Crystallography Open Database

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4515554 CIFC23 H25 N O2P 1 21 19.356; 10.7541; 9.6715
90; 96.3296; 90
967.17Huang, Liang-Zhu; Xuan, Zi; Jeon, Hyun Ji; Du, Zhen-Ting; Kim, Ju Hyun; Lee, Sang-gi
Asymmetric Rh(II)/Pd(0) Relay Catalysis: Synthesis of α-Quaternary Chiral β-Lactams through Enantioselective C‒H Insertion/Diastereoselective Allylation of Diazoamides
ACS Catalysis, 2018, 8, 7340
4515555 CIFC11 H17 B Cl N OP n a 2119.738; 5.4134; 11.384
90; 90; 90
1216.4Yang, Ji-Min; Zhao, Yu-Tao; Li, Zi-Qi; Gu, Xue-Song; Zhu, Shou-Fei; Zhou, Qi-Lin
Gold-Catalyzed Oxidative Coupling of Terminal Alkynes and Borane Adducts: Efficient Synthesis of α-Boryl Ketones
ACS Catalysis, 2018, 8, 7351
4515556 CIFC62 H42 O6 Ru2P -112.7987; 15.0974; 25.8586
104.39; 95.12; 100
4720.16Gusev, Dmitry G.; Spasyuk, Denis M.
Revised Mechanisms for Aldehyde Disproportionation and the Related Reactions of the Shvo Catalyst
ACS Catalysis, 2018, 8, 6851
4515557 CIFC31 H22 O3 RuP 1 21/n 115.7952; 7.4857; 20.8655
90; 100.47; 90
2426.02Gusev, Dmitry G.; Spasyuk, Denis M.
Revised Mechanisms for Aldehyde Disproportionation and the Related Reactions of the Shvo Catalyst
ACS Catalysis, 2018, 8, 6851
4515558 CIFC57 H75 Cl3 Fe3 N6P -112.6922; 13.0313; 16.647
76.0639; 84.1498; 84.0536
2649.46Ferreira, Ricardo B.; Cook, Brian J.; Knight, Brian J.; Catalano, Vincent J.; García-Serres, Ricardo; Murray, Leslie J.
Catalytic Silylation of Dinitrogen by a Family of Triiron Complexes.
ACS catalysis, 2018, 8, 7208-7212
4515559 CIFC21 H18 Mn N5 O4P 1 21/c 113.4325; 11.7346; 13.7646
90; 92.32; 90
2167.87Liu, Tingting; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Manganese-Catalyzed β-Alkylation of Secondary Alcohols with Primary Alcohols under Phosphine-Free Conditions
ACS Catalysis, 2018, 8, 7201
4515560 CIFC21 H26 N2 OP 1 21/c 117.2156; 7.3295; 13.8834
90; 90.807; 90
1751.66Fernández, David F.; Rodrigues, Catarina A. B.; Calvelo, Martín; Gulías, Moisés; Mascareñas, José L.; López, Fernando
Iridium(I)-Catalyzed Intramolecular Cycloisomerization of Enynes: Scope and Mechanistic Course
ACS Catalysis, 2018, 8, 7397
4515561 CIFC22 H23 N O2P 1 21/c 112.2561; 9.8925; 15.8384
90; 110.254; 90
1801.6Fernández, David F.; Rodrigues, Catarina A. B.; Calvelo, Martín; Gulías, Moisés; Mascareñas, José L.; López, Fernando
Iridium(I)-Catalyzed Intramolecular Cycloisomerization of Enynes: Scope and Mechanistic Course
ACS Catalysis, 2018, 8, 7397
4515562 CIFC37 H46 Cu N3P 1 21/n 112.411; 12.765; 21.416
90; 95.043; 90
3379.7Nakamura, Kimiaki; Hara, Reina; Sunada, Yusuke; Nishikata, Takashi
Radical-Organometallic Hybrid Reaction System Enabling Couplings between Tertiary-Alkyl Groups and 1-Alkenyl Groups
ACS Catalysis, 2018, 8, 6791
4515563 CIFC26 H24 Cu N4 O7 S2P b c a17.7588; 13.939; 20.7682
90; 90; 90
5140.96Hardouin Duparc, Valérie; Bano, Guillaume L.; Schaper, Frank
Chan‒Evans‒Lam Couplings with Copper Iminoarylsulfonate Complexes: Scope and Mechanism
ACS Catalysis, 2018, 8, 7308
4515564 CIFC14 H13 Cu F3 N2 O7 S2P -17.9814; 11.0894; 11.102
