Crystallography Open Database
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Searching journal of publication like 'ACS catalysis' volume of publication is 8
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
4514384 | CIF | C24 H29 N2 O3 Rh S | P 1 21/n 1 | 9.8164; 14.358; 17.0526 90; 90.736; 90 | 2403.26 | Ran, You; Yang, Yudong; You, Huansha; You, Jingsong RhCl3-Catalyzed Oxidative C‒H/C‒H Cross-Coupling of (Hetero)aromatic Sulfonamides with (Hetero)arenes ACS Catalysis, 2018, 8, 1796 |
4514387 | CIF | C26 H24 Br N O | P 1 21 1 | 11.693; 6.314; 15.57 90; 103.875; 90 | 1116 | Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation ACS Catalysis, 2018, 8, 1964 |
4514388 | CIF | C23 H22 F6 N3 P Pd | P 1 21/n 1 | 11.7229; 13.9765; 13.8227 90; 91.721; 90 | 2263.8 | Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation ACS Catalysis, 2018, 8, 1964 |
4514394 | CIF | C24 H33 Ir N2 O6 | P 1 21/n 1 | 14.1793; 34.531; 16.0684 90; 113.726; 90 | 7202.5 | Yuan, Hongmei; Brennessel, William W.; Jones, William D. Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes ACS Catalysis, 2018, 8, 2326 |
4514395 | CIF | C28 H43 Ir N2 O7 | P 1 21/c 1 | 17.9996; 11.5553; 15.0325 90; 100.311; 90 | 3076.1 | Yuan, Hongmei; Brennessel, William W.; Jones, William D. Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes ACS Catalysis, 2018, 8, 2326 |
4514396 | CIF | C34 H39 Ir N2 O7 | P -1 | 10.4412; 11.3139; 13.9001 75.379; 83.373; 84.494 | 1574.4 | Yuan, Hongmei; Brennessel, William W.; Jones, William D. Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes ACS Catalysis, 2018, 8, 2326 |
4514397 | CIF | C28 H39 Ir N2 O7 | P 1 21/c 1 | 12.1132; 39.536; 11.7754 90; 94.196; 90 | 5624.2 | Yuan, Hongmei; Brennessel, William W.; Jones, William D. Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes ACS Catalysis, 2018, 8, 2326 |
4514398 | CIF | C87 H190 N3 O38 P Si3 Ti W9 | P b c a | 20.2301; 28.431; 43.025 90; 90; 90 | 24746 | Zhang, Teng; Mazaud, Louis; Chamoreau, Lise-Marie; Paris, Céline; Proust, Anna; Guillemot, Geoffroy Unveiling the Active Surface Sites in Heterogeneous Titanium-Based Silicalite Epoxidation Catalysts: Input of Silanol-Functionalized Polyoxotungstates as Soluble Analogues ACS Catalysis, 2018, 8, 2330 |
4514400 | CIF | C27 H18 O2 | P 1 21/c 1 | 17.4516; 7.5513; 15.134 90; 107.604; 90 | 1900.99 | Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V. Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes ACS Catalysis, 2018, 8, 2748 |
4514401 | CIF | C61 H51 Cl3 F6 N3 P3 Ru | P 1 21/c 1 | 10.0272; 23.326; 22.7595 90; 95.922; 90 | 5294.9 | Paul, Bhaskar; Shee, Sujan; Panja, Dibyajyoti; Chakrabarti, Kaushik; Kundu, Sabuj Direct Synthesis of N,N-Dimethylated and β-Methyl N,N-Dimethylated Amines from Nitriles Using Methanol: Experimental and Computational Studies ACS Catalysis, 2018, 8, 2890 |
4515514 | CIF | C25 H38 B N O6 S | P -1 | 11.446; 11.5967; 12.3843 112.094; 115.7; 93.978 | 1318.18 | Kim-Lee, Shin-Ho; Alonso, Inés; Mauleón, Pablo; Arrayás, Ramón Gómez; Carretero, Juan C. Rationalizing the Role of NaOtBu in Copper-Catalyzed Carboboration of Alkynes: Assembly of Allylic All-Carbon Quaternary Stereocenters ACS Catalysis, 2018, 8, 8993 |
4515515 | CIF | C21 H22 F N O4 | P 1 21/c 1 | 27.4465; 6.4873; 22.0138 90; 112.954; 90 | 3609.3 | Park, Hojoon; Chekshin, Nikita; Shen, Peng-Xiang; Yu, Jin-Quan Ligand-Enabled, Palladium-Catalyzed β-C(sp<sup>3</sup>)-H Arylation of Weinreb Amides. ACS catalysis, 2018, 8, 9292-9297 |
