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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 4513811 | CIF | C22 H17 N O3 S | P 1 21/n 1 | 10.3225; 20.9863; 16.6431 90; 95.815; 90 | 3586.9 | Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams ACS Catalysis, 2016, 6, 1565 |
| 4513812 | CIF | C22 H17 N O3 S | P -1 | 8.5582; 10.1474; 11.3665 114.204; 92.3803; 95.0132 | 893.63 | Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams ACS Catalysis, 2016, 6, 1565 |
| 4513813 | CIF | C13 H15 N O3 S | P 1 21/c 1 | 15.7908; 6.1888; 13.6788 90; 106.523; 90 | 1281.57 | Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams ACS Catalysis, 2016, 6, 1565 |
| 4513814 | CIF | C13 H15 N O3 S | P 21 21 21 | 6.4715; 12.2935; 16.0625 90; 90; 90 | 1277.89 | Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams ACS Catalysis, 2016, 6, 1565 |
| 4513815 | CIF | C17 H17 N3 O | P 1 21 1 | 8.6937; 8.2505; 9.8923 90; 96.8229; 90 | 704.524 | Singh, Manish K.; Akula, Hari K.; Satishkumar, Sakilam; Stahl, Lothar; Lakshman, Mahesh K. Ruthenium-Catalyzed C-H Bond Activation Approach to Azolyl Aminals and Hemiaminal Ethers, Mechanistic Evaluations, and Isomer Interconversion. ACS catalysis, 2016, 6, 1921-1928 |
| 4513816 | CIF | C33 H27 F2 N O4 | P -1 | 7.9794; 12.355; 27.87 83.268; 84.119; 89.549 | 2714.2 | Wang, Qiang; Li, Yingzi; Qi, Zisong; Xie, Fang; Lan, Yu; Li, Xingwei Rhodium(III)-Catalyzed Annulation betweenN-Sulfinyl Ketoimines and Activated Olefins: C‒H Activation Assisted by an Oxidizing N‒S Bond ACS Catalysis, 2016, 6, 1971 |
| 4513817 | CIF | C63 H53 B Cl N4 O3 P Ru | P 1 21/c 1 | 10.0715; 28.3272; 21.8875 90; 92.226; 90 | 6239.7 | Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K. Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals ACS Catalysis, 2016, 6, 1981 |
| 4513818 | CIF | C38 H36 Cl F6 N3 O4 P2 Ru | P 1 21/n 1 | 14.0112; 9.7442; 27.2179 90; 94.215; 90 | 3706 | Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K. Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals ACS Catalysis, 2016, 6, 1981 |
| 4513819 | CIF | C21 H29 Cl F6 N3 O2 P3 Ru | P 1 21/n 1 | 12.1467; 17.3624; 12.8848 90; 90.182; 90 | 2717.3 | Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K. Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals ACS Catalysis, 2016, 6, 1981 |
| 4513820 | CIF | C33 H26 Cl2 N3 O2 P Ru | P 1 21/n 1 | 11.6136; 17.269; 14.4146 90; 90.128; 90 | 2890.9 | Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K. Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals ACS Catalysis, 2016, 6, 1981 |
| 4513821 | CIF | C69 H53 N6 O5 P2 Ru2 | C 1 2/c 1 | 38.209; 13.4891; 24.3071 90; 118.199; 90 | 11041.1 | Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K. Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals ACS Catalysis, 2016, 6, 1981 |
