Crystallography Open Database
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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 4514799 | CIF | C24 H22 N2 O | P b c a | 10.4266; 18.053; 19.734 90; 90; 90 | 3714.6 | Sahani, Rajkumar Lalji; Liu, Rai-Shung Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring ACS Catalysis, 2019, 9, 5890 |
| 4514800 | CIF | C26 H24 N2 O | P 1 21 1 | 8.7098; 8.9173; 13.0467 90; 93.444; 90 | 1011.48 | Sahani, Rajkumar Lalji; Liu, Rai-Shung Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring ACS Catalysis, 2019, 9, 5890 |
| 4514801 | CIF | C18 H19 N O2 | P -1 | 9.859; 10.008; 15.838 93.054; 90.75; 99.872 | 1537 | Sahani, Rajkumar Lalji; Liu, Rai-Shung Gold-Catalyzed Oxidative Arylations of 3-Butyn-1-ols and 2-Propyn-1-ols with Nitrones to Yield Distinct Fused Indoles Bearing a Heterocyclic Ring ACS Catalysis, 2019, 9, 5890 |
| 4514802 | CIF | C30 H36 B N3 O3 | P 1 21 1 | 6.5399; 23.9124; 9.103 90; 102.293; 90 | 1390.93 | Bai, Zibo; Zheng, Sujuan; Bai, Ziqian; Song, Fangfang; Wang, Hao; Peng, Qian; Chen, Gong; He, Gang Palladium-Catalyzed Amide-Directed Enantioselective Carboboration of Unactivated Alkenes Using a Chiral Monodentate Oxazoline Ligand ACS Catalysis, 2019, 9, 6502 |
| 4514803 | CIF | C30 H36 B N3 O3 | P 41 21 2 | 9.0322; 9.0322; 68.9818 90; 90; 90 | 5627.58 | Bai, Zibo; Zheng, Sujuan; Bai, Ziqian; Song, Fangfang; Wang, Hao; Peng, Qian; Chen, Gong; He, Gang Palladium-Catalyzed Amide-Directed Enantioselective Carboboration of Unactivated Alkenes Using a Chiral Monodentate Oxazoline Ligand ACS Catalysis, 2019, 9, 6502 |
| 4514804 | CIF | C34 H36 O S2 | P 1 21/c 1 | 12.8072; 13.6963; 17.6483 90; 110.451; 90 | 2900.59 | Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes ACS Catalysis, 2019, 9, 6188 |
| 4514805 | CIF | C19 H14 S2 | P -1 | 7.9503; 8.3038; 12.6012 78.352; 79.15; 72.944 | 771.51 | Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes ACS Catalysis, 2019, 9, 6188 |
| 4514806 | CIF | C19 H14 O S2 | C 1 2/c 1 | 16.653; 5.92231; 33.4022 90; 104.977; 90 | 3182.36 | Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes ACS Catalysis, 2019, 9, 6188 |
| 4514807 | CIF | C21 H24 Cl Rh S | P 1 21 1 | 7.74658; 14.0941; 9.1196 90; 108.015; 90 | 946.87 | Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes ACS Catalysis, 2019, 9, 6188 |
| 4514808 | CIF | C18 H10 S2 | P 1 21/c 1 | 3.95493; 12.7072; 25.5848 90; 91.496; 90 | 1285.35 | Yang, Shiping; Cheng, Rui; Zhang, Min; Bin, Zhengyang; You, Jingsong Rh/Ag-Mediated Peri-Selective Heteroarylation/Single Electron Transfer Annulation Cascade of 1-(Methylthio)naphthalenes and Analogues: Road Less Traveled to Benzo[de]thioacenes ACS Catalysis, 2019, 9, 6188 |
| 4514809 | CIF | C42 H78 N6 O Si6 Th | P -1 | 11.208; 13.909; 19.199 69.17; 83.14; 71.15 | 2647.3 | Saha, Sayantani; Eisen, Moris S. Catalytic Recycling of a Th‒H Bond via Single or Double Hydroboration of Inactivated Imines or Nitriles ACS Catalysis, 2019, 9, 5947 |
| 4514810 | CIF | C10 H10 F2 O2 | P 1 21/c 1 | 9.946; 9.088; 10.222 90; 102.351; 90 | 902.6 | Nakayama, Yoshiki; Ando, Gaku; Abe, Manabu; Koike, Takashi; Akita, Munetaka Keto-Difluoromethylation of Aromatic Alkenes by Photoredox Catalysis: Step-Economical Synthesis of α-CF2H-Substituted Ketones in Flow ACS Catalysis, 2019, 9, 6555 |
| 4514811 | CIF | C15 H18 O2 | P n a 21 | 25.8841; 7.333; 6.343 90; 90; 90 | 1203.95 | Luo, Youran; Gutiérrez-Bonet, Álvaro; Matsui, Jennifer K.; Rotella, Madeline E.; Dykstra, Ryan; Gutierrez, Osvaldo; Molander, Gary A. Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis ACS Catalysis, 2019, 9, 8835 |
| 4514812 | CIF | C21 H29 N O2 | P 1 21 1 | 5.5974; 16.9126; 19.3211 90; 90.056; 90 | 1829.1 | Luo, Youran; Gutiérrez-Bonet, Álvaro; Matsui, Jennifer K.; Rotella, Madeline E.; Dykstra, Ryan; Gutierrez, Osvaldo; Molander, Gary A. Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis ACS Catalysis, 2019, 9, 8835 |
| 4514813 | CIF | C93 H84 F3 O31 P4 S Yb2 | P 1 21 1 | 17.0655; 17.2352; 23.1949 90; 95.16; 90 | 6794.6 | Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir N.; Cundari, Thomas R.; Wang, Hong Asymmetric Ring-Opening of Donor‒Acceptor Cyclopropanes with Primary Arylamines Catalyzed by a Chiral Heterobimetallic Catalyst ACS Catalysis, 2019, 9, 8285 |
| 4514814 | CIF | C20 H23 N O5 | P 21 21 21 | 5.78428; 12.07053; 25.84988 90; 90; 90 | 1804.82 | Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir N.; Cundari, Thomas R.; Wang, Hong Asymmetric Ring-Opening of Donor‒Acceptor Cyclopropanes with Primary Arylamines Catalyzed by a Chiral Heterobimetallic Catalyst ACS Catalysis, 2019, 9, 8285 |
