodides to gold(I) by ligand design: Bending turns on reactivity
-
Joost, M. et al. Facile oxidative addition of aryl iodides to gold(I) by ligand design: bending turns on reactivity. J. Am. Chem. Soc. 136, 14654-14657 (2014).
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 14654-14657
-
-
Joost, M.1
-
31
-
-
84861793225
-
Isolated silver intermediate of gold precatalyst activation
-
Weber, S. G., Rominger, F. & Straub, B. F. Isolated silver intermediate of gold precatalyst activation. Eur. J. Inorg. Chem. 2863-2867 (2012).
-
(2012)
Eur. J. Inorg. Chem.
, pp. 2863-2867
-
-
Weber, S.G.1
Rominger, F.2
Straub, B.F.3
-
32
-
-
60749104310
-
Lewis acid catalyzed asymmetric cyanohydrin synthesis
-
North, M., Usanov, D. L. & Young, C. Lewis acid catalyzed asymmetric cyanohydrin synthesis. Chem. Rev. 108, 5146-5226 (2008).
-
(2008)
Chem. Rev.
, vol.108
, pp. 5146-5226
-
-
North, M.1
Usanov, D.L.2
Young, C.3
-
34
-
-
0001196589
-
Diastereoselection in Lewis-acid-mediated aldol reactions
-
Mahrwald, R. Diastereoselection in Lewis-acid-mediated aldol reactions. Chem. Rev. 99, 1095-1120 (1999).
-
(1999)
Chem. Rev.
, vol.99
, pp. 1095-1120
-
-
Mahrwald, R.1
-
35
-
-
0001280755
-
Virtually complete blocking of a,b-unsaturated aldehyde carbonyls by complexation with aluminum tris(2,6-diphenylphenoxide)
-
Maruoka, K., Imoto, H., Saito, S. & Yamamoto, H. Virtually complete blocking of a,b-unsaturated aldehyde carbonyls by complexation with aluminum tris(2,6-diphenylphenoxide). J. Am. Chem. Soc. 116, 4131-4132 (1994).
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4131-4132
-
-
Maruoka, K.1
Imoto, H.2
Saito, S.3
Yamamoto, H.4
-
36
-
-
78651292341
-
Gold(I)-catalyzed synthesis of conjugated trienes
-
Hadfield, M. S.&Lee, A.-L. Gold(I)-catalyzed synthesis of conjugated trienes. Chem. Commun. 47, 1333-1335 (2011).
-
(2011)
Chem. Commun.
, vol.47
, pp. 1333-1335
-
-
Hadfield, M.S.1
Lee, A.-L.2
-
37
-
-
84900801729
-
Peptide-catalyzed consecutive 1,6-and 1,4-additions of thiols to a,b,c,d-unsaturated aldehydes
-
Akagawa, K., Nishi, N., Sen, J. & Kudo, K. Peptide-catalyzed consecutive 1,6-and 1,4-additions of thiols to a,b,c,d-unsaturated aldehydes. Org. Biomol. Chem. 12, 3581-3585 (2014).
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 3581-3585
-
-
Akagawa, K.1
Nishi, N.2
Sen, J.3
Kudo, K.4
-
38
-
-
84885967689
-
Peptide-catalyzed regio-and enantioselective reduction of a,b,c,d-diunsaturated aldehydes
-
Akagawa, K., Sen, J. & Kudo, K. Peptide-catalyzed regio-and enantioselective reduction of a,b,c,d-diunsaturated aldehydes. Angew. Chem. Int. Ed. 52, 11585-11588 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 11585-11588
-
-
Akagawa, K.1
Sen, J.2
Kudo, K.3
-
39
-
-
0034600250
-
New strategies for organic synthesis: The first highly enantioselective organocatalytic Diels-Alder reaction
-
Ahrendt, K. A., Borths, C. J. & MacMillan, D. W. C. New strategies for organic synthesis: the first highly enantioselective organocatalytic Diels-Alder reaction. J. Am. Chem. Soc. 122, 4243-4244 (2000).
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 4243-4244
-
-
Ahrendt, K.A.1
Borths, C.J.2
MacMillan, D.W.C.3
-
40
-
-
84862726543
-
Organocatalytic 1,4-addition reaction of a,b,c,d-diunsaturated aldehydes versus 1,6-addition reaction
-
Hayashi, Y., Okamura, D.,Umemiya, S.&Uchimaru, T. Organocatalytic 1,4-addition reaction of a,b,c,d-diunsaturated aldehydes versus 1,6-addition reaction. ChemCatChem 4, 959-962 (2012).
-
(2012)
ChemCatChem
, vol.4
, pp. 959-962
-
-
Hayashi, Y.1
Okamura, D.2
Umemiya, S.3
Uchimaru, T.4
-
41
-
-
75749141777
-
Exploiting [212] cycloaddition chemistry: Achievements with allenes
-
Alcaide, B., Almendros, P. & Arancillo, C. Exploiting [212] cycloaddition chemistry: achievements with allenes. Chem. Soc. Rev. 39, 783-816 (2010).
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 783-816
-
-
Alcaide, B.1
Almendros, P.2
Arancillo, C.3
-
42
-
-
84856853378
-
On homogeneous gold/palladium catalytic systems
-
Hashmi, A. S. K. et al. On homogeneous gold/palladium catalytic systems. Adv. Synth. Catal. 354, 133-147 (2012).
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 133-147
-
-
Hashmi, A.S.K.1
-
43
-
-
84892640802
-
Rationale for the sluggish oxidative addition of aryl halides to Au(I)
-
Livendahl, M., Goehry, C.,Maseras, F.& Echavarren, A. M. Rationale for the sluggish oxidative addition of aryl halides to Au(I). Chem. Commun. 50, 1533-1536 (2014).
-
(2014)
Chem. Commun.
, vol.50
, pp. 1533-1536
-
-
Livendahl, M.1
Goehry, C.2
Maseras, F.3
Echavarren, A.M.4
-
44
-
-
0034703716
-
Highly selective gold-catalyzed arene synthesis
-
Hashmi, A. S. K., Frost, T. M. & Bats, J. W. Highly selective gold-catalyzed arene synthesis. J. Am. Chem. Soc. 122, 11553-11554 (2000).
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11553-11554
-
-
Hashmi, A.S.K.1
Frost, T.M.2
Bats, J.W.3
|