Crystallography Open Database

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1517271 CIFC371 H328 B16 Co8 F64 N72 O26C 1 2/c 127.3936; 39.1227; 41.964
90; 107.152; 90
42973Cullen, William; Turega, Simon; Hunter, Christopher A.; Ward, Michael D.
pH-dependent binding of guests in the cavity of a polyhedral coordination cage: reversible uptake and release of drug molecules
Chem. Sci., 2015, 6, 625
1517459 CIFC46 H44 Cl2 F6 N O7 P3 Ru S2P 1 21 112.731; 15.301; 13.247
90; 109.038; 90
2439.3Wesselbaum, Sebastian; Moha, Verena; Meuresch, Markus; Brosinski, Sandra; Thenert, Katharina M.; Kothe, Jens; Stein, Thorsten vom; Englert, Ulli; Hölscher, Markus; Klankermayer, Jürgen; Leitner, Walter
Hydrogenation of carbon dioxide to methanol using a homogeneous ruthenium‒Triphos catalyst: from mechanistic investigations to multiphase catalysis
Chem. Sci., 2015, 6, 693
1517514 CIFC12 H12 F6 P TcP 1 21/c 113.8831; 9.8745; 9.719
90; 94.232; 90
1328.73Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517515 CIFC14 H16 F6 P TcP 1 21/n 17.7559; 11.003; 8.9353
90; 98.474; 90
754.2Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517516 CIFC18 H24 F6 P TcP 21 21 219.2697; 13.0695; 15.815
90; 90; 90
1916Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517517 CIFC20 H24 F6 P TcP 1 21/n 18.7563; 12.1899; 9.5187
90; 108.089; 90
965.8Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517518 CIFC21 H49 Al Cl7 N7 O7 TcP 1 21 18.8724; 23.5963; 9.6318
90; 96.888; 90
2001.92Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517671 CIFC22 H19 F O2P 1 21/c 115.5436; 8.7069; 12.5382
90; 92.769; 90
1694.9Alza, Esther; Laraia, Luca; Ibbeson, Brett M.; Collins, Súil; Galloway, Warren R. J. D.; Stokes, Jamie E.; Venkitaraman, Ashok R.; Spring, David R.
Synthesis of a novel polycyclic ring scaffold with antimitotic properties via a selective domino Heck‒Suzuki reaction
Chem. Sci., 2015, 6, 390
1517679 CIFC18 H18 B2 F8 N4P 1 21/n 17.9704; 9.6387; 26.395
90; 98.556; 90
2005.2Jo, Hyun Hwa; Edupuganti, Ramakrishna; You, Lei; Dalby, Kevin N.; Anslyn, Eric V.
Mechanistic Studies on Covalent Assemblies of Metal-Mediated Hemi-Aminal Ethers.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 158-164
1517680 CIFC39 H36 Ag3 F9 N12 O9.5 S3P 1 21/n 113.528; 20.05; 18.26
90; 107.1; 90
4733.8He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517681 CIFC40 H36 Ag5 F9 N12 O10 S4P 21 21 2110.57; 21.277; 23.103
90; 90; 90
5195.8He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517682 CIFC75 H72 Ag5 F9 N24 O9 S4C 1 2/c 123.725; 19.387; 18.732
90; 90.71; 90
8615He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517683 CIFC40 H36 Ag6 F10.5 N12 O16 S4.5P b c n12.772; 35.464; 25.664
90; 90; 90
11624He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517789 CIFC51 H54 O6P -113.7149; 15.9855; 20.8687
103.455; 105.879; 93.251
4244.3Chen, Huanqing; Fan, Jiazeng; Hu, Xiaoshi; Ma, Junwei; Wang, Shilu; Li, Jian; Yu, Yihua; Jia, Xueshun; Li, Chunju
Biphen[n]arenes
Chem. Sci., 2015, 6, 197
1517790 CIFC68 H72 O8P 1 21/c 111.5532; 30.664; 7.71
90; 90.771; 90
2731.2Chen, Huanqing; Fan, Jiazeng; Hu, Xiaoshi; Ma, Junwei; Wang, Shilu; Li, Jian; Yu, Yihua; Jia, Xueshun; Li, Chunju
Biphen[n]arenes
Chem. Sci., 2015, 6, 197
1517812 CIFC33 H30 Cl Co N4 O7P -110.4178; 12.0725; 13.2955
90.683; 110.55; 96.916
1551.7Liu, Dengfeng; Zhang, Xingmei; Zhu, Luqun; Wu, Jing; Lü, Xingqiang
Alternating ring-opening copolymerization of styrene oxide and maleic anhydride using asymmetrical bis-Schiff-base metal(iii) catalysts
Catal. Sci. Technol., 2015, 5, 562
1517813 CIFC35 H33 Br Cl Co N4 O7P -112.326; 12.7391; 13.0205
62.534; 82.794; 79.008
1779.1Liu, Dengfeng; Zhang, Xingmei; Zhu, Luqun; Wu, Jing; Lü, Xingqiang
Alternating ring-opening copolymerization of styrene oxide and maleic anhydride using asymmetrical bis-Schiff-base metal(iii) catalysts
Catal. Sci. Technol., 2015, 5, 562
1517834 CIFC16 H15 N5 O2P 1 21/c 111.641; 8.7512; 14.7356
90; 92.598; 90
1499.61Foy, Justin T.; Ray, Debdas; Aprahamian, Ivan
Regulating signal enhancement with coordination-coupled deprotonation of a hydrazone switch
Chem. Sci., 2015, 6, 209
1517835 CIFC19 H20.5 Cl N6.5 O7 ZnC 1 2/c 122.782; 7.5608; 26.996
90; 102.942; 90
4531.9Foy, Justin T.; Ray, Debdas; Aprahamian, Ivan
Regulating signal enhancement with coordination-coupled deprotonation of a hydrazone switch
Chem. Sci., 2015, 6, 209
1517851 CIFC23 H17 N O6P b c a21.073; 7.448; 23.393
90; 90; 90
3671.6Velasco, V.; Aguilà, D.; Barrios, L. A.; Borilovic, I.; Roubeau, O.; Ribas-Ariño, J.; Fumanal, M.; Teat, S. J.; Aromí, G.
New coordination features; a bridging pyridine and the forced shortest non-covalent distance between two CO32−species
Chem. Sci., 2015, 6, 123
1517852 CIFC111 H92 Co4 N16 O16C 1 2/c 116.833; 19.112; 30.84
90; 101.398; 90
9726Velasco, V.; Aguilà, D.; Barrios, L. A.; Borilovic, I.; Roubeau, O.; Ribas-Ariño, J.; Fumanal, M.; Teat, S. J.; Aromí, G.
New coordination features; a bridging pyridine and the forced shortest non-covalent distance between two CO32−species
Chem. Sci., 2015, 6, 123
1517853 CIFC194 H158 B2 Co8 F8 N24 Na4 O34P 1 21/c 118.4101; 17.6277; 30.4003
90; 106.78; 90
9445.7Velasco, V.; Aguilà, D.; Barrios, L. A.; Borilovic, I.; Roubeau, O.; Ribas-Ariño, J.; Fumanal, M.; Teat, S. J.; Aromí, G.
New coordination features; a bridging pyridine and the forced shortest non-covalent distance between two CO32−species
Chem. Sci., 2015, 6, 123
1517854 CIFC62 H87 N O7 S UP -114.4228; 14.8678; 15.4212
112.831; 96.488; 108.933
2772.5Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517855 CIFC64 H83 N O5 Se UP -116.827; 17.007; 19.804
88.022; 80.746; 82.903
5550.2Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517856 CIFC58 H77 N O5 Te UP -111.2439; 12.9994; 18.636
102.273; 101.519; 100.806
2531.7Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517857 CIFC124.5 H154.5 N2 O6 S2 U2P -111.1756; 16.817; 28.662
85.233; 87.451; 88.366
5361.1Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517858 CIFC126 H156 N2 O6 Se2 U2P -111.217; 16.815; 28.68
85.324; 87.434; 88.412
5384.5Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517859 CIFC150 H179.5 N2 O6.35 Te2 U2P -116.773; 16.923; 25.039
105.196; 102.968; 101.507
6426.8Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517870 CIFC21 H29 Cl N RhP -111.7956; 12.394; 13.9527
85.713; 81.671; 80.615
1988.5Hyster, Todd K.; Dalton, Derek M.; Rovis, Tomislav
Ligand Design for Rh(III)-Catalyzed C-H Activation: An Unsymmetrical Cyclopentadienyl Enables a Regioselective Synthesis of Dihydroisoquinolones.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 254-258
1517871 CIFC29 H17 Cl2 F12 Fe Hg3 P5P -111.733; 12.1852; 13.1641
85.129; 80.243; 74.103
1782.43Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517872 CIFC29 H17 As5 Cl2 F12 Fe Hg3P -111.9982; 13.3448; 14.1016
65.329; 78.072; 66.415
1878.24Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517873 CIFC9 H13 Fe P5P n m a11.4347; 23.4865; 15.1315
90; 90; 90
4063.73Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517874 CIFC13 H21 Fe P5P c a 2118.7588; 6.5778; 14.1509
90; 90; 90
1746.1Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517875 CIFC17 H29 Fe P5P 1 21/c 19.0507; 25.602; 10.1648
90; 115.783; 90
2120.87Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517876 CIFC31 H21 F12 Fe Hg3 P5P -112.0744; 12.2486; 14.5238
69.244; 82.395; 65.44
1826.58Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517877 CIFC36.5 H32 Cl3 F12 Fe Hg3 P5P 1 21 112.3145; 26.4751; 14.4338
90; 107.168; 90
4496.14Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517878 CIFC55 H53 As15 F12 Fe3 Hg3C 1 2/c 148.2155; 14.138; 22.3159
90; 109.887; 90
14304.9Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517879 CIFC19 H2 Cl2 F12 Hg3P -19.2776; 9.7199; 12.7689
103.463; 100.8; 97.447
1081.75Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517880 CIFC28 H15 Cl2 F12 Fe Hg3 P5P -111.6373; 11.8015; 15.7005
89.754; 68.252; 66.286
1806.94Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517881 CIFC26 H24 F18 Li2 O2P -19.0486; 12.7853; 14.6892
84.024; 74.906; 69.739
1539.05Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517882 CIFC28 H17 B F18P 1 21/n 19.1239; 24.4308; 12.5042
90; 97.114; 90
2765.78Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517883 CIFC36 H36 B NP 1 21/n 18.8391; 34.0268; 9.5807
90; 100.72; 90
2831.26Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517884 CIFC36 H18 B F18 NI 4123.5023; 23.5023; 25.182
90; 90; 90
13909.5Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517885 CIFC24 H9 B F18P b c a15.56; 8.7136; 35.624
90; 90; 90
4830Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517889 CIFC20 H20 N2 O3P 1 21 15.7962; 29.2094; 15.6928
90; 97.272; 90
2635.5Nelson, H. M.; Patel, J. S.; Shunatona, H. P.; Toste, F. D.
Enantioselective α-Amination Enabled by a BINAM-Derived Phase-Transfer Catalyst.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 170-173
1517951 CIFC252 H276 Co4 F36 N48 P6R -330.5162; 30.5162; 71.022
90; 90; 120
57278Symmers, P. R.; Burke, M. J.; August, D. P.; Thomson, P. I. T.; Nichol, G. S.; Warren, M. R.; Campbell, C. J.; Lusby, P. J.