| 4513822 | CIF | C19 H23 F3 Ir N3 O3 S | P 1 21/c 1 | 14.9292; 12.2212; 12.2965 90; 109.506; 90 | 2114.8 | Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J. A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid ACS Catalysis, 2016, 6, 2014 |
| 4513823 | CIF | C27 H31 F3 Ir N3 O3 S | P 1 21/c 1 | 11.0313; 26.4631; 19.9865 90; 98.415; 90 | 5771.7 | Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J. A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid ACS Catalysis, 2016, 6, 2014 |
| 4513824 | CIF | C2 H5 Na3 O8 | C 1 2/c 1 | 20.3758; 3.4577; 10.3049 90; 106.491; 90 | 696.15 | Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J. A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid ACS Catalysis, 2016, 6, 2014 |
| 4513825 | CIF | C28 H33 B O2 Si | P -1 | 9.8337; 11.7927; 12.4336 112.475; 96.966; 104.18 | 1254 | Ansell, Melvyn B.; Spencer, John; Navarro, Oscar (N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies ACS Catalysis, 2016, 6, 2192 |
| 4513826 | CIF | C33 H49 N4 Pd Si2 | P -1 | 11.8802; 12.1897; 13.9679 86.341; 73.708; 63.295 | 1729.87 | Ansell, Melvyn B.; Spencer, John; Navarro, Oscar (N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies ACS Catalysis, 2016, 6, 2192 |
| 4513827 | CIF | C28 H47 B N4 O2 Pd Si | P 1 21/n 1 | 12.9381; 17.8318; 14.8311 90; 113.454; 90 | 3138.98 | Ansell, Melvyn B.; Spencer, John; Navarro, Oscar (N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies ACS Catalysis, 2016, 6, 2192 |
| 4513837 | CIF | C23 H26 I2 Ir N3 | P 1 21/c 1 | 17.0173; 7.793; 19.3018 90; 103.52; 90 | 2488.79 | Semwal, Shrivats; Choudhury, Joyanta Molecular Coordination-Switch in a New Role: Controlling Highly Selective Catalytic Hydrogenation with Switchability Function ACS Catalysis, 2016, 6, 2424 |
| 4513838 | CIF | C23 H25 I Ir N3 | P -1 | 9.2675; 10.21; 12.0027 79.971; 78.553; 83.299 | 1092.13 | Semwal, Shrivats; Choudhury, Joyanta Molecular Coordination-Switch in a New Role: Controlling Highly Selective Catalytic Hydrogenation with Switchability Function ACS Catalysis, 2016, 6, 2424 |
| 4513839 | CIF | C21 H19 N O4 | P 21 21 21 | 7.32516; 13.4286; 19.6168 90; 90; 90 | 1929.64 | Wang, Gang; Liu, Xiaohua; Chen, Yushuang; Yang, Jian; Li, Jun; Lin, Lili; Feng, Xiaoming Diastereoselective and Enantioselective Alleno-aldol Reaction of Allenoates with Isatins to Synthesis of Carbinol Allenoates Catalyzed by Gold ACS Catalysis, 2016, 6, 2482 |
| 4513840 | CIF | C17 H10 F6 O2 | P 1 21/c 1 | 5.622; 15.483; 18.549 90; 94.841; 90 | 1608.8 | Fu, Ming-Chen; Shang, Rui; Cheng, Wan-Min; Fu, Yao Nickel-Catalyzed Regio- and Stereoselective Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling ACS Catalysis, 2016, 6, 2501 |
| 4513841 | CIF | C12 H12 O4 | P 1 21/n 1 | 4.5824; 19.9078; 12.0067 90; 94.374; 90 | 1092.13 | Fu, Ming-Chen; Shang, Rui; Cheng, Wan-Min; Fu, Yao Nickel-Catalyzed Regio- and Stereoselective Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling ACS Catalysis, 2016, 6, 2501 |
