Crystallography Open Database

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Searching journal of publication like 'ACS Catalysis' volume of publication is 10

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4517169 CIFC11 H22 O2P b c a9.6851; 7.3807; 31.3965
90; 90; 90		2244.31Wu, Bin; Zhu, Rong
Radical Philicity Inversion in Co- and Fe-Catalyzed Hydrogen-Atom-Transfer-Initiated Cyclizations of Unsaturated Acylsilanes
ACS Catalysis, 2019, 10, 510
4517213 CIFC58 H52 F6 O4 P4 PdP 1 21/n 111.0969; 18.3586; 12.3866
90; 94.46; 90		2515.8Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517214 CIFC29 H30 Cl2 P2 PdP 1 21/c 111.3082; 17.6113; 13.8182
90; 92.789; 90		2748.7Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517215 CIFC36 H44 Cl4 P2 PdP b c a21.8565; 14.7082; 22.7524
90; 90; 90		7314.2Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517216 CIFC33 H38 Cl2 P2 PdP 1 21/n 111.2984; 20.6157; 14.14
90; 110.081; 90		3093.3Tay, Dillon W. P.; Nobbs, James D.; Romain, Charles; White, Andrew J. P.; Aitipamula, Srinivasulu; van Meurs, Martin; Britovsek, George J. P.
gem-Dialkyl Effect in Diphosphine Ligands: Synthesis, Coordination Behavior, and Application in Pd-Catalyzed Hydroformylation
ACS Catalysis, 2019, 10, 663
4517217 CIFC63 H56 B8 O16P -15.1932; 15.4161; 18.5227
72.871; 83.638; 89.832		1407.71Michigami, Kenichi; Sakaguchi, Tatsuhiko; Takemoto, Yoshiji
Catalytic Dehydrative Peptide Synthesis with gem-Diboronic Acids
ACS Catalysis, 2019, 10, 683
4517218 CIFC20 H40 O4 S Si4P 1 21/c 122.0893; 9.47947; 14.2315
90; 107.915; 90		2835.51Zhang, Zhikun; Hu, Xile
Arylsilylation of Electron-Deficient Alkenes via Cooperative Photoredox and Nickel Catalysis
ACS Catalysis, 2019, 10, 777
4517365 CIFC37 H36 Fe N O P SP 1 21 110.9997; 10.5162; 14.1245
90; 106.586; 90		1565.87Ji, Wangqin; Wu, Hai-Hong; Zhang, Junliang
Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki‒Miyaura Cross-coupling
ACS Catalysis, 2020, 10, 1548-1554
4517366 CIFC32 H23 O PP 1 21 19.5052; 11.4481; 11.0312
90; 93.722; 90		1197.84Ji, Wangqin; Wu, Hai-Hong; Zhang, Junliang
Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki‒Miyaura Cross-coupling
ACS Catalysis, 2020, 10, 1548-1554
4517367 CIFC38 H37 Cl3 Fe N O2 P SP 1 21 110.3729; 11.5112; 15.6134
90; 106.888; 90		1783.91Ji, Wangqin; Wu, Hai-Hong; Zhang, Junliang
Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki‒Miyaura Cross-coupling
ACS Catalysis, 2020, 10, 1548-1554
4517368 CIFC27 H24 F3 N O6 SP b c a13.5499; 15.2341; 24.4346
90; 90; 90		5043.8Uno, Hiroto; Imai, Takanori; Harada, Kyosuke; Shibata, Norio
Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
ACS Catalysis, 2020, 10, 1454-1459
4517369 CIFC16 H12 F3 N O4 SP -18.4561; 8.5762; 12.4229
110.047; 111.941; 90.1156		776.24Uno, Hiroto; Imai, Takanori; Harada, Kyosuke; Shibata, Norio
Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
ACS Catalysis, 2020, 10, 1454-1459
4517370 CIFC29 H29 F4 N O6 SP -19.4313; 11.4154; 13.8509
84.332; 74.645; 85.308		1428.55Uno, Hiroto; Imai, Takanori; Harada, Kyosuke; Shibata, Norio
Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
ACS Catalysis, 2020, 10, 1454-1459
4517383 CIFC31 H26 Br2 O4P 21 21 219.6286; 10.7523; 25.4679
90; 90; 90		2636.68Liu, Na; Zhu, Wanjiang; Yao, Jian; Yin, Long; Lu, Tao; Dou, Xiaowei
Catalyst-Controlled Chemodivergent Synthesis of Spirochromans from Diarylideneacetones and Organoboronic Acids
ACS Catalysis, 2020, 10, 2596-2602
4517384 CIFC24 H20 O3P -17.712; 10.915; 12.298
114.959; 99.228; 100.157		891.3Liu, Na; Zhu, Wanjiang; Yao, Jian; Yin, Long; Lu, Tao; Dou, Xiaowei
Catalyst-Controlled Chemodivergent Synthesis of Spirochromans from Diarylideneacetones and Organoboronic Acids
ACS Catalysis, 2020, 10, 2596-2602
4517385 CIFC53 H42 O2 P2P 1 21 18.89; 21.1643; 11.0358
90; 104.694; 90		2008.48Liu, Na; Zhu, Wanjiang; Yao, Jian; Yin, Long; Lu, Tao; Dou, Xiaowei
Catalyst-Controlled Chemodivergent Synthesis of Spirochromans from Diarylideneacetones and Organoboronic Acids
ACS Catalysis, 2020, 10, 2596-2602
4517476 CIFC23 H33 Br OP 1 21/c 115.7036; 13.5822; 9.9735
90; 97.264; 90		2110.2Takahashi, Toshifumi; Kurahashi, Takuya; Matsubara, Seijiro
Nickel-Catalyzed Intermolecular Carbobromination of Alkynes
ACS Catalysis, 2020, 10, 3773-3777
4517477 CIFC20 H21 Br OP -19.0497; 11.0964; 17.4034
80.749; 86.494; 89.645		1721.66Takahashi, Toshifumi; Kurahashi, Takuya; Matsubara, Seijiro
Nickel-Catalyzed Intermolecular Carbobromination of Alkynes
ACS Catalysis, 2020, 10, 3773-3777
4517481 CIFC21 H24 N4 OP -19.6626; 10.1376; 11.1294
97.909; 105.084; 114.113		923.2Tan, Jin-Fay; Bormann, Carl Thomas; Severin, Kay; Cramer, Nicolai
Alkynyl Triazenes as Fluoroalkyne Surrogates: Regioselective Access to 4-Fluoro-2-pyridones by a Rh(III)-Catalyzed C‒H Activation‒Lossen Rearrangement‒Wallach Reaction
ACS Catalysis, 2020, 10, 3790-3796
4517482 CIFC18 H14 F N OP -110.2367; 11.4102; 13.7829
109.851; 92.169; 112.466		1373.04Tan, Jin-Fay; Bormann, Carl Thomas; Severin, Kay; Cramer, Nicolai
Alkynyl Triazenes as Fluoroalkyne Surrogates: Regioselective Access to 4-Fluoro-2-pyridones by a Rh(III)-Catalyzed C‒H Activation‒Lossen Rearrangement‒Wallach Reaction
ACS Catalysis, 2020, 10, 3790-3796

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