4515516 | CIF | C41 H51 Co K N6 O11 | P 21 21 21 | 11.0919; 18.3376; 21.9261 90; 90; 90 | 4459.7 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515517 | CIF | C45 H36 K Mn N7 O3 | P 1 21/n 1 | 11.7651; 21.2221; 16.4682 90; 95.468; 90 | 4093.1 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515518 | CIF | C45 H48 N4 | P -1 | 9.1381; 12.0237; 17.8361 96.278; 90.36; 111.214 | 1813.7 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515519 | CIF | C50 H55 K Mn N4 O2 | P 1 21/n 1 | 11.527; 13.729; 27.724 90; 92.471; 90 | 4383.4 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515520 | CIF | C53 H47.5 F9 K Mn N4.5 O6.5 | P 1 21/n 1 | 12.3883; 18.995; 21.656 90; 101.457; 90 | 4994.5 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515521 | CIF | C48 H39 F9 N4 O6 | P 1 21/c 1 | 19.36; 10.0615; 29.486 90; 128.675; 90 | 4484 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515522 | CIF | C88 H131 K Mn N4 O7 | P -1 | 13.4244; 15.4608; 21.041 92.203; 93.474; 102.805 | 4244.6 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515523 | CIF | C54 H45 F18 K Mn N4 O3 | P -1 | 12.729; 14.584; 16.701 112.045; 92.891; 99.02 | 2817.9 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515524 | CIF | C148 H198 Cl0 K4 Mn4 N20 O19 | P -1 | 12.421; 13.222; 24.754 89.65; 77.831; 72.506 | 3783.1 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515525 | CIF | C64.75 H86 K Mn N4 O4 | P -1 | 11.719; 12.417; 21.77 91.221; 100.827; 100.424 | 3055 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515526 | CIF | C58 H71 K Mn N4 O4 | P 1 21/n 1 | 12.4818; 21.792; 20.039 90; 105.708; 90 | 5247.1 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515527 | CIF | C32 H29 F9 K Mn N6 O5 | C 1 c 1 | 18.3717; 10.8662; 19.0286 90; 94.307; 90 | 3788 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515528 | CIF | C41 H51 Fe K N6 O11 | P 21 21 21 | 11.1683; 18.406; 21.83 90; 90; 90 | 4487.5 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515529 | CIF | C56 H61 Cl6 K Mn N4 O5 | P 1 21/n 1 | 11.391; 20.1796; 24.488 90; 93.742; 90 | 5617 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515530 | CIF | C28 H18 Co F9 K N6 O3 | P 1 21/c 1 | 10.696; 18.855; 15.813 90; 101.378; 90 | 3126.4 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515531 | CIF | C86 H118 K2 Mn2 N8 O17 | C 1 2/c 1 | 18.8633; 21.7465; 22.5199 90; 102.759; 90 | 9009.8 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515532 | CIF | C36 H39 F9 K N7 Ni O6 | P 1 21/n 1 | 9.133; 29.15; 16.125 90; 95.392; 90 | 4274 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515533 | CIF | C28 H18 F9 K Mn N6 O3 | P 1 21/c 1 | 10.661; 18.766; 15.752 90; 100.699; 90 | 3097 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515534 | CIF | C78 H105 K2 Mn2 N11 O9 | P -1 | 11.759; 13.541; 26.426 86.003; 80.023; 73.719 | 3977 | Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes ACS Catalysis, 2018, 8, 9183 |
4515535 | CIF | C15 H13 N O2 | P 1 21/c 1 | 5.8829; 8.228; 25.846 90; 96.056; 90 | 1244.08 | Liu, Chengwei; Li, Guangchen; Shi, Shicheng; Meng, Guangrong; Lalancette, Roger; Szostak, Roman; Szostak, Michal Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon‒Nitrogen Bond Cleavage ACS Catalysis, 2018, 8, 9131 |
4515536 | CIF | C30 H27 N2 O4 P | P 1 21/c 1 | 12.148; 10.6001; 19.4764 90; 96.366; 90 | 2492.5 | Meyer, Tjark H.; Oliveira, João C. A.; Sau, Samaresh Chandra; Ang, Nate W. J.; Ackermann, Lutz Electrooxidative Allene Annulations by Mild Cobalt-Catalyzed C‒H Activation ACS Catalysis, 2018, 8, 9140 |