Non-equilibrium cobalt(iii) “click” capsules
Chem. Sci., 2015, 6, 756
1517963 CIFF0.5 O32.5 Si16I m m m26.585; 24.926; 15.939
90; 90; 90
10562.1Jiang, Jiuxing; Yun, Yifeng; Zou, Xiaodong; Jorda, Jose Luis; Corma, Avelino
ITQ-54: a multi-dimensional extra-large pore zeolite with 20 ×14 ×12-ring channels
Chem. Sci., 2015, 6, 480
1517964 CIFC36 H30 Cl4 Ni P2P b c a17.435; 15.662; 24.139
90; 90; 90
6592Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517965 CIFC18 H15 Cl2 PP 1 21/c 113.338; 14.376; 8.7454
90; 102.53; 90
1637Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517966 CIFC19 H15 Cl F3 O3 P SP 1 21/n 111.255; 9.1501; 18.658
90; 93.04; 90
1918.8Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517967 CIFC40 H48 Cl4 Ni O4 P2P 1 21/n 110.1261; 23.4579; 17.8192
90; 106.355; 90
4061.4Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517970 CIFC12 H12 Au Br2 N OP -17.0801; 10.0993; 10.1771
97.689; 99.69; 92.96
708.82Wu, Qian; Du, Chenglong; Huang, Yumin; Liu, Xingyan; Long, Zhen; Song, Feijie; You, Jingsong
Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: insight into the mechanism of gold-catalyzed oxidative C(sp2)‒H arylation
Chem. Sci., 2015, 6, 288
1517971 CIFC18 H15 Au Br NP b c a15.9554; 11.7205; 16.839
90; 90; 90
3148.98Wu, Qian; Du, Chenglong; Huang, Yumin; Liu, Xingyan; Long, Zhen; Song, Feijie; You, Jingsong
Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: insight into the mechanism of gold-catalyzed oxidative C(sp2)‒H arylation
Chem. Sci., 2015, 6, 288
1517972 CIFC18 H16 Au Cl2 NP -17.8572; 8.2744; 15.3789
93.413; 103.381; 113.776
876.93Wu, Qian; Du, Chenglong; Huang, Yumin; Liu, Xingyan; Long, Zhen; Song, Feijie; You, Jingsong
Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: insight into the mechanism of gold-catalyzed oxidative C(sp2)‒H arylation
Chem. Sci., 2015, 6, 288
1517979 CIFC19 H16 N2 O3P 1 21 16.8436; 26.8023; 8.3932
90; 90.9; 90
1539.33Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517980 CIFC19 H16 N2 O3P 1 21 16.8507; 26.777; 8.4103
90; 90.84; 90
1542.63Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517981 CIFC26 H22 N2 O3P 1 21 15.4249; 16.5948; 11.417
90; 98.277; 90
1017.11Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517982 CIFC26 H22 N2 O3P 1 21 15.4288; 16.6067; 11.4114
90; 98.2867; 90
1018.05Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517983 CIFC57 H49.5 Eu N6 O11.5C 2 2 2126.0015; 26.4029; 30.8305
90; 90; 90
21165.6Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517990 CIFC197.82 H137.82 Cl5.46C 1 2 153.108; 21.244; 26.197
90; 98.53; 90
29229Matsuno, Taisuke; Sato, Sota; Iizuka, Ryosuke; Isobe, Hiroyuki
Molecular recognition in curved π-systems: effects of π-lengthening of tubular molecules on thermodynamics and structures
Chem. Sci., 2015, 6, 909
1518019 CIFC36 H66 Al Cl5 P2 Pb PtP c a 2125.2527; 13.9068; 24.7327
90; 90; 90
8685.7Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518020 CIFC120 H156 B2 Cl18 P4 Pb2 Pt2P -110.5092; 15.3892; 20.0776
109.785; 90.439; 90.796
3054.9Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518021 CIFC36 H66 Al Cl4 I P2 Pb PtP -113.381; 13.612; 13.987
92.698; 111.864; 101.984
2291Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518022 CIFC36 H66 Al2 Cl8 P2 Pb PtC 1 2/c 120.719; 10.6901; 23.859
90; 111.311; 90
4923.1Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518023 CIFC72 H132 Br2 P4 Pt2 SnP -113.9687; 14.2448; 21.1628
96.439; 101.9; 114.878
3643.1Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518024 CIFC36 H66 Al Br5 P2 Pt SnP -111.5394; 12.469; 17.7
105.191; 100.053; 107.994
2245.2Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518025 CIFC60 H78 B Br Cl8 P2 Pt SnP -113.5049; 15.4437; 15.6528
82.203; 78.913; 85.651
3169.9Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518026 CIFC36 H66 Al2 Br8 P2 Pt SnP 1 21/n 113.2989; 22.907; 16.964
90; 99.008; 90
5104.1Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518027 CIFC56 H110 Br3 N O P2 Pt SnP -115.687; 20.715; 21.567
75.297; 82.231; 78.538
6617Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518028 CIFC36 H49.5 Cl F12 Fe Li2 N O6P -112.26; 12.5792; 15.8788
75.171; 71.664; 67.768
2125.4Pascualini, M. E.; Di Russo, N. V.; Thuijs, A. E.; Ozarowski, A.; Stoian, S. A.; Abboud, K. A.; Christou, G.; Veige, A. S.
A high-spin square-planar Fe(ii) complex stabilized by a trianionic pincer-type ligand and conclusive evidence for retention of geometry and spin state in solution
Chem. Sci., 2015, 6, 608
1518079 CIFC12 As2 F21 Se2P -18.5406; 8.5891; 14.093
84.9; 84.781; 88.091
1025.1Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518080 CIFC48 H50 S2P 1 21/n 115.695; 15.264; 16.274
90; 93.45; 90
3891.7Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518081 CIFC48 H50 F6 S2 SbP 1 21/n 116.17; 15.837; 17.339
90; 92.97; 90
4434.3Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518082 CIFC49 H52 Cl2 F6 Sb Se2P 1 21/c 119.147; 15.238; 16.653
90; 90.08; 90
4859Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518083 CIFC51 H55 F6 N Sb Te2C 1 2/c 119.854; 14.726; 17.178
90; 92.07; 90
5019Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518084 CIFC12 F21 S2 Sb2P 1 21/n 112.029; 12.276; 14.44
90; 97.662; 90
2113.3Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518097 CIFC60 H78 Cl2 Ir N2 O6.5 P2 S2P -111.6106; 17.2668; 18.6161
113.198; 95.475; 105.211
3226Oldenhof, Sander; Lutz, Martin; de Bruin, Bas; Ivar van der Vlugt, Jarl; Reek, Joost N. H.
Dehydrogenation of formic acid by Ir‒bisMETAMORPhos complexes: experimental and computational insight into the role of a cooperative ligand
Chem. Sci., 2015, 6, 1027
1518098 CIFC30 H25 N O4P -112.1231; 12.9429; 17.2915
95.734; 108.021; 113.144
2295Berger, Reinhard; Wagner, Manfred; Feng, Xinliang; Müllen, Klaus
Polycyclic aromatic azomethine ylides: a unique entry to extended polycyclic heteroaromatics
Chem. Sci., 2015, 6, 436
1518099 CIFC38.5 H20 Cl F10 NP -112.6166; 16.35; 16.738
87.227; 75.478; 67.501
3083.7Berger, Reinhard; Wagner, Manfred; Feng, Xinliang; Müllen, Klaus
Polycyclic aromatic azomethine ylides: a unique entry to extended polycyclic heteroaromatics
Chem. Sci., 2015, 6, 436
1518122 CIFC28 H39 Br O4P 1 21/c 19.3571; 16.7917; 17.242
90; 101.238; 90
2657.1Ghiggino, Kenneth P.; Tilley, Andrew J.; Robotham, Benjamin; White, Jonathan M.
Excited state dynamics of organic semi-conducting materials.
Faraday discussions, 2015, 177, 111-119
1518139 CIFC40 H60 Cu3 K N8 O54 Ru Si W11P -4 21 m24.415; 24.415; 15.337
90; 90; 90
9142Shi, Dongying; He, Cheng; Qi, Bo; Chen, Cong; Niu, Jingyang; Duan, Chunying
Merging of the photocatalysis and copper catalysis in metal‒organic frameworks for oxidative C‒C bond formation
Chem. Sci., 2015, 6, 1035
1518140 CIFC40 H58 Cu2 K N8 O52 Ru Si W11P c c n17.8663; 22.1923; 22.2835
90; 90; 90
8835.3Shi, Dongying; He, Cheng; Qi, Bo; Chen, Cong; Niu, Jingyang; Duan, Chunying
Merging of the photocatalysis and copper catalysis in metal‒organic frameworks for oxidative C‒C bond formation
Chem. Sci., 2015, 6, 1035
1518141 CIFC13 H14 N2 O2P 1 21/c 111.6434; 10.03245; 20.857
90; 103.161; 90
2372.35Brachet, E.; Ghosh, T.; Ghosh, I.; König, B.
