Crystallography Open Database

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4515654 CIFC26 H21 F3 O2 SP 1 21 17.7702; 7.7862; 17.9926
90; 100.144; 90		1071.54Maddox, 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 CIFC23.7 H15 Cl2.1 D0.7 F3 O4 SP 21 21 219.3182; 10.5061; 24.8751
90; 90; 90		2435.2Maddox, 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 CIFC21 H20 N2 O3P 1 21/n 113.218; 8.696; 16.546
90; 98.483; 90		1881.1Pang, 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 CIFC22 H22 N2 O4P 1 21/n 110.559; 8.848; 20.03
90; 91.424; 90		1870.7Pang, 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 CIFC16 H21 Cl2 Fe N9 O2P n a 2113.7551; 18.856; 8.4263
90; 90; 90		2185.5Zhu, 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 CIFC15 H19 F3 N2 O4 SP -17.6537; 10.3038; 11.7
69.471; 74.774; 75.983		822.2Zhu, 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 CIFC18 H22 Cl3 F3 N2 O4 SP 21 21 216.1287; 17.2349; 21.6302
90; 90; 90		2284.74Zhu, 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 CIFC14 H22 F3 N O2P 1 21/c 111.8893; 5.2263; 24.518
90; 96.137; 90		1514.75Zhu, 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 CIFC16 H26 F3 N O2P 21 21 2111.579; 16.9733; 18.2465
90; 90; 90		3586.05Zhu, 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 CIFC19 H25 F3 N2 O4P 1 21/c 114.9198; 13.8571; 9.9498
90; 95.4351; 90		2047.82Zhu, 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 CIFC17 H39 As Co K2 Mo6 N O39.5P -112.0872; 12.5682; 17.2255
76.7; 74.058; 76.399		2407Hou, 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 CIFC17 H44 As K2 Mo6 N Ni O42P -111.9612; 12.5318; 17.1943
76.499; 74.053; 76.535		2370.12Hou, 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 CIFC17 H40 As K2 Mo6 N O41 ZnP -112.1425; 12.5739; 17.2226
76.443; 74.062; 76.225		2415.16Hou, 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 CIFC17 H39 As K2 Mn Mo6 N O40P -112.2865; 12.6065; 17.2145
76.319; 73.933; 76.064		2445.2Hou, 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 CIFC18 H87 As2 Co0.5 K3 Mo12 N6 Na O77.5P -116.1055; 18.5246; 19.0707
75.701; 65.877; 64.845		4681.8Hou, 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 CIFC21 H44 As Co0.5 K5 Mo6 O44.5P -112.6575; 12.671; 18.5916
105.723; 91.318; 106.19		2740.7Hou, 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 CIFC47.5 H70 N2 Ni O8P -111.54858; 30.1957; 32.8403
64.8392; 80.3426; 86.1838		10218.4Nett, 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 CIFC97 H92 N2 Ni O8.5P -114.0561; 14.806; 22.1265
93.854; 102.679; 118.29		3876.59Nett, 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 CIFC27 H22 N2 O3C 1 2/c 114.2005; 10.38306; 28.0529
90; 102.226; 90		4042.44Rej, 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 CIFC27 H36 I4 N2 SP -110.6361; 16.8158; 19.6467
91.7164; 105.424; 93.774		3375.9Horibe, 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
4515674 CIFC27 H36 Cl I3 N2 SP 1 21/n 110.689; 18.743; 16.225
90; 102.555; 90		3172.9Horibe, 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
4515675 CIFC17 H20 O7P c a 2112.9176; 15.173; 16.7769
90; 90; 90		3288.25Shu, Wei; Merino, Estíbaliz; Nevado, Cristina
Visible Light Mediated, Redox Neutral Remote 1,6-Difunctionalizations of Alkenes
ACS Catalysis, 2018, 8, 6401
4515676 CIFC27 H39 N2 Sc Si2P 1 21/c 116.7493; 17.9477; 9.7237
90; 105.053; 90		2822.8Li, Shihui; Liu, Dongtao; Wang, Zichuan; Cui, Dongmei
Development of Group 3 Catalysts for Alternating Copolymerization of Ethylene and Styrene Derivatives
ACS Catalysis, 2018, 8, 6086
4515677 CIFC33 H41 N3 O3P -111.5304; 11.8994; 12.6132
107.862; 96.62; 114.133		1444.35Li, Zhenghua; Song, Liangliang; Van Meervelt, Luc; Tian, Guilong; Van der Eycken, Erik V.