| 4513842 | CIF | C67 H16 B2 Cl2 F40 Fe4 O12 S4 | P c a 21 | 17.7344; 14.2966; 30.6824 90; 90; 90 | 7779.3 | Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation ACS Catalysis, 2016, 6, 2559 |
| 4513843 | CIF | C36 H5 B F20 Fe2 O6 S2 | P b c a | 16.0418; 20.9445; 23.0959 90; 90; 90 | 7759.9 | Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation ACS Catalysis, 2016, 6, 2559 |
| 4513844 | CIF | C33 H7 B Cl2 F20 Fe2 O6 S2 | C 1 c 1 | 22.9134; 12.3868; 17.2161 90; 124.699; 90 | 4017.3 | Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation ACS Catalysis, 2016, 6, 2559 |
| 4513845 | CIF | C11 H7 F9 Fe2 O15 S5 | P 1 21/m 1 | 6.4147; 18.5996; 11.5206 90; 104.145; 90 | 1332.85 | Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation ACS Catalysis, 2016, 6, 2559 |
| 4513846 | CIF | C18 H16 O | P 1 21 1 | 10.5879; 4.8182; 13.6534 90; 96.876; 90 | 691.51 | Rodríguez, Elsa; Grayson, Matthew N.; Asensio, Amparo; Barrio, Pablo; Houk, K. N.; Fustero, Santos Chiral Brønsted Acid-Catalyzed Asymmetric Allyl(propargyl)boration Reaction ofortho-Alkynyl Benzaldehydes: Synthetic Applications and Factors Governing the Enantioselectivity ACS Catalysis, 2016, 6, 2506 |
| 4513847 | CIF | C18 H14 O | P 1 21 1 | 10.5044; 4.7708; 13.7318 90; 97.605; 90 | 682.11 | Rodríguez, Elsa; Grayson, Matthew N.; Asensio, Amparo; Barrio, Pablo; Houk, K. N.; Fustero, Santos Chiral Brønsted Acid-Catalyzed Asymmetric Allyl(propargyl)boration Reaction ofortho-Alkynyl Benzaldehydes: Synthetic Applications and Factors Governing the Enantioselectivity ACS Catalysis, 2016, 6, 2506 |
| 4513848 | CIF | C23 H33 Co N3 O4 | P 1 21/c 1 | 8.9984; 21.6663; 12.2395 90; 90.0826; 90 | 2386.24 | Schuster, Christopher H.; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J. Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes ACS Catalysis, 2016, 6, 2632 |
| 4513849 | CIF | C21 H35 Co N3 O5 | P 1 21/c 1 | 8.9806; 29.3177; 8.8612 90; 97.9533; 90 | 2310.63 | Schuster, Christopher H.; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J. Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes ACS Catalysis, 2016, 6, 2632 |
| 4513850 | CIF | C22 H23 Cl Ir N3 O3 | P 1 21/c 1 | 15.229; 8.446; 17.388 90; 108.03; 90 | 2126.7 | Ngo, Anh H.; Ibañez, Miguel; Do, Loi H. Catalytic Hydrogenation of Cytotoxic Aldehydes Using Nicotinamide Adenine Dinucleotide (NADH) in Cell Growth Media ACS Catalysis, 2016, 6, 2637 |
| 4513853 | CIF | C20 H38 Br Fe N3 O P2 | P 1 21 1 | 11.7189; 12.5863; 16.7721 90; 99.602; 90 | 2439.2 | Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity. ACS catalysis, 2016, 6, 2664-2672 |
| 4513854 | CIF | C20 H39 Fe N3 O P2 | P 1 21/c 1 | 13.7848; 11.7982; 15.4447 90; 113.332; 90 | 2306.5 | Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity. ACS catalysis, 2016, 6, 2664-2672 |