96.461; 100.176; 110.007
892.77Hardouin Duparc, Valérie; Bano, Guillaume L.; Schaper, Frank
Chan‒Evans‒Lam Couplings with Copper Iminoarylsulfonate Complexes: Scope and Mechanism
ACS Catalysis, 2018, 8, 7308
4515565 CIFC14 H14 O3P c a 2111.7373; 4.431; 21.078
90; 90; 90
1096.2Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515566 CIFC14 H14 O3P c c n6.6399; 17.0733; 19.2759
90; 90; 90
2185.2Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515567 CIFC15 H18 O2P 1 21/c 114.435; 5.4011; 16.2501
90; 104.851; 90
1224.62Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515568 CIFC15 H20 O2P 1 21 19.1834; 5.2643; 13.7823
90; 107.711; 90
634.72Teng, Shenghan; Tessensohn, Malcolm E.; Webster, Richard D.; Zhou, Jianrong Steve
Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides
ACS Catalysis, 2018, 8, 7439
4515569 CIFC42 H70 Ce N7 O8P -110.5305; 11.181; 20.761
101.915; 91.944; 94.462
2381.4Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515570 CIFC32 H51 Ce N6 O8P -111.5006; 17.4646; 20.0865
67.599; 80.635; 78.648
3639.9Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515571 CIFC49 H66 Ce2 N11 O17C 1 2/c 122.935; 19.6202; 13.5095
90; 114.142; 90
5547.4Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515572 CIFC124 H174 Ce4 N21 O32C 1 2/c 115.263; 27.226; 17.096
90; 96.089; 90
7064Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515573 CIFC68 H102 Ce2 N8 O11C 1 2/c 127.711; 19.4594; 15.5984
90; 122.044; 90
7129.7Shirase, Satoru; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi
Oxidation of Alcohols to Carbonyl Compounds Catalyzed by Oxo-Bridged Dinuclear Cerium Complexes with Pentadentate Schiff-Base Ligands under a Dioxygen Atmosphere
ACS Catalysis, 2018, 8, 6939
4515574 CIFC34 H30 N2 O4P 1 21/c 113.746; 11.435; 18.615
90; 110.457; 90
2741.5Usui, Kenji; Haines, Brandon E.; Musaev, Djamaladdin G.; Sarpong, Richmond
Understanding Regiodivergence in a Pd(II)-Mediated Site-Selective C‒H Alkynylation
ACS Catalysis, 2018, 8, 4516
4515575 CIFC25 H25 N3 O PdP 1 21/n 112.551; 9.9456; 17.6307
90; 106.171; 90
2113.72Usui, Kenji; Haines, Brandon E.; Musaev, Djamaladdin G.; Sarpong, Richmond
Understanding Regiodivergence in a Pd(II)-Mediated Site-Selective C‒H Alkynylation
ACS Catalysis, 2018, 8, 4516
4515576 CIFC19 H17 Cl OP 21 21 215.612; 7.5305; 37.033
90; 90; 90
1565.1Teng, Huai-Long; Ma, Yuanhong; Zhan, Gu; Nishiura, Masayoshi; Hou, Zhaomin
Asymmetric C(sp)‒H Addition of Terminal Alkynes to Cyclopropenes by a Chiral Gadolinium Catalyst
ACS Catalysis, 2018, 8, 4705
4515577 CIFC21 H49 N O3 P2 RuP 1 21/n 113.2573; 13.3386; 15.3535
90; 92.948; 90
2711.4Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515578 CIFC51 H125 N3 O10 P6 Ru3P -115.1793; 16.5074; 16.664
88.609; 71.881; 62.825
3496Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515579 CIFC19 H41 N O3 P2 RuP b c a14.17; 15.3918; 21.741
90; 90; 90
4741.8Nguyen, Duc Hanh; Trivelli, Xavier; Capet, Frédéric; Swesi, Youssef; Favre-Réguillon, Alain; Vanoye, Laurent; Dumeignil, Franck; Gauvin, Régis M.