Visible light C‒H amidation of heteroarenes with benzoyl azides
Chem. Sci., 2015, 6, 987
1518142 CIFC13 H10 N2 O4P 1 21/n 18.3156; 9.9732; 14.574
90; 102.762; 90
1178.81Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518143 CIFC13 H9 N2 O4P 1 21 18.3745; 10.0838; 14.5833
90; 103.496; 90
1197.51Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518144 CIFC13 H9 F N2 O4P 1 21/c 17.24677; 14.8112; 11.0943
90; 99.3083; 90
1175.11Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518145 CIFC13 H9 F N2 O4P 1 21 17.1667; 5.2718; 15.7374
90; 101.26; 90
583.14Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518146 CIFC13 H9 F N2 O4P 1 21 17.1322; 5.2282; 15.7662
90; 101.237; 90
576.63Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518147 CIFC13 H9 F N2 O4P 21 21 216.56098; 13.5445; 13.6122
90; 90; 90
1209.65Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518148 CIFC12 H40 B4 N4 O6P 1 21/n 116.026; 8.7017; 17.485
90; 115.469; 90
2201.4Kalviri, Hassan A.; Gärtner, Felix; Ye, Gang; Korobkov, Ilia; Baker, R. Tom
Probing the second dehydrogenation step in ammonia-borane dehydrocoupling: characterization and reactivity of the key intermediate, B-(cyclotriborazanyl)amine-borane
Chem. Sci., 2015, 6, 618
1518149 CIFC4 H26 B4 N4 O2P -16.9419; 8.8077; 12.4471
91.79; 103.761; 111.731
680.64Kalviri, Hassan A.; Gärtner, Felix; Ye, Gang; Korobkov, Ilia; Baker, R. Tom
Probing the second dehydrogenation step in ammonia-borane dehydrocoupling: characterization and reactivity of the key intermediate, B-(cyclotriborazanyl)amine-borane
Chem. Sci., 2015, 6, 618
1518154 CIFC22 H22.5 B Cl Cr F4 N4.5 O3P b c n14.5572; 13.9044; 24.0822
90; 90; 90
4874.5Kotani, Hiroaki; Kaida, Suzue; Ishizuka, Tomoya; Sakaguchi, Miyuki; Ogura, Takashi; Shiota, Yoshihito; Yoshizawa, Kazunari; Kojima, Takahiko
Formation and characterization of a reactive chromium(v)‒oxo complex: mechanistic insight into hydrogen-atom transfer reactions
Chem. Sci., 2015, 6, 945
1518155 CIFC21 H20 B2 Cr F8 N5 O2P 1 21/c 19.683; 22.83; 11.317
90; 104.712; 90
2419.7Kotani, Hiroaki; Kaida, Suzue; Ishizuka, Tomoya; Sakaguchi, Miyuki; Ogura, Takashi; Shiota, Yoshihito; Yoshizawa, Kazunari; Kojima, Takahiko
Formation and characterization of a reactive chromium(v)‒oxo complex: mechanistic insight into hydrogen-atom transfer reactions
Chem. Sci., 2015, 6, 945
1518167 CIFC51 H99 K N2 O6 Si6 ThP -112.1595; 12.7622; 22.2587
100.93; 104.448; 95.5814
3246.1Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518168 CIFC53 H103 K O8 Si6 ThP 1 21/n 117.1884; 18.0161; 22.654
90; 99.6558; 90
6915.8Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518169 CIFC33 H63 Si6 ThP 1 21/c 117.547; 13.6955; 19.1293
90; 112.595; 90
4244.2Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518170 CIFC30 H50 Si4 ThC 1 2/c 120.2007; 8.1694; 19.9544
90; 91.3531; 90
3292.1Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518200 CIFC28 H20 N4P -17.8497; 10.7861; 14.7876
109.56; 91.8983; 111.312
1081.87Rijeesh, K.; Hashim, P. K.; Noro, Shin-ichiro; Tamaoki, Nobuyuki
Dynamic induction of enantiomeric excess from a prochiral azobenzene dimer under circularly polarized light
Chem. Sci., 2015, 6, 973
1518209 CIFC11 H7 Au Cl2 F NP 1 21/c 19.1445; 7.8648; 15.71
90; 106.294; 90
1084.5Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518210 CIFC24 H18 Au F2 NP -114.8527; 16.3867; 17.62
90.156; 91.414; 114.256
3908.3Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518211 CIFC27 H20 Au Cl2 F6 NP -19.334; 11.4331; 12.8416
73.407; 81.938; 73.869
1258.9Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518212 CIFC24 H18 Au N3 O4P b c n11.1263; 14.1527; 26.2319
90; 90; 90
4130.7Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518213 CIFC28 H20 Au N S2I 41/a35.5669; 35.5669; 7.2973
90; 90; 90
9231.1Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518214 CIFC26 H24 Au NP 1 21/n 17.5722; 16.2301; 16.7076
90; 93.349; 90
2049.8Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518215 CIFC30 H32 Au N O2C 1 2/c 119.4071; 15.6565; 19.6251
90; 112.078; 90
5525.8Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518216 CIFC18 H14 Au Cl F NP 1 21/c 19.4066; 13.227; 13.1786
90; 110.251; 90
1538.3Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518217 CIFC22 H17 Au Cl NP 1 21/c 110.34; 18.881; 9.579
90; 110.408; 90
1752.7Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518218 CIFC20.62 H17.23 Au Cl1.23 N OP c a 2122.3204; 11.4097; 7.0554
90; 90; 90
1796.79Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518219 CIFC34 H30 Br2 N2 O2 S2P 1 21/c 16.8071; 21.415; 10.9248
90; 102.159; 90
1556.8Welterlich, Irina; Neudörfl, Jörg-Martin; Tieke, Bernd
Electrochemical polymerization of 1,3,4,6-tetraarylpyrrolo[3,2-b]pyrrole-2,5-dione (isoDPP) derivatives
Polym. Chem., 2015, 6, 1005
1518232 CIFC48 H30 F6 O4C 1 2/c 113.07527; 16.18867; 19.01027
90; 100.1; 90
3961.57Rives, Arnaud; Baglai, Iaroslav; Barthes, Cécile; Maraval, Valérie; Saffon-Merceron, Nathalie; Saquet, Alix; Voitenko, Zoia; Volovenko, Yulian; Chauvin, Remi
Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties
Chem. Sci., 2015, 6, 1139
1518233 CIFC47 H28 Cl2 F6 O2P -112.5119; 12.6648; 14.9565
70.805; 66.621; 67.665
1967.5Rives, Arnaud; Baglai, Iaroslav; Barthes, Cécile; Maraval, Valérie; Saffon-Merceron, Nathalie; Saquet, Alix; Voitenko, Zoia; Volovenko, Yulian; Chauvin, Remi
Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties
Chem. Sci., 2015, 6, 1139
1518234 CIFC49 H25 Cl3 F12 O2P 1 21/c 112.8182; 35.815; 9.7626
90; 92.841; 90
4476.3Rives, Arnaud; Baglai, Iaroslav; Barthes, Cécile; Maraval, Valérie; Saffon-Merceron, Nathalie; Saquet, Alix; Voitenko, Zoia; Volovenko, Yulian; Chauvin, Remi
Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties
Chem. Sci., 2015, 6, 1139
1518239 CIFC42 H44 Cl6 Fe N4F d d 219.23; 43.035; 10.2776
90; 90; 90
8505.4Fillman, Kathlyn L.; Przyojski, Jacob A.; Al-Afyouni, Malik H; Tonzetich, Zachary J.; Neidig, Michael L.
A combined magnetic circular dichroism and density functional theory approach for the elucidation of electronic structure and bonding in three- and four-coordinate iron(II)-N-heterocyclic carbene complexes.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1178-1188
1518240 CIFC35 H54 Fe N2 Si2C 1 2/c 110.777; 19.521; 18.542
90; 103.339; 90
3796Fillman, Kathlyn L.; Przyojski, Jacob A.; Al-Afyouni, Malik H; Tonzetich, Zachary J.; Neidig, Michael L.
A combined magnetic circular dichroism and density functional theory approach for the elucidation of electronic structure and bonding in three- and four-coordinate iron(II)-N-heterocyclic carbene complexes.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1178-1188
1518241 CIFC6 H18 Cl2 Fe P2P -17.6475; 12.4439; 15.3186
102.743; 95.406; 101.351
1379.6Fillman, Kathlyn L.; Przyojski, Jacob A.; Al-Afyouni, Malik H; Tonzetich, Zachary J.; Neidig, Michael L.
A combined magnetic circular dichroism and density functional theory approach for the elucidation of electronic structure and bonding in three- and four-coordinate iron(II)-N-heterocyclic carbene complexes.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1178-1188
1518242 CIFC81 H86 Cl6 N6 O8 Rh2P 21 21 2113.919; 19.144; 28.616
90; 90; 90
7625Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518243 CIFC39 H40 Cl2 F6 N4 O2 P RhP 21 21 2113.1445; 13.6427; 22.5166
90; 90; 90
4037.8Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518244 CIFC14 H18 N2 O5P 21 21 215.4571; 15.3289; 17.4084
90; 90; 90
1456.24Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518245 CIFC22 H26 N2 O4P 1 21/c 110.1905; 11.5731; 17.4203
90; 97.5045; 90
2036.88Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518246 CIFC51 H52 Cl4 F6 N4 O3 P RhP n a 2117.7761; 22.9437; 13.1111
90; 90; 90
5347.4Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518247 CIFC47 H45 Cl2 Ir N4 O3C 1 2/c 138.9286; 13.3583; 17.0015
90; 111.479; 90
8227.1Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518248 CIFC98 H110 B Cl2 F20 N6 Nb2P 1 21/c 114.224; 21.737; 31.247
90; 90.83; 90
9660Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518249 CIFC65 H66 B F20 N3 Nb O2P 1 21/c 118.1669; 17.1279; 19.7092
90; 90.559; 90
6132.4Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518250 CIFC95 H110 B Cl9 F20 N6 Nb2P 1 21/c 120.744; 20.888; 22.683
90; 90.709; 90
9827.8Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518251 CIFC61 H60 B Cl0 F20 N4 NbP 1 n 115.2666; 16.9177; 25.577
90; 97.658; 90
6547Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518252 CIFC24 H28 B2 Cl6 Fe N8 O6C 1 2/c 124.287; 8.1945; 20.396
90; 120.269; 90
3505.8Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518253 CIFC31 H44 B2 Fe N8 O9P -110.435; 12.522; 14.568
110.05; 98.25; 92.93
1759.4Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518254 CIFC270 H327 B29.5 F22 Fe12 N96 O73.5 Pd6F 4 3 277.1812; 77.1812; 77.1812
90; 90; 90
459764Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518255 CIFC193 H230 B12 Fe6 N59 O53 Pd3P -124.07; 25.09; 26.26
111.25; 101.84; 110.6
12790Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518256 CIFC453.5 H476.75 B33.75 F9 Fe12 N100.75 O83.5 Pd6P -137.76; 37.914; 49.64
109.87; 111.57; 90.72
61382Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518257 CIFC350 H400 B24 Fe12 N105 O99 Pd6P -126.3697; 37.7311; 41.401
113.826; 96.68; 90.021
37375Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518275 CIFC14 H19 N OC 1 2 17.0592; 9.6718; 18.5618
90; 91.179; 90
1267.04Cui, Xin; Xu, Xue; Jin, Li-Mei; Wojtas, Lukasz; Zhang, X. Peter
Stereoselective Radical C-H Alkylation with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1219-1224
1518276 CIFC12 H14 O4 SP 1 21 16.7037; 10.0938; 9.5452
90; 108.132; 90
613.81Cui, Xin; Xu, Xue; Jin, Li-Mei; Wojtas, Lukasz; Zhang, X. Peter
Stereoselective Radical C-H Alkylation with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1219-1224
1518277 CIFC12 H11 Cl2 F O4 SP 21 21 217.7539; 8.4364; 22.2865
90; 90; 90
1457.87Cui, Xin; Xu, Xue; Jin, Li-Mei; Wojtas, Lukasz; Zhang, X. Peter
Stereoselective Radical C-H Alkylation with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1219-1224
1518278 CIFC20 H20 N2 O3 SC 1 2/c 111.5572; 15.5085; 20.8957
90; 94.733; 90
3732.5Zhou, Ai-Hua; He, Qiao; Shu, Chao; Yu, Yong-Fei; Liu, Shuang; Zhao, Tian; Zhang, Wei; Lu, Xin; Ye, Long-Wu
Atom-economic generation of gold carbenes: gold-catalyzed formal [3+2] cycloaddition between ynamides and isoxazoles
Chem. Sci., 2015, 6, 1265
1518279 CIFC24 H20 N2 O2P 21 21 217.58; 13.2149; 18.5282
90; 90; 90
1855.95Hesping, Lena; Biswas, Anup; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Studer, Armido
Stereoselective Lewis base catalyzed formal 1,3-dipolar cycloaddition of azomethine imines with mixed anhydrides
Chem. Sci., 2015, 6, 1252
1518280 CIFC12 H12 O6P 1 21/c 17.6482; 7.4766; 10.4304
90; 102.535; 90
582.22Zhang, Quanxuan; Ren, Hong; Baker, Gregory L.
Synthesis and click chemistry of a new class of biodegradable polylactide towards tunable thermo-responsive biomaterials.
Polymer chemistry, 2015, 6, 1275-1285
1518308 CIFC90 H64 F24 N14 P4 Ru2P -113.811; 18.252; 20.803
84.81; 82.76; 72.33
4949Cui, Bin-Bin; Mao, Zupan; Chen, Yuxia; Zhong, Yu-Wu; Yu, Gui; Zhan, Chuanlang; Yao, Jiannian
Tuning of resistive memory switching in electropolymerized metallopolymeric films
Chem. Sci., 2015, 6, 1308
1518309 CIFC12 H26 Co3 N2 O14 P2C 1 2/c 123.446; 9.956; 19.018
90; 98.983; 90
4385Zhou, Tianhua; Wang, Danping; Chun-Kiat Goh, Simon; Hong, Jindui; Han, Jianyu; Mao, Jianggao; Xu, Rong
Bio-inspired organic cobalt(ii) phosphonates toward water oxidation
Energy Environ. Sci., 2015, 8, 526
1518310 CIFC12 H28 Ba3 O26I 1 2/a 113.4109; 16.2568; 27.9028
90; 98.984; 90
6008.7Boon, Matthew P.; Freeman, Sandra; Ogden, Mark I.; Oliveira, Allan; Richmond, William R.; Skelton, Brian W.; Jones, Franca
The many roles of mellitic acid during barium sulfate crystallization.
