Crystallography Open Database

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4513030 CIFC19 H9 Ag B Br3 F18 N6 OP -19.5396; 12.6988; 12.9452
100.867; 94.371; 98.592
1514Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C‒H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513043 CIFC24 H20 N4 O5 Ru SP -18.7507; 10.3497; 14.1618
79.212; 73.228; 77.234
1187.17Wang, Ying; Duan, Lele; Wang, Lei; Chen, Hong; Sun, Junliang; Sun, Licheng; Ahlquist, Mårten S. G.
Alkene Epoxidation Catalysts [Ru(pdc)(tpy)] and [Ru(pdc)(pybox)] Revisited: Revealing a Unique RuIV═O Structure from a Dimethyl Sulfoxide Coordinating Complex
ACS Catalysis, 2015, 5, 3966
4513044 CIFC45 H57 Cl F N2 O3 P RuP -19.25; 10.543; 21.668
84.919; 89.766; 81.66
2082.5Guidone, Stefano; Songis, Olivier; Falivene, Laura; Nahra, Fady; Slawin, Alexandra M. Z.; Jacobsen, Heiko; Cavallo, Luigi; Cazin, Catherine S. J.
Ruthenium Olefin Metathesis Catalysts Containing Fluoride
ACS Catalysis, 2015, 5, 3932
4513045 CIFC45 H57 F2 N2 O3 P RuP -19.123; 10.569; 21.751
94.901; 90.209; 99.166
2062.6Guidone, Stefano; Songis, Olivier; Falivene, Laura; Nahra, Fady; Slawin, Alexandra M. Z.; Jacobsen, Heiko; Cavallo, Luigi; Cazin, Catherine S. J.
Ruthenium Olefin Metathesis Catalysts Containing Fluoride
ACS Catalysis, 2015, 5, 3932
4513186 CIFC49 H47 Cl F6 N2 P2 RuP -111.185; 12.2337; 15.712
87.763; 85.343; 75.988
2078.7Xie, Xiaoke; Huynh, Han Vinh
Tunable Dehydrogenative Amidation versus Amination Using a Single Ruthenium-NHC Catalyst
ACS Catalysis, 2015, 5, 4143
4513187 CIFC45 H47 Cl F6 N2 P2 RuC 1 c 118.524; 15.304; 14.862
90; 98.269; 90
4169.4Xie, Xiaoke; Huynh, Han Vinh
Tunable Dehydrogenative Amidation versus Amination Using a Single Ruthenium-NHC Catalyst
ACS Catalysis, 2015, 5, 4143
4513215 CIFC32 H28 B Fe PP 21 21 217.8373; 11.1807; 28.7574
90; 90; 90
2519.91Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513216 CIFC20 H25 NP 1 21 18.4925; 18.0565; 21.7726
90; 92.034; 90
3336.61Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513217 CIFC18 H21 NP -17.6079; 9.9255; 10.7036
113.746; 100.964; 95.416
713.05Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513218 CIFC25 H29 Fe N OP 21 21 2110.843; 12.6988; 15.1797
90; 90; 90
2090.14Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513219 CIFC43 H38 N O3.5 P Pd SP 41 21 214.5165; 14.5165; 37.1387
90; 90; 90
7826.2Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513383 CIFC72 H78 N4 O11 Ti2P 43 21 212.3687; 12.3687; 44.436
90; 90; 90
6798Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513384 CIFC76 H78 N4 O11 Ti2P 31 2 119.0457; 19.0457; 41.0671
90; 90; 120
12900.9Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513385 CIFC65 H61 Cl3 N4 O6 Ti2P 1 21 111.5315; 19.176; 13.4627
90; 98.481; 90
2944.4Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513386 CIFC68 H66 Br4 N4 O7 Ti2P 43 21 212.2324; 12.2324; 45.9762
90; 90; 90
6879.5Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513387 CIFC64 H56 Br4 N4 O6 Ti2P 113.8302; 15.4438; 16.7517
108.353; 90.647; 116.089
3002.56Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513439 CIFC54 H47 N4 O7P 21 21 2112.3766; 16.424; 28.578
90; 90; 90
5809.1Alcaide, Benito; Almendros, Pedro; Fernández, Israel; Martín-Montero, Raúl; Martínez-Peña, Francisco; Ruiz, M. Pilar; Torres, M. Rosario
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
ACS Catalysis, 2015, 5, 4842
4513440 CIFC22 H22 N2 O3P 1 21 110.202; 7.487; 11.933
90; 100.922; 90
895Alcaide, Benito; Almendros, Pedro; Fernández, Israel; Martín-Montero, Raúl; Martínez-Peña, Francisco; Ruiz, M. Pilar; Torres, M. Rosario
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
ACS Catalysis, 2015, 5, 4842
4513441 CIFC22 H16 F3 N O3 SC 1 2/c 140.887; 9.2404; 27.6197
90; 131.709; 90
7790.1Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)‒H and C(sp2)‒H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513442 CIFC21 H16 B F4 NP 21 21 216.1068; 15.2343; 18.4646
90; 90; 90
1717.81Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)‒H and C(sp2)‒H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837

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