-
3
-
-
0030984556
-
Kinetic resolution of racemic secondary alcohols by Ru″-catalyzed hydrogen transfer
-
Hashiguchi, S. et al. Kinetic resolution of racemic secondary alcohols by Ru″-catalyzed hydrogen transfer. Angew. Chem. Int. Ed. 36, 288-290 (1997).
-
(1997)
Angew. Chem. Int. Ed.
, vol.36
, pp. 288-290
-
-
Hashiguchi, S.1
-
4
-
-
0030984352
-
The catalyst precursor, catalyst, and intermediate in the Ru″-promoted asymmetric hydrogen transfer between alcohols and ketones
-
Haack, K. J., Hashiguchi, S., Fujii, A., Ikariya, T. & Noyori, R. The catalyst precursor, catalyst, and intermediate in the Ru″-promoted asymmetric hydrogen transfer between alcohols and ketones. Angew. Chem. Int. Ed. 36, 285-288 (1997).
-
(1997)
Angew. Chem. Int. Ed.
, vol.36
, pp. 285-288
-
-
Haack, K.J.1
Hashiguchi, S.2
Fujii, A.3
Ikariya, T.4
Noyori, R.5
-
5
-
-
84930481235
-
Cisplatin resistance: A cellular self-defense mechanism resulting from multiple epigenetic and genetic changes
-
Shen, D. W., Pouliot, L. M., Hall, M. D. & Gottesman, M. M. Cisplatin resistance: a cellular self-defense mechanism resulting from multiple epigenetic and genetic changes. Pharmacol. Rev. 64, 706-721 (2012).
-
(2012)
Pharmacol. Rev.
, vol.64
, pp. 706-721
-
-
Shen, D.W.1
Pouliot, L.M.2
Hall, M.D.3
Gottesman, M.M.4
-
6
-
-
33646510110
-
Platinum group antitumor chemistry: Design and development of new anticancer drugs complementary to cisplatin
-
Abu-Surrah, A. S. & Kettunen, M. Platinum group antitumor chemistry: design and development of new anticancer drugs complementary to cisplatin. Cur. Med. Chem. 13, 1337-1357 (2006).
-
(2006)
Cur. Med. Chem.
, vol.13
, pp. 1337-1357
-
-
Abu-Surrah, A.S.1
Kettunen, M.2
-
7
-
-
84927570163
-
-
ed. Gasser, G. Wiley
-
Furrer, J., Smith, G. S. & Therrien, B. in Inorganic Chemical Biology: Principles, Techniques and Applications (ed. Gasser, G.) 341-364 (Wiley, 2014).
-
(2014)
Inorganic Chemical Biology: Principles, Techniques and Applications
, pp. 341-364
-
-
Furrer, J.1
Smith, G.S.2
Therrien, B.3
-
8
-
-
84898063153
-
The potent oxidant anticancer activity of organoiridium catalysts
-
Liu, Z. et al. The potent oxidant anticancer activity of organoiridium catalysts. Angew. Chem. Int. Ed. 53, 3941-3946 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 3941-3946
-
-
Liu, Z.1
-
9
-
-
0345817539
-
Regeneration of nicotinamide cofactors for use in organic synthesis
-
Chenault, H. K. & Whitesides, G. M. Regeneration of nicotinamide cofactors for use in organic synthesis. Appl. Biochem. Biotechnol. 14, 147-197 (1987).
-
(1987)
Appl. Biochem. Biotechnol.
, vol.14
, pp. 147-197
-
-
Chenault, H.K.1
Whitesides, G.M.2
-
10
-
-
84884183601
-
Methods for the regeneration on NAD coenzymes
-
Wu, H. et al. Methods for the regeneration on NAD coenzymes. Green Chem. 15, 1773-1789 (2013).
-
(2013)
Green Chem.