| 4514815 | CIF | C25 H9 B F15 N O | P 1 21/c 1 | 15.7548; 8.5218; 17.5186 90; 91.195; 90 | 2351.52 | Meng, Shan-Shui; Tang, Xiaowen; Luo, Xiang; Wu, Ruibo; Zhao, Jun-Ling; Chan, Albert S. C. Borane-Catalyzed Chemoselectivity-Controllable N-Alkylation and ortho C-Alkylation of Unprotected Arylamines Using Benzylic Alcohols ACS Catalysis, 2019, 9, 8397 |
| 4514816 | CIF | C44 H55 Au N O2 P | P -1 | 11.7663; 12.5195; 15.6679 101.971; 95.869; 117.925 | 1941.11 | Verlee, Arno; Heugebaert, Thomas; van der Meer, Tom; Kerchev, Pavel; Van Hecke, Kristof; Van Breusegem, Frank; Stevens, Christian V. Gold and Palladium Mediated Bimetallic Catalysis: Mechanistic Investigation through the Isolation of the Organogold(I) Intermediates ACS Catalysis, 2019, 9, 7862 |
| 4514817 | CIF | C30 H25 Au N O2 P | P 1 21/c 1 | 12.35599; 11.5441; 17.5685 90; 98.0363; 90 | 2481.34 | Verlee, Arno; Heugebaert, Thomas; van der Meer, Tom; Kerchev, Pavel; Van Hecke, Kristof; Van Breusegem, Frank; Stevens, Christian V. Gold and Palladium Mediated Bimetallic Catalysis: Mechanistic Investigation through the Isolation of the Organogold(I) Intermediates ACS Catalysis, 2019, 9, 7862 |
| 4514818 | CIF | C19 H20 O | P 1 21 1 | 8.803; 5.4591; 15.567 90; 104.94; 90 | 722.8 | Yu, Zhunzhun; Mendoza, Abraham Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates ACS Catalysis, 2019, 9, 7870 |
| 4514819 | CIF | C24 H16 Br N O4 | P 1 21 1 | 9.7213; 9.12937; 12.1367 90; 102.827; 90 | 1050.24 | Yu, Zhunzhun; Mendoza, Abraham Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates ACS Catalysis, 2019, 9, 7870 |
| 4514820 | CIF | C25 H15 N3 O | C 1 2/c 1 | 39.582; 6.6842; 13.9095 90; 97.656; 90 | 3647.3 | Tian, Cong; Dhawa, Uttam; Scheremetjew, Alexej; Ackermann, Lutz Cupraelectro-Catalyzed Alkyne Annulation: Evidence for Distinct C‒H Alkynylation and Decarboxylative C‒H/C‒C Manifolds ACS Catalysis, 2019, 9, 7690 |
| 4514821 | CIF | C14 H17 N O2 | P 1 21/c 1 | 10.9605; 9.5967; 11.9487 90; 93.832; 90 | 1254 | Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes ACS Catalysis, 2019, 9, 8555 |
| 4514822 | CIF | C16 H21 N O2 | P n a 21 | 23.054; 8.4318; 7.3235 90; 90; 90 | 1423.6 | Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes ACS Catalysis, 2019, 9, 8555 |
| 4514823 | CIF | C15 H18 O3 | P 1 21/c 1 | 12.827; 20.383; 5.0473 90; 96.027; 90 | 1312.3 | Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes ACS Catalysis, 2019, 9, 8555 |
| 4514824 | CIF | C16 H20 O3 | C 1 2/c 1 | 31.2814; 6.1424; 15.8248 90; 111.709; 90 | 2825 | Pang, Hailiang; Wu, Dong; Cong, Hengjiang; Yin, Guoyin Stereoselective Palladium-Catalyzed 1,3-Arylboration of Unconjugated Dienes for Expedient Synthesis of 1,3-Disubstituted Cyclohexanes ACS Catalysis, 2019, 9, 8555 |
| 4514825 | CIF | C19 H28 Cl Cu N3 O4 | P n a 21 | 23.1742; 9.9101; 9.2756 90; 90; 90 | 2130.22 | Hunt, Andrew P.; Batka, Allison E.; Hosseinzadeh, Marjan; Gregory, Jordan D.; Haque, Halima K.; Ren, Hang; Meyerhoff, Mark E.; Lehnert, Nicolai Nitric Oxide Generation On Demand for Biomedical Applications via Electrocatalytic Nitrite Reduction by Copper BMPA- and BEPA-Carboxylate Complexes. ACS catalysis, 2019, 9, 7746-7758 |
| 4514826 | CIF | C50 H52 Ir N4 | P 1 21/c 1 | 20.5401; 12.5368; 16.2915 90; 100.551; 90 | 4124.2 | Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S. Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination ACS Catalysis, 2019, 9, 8646 |
| 4514827 | CIF | C43 H42 Ir N6 | P -1 | 10.1805; 13.1835; 14.4356 85.2561; 69.5849; 77.2239 | 1770.8 | Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S. Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination ACS Catalysis, 2019, 9, 8646 |
| 4514828 | CIF | C41 H36 Ir N6 | P 1 21/n 1 | 14.476; 14.367; 34.464 90; 101.797; 90 | 7016.3 | Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S. Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination ACS Catalysis, 2019, 9, 8646 |
| 4514829 | CIF | C39 H45 Ir N4 | P 1 21/c 1 | 11.3918; 14.4386; 20.4434 90; 99.64; 90 | 3315.1 | Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S. Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination ACS Catalysis, 2019, 9, 8646 |
| 4514830 | CIF | C49 H55 Ir N6 | P 1 21/c 1 | 17.6455; 12.6291; 20.6034 90; 111.016; 90 | 4286 | Shon, Jong-Hwa; Sittel, Steven; Teets, Thomas S. Synthesis and Characterization of Strong Cyclometalated Iridium Photoreductants for Application in Photocatalytic Aryl Bromide Hydrodebromination ACS Catalysis, 2019, 9, 8646 |
| 4514831 | CIF | C11 H23 N3 O3 S | P 21 21 21 | 8.3707; 11.4502; 14.6387 90; 90; 90 | 1403.06 | Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian 1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination ACS Catalysis, 2019, 9, 7741 |