Deeper Mechanistic Insight into Ru Pincer-Mediated Acceptorless Dehydrogenative Coupling of Alcohols: Exchanges, Intermediates, and Deactivation Species
ACS Catalysis, 2018, 8, 4719
4515580 CIFC19 H35 Cl2 Mn N P2P 1 21/c 112.4393; 11.9755; 15.9077
90; 91.637; 90
2368.8Brzozowska, Aleksandra; Azofra, Luis Miguel; Zubar, Viktoriia; Atodiresei, Iuliana; Cavallo, Luigi; Rueping, Magnus; El-Sepelgy, Osama
Highly Chemo- and Stereoselective Transfer Semihydrogenation of Alkynes Catalyzed by a Stable, Well-Defined Manganese(II) Complex
ACS Catalysis, 2018, 8, 4103
4515581 CIFC7 H9 Co O5 PP 1 21/n 14.8553; 32.281; 5.6773
90; 91.788; 90
889.39Cai, Zhong-Sheng; Shi, Yi; Bao, Song-Song; Shen, Yang; Xia, Xing-Hua; Zheng, Li-Min
Bioinspired Engineering of Cobalt-Phosphonate Nanosheets for Robust Hydrogen Evolution Reaction
ACS Catalysis, 2018, 8, 3895
4515582 CIFC25 H40 N3 O2 P2 ReP 21 21 2110.1881; 13.7426; 20.6392
90; 90; 90
2889.7Glatz, Mathias; Stöger, Berthold; Himmelbauer, Daniel; Veiros, Luis F.; Kirchner, Karl
Chemoselective Hydrogenation of Aldehydes under Mild, Base-Free Conditions: Manganese Outperforms Rhenium.
ACS catalysis, 2018, 8, 4009-4016
4515583 CIFC72 H87 B N3 O2 YP 1 21/n 112.047; 17.64; 32.956
90; 96.116; 90
6964Yu, Xiaying; You, Qing; Zhou, Xigeng; Zhang, Lixin
Isoprene Regioblock Copolymerization: Switching the Regioselectivity by the in Situ Ancillary Ligand Transmetalation of Active Yttrium Species
ACS Catalysis, 2018, 8, 4465
4515584 CIFC12 H6 In0.54 N O2.25C m m m7.0996; 33.5115; 16.7335
90; 90; 90
3981.2Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515585 CIFC12 H6 In0.75 N O2.73C m m m7.125; 33.622; 16.583
90; 90; 90
3972.57Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515586 CIFC48 H24 In2 N4 Ni O10C m m m7.0725; 33.2883; 16.666
90; 90; 90
3923.7Leng, Fucheng; Liu, Hang; Ding, Meili; Lin, Qi-Pu; Jiang, Hai-Long
Boosting Photocatalytic Hydrogen Production of Porphyrinic MOFs: The Metal Location in Metalloporphyrin Matters
ACS Catalysis, 2018, 8, 4583
4515587 CIFC26 H28 F6 Mn N4 O6 S2P 4318.28107; 18.28107; 36.923
90; 90; 90
12339.6Du, Junyi; Miao, Chengxia; Xia, Chungu; Lee, Yong-Min; Nam, Wonwoo; Sun, Wei
Mechanistic Insights into the Enantioselective Epoxidation of Olefins by Bioinspired Manganese Complexes: Role of Carboxylic Acid and Nature of Active Oxidant
ACS Catalysis, 2018, 8, 4528
4515588 CIFC28 H24 B F12 PP -113.414; 13.786; 18.1493
101.69; 106.173; 109.985
2859.7Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515589 CIFC28 H26 B F12 PP 1 21/n 110.6496; 15.3406; 18.042