, vol.15
, pp. 1773-1789
-
-
Wu, H.1
-
11
-
-
84896556750
-
Recent trends in biomimetic NADH regeneration
-
Quinto, T., Köhler, V. & Ward, T. R. Recent trends in biomimetic NADH regeneration. Top. Catal. 57, 321-331 (2014).
-
(2014)
Top. Catal.
, vol.57
, pp. 321-331
-
-
Quinto, T.1
Köhler, V.2
Ward, T.R.3
-
12
-
-
0033577884
-
+: Structure-activity relationships and mechanistic aspects in the formation of the 1, 4-NADH derivatives
-
+: structure-activity relationships and mechanistic aspects in the formation of the 1, 4-NADH derivatives. Angew. Chem. Int. Ed. 38, 1997-2000 (1999).
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 1997-2000
-
-
Buriez, O.1
Kerr, J.2
Fish, R.3
-
13
-
-
0036462504
-
+ models for tandem cofactor regeneration, horse liver alcohol dehydrogenase recognition of 1,4-NADH derivatives, and chiral synthesis
-
+ models for tandem cofactor regeneration, horse liver alcohol dehydrogenase recognition of 1,4-NADH derivatives, and chiral synthesis. Angew. Chem. Int. Ed. 41, 478-481 (2002).
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 478-481
-
-
Lo, H.C.1
Fish, R.H.2
-
14
-
-
0035904986
-
+: Structure-activity relationships, kinetics, and mechanist
-
+: structure-activity relationships, kinetics, and mechanist. Inorg. Chem. 40, 6705-6716 (2001).
-
(2001)
Inorg. Chem.
, vol.40
, pp. 6705-6716
-
-
Lo, H.C.1
-
15
-
-
72749104428
-
2 as the precatalyst and sodium formate as the hydride source: Kinetic and activation parameters, and the significance of steric and electronic effects
-
2 as the precatalyst and sodium formate as the hydride source: Kinetic and activation parameters, and the significance of steric and electronic effects. J. Organomet. Chem. 695, 145-150 (2010).
-
(2010)
J. Organomet. Chem.
, vol.695
, pp. 145-150
-
-
Leiva, C.1
Lo, H.C.2
Fish, R.H.3
-
16
-
-
11844296083
-
+ for selective organic synthesis
-
+ for selective organic synthesis. J. Organomet. Chem. 689, 4783-4790 (2004).
-
(2004)
J. Organomet. Chem.
, vol.689
, pp. 4783-4790
-
-
Lutz, J.1
-
17
-
-
35848962068
-
Water-soluble phenanthroline complexes of rhodium, iridium and ruthenium for the regeneration of NADH in the enzymatic reduction of ketones
-
Canivet, J., Süss-Fink, G. & Štěpnička, P. Water-soluble phenanthroline complexes of rhodium, iridium and ruthenium for the regeneration of NADH in the enzymatic reduction of ketones. Eur. J. Inorg. Chem. 2007, 4736-4742 (2007).
-
(2007)
Eur. J. Inorg. Chem.
, vol.2007
, pp. 4736-4742
-
-
Canivet, J.1
Süss-Fink, G.2
Štěpnička, P.3
-
18
-
-
79960999137
-
Chemically engineered papain as artificial formate dehydrogenase for NAD(P)H regeneration
-
Haquette, P. et al. Chemically engineered papain as artificial formate dehydrogenase for NAD(P)H regeneration. Org. Biomol. Chem. 9, 5720-5727 (2011).
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 5720-5727
-
-
Haquette, P.1
-
19
-
-
84865491051
-
Towards recyclable NAD(P)H regeneration catalysts
-
de Torres, M., Dimroth, J., Arends, I. W. C. E., Keilitz, J. & Hollmann, F. Towards recyclable NAD(P)H regeneration catalysts. Molecules 17, 9835-9841 (2012).