Cationic Gold(I)-Catalyzed Cascade Bicyclizations for Divergent Synthesis of (Spiro)polyheterocycles
ACS Catalysis, 2018, 8, 6388
4515678 CIFC21 H22 N2 O2 SP 21 21 219.2626; 11.273; 36.0958
90; 90; 90		3769Rigotti, Thomas; Casado-Sánchez, Antonio; Cabrera, Silvia; Pérez-Ruiz, Raúl; Liras, Marta; de la Peña O’Shea, Víctor A.; Alemán, José
A Bifunctional Photoaminocatalyst for the Alkylation of Aldehydes: Design, Analysis, and Mechanistic Studies
ACS Catalysis, 2018, 8, 5928
4515679 CIFC24 H20 N2 O2 SP 1 21 17.3859; 14.0495; 19.8207
90; 95.797; 90		2046.24Rigotti, Thomas; Casado-Sánchez, Antonio; Cabrera, Silvia; Pérez-Ruiz, Raúl; Liras, Marta; de la Peña O’Shea, Víctor A.; Alemán, José
A Bifunctional Photoaminocatalyst for the Alkylation of Aldehydes: Design, Analysis, and Mechanistic Studies
ACS Catalysis, 2018, 8, 5928
4515680 CIFC22 H17 N3 O2P 1 21/c 16.0252; 14.9032; 19.2088
90; 93.713; 90		1721.23Zhai, Shengxian; Qiu, Shuxian; Chen, Xiaoming; Tao, Cheng; Li, Yun; Cheng, Bin; Wang, Huifei; Zhai, Hongbin
Trifunctionalization of Allenes via Cobalt-Catalyzed MHP-Assisted C‒H Bond Functionalization and Molecular Oxygen Activation
ACS Catalysis, 2018, 8, 6645
4515681 CIFC38 H22 Cl2C 1 2/c 115.8675; 11.3225; 16.9255
90; 116.905; 90		2711.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515682 CIFC40 H26 Cl2C 1 2/c 116.6618; 12.3936; 16.076
90; 119.312; 90		2894.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515683 CIFC45 H54 OP -113.048; 15.9745; 20.3351
69.8393; 74.7061; 79.3386		3817.17Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515684 CIFC115 H108 Cl2 F36 N6 O8 P2 Sb2P 4 21 223.156; 23.156; 45.3164
90; 90; 90		24298.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515685 CIFC40 H28C 1 2/c 124.6931; 9.8945; 11.3008
90; 107.002; 90		2640.4Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515686 CIFC57 H53 Au Cl F18 N3 O4 P SbP 21 21 2111.625; 21.7951; 24.924
90; 90; 90		6314.9Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515687 CIFC85 H148 Au4 Cl4 F24 N4 O10 P4 S2 Sb4P -114.1224; 14.3201; 16.3265
111.05; 108.05; 90.835		2900.2Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515688 CIFC42 H50 Cl2 F6 N2 O4 P SbP 21 21 2114.5593; 16.985; 18.089
90; 90; 90		4473.2Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515689 CIFC64 H59 Cl2 F18 N3 O4 P SbP 1 21 111.2724; 25.712; 22.718
90; 98.349; 90		6514.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515690 CIFC28 H18 Br2P 21 21 216.7543; 9.853; 31.4363
90; 90; 90		2092.09Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515691 CIFC63 H59 Au Cl3 F18 N3 O4 P SbP 1 21 111.5608; 22.3675; 14.1582
90; 95.008; 90		3647.1Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515692 CIFC56 H48 Au Cl5 F18 N2 O4 P SbP 21 21 2111.8911; 20.269; 26.818
90; 90; 90		6463.7Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515693 CIFC40 H25.94 Cl2.06P 1 21/c 117.9011; 8.3634; 19.4197
90; 90.871; 90		2907.1Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515694 CIFC21 H25 N3P -18.0652; 8.3219; 14.129
77.347; 83.454; 80.93		910.59Nicholls, Leo D. M.; Marx, Maximilian; Hartung, Thierry; González-Fernández, Elisa; Golz, Christopher; Alcarazo, Manuel
TADDOL-Derived Cationic Phosphonites: Toward an Effective Enantioselective Synthesis of [6]Helicenes via Au-Catalyzed Alkyne Hydroarylation
ACS Catalysis, 2018, 8, 6079
4515695 CIFC23 H21 N OP -111.8311; 12.7714; 12.7734
69.209; 81.613; 86.471		1785Li, Deng-Yuan; Liu, Shuo; Chen, Shuang; Wang, An; Zhu, Xiao-Ping; Liu, Pei-Nian
Dual Role of Aryl Iodide in Cascade C‒H Arylation/Amination: Arylation Reagent and Cocatalyst for C‒N Formation
ACS Catalysis, 2018, 8, 6407
4515696 CIFC20 H26 N O4 ZnP 1 21/n 110.811; 16.451; 11.445
90; 101.668; 90		1993.5Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515697 CIFC28 H47 Ni O4 PP -110.2938; 16.839; 17.23
73.123; 78.321; 87.036		2798.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515698 CIFC13 H22 B N O2P 1 21/n 17.204; 34.935; 11.091
90; 92.218; 90		2789Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515699 CIFC24 H32 N2 Ni O4P -17.96; 8.085; 9.656
108.25; 93.812; 94.208		585.9Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515700 CIFC25 H41 Ni O4 PP -110.001; 10.415; 13.862
76.659; 77.984; 62.798		1240.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515701 CIFC22 H22 F6 N2 Ni O4P -16.3927; 8.606; 10.965
86.398; 79.115; 86.957		590.7Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515702 CIFC24 H28 N2 Ni O8P -16.736; 8.129; 11.969
101.952; 99.095; 99.806		619Tamang, Sem Raj; Singh, Arpita; Unruh, Daniel K.; Findlater, Michael
Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes
ACS Catalysis, 2018, 8, 6186
4515703 CIFC24 H20 N2 O6 PdP -18.78; 10; 13.272
101.969; 98.6857; 103.084		1086.1Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515704 CIFC22 H17 I N2 O4 PdP 1 21/c 17.939; 16.611; 16.219
90; 93.262; 90		2135.4Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515705 CIFC20 H18 O8C 1 2/c 118.828; 8.059; 12.153
90; 91.24; 90		1844Hirano, Masafumi; Sano, Kosuke; Kanazawa, Yuki; Komine, Nobuyuki; Maeno, Zen; Mitsudome, Takato; Takaya, Hikaru
Mechanistic Insights on Pd/Cu-Catalyzed Dehydrogenative Coupling of Dimethyl Phthalate
ACS Catalysis, 2018, 8, 5827
