Crystallography Open Database

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4514384 CIFC24 H29 N2 O3 Rh SP 1 21/n 19.8164; 14.358; 17.0526
90; 90.736; 90
2403.26Ran, You; Yang, Yudong; You, Huansha; You, Jingsong
RhCl3-Catalyzed Oxidative C‒H/C‒H Cross-Coupling of (Hetero)aromatic Sulfonamides with (Hetero)arenes
ACS Catalysis, 2018, 8, 1796
4514387 CIFC26 H24 Br N OP 1 21 111.693; 6.314; 15.57
90; 103.875; 90
1116Huang, Jian-Qiang; Liu, Wei; Zheng, Bao-Hui; Liu, Xiu Yan; Yang, Zhen; Ding, Chang-Hua; Li, Hao; Peng, Qian; Hou, Xue-Long
Pd-Catalyzed Asymmetric Cyclopropanation Reaction of Acyclic Amides with Allyl and Polyenyl Carbonates. Experimental and Computational Studies for the Origin of Cyclopropane Formation
ACS Catalysis, 2018, 8, 1964
4514388 CIFC23 H22 F6 N3 P PdP 1 21/n 111.7229; 13.9765; 13.8227
90; 91.721; 90
2263.8Huang, 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
4514394 CIFC24 H33 Ir N2 O6P 1 21/n 114.1793; 34.531; 16.0684
90; 113.726; 90
7202.5Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514395 CIFC28 H43 Ir N2 O7P 1 21/c 117.9996; 11.5553; 15.0325
90; 100.311; 90
3076.1Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514396 CIFC34 H39 Ir N2 O7P -110.4412; 11.3139; 13.9001
75.379; 83.373; 84.494
1574.4Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514397 CIFC28 H39 Ir N2 O7P 1 21/c 112.1132; 39.536; 11.7754
90; 94.196; 90
5624.2Yuan, Hongmei; Brennessel, William W.; Jones, William D.
Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes
ACS Catalysis, 2018, 8, 2326
4514398 CIFC87 H190 N3 O38 P Si3 Ti W9P b c a20.2301; 28.431; 43.025
90; 90; 90
24746Zhang, Teng; Mazaud, Louis; Chamoreau, Lise-Marie; Paris, Céline; Proust, Anna; Guillemot, Geoffroy
Unveiling the Active Surface Sites in Heterogeneous Titanium-Based Silicalite Epoxidation Catalysts: Input of Silanol-Functionalized Polyoxotungstates as Soluble Analogues
ACS Catalysis, 2018, 8, 2330
4514400 CIFC27 H18 O2P 1 21/c 117.4516; 7.5513; 15.134
90; 107.604; 90
1900.99Mondal, Atanu; Hazra, Raju; Grover, Jagdeep; Raghu, Moluguri; Ramasastry, S. S. V.
Organophosphine-Catalyzed Intramolecular Hydroacylation of Activated Alkynes
ACS Catalysis, 2018, 8, 2748
4514401 CIFC61 H51 Cl3 F6 N3 P3 RuP 1 21/c 110.0272; 23.326; 22.7595
90; 95.922; 90
5294.9Paul, Bhaskar; Shee, Sujan; Panja, Dibyajyoti; Chakrabarti, Kaushik; Kundu, Sabuj
Direct Synthesis of N,N-Dimethylated and β-Methyl N,N-Dimethylated Amines from Nitriles Using Methanol: Experimental and Computational Studies
ACS Catalysis, 2018, 8, 2890
4515514 CIFC25 H38 B N O6 SP -111.446; 11.5967; 12.3843
112.094; 115.7; 93.978
1318.18Kim-Lee, Shin-Ho; Alonso, Inés; Mauleón, Pablo; Arrayás, Ramón Gómez; Carretero, Juan C.
Rationalizing the Role of NaOtBu in Copper-Catalyzed Carboboration of Alkynes: Assembly of Allylic All-Carbon Quaternary Stereocenters
ACS Catalysis, 2018, 8, 8993
4515515 CIFC21 H22 F N O4P 1 21/c 127.4465; 6.4873; 22.0138
90; 112.954; 90
3609.3Park, Hojoon; Chekshin, Nikita; Shen, Peng-Xiang; Yu, Jin-Quan
Ligand-Enabled, Palladium-Catalyzed β-C(sp<sup>3</sup>)-H Arylation of Weinreb Amides.