-
(2012)
Molecules
, vol.17
, pp. 9835-9841
-
-
De Torres, M.1
Dimroth, J.2
Arends, I.W.C.E.3
Keilitz, J.4
Hollmann, F.5
-
22
-
-
33750193289
-
On water and in air: Fast and highly chemoselective transfer hydrogenation of aldehydes with iridium catalysts
-
Wu, X. et al. On water and in air: fast and highly chemoselective transfer hydrogenation of aldehydes with iridium catalysts. Angew. Chem. Int. Ed. 45, 6718-6722 (2006).
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6718-6722
-
-
Wu, X.1
-
23
-
-
79960570536
-
pH-regulated transfer hydrogenation of quinoxalines with a Cp∗Ir-diamine catalyst in aqueous media
-
Tan, J. et al. pH-regulated transfer hydrogenation of quinoxalines with a Cp∗Ir-diamine catalyst in aqueous media. Tetrahedron 67, 6206-6213 (2011).
-
(2011)
Tetrahedron
, vol.67
, pp. 6206-6213
-
-
Tan, J.1
-
24
-
-
51849098200
-
Cytotoxicity, cellular uptake, and DNA interactions of new monodentate ruthenium(II) complexes containing terphenyl arenes
-
Bugarcic, T. et al. Cytotoxicity, cellular uptake, and DNA interactions of new monodentate ruthenium(II) complexes containing terphenyl arenes. J. Med. Chem. 51, 5310-5319 (2008).
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5310-5319
-
-
Bugarcic, T.1
-
25
-
-
0037425530
-
Highly selective binding of organometallic ruthenium ethylenediamine complexes to nucleic acids: Novel recognition mechanisms
-
Chen, H., Parkinson, J. A., Morris, R. E. & Sadler, P. J. Highly selective binding of organometallic ruthenium ethylenediamine complexes to nucleic acids: novel recognition mechanisms. J. Am. Chem. Soc. 173-186 (2003).
-
(2003)
J. Am. Chem. Soc.
, pp. 173-186
-
-
Chen, H.1
Parkinson, J.A.2
Morris, R.E.3
Sadler, P.J.4
-
26
-
-
0037181357
-
Organometallic ruthenium(II) diamine anticancer complexes: Arene-nucleobase stacking and stereospecific hydrogen-bonding in guanine adducts
-
Chen, H. et al. Organometallic ruthenium(II) diamine anticancer complexes: arene-nucleobase stacking and stereospecific hydrogen-bonding in guanine adducts. J. Am. Chem. Soc. 124, 3064-3082 (2002).
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3064-3082
-
-
Chen, H.1
-
27
-
-
33750969384
-
Structure-activity relationships for cytotoxic ruthenium(II) arene complexes containing N,N-, N,O-, and O,O-chelating ligands
-
Habtemariam, A. et al. Structure-activity relationships for cytotoxic ruthenium(II) arene complexes containing N,N-, N,O-, and O,O-chelating ligands. J. Med. Chem. 49, 6858-6868 (2006).
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6858-6868
-
-
Habtemariam, A.1
-
28
-
-
29344458540
-
Competition between glutathione and guanine for a ruthenium(II) arene anticancer complex: Detection of a sulfenato intermediate
-
Wang, F., Xu, J., Habtemariam, A. & Sadler, P. J. Competition between glutathione and guanine for a ruthenium(II) arene anticancer complex: detection of a sulfenato intermediate. J. Am. Chem. Soc. 127, 17734-17743 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17734-17743
-
-
Wang, F.1
Xu, J.2
Habtemariam, A.3
Sadler, P.J.4
-
29
-
-
84873687037
-
Competition between glutathione and DNA oligonucleotides for ruthenium(II) arene anticancer complexes
-
Wang, F. et al. Competition between glutathione and DNA oligonucleotides for ruthenium(II) arene anticancer complexes. Dalton Trans. 42, 3188-3195 (2013).
-
(2013)
Dalton Trans.
, vol.42
, pp. 3188-3195
-
-
Wang, F.1
-
30
-
-
0037141471
-
In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer
-
Aird, R. E. et al. In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer. Br. J. Cancer 86, 1652-1657 (2002).