| 4514832 | CIF | C12 H18 N2 O2 S | P b c a | 17.0285; 6.9101; 21.3006 90; 90; 90 | 2506.41 | Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian 1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination ACS Catalysis, 2019, 9, 7741 |
| 4514833 | CIF | C29 H47 N3 O6 S | P 1 | 7.0841; 14.1779; 15.2277 98.32; 100.672; 103.356 | 1433.94 | Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian 1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination ACS Catalysis, 2019, 9, 7741 |
| 4514834 | CIF | C17 H20 N2 O2 S | P 1 21/n 1 | 10.2981; 7.0578; 21.651 90; 94.024; 90 | 1569.8 | Duhamel, Thomas; Martínez, Mario D.; Sideri, Ioanna K.; Muñiz, Kilian 1,3-Diamine Formation from an Interrupted Hofmann‒Löffler Reaction: Iodine Catalyst Turnover through Ritter-Type Amination ACS Catalysis, 2019, 9, 7741 |
| 4514835 | CIF | C20 H30 Cl N3 O3 S | P b c a | 15.2153; 14.9228; 18.7632 90; 90; 90 | 4260.3 | Lam, Ying-Pong; Wang, Xinyan; Tan, Fei; Ng, Wing-Hin; Tse, Ying-Lung Steve; Yeung, Ying-Yeung Amide/Iminium Zwitterionic Catalysts for (Trans)esterification: Application in Biodiesel Synthesis ACS Catalysis, 2019, 9, 8083 |
| 4514836 | CIF | C32 H29 N O4 S | P 1 21/c 1 | 13.6328; 9.7259; 19.2323 90; 94.976; 90 | 2540.42 | Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis ACS Catalysis, 2019, 9, 8256 |
| 4514837 | CIF | C27 H27 N O4 S | P 1 21/c 1 | 37.0525; 12.0473; 10.4128 90; 90.415; 90 | 4647.97 | Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis ACS Catalysis, 2019, 9, 8256 |
| 4514838 | CIF | C25 H23 N O2 | P 1 21/c 1 | 18.0757; 14.6438; 7.2015 90; 101.012; 90 | 1871.12 | Zeng, Rong; Li, Jun-Long; Zhang, Xiang; Liu, Yan-Qing; Jia, Zhi-Qiang; Leng, Hai-Jun; Huang, Qian-Wei; Liu, Yue; Li, Qing-Zhu Diastereoselective Construction of 6,8-Dioxabicyclo[3.2.1]octane Frameworks from Vinylethylene Carbonates via Palladium-Organo Relay Catalysis ACS Catalysis, 2019, 9, 8256 |
| 4514839 | CIF | C21 H26 B N O4 S | P 21 21 21 | 10.4319; 14.2343; 29.1953 90; 90; 90 | 4335.2 | Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters ACS Catalysis, 2019, 9, 8503 |
| 4514840 | CIF | C21 H26 B N O5 S | P 31 | 9.9417; 9.9417; 18.9939 90; 90; 120 | 1625.8 | Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters ACS Catalysis, 2019, 9, 8503 |
| 4514841 | CIF | C23 H36 B F3 N2 O6 S | P 21 21 21 | 9.2674; 10.7476; 28.5667 90; 90; 90 | 2845.3 | Kim, Jeongho; Shin, Minkyeong; Cho, Seung Hwan Copper-Catalyzed Diastereoselective and Enantioselective Addition of 1,1-Diborylalkanes to Cyclic Ketimines and α-Imino Esters ACS Catalysis, 2019, 9, 8503 |
| 4514842 | CIF | C31 H65 K N3 Si6 Y | P -1 | 9.999; 11.964; 19.292 83.01; 85.8; 82.27 | 2266.1 | Zhai, Dan-Dan; Du, Hui-Zhen; Zhang, Xiang-Yu; Liu, Yu-Feng; Guan, Bing-Tao Potassium Yttrium Ate Complexes: Synergistic Effect Enabled Reversible H2 Activation and Catalytic Hydrogenation ACS Catalysis, 2019, 9, 8766 |
| 4514843 | CIF | C29 H69 K N3 O Si6 Y | P 1 21/c 1 | 11.344; 11.734; 31.997 90; 92.915; 90 | 4253.6 | Zhai, Dan-Dan; Du, Hui-Zhen; Zhang, Xiang-Yu; Liu, Yu-Feng; Guan, Bing-Tao Potassium Yttrium Ate Complexes: Synergistic Effect Enabled Reversible H2 Activation and Catalytic Hydrogenation ACS Catalysis, 2019, 9, 8766 |
| 4514844 | CIF | C38 H30 F6 N2 O4 Pd S4 | C 1 2/c 1 | 15.336; 10.1947; 24.0955 90; 98.408; 90 | 3726.7 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514845 | CIF | C34 H26 Cl2 F6 N2 O4 Pd S4 | P -1 | 9.0381; 10.3207; 10.3832 68.768; 89.673; 88.327 | 902.4 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514846 | CIF | C17 H15 N O2 S2 | C 1 2/c 1 | 32.753; 4.888; 23.981 90; 124.967; 90 | 3146.2 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514847 | CIF | C22 H23 N O2 S2 | P -1 | 8.6349; 9.3163; 13.5605 70.251; 85.755; 83.165 | 1018.75 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514848 | CIF | C22 H24 O6 | P 1 21/c 1 | 19.271; 4.5166; 23.345 90; 107.803; 90 | 1934.6 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514849 | CIF | C24 H23 N O4 S2 | P 1 21/c 1 | 15.796; 15.246; 9.849 90; 105.81; 90 | 2282.17 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514850 | CIF | C23 H26 O6 | P -1 | 9.7261; 10.89; 11.528 65.75; 69.528; 86.877 | 1037.3 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514851 | CIF | C23 H19 N S2 | P 1 21/n 1 | 10.584; 4.346; 40.473 90; 95.273; 90 | 1853.8 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514852 | CIF | C20 H18 F N O2 S2 | P -1 | 7.0055; 10.2801; 13.131 79.22; 84.888; 80.238 | 913.91 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514853 | CIF | C24 H32 O10 | P 1 21 1 | 11.2; 5.0559; 11.554 90; 115.351; 90 | 591.25 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514854 | CIF | C28 H25 N O4 S2 | P -1 | 8.4844; 12.3314; 12.7997 112.337; 94.171; 98.558 | 1212.59 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514855 | CIF | C19 H16 Cl N O2 S2 | P -1 | 6.5696; 10.4589; 13.1664 79.911; 84.189; 81.356 | 877.96 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514856 | CIF | C23 H19 N O2 S3 | P 1 21/n 1 | 6.9999; 10.6761; 27.063 90; 92.75; 90 | 2020.1 | Romine, Andrew M.; Yang, Kin S.; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis ACS Catalysis, 2019, 9, 7626 |