90; 95.278; 90
2935Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515590 CIFC28 H27 B2 F12 PP -111.7104; 12.4425; 12.4488
71.092; 69.578; 64.329
1499.65Boudjelel, Maxime; Sosa Carrizo, E. Daiann; Mallet−Ladeira, Sonia; Massou, Stéphane; Miqueu, Karinne; Bouhadir, Ghenwa; Bourissou, Didier
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geometrically Constrained Phosphine-Borane Lewis Pair
ACS Catalysis, 2018, 8, 4459
4515591 CIFC72 H94 Co2 N6P 1 21/n 111.1904; 12.5885; 22.6178
90; 99.722; 90
3140.42Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515592 CIFC31 H48 Co N2 O SiP 1 21/n 117.0369; 10.7343; 17.0418
90; 93.483; 90
3110.83Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515593 CIFC31 H45 Cl2 Co Li N2 O2P 41 21 212.0633; 12.0633; 21.8421
90; 90; 90
3178.53Lepori, Clément; Gómez-Orellana, Pablo; Ouharzoune, Allissa; Guillot, Régis; Lledós, Agusti; Ujaque, Gregori; Hannedouche, Jérôme
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines
ACS Catalysis, 2018, 8, 4446
4515594 CIFC39 H49 N3 O Si ZnP 1 21/n 18.8505; 21.914; 19.0059
90; 100.646; 90
3622.7Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515595 CIFC22.5 H38.5 N3 ZnP 1 21/c 114.8856; 21.731; 16.0804
90; 113.482; 90
4770.9Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515596 CIFC22 H35 N3 O2 ZnP 1 21/c 123.041; 10.016; 22.532
90; 117.531; 90
4611Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515597 CIFC50 H86 N6 Zn2C 1 2/c 121.7365; 14.2049; 20.3579
90; 102.81; 90
6129.4Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515598 CIFC55 H93 N6 O4 Zn2P -112.7688; 13.881; 17.4955
76.808; 73.779; 84.324
2896.9Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515599 CIFC51 H86 N6 O2 Zn2P -116.1366; 16.5978; 23.3164
98.9; 90.984; 119.052
5362.53Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515600 CIFC60 H84 N4 O4 Zn2P -113.4707; 14.5272; 16.2991
88.145; 89.86; 65.496
2900.6Feng, Guoqin; Du, Chongyang; Xiang, Li; del Rosal, Iker; Li, Guangyu; Leng, Xuebing; Chen, Eugene Y.-X.; Maron, Laurent; Chen, Yaofeng
Side Arm Twist on Zn-Catalyzed Hydrosilylative Reduction of CO2 to Formate and Methanol Equivalents with High Selectivity and Activity
ACS Catalysis, 2018, 8, 4710
4515601 CIFC10 H12 Fe N11 OP 1 21/n 110.82; 12.675; 11.662
90; 106.559; 90
1533Shen, Shou-Jie; Zhu, Cheng-Liang; Lu, Deng-Fu; Xu, Hao
Iron-Catalyzed Direct Olefin Diazidation via Peroxyester Activation Promoted by Nitrogen-Based Ligands.