4515706 CIFC21 H18 Br2P 1 21/c 17.258; 18.732; 12.399
90; 93.746; 90		1682.1Su, Xiang; Chen, Bifeng; Wang, Shaohong; Chen, Hui; Chen, Chao
Atom- and Step-Efficient Construction of Five-Membered Carbocycles with Alkenes and Alkynes Catalyzed by AgSbF6
ACS Catalysis, 2018, 8, 7760
4515707 CIFC17 H15 N O5C 1 2 121.4471; 6.4084; 12.069
90; 113.464; 90		1521.62Li, Kaizhi; Jin, Zhichao; Chan, Wai-Lun; Lu, Yixin
Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut‒Currier Reactions Catalyzed by Thiourea-Phosphines
ACS Catalysis, 2018, 8, 8810
4515708 CIFC19 H17 Br O3P 21 21 218.8312; 11.2095; 16.7904
90; 90; 90		1662.14Li, Kaizhi; Jin, Zhichao; Chan, Wai-Lun; Lu, Yixin
Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut‒Currier Reactions Catalyzed by Thiourea-Phosphines
ACS Catalysis, 2018, 8, 8810
4515709 CIFC17 H12 N2 O4P 1 21/c 16.8554; 18.0992; 11.1588
90; 92.472; 90		1383.26Chen, Fei; Lai, Sheng-Qiang; Zhu, Fei-Fei; Meng, Qiang; Jiang, Yu; Yu, Wei; Han, Bing
Cu-Catalyzed Radical Cascade Annulations of Alkyne-Tethered N-Alkoxyamides with Air: Facile Access to Isoxazolidine/1,2-Oxazinane-Fused Isoquinolin-1(2H)-ones
ACS Catalysis, 2018, 8, 8925
4515710 CIFC18 H29 Cl Ir N OP -18.6737; 8.7731; 13.6686
78.458; 75.85; 88.359		987.94Tan, Guangying; You, Qiulin; You, Jingsong
Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates
ACS Catalysis, 2018, 8, 8709
4515711 CIFC32 H38 N2 O2 S2P 1 21/n 112.5365; 14.4554; 17.4788
90; 103.091; 90		3085.19Tan, Guangying; You, Qiulin; You, Jingsong
Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates
ACS Catalysis, 2018, 8, 8709
4515712 CIFC30 H12.5 Al Cl F15.5 NP 1 21/c 110.307; 26.879; 20.89
90; 101.156; 90		5678Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515713 CIFC22 H21 N SiP -19.3329; 10.0874; 11.22
67.672; 88.245; 65.949		882.58Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515714 CIFC27 H14 Al F16 N4P -110.4075; 10.6369; 13.0972
79.781; 79.01; 71.612		1339.9Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515715 CIFC27 H9 Al F15 NP 1 21 17.4782; 17.022; 9.979
90; 107.975; 90		1208.3Han, Yuxi; Zhang, Sutao; He, Jianghua; Zhang, Yuetao
Switchable C‒H Silylation of Indoles Catalyzed by a Thermally Induced Frustrated Lewis Pair
ACS Catalysis, 2018, 8, 8765
4515716 CIFC15 H11 F3 O2 S2P 1 21/c 111.7791; 5.8649; 21.894
90; 92.863; 90		1510.6Li, Haoyu; Cheng, Zengrui; Tung, Chen-Ho; Xu, Zhenghu
Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
ACS Catalysis, 2018, 8, 8237
4515717 CIFC21 H20 F4 O3 S2P 1 21/c 110.219; 20.254; 10.852
90; 107.747; 90		2139Li, Haoyu; Cheng, Zengrui; Tung, Chen-Ho; Xu, Zhenghu
Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
ACS Catalysis, 2018, 8, 8237
4515718 CIFC21 H36 Mn N O2 P2C 1 2/c 118.6272; 10.623; 23.1001
90; 101.192; 90		4484.04Zou, You-Quan; Chakraborty, Subrata; Nerush, Alexander; Oren, Dror; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal-Ligand Cooperation.
ACS catalysis, 2018, 8, 8014-8019
4515719 CIFC42 H68 Mn2 N4 O4 P4P 1 21/c 111.6109; 18.5885; 21.5322
90; 99.218; 90		4587.26Zou, You-Quan; Chakraborty, Subrata; Nerush, Alexander; Oren, Dror; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal-Ligand Cooperation.
ACS catalysis, 2018, 8, 8014-8019
4515720 CIFC29 H55 Fe N3 P2 Si2P 1 21/c 112.7712; 19.068; 15.4049
90; 110.526; 90		3513.3Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515721 CIFC35 H67 Fe N3 P3 Si2P -110.589; 12.811; 15.92
92.93; 104.249; 99.001		2058.3Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515722 CIFC31 H58 Fe N4 P2 Si2P 1 21/c 116.778; 15.4527; 16.706
90; 99.322; 90		4274.1Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515723 CIFC40 H50 Fe N6 P2P 1 21/n 118.6843; 11.1179; 18.9515
90; 110.665; 90		3683.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515724 CIFC39 H58 B Fe N5 O2 P2P 1 21/c 118.764; 11.2867; 20.592
90; 114.08; 90		3981.5Gorgas, Nikolaus; Stöger, Berthold; Veiros, Luis F.; Kirchner, Karl
Iron(II) Bis(acetylide) Complexes as Key Intermediates in the Catalytic Hydrofunctionalization of Terminal Alkynes
ACS Catalysis, 2018, 8, 7973
4515725 CIFC22 H24 Cl N O RuP 1 21/n 111.6782; 8.2226; 20.44
90; 99.939; 90		1933.3Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515726 CIFC23 H24 N2 O2P 1 21/c 18.295; 11.086; 21.615
90; 93.5; 90		1984Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515727 CIFC33 H39 F6 N2 O2 Ru SbP 1 21/c 113.2275; 10.9193; 24.4944
90; 98.3993; 90		3499.9Zhang, Luoqiang; Zhu, Lei; Zhang, Yuming; Yang, Yudong; Wu, Yimin; Ma, Weixin; Lan, Yu; You, Jingsong
Experimental and Theoretical Studies on Ru(II)-Catalyzed Oxidative C‒H/C‒H Coupling of Phenols with Aromatic Amides Using Air as Oxidant: Scope, Synthetic Applications, and Mechanistic Insights
ACS Catalysis, 2018, 8, 8324
4515728 CIFC47 H43 Br Mn N O4 P2P -112.0659; 12.6901; 13.3087
94.285; 102.738; 90.704		1981.22Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515729 CIFC39 H31 B Mn N O2 P2P -110.0379; 11.3687; 15.6568
73.97; 77.542; 72.82		1623.02Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515730 CIFC39 H31 Mn N2 O2 P2R -3 :H37.5012; 37.5012; 11.98047
90; 90; 120		14591.3Daw, Prosenjit; Kumar, Amit; Espinosa-Jalapa, Noel Angel; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes.