4515537 | CIF | C25 H20 Cl N O2 | P 21 21 21 | 6.1285; 10.8042; 30.5592 90; 90; 90 | 2023.43 | Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles ACS Catalysis, 2018, 8, 9543 |
4515538 | CIF | C25 H20 Br N O2 | P 1 21 1 | 13.288; 5.6; 14.983 90; 114.29; 90 | 1016.23 | Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles ACS Catalysis, 2018, 8, 9543 |
4515539 | CIF | C88 H44 Mo0.96 O32 S1.92 Zr6 | P 6/m m m | 39.254; 39.254; 16.542 90; 90; 120 | 22074 | Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T. Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework ACS Catalysis, 2018, 8, 9848 |
4515540 | CIF | C88 H44 Mo2.24 O36.88 Zr6 | P 6/m m m | 39.4657; 39.4657; 16.3953 90; 90; 120 | 22115.1 | Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T. Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework ACS Catalysis, 2018, 8, 9848 |
4515541 | CIF | C28 H26 N4 O7 | P 21 21 21 | 9.0462; 11.8256; 23.9232 90; 90; 90 | 2559.23 | Wang, Jilan; Li, Yongjia; Sun, Jun; Wang, Hongling; Jin, Zhichao; Chi, Yonggui Robin Carbene-Catalyzed Enantioselective Addition of Benzylic Carbon to Unsaturated Acyl Azolium for Rapid Synthesis of Pyrrolo[3,2-c]quinolines ACS Catalysis, 2018, 8, 9859 |
4515542 | CIF | C14 H21 Ge N O3 | P b c a | 13.7717; 11.1518; 18.9206 90; 90; 90 | 2905.81 | Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis ACS Catalysis, 2018, 8, 9287 |
4515543 | CIF | C14 H20 Cl Ge N O3 | P 1 21/n 1 | 14.8342; 13.3798; 16.4653 90; 96.777; 90 | 3245.18 | Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis ACS Catalysis, 2018, 8, 9287 |
4515544 | CIF | C54 H60 N2 | P -1 | 8.3369; 9.3962; 14.592 100.111; 103.43; 98.334 | 1073.8 | Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation ACS Catalysis, 2018, 8, 9408 |
4515545 | CIF | C12 H14 F3 N O | P c a 21 | 8.8458; 14.526; 9.5388 90; 90; 90 | 1225.7 | Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation ACS Catalysis, 2018, 8, 9408 |
4515546 | CIF | C28 H23 N S | P 1 | 10.1611; 10.3192; 12.2146 73.14; 71.609; 61.296 | 1051.13 | Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction ACS Catalysis, 2018, 8, 9364 |
4515547 | CIF | C28 H23 N S | P 1 | 10.082; 10.316; 12.247 73.57; 71.546; 61.603 | 1049.43 | Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction ACS Catalysis, 2018, 8, 9364 |
4515548 | CIF | C15 H14 N2 O3 | P 1 21/c 1 | 8.085; 16.9819; 10.0705 90; 110.13; 90 | 1298.2 | Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity ACS Catalysis, 2018, 8, 9697 |
4515549 | CIF | C23 H19 Cl N2 O3 S | P 1 21/c 1 | 7.0746; 19.195; 15.3264 90; 100.918; 90 | 2043.6 | Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity ACS Catalysis, 2018, 8, 9697 |
4515550 | CIF | C27 H22 N2 O3 S | P n a 21 | 33.95; 8.4972; 7.9321 90; 90; 90 | 2288.3 | Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity ACS Catalysis, 2018, 8, 9697 |
4515551 | CIF | C26 H24 N2 O5 S | P 1 21/c 1 | 12.008; 7.0368; 30.631 90; 92.288; 90 | 2586.2 | Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity ACS Catalysis, 2018, 8, 9697 |
4515552 | CIF | C28 H28 N2 O3 S | C 1 2/c 1 | 33.457; 7.1395; 20.377 90; 103.524; 90 | 4732.4 | Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity ACS Catalysis, 2018, 8, 9697 |
4515553 | CIF | C24 H22 Cl N3 O2 | P -1 | 9.5004; 11.278; 11.5979 104.256; 109.363; 106.026 | 1045.71 | Liu, Bingxian; Li, Jie; Hu, Panjie; Zhou, Xukai; Bai, Dachang; Li, Xingwei Divergent Annulative C‒C Coupling of Indoles Initiated by Manganese-Catalyzed C‒H Activation ACS Catalysis, 2018, 8, 9463 |
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