| 4513855 | CIF | C29 H26 F3 N3 O6 S | P 21 21 21 | 8.33; 21.758; 15.532 90; 90; 90 | 2815.08 | Montesinos-Magraner, Marc; Vila, Carlos; Rendón-Patiño, Alejandra; Blay, Gonzalo; Fernández, Isabel; Muñoz, M. Carmen; Pedro, José R. Organocatalytic Enantioselective Friedel‒Crafts Aminoalkylation of Indoles in the Carbocyclic Ring ACS Catalysis, 2016, 6, 2689 |
| 4513856 | CIF | C29 H29 N3 O6 S | P 21 21 21 | 8.592; 11.328; 27.778 90; 90; 90 | 2703.64 | Montesinos-Magraner, Marc; Vila, Carlos; Rendón-Patiño, Alejandra; Blay, Gonzalo; Fernández, Isabel; Muñoz, M. Carmen; Pedro, José R. Organocatalytic Enantioselective Friedel‒Crafts Aminoalkylation of Indoles in the Carbocyclic Ring ACS Catalysis, 2016, 6, 2689 |
| 4513857 | CIF | C29 H26 F3 N3 O6 S | P -1 | 10.512; 10.602; 13.589 104.085; 99.52; 91.757 | 1444.7 | Montesinos-Magraner, Marc; Vila, Carlos; Rendón-Patiño, Alejandra; Blay, Gonzalo; Fernández, Isabel; Muñoz, M. Carmen; Pedro, José R. Organocatalytic Enantioselective Friedel‒Crafts Aminoalkylation of Indoles in the Carbocyclic Ring ACS Catalysis, 2016, 6, 2689 |
| 4513858 | CIF | C20 H19 N O2 | P 21 21 21 | 7.23695; 9.22435; 23.1301 90; 90; 90 | 1544.08 | Ghosh, Avipsa; Walker, James A.; Ellern, Arkady; Stanley, Levi M. Coupling Catalytic Alkene Hydroacylation and α-Arylation: Enantioselective Synthesis of Heterocyclic Ketones with α-Chiral Quaternary Stereocenters ACS Catalysis, 2016, 6, 2673 |
| 4513863 | CIF | C33 H38 B Li O2 P2 S2 | P -1 | 9.0615; 10.7999; 17.4441 88.376; 79.606; 82.091 | 1663.14 | Lafage, Mathieu; Pujol, Anthony; Saffon-Merceron, Nathalie; Mézailles, Nicolas BH3Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2Reduction into Methanol Derivatives ACS Catalysis, 2016, 6, 3030 |
| 4513864 | CIF | C29 H35 B2 Li O P2 S2 | C 1 2/c 1 | 15.4208; 14.8446; 13.1339 90; 92.9702; 90 | 3002.52 | Lafage, Mathieu; Pujol, Anthony; Saffon-Merceron, Nathalie; Mézailles, Nicolas BH3Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2Reduction into Methanol Derivatives ACS Catalysis, 2016, 6, 3030 |
| 4513865 | CIF | C20 H20 O | P 21 21 21 | 8.4103; 8.8487; 20.8277 90; 90; 90 | 1550 | Casanova, Noelia; Del Rio, Karina P.; García-Fandiño, Rebeca; Mascareñas, José L; Gulías, Moisés Palladium(II)-Catalyzed Annulation between ortho-Alkenylphenols and Allenes. Key Role of the Metal Geometry in Determining the Reaction Outcome. ACS catalysis, 2016, 6, 3349-3353 |
| 4513866 | CIF | C36 H32 O2 | P 1 21/c 1 | 9.4194; 7.0858; 19.435 90; 95.373; 90 | 1291.5 | Casanova, Noelia; Del Rio, Karina P.; García-Fandiño, Rebeca; Mascareñas, José L; Gulías, Moisés Palladium(II)-Catalyzed Annulation between ortho-Alkenylphenols and Allenes. Key Role of the Metal Geometry in Determining the Reaction Outcome. ACS catalysis, 2016, 6, 3349-3353 |