ACS catalysis, 2018, 8, 7734-7741
4515731 CIFC20 H20 Br Cl2 N O PtP 1 21/c 19.7404; 13.3126; 17.0002
90; 104.115; 90		2137.9Shimbayashi, Takuya; Matsushita, Gaku; Nanya, Atsushi; Eguchi, Akira; Okamoto, Kazuhiro; Ohe, Kouichi
Divergent Catalytic Approach from Cyclic Oxime Esters to Nitrogen-Containing Heterocycles with Group 9 Metal Catalysts
ACS Catalysis, 2018, 8, 7773
4515732 CIFC33 H41 Cl2 N Ru SP 4310.0186; 10.0186; 30.9734
90; 90; 90		3108.87Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515733 CIFC28 H36 Cl2 F3 N Ru SP n a 2116.3382; 16.5805; 10.4655
90; 90; 90		2835.1Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515734 CIFC26 H32 Cl2 F3 N Ru SP -111.0669; 14.1689; 17.6536
103.228; 94.276; 100.447		2630.52Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515735 CIFC32 H39 Cl4 N Ru SP c a 2119.868; 9.2131; 17.5258
90; 90; 90		3208Rozenberg, Illya; Eivgi, Or; Frenklah, Alexander; Butilkov, Danielle; Kozuch, Sebastian; Goldberg, Israel; Lemcoff, N. Gabriel
Synthesis and Catalytic Properties of Sulfur-Chelated Ruthenium Benzylidenes Bearing a Cyclic (Alkyl)(amino)carbene Ligand
ACS Catalysis, 2018, 8, 8182
4515736 CIFC43 H60 S Y2P 1 21/n 112.6411; 16.3119; 19.7095
90; 106.372; 90		3899.3Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515737 CIFC25 H33 S YP 1 21/c 116.796; 8.4624; 16.616
90; 102.549; 90		2305.3Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515738 CIFC50 H66 S2 Y2P -110.343; 10.6225; 10.683
94.507; 108.927; 92.924		1103.18Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515739 CIFC20 H20 S SiP 1 21/n 19.7426; 9.7458; 18.818
90; 90.465; 90		1786.7Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515740 CIFC23 H23 N S SiP 1 21/n 110.304; 17.9385; 11.4674
90; 107.757; 90		2018.6Luo, Yong; Teng, Huai-Long; Xue, Can; Nishiura, Masayoshi; Hou, Zhaomin
Yttrium-Catalyzed Regioselective α-C‒H Silylation of Methyl Sulfides with Hydrosilanes
ACS Catalysis, 2018, 8, 8027
4515741 CIFC21 H25 Cl3 Ir N O3P 21 21 219.6875; 13.7823; 17.6769
90; 90; 90		2360.1Zhou, Gang; Aboo, Ahmed H.; Robertson, Craig M.; Liu, Ruixia; Li, Zhenhua; Luzyanin, Konstantin; Berry, Neil G.; Chen, Weiping; Xiao, Jianliang
N,O- vs N,C-Chelation in Half-Sandwich Iridium Complexes: A Dramatic Effect on Enantioselectivity in Asymmetric Transfer Hydrogenation of Ketones
ACS Catalysis, 2018, 8, 8020
4515742 CIFC21 H25 Cl Ir N O3P 6118.4094; 18.4094; 11.3169
90; 90; 120		3321.5Zhou, Gang; Aboo, Ahmed H.; Robertson, Craig M.; Liu, Ruixia; Li, Zhenhua; Luzyanin, Konstantin; Berry, Neil G.; Chen, Weiping; Xiao, Jianliang
N,O- vs N,C-Chelation in Half-Sandwich Iridium Complexes: A Dramatic Effect on Enantioselectivity in Asymmetric Transfer Hydrogenation of Ketones
ACS Catalysis, 2018, 8, 8020
4515743 CIFC20 H24 Cl N O4P 1 21 17.421; 16.048; 8.176
90; 101.174; 90		955.2Schmid, Steven C.; Guzei, Ilia A.; Fernández, Israel; Schomaker, Jennifer M.
Ring Expansion of Bicyclic Methyleneaziridines via Concerted, Near-Barrierless [2,3]-Stevens Rearrangements of Aziridinium Ylides.
ACS catalysis, 2018, 8, 7907-7914
4515744 CIFC29 H43 F6 N P SbP b c a16.4612; 13.7221; 26.85
90; 90; 90		6064.9Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515745 CIFC30 H21 F18 N P SbC 1 2/c 127.034; 8.1387; 29.826
90; 95.017; 90		6537.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515746 CIFC32 H24 Au Cl F18 N2 P SbP 1 21/n 18.7962; 27.1915; 16.076
90; 103.535; 90		3738.3Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515747 CIFC27 H27 Cl2 F6 N P SbP -18.4844; 13.1717; 13.5679
92.667; 105.963; 100.874		1423.8Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515748 CIFC26 H37 Au Cl F6 N P SbP -110.6409; 16.737; 17.0626
82.428; 84.084; 87.346		2994.6Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515749 CIFC26 H37 F6 N P SbP 1 21/n 113.8885; 13.3919; 15.6069
90; 112.626; 90		2679.4Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515750 CIFC26 H29 Cl F6 Ir N P SbP 1 21/c 111.9033; 8.2433; 28.535
90; 99.672; 90		2760.1Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515751 CIFC26 H25 Au Cl F6 N P SbP -110.004; 10.1489; 15.7193
107.808; 92.182; 112.364		1383.43Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515752 CIFC31.5 H24 Au Cl6 F18 N O2 P SbP -18.9106; 12.9646; 19.744
73.397; 82.399; 85.849		2165.1Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515753 CIFC46 H40 O5P -111.0227; 11.4514; 15.2564
69.58; 76.609; 74.008		1715.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515754 CIFC25 H23 F6 N O2 P SbP -18.3643; 11.8205; 13.1583
91.321; 104.359; 99.991		1238.2Tinnermann, Hendrik; Nicholls, Leo D. M.; Johannsen, Tim; Wille, Christian; Golz, Christopher; Goddard, Richard; Alcarazo, Manuel
N-Arylpyridiniophosphines: Synthesis, Structure, and Applications in Au(I) Catalysis
ACS Catalysis, 2018, 8, 10457
4515755 CIFC25 H21 N O2 SC 1 2 126.96; 8.264; 9.337
90; 107.363; 90		1985.5Liu, Xihong; Wang, Pengxin; Bai, Lutao; Li, Dan; Wang, Linqing; Yang, Dongxu; Wang, Rui
Construction of Vicinal All-Carbon Quaternary Stereocenters Enabled by a Catalytic Asymmetric Dearomatization Reaction of β-Naphthols with 3-Bromooxindoles
ACS Catalysis, 2018, 8, 10888
4515756 CIFC22 H22 N4 OP 1 21 16.4088; 7.0686; 19.8625
90; 93.865; 90		897.75Marichev, Kostiantyn O.; Adly, Frady G.; Carranco, Alejandra M.; Garcia, Estevan C.; Arman, Hadi; Doyle, Michael P.