ACS catalysis, 2018, 8, 9292-9297
4515516 CIFC41 H51 Co K N6 O11P 21 21 2111.0919; 18.3376; 21.9261
90; 90; 90
4459.7Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515517 CIFC45 H36 K Mn N7 O3P 1 21/n 111.7651; 21.2221; 16.4682
90; 95.468; 90
4093.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515518 CIFC45 H48 N4P -19.1381; 12.0237; 17.8361
96.278; 90.36; 111.214
1813.7Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515519 CIFC50 H55 K Mn N4 O2P 1 21/n 111.527; 13.729; 27.724
90; 92.471; 90
4383.4Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515520 CIFC53 H47.5 F9 K Mn N4.5 O6.5P 1 21/n 112.3883; 18.995; 21.656
90; 101.457; 90
4994.5Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515521 CIFC48 H39 F9 N4 O6P 1 21/c 119.36; 10.0615; 29.486
90; 128.675; 90
4484Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515522 CIFC88 H131 K Mn N4 O7P -113.4244; 15.4608; 21.041
92.203; 93.474; 102.805
4244.6Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515523 CIFC54 H45 F18 K Mn N4 O3P -112.729; 14.584; 16.701
112.045; 92.891; 99.02
2817.9Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515524 CIFC148 H198 Cl0 K4 Mn4 N20 O19P -112.421; 13.222; 24.754
89.65; 77.831; 72.506
3783.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515525 CIFC64.75 H86 K Mn N4 O4P -111.719; 12.417; 21.77
91.221; 100.827; 100.424
3055Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515526 CIFC58 H71 K Mn N4 O4P 1 21/n 112.4818; 21.792; 20.039
90; 105.708; 90
5247.1Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515527 CIFC32 H29 F9 K Mn N6 O5C 1 c 118.3717; 10.8662; 19.0286
90; 94.307; 90
3788Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515528 CIFC41 H51 Fe K N6 O11P 21 21 2111.1683; 18.406; 21.83
90; 90; 90
4487.5Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515529 CIFC56 H61 Cl6 K Mn N4 O5P 1 21/n 111.391; 20.1796; 24.488
90; 93.742; 90
5617Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515530 CIFC28 H18 Co F9 K N6 O3P 1 21/c 110.696; 18.855; 15.813
90; 101.378; 90
3126.4Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515531 CIFC86 H118 K2 Mn2 N8 O17C 1 2/c 118.8633; 21.7465; 22.5199
90; 102.759; 90
9009.8Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515532 CIFC36 H39 F9 K N7 Ni O6P 1 21/n 19.133; 29.15; 16.125
90; 95.392; 90
4274Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515533 CIFC28 H18 F9 K Mn N6 O3P 1 21/c 110.661; 18.766; 15.752
90; 100.699; 90
3097Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515534 CIFC78 H105 K2 Mn2 N11 O9P -111.759; 13.541; 26.426
86.003; 80.023; 73.719
3977Bagchi, Vivek; Kalra, Anshika; Das, Purak; Paraskevopoulou, Patrina; Gorla, Saidulu; Ai, Lin; Wang, Qiuwen; Mohapatra, Sudip; Choudhury, Amitava; Sun, Zhicheng; Cundari, Thomas R.; Stavropoulos, Pericles
Comparative Nitrene-Transfer Chemistry to Olefinic Substrates Mediated by a Library of Anionic Mn(II) Triphenylamido-Amine Reagents and M(II) Congeners (M = Fe, Co, Ni) Favoring Aromatic over Aliphatic Alkenes
ACS Catalysis, 2018, 8, 9183
4515535 CIFC15 H13 N O2P 1 21/c 15.8829; 8.228; 25.846
90; 96.056; 90
1244.08Liu, Chengwei; Li, Guangchen; Shi, Shicheng; Meng, Guangrong; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon‒Nitrogen Bond Cleavage
ACS Catalysis, 2018, 8, 9131
4515536 CIFC30 H27 N2 O4 PP 1 21/c 112.148; 10.6001; 19.4764
90; 96.366; 90
2492.5Meyer, Tjark H.; Oliveira, João C. A.; Sau, Samaresh Chandra; Ang, Nate W. J.; Ackermann, Lutz
Electrooxidative Allene Annulations by Mild Cobalt-Catalyzed C‒H Activation
ACS Catalysis, 2018, 8, 9140
4515537 CIFC25 H20 Cl N O2P 21 21 216.1285; 10.8042; 30.5592
90; 90; 90
2023.43Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang
Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles
ACS Catalysis, 2018, 8, 9543
4515538 CIFC25 H20 Br N O2P 1 21 113.288; 5.6; 14.983
90; 114.29; 90
1016.23Dong, Kuiyong; Pei, Chao; Zeng, Qian; Wei, Hanlin; Doyle, Michael P.; Xu, Xinfang
Selective C(sp3)‒H Bond Insertion in Carbene/Alkyne Metathesis Reactions. Enantioselective Construction of Dihydroindoles
ACS Catalysis, 2018, 8, 9543
4515539 CIFC88 H44 Mo0.96 O32 S1.92 Zr6P 6/m m m39.254; 39.254; 16.542
90; 90; 120
22074Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T.
Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework
ACS Catalysis, 2018, 8, 9848
4515540 CIFC88 H44 Mo2.24 O36.88 Zr6P 6/m m m39.4657; 39.4657; 16.3953
90; 90; 120
22115.1Noh, Hyunho; Kung, Chung-Wei; Otake, Ken-ichi; Peters, Aaron W.; Li, Zhanyong; Liao, Yijun; Gong, Xinyi; Farha, Omar K.; Hupp, Joseph T.
Redox-Mediator-Assisted Electrocatalytic Hydrogen Evolution from Water by a Molybdenum Sulfide-Functionalized Metal‒Organic Framework
ACS Catalysis, 2018, 8, 9848
4515541 CIFC28 H26 N4 O7P 21 21 219.0462; 11.8256; 23.9232
90; 90; 90
2559.23Wang, Jilan; Li, Yongjia; Sun, Jun; Wang, Hongling; Jin, Zhichao; Chi, Yonggui Robin
Carbene-Catalyzed Enantioselective Addition of Benzylic Carbon to Unsaturated Acyl Azolium for Rapid Synthesis of Pyrrolo[3,2-c]quinolines
ACS Catalysis, 2018, 8, 9859
4515542 CIFC14 H21 Ge N O3P b c a13.7717; 11.1518; 18.9206
90; 90; 90
2905.81Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin
Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis
ACS Catalysis, 2018, 8, 9287
4515543 CIFC14 H20 Cl Ge N O3P 1 21/n 114.8342; 13.3798; 16.4653
90; 96.777; 90
3245.18Song, Hai-Jie; Jiang, Wei-Tao; Zhou, Qiao-Lan; Xu, Meng-Yu; Xiao, Bin
Structure-Modified Germatranes for Pd-Catalyzed Biaryl Synthesis
ACS Catalysis, 2018, 8, 9287
4515544 CIFC54 H60 N2P -18.3369; 9.3962; 14.592
100.111; 103.43; 98.334
1073.8Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka
Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation
ACS Catalysis, 2018, 8, 9408
4515545 CIFC12 H14 F3 N OP c a 218.8458; 14.526; 9.5388
90; 90; 90
1225.7Noto, Naoki; Tanaka, Yuya; Koike, Takashi; Akita, Munetaka
Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation
ACS Catalysis, 2018, 8, 9408
4515546 CIFC28 H23 N SP 110.1611; 10.3192; 12.2146
73.14; 71.609; 61.296
1051.13Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong
Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction
ACS Catalysis, 2018, 8, 9364
4515547 CIFC28 H23 N SP 110.082; 10.316; 12.247
73.57; 71.546; 61.603
1049.43Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong
Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction
ACS Catalysis, 2018, 8, 9364
4515548 CIFC15 H14 N2 O3P 1 21/c 18.085; 16.9819; 10.0705
90; 110.13; 90
1298.2Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515549 CIFC23 H19 Cl N2 O3 SP 1 21/c 17.0746; 19.195; 15.3264
90; 100.918; 90
2043.6Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515550 CIFC27 H22 N2 O3 SP n a 2133.95; 8.4972; 7.9321
90; 90; 90
2288.3Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515551 CIFC26 H24 N2 O5 SP 1 21/c 112.008; 7.0368; 30.631
90; 92.288; 90
2586.2Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515552 CIFC28 H28 N2 O3 SC 1 2/c 133.457; 7.1395; 20.377
90; 103.524; 90
4732.4Jadhav, Prakash D.; Lu, Xin; Liu, Rai-Shung
Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity
ACS Catalysis, 2018, 8, 9697
4515553 CIFC24 H22 Cl N3 O2P -19.5004; 11.278; 11.5979
104.256; 109.363; 106.026
1045.71Liu, Bingxian; Li, Jie; Hu, Panjie; Zhou, Xukai; Bai, Dachang; Li, Xingwei
Divergent Annulative C‒C Coupling of Indoles Initiated by Manganese-Catalyzed C‒H Activation
ACS Catalysis, 2018, 8, 9463

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