-
(2002)
Br. J. Cancer
, vol.86
, pp. 1652-1657
-
-
Aird, R.E.1
-
31
-
-
0347624091
-
Kinetics of aquation and anation of ruthenium(II) arene anticancer complexes, acidity and X-ray structures of aqua adducts
-
Wang, F. et al. Kinetics of aquation and anation of ruthenium(II) arene anticancer complexes, acidity and X-ray structures of aqua adducts. Chem. Eur. J. 9, 5810-5820 (2003).
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 5810-5820
-
-
Wang, F.1
-
32
-
-
64749093574
-
Association of reactive oxygen species levels and radioresistance in cancer stem cells
-
Diehn, M. et al. Association of reactive oxygen species levels and radioresistance in cancer stem cells. Nature 458, 780-783 (2009).
-
(2009)
Nature
, vol.458
, pp. 780-783
-
-
Diehn, M.1
-
33
-
-
79960419089
-
Anticancer activity of metal complexes: Involvement of redox processes
-
Jungwirth, U. et al. Anticancer activity of metal complexes: involvement of redox processes. Antioxid. Redox Signal. 15, 1085-1127 (2011).
-
(2011)
Antioxid. Redox Signal.
, vol.15
, pp. 1085-1127
-
-
Jungwirth, U.1
-
34
-
-
84887126272
-
Next-generation metal anticancer complexes: Multitargeting via redox modulation
-
Romero-Canelón, I. & Sadler, P. J. Next-generation metal anticancer complexes: multitargeting via redox modulation. Inorg. Chem. 52, 12276-12291 (2013).
-
(2013)
Inorg. Chem.
, vol.52
, pp. 12276-12291
-
-
Romero-Canelón, I.1
Sadler, P.J.2
-
35
-
-
84875181661
-
Oxidants, antioxidants and the current incurability of metastatic cancers
-
Watson, J. Oxidants, antioxidants and the current incurability of metastatic cancers. Open Biol. 3, 1-9 (2013).
-
(2013)
Open Biol.
, vol.3
, pp. 1-9
-
-
Watson, J.1
-
36
-
-
67650071137
-
Targeting cancer cells by ROS-mediated mechanisms: A radical therapeutic approach?
-
Trachootham, D., Alexandre, J. & Huang, P. Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach? Nat. Rev. Drug. Discov. 8, 579-591 (2009).
-
(2009)
Nat. Rev. Drug. Discov.
, vol.8
, pp. 579-591
-
-
Trachootham, D.1
Alexandre, J.2
Huang, P.3
-
37
-
-
84859768496
-
Organometallic ruthenium and iridium transfer-hydrogenation catalysts using coenzyme NADH as a cofactor
-
Betanzos-Lara, S. et al. Organometallic ruthenium and iridium transfer-hydrogenation catalysts using coenzyme NADH as a cofactor. Angew. Chem. Int. Ed. 51, 3897-3900 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 3897-3900
-
-
Betanzos-Lara, S.1
-
38
-
-
84875871087
-
Reduction of quinones by NADH catalyzed by organoiridium complexes
-
Liu, Z. et al. Reduction of quinones by NADH catalyzed by organoiridium complexes. Angew. Chem. Int. Ed. 52, 4194-4197 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 4194-4197
-
-
Liu, Z.1
-
39
-
-
33745727023
-
Apoptotic interactions of cytochrome c: Redox flirting with anionic phospholipids within and outside of mitochondria
-
Bayir, H. et al. Apoptotic interactions of cytochrome c: redox flirting with anionic phospholipids within and outside of mitochondria. Biochim. Biophys. Acta 1757, 648-659 (2006).
