Crystallography Open Database
Search results
Result: there are 375 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
Searching journal of publication like 'ACS catalysis' volume of publication is 8
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 4515654 | CIF | C26 H21 F3 O2 S | P 1 21 1 | 7.7702; 7.7862; 17.9926 90; 100.144; 90 | 1071.54 | Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L. Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones. ACS catalysis, 2018, 8, 5443-5447 |
| 4515655 | CIF | C23.7 H15 Cl2.1 D0.7 F3 O4 S | P 21 21 21 | 9.3182; 10.5061; 24.8751 90; 90; 90 | 2435.2 | Maddox, Sean M.; Dawson, Gregory A.; Rochester, Nicholas C.; Ayonon, Arianna B.; Moore, Curtis E.; Rheingold, Arnold L.; Gustafson, Jeffrey L. Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones. ACS catalysis, 2018, 8, 5443-5447 |
| 4515656 | CIF | C21 H20 N2 O3 | P 1 21/n 1 | 13.218; 8.696; 16.546 90; 98.483; 90 | 1881.1 | Pang, Shuai; Yang, Xing; Cao, Ze-Hun; Zhang, Yu-Long; Zhao, Yan; Huang, Yi-Yong Intermolecular [2 + 2] Cycloaddition/Isomerization of Allenyl Imides and Unactivated Imines for the Synthesis of 1-Azadienes Catalyzed by a Ni(ClO4)2·6H2O Lewis Acid ACS Catalysis, 2018, 8, 5193 |
| 4515657 | CIF | C22 H22 N2 O4 | P 1 21/n 1 | 10.559; 8.848; 20.03 90; 91.424; 90 | 1870.7 | Pang, Shuai; Yang, Xing; Cao, Ze-Hun; Zhang, Yu-Long; Zhao, Yan; Huang, Yi-Yong Intermolecular [2 + 2] Cycloaddition/Isomerization of Allenyl Imides and Unactivated Imines for the Synthesis of 1-Azadienes Catalyzed by a Ni(ClO4)2·6H2O Lewis Acid ACS Catalysis, 2018, 8, 5193 |
| 4515658 | CIF | C16 H21 Cl2 Fe N9 O2 | P n a 21 | 13.7551; 18.856; 8.4263 90; 90; 90 | 2185.5 | Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS catalysis, 2018, 8, 5032-5037 |
| 4515659 | CIF | C15 H19 F3 N2 O4 S | P -1 | 7.6537; 10.3038; 11.7 69.471; 74.774; 75.983 | 822.2 | Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS catalysis, 2018, 8, 5032-5037 |
| 4515660 | CIF | C18 H22 Cl3 F3 N2 O4 S | P 21 21 21 | 6.1287; 17.2349; 21.6302 90; 90; 90 | 2284.74 | Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS catalysis, 2018, 8, 5032-5037 |
| 4515661 | CIF | C14 H22 F3 N O2 | P 1 21/c 1 | 11.8893; 5.2263; 24.518 90; 96.137; 90 | 1514.75 | Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS catalysis, 2018, 8, 5032-5037 |
| 4515662 | CIF | C16 H26 F3 N O2 | P 21 21 21 | 11.579; 16.9733; 18.2465 90; 90; 90 | 3586.05 | Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS catalysis, 2018, 8, 5032-5037 |
| 4515663 | CIF | C19 H25 F3 N2 O4 | P 1 21/c 1 | 14.9198; 13.8571; 9.9498 90; 95.4351; 90 | 2047.82 | Zhu, Cheng-Liang; Wang, Cheng; Qin, Qi-Xue; Yruegas, Sam; Martin, Caleb D.; Xu, Hao Iron(II)-Catalyzed Azidotrifluoromethylation of Olefins and N-Heterocycles for Expedient Vicinal Trifluoromethyl Amine Synthesis. ACS catalysis, 2018, 8, 5032-5037 |
| 4515664 | CIF | C17 H39 As Co K2 Mo6 N O39.5 | P -1 | 12.0872; 12.5682; 17.2255 76.7; 74.058; 76.399 | 2407 | Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands ACS Catalysis, 2018, 8, 6062 |
| 4515665 | CIF | C17 H44 As K2 Mo6 N Ni O42 | P -1 | 11.9612; 12.5318; 17.1943 76.499; 74.053; 76.535 | 2370.12 | Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands ACS Catalysis, 2018, 8, 6062 |
| 4515666 | CIF | C17 H40 As K2 Mo6 N O41 Zn | P -1 | 12.1425; 12.5739; 17.2226 76.443; 74.062; 76.225 | 2415.16 | Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands ACS Catalysis, 2018, 8, 6062 |
| 4515667 | CIF | C17 H39 As K2 Mn Mo6 N O40 | P -1 | 12.2865; 12.6065; 17.2145 76.319; 73.933; 76.064 | 2445.2 | Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands ACS Catalysis, 2018, 8, 6062 |
| 4515668 | CIF | C18 H87 As2 Co0.5 K3 Mo12 N6 Na O77.5 | P -1 | 16.1055; 18.5246; 19.0707 75.701; 65.877; 64.845 | 4681.8 | Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands ACS Catalysis, 2018, 8, 6062 |
| 4515669 | CIF | C21 H44 As Co0.5 K5 Mo6 O44.5 | P -1 | 12.6575; 12.671; 18.5916 105.723; 91.318; 106.19 | 2740.7 | Hou, Yujiao; An, Haiyan; Zhang, Yumeng; Hu, Tao; Yang, Wei; Chang, Shenzhen Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands ACS Catalysis, 2018, 8, 6062 |
| 4515670 | CIF | C47.5 H70 N2 Ni O8 | P -1 | 11.54858; 30.1957; 32.8403 64.8392; 80.3426; 86.1838 | 10218.4 | Nett, Alex J.; Cañellas, Santiago; Higuchi, Yuki; Robo, Michael T.; Kochkodan, Jeanne M.; Haynes, 2nd, M Taylor; Kampf, Jeff W.; Montgomery, John Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation. ACS catalysis, 2018, 8, 6606-6611 |
| 4515671 | CIF | C97 H92 N2 Ni O8.5 | P -1 | 14.0561; 14.806; 22.1265 93.854; 102.679; 118.29 | 3876.59 | Nett, Alex J.; Cañellas, Santiago; Higuchi, Yuki; Robo, Michael T.; Kochkodan, Jeanne M.; Haynes, 2nd, M Taylor; Kampf, Jeff W.; Montgomery, John Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation. ACS catalysis, 2018, 8, 6606-6611 |
| 4515672 | CIF | C27 H22 N2 O3 | C 1 2/c 1 | 14.2005; 10.38306; 28.0529 90; 102.226; 90 | 4042.44 | Rej, Supriya; Chatani, Naoto Rhodium(I)-Catalyzed C8-Alkylation of 1-Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System ACS Catalysis, 2018, 8, 6699 |
| 4515673 | CIF | C27 H36 I4 N2 S | P -1 | 10.6361; 16.8158; 19.6467 91.7164; 105.424; 93.774 | 3375.9 | Horibe, Takahiro; Tsuji, Yasutaka; Ishihara, Kazuaki Thiourea‒I2 as Lewis Base‒Lewis Acid Cooperative Catalysts for Iodochlorination of Alkene with In Situ-Generated I‒Cl ACS Catalysis, 2018, 8, 6362 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!