Catalyst Choice for Highly Enantioselective [3 + 3]-Cycloaddition of Enoldiazocarbonyl Compounds
ACS Catalysis, 2018, 8, 10392
4515757 CIFC50.31 H48.22 B Cl1.39 F4 Fe N2 Ni O1.31 S2C 1 2/c 125.286; 23.295; 20.693
90; 127.48; 90		9673Brazzolotto, Deborah; Wang, Lianke; Tang, Hao; Gennari, Marcello; Queyriaux, Nicolas; Philouze, Christian; Demeshko, Serhiy; Meyer, Franc; Orio, Maylis; Artero, Vincent; Hall, Michael B.; Duboc, Carole
Tuning Reactivity of Bioinspired [NiFe]-Hydrogenase Models by Ligand Design and Modeling the CO Inhibition Process
ACS Catalysis, 2018, 8, 10658
4515758 CIFC20 H18 N O2 PP 21 21 219.1903; 10.9348; 17.0654
90; 90; 90		1714.97Wang, Huamin; Li, Yongli; Tang, Zilu; Wang, Shengchun; Zhang, Heng; Cong, Hengjiang; Lei, Aiwen
Z-Selective Addition of Diaryl Phosphine Oxides to Alkynes via Photoredox Catalysis
ACS Catalysis, 2018, 8, 10599
4515759 CIFC58 H94 F9 Ho N4 O22 S3P 1 21 112.992; 16.505; 17.872
90; 102.41; 90		3742.8Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515760 CIFC30 H31 N2 O6 SP 1 21 113.9107; 13.9185; 15.4002
90; 109.507; 90		2810.6Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515761 CIFC42 H60 Br2 F9 N4 O16 S3 TmP 1 21 19.458; 25.399; 11.67
90; 93.281; 90		2798.8Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515762 CIFC36 H36 N2 O6 SP 1 21 19.3322; 18.7754; 9.4931
90; 107.649; 90		1585.05Xu, Yali; Chang, Fenzhen; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Catalytic Asymmetric Chemodivergent C2 Alkylation and [3 + 2]-Cycloaddition of 3-Methylindoles with Aziridines
ACS Catalysis, 2018, 8, 10261
4515763 CIFC27 H28 Cl F N4 O8P 21 21 2112.2999; 14.3668; 15.8349
90; 90; 90		2798.2Guo, Wengang; Li, Lu; Ding, Qian; Lin, Xiangfeng; Liu, Xianghui; Wang, Kai; Liu, Yan; Fan, Hongjun; Li, Can
Synthesis of Chiral Trispirocyclic Oxindoles via Organic-Base/Au(I)-Catalyzed Sequential Reactions
ACS Catalysis, 2018, 8, 10180
4515764 CIFC27 H28 Cl2 N4 O8P 21 21 2112.4437; 15.4069; 15.5019
90; 90; 90		2972Guo, Wengang; Li, Lu; Ding, Qian; Lin, Xiangfeng; Liu, Xianghui; Wang, Kai; Liu, Yan; Fan, Hongjun; Li, Can
Synthesis of Chiral Trispirocyclic Oxindoles via Organic-Base/Au(I)-Catalyzed Sequential Reactions
ACS Catalysis, 2018, 8, 10180
4515765 CIFC30 H31 N5 O7C 2 2 2110.4443; 14.5326; 38.8497
90; 90; 90		5896.7Guo, Wengang; Li, Lu; Ding, Qian; Lin, Xiangfeng; Liu, Xianghui; Wang, Kai; Liu, Yan; Fan, Hongjun; Li, Can
Synthesis of Chiral Trispirocyclic Oxindoles via Organic-Base/Au(I)-Catalyzed Sequential Reactions
ACS Catalysis, 2018, 8, 10180
4515766 CIFC32 H39 N O4 SP 1 21/c 111.7118; 39.9043; 6.266
90; 97.254; 90		2905Jiang, Fei; Yuan, Fu-Ru; Jin, Li-Wen; Mei, Guang-Jian; Shi, Feng
Metal-Catalyzed (4 + 3) Cyclization of Vinyl Aziridines withpara-Quinone Methide Derivatives
ACS Catalysis, 2018, 8, 10234
4515767 CIFC22 H22 N2 O3 PdP -16.7169; 11.3747; 13.8249
67.899; 87.885; 79.889		962.96Maji, Arun; Reddi, Yernaidu; Sunoj, Raghavan B.; Maiti, Debabrata
Mechanistic Insights on Orthogonal Selectivity in Heterocycle Synthesis
ACS Catalysis, 2018, 8, 10111
4515768 CIFC38 H51 Bi O8 P RhP -110.4797; 13.5923; 13.9879
91.294; 92.227; 91.361		1989.86Ren, Zhi; Sunderland, Travis L.; Tortoreto, Cecilia; Yang, Tzuhsiung; Berry, John F.; Musaev, Djamaladdin G.; Davies, Huw M. L.
Comparison of Reactivity and Enantioselectivity between Chiral Bimetallic Catalysts: Bismuth‒Rhodium- and Dirhodium-Catalyzed Carbene Chemistry
ACS Catalysis, 2018, 8, 10676
4515769 CIFC67.84 H95.68 Bi N4 O17.96 Rh S4I 422.2169; 22.2169; 10.9063
90; 90; 90		5383.2Ren, Zhi; Sunderland, Travis L.; Tortoreto, Cecilia; Yang, Tzuhsiung; Berry, John F.; Musaev, Djamaladdin G.; Davies, Huw M. L.