| 4514857 | CIF | C23 H17 Br N2 | P 1 21 1 | 11.03; 5.7133; 14.591 90; 92.925; 90 | 918.3 | Hatano, Manabu; Nishio, Kosuke; Mochizuki, Takuya; Nishikawa, Keisuke; Ishihara, Kazuaki Highly Active Chiral Dilithium(I) Binaphthyldisulfonate Catalysts for Enantio- and Chemoselective Strecker-Type Reactions ACS Catalysis, 2019, 9, 8178 |
| 4514858 | CIF | C20 H19 N O3 S | P 1 21/c 1 | 8.2877; 14.334; 14.903 90; 103.09; 90 | 1724.4 | Liu, Jibing; Chakraborty, Pushkin; Zhang, Heng; Zhong, Liang; Wang, Zhi-Xiang; Huang, Xueliang Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration ACS Catalysis, 2019, 9, 2610 |
| 4514859 | CIF | C17 H19 N O6 S | P 1 21/c 1 | 7.5531; 28.802; 8.5314 90; 113.57; 90 | 1701.1 | Liu, Jibing; Chakraborty, Pushkin; Zhang, Heng; Zhong, Liang; Wang, Zhi-Xiang; Huang, Xueliang Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration ACS Catalysis, 2019, 9, 2610 |
| 4514860 | CIF | C22 H25 I N2 O2 Ru | P -1 | 8.8149; 10.4274; 12.2762 74.663; 83.855; 77.212 | 1059.8 | Kumar, Abhishek; Semwal, Shrivats; Choudhury, Joyanta Catalytic Conversion of CO2 to Formate with Renewable Hydrogen Donors: An Ambient-Pressure and H2-Independent Strategy ACS Catalysis, 2019, 9, 2164 |
| 4514861 | CIF | C20 H14 Cl N O | P 1 | 8.6566; 11.3426; 16.584 89.235; 77.991; 89.031 | 1592.41 | Fan, Xiaozhong; Zhang, Xue; Li, Chunyu; Gu, Zhenhua Enantioselective Atropisomeric Anilides Synthesis via Cu-Catalyzed Intramolecular Adjacent C‒N Coupling ACS Catalysis, 2019, 9, 2286 |
| 4514862 | CIF | C28 H32 N2 O2 | P 1 21/c 1 | 13.969; 27.1371; 6.25424 90; 99.738; 90 | 2336.69 | Wu, Xiao; Chen, Chentuo; Guo, Ziyang; North, Michael; Whitwood, Adrian C. Metal- and Halide-Free Catalyst for the Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide ACS Catalysis, 2019, 9, 1895 |
| 4514863 | CIF | C13 H12 Br Mn N2 O4 | P 1 21/c 1 | 11.071; 10.4143; 13.4557 90; 105.015; 90 | 1498.43 | Steinlechner, Christoph; Roesel, Arend F.; Oberem, Elisabeth; Päpcke, Ayla; Rockstroh, Nils; Gloaguen, Frédéric; Lochbrunner, Stefan; Ludwig, Ralf; Spannenberg, Anke; Junge, Henrik; Francke, Robert; Beller, Matthias Selective Earth-Abundant System for CO2 Reduction: Comparing Photo- and Electrocatalytic Processes ACS Catalysis, 2019, 9, 2091 |
| 4514864 | CIF | C15 H10 Br Mn N2 O4 | P -1 | 7.1769; 9.2213; 11.5716 85.6351; 84.0784; 82.509 | 753.7 | Steinlechner, Christoph; Roesel, Arend F.; Oberem, Elisabeth; Päpcke, Ayla; Rockstroh, Nils; Gloaguen, Frédéric; Lochbrunner, Stefan; Ludwig, Ralf; Spannenberg, Anke; Junge, Henrik; Francke, Robert; Beller, Matthias Selective Earth-Abundant System for CO2 Reduction: Comparing Photo- and Electrocatalytic Processes ACS Catalysis, 2019, 9, 2091 |
| 4514865 | CIF | C17 H13 Br O3 | P c a 21 | 10.7383; 18.1542; 7.5303 90; 90; 90 | 1468 | Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols ACS Catalysis, 2019, 9, 2440 |
| 4514866 | CIF | C27 H32 O3 | P 1 21 1 | 9.72; 7.5084; 16.171 90; 94.588; 90 | 1176.4 | Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols ACS Catalysis, 2019, 9, 2440 |
| 4514867 | CIF | C18 H12 F3 N3 O3 | P 1 21/c 1 | 10.5383; 19.337; 7.9828 90; 92.029; 90 | 1625.7 | Zhang, Cheng; Li, Hongli; Pei, Chao; Qiu, Lihua; Hu, Wenhao; Bao, Xiaoguang; Xu, Xinfang Selective Vinylogous Reactivity of Carbene Intermediate in Gold-Catalyzed Alkyne Carbocyclization: Synthesis of Indenols ACS Catalysis, 2019, 9, 2440 |
| 4514868 | CIF | C50 H39 N Ni O P2 | P -1 | 13.3161; 14.0105; 15.2863 72.192; 64.226; 62.74 | 2262.59 | Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization. ACS catalysis, 2019, 9, 2458-2481 |
| 4514869 | CIF | C49 H39 N Ni O P2 | P -1 | 9.5744; 11.9148; 18.1503 102.462; 103.789; 97.605 | 1926.26 | Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization. ACS catalysis, 2019, 9, 2458-2481 |
| 4514870 | CIF | C54 H47 Ni P3 | P 1 21/c 1 | 20.6558; 9.9242; 22.517 90; 109.612; 90 | 4348 | Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization. ACS catalysis, 2019, 9, 2458-2481 |