| 4513867 | CIF | C20 H19 F O | P 21 21 21 | 6.489; 7.157; 32.722 90; 90; 90 | 1519.7 | Casanova, Noelia; Del Rio, Karina P.; García-Fandiño, Rebeca; Mascareñas, José L; Gulías, Moisés Palladium(II)-Catalyzed Annulation between ortho-Alkenylphenols and Allenes. Key Role of the Metal Geometry in Determining the Reaction Outcome. ACS catalysis, 2016, 6, 3349-3353 |
| 4513868 | CIF | C16 H19.16 N2 O4.58 Pd | P 1 21/c 1 | 14.136; 9.529; 25.085 90; 94.09; 90 | 3370.4 | White, Paul B.; Jaworski, Jonathan N.; Zhu, Geyunjian Harry; Stahl, Shannon S. Diazafluorenone-Promoted Oxidation Catalysis: Insights into the Role of Bidentate Ligands in Pd-Catalyzed Aerobic Aza-Wacker Reactions. ACS catalysis, 2016, 6, 3340-3348 |
| 4513869 | CIF | C20 H17 N3 O5 Pd | P 1 21/n 1 | 11.06; 10.703; 15.879 90; 102.713; 90 | 1833.6 | White, Paul B.; Jaworski, Jonathan N.; Zhu, Geyunjian Harry; Stahl, Shannon S. Diazafluorenone-Promoted Oxidation Catalysis: Insights into the Role of Bidentate Ligands in Pd-Catalyzed Aerobic Aza-Wacker Reactions. ACS catalysis, 2016, 6, 3340-3348 |
| 4513870 | CIF | C22 H23 N3 O4 Pd | P 1 21/c 1 | 12.472; 8.829; 19.26 90; 90.22; 90 | 2120.8 | White, Paul B.; Jaworski, Jonathan N.; Zhu, Geyunjian Harry; Stahl, Shannon S. Diazafluorenone-Promoted Oxidation Catalysis: Insights into the Role of Bidentate Ligands in Pd-Catalyzed Aerobic Aza-Wacker Reactions. ACS catalysis, 2016, 6, 3340-3348 |
| 4513871 | CIF | C19 H26 B N O2 | P 1 21 1 | 9.8601; 17.3729; 10.9482 90; 111.164; 90 | 1748.92 | Zhan, Miao; Li, Ren-Zhe; Mou, Ze-Dong; Cao, Chao-Guo; Liu, Jie; Chen, Yuan-Wei; Niu, Dawen Silver-Assisted, Iridium-Catalyzed Allylation of Bis[(pinacolato)boryl]methane Allows the Synthesis of Enantioenriched Homoallylic Organoboronic Esters ACS Catalysis, 2016, 6, 3381 |
| 4513872 | CIF | C51 H32 N4 O9 Zn2 | P 42/m n m | 36.0683; 36.0683; 27.0566 90; 90; 90 | 35199 | Hall, Edward A.; Redfern, Louis R.; Wang, Michael H.; Scheidt, Karl A. Lewis Acid Activation of a Hydrogen Bond Donor Metal‒Organic Framework for Catalysis ACS Catalysis, 2016, 6, 3248 |
| 4513873 | CIF | C15 H19 Ir N2 O6 S | P 1 21/c 1 | 8.7413; 14.2966; 15.2329 90; 98.084; 90 | 1884.75 | Koelewijn, Jacobus M.; Lutz, Martin; Dzik, Wojciech I.; Detz, Remko J.; Reek, Joost N. H. Reaction Progress Kinetic Analysis as a Tool To Reveal Ligand Effects in Ce(IV)-Driven IrCp*-Catalyzed Water Oxidation ACS Catalysis, 2016, 6, 3418 |
| 4513878 | CIF | C30 H20 N2 O | P 21 21 21 | 9.0933; 20.0387; 23.2417 90; 90; 90 | 4235.05 | Kumar, Dinesh; Vemula, Sandeep R.; Cook, Gregory R. Merging C‒H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines ACS Catalysis, 2016, 6, 3531 |
| 4513879 | CIF | C33 H23 F3 N2 O4 | P 1 21/c 1 | 21.6794; 5.8892; 20.8559 90; 98.889; 90 | 2630.78 | Kumar, Dinesh; Vemula, Sandeep R.; Cook, Gregory R. Merging C‒H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines ACS Catalysis, 2016, 6, 3531 |
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