Faraday discussions, 2015, 179, 343-357
1518313 CIFC72 H68 F24 N26 O2 P4 Ru2I 1 2/a 124.007; 14.6606; 26.57
90; 92.563; 90
9342.1Kumar, Sreedhar V.; Lo, Warrick K.C.; Brooks, Heather J.L.; Crowley, James D.
Synthesis, structure, stability and antimicrobial activity of a ruthenium(II) helicate derived from a bis-bidentate "click" pyridyl-1,2,3-triazole ligand
Inorganica Chimica Acta, 2015, 425, 1-6
1518314 CIFC18 H17 Cd N2 O4P 1 21/c 17.3532; 15.123; 15.554
90; 103.11; 90
1684.6Ran, Yungen; Xie, Jixing; Mu, Yajuan; Zhang, Linfen; Han, Bo
A series of 2D Cd(II) coordination polymers constructed from dicarboxylate acids and a flexible imidazole-based ligand
Inorganica Chimica Acta, 2015, 425, 17-27
1518315 CIFC29 H34 Cd N4 O5P b c a17.061; 14.6879; 22.0163
90; 90; 90
5517.1Ran, Yungen; Xie, Jixing; Mu, Yajuan; Zhang, Linfen; Han, Bo
A series of 2D Cd(II) coordination polymers constructed from dicarboxylate acids and a flexible imidazole-based ligand
Inorganica Chimica Acta, 2015, 425, 17-27
1518316 CIFC56 H66 Cd2 N8 O11P 1 2/n 115.69; 9.0941; 21.264
90; 101.23; 90
2976Ran, Yungen; Xie, Jixing; Mu, Yajuan; Zhang, Linfen; Han, Bo
A series of 2D Cd(II) coordination polymers constructed from dicarboxylate acids and a flexible imidazole-based ligand
Inorganica Chimica Acta, 2015, 425, 17-27
1518317 CIFC24 H32 Cd N2 O5P -17.7525; 12.7608; 13.0438
71.42; 82.875; 74.766
1179Ran, Yungen; Xie, Jixing; Mu, Yajuan; Zhang, Linfen; Han, Bo
A series of 2D Cd(II) coordination polymers constructed from dicarboxylate acids and a flexible imidazole-based ligand
Inorganica Chimica Acta, 2015, 425, 17-27
1518318 CIFC26 H38 Cd N4 O6P -111.4475; 11.593; 13.3747
76.497; 78.592; 64.39
1546.82Ran, Yungen; Xie, Jixing; Mu, Yajuan; Zhang, Linfen; Han, Bo
A series of 2D Cd(II) coordination polymers constructed from dicarboxylate acids and a flexible imidazole-based ligand
Inorganica Chimica Acta, 2015, 425, 17-27
1518319 CIFC4 H5 Cd Cl N2 O3P 1 21/n 17.0184; 10.3158; 10.6545
90; 107.051; 90
737.48Liu, Guang-Ning; Zhu, Wen-Juan; Chu, Ya-Nan; Li, Cuncheng
Three d10 metal coordination compounds based on pyrazole-3-carboxylic acid showing mixed-ligand characteristic: Syntheses, crystal structures, and photoluminescent properties
Inorganica Chimica Acta, 2015, 425, 28-35
1518320 CIFC28 H19 Cd Cl N6 O6P 1 21/n 115.0658; 13.145; 15.5206
90; 112.932; 90
2830.78Liu, Guang-Ning; Zhu, Wen-Juan; Chu, Ya-Nan; Li, Cuncheng
Three d10 metal coordination compounds based on pyrazole-3-carboxylic acid showing mixed-ligand characteristic: Syntheses, crystal structures, and photoluminescent properties
Inorganica Chimica Acta, 2015, 425, 28-35
1518321 CIFC28 H28 N8 O8 Zn2P -18.8834; 9.2233; 9.4907
95.785; 100.198; 101.908
741.21Liu, Guang-Ning; Zhu, Wen-Juan; Chu, Ya-Nan; Li, Cuncheng
Three d10 metal coordination compounds based on pyrazole-3-carboxylic acid showing mixed-ligand characteristic: Syntheses, crystal structures, and photoluminescent properties
Inorganica Chimica Acta, 2015, 425, 28-35
1518322 CIFC16 H17 N3 O2P b c a11.4611; 8.8278; 28.757
90; 90; 90
2909.5Mishra, Monika; Tiwari, Karishma; Singh, Ashish Kumar; Singh, Vinod P.
Versatile coordination behaviour of a multi-dentate Schiff base with manganese(II), copper(II) and zinc(II) ions and their corrosion inhibition study
Inorganica Chimica Acta, 2015, 425, 36-45
1518323 CIFC19 H21 N3 O2C 1 2/c 126.243; 10.56; 13.89
90; 119.44; 90
3352Mishra, Monika; Tiwari, Karishma; Singh, Ashish Kumar; Singh, Vinod P.
Versatile coordination behaviour of a multi-dentate Schiff base with manganese(II), copper(II) and zinc(II) ions and their corrosion inhibition study
Inorganica Chimica Acta, 2015, 425, 36-45
1518324 CIFC32 H32 Mn N6 O4P n a 2120.213; 11.155; 13.117
90; 90; 90
2958Mishra, Monika; Tiwari, Karishma; Singh, Ashish Kumar; Singh, Vinod P.
Versatile coordination behaviour of a multi-dentate Schiff base with manganese(II), copper(II) and zinc(II) ions and their corrosion inhibition study
Inorganica Chimica Acta, 2015, 425, 36-45
1518325 CIFC18 H21 Cu N3 O3 SP 1 21/c 110.1639; 9.6526; 18.9701
90; 91.74; 90
1860.26Mishra, Monika; Tiwari, Karishma; Singh, Ashish Kumar; Singh, Vinod P.
Versatile coordination behaviour of a multi-dentate Schiff base with manganese(II), copper(II) and zinc(II) ions and their corrosion inhibition study
Inorganica Chimica Acta, 2015, 425, 36-45
1518326 CIFC18 H21 N3 O3 S ZnP -19.004; 13.522; 17.296
79.133; 75.504; 71.182
1916.4Mishra, Monika; Tiwari, Karishma; Singh, Ashish Kumar; Singh, Vinod P.
Versatile coordination behaviour of a multi-dentate Schiff base with manganese(II), copper(II) and zinc(II) ions and their corrosion inhibition study
Inorganica Chimica Acta, 2015, 425, 36-45
1518327 CIFC10 H8 N10 O4 ZnP 1 21/c 18.06; 14.0316; 13.4153
90; 97.456; 90
1504.4Mautner, Franz A.; Scherzer, Michael; Berger, Christian; Fischer, Roland C.; Massoud, Salah S.
Synthesis, characterization and luminescence properties of zinc(II) complexes of pseudohalides and nitrite derived from 4-azidopyridine
Inorganica Chimica Acta, 2015, 425, 46-51
1518328 CIFC12 H8 N10 O2 ZnP -15.5546; 9.0633; 15.527
74.72; 80.86; 78.21
733.6Mautner, Franz A.; Scherzer, Michael; Berger, Christian; Fischer, Roland C.; Massoud, Salah S.
Synthesis, characterization and luminescence properties of zinc(II) complexes of pseudohalides and nitrite derived from 4-azidopyridine
Inorganica Chimica Acta, 2015, 425, 46-51
1518329 CIFC10 H8 N14 ZnP -18.1876; 8.2228; 11.8147
109.876; 91.188; 98.745
737.1Mautner, Franz A.; Scherzer, Michael; Berger, Christian; Fischer, Roland C.; Massoud, Salah S.
Synthesis, characterization and luminescence properties of zinc(II) complexes of pseudohalides and nitrite derived from 4-azidopyridine
Inorganica Chimica Acta, 2015, 425, 46-51
1518330 CIFC22 H16 N18 S2 ZnP 1 21/c 119.0082; 7.8756; 20.9499
90; 115.916; 90
2820.83Mautner, Franz A.; Scherzer, Michael; Berger, Christian; Fischer, Roland C.; Massoud, Salah S.
Synthesis, characterization and luminescence properties of zinc(II) complexes of pseudohalides and nitrite derived from 4-azidopyridine
Inorganica Chimica Acta, 2015, 425, 46-51
1518331 CIFC5 H8 Ag Br2 N2P 1 21/a 18.2464; 12.5278; 9.1307
90; 104.737; 90
912.26Zhang, Wen-Li; Huang, Zhi-Peng; Ma, Cheng-Jie; Zai, Yu-Xia; Yang, Qing; Niu, Yun-Yin
Novel bis(methylimidazolium) alkane bolaamphiphiles as templates for the construction of haloclusters supramolecules
Inorganica Chimica Acta, 2015, 425, 52-60
1518332 CIFC10 H16 Ag2 I4 N4P -17.061; 7.702; 9.321
87.062; 85.931; 69.444
473.3Zhang, Wen-Li; Huang, Zhi-Peng; Ma, Cheng-Jie; Zai, Yu-Xia; Yang, Qing; Niu, Yun-Yin
Novel bis(methylimidazolium) alkane bolaamphiphiles as templates for the construction of haloclusters supramolecules
Inorganica Chimica Acta, 2015, 425, 52-60
1518333 CIFC12 H20 Ag2 Br4 N4P 1 21/a 17.049; 21.8537; 13.1219
90; 93.54; 90
2017.53Zhang, Wen-Li; Huang, Zhi-Peng; Ma, Cheng-Jie; Zai, Yu-Xia; Yang, Qing; Niu, Yun-Yin
Novel bis(methylimidazolium) alkane bolaamphiphiles as templates for the construction of haloclusters supramolecules
Inorganica Chimica Acta, 2015, 425, 52-60
1518334 CIFC11 H14 Cu2 N5 S3P -18.1184; 10.2788; 11.1619
107.439; 104.091; 94.198
851.06Zhang, Wen-Li; Huang, Zhi-Peng; Ma, Cheng-Jie; Zai, Yu-Xia; Yang, Qing; Niu, Yun-Yin
Novel bis(methylimidazolium) alkane bolaamphiphiles as templates for the construction of haloclusters supramolecules
Inorganica Chimica Acta, 2015, 425, 52-60
1518335 CIFC11 H16 Cu N4 S2P 1 21/c 15.9561; 12.4658; 20.3391
90; 98.649; 90
1492.96Zhang, Wen-Li; Huang, Zhi-Peng; Ma, Cheng-Jie; Zai, Yu-Xia; Yang, Qing; Niu, Yun-Yin
Novel bis(methylimidazolium) alkane bolaamphiphiles as templates for the construction of haloclusters supramolecules
Inorganica Chimica Acta, 2015, 425, 52-60
1518336 CIFC75 H45 Fe11 O62.23P -114.6; 14.602; 23.236
99.165; 99.281; 94.805
4795.9Mal, Sunit K.; Mitra, Merry; Biswas, Bhaskar; Kaur, Gurpreet; Bag, Partha P.; Reddy, C. Malla; Choudhury, Angshuman Roy; Aliaga-Alcalde, Nuria; Ghosh, Rajarshi
Ligand template synthesis of an undecametallic iron(III) complex: X-ray structure, magnetism and catecholase activity
Inorganica Chimica Acta, 2015, 425, 61-66
1518337 CIFC75 H60 B Cl3 F24 Ir2 N2P -119.0059; 21.9914; 22.092
114.003; 107.666; 99.412
7588Corre, Y.; Iali, W.; Hamdaoui, M.; Trivelli, X.; Djukic, J.-P.; Agbossou-Niedercorn, F.; Michon, C.