| 4514871 | CIF | C54.5 H46 Ni O P2 | P -1 | 10.3659; 14.4217; 16.331 102.781; 99.4257; 110.567 | 2149.77 | Orsino, Alessio F.; Gutiérrez Del Campo, Manuel; Lutz, Martin; Moret, Marc-Etienne Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization. ACS catalysis, 2019, 9, 2458-2481 |
| 4514872 | CIF | C210 H154 Br2 Cu6 F18 N30 O24 | P -1 | 15.8225; 19.4848; 21.1157 70.092; 81.078; 72.501 | 5827.6 | Prakasam, Thirumurugan; Devaraj, Anthonisamy; Saha, Rupak; Lusi, Matteo; Brandel, Jeremy; Esteban-Gómez, David; Platas-Iglesias, Carlos; Olson, Mark Anthony; Mukherjee, Partha Sarathi; Trabolsi, Ali Metal‒Organic Self-Assembled Trefoil Knots for C—Br Bond Activation ACS Catalysis, 2019, 9, 1907 |
| 4514873 | CIF | C18 H28 O2 | P 3 | 15.378; 15.378; 5.9449 90; 90; 120 | 1217.5 | Yang, Junfeng; Sun, Qiao; Yoshikai, Naohiko Cobalt-Catalyzed Regio- and Diastereoselective Formal [3 + 2] Cycloaddition between Cyclopropanols and Allenes ACS Catalysis, 2019, 9, 1973 |
| 4514874 | CIF | C19 H26 O | I -4 c 2 | 15.4852; 15.4852; 26.1457 90; 90; 90 | 6269.5 | Yang, Junfeng; Sun, Qiao; Yoshikai, Naohiko Cobalt-Catalyzed Regio- and Diastereoselective Formal [3 + 2] Cycloaddition between Cyclopropanols and Allenes ACS Catalysis, 2019, 9, 1973 |
| 4514875 | CIF | C21 H22 O | P 1 21/n 1 | 8.787; 11.718; 14.849 90; 95.361; 90 | 1522.3 | Yang, Junfeng; Sun, Qiao; Yoshikai, Naohiko Cobalt-Catalyzed Regio- and Diastereoselective Formal [3 + 2] Cycloaddition between Cyclopropanols and Allenes ACS Catalysis, 2019, 9, 1973 |
| 4514876 | CIF | C20 H19 N3 O2 | P 21 21 21 | 7.1039; 11.823; 19.698 90; 90; 90 | 1654.4 | Zhang, Lin-Bao; Zhu, Ming-Hui; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming Silver-Mediated Indole (4 + 2) Dearomative Annulation with N-Radicals: A Strategy To Construct Heterocycle-Fused Indolines ACS Catalysis, 2019, 9, 1680 |
| 4514877 | CIF | C27 H31 O2 Si | C 1 2/c 1 | 27.6888; 8.415; 21.6977 90; 90.427; 90 | 5055.5 | Zhang, Shuo; Yao, Qi-Jun; Liao, Gang; Li, Xin; Li, Han; Chen, Hao-Ming; Hong, Xin; Shi, Bing-Feng Enantioselective Synthesis of Atropisomers Featuring Pentatomic Heteroaromatics by Pd-Catalyzed C‒H Alkynylation ACS Catalysis, 2019, 9, 1956 |
| 4514878 | CIF | C30 H32 O S Si | P 21 21 21 | 10.8692; 13.9222; 17.5154 90; 90; 90 | 2650.49 | Zhang, Shuo; Yao, Qi-Jun; Liao, Gang; Li, Xin; Li, Han; Chen, Hao-Ming; Hong, Xin; Shi, Bing-Feng Enantioselective Synthesis of Atropisomers Featuring Pentatomic Heteroaromatics by Pd-Catalyzed C‒H Alkynylation ACS Catalysis, 2019, 9, 1956 |
| 4514879 | CIF | C32 H33 N O Si | P 1 21 1 | 7.3547; 43.2835; 8.7345 90; 93.821; 90 | 2774.3 | Zhang, Shuo; Yao, Qi-Jun; Liao, Gang; Li, Xin; Li, Han; Chen, Hao-Ming; Hong, Xin; Shi, Bing-Feng Enantioselective Synthesis of Atropisomers Featuring Pentatomic Heteroaromatics by Pd-Catalyzed C‒H Alkynylation ACS Catalysis, 2019, 9, 1956 |
| 4514880 | CIF | C23 H30 Br Mn N2 O9 P2 | P -1 | 11.5014; 12.237; 12.4559 61.15; 71.428; 73.307 | 1436.6 | Woo, Sung-Jun; Choi, Sunghan; Kim, So-Yoen; Kim, Pil Soo; Jo, Ju Hyoung; Kim, Chul Hoon; Son, Ho-Jin; Pac, Chyongjin; Kang, Sang Ook Highly Selective and Durable Photochemical CO2 Reduction by Molecular Mn(I) Catalyst Fixed on a Particular Dye-Sensitized TiO2 Platform ACS Catalysis, 2019, 9, 2580 |
| 4514881 | CIF | C17 H16 Br2 O5 | P 1 21/c 1 | 20.647; 10.3884; 17.2385 90; 114.021; 90 | 3377.26 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514882 | CIF | C17 H15 Cl O5 | P 1 21 1 | 6.1976; 17.271; 7.158 90; 103.688; 90 | 744.4 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514883 | CIF | C30 H25 Br N2 O5 | P 1 21 1 | 11.584; 7.7058; 15.1367 90; 109.376; 90 | 1274.63 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514884 | CIF | C11 H12 O5 | P 21 21 21 | 6.0801; 8.1103; 22.242 90; 90; 90 | 1096.8 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514885 | CIF | C33 H33 N3 O8 S | P 21 21 21 | 8.7971; 17.2916; 20.3839 90; 90; 90 | 3100.7 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514886 | CIF | C27 H26 Cl N O7 | P 1 21/c 1 | 6.2963; 32.789; 11.523 90; 100.644; 90 | 2338 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514887 | CIF | C11 H12 O5 | C 1 c 1 | 6.0855; 12.683; 13.554 90; 93.29; 90 | 1044.4 | Gao, Xing; Xia, Miaoren; Yuan, Chunhao; Zhou, Leijie; Sun, Wei; Li, Cheng; Wu, Bo; Zhu, Dongyu; Zhang, Cheng; Zheng, Bing; Wang, Dongqi; Guo, Hongchao Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy ACS Catalysis, 2019, 9, 1645 |
| 4514888 | CIF | C28 H26 F6 N2 O8 | P 21 21 21 | 11.7248; 13.6488; 19.0159 90; 90; 90 | 3043.1 | Sletten, Eric T.; Tu, Yi-Jung; Schlegel, H. Bernhard; Nguyen, Hien M. Are Brønsted Acids the True Promoter of Metal-Triflate-Catalyzed Glycosylations? A Mechanistic Probe into 1,2-cis-Aminoglycoside Formation by Nickel Triflate ACS Catalysis, 2019, 9, 2110 |