Comparison of Reactivity and Enantioselectivity between Chiral Bimetallic Catalysts: Bismuth‒Rhodium- and Dirhodium-Catalyzed Carbene Chemistry
ACS Catalysis, 2018, 8, 10676
4515770 CIFC14 H28 Cl Ir P2P 1 21/m 17.1256; 13.4641; 8.7896
90; 102.373; 90		823.69Ahn, Seihwan; Sorsche, Dieter; Berritt, Simon; Gau, Michael R.; Mindiola, Daniel J.; Baik, Mu-Hyun
Rational Design of a Catalyst for the Selective Monoborylation of Methane
ACS Catalysis, 2018, 8, 10021
4515771 CIFC18 H26 N2 O3P 1 21/n 19.2992; 15.198; 12.6751
90; 99.38; 90		1767.4Zhang, Bo-Sheng; Li, Yuke; An, Yang; Zhang, Zhe; Liu, Ce; Wang, Xin-Gang; Liang, Yong-Min
Carboxylate Ligand-Exchanged Amination/C(sp3)‒H Arylation Reaction via Pd/Norbornene Cooperative Catalysis
ACS Catalysis, 2018, 8, 11827
4515772 CIFC16 H22 N2 O3P n a 2110.5957; 18.8441; 7.6415
90; 90; 90		1525.8Zhang, Bo-Sheng; Li, Yuke; An, Yang; Zhang, Zhe; Liu, Ce; Wang, Xin-Gang; Liang, Yong-Min
Carboxylate Ligand-Exchanged Amination/C(sp3)‒H Arylation Reaction via Pd/Norbornene Cooperative Catalysis
ACS Catalysis, 2018, 8, 11827
4515773 CIFC30 H28 O4P -19.097; 12.191; 13.111
114.466; 95.343; 108.732		1209.5Zuo, Zhijun; Wang, Hui; Diao, Yunxia; Ge, Yicong; Liu, Jingjing; Luan, Xinjun
Palladium-Catalyzed Aryne Insertion/Arene Dearomatization Domino Reaction: A Highly Chemoselective Route to Spirofluorenes
ACS Catalysis, 2018, 8, 11029
4515774 CIFC26 H20 O2P 1 21/n 112.157; 12.525; 12.945
90; 91.141; 90		1970.7Zuo, Zhijun; Wang, Hui; Diao, Yunxia; Ge, Yicong; Liu, Jingjing; Luan, Xinjun
Palladium-Catalyzed Aryne Insertion/Arene Dearomatization Domino Reaction: A Highly Chemoselective Route to Spirofluorenes
ACS Catalysis, 2018, 8, 11029
4515775 CIFC8 H7 N O2P 1 21/c 111.6456; 5.1414; 13.0095
90; 110.064; 90		731.67Hota, Pradip Kumar; Sau, Samaresh Chandra; Mandal, Swadhin K.
Metal-Free Catalytic Formylation of Amides Using CO2 under Ambient Conditions
ACS Catalysis, 2018, 8, 11999
4515776 CIFC24 H22 Br I N2 O4 SP 21 21 217.4546; 13.367; 24.063
90; 90; 90		2397.8Struble, Thomas J.; Lankswert, Hannah M.; Pink, Maren; Johnston, Jeffrey N.
Enantioselective Organocatalytic Amine-Isocyanate Capture-Cyclization: Regioselective Alkene Iodoamination for the Synthesis of Chiral Cyclic Ureas.
ACS catalysis, 2018, 8, 11926-11931
4515777 CIFC26 H25 I N2 O4 SP 1 21 16.8374; 14.8665; 12.6176
90; 105.716; 90		1234.61Struble, Thomas J.; Lankswert, Hannah M.; Pink, Maren; Johnston, Jeffrey N.
Enantioselective Organocatalytic Amine-Isocyanate Capture-Cyclization: Regioselective Alkene Iodoamination for the Synthesis of Chiral Cyclic Ureas.
ACS catalysis, 2018, 8, 11926-11931
4515778 CIFC26 H18 O3C 1 2/c 124.897; 5.8589; 26.361
90; 100.161; 90		3784.9Lad, Bapurao Sudam; Katukojvala, Sreenivas
Piano-Stool Rhodium Enalcarbenoids: Application to Catalyst-Controlled Metal-Templated Annulations of Diazoenals and 1,3-Dicarbonyls
ACS Catalysis, 2018, 8, 11807
4515779 CIFC12 H14 O5P -15.8118; 7.6603; 13.506
82.491; 89.314; 82.461		590.97Lad, Bapurao Sudam; Katukojvala, Sreenivas
Piano-Stool Rhodium Enalcarbenoids: Application to Catalyst-Controlled Metal-Templated Annulations of Diazoenals and 1,3-Dicarbonyls
ACS Catalysis, 2018, 8, 11807
4515780 CIFC4 H10 Cl8 N2 W2P -17.7134; 7.817; 7.9908
97.754; 108.946; 112.35		402.67Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515781 CIFC26 H20 Cl8 F6 N2 W2P -17.1984; 9.6255; 12.8058
68.524; 86.291; 81.137		815.79Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515782 CIFC24 H34 Cl8 N2 W2P -19.6082; 9.7882; 10.2905
106.301; 106.481; 110.355		788.82Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515783 CIFC30 H34 Cl8 D6 N2 W2P 1 21/n 19.7378; 11.39; 16.7268
90; 93.494; 90		1851.78Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515784 CIFC10 H10 Cl4 F3 N O WP 1 21/c 111.3589; 11.3408; 11.9422
90; 100.845; 90		1510.91Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515785 CIFC16 H25 Cl4 N O WP -18.5798; 14.0708; 17.3875
95.674; 98.423; 97.281		2044.9Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515786 CIFC32 H54 Cl7 N3 W2P c c n9.5696; 10.714; 40.8756
90; 90; 90		4190.9Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515787 CIFC21 H45 Cl N P3 WP n m a15.7347; 13.6973; 12.7686
90; 90; 90		2751.93Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515788 CIFC9 H14 Cl N WP 1 21/m 16.3483; 7.2804; 11.9671
90; 93.604; 90		552Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515789 CIFC15 H26 Al Cl4 N WP 1 21/c 110.0824; 16.3429; 13.3029
90; 96.616; 90		2177.4Messinis, Antonis M.; Wright, William R. H.; Batsanov, Andrei S.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Exploration of Homogeneous Ethylene Dimerization Mediated by Tungsten Mono(imido) Complexes
ACS Catalysis, 2018, 8, 11235
4515790 CIFC56 H120 Co2 N7 O34 V W9P 1 21/n 114.4162; 32.8597; 20.2434
90; 109.886; 90		9017.7Sullivan, Kevin P.; Wieliczko, Marika; Kim, Mooeung; Yin, Qiushi; Collins-Wildman, Daniel L.; Mehta, Anil K.; Bacsa, John; Lu, Xinlin; Geletii, Yurii V.; Hill, Craig L.