-
(2006)
Biochim. Biophys. Acta
, vol.1757
, pp. 648-659
-
-
Bayir, H.1
-
40
-
-
84255210700
-
Molecular definitions of cell death subroutines: Recommendations of the Nomenclature Committee on Cell Death 2012
-
Galluzzi, L. et al. Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012. Cell Death Differ. 19, 107-120 (2012).
-
(2012)
Cell Death Differ.
, vol.19
, pp. 107-120
-
-
Galluzzi, L.1
-
41
-
-
84860904314
-
Glutathione-dependent reductive stress triggers mitochondrial oxidation and cytotoxicity
-
Zhang, H. et al. Glutathione-dependent reductive stress triggers mitochondrial oxidation and cytotoxicity. FASEB J. 26, 1442-1451 (2012).
-
(2012)
FASEB J.
, vol.26
, pp. 1442-1451
-
-
Zhang, H.1
-
42
-
-
69749101546
-
Metallotherapeutics: Novel strategies in drug design
-
Hocharoen, L. & Cowan, J. A. Metallotherapeutics: novel strategies in drug design. Chem. Eur. J. 15, 8670-8676 (2009).
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 8670-8676
-
-
Hocharoen, L.1
Cowan, J.A.2
-
43
-
-
84864770769
-
Moving Pd-mediated protein cross coupling to living systems
-
Li, J. & Chen, P. R. Moving Pd-mediated protein cross coupling to living systems. Chembiochem 13, 1728-1731 (2012).
-
(2012)
Chembiochem
, vol.13
, pp. 1728-1731
-
-
Li, J.1
Chen, P.R.2
-
44
-
-
84860817510
-
Designing organometallic compounds for catalysis and therapy
-
Noffke, A. L., Habtemariam, A., Pizarro, A. M. & Sadler, P. J. Designing organometallic compounds for catalysis and therapy. Chem. Commun. 48, 5219-5246 (2012).
-
(2012)
Chem. Commun.
, vol.48
, pp. 5219-5246
-
-
Noffke, A.L.1
Habtemariam, A.2
Pizarro, A.M.3
Sadler, P.J.4
-
45
-
-
84873279753
-
Metal complex catalysis in living biological systems
-
Sasmal, P. K., Streu, C. N. & Meggers, E. Metal complex catalysis in living biological systems. Chem. Commun. 49, 1581-1587 (2013).
-
(2013)
Chem. Commun.
, vol.49
, pp. 1581-1587
-
-
Sasmal, P.K.1
Streu, C.N.2
Meggers, E.3
-
46
-
-
0033536644
-
A nonpeptidyl mimic of superoxide dismutase with therapeutic activity in rats
-
Salvemini, D. et al. A nonpeptidyl mimic of superoxide dismutase with therapeutic activity in rats. Science 286, 304-306 (1999).
-
(1999)
Science
, vol.286
, pp. 304-306
-
-
Salvemini, D.1
-
47
-
-
77953485055
-
Striking inflammation from both sides: Manganese(II) pentaazamacrocyclic SOD mimics act also as nitric oxide dismutases: A single-cell study
-
Filipović, M. R. et al. Striking inflammation from both sides: manganese(II) pentaazamacrocyclic SOD mimics act also as nitric oxide dismutases: a single-cell study. Angew. Chem. Int. Ed. 49, 4228-4232 (2010).
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 4228-4232
-
-
Filipović, M.R.1
-
48
-
-
84861418856
-
Catalytic azide reduction in biological environments
-
Sasmal, P. K. et al. Catalytic azide reduction in biological environments. Chem. Bio. Chem. 13, 1116-1120 (2012).
-
(2012)
Chem. Bio. Chem.
, vol.13
, pp. 1116-1120
-
-
Sasmal, P.K.1
-
49
-
-
84857708155
-
Catalytic metallodrugs targeting HCV IRES RNA
-
Bradford, S. & Cowan, J. A. Catalytic metallodrugs targeting HCV IRES RNA. Chem. Commun. 48, 3118-3120 (2012).
-
(2012)
Chem. Commun.