Efficient hydrosilylation of imines using catalysts based on iridium(iii) metallacycles
Catal. Sci. Technol., 2015, 5, 1452
1518338 CIFC36 H54 F18 N15 P3 Ru3 S9C 1 2 127.5079; 16.0629; 14.4082
90; 108.033; 90
6053.6Zubi, Ahmed; Wragg, Ashley; Turega, Simon; Adams, Harry; Costa, Paulo J.; Félix, Vítor; Thomas, Jim A.
Modulating the electron-transfer properties of a mixed-valence system through host‒guest chemistry
Chem. Sci., 2015, 6, 1334
1518339 CIFC15 H12 Au N O2P -17.3807; 11.755; 15.94
102.912; 92.025; 100.595
1320.8Seki, Tomohiro; Sakurada, Kenta; Muromoto, Mai; Ito, Hajime
Photoinduced single-crystal-to-single-crystal phase transition and photosalient effect of a gold(i) isocyanide complex with shortening of intermolecular aurophilic bonds
Chem. Sci., 2015, 6, 1491
1518340 CIFC15 H12 Au N O2P -16.0552; 7.0297; 15.9689
96.315; 93.979; 90.279
673.93Seki, Tomohiro; Sakurada, Kenta; Muromoto, Mai; Ito, Hajime
Photoinduced single-crystal-to-single-crystal phase transition and photosalient effect of a gold(i) isocyanide complex with shortening of intermolecular aurophilic bonds
Chem. Sci., 2015, 6, 1491
1518341 CIFC88 H92 Cd3 N8 O23C 1 2/c 131.136; 20.048; 15.849
90; 108.347; 90
9390Yi, Fei-Yan; Wang, Ying; Li, Jian-Ping; Wu, Dai; Lan, Ya-Qian; Sun, Zhong-Ming
An ultrastable porous metal‒organic framework luminescent switch towards aromatic compounds
Mater. Horiz., 2015, 2, 245
1518342 CIFC33 H27 Br N2 O4P 1 21 19.7143; 22.5934; 12.6641
90; 106.703; 90
2662.23Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518343 CIFC33 H28 N2 O4P 21 21 2112.1648; 12.4912; 17.107
90; 90; 90
2599.46Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518344 CIFC24 H26 N2 O5P 16.25441; 12.592; 13.61853
100.755; 92.7028; 95.0674
1047.35Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518345 CIFC22 H22 N2 O5P 1 21 112.14306; 6.28576; 13.0165
90; 108.566; 90
941.82Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518346 CIFC8 H4 Cr2 O8 P2C m c a12.2545; 11.5949; 9.7196
90; 90; 90
1381.06Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518347 CIFC8 H4 O8 P2 W2C m c a12.4977; 12.0462; 10.1185
90; 90; 90
1523.3Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518348 CIFC7 H7 Cr2 O7 P3P -16.9134; 7.3239; 8.761
111.796; 92.15; 115.204
362.43Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518352 CIFC3 H3 Cl Cu N3 S3P a -311.70071; 11.70071; 11.70071
90; 90; 90
1601.9Tominaka, S.; Hamoudi, H.; Suga, T.; Bennett, T. D.; Cairns, A. B.; Cheetham, A. K.
Topochemical conversion of a dense metal‒organic framework from a crystalline insulator to an amorphous semiconductor
Chem. Sci., 2015, 6, 1465
1518353 CIFC3 H3 Cl Cu N3 S3P a -311.74713; 11.74713; 11.74713
90; 90; 90
1621.05Tominaka, S.; Hamoudi, H.; Suga, T.; Bennett, T. D.; Cairns, A. B.; Cheetham, A. K.
Topochemical conversion of a dense metal‒organic framework from a crystalline insulator to an amorphous semiconductor
Chem. Sci., 2015, 6, 1465
1518354 CIFC3 H3 Cl Cu N3 S3P a -311.78842; 11.78842; 11.78842
90; 90; 90
1638.2Tominaka, S.; Hamoudi, H.; Suga, T.; Bennett, T. D.; Cairns, A. B.; Cheetham, A. K.
Topochemical conversion of a dense metal‒organic framework from a crystalline insulator to an amorphous semiconductor
Chem. Sci., 2015, 6, 1465
1518355 CIFC32 H44 K N2 O13 RhC 1 c 113.6052; 19.6523; 14.3113
90; 105.559; 90
3686.2Murphy, Stephen K.; Bruch, Achim; Dong, Vy M.
Mechanistic insights into hydroacylation with non-chelating aldehydes
Chemical Science, 2015, 6, 174-180
1518357 CIFC19 H21 N O2 SP 1 21/n 19.952; 15.043; 11.1
90; 90.067; 90
1661.8Labed, I.; Labed, A.; Sun, Y.; Jiang, F.; Achard, M.; Dérien, S.; Kabouche, Z.; Bruneau, C.
[Cp*Ru]-catalyzed selective coupling/hydrogenation
Catal. Sci. Technol., 2015, 5, 1650
1518358 CIFC18 H32 N4 PdP 1 21/c 19.5147; 8.7236; 12.2763
90; 96.21; 90
1012.98Hering, Florian; Nitsch, Jörn; Paul, Ursula; Steffen, Andreas; Bickelhaupt, F. Matthias; Radius, Udo
Bite-angle bending as a key for understanding group-10 metal reactivity of d10-[M(NHC)2] complexes with sterically modest NHC ligands
Chem. Sci., 2015, 6, 1426
1518359 CIFC28 H50 Cl4 N6 PdP -19.5437; 12.6519; 14.7569
81.229; 83.044; 81.137
1731.26Hering, Florian; Nitsch, Jörn; Paul, Ursula; Steffen, Andreas; Bickelhaupt, F. Matthias; Radius, Udo
Bite-angle bending as a key for understanding group-10 metal reactivity of d10-[M(NHC)2] complexes with sterically modest NHC ligands
Chem. Sci., 2015, 6, 1426
1518360 CIFC145 H149 Cl6 Cs3 N8 O14P -111.649; 18.299; 18.362
60.833; 80.132; 86.221
3366.6Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518361 CIFC74 H78 Cl6 Cs F N4 O8P -112.5824; 16.3849; 18.0859
89.08; 89.123; 70.854
3521.7Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518362 CIFC82 H92 N4 O12P -116.284; 21.681; 24.254
65.823; 87.933; 77.172
7602Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518363 CIFC75 H71 Cl3 N4 O12P 1 21/c 118.865; 17.828; 20.315
90; 107.064; 90
6532Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518364 CIFC81 H94 Cl6 F N5 O6P 1 21/n 118.1082; 20.262; 21.408
90; 105.284; 90
7577Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518365 CIFC78 H81 N7 O6P 1 21/n 119.8344; 17.7442; 20.5845
90; 109.128; 90
6844.6Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518366 CIFC74 H77 Cl4 Cs N4 O7P 1 2/n 128.4416; 17.3237; 28.5922
90; 90.135; 90
14087.7Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518367 CIFC74 H77 Cl3 Cs F N4 O7P 1 21/n 117.1643; 20.272; 20.1109
90; 99.129; 90
6909Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518368 CIFC163 H193 Cl6 F2 N10 O15P -117.7069; 19.2391; 27.8205
71.903; 75.381; 69.249
8315.5Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518371 CIFC279.28 H164 N37 O100C 1 2/c 133.067; 14.8252; 17.1809
90; 121.19; 90
7205.1Mallick, Arijit; Garai, Bikash; Addicoat, Matthew A.; Petkov, Petko St.; Heine, Thomas; Banerjee, Rahul
Solid state organic amine detection in a photochromic porous metal organic framework
Chem. Sci., 2015, 6, 1420
1518372 CIFC69 H35 Mg4 N7 O30P 1 2/c 134.3413; 10.0447; 17.7382
90; 96.234; 90
6082.6Mallick, Arijit; Garai, Bikash; Addicoat, Matthew A.; Petkov, Petko St.; Heine, Thomas; Banerjee, Rahul
Solid state organic amine detection in a photochromic porous metal organic framework
Chem. Sci., 2015, 6, 1420
1518403 CIFC25 H17 N OP -18.2167; 16.3939; 25.795
90; 86.989; 90
3469.9Wang, Zhen; Li, Ting
Facile Synthesis of 6-Acylated Pyrido[2,1-a]isoindoles from 2-Arylpyridines and γ-Substituted tert-Propargyl Alcohols via Rhodium-Catalyzed C-H Bond Activation and β-Carbon Elimination.
Organic letters, 2015, 17, 1348
1518406 CIFC28 H36 N2 P2P -111.4796; 15.5902; 15.8639
98.551; 106.145; 104.953
2559.42Härzschel, Stefan; Kühn, Fritz E.; Wöhl, Anina; Müller, Wolfgang; Al-Hazmi, Mohammed H.; Alqahtani, Abdullah M.; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
Comparative study of new chromium-based catalysts for the selective tri- and tetramerization of ethylene
Catal. Sci. Technol., 2015, 5, 1678
1518407 CIFC74 H86 N6 O3P -19.827; 16.9659; 21.6298
69.273; 81.505; 87.976
3335.2Slater, Anna G.; Hu, Ya; Yang, Lixu; Argent, Stephen P.; Lewis, William; Blunt, Matthew O.; Champness, Neil R.
Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly
Chem. Sci., 2015, 6, 1562
1518408 CIFC86 H92 Cl18 N6 O3P -115.4721; 16.3717; 19.0278
92.068; 110.731; 99.28
4426Slater, Anna G.; Hu, Ya; Yang, Lixu; Argent, Stephen P.; Lewis, William; Blunt, Matthew O.; Champness, Neil R.
Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly
Chem. Sci., 2015, 6, 1562
1518409 CIFC28 H20 N2P 21 21 215.9763; 11.5786; 29.273
90; 90; 90
2025.6Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518410 CIFC40 H28 N2P -110.6571; 11.1264; 13.1685
88; 76.566; 74.575
1463.4Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518411 CIFC42 H32 N2 O2P -111.1806; 11.4458; 12.861
101.527; 91.283; 99.274
1589.02Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518412 CIFC32 H28 N2 O4P -19.768; 12.3063; 12.4687
68.542; 70.492; 88.089
1308.1Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518413 CIFC41 H39 N7 O5P -110.244; 13.8307; 14.5665
72.3415; 70.128; 75.9246
1826.7Mahapatra, Ajit Kumar; Manna, Saikat Kumar; Maiti, Kalipada; Mondal, Sanchita; Maji, Rajkishor; Mandal, Debasish; Mandal, Sukhendu; Uddin, Md Raihan; Goswami, Shyamaprosad; Quah, Ching Kheng; Fun, Hoong-Kun
An azodye-rhodamine-based fluorescent and colorimetric probe specific for the detection of Pd(2+) in aqueous ethanolic solution: synthesis, XRD characterization, computational studies and imaging in live cells.