ACS catalysis, 2018, 8, 4473-4482
4515602 CIFC44 H54 N4 NiP 21 21 2110.1006; 18.0014; 42.163
90; 90; 90
7666.3Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515603 CIFC110 H136 Cl3 N9 Ni3P 1 21/c 126.6781; 16.5463; 22.7174
90; 90.462; 90
10027.7Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515604 CIFC64 H80 Cl2 N6 Ni2P 21 21 2112.855; 21.217; 24.26
90; 90; 90
6617Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515605 CIFC43 H56 Cl N3 NiC 1 2/c 127.4949; 19.0191; 16.9558
90; 108.589; 90
8404.1Rull, Silvia G.; Funes-Ardoiz, Ignacio; Maya, Celia; Maseras, Feliu; Fructos, Manuel R.; Belderrain, Tomás R.; Nicasio, M. Carmen
Elucidating the Mechanism of Aryl Aminations Mediated by NHC-Supported Nickel Complexes: Evidence for a Nonradical Ni(0)/Ni(II) Pathway
ACS Catalysis, 2018, 8, 3733
4515606 CIFC22 H37 Ir N PP 21 21 2110.5276; 10.7464; 18.567
90; 90; 90
2100.6Cherepakhin, Valeriy; Williams, Travis J.
Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.
ACS catalysis, 2018, 8, 3754-3763
4515607 CIFC29 H48 Ir2 N2 O P2P 1 21/c 114.836; 15.464; 15.385
90; 114.159; 90
3220.5Cherepakhin, Valeriy; Williams, Travis J.
Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.
ACS catalysis, 2018, 8, 3754-3763
4515608 CIFC34 H26 F6 N6 O9 P Ru2P 1 21/c 113.8587; 23.8714; 12.5805
90; 115.201; 90
3765.8Daniel, Quentin; Duan, Lele; Timmer, Brian J. J.; Chen, Hong; Luo, Xiaodan; Ambre, Ram; Wang, Ying; Zhang, Biaobiao; Zhang, Peili; Wang, Lei; Li, Fusheng; Sun, Junliang; Ahlquist, Mårten; Sun, Licheng
Water Oxidation Initiated by In Situ Dimerization of the Molecular Ru(pdc) Catalyst
ACS Catalysis, 2018, 8, 4375
4515609 CIFC21 H23 Br N OP -18.6881; 9.8467; 11.0731
94.586; 91.58; 105.361
909.36Bai, Dachang; Xu, Teng; Ma, Chaorui; Zheng, Xin; Liu, Bingxian; Xie, Fang; Li, Xingwei
Rh(III)-Catalyzed Mild Coupling of Nitrones and Azomethine Imines with Alkylidenecyclopropanes via C‒H Activation: Facile Access to Bridged Cycles
ACS Catalysis, 2018, 8, 4194
4515610 CIFC8 H7 Cl O3P n a 2114.4042; 3.8522; 14.6641
90; 90; 90
813.68Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515611 CIFC25 H25 Cl O4P 1 21 110.936; 6.5014; 14.9916
90; 95.8987; 90
1060.25Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515612 CIFC6 H3 Br Cl I OP 1 21 17.2559; 4.5474; 13.321
90; 100.781; 90
431.77Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515613 CIFC12 H8 Cl2 O2P b c n6.3191; 15.8114; 21.7404
90; 90; 90
2172.17Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515614 CIFC8 H7 Cl O2P 1 21/c 16.7838; 16.4432; 7.2539
90; 108.069; 90
769.25Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515615 CIFC25 H21 Cl O3C 1 2/c 113.6694; 14.6546; 21.7416
90; 104.277; 90
4220.76Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515616 CIFC8 H6 Br Cl O3P 1 21/c 14.1058; 17.9301; 12.4296
90; 93.138; 90
913.66Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515617 CIFC12 H8 F2 O SeP -15.6425; 9.1159; 11.1839
106.666; 102.943; 93.95
531.61Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515618 CIFC7 H4 Br Cl O2P 1 21/n 17.7896; 13.5178; 15.0171
90; 101.499; 90
1549.54Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515619 CIFC19 H17 Cl O3P 1 21 19.6791; 7.1917; 12.2628
90; 107.906; 90
812.26Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515620 CIFC12 H9 Cl OP 1 21/n 15.7829; 20.3532; 8.3091
90; 97.502; 90
969.61Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515621 CIFC12 H16 B Cl O3I -419.7094; 19.7094; 6.8557
90; 90; 90
2663.2Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515622 CIFC6 H4 Br Cl OP 21 21 215.2204; 11.214; 11.717
90; 90; 90
685.9Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515623 CIFC12 H10 Br2 Cl2 O4C 1 2/c 132.7811; 3.926; 21.7084
90; 91.5018; 90
2792.9Xiong, Xiaodong; Yeung, Ying-Yeung
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
ACS Catalysis, 2018, 8, 4033
4515624 CIFC48 H38 B Cl2 F27 Fe N4 O3 SP -112.695; 13.3351; 17.1823
102.363; 97.011; 92.487
2812.8Postils, Verònica; Rodríguez, Mònica; Sabenya, Gerard; Conde, Ana; Díaz-Requejo, M. Mar; Pérez, Pedro J.; Costas, Miquel; Solà, Miquel; Luis, Josep M.