| 4514889 | CIF | C16 H12 Cl N S | P n a 21 | 7.6912; 23.747; 7.518 90; 90; 90 | 1373.1 | Wang, Huamin; Li, Yongli; Lu, Qingquan; Yu, Mingming; Bai, Xudong; Wang, Shengchun; Cong, Hengjiang; Zhang, Heng; Lei, Aiwen Oxidation-Induced β-Selective C‒H Bond Functionalization: Thiolation and Selenation of N-Heterocycles ACS Catalysis, 2019, 9, 1888 |
| 4515457 | CIF | C27 H25 N | P -1 | 11.627; 11.659; 15.889 85.73; 77.49; 69.54 | 1970.1 | Tian, Jun-Jie; Zeng, Ning-Ning; Liu, Ning; Tu, Xian-Shuang; Wang, Xiao-Chen Intramolecular Cyclizations of Vinyl-Substituted N,N-Dialkyl Arylamines Enabled by Borane-Assisted Hydride Transfer ACS Catalysis, 2018, 9, 295 |
| 4515458 | CIF | C25 H19 Br Mn N2 O2 P | P 1 21/c 1 | 12.9669; 13.874; 12.3572 90; 93.057; 90 | 2219.93 | Das, Uttam Kumar; Ben-David, Yehoshoa; Leitus, Gregory; Diskin-Posner, Yael; Milstein, David Dehydrogenative Cross-Coupling of Primary Alcohols To Form Cross-Esters Catalyzed by a Manganese Pincer Complex ACS Catalysis, 2018, 9, 479 |
| 4515459 | CIF | C32 H26 Mn N2 O3 P | P 1 21/c 1 | 9.7663; 16.9042; 16.0896 90; 97.951; 90 | 2630.72 | Das, Uttam Kumar; Ben-David, Yehoshoa; Leitus, Gregory; Diskin-Posner, Yael; Milstein, David Dehydrogenative Cross-Coupling of Primary Alcohols To Form Cross-Esters Catalyzed by a Manganese Pincer Complex ACS Catalysis, 2018, 9, 479 |
| 4515460 | CIF | C18 H23 N3 O2 | P 1 21/c 1 | 8.3986; 10.167; 18.964 90; 101.38; 90 | 1587.5 | van der Puyl, Vincent A.; Derosa, Joseph; Engle, Keary M. Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds ACS Catalysis, 2018, 9, 224 |
| 4515461 | CIF | C20 H27 N3 O2 | P -1 | 9.4368; 11.2965; 18.1549 81.081; 81.652; 73.77 | 1825.2 | van der Puyl, Vincent A.; Derosa, Joseph; Engle, Keary M. Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds ACS Catalysis, 2018, 9, 224 |
| 4515462 | CIF | C22 H33 B F2 O4 Si | P 21 21 21 | 7.4443; 10.4007; 31.5827 90; 90; 90 | 2445.32 | Guo, Wen-Hao; Zhao, Hai-Yang; Luo, Zhi-Ji; Zhang, Shu; Zhang, Xingang Fluoroalkylation‒Borylation of Alkynes: An Efficient Method To Obtain (Z)-Tri- and Tetrasubstituted Fluoroalkylated Alkenylboronates ACS Catalysis, 2018, 9, 38 |
| 4515463 | CIF | C28 H47 B O8 P2 Pd | C 1 2/c 1 | 26.0162; 11.1134; 23.2857 90; 108.358; 90 | 6389.9 | Espinosa, Matthew R.; Charboneau, David J.; Garcia de Oliveira, André; Hazari, Nilay Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels ACS Catalysis, 2018, 9, 301 |
| 4515464 | CIF | C9 H15 B O2 | I 41/a c d :2 | 13.2301; 13.2301; 38.893 90; 90; 90 | 6807.7 | Espinosa, Matthew R.; Charboneau, David J.; Garcia de Oliveira, André; Hazari, Nilay Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels ACS Catalysis, 2018, 9, 301 |
| 4515465 | CIF | C15 H15 Cl N2 | P 1 21/n 1 | 8.473; 17.4446; 9.0374 90; 94.072; 90 | 1332.43 | Fu, Niankai; Shen, Yifan; Allen, Anthony R.; Song, Lu; Ozaki, Atsushi; Lin, Song Mn-Catalyzed Electrochemical Chloroalkylation of Alkenes. ACS catalysis, 2019, 9, 746-754 |
| 4515466 | CIF | C18 H14 F3 N O4 | P 1 21 1 | 11.8498; 9.5906; 14.708 90; 96.008; 90 | 1662.33 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515467 | CIF | C17 H15 N O4 | P 1 21 1 | 13.5517; 9.2461; 11.8061 90; 106.796; 90 | 1416.2 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515468 | CIF | C60 H79 N6 O15 P | P 21 21 21 | 9.8665; 19.0145; 31.36 90; 90; 90 | 5883.3 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515469 | CIF | C17 H14 Br N O4 | I 1 2 1 | 22.7393; 5.2121; 14.2943 90; 93.045; 90 | 1691.76 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515470 | CIF | C17 H15 N O4 | P 1 21 1 | 10.8042; 8.4963; 15.825 90; 103.232; 90 | 1414.1 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515471 | CIF | C18 H17 N O4 | P -1 | 9.806; 14.9855; 21.2136 89.141; 86.664; 88.303 | 3110.4 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515472 | CIF | C36 H57 N7 O7 | C 1 2 1 | 26.466; 17.7566; 22.8328 90; 124.789; 90 | 8812.3 | Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J. Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones. ACS catalysis, 2019, 9, 242-252 |
| 4515473 | CIF | C20 H23 N O2 | P b c a | 13.76; 7.1297; 34.2631 90; 90; 90 | 3361.37 | Ho, Hon Eong; Stephens, Thomas C.; Payne, Thomas J.; O’Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics ACS Catalysis, 2018, 9, 504 |
| 4515474 | CIF | C45.67 H35.35 Cl3.35 N2 O2 | I 1 2/a 1 | 7.38319; 26.3138; 19.6731 90; 93.6518; 90 | 3814.33 | Ho, Hon Eong; Stephens, Thomas C.; Payne, Thomas J.; O’Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics ACS Catalysis, 2018, 9, 504 |