, vol.48
, pp. 3118-3120
-
-
Bradford, S.1
Cowan, J.A.2
-
50
-
-
44149124272
-
Cleavage agents for a-synuclein
-
Lee, J. et al. Cleavage agents for a-synuclein. Bull. Korean Chem. Soc. 29, 882-884 (2008).
-
(2008)
Bull. Korean Chem. Soc.
, vol.29
, pp. 882-884
-
-
Lee, J.1
-
51
-
-
44549088206
-
Cleavage agents for soluble oligomers of human islet amyloid polypeptide
-
Suh, J. et al. Cleavage agents for soluble oligomers of human islet amyloid polypeptide. J. Biol. Inorg. Chem. 13, 693-701 (2008).
-
(2008)
J. Biol. Inorg. Chem.
, vol.13
, pp. 693-701
-
-
Suh, J.1
-
52
-
-
34848913126
-
Cleavage agents for soluble oligomers of amyloid beta peptides
-
Suh, J. et al. Cleavage agents for soluble oligomers of amyloid beta peptides. Angew. Chem. Int. Ed. 46, 7064-7067 (2007).
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 7064-7067
-
-
Suh, J.1
-
53
-
-
68949179788
-
Target-selective peptide-cleaving catalysts as a new paradigm in drug design
-
Lee, T. Y. & Suh, J. Target-selective peptide-cleaving catalysts as a new paradigm in drug design. Chem. Soc. Rev. 38, 1949-1957 (2009).
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 1949-1957
-
-
Lee, T.Y.1
Suh, J.2
-
54
-
-
0242668337
-
Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis
-
Kayed, R. et al. Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science 300, 486-489 (2003).
-
(2003)
Science
, vol.300
, pp. 486-489
-
-
Kayed, R.1
-
55
-
-
50149099558
-
Catalytic organometallic anticancer complexes
-
Dougan, S. J., Habtemariam, A., McHale, S. E., Parsons, S. & Sadler, P. J. Catalytic organometallic anticancer complexes. Proc. Natl Acad. Sci. USA 105, 11628-11633 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 11628-11633
-
-
Dougan, S.J.1
Habtemariam, A.2
McHale, S.E.3
Parsons, S.4
Sadler, P.J.5
-
56
-
-
33748620928
-
Ruthenium-induced allylcarbamate cleavage in living cells
-
Streu, C. & Meggers, E. Ruthenium-induced allylcarbamate cleavage in living cells. Angew. Chem. Int. Ed. 45, 5645-5648 (2006).
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5645-5648
-
-
Streu, C.1
Meggers, E.2
-
57
-
-
84865495920
-
Light-triggered ruthenium-catalyzed allylcarbamate cleavage in biological environments
-
Sasmal, P. K., Carregal-Romero, S., Parak, W. J. & Meggers, E. Light-triggered ruthenium-catalyzed allylcarbamate cleavage in biological environments. Organometallics 31, 5968-5970 (2012).
-
(2012)
Organometallics
, vol.31
, pp. 5968-5970
-
-
Sasmal, P.K.1
Carregal-Romero, S.2
Parak, W.J.3
Meggers, E.4
-
58
-
-
84908552170
-
Progress towards bioorthogonal catalysis with organometallic compounds
-
Völker, T., Dempwolff, F., Graumann, P. L. & Meggers, E. Progress towards bioorthogonal catalysis with organometallic compounds. Angew. Chem. Int. Ed. 53, 10536-10540 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 10536-10540
-
-
Völker, T.1
Dempwolff, F.2
Graumann, P.L.3
Meggers, E.4
-
59
-
-
84873872136
-
Synthetic cascades are enabled by combining biocatalysts with artificial metalloenzymes
-
Köhler, V. et al. Synthetic cascades are enabled by combining biocatalysts with artificial metalloenzymes. Nat. Chem. 5, 93-99 (2013).
-
(2013)
Nat. Chem.
, vol.5
, pp. 93-99
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