Mechanism of the Selective Fe-Catalyzed Arene Carbon‒Hydrogen Bond Functionalization
ACS Catalysis, 2018, 8, 4313
4515625 CIFC26 H36 O4 SP 1 21 19.0489; 8.4426; 15.648
90; 94.577; 90
1191.6Yu, Fei-Le; Bai, Da-Chang; Liu, Xiu-Yan; Jiang, Yang-Jie; Ding, Chang-Hua; Hou, Xue-Long
Pd-Catalyzed Allylic Alkylation of gem-Alkyl,Aryl-Disubstituted Allyl Reagents with Ketones: Diastereoselective Construction of Vicinal Tertiary and Quaternary Carbon Centers
ACS Catalysis, 2018, 8, 3317
4515626 CIFC16 H20 OP 1 21/c 18.6633; 8.4114; 17.9313
90; 99.6888; 90
1288Yu, Fei-Le; Bai, Da-Chang; Liu, Xiu-Yan; Jiang, Yang-Jie; Ding, Chang-Hua; Hou, Xue-Long
Pd-Catalyzed Allylic Alkylation of gem-Alkyl,Aryl-Disubstituted Allyl Reagents with Ketones: Diastereoselective Construction of Vicinal Tertiary and Quaternary Carbon Centers
ACS Catalysis, 2018, 8, 3317
4515627 CIFC21 H21 N3 O3 SP -16.3615; 10.4427; 15.1313
85.229; 87.86; 76.106
972.24Guin, Srimanta; Deb, Arghya; Dolui, Pravas; Chakraborty, Souvik; Singh, Vikas Kumar; Maiti, Debabrata
Promoting Highly Diastereoselective γ-C‒H Chalcogenation of α-Amino Acids and Aliphatic Carboxylic Acids
ACS Catalysis, 2018, 8, 2664
4515628 CIFC16 H20 O5P 21 21 218.793; 10.1042; 16.0484
90; 90; 90
1425.8Biosca, Maria; Margalef, Jèssica; Caldentey, Xisco; Besora, Maria; Rodríguez-Escrich, Carles; Saltó, Joan; Cambeiro, Xacobe C.; Maseras, Feliu; Pàmies, Oscar; Diéguez, Montserrat; Pericàs, Miquel A.
Computationally Guided Design of a Readily Assembled Phosphite‒Thioether Ligand for a Broad Range of Pd-Catalyzed Asymmetric Allylic Substitutions
ACS Catalysis, 2018, 8, 3587
4515629 CIFC13 H15 B F3 KP 19.0823; 10.0446; 16.7815
72.627; 75.846; 89.976
1412.38Gao, De-Wei; Xiao, Yiyang; Liu, Mingyu; Liu, Zhen; Karunananda, Malkanthi K.; Chen, Jason S.; Engle, Keary M.
Catalytic, Enantioselective Synthesis of Allenyl Boronates.
ACS catalysis, 2018, 8, 3650-3654
4515630 CIFC14 H13 N O4P 21 21 216.6275; 8.0167; 22.6419
90; 90; 90
1202.98Brandenberg, Oliver F.; Prier, Christopher K.; Chen, Kai; Knight, Anders M.; Wu, Zachary; Arnold, Frances H.