The Analyst, 2015, 140, 1229-1236
1518416 CIFC34 H35 N O14P 17.4957; 12.0298; 17.8347
87.387; 87.555; 74.708
1548.85Moon, Kyuho; Chung, Beomkoo; Shin, Yoonho; Rheingold, Arnold L.; Moore, Curtis E.; Park, Sung Jean; Park, Sunghyouk; Lee, Sang Kook; Oh, Ki-Bong; Shin, Jongheon; Oh, Dong-Chan
Pentacyclic antibiotics from a tidal mud flat-derived actinomycete.
Journal of natural products, 2015, 78, 524-529
1518421 CIFC23 H28 N2 O4 SP 1 21/n 110.543; 9.344; 22.465
90; 92.128; 90
2211.6Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua
One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.
Organic letters, 2015, 17, 66-69
1518422 CIFC23 H28 N2 O4 SP n a 2126.688; 18.145; 9.062
90; 90; 90
4388.3Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua
One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.
Organic letters, 2015, 17, 66-69
1518427 CIFC15 H9 F3 N2 O2P 1 21/n 116.6085; 7.853; 20.7239
90; 103.721; 90
2625.8Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit
KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.
Organic letters, 2015, 17, 82-85
1518428 CIFC15 H11 Cl N2 O2C 1 2/c 119.16; 11.3942; 15.345
90; 126.612; 90
2689Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit
KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.
Organic letters, 2015, 17, 82-85
1518432 CIFC6 H12 O6P 21 21 2110.336; 14.852; 4.924
90; 90; 90
755.9Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518433 CIFC6 H12 O6P 21 21 2110.26; 14.837; 4.8169
90; 90; 90
733.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518434 CIFC6 H12 O6P 21 21 2110.22; 14.832; 4.7689
90; 90; 90
722.9Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518435 CIFC6 H12 O6P 21 21 2110.218; 14.823; 4.7439
90; 90; 90
718.5Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518436 CIFC6 H12 O6P 21 21 2110.181; 14.808; 4.693
90; 90; 90
707.5Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518437 CIFC6 H12 O6P 21 21 2110.11; 14.808; 4.5801
90; 90; 90
685.7Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518438 CIFC6 H12 O6P 21 21 2110.06; 14.798; 4.537
90; 90; 90
675.4Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518439 CIFC6 H12 O6P 21 21 2110.05; 14.807; 4.4206
90; 90; 90
657.8Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518440 CIFC6 H12 O6P 21 21 2110.04; 14.796; 4.3879
90; 90; 90
651.8Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518441 CIFC6 H12 O6P 21 21 2110.056; 14.779; 4.275
90; 90; 90
635.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518442 CIFC6 H12 O6P 21 21 2110.059; 14.776; 4.261
90; 90; 90
633.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518443 CIFC6 H12 O6P 21 21 2110.063; 14.787; 4.256
90; 90; 90
633.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518444 CIFC6 H12 O6P 21 21 219.714; 14.99; 4.262
90; 90; 90
621Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518445 CIFC6 H12 O6P 21 21 219.73; 14.987; 4.234
90; 90; 90
617.4Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518446 CIFC6 H12 O6P 21 21 219.694; 14.931; 4.2234
90; 90; 90
611.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518447 CIFC67 F6P b c a9.9998; 20.6538; 31.3512
90; 90; 90
6475.1San, Long K.; Bukovsky, Eric V.; Larson, Bryon W.; Whitaker, James B.; Deng, S. H. M.; Kopidakis, Nikos; Rumbles, Garry; Popov, Alexey A.; Chen, Yu-Sheng; Wang, Xue-Bin; Boltalina, Olga V.; Strauss, Steven H.
A faux hawk fullerene with PCBM-like properties
Chem. Sci., 2015, 6, 1801
1518448 CIFC60 H60 Li4 O5 Rb4C m c m14.166; 13.519; 25.901
90; 90; 90
4960Filatov, Alexander S.; Spisak, Sarah N.; Zabula, Alexander V.; McNeely, James; Rogachev, Andrey Yu.; Petrukhina, Marina A.
Self-assembly of tetrareduced corannulene with mixed Li‒Rb clusters: dynamic transformations, unique structures and record7Li NMR shifts
Chem. Sci., 2015, 6, 1959
1518449 CIFC66 H80 Li3 O12.5 Rb5P -110.064; 15.27; 22.129
90.416; 93.102; 94.532
3384.9Filatov, Alexander S.; Spisak, Sarah N.; Zabula, Alexander V.; McNeely, James; Rogachev, Andrey Yu.; Petrukhina, Marina A.
Self-assembly of tetrareduced corannulene with mixed Li‒Rb clusters: dynamic transformations, unique structures and record7Li NMR shifts
Chem. Sci., 2015, 6, 1959
1518450 CIFC28 H46 N4 O19 TmC 1 c 123.1686; 9.677; 16.8001
90; 118.272; 90
3317.3Funk, Alexander M.; Finney, Katie-Louise N. A.; Harvey, Peter; Kenwright, Alan M.; Neil, Emily R.; Rogers, Nicola J.; Kanthi Senanayake, P.; Parker, David
Critical analysis of the limitations of Bleaney's theory of magnetic anisotropy in paramagnetic lanthanide coordination complexes
Chem. Sci., 2015, 6, 1655
1518451 CIFC33 H31.75 N2 O5.88C 1 2 152.27; 5.01; 22.83
90; 105.49; 90
5761Raeburn, Jaclyn; Mendoza-Cuenca, Cristina; Cattoz, Beatrice N.; Little, Marc A.; Terry, Ann E.; Zamith Cardoso, Andre; Griffiths, Peter C.; Adams, Dave J.
The effect of solvent choice on the gelation and final hydrogel properties of Fmoc-diphenylalanine.
Soft matter, 2015, 11, 927-935
1518452 CIFC36 H58 Cl N3 O2P 3215.865; 15.865; 11.7214
90; 90; 120
2555Bandar, Jeffrey S.; Barthelme, Alexandre P.; Mazori, Alon Y.; Lambert, Tristan H.
Structure-Activity Relationship Studies of Cyclopropenimines as Enantioselective Brønsted Base Catalysts.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1537-1547
1518453 CIFC32 H31 F3 N4 O6I 41/a28.1062; 28.1062; 14.709
90; 90; 90
11619.5Jiao, Wei-Hua; Chen, Guo-Dong; Gao, Hao; Li, Jing; Gu, Bin-Bin; Xu, Ting-Ting; Yu, Hao-Bing; Shi, Guo-Hua; Yang, Fan; Yao, Xin-Sheng; Lin, Hou-Wen
(±)-Quassidines I and J, Two Pairs of Cytotoxic Bis-β-carboline Alkaloid Enantiomers from Picrasma quassioides.
Journal of natural products, 2015, 78, 125-130
1518454 CIFC11 H18 N8 O3P m n 219.5289; 9.1191; 8.667
90; 90; 90
753.12Gryl, Marlena; Cenedese, Simone; Stadnicka, Katarzyna
Crystal Engineering and Charge Density Study of Pharmaceutical Nonlinear Optical Material: Melamine-Barbital Co-Crystal
The Journal of Physical Chemistry C, 2015, 119, 590
1518455 CIFC29 H37 N3 O4P 21 21 217.788; 16.0615; 20.7023
90; 90; 90
2589.6Lee, Pin-Sheng; Yoshikai, Naohiko
Cobalt-catalyzed enantioselective directed C-h alkylation of indole with styrenes.
Organic letters, 2015, 17, 22-25
1518456 CIFC21 H28 O4 SC 1 2 119.3925; 6.0017; 17.9993
90; 107.635; 90
1996.45Lan, Ping; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.
Organic letters, 2015, 17, 166-169
1518457 CIFC21 H28 O4P 21 21 216.2688; 16.308; 18.2849
90; 90; 90
1869.29Lan, Ping; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.
Organic letters, 2015, 17, 166-169
1518458 CIFC24 H25 N O5P 21 21 219.0419; 12.2803; 19.0748
90; 90; 90
2118.01Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518459 CIFC24 H23 N O4P 1 21/c 19.6257; 24.6776; 9.1983
90; 108.936; 90
2066.71Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518460 CIFC25 H25 N O4P -110.1067; 11.5787; 19.2079
83.811; 82.159; 76.354
2157.2Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518461 CIFC24 H21 Cl2 N O4C 1 2 121.3083; 16.6395; 17.8923
90; 118.967; 90
5550.3Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518462 CIFC21 H21 Br N2 O3 SP c a 2124.0183; 11.2598; 7.4174
90; 90; 90
2005.97Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi
Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.
Organic letters, 2015, 17, 86-89
1518463 CIFC21 H21 Br N2 O3 SP 1 21/n 18.12; 11.101; 21.7055
90; 94.955; 90
1949.2Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi
Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.
Organic letters, 2015, 17, 86-89
1518464 CIFC19 H26 O7P 21 21 219.1452; 12.5627; 16.2841
90; 90; 90
1870.85Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi
(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.
Organic letters, 2015, 17, 146-149
1518465 CIFC19 H26 O7P 329.2683; 9.2683; 18.5901
90; 90; 120
1382.97Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi
(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.
Organic letters, 2015, 17, 146-149
1518466 CIFC24.5 H26.52 O7C 1 2 143.491; 5.5109; 18.3225
90; 95.331; 90
4372.4McDonald, Benjamin R.; Nibbs, Antoinette E.; Scheidt, Karl A.
A biomimetic strategy to access the silybins: total synthesis of (-)-isosilybin a.
Organic letters, 2015, 17, 98-101
1518467 CIFC18 H26 O4P -17.1391; 7.5445; 15.455
88.709; 83.268; 76.661
804.4Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko
Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.
Organic letters, 2015, 17, 126-129
1518468 CIFC19 H24 O7 SP 1 21/n 116.194; 6.597; 18.175
90; 102.603; 90
1894.9Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko
Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.
Organic letters, 2015, 17, 126-129
1518469 CIFC21 H10 Au B Cl10 N6 PbP -18.5794; 13.7444; 13.7913
110.805; 93.371; 101.13
1477.17Echeverría, Raquel; López-de-Luzuriaga, José M.; Monge, Miguel; Olmos, M. Elena
The gold(i)⋯lead(ii) interaction: a relativistic connection
Chem. Sci., 2015, 6, 2022
1518470 CIFC18 H21 N3 O13P 1 21/c 110.0519; 11.0764; 19.917
90; 115.105; 90
2008Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518471 CIFC8 H15 N2 O3P 1 21/n 18.504; 11.8666; 9.5595
90; 96.868; 90
957.8Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518472 CIFC9 H17 N2 O2P 1 21/c 110.928; 6.85; 14.18
90; 91.265; 90
1061.2Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518473 CIFC28 H27 N4 O16C 1 2/c 117.65; 7.5376; 22.793
90; 91.608; 90
3031.2Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518474 CIFC8 H15 N2 O3P 1 21/c 110.028; 9.435; 11.76
90; 122.95; 90
934Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518475 CIFC19 H22 N2 O13P 1 21/n 19.975; 11.085; 18.066
90; 94.823; 90
1990.5Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518476 CIFC14 H23 F6 O6 Pd SbP -19.539; 10.408; 11.253
115.767; 97.422; 91.945
992.6Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518477 CIFC15 H22 F6 N O6 Pd SbP n m a18.89; 16.805; 13.196
90; 90; 90
4189Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518478 CIFC22 H35 F6 O6 Pd SbP n a 2116.758; 16.947; 9.5046
90; 90; 90
2699.3Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518479 CIFC17 H28 F6 N3 O10 Pd SbP 1 21/c 110.0271; 19.0026; 14.5138
90; 92.747; 90
2762.3Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518480 CIFC66 H86 Cl20 F24 O16 Pd4 Sb4P -116.4284; 19.3745; 21.4447
66.181; 88.434; 72.775
5930.9Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518481 CIFC12 H15 Cl O6P 1 21 14.6451; 11.3065; 12.3885
90; 94.458; 90
648.67Wu, Jing; Tokunaga, Taiki; Kondo, Mitsuru; Ishigami, Kota; Tokuyama, Shinji; Suzuki, Tomohiro; Choi, Jae-Hoon; Hirai, Hirofumi; Kawagishi, Hirokazu
Erinaceolactones A to C, from the Culture Broth of Hericium erinaceus.