| 4515475 | CIF | C22 H40 Mn N3 O5 P2 S | P b c a | 11.5; 14.765; 34.41 90; 90; 90 | 5843 | Bertini, Federica; Glatz, Mathias; Stöger, Berthold; Peruzzini, Maurizio; Veiros, Luis F.; Kirchner, Karl; Gonsalvi, Luca Carbon Dioxide Reduction to Methanol Catalyzed by Mn(I) PNP Pincer Complexes under Mild Reaction Conditions ACS Catalysis, 2018, 9, 632 |
| 4515476 | CIF | C27 H29 N | P -1 | 8.9763; 10.84; 11.572 109.84; 99.23; 93.29 | 1037.8 | Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation ACS Catalysis, 2018, 9, 599 |
| 4515477 | CIF | C23 H40 N Sc Si2 | P -1 | 9.616; 10.433; 13.436 100.936; 95.927; 95.808 | 1306.3 | Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation ACS Catalysis, 2018, 9, 599 |
| 4515478 | CIF | C15 H24 F6 N P | C 1 c 1 | 19.003; 10.452; 8.8763 90; 96.73; 90 | 1750.9 | Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation ACS Catalysis, 2018, 9, 599 |
| 4515479 | CIF | C29 H20 B F18 N6 Rh | P 1 21/c 1 | 18.0106; 9.0679; 19.7109 90; 96.859; 90 | 3196.1 | Avullala, Thirupataiah; Asgari, Parham; Hua, Yuanda; Bokka, Apparao; Ridlen, Shawn G.; Yum, Kyungsuk; Dias, H. V. Rasika; Jeon, Junha Umpolung <i>α</i>-Silylation of Cyclopropyl Acetates via Low-Temperature Catalytic C-C Activation. ACS catalysis, 2019, 9, 402-408 |
| 4515480 | CIF | C36 H48 Cl2 N2 O Ru | P 1 21/c 1 | 19.3364; 10.43031; 16.58648 90; 95.7369; 90 | 3328.48 | Małecki, Paweł; Gajda, Katarzyna; Gajda, Roman; Woźniak, Krzysztof; Trzaskowski, Bartosz; Kajetanowicz, Anna; Grela, Karol Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application ACS Catalysis, 2018, 9, 587 |
| 4515481 | CIF | C53 H50 Cl2 N2 O Ru | P 1 21/n 1 | 13.16; 10.12687; 37.8176 90; 98.1376; 90 | 4989.19 | Małecki, Paweł; Gajda, Katarzyna; Gajda, Roman; Woźniak, Krzysztof; Trzaskowski, Bartosz; Kajetanowicz, Anna; Grela, Karol Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application ACS Catalysis, 2018, 9, 587 |
| 4515482 | CIF | C41 H48 Br N3 O7 | P 21 21 21 | 11.6704; 12.4895; 24.8148 90; 90; 90 | 3616.94 | Paria, Suva; Kang, Qi-Kai; Hatanaka, Miho; Maruoka, Keiji Design of Efficient Chiral Bifunctional Phase-Transfer Catalysts Possessing an Amino Functionality for Asymmetric Aminations ACS Catalysis, 2018, 9, 78 |
| 4515483 | CIF | C71 H72 N2 Ni | P 21 21 21 | 14.9159; 18.747; 20.4012 90; 90; 90 | 5704.8 | Cai, Yuan; Zhang, Jia-Wen; Li, Feng; Liu, Jia-Ming; Shi, Shi-Liang Nickel/N-Heterocyclic Carbene Complex-Catalyzed Enantioselective Redox-Neutral Coupling of Benzyl Alcohols and Alkynes to Allylic Alcohols ACS Catalysis, 2018, 9, 1 |
| 4515484 | CIF | C23 H22 N2 O4 S2 | P 1 | 9.0036; 10.9036; 11.9944 103.063; 98.741; 91.068 | 1132 | Yang, Shengbiao; Wang, Lihong; Zhang, Hongwei; Liu, Chunyang; Zhang, Linli; Wang, Xiaomin; Zhang, Ge; Li, Yan; Zhang, Qian Copper-Catalyzed Asymmetric Aminocyanation of Arylcyclopropanes for Synthesis of γ-Amino Nitriles ACS Catalysis, 2018, 9, 716 |
| 4515485 | CIF | C37 H31 F2 I P2 Pd | C 1 2/c 1 | 12.09; 15.2246; 20.0614 90; 91.35; 90 | 3691.6 | Hori, Kaishi; Motohashi, Hirotaka; Saito, Daichi; Mikami, Koichi Precatalyst Effects on Pd-Catalyzed Cross-Coupling Difluoromethylation of Aryl Boronic Acids ACS Catalysis, 2018, 9, 417 |
| 4515486 | CIF | C56 H34 F16 Ir N4 P | C 1 2/c 1 | 16.49; 22.606; 13.5064 90; 90.007; 90 | 5034.8 | Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes ACS Catalysis, 2018, 9, 1320 |
| 4515487 | CIF | C49 H32 Cl2 F16 Ir N4 P | P -1 | 11.7565; 12.8586; 18.657 81.314; 80.238; 73.409 | 2648.1 | Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes ACS Catalysis, 2018, 9, 1320 |
| 4515488 | CIF | C56 H34 F16 Ir N4 P | R -3 :H | 26.5472; 26.5472; 38.495 90; 90; 120 | 23494.8 | Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes ACS Catalysis, 2018, 9, 1320 |
| 4515489 | CIF | C27 H43 Al Cl N3 Si3 | P -1 | 9.6279; 10.9013; 17.0857 98.271; 102.568; 108.408 | 1616.39 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515490 | CIF | C24 H24 Al N3 | P 21 21 21 | 7.3795; 13.4511; 21.1096 90; 90; 90 | 2095.39 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515491 | CIF | C18 H19 Al Cl N3 | P 1 21/c 1 | 8.9033; 22.602; 8.763 90; 100.967; 90 | 1731.2 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515492 | CIF | C35 H44 Al N4 | P -1 | 9.0364; 10.9957; 16.5417 91.033; 97.953; 107.345 | 1550.72 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515493 | CIF | C29 H33 Al N3 | P 1 21/n 1 | 9.6204; 24.1661; 10.8834 90; 94.131; 90 | 2523.68 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515494 | CIF | C33 H48 Al N3 Si3 | P -1 | 9.2076; 12.1268; 16.763 98.513; 98.865; 103.694 | 1763.3 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515495 | CIF | C15 H24 Al Cl4 N3 O7 | P 1 21/n 1 | 7.0617; 25.6486; 13.413 90; 105.218; 90 | 2344.2 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515496 | CIF | C27 H37 Al Cl N3 | P 1 21/n 1 | 9.2525; 15.9339; 17.4939 90; 95.425; 90 | 2567.5 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515497 | CIF | C27 H38 Al N3 | P -1 | 8.9098; 9.0012; 17.5788 89.93; 76.945; 69.158 | 1278.64 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515498 | CIF | C33 H42 Al N3 | P 1 21/c 1 | 16.055; 10.4568; 35.146 90; 98.496; 90 | 5835.7 | Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A. Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration ACS Catalysis, 2018, 9, 874 |