Stereoselective Enzymatic Synthesis of Heteroatom-Substituted Cyclopropanes
ACS Catalysis, 2018, 8, 2629
4515631 CIFC70 H110 Cl2 Co2 N4 P4P 1 21/n 110.4784; 22.1575; 15.6461
90; 105.074; 90
3507.6Suzuki, Tatsuya; Fujimoto, Keisuke; Takemoto, Yoshiyuki; Wasada-Tsutsui, Yuko; Ozawa, Tomohiro; Inomata, Tomohiko; Fryzuk, Michael D.; Masuda, Hideki
Efficient Catalytic Conversion of Dinitrogen to N(SiMe3)3 Using a Homogeneous Mononuclear Cobalt Complex
ACS Catalysis, 2018, 8, 3011
4515632 CIFC70 H110 Co2 N4 P4P 1 21/c 110.7673; 29.054; 12.6363
90; 117.372; 90
3510.5Suzuki, Tatsuya; Fujimoto, Keisuke; Takemoto, Yoshiyuki; Wasada-Tsutsui, Yuko; Ozawa, Tomohiro; Inomata, Tomohiko; Fryzuk, Michael D.; Masuda, Hideki
Efficient Catalytic Conversion of Dinitrogen to N(SiMe3)3 Using a Homogeneous Mononuclear Cobalt Complex
ACS Catalysis, 2018, 8, 3011
4515633 CIFC23 H34 N6 O3 SP 1 21 19.2161; 12.7576; 10.9094
90; 95.835; 90
1276.03Nicholls, Rachel L.; McManus, James A.; Rayner, Christopher M.; Morales-Serna, José A.; White, Andrew J. P.; Nguyen, Bao N.
Guanidine-Catalyzed Reductive Amination of Carbon Dioxide with Silanes: Switching between Pathways and Suppressing Catalyst Deactivation
ACS Catalysis, 2018, 8, 3678
4515634 CIFC23 H16 O2C 1 2/c 115.5099; 7.5217; 28.568
90; 99.09; 90
3290.9Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V.
Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes
ACS Catalysis, 2018, 8, 2748
4515635 CIFC15 H22 Br N OP 1 21 17.5964; 16.0907; 12.1098
90; 99.736; 90
1458.88Liu, Ze-Shui; Qian, Guangyin; Gao, Qianwen; Wang, Peng; Cheng, Hong-Gang; Wei, Qiang; Liu, Qi; Zhou, Qianghui
Palladium/Norbornene Cooperative Catalysis To Access Tetrahydronaphthalenes and Indanes with a Quaternary Center
ACS Catalysis, 2018, 8, 4783
4515636 CIFC29 H30 O5P 1 21/n 110.573; 16.555; 14.695
90; 104.784; 90
2487Liu, Ze-Shui; Qian, Guangyin; Gao, Qianwen; Wang, Peng; Cheng, Hong-Gang; Wei, Qiang; Liu, Qi; Zhou, Qianghui
Palladium/Norbornene Cooperative Catalysis To Access Tetrahydronaphthalenes and Indanes with a Quaternary Center
ACS Catalysis, 2018, 8, 4783
4515637 CIFC13 H17 N O5 SP 1 21/n 15.923; 16.864; 14.255
90; 92.357; 90
1422.7Kishi, Kenta; Takizawa, Shinobu; Sasai, Hiroaki
Phosphine-Catalyzed Dual Umpolung Domino Michael Reaction: Facile Synthesis of Hydroindole- and Hydrobenzofuran-2-Carboxylates
ACS Catalysis, 2018, 8, 5228
4515638 CIFC37 H47 Mo N3 OP 1 21/n 115.8128; 13.0267; 16.0929
90; 98.231; 90
3280.8Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515639 CIFC47 H60 Mo N5 OF d d 232.0833; 33.7453; 17.8428
90; 90; 90
19317.7Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515640 CIFC41 H65 Mo N3 Si2P 1 21/c 111.264; 17.5505; 23.2268
90; 115.23; 90
4153.65Joannou, Matthew V.; Bezdek, Máté J.; Chirik, Paul J.