Journal of natural products, 2015, 78, 155-158
1518482 CIFC24 H20 N2 OP b c a8.8127; 13.2298; 32.5
90; 90; 90
3789.2Fan, Zhoulong; Song, Shanshan; Li, Wei; Geng, Kaijun; Xu, Youjun; Miao, Ze-Hong; Zhang, Ao
Rh(III)-Catalyzed Redox-Neutral C-H Activation of Pyrazolones: An Economical Approach for the Synthesis of N-Substituted Indoles.
Organic letters, 2015, 17, 310-313
1518483 CIFC23 H24 Cl N O4P -110.0098; 10.1777; 12.0505
67.347; 70.617; 79.738
1066.95Craig, Alexander J.; van der Salm, Louise; Stevens-Cullinane, Lars; Lucas, Nigel T.; Tan, Eng Wui; Hawkins, Bill C.
Expedient Metal-Free Synthesis of 1,3-Oxazinen-4-ones.
Organic letters, 2015, 17, 234-237
1518484 CIFC54 H75 N8 O16 SP 19.1948; 12.5947; 13.668
79.379; 77.83; 78.547
1499.6Ganesh Kumar, Mothukuri; Mali, Sachitanand M.; Raja, K. Muruga Poopathi; Gopi, Hosahudya N.
Design of Stable β-Hairpin Mimetics through Backbone Disulfide Bonds.
Organic letters, 2015, 17, 230-233
1518485 CIFC22 H16 I N O2 SP 1 21/c 18.0428; 19.587; 12.8121
90; 104.921; 90
1950.29Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang
Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.
Organic letters, 2015, 17, 242-245
1518486 CIFC21 H14 I N O2 SP -18.195; 10.1773; 11.9407
86.942; 83.912; 76.661
963.13Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang
Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.
Organic letters, 2015, 17, 242-245
1518487 CIFC24 H24 O6C 1 c 117.142; 9.0363; 12.653
90; 90.03; 90
1960Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518488 CIFC16 H16 O5P n a 2114.969; 7.307; 12.761
90; 90; 90
1395.8Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518489 CIFC22 H14 Co2 O11P -18.0572; 8.3258; 17.63
88.79; 84.64; 75.45
1139.7Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518490 CIFC36 H34 Co2 F6 N O5 P2P 21 21 215.8829; 19.5684; 11.5831
90; 90; 90
3600.1Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier
Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.
Organic letters, 2015, 17, 250-253
1518491 CIFC30 H37 Co2 N3 O5 P2 SiP 1 21 18.8649; 20.8055; 9.1083
90; 101.487; 90
1646.3Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier
Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.
Organic letters, 2015, 17, 250-253
1518492 CIFC32 H22 B Cl3 F4 N2 O2C 1 2/c 130.8526; 11.997; 18.7562
90; 113.744; 90
6354.75Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518493 CIFC15 H10 Cl N O3P 1 21/n 18.5347; 14.9824; 10.2813
90; 96.632; 90
1305.88Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518494 CIFC18 H20 N2 O2 SP c a 2112.7796; 13.8018; 18.4448
90; 90; 90
3253.32Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518495 CIFC16 H12 Br N3P 3210.18; 10.18; 10.954
90; 90; 120
983.1Tang, Hai-Tao; Xiong, Kai; Li, Ren-Hao; Ding, Zong-Cang; Zhan, Zhuang-Ping
Synthesis of 5,6-Dihydropyrazolo[1,5-c]quinazolines through Gold-Catalyzed Chemoselective Bicyclization of N-Propargylic Sulfonylhydrazones.
Organic letters, 2015, 17, 326-329
1518496 CIFC34 H58 As4 Co2P 1 21/n 18.4386; 13.7676; 16.0276
90; 100.27; 90
1832.24Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518497 CIFC35 H60 As4 Cl2 Co2C 1 2/c 117.893; 19.9249; 11.6299
90; 107.903; 90
3945.5Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518498 CIFC68 H116 As10 Co4P -110.3921; 14.3707; 14.8262
62.53; 76.535; 79.819
1904.35Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518499 CIFC72 H124 As10 Cl8 Co4P -113.7956; 14.0892; 15.0382
62.971; 69.895; 61.292
2254Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518500 CIFC51 H87 As12 Co3C 1 2/c 128.9202; 15.7899; 29.9375
90; 112.752; 90
12607.1Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518501 CIFC23 H32 N2 SeP n a 2123.3; 7.0807; 11.6415
90; 90; 90
1920.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518502 CIFC15 H24 N2 SeP 1 21/c 111.8147; 11.1443; 12.2088
90; 108.21; 90
1527Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518503 CIFC27 H48 N2 SeP 1 21/n 114.4058; 7.4133; 25.023
90; 97.856; 90
2647.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518504 CIFC19 H20 N2 SeP 1 2/n 18.3318; 7.4265; 13.6459
90; 98.798; 90
834.42Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518505 CIFC21 H24 N2 SeP b c n16.043; 7.3937; 16.055
90; 90; 90
1904.4Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518506 CIFC35 H52 N2 SeP 1 21/c 120.433; 7.6327; 21.563
90; 106.66; 90
3221.8Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518507 CIFC27 H34 Cl2 N2 SeI 1 2/a 117.366; 9.4565; 21.295
90; 109.08; 90
3305Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518508 CIFC21 H26 N2 SeP b c n15.9194; 7.4418; 16.1915
90; 90; 90
1918.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518509 CIFC11 H6 F5 N3 SeP 1 21/c 19.3746; 15.527; 8.3524
90; 90.357; 90
1215.7Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518510 CIFC11 H11 N3 O SeP -17.8283; 7.9731; 18.447
97.93; 94.637; 90.042
1136.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518511 CIFC21 H21 N3 O SeP -18.5326; 10.637; 11.589
107.558; 101.546; 107.498
906.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518512 CIFC30 H35 N3 O Se SiP b c a13.2692; 19.8926; 20.979
90; 90; 90
5537.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518526 CIFC12 H11 N O2P -14.00444; 11.1381; 12.202
71.955; 89.514; 80.992
510.62Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518527 CIFC38 H48 N2 O4P 1 21/c 114.93217; 14.22602; 15.93712
90; 100.89; 90
3324.49Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518528 CIFC30 H40 N2 O4 Si4P -18.5558; 11.887; 17.0071
99.115; 92.129; 94.397
1700.67Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518529 CIFC34 H52 N2 O4 Si6P -18.6514; 11.8373; 20.4256
82.751; 87.339; 86.175
2068.9Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518530 CIFC152.05 H75.74 Cl2.21 F40 N12 S8P -118.9073; 20.7452; 21.091
67.38; 77.21; 65.257
6917.2Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518531 CIFC87.05 H40.13 Cl3.96 F20 N6 S6C 1 2/c 149.998; 12.402; 35.242
90; 131.613; 90
16338Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518532 CIFC95.3 H48 Cl2.3 F20 N6 O0.5 S8P -117.2734; 18.9028; 30.1289
105; 92.92; 107.23
8989Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518533 CIFC90 H72 Ag12 F18 N6 O12 S6R -3 :H23.9571; 23.9571; 16.5415
90; 90; 120
8221.9Xu, Qing-Qing; Dong, Xi-Yan; Huang, Ren-Wu; Li, Bo; Zang, Shuang-Quan; Mak, Thomas C. W.
A thermochromic silver nanocluster exhibiting dual emission character.
Nanoscale, 2015, 7, 1650-1654
1518534 CIFC6 H4 F9 N3 O3 SP 1 21/n 15.2742; 8.2719; 29.673
90; 93.124; 90
1292.64Luo, Jiangshui; Jensen, Annemette H.; Brooks, Neil R.; Sniekers, Jeroen; Knipper, Martin; Aili, David; Li, Qingfeng; Vanroy, Bram; Wübbenhorst, Michael; Yan, Feng; Van Meervelt, Luc; Shao, Zhigang; Fang, Jianhua; Luo, Zheng-Hong; De Vos, Dirk E.; Binnemans, Koen; Fransaer, Jan
1,2,4-Triazolium perfluorobutanesulfonate as an archetypal pure protic organic ionic plastic crystal electrolyte for all-solid-state fuel cells
Energy Environ. Sci., 2015, 8, 1276
1518535 CIFC6 H4 F9 N3 O3 SP 1 21/n 15.351; 8.2492; 30.2383
90; 93.95; 90
1331.59Luo, Jiangshui; Jensen, Annemette H.; Brooks, Neil R.; Sniekers, Jeroen; Knipper, Martin; Aili, David; Li, Qingfeng; Vanroy, Bram; Wübbenhorst, Michael; Yan, Feng; Van Meervelt, Luc; Shao, Zhigang; Fang, Jianhua; Luo, Zheng-Hong; De Vos, Dirk E.; Binnemans, Koen; Fransaer, Jan
1,2,4-Triazolium perfluorobutanesulfonate as an archetypal pure protic organic ionic plastic crystal electrolyte for all-solid-state fuel cells
Energy Environ. Sci., 2015, 8, 1276
1518536 CIFC18 H11 F6 N O3C 1 2/c 132.403; 6.8959; 15.25
90; 97.03; 90
3382Lu, Yi; Wang, Huai-Wei; Spangler, Jillian E.; Chen, Kai; Cui, Pei-Pei; Zhao, Yue; Sun, Wei-Yin; Yu, Jin-Quan
Rh(iii)-catalyzed C‒H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant
Chem. Sci., 2015, 6, 1923
1518537 CIFC22 H23 Cl3 N4 O2P -17.4245; 13.2237; 24.7183
96.898; 96.177; 90.664
2394.5Fours, Baptiste; Cartigny, Yohann; Petit, Samuel; Coquerel, Gérard
Formation of new polymorphs without any nucleation step. Desolvation of the rimonabant monohydrate: directional crystallisation concomitant to smooth dehydration.
Faraday discussions, 2015, 179, 475-488
1518538 CIFC19 H33 Cl3 Fe N5 O3P -17.2528; 12.6837; 14.9215
106.95; 99.766; 99.208
1261.66Nesterov, Dmytro S.; Nesterova, Oksana V.; Guedes da Silva, M. Fátima C.; Pombeiro, Armando J. L.
Catalytic behaviour of a novel Fe(iii) Schiff base complex in the mild oxidation of cyclohexane
Catal. Sci. Technol., 2015, 5, 1801
1518539 CIFC17 H24 N2 O5C 1 2/c 114.2575; 13.1713; 20.8636
90; 108.856; 90
3707.7Kar, Sudeshna; Tai, Yian
Marked difference in self-assembly, morphology, and cell viability of positional isomeric dipeptides generated by reversal of sequence.