Speciation and Dynamics in the [Co4V2W18O68]10‒/Co(II)aq/CoOx Catalytic Water Oxidation System
ACS Catalysis, 2018, 8, 11952
4515791 CIFC24 H24 N2 O2 SP 1 21/c 19.9646; 31.521; 6.9339
90; 101.603; 90		2133.4Wang, Huifei; Qiu, Shuxian; Wang, Sasa; Zhai, Hongbin
Pd-Catalyzed Umpolung of π‒Allylpalladium Intermediates: Assembly of All-Carbon α-Vinyl Quaternary Aldehydes through C(sp3)‒C(sp3) Coupling
ACS Catalysis, 2018, 8, 11960
4515792 CIFC60 H42 Br2 Cu F12 N6 O8 Sb2C 1 2/c 111.7665; 26.084; 21.832
90; 92.097; 90		6696.1Ng, Yik Yie; Tan, Lisa Jiaying; Ng, Shue Mei; Chai, Yoke Tin; Ganguly, Rakesh; Du, Yonghua; Yeow, Edwin Kok Lee; Soo, Han Sen
Spectroscopic Characterization and Mechanistic Studies on Visible Light Photoredox Carbon‒Carbon Bond Formation by Bis(arylimino)acenaphthene Copper Photosensitizers
ACS Catalysis, 2018, 8, 11277
4515793 CIFC76 H92 Br2 Cu F6 N12 O15 PC 1 2/c 126.796; 14.7426; 22.903
90; 114.796; 90		8213.5Ng, Yik Yie; Tan, Lisa Jiaying; Ng, Shue Mei; Chai, Yoke Tin; Ganguly, Rakesh; Du, Yonghua; Yeow, Edwin Kok Lee; Soo, Han Sen
Spectroscopic Characterization and Mechanistic Studies on Visible Light Photoredox Carbon‒Carbon Bond Formation by Bis(arylimino)acenaphthene Copper Photosensitizers
ACS Catalysis, 2018, 8, 11277
4515794 CIFC24 H18 Br N2 OP 15.6607; 8.2437; 10.596
96.24; 99.41; 96.49		480.59Tong, Hua-Rong; Zheng, Sujuan; Li, Xinghua; Deng, Zhiqiang; Wang, Hao; He, Gang; Peng, Qian; Chen, Gong
Pd(0)-Catalyzed Bidentate Auxiliary Directed Enantioselective Benzylic C‒H Arylation of 3-Arylpropanamides Using the BINOL Phosphoramidite Ligand
ACS Catalysis, 2018, 8, 11502
4515795 CIFC40 H32 N12 Ni2P 41 21 211.3157; 11.3157; 31.5787
90; 90; 90		4043.5Ghorai, Debasish; Finger, Lars H.; Zanoni, Giuseppe; Ackermann, Lutz
Bimetallic Nickel Complexes for Aniline C–H Alkylations
ACS Catalysis, 2018, 8, 11657
4515796 CIFC14 H14 F N3P 1 21/c 113.3888; 8.0065; 22.9811
90; 95.656; 90		2451.5Ghorai, Debasish; Finger, Lars H.; Zanoni, Giuseppe; Ackermann, Lutz
Bimetallic Nickel Complexes for Aniline C‒H Alkylations
ACS Catalysis, 2018, 8, 11657
4515797 CIFC40 H28 F4 N12 Ni2P c c n9.5253; 16.5175; 22.4483
90; 90; 90		3531.9Ghorai, Debasish; Finger, Lars H.; Zanoni, Giuseppe; Ackermann, Lutz
Bimetallic Nickel Complexes for Aniline C‒H Alkylations
ACS Catalysis, 2018, 8, 11657
4515798 CIFC90 H64 Cu2 F6 P4 S2P -111.1442; 12.9041; 13.9829
101.643; 97.123; 109.481		1816.4He, Jian; Chen, Caiyou; Fu, Gregory C.; Peters, Jonas C.
Visible-Light-Induced, Copper-Catalyzed Three-Component Coupling of Alkyl Halides, Olefins, and Trifluoromethylthiolate to Generate Trifluoromethyl Thioethers.
ACS catalysis, 2018, 8, 11741-11748
4515799 CIFC24 H18 Fe S2P 1 21 110.1167; 9.2912; 10.2864
90; 105.881; 90		930Xu, Bing-Bin; Ye, Jie; Yuan, Yu; Duan, Wei-Liang
Palladium-Catalyzed Asymmetric C‒H Arylation for the Synthesis of Planar Chiral Benzothiophene-Fused Ferrocenes
ACS Catalysis, 2018, 8, 11735
4515800 CIFC45 H51 Cl N4 Ni O PP 1 21/c 117.8919; 12.6768; 19.8115
90; 114.361; 90		4093.4Wang, Ting-Hsuan; Ambre, Ram; Wang, Qing; Lee, Wei-Chih; Wang, Pen-Cheng; Liu, Yuhua; Zhao, Lili; Ong, Tiow-Gan
Nickel-Catalyzed Heteroarenes Cross Coupling via Tandem C‒H/C‒O Activation
ACS Catalysis, 2018, 8, 11368
4515801 CIFC34 H44 Cl2 N4 WP 21 21 219.8622; 17.5716; 19.3465
90; 90; 90		3352.6Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515802 CIFC27 H43 Cl2 N2 P WP 21 21 2110.5486; 16.4202; 17.086
90; 90; 90		2959.5Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515803 CIFC16 H14 Cl2 F6 N2 O2 WP 21 21 2112.0005; 12.4893; 13.5857
90; 90; 90		2036.2Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515804 CIFC52.4 H45 Cl2 N2 O2.2 WR -3 :H32.8492; 32.8492; 20.7376
90; 90; 120		19379.3Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515805 CIFC22 H14 Cl2 F18 N2 O2 WP 1 21/c 112.5254; 27.3985; 9.0867
90; 105.516; 90		3004.7Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515806 CIFC16 H10 Cl2 F10 N2 O2 WP -17.3379; 7.8387; 17.8616
87.953; 81.828; 87.079		1015.22Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515807 CIFC19 H34 Cl2 N2 O2 WP 1 21/n 113.4052; 9.8029; 18.7197
90; 109.016; 90		2325.7Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515808 CIFC20 H36 Cl2 N2 O2 WP -19.8343; 9.9604; 13.7645
70.528; 85.509; 71.846		1207.4Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515809 CIFC27.5 H43.75 Cl2.5 N2 O2 WP -19.0974; 12.8175; 14.1008
112.357; 90.965; 99.035		1496.5Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515810 CIFC28 H35 Cl5 N2 O2 WP 1 21/c 112.1544; 10.4027; 24.447
90; 91.001; 90		3090.6Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515811 CIFC22 H29 Cl2 F3 N2 O2 WP -18.8303; 11.5526; 12.8453
77.061; 85.454; 74.916		1232.81Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515812 CIFC23 H32 Cl4 N4 O6 WP c a 2116.4344; 10.2454; 17.7291
90; 90; 90		2985.17Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515813 CIFC40 H44 Cl2 N2 O2 WP 1 21/n 116.2309; 10.3469; 22.3012
90; 103.618; 90		3640Messinis, Antonis M.; Batsanov, Andrei S.; Wright, William R. H.; Howard, Judith A. K.; Hanton, Martin J.; Dyer, Philip W.