Pyridine(diimine) Molybdenum-Catalyzed Hydrogenation of Arenes and Hindered Olefins: Insights into Precatalyst Activation and Deactivation Pathways
ACS Catalysis, 2018, 8, 5276
4515641 CIFC41 H50 Cl6 N P PdP 21 21 2113.8095; 15.6122; 19.5369
90; 90; 90
4212.1Ding, Linlin; Sui, Xianwei; Gu, Zhenhua
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
ACS Catalysis, 2018, 8, 5630
4515642 CIFC25.5 H15 Cl5 O3P 1 21 111.39996; 31.0942; 19.9369
90; 96.7204; 90
7018.53Ding, Linlin; Sui, Xianwei; Gu, Zhenhua
Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings
ACS Catalysis, 2018, 8, 5630
4515643 CIFC29 H34 Cl N O5P 1 21 18.4142; 14.046; 11.3304
90; 104.324; 90
1297.5Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515644 CIFC21 H27 N O5P 1 21/c 112.432; 11.174; 14.1728
90; 96.117; 90
1957.6Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515645 CIFC21 H27 N O5P 1 21/c 18.3767; 12.1262; 39.035
90; 93.093; 90
3959.3Kuang, Xiao-Kang; Zhu, Jun; Zhou, Li; Wang, Lijia; Wang, Sunewang R.; Tang, Yong
Synergetic Tandem Enantiomeric Enrichment in Catalytic Asymmetric Multi-Component Reactions (AMCRs): Highly Enantioselective Construction of Tetracyclic Indolines with Four Continuous Stereocenters
ACS Catalysis, 2018, 8, 4991
4515646 CIFC39 H38 Br N O Si2P 21 21 219.6879; 9.8487; 34.927
90; 90; 90
3332.5Meng, Fei-Fan; Xie, Jia-Hao; Xu, Yun-He; Loh, Teck-Peng
Catalytically Asymmetric Synthesis of 1,3-Bis(silyl)propenes via Copper-Catalyzed Double Proto-Silylations of Polar Enynes
ACS Catalysis, 2018, 8, 5306
4515647 CIFC15 H21 N O2 SP 1 21/c 116.125; 6.8205; 13.1663
90; 96.287; 90
1439.33Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515648 CIFC30 H42 N2 O4 S2P 1 21/n 119.6621; 8.3363; 19.9464
90; 112.146; 90
3028.2Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515649 CIFC30 H42 N2 O4 S2P n a 2132.802; 8.4124; 10.9145
90; 90; 90
3011.8Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515650 CIFC13 H17 N O2 SP 1 21/n 17.851; 10.524; 15.813
90; 98.263; 90
1293Liu, Ruzhang; Ge, Hua; Chen, Kuanwei; Xue, Huaiguo
Selectivity in Olefin-Intervened Macrocyclic Ring-Closing Metathesis
ACS Catalysis, 2018, 8, 5574
4515651 CIFC16 H25 O2 PP 1 21 18.589; 5.946; 15.333
90; 100.966; 90
768.8Smaligo, Andrew J.; Vardhineedi, Sriramurthy; Kwon, Ohyun
Carvone-Derived P-Stereogenic Phosphines: Design, Synthesis, and Use in Allene-Imine [3 + 2] Annulation.
ACS catalysis, 2018, 8, 5188-5192
4515652 CIFC16 H23 O3 PP 1 21 110.2543; 10.9798; 13.7645
90; 90.59; 90
1549.67Smaligo, Andrew J.; Vardhineedi, Sriramurthy; Kwon, Ohyun
Carvone-Derived P-Stereogenic Phosphines: Design, Synthesis, and Use in Allene-Imine [3 + 2] Annulation.
ACS catalysis, 2018, 8, 5188-5192
4515653 CIFC25 H18 Cl F3 O2 SP 21 21 217.8069; 7.8369; 35.3156
90; 90; 90
2160.68Maddox, 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

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