| 4515499 | CIF | C57 H34 B2 F30 Nd Si3 | C 1 2/c 1 | 39.687; 12.1443; 26.344 90; 98.409; 90 | 12561 | Schmidt, Bradley M.; Pindwal, Aradhana; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D. Zwitterionic Trivalent (Alkyl)lanthanide Complexes in Ziegler-Type Butadiene Polymerization ACS Catalysis, 2018, 9, 827 |
| 4515500 | CIF | C20 H16 O4 | I 1 a 1 | 6.101; 7.1857; 36.046 90; 94.848; 90 | 1574.6 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515501 | CIF | C23 H31 Cl Fe N2 | P 1 2/c 1 | 14.4785; 9.0523; 16.7522 90; 92.179; 90 | 2194 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515502 | CIF | C29 H35 Cl Fe N2 | P b c a | 16.5485; 10.4399; 31.246 90; 90; 90 | 5398.2 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515503 | CIF | C26 H38 Cl Fe N3 | P b c a | 11.9206; 15.6644; 27.735 90; 90; 90 | 5178.93 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515504 | CIF | C37 H40 Fe N2 | P 1 21/c 1 | 12.631; 15.5444; 16.5595 90; 105.365; 90 | 3135.1 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515505 | CIF | C25 H35 Cl Fe N2 | P 1 21/c 1 | 17.827; 15.8552; 11.0869 90; 104.133; 90 | 3038.9 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515506 | CIF | C24 H20 Fe2 | P 1 21/n 1 | 11.736; 10.478; 14.979 90; 102.775; 90 | 1796.4 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515507 | CIF | C28 H41 Cl Fe N2 | P 21 21 21 | 8.6146; 17.039; 19.7629 90; 90; 90 | 2900.9 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515508 | CIF | C32 H41 Cl Fe N2 | P 1 21/c 1 | 8.4344; 22.681; 15.3166 90; 90.017; 90 | 2930.1 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515509 | CIF | C26 H37 Cl Fe N2 | P 1 21/c 1 | 8.5309; 16.6841; 17.0048 90; 91.196; 90 | 2419.8 | Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes ACS Catalysis, 2018, 9, 810 |
| 4515510 | CIF | C19 H13 N O4 S | P -1 | 7.0423; 9.2936; 12.8025 89.117; 75.476; 77.243 | 790.39 | Shu, Chao; Shi, Chong-Yang; Sun, Qing; Zhou, Bo; Li, Tian-You; He, Qiao; Lu, Xin; Liu, Rai-Shung; Ye, Long-Wu Generation of Endocyclic Vinyl Carbene Complexes via Gold-Catalyzed Oxidative Cyclization of Terminal Diynes: Toward Naphthoquinones and Carbazolequinones ACS Catalysis, 2018, 9, 1019 |
| 4515511 | CIF | C30 H29 Al N4 O | P -1 | 9.633; 11.189; 12.051 89.56; 71.1; 83.22 | 1220 | Mandal, Mukunda; Luke, Anna M.; Dereli, Büşra; Elwell, Courtney E.; Reineke, Theresa M.; Tolman, William B.; Cramer, Christopher J. Computational Prediction and Experimental Verification of ε-Caprolactone Ring-Opening Polymerization Activity by an Aluminum Complex of an Indolide/Schiff-Base Ligand ACS Catalysis, 2018, 9, 885 |
| 4515512 | CIF | C26 H30 N2 O3 | P 21 21 21 | 9.1036; 13.3256; 36.2038 90; 90; 90 | 4391.92 | Shen, Hong-Cheng; Zhang, Ling; Chen, Shu-Sen; Feng, Jiajie; Zhang, Bo-Wen; Zhang, Ying; Zhang, Xinhao; Wu, Yun-Dong; Gong, Liu-Zhu Enantioselective Addition of Cyclic Ketones to Unactivated Alkenes Enabled by Amine/Pd(II) Cooperative Catalysis ACS Catalysis, 2018, 9, 791 |
| 4515513 | CIF | C25 H27 Br N2 O2 | P 21 21 21 | 9.0909; 13.2501; 36.0908 90; 90; 90 | 4347.3 | Shen, Hong-Cheng; Zhang, Ling; Chen, Shu-Sen; Feng, Jiajie; Zhang, Bo-Wen; Zhang, Ying; Zhang, Xinhao; Wu, Yun-Dong; Gong, Liu-Zhu Enantioselective Addition of Cyclic Ketones to Unactivated Alkenes Enabled by Amine/Pd(II) Cooperative Catalysis ACS Catalysis, 2018, 9, 791 |
| 4516742 | CIF | C78 H60 Cu3 N8 O15 | R -3 :H | 15.598; 15.598; 59.01 90; 90; 120 | 12434 | Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction ACS Catalysis, 2019, 9, 1726 |
| 4516743 | CIF | C78 H66 Co3 N8 O18 | R -3 :H | 15.7439; 15.7439; 61.146 90; 90; 120 | 13125.7 | Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction ACS Catalysis, 2019, 9, 1726 |
| 4516744 | CIF | C468 H450 N48 Ni18 O135 | R -3 :H | 15.7128; 15.7128; 60.539 90; 90; 120 | 12944.1 | Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction ACS Catalysis, 2019, 9, 1726 |
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