Crystallography Open Database

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Searching journal of publication like 'ACS Catalysis' volume of publication is 6

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4513821 CIFC69 H53 N6 O5 P2 Ru2C 1 2/c 138.209; 13.4891; 24.3071
90; 118.199; 90
11041.1Moore, Cameron M.; Bark, Byongjoo; Szymczak, Nathaniel K.
Simple Ligand Modifications with Pendent OH Groups Dramatically Impact the Activity and Selectivity of Ruthenium Catalysts for Transfer Hydrogenation: The Importance of Alkali Metals
ACS Catalysis, 2016, 6, 1981
4513822 CIFC19 H23 F3 Ir N3 O3 SP 1 21/c 114.9292; 12.2212; 12.2965
90; 109.506; 90
2114.8Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J.
A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid
ACS Catalysis, 2016, 6, 2014
4513823 CIFC27 H31 F3 Ir N3 O3 SP 1 21/c 111.0313; 26.4631; 19.9865
90; 98.415; 90
5771.7Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J.
A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid
ACS Catalysis, 2016, 6, 2014
4513824 CIFC2 H5 Na3 O8C 1 2/c 120.3758; 3.4577; 10.3049
90; 106.491; 90
696.15Lu, Zhiyao; Demianets, Ivan; Hamze, Rasha; Terrile, Nicholas J.; Williams, Travis J.
A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid
ACS Catalysis, 2016, 6, 2014
4513825 CIFC28 H33 B O2 SiP -19.8337; 11.7927; 12.4336
112.475; 96.966; 104.18
1254Ansell, Melvyn B.; Spencer, John; Navarro, Oscar
(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies
ACS Catalysis, 2016, 6, 2192
4513826 CIFC33 H49 N4 Pd Si2P -111.8802; 12.1897; 13.9679
86.341; 73.708; 63.295
1729.87Ansell, Melvyn B.; Spencer, John; Navarro, Oscar
(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies
ACS Catalysis, 2016, 6, 2192
4513827 CIFC28 H47 B N4 O2 Pd SiP 1 21/n 112.9381; 17.8318; 14.8311
90; 113.454; 90
3138.98Ansell, Melvyn B.; Spencer, John; Navarro, Oscar
(N-Heterocyclic Carbene)2-Pd(0)-Catalyzed Silaboration of Internal and Terminal Alkynes: Scope and Mechanistic Studies
ACS Catalysis, 2016, 6, 2192
4513837 CIFC23 H26 I2 Ir N3P 1 21/c 117.0173; 7.793; 19.3018
90; 103.52; 90
2488.79Semwal, Shrivats; Choudhury, Joyanta
Molecular Coordination-Switch in a New Role: Controlling Highly Selective Catalytic Hydrogenation with Switchability Function
ACS Catalysis, 2016, 6, 2424
4513838 CIFC23 H25 I Ir N3P -19.2675; 10.21; 12.0027
79.971; 78.553; 83.299
1092.13Semwal, Shrivats; Choudhury, Joyanta
Molecular Coordination-Switch in a New Role: Controlling Highly Selective Catalytic Hydrogenation with Switchability Function
ACS Catalysis, 2016, 6, 2424
4513839 CIFC21 H19 N O4P 21 21 217.32516; 13.4286; 19.6168
90; 90; 90
1929.64Wang, Gang; Liu, Xiaohua; Chen, Yushuang; Yang, Jian; Li, Jun; Lin, Lili; Feng, Xiaoming
Diastereoselective and Enantioselective Alleno-aldol Reaction of Allenoates with Isatins to Synthesis of Carbinol Allenoates Catalyzed by Gold
ACS Catalysis, 2016, 6, 2482
4513840 CIFC17 H10 F6 O2P 1 21/c 15.622; 15.483; 18.549
90; 94.841; 90
1608.8Fu, Ming-Chen; Shang, Rui; Cheng, Wan-Min; Fu, Yao
Nickel-Catalyzed Regio- and Stereoselective Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling
ACS Catalysis, 2016, 6, 2501
4513841 CIFC12 H12 O4P 1 21/n 14.5824; 19.9078; 12.0067
90; 94.374; 90
1092.13Fu, Ming-Chen; Shang, Rui; Cheng, Wan-Min; Fu, Yao
Nickel-Catalyzed Regio- and Stereoselective Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling
ACS Catalysis, 2016, 6, 2501
4513842 CIFC67 H16 B2 Cl2 F40 Fe4 O12 S4P c a 2117.7344; 14.2966; 30.6824
90; 90; 90
7779.3Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513843 CIFC36 H5 B F20 Fe2 O6 S2P b c a16.0418; 20.9445; 23.0959
90; 90; 90
7759.9Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513844 CIFC33 H7 B Cl2 F20 Fe2 O6 S2C 1 c 122.9134; 12.3868; 17.2161
90; 124.699; 90
4017.3Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513845 CIFC11 H7 F9 Fe2 O15 S5P 1 21/m 16.4147; 18.5996; 11.5206
90; 104.145; 90
1332.85Liu, Yu-Chiao; Chu, Kai-Ti; Huang, Yi-Lan; Hsu, Cheng-Huey; Lee, Gene-Hsiang; Tseng, Mei-Chun; Chiang, Ming-Hsi
Protonation/Reduction of Carbonyl-Rich Diiron Complexes and the Direct Observation of Triprotonated Species: Insights into the Electrocatalytic Mechanism of Hydrogen Formation
ACS Catalysis, 2016, 6, 2559
4513846 CIFC18 H16 OP 1 21 110.5879; 4.8182; 13.6534
90; 96.876; 90
691.51Rodríguez, Elsa; Grayson, Matthew N.; Asensio, Amparo; Barrio, Pablo; Houk, K. N.; Fustero, Santos
Chiral Brønsted Acid-Catalyzed Asymmetric Allyl(propargyl)boration Reaction ofortho-Alkynyl Benzaldehydes: Synthetic Applications and Factors Governing the Enantioselectivity
ACS Catalysis, 2016, 6, 2506
4513847 CIFC18 H14 OP 1 21 110.5044; 4.7708; 13.7318
90; 97.605; 90
682.11Rodríguez, Elsa; Grayson, Matthew N.; Asensio, Amparo; Barrio, Pablo; Houk, K. N.; Fustero, Santos
Chiral Brønsted Acid-Catalyzed Asymmetric Allyl(propargyl)boration Reaction ofortho-Alkynyl Benzaldehydes: Synthetic Applications and Factors Governing the Enantioselectivity
ACS Catalysis, 2016, 6, 2506
4513848 CIFC23 H33 Co N3 O4P 1 21/c 18.9984; 21.6663; 12.2395
90; 90.0826; 90
2386.24Schuster, Christopher H.; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes
ACS Catalysis, 2016, 6, 2632
4513849 CIFC21 H35 Co N3 O5P 1 21/c 18.9806; 29.3177; 8.8612
90; 97.9533; 90
2310.63Schuster, Christopher H.; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes
ACS Catalysis, 2016, 6, 2632

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