Bis(Imido) Tungsten Complexes: Efficient Precatalysts for the Homogeneous Dimerization of Ethylene
ACS Catalysis, 2018, 8, 11249
4515814 CIFC25 H23 N O4P -18.535; 10.595; 11.444
79.5; 87.548; 81.464		1006.1Li, Guo-Xing; Hu, Xiafei; He, Gang; Chen, Gong
Photoredox-Mediated Minisci-type Alkylation of N-Heteroarenes with Alkanes with High Methylene Selectivity
ACS Catalysis, 2018, 8, 11847
4515815 CIFC25 H23 N O4P -19.737; 10.551; 11.09
68.032; 80.699; 75.858		1021.5Li, Guo-Xing; Hu, Xiafei; He, Gang; Chen, Gong
Photoredox-Mediated Minisci-type Alkylation of N-Heteroarenes with Alkanes with High Methylene Selectivity
ACS Catalysis, 2018, 8, 11847
4515816 CIFC27 H33 N O4P 1 21 18.9557; 9.9317; 13.533
90; 104.289; 90		1166.5Li, Guo-Xing; Hu, Xiafei; He, Gang; Chen, Gong
Photoredox-Mediated Minisci-type Alkylation of N-Heteroarenes with Alkanes with High Methylene Selectivity
ACS Catalysis, 2018, 8, 11847
4515817 CIFC28 H44 O3 Os P2P 1 21/c 115.878; 10.9673; 16.462
90; 90.174; 90		2866.7Esteruelas, Miguel A.; García-Yebra, Cristina; Martín, Jaime; Oñate, Enrique
Dehydrogenation of Formic Acid Promoted by a Trihydride-Hydroxo-Osmium(IV) Complex: Kinetics and Mechanism
ACS Catalysis, 2018, 8, 11314
4515818 CIFC23 H21.5 F6 N3.5 P PdP 21 21 2111.993; 17.981; 22.586
90; 90; 90		4871Huang, 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
4515819 CIFC47 H44 F3 Fe N2 O6 P Pd SP 21 21 2111.4924; 18.4018; 20.7858
90; 90; 90		4395.8Huang, 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
4515820 CIFC48 H45 Cl3 F3 Fe N2 O6 P Pd SP 21 21 2111.5846; 16.3753; 25.133
90; 90; 90		4767.8Huang, 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
4515821 CIFC53 H61 Fe Ni O P2P 1 21/c 114.2235; 16.3932; 19.5487
90; 98.023; 90		4513.5Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515822 CIFC43 H39 Fe Ni P2C 1 2/c 123.2567; 16.9768; 21.0881
90; 106.649; 90		7977Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515823 CIFC56 H53 Fe Ni P2I 1 2/a 114.0344; 13.358; 23.5713
90; 95.985; 90		4394.9Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515824 CIFC63 H67 Br Fe Ni P2P -110.4283; 13.6108; 19.5796
77.34; 81.336; 88.445		2680.5Beromi, Megan Mohadjer; Banerjee, Gourab; Brudvig, Gary W.; Hazari, Nilay; Mercado, Brandon Q.
Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.
ACS catalysis, 2018, 8, 2526-2533
4515825 CIFC31 H24 N6 O4 RuP n a 2117.4154; 17.0027; 9.3236
90; 90; 90		2760.8Matheu, Roc; Ertem, Mehmed Z.; Pipelier, Muriel; Lebreton, Jacques; Dubreuil, Didier; Benet-Buchholz, Jordi; Sala, Xavier; Tessier, Arnaud; Llobet, Antoni
The Role of Seven-Coordination in Ru-Catalyzed Water Oxidation
ACS Catalysis, 2018, 8, 2039
4515826 CIFC28.5 H28 N5 O6.5 RuP 1 21/c 111.7638; 16.7628; 15.8332
90; 107.656; 90		2975.1Matheu, Roc; Ertem, Mehmed Z.; Pipelier, Muriel; Lebreton, Jacques; Dubreuil, Didier; Benet-Buchholz, Jordi; Sala, Xavier; Tessier, Arnaud; Llobet, Antoni
The Role of Seven-Coordination in Ru-Catalyzed Water Oxidation
ACS Catalysis, 2018, 8, 2039
4515827 CIFC55 H48 Ce N15 O26 Ru2P c a 2117.9909; 22.189; 15.3463
90; 90; 90		6126.24Matheu, Roc; Ertem, Mehmed Z.; Pipelier, Muriel; Lebreton, Jacques; Dubreuil, Didier; Benet-Buchholz, Jordi; Sala, Xavier; Tessier, Arnaud; Llobet, Antoni
The Role of Seven-Coordination in Ru-Catalyzed Water Oxidation
ACS Catalysis, 2018, 8, 2039
4515828 CIFC2.778 H2.333 Cu0.111 N0.444 O0.778 S0.222C 1 2/c 122.2892; 22.2235; 15.7911
90; 101.936; 90		7652.9Zhang, Guiyang; Yang, Huimin; Fei, Honghan
Unusual Missing Linkers in an Organosulfonate-Based Primitive‒Cubic (pcu)-Type Metal‒Organic Framework for CO2 Capture and Conversion under Ambient Conditions
ACS Catalysis, 2018, 8, 2519

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