Soft matter, 2015, 11, 1345-1351
1518540 CIFC18 H33 N2 O8 S2P -17.8956; 9.6557; 14.916
77.311; 81.835; 86.214
1097.43Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518541 CIFC36 H66 N4 O16 S4I 1 2/c 119.4827; 7.7013; 30.1416
90; 101.758; 90
4427.61Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518542 CIFC28.7552 H49.5104 N8 O14 S4P -19.7673; 9.8143; 10.2046
94.88; 96.822; 95.184
962.76Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518543 CIFC58 H76 Mo2 O10P 1 21/c 19.9404; 15.744; 17.7587
90; 100.059; 90
2736.54Brown-Xu, Samantha E; Chisholm, Malcolm H.; Durr, Christopher B.; Spilker, Thomas F.; Young, Philip J.
MM Quadruply Bonded Complexes Supported by Vinylbenzoate Ligands: Synthesis, Characterization, Photophysical Properties and Application as Synthons.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1780-1791
1518544 CIFC58 H76 Mo2 O10P -19.8343; 11.252; 15.714
107; 105.165; 90.114
1599.14Brown-Xu, Samantha E; Chisholm, Malcolm H.; Durr, Christopher B.; Spilker, Thomas F.; Young, Philip J.
MM Quadruply Bonded Complexes Supported by Vinylbenzoate Ligands: Synthesis, Characterization, Photophysical Properties and Application as Synthons.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1780-1791
1518545 CIFC14 H34 Cl Mo P3P 21 21 2111.8282; 12.449; 13.6005
90; 90; 90
2002.7Neary, Michelle C.; Parkin, Gerard
Dehydrogenation, disproportionation and transfer hydrogenation reactions of formic acid catalyzed by molybdenum hydride compounds
Chem. Sci., 2015, 6, 1859
1518546 CIFC9 H5 F3 Mo O3P 16.453; 6.544; 6.7851
107.752; 97.132; 107.192
253.356Hauser, Simone A.; Reich, Robert M.; Mink, János; Pöthig, Alexander; Cokoja, Mirza; Kühn, Fritz E.
Influence of structural and electronic properties of organomolybdenum(ii) complexes of the type [CpMo(CO)3R] and [CpMo(O2)(O)R] (R = Cl, CH3, CF3) on the catalytic olefin epoxidation
Catal. Sci. Technol., 2015, 5, 2282
1518547 CIFC6 H5 F3 Mo O3C 1 2/c 120.5911; 6.9325; 12.3919
90; 117.372; 90
1570.87Hauser, Simone A.; Reich, Robert M.; Mink, János; Pöthig, Alexander; Cokoja, Mirza; Kühn, Fritz E.
Influence of structural and electronic properties of organomolybdenum(ii) complexes of the type [CpMo(CO)3R] and [CpMo(O2)(O)R] (R = Cl, CH3, CF3) on the catalytic olefin epoxidation
Catal. Sci. Technol., 2015, 5, 2282
1518548 CIFC44.71 H22.16 Cl4 F14 N6 Na2 O7.22P -114.6741; 15.8676; 24.1918
91.946; 106.327; 115.228
4812.8Seifert, Sabine; Schmidt, David; Würthner, Frank
An ambient stable core-substituted perylene bisimide dianion: isolation and single crystal structure analysis
Chem. Sci., 2015, 6, 1663
1518549 CIFC22 H24 O6P -16.0103; 8.0802; 22.1231
94.344; 93.489; 111.753
990.42Merlani, Maia; Koyama, Yasuhito; Sato, Hiroyasu; Geng, Li; Barbakadze, Vakhtang; Chankvetadze, Bezhan; Nakano, Tamaki
Ring-opening polymerization of a 2,3-disubstituted oxirane leading to a polyether having a carbonyl‒aromatic π-stacked structure
Polym. Chem., 2015, 6, 1932
1518550 CIFC20 H18 O5P -19.6559; 9.9869; 18.8822
84.288; 81.394; 73.131
1719.86Merlani, Maia; Koyama, Yasuhito; Sato, Hiroyasu; Geng, Li; Barbakadze, Vakhtang; Chankvetadze, Bezhan; Nakano, Tamaki
Ring-opening polymerization of a 2,3-disubstituted oxirane leading to a polyether having a carbonyl‒aromatic π-stacked structure
Polym. Chem., 2015, 6, 1932
1518551 CIFC14 H26 F6 Li N O10 S2P -19.2411; 9.6767; 13.9904
95.234; 97.155; 95.662
1228.46Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518552 CIFC14 H26 F6 K N O10 S2P -19.4304; 16.507; 18.079
66.416; 78.33; 81.019
2517.1Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518553 CIFC10 H16 F6 Li N O8 S2P -18.838; 9.535; 11.379
81.162; 78.012; 79.457
915.5Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518554 CIFC14 H24 F6 K N O10 S2P -18.7544; 8.9026; 9.1253
113.587; 95.75; 106.568
605.85Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518555 CIFC12 H26 F6 K O6 PP b c a15.404; 15.758; 16.51
90; 90; 90
4007.6Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518556 CIFC14 H30 F6 K O7 PP 1 21/c 117.084; 13.183; 20.904
90; 105.027; 90
4547Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518557 CIFC7 H6 I Li O3P -16.65059; 6.89548; 18.4951
81.559; 84.29; 84.975
832.52Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518558 CIFC7 H6 I Na O3P -16.86202; 7.02675; 18.4262
84.11; 82.711; 89.611
876.62Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518559 CIFC7 H5 I K O2.5P -16.3689; 7.4984; 18.6977
83.832; 83.446; 84.606
878.942Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518560 CIFC7 H6 I O3 RbP 1 21/c 119.6879; 4.001; 12.0832
90; 105.805; 90
915.83Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518561 CIFC7 H6 Cs I O3P 1 21/c 119.6351; 4.13863; 12.4789
90; 106.518; 90
972.22Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518562 CIFC30 H23 F3 N2 O2P 1 21/c 112.476; 8.8085; 23.896
90; 103.508; 90
2553.4Jeżewski, Artur; Hammann, Tommy; Cywiński, Piotr J; Gryko, Daniel T.
Optical Behavior of Substituted 4-(2'-Hydroxyphenyl)imidazoles.
The journal of physical chemistry. B, 2015, 119, 2507-2514
1518563 CIFC60 H48 F6 N4 O5P 1 21/n 116.6424; 9.314; 17.808
90; 99.221; 90
2724.7Jeżewski, Artur; Hammann, Tommy; Cywiński, Piotr J; Gryko, Daniel T.
Optical Behavior of Substituted 4-(2'-Hydroxyphenyl)imidazoles.
The journal of physical chemistry. B, 2015, 119, 2507-2514
1518564 CIFC21 H14 Br NP c a 217.6677; 10.2755; 19.816
90; 90; 90
1561.3Dibble, David J.; Umerani, Mehran J.; Mazaheripour, Amir; Park, Young S.; Ziller, Joseph W.; Gorodetsky, Alon A.
An Aza-Diels‒Alder Route to Polyquinolines
Macromolecules, 2015, 48, 557
1518565 CIFC24 H23 N O3P -112.483; 12.4917; 14.6608
71.195; 68.259; 69.138
1935.93Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518566 CIFC24 H27 N O3P 1 21/n 113.1285; 8.9817; 17.2111
90; 107.754; 90
1932.8Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518567 CIFC24 H22 Br N O3P 21 21 218.9945; 12.4644; 17.7143
90; 90; 90
1985.97Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518568 CIFC31 H37 N5 O8 SP 1 21 110.9519; 18.6953; 14.864
90; 100.907; 90
2988.4Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518569 CIFC15 H19 N O2P -16.6977; 8.9166; 11.8671
97.4234; 102.013; 108.163
644.13Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518570 CIFC13 H15 N O2P 21 21 219.0807; 9.5935; 12.844
90; 90; 90
1118.91Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518571 CIFC8 H13 N O3P -17.0255; 8.3274; 8.5054
64.8193; 75.8585; 86.3999
436.19Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518572 CIFC18 H17 N O2C 1 2/c 116.694; 9.6688; 18.2592
90; 101.972; 90
2883.1Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518573 CIFC25 H20 N2 O4P 1 21/c 110.359; 8.616; 22.998
90; 98.931; 90
2027.8Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518574 CIFC26 H22 N2 O4P -18.5149; 11.4869; 11.4981
90.53; 111.599; 91.352
1045.17Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518575 CIFC26 H22 N2 O4P 1 21/c 18.1999; 23.636; 10.7112
90; 97.847; 90
2056.5Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518576 CIFC25 H21 N5 O4P n a 2115.0058; 16.0652; 9.235
90; 90; 90
2226.29Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518577 CIFC26 H21 N3 O4 SP 1 21/n 113.7112; 7.9341; 22.1644
90; 101.626; 90
2361.71Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518578 CIFC25 H22 N2 O5P 1 21/n 112.2086; 8.2983; 20.1576
90; 94.952; 90
2034.56Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518579 CIFC25 H19 N3 O4I 41/a :225.4401; 25.4401; 14.9071
90; 90; 90
9647.9Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518580 CIFC25 H19 N3 O4P -18.2122; 14.1107; 17.9598
100.563; 95.565; 90.101
2035.86Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518581 CIFC14 H16 F N O3P 1 21 110.68; 10.806; 12.352
90; 107.01; 90
1363.2Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.
A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.
Organic letters, 2015, 17, 572-575
1518582 CIFC17 H14 F N O3P 1 21 16.5754; 10.311; 11.071
90; 95.19; 90
747.5Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.
A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.
Organic letters, 2015, 17, 572-575
1518583 CIFC14 H18 O2P 21 21 218.0591; 9.6081; 15.5767
90; 90; 90
1206.14Homs, Anna; Muratore, Michael E.; Echavarren, Antonio M.
Enantioselective Total Synthesis of (-)-Nardoaristolone B via a Gold(I)-Catalyzed Oxidative Cyclization.
Organic letters, 2015, 17, 461-463
1518584 CIFC32 H33 Br N O2 PP 1 21/n 18.4438; 10.9189; 32.745
90; 95.201; 90
3006.6Barrett, Kimberly T.; Miller, Scott J.
Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.
Organic letters, 2015, 17, 580-583
1518585 CIFC33 H35 Au Br Cl3 N O2 PP 1 21/n 19.848; 24.3169; 15.0477
90; 104.667; 90
3486.1Barrett, Kimberly T.; Miller, Scott J.
Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.
Organic letters, 2015, 17, 580-583
1518586 CIFC60.5 H56 N4 O6C 1 c 116.1723; 24.7158; 24.1251
90; 90.474; 90
9642.7Liu, Lei; Carroll, Patrick J.; Kozlowski, Marisa C.
Vanadium-catalyzed regioselective oxidative coupling of 2-hydroxycarbazoles.
Organic letters, 2015, 17, 508-511
1518587 CIFC56 H92 Cl2 Co2 I2 N4 P4 Ti2P b c a18.6991; 16.4217; 21.8753
90; 90; 90
6717.3Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518588 CIFC31 H55 Cl Co N2 P3 TiP 1 21/n 19.0138; 18.8395; 21.5085
90; 90.54; 90
3652.3Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518589 CIFC68 H104 Co2 I2 N4 O2 P4 Ti2P -112.5912; 13.4571; 13.5956
110.682; 94.623; 117.15
1835.07Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518590 CIFC24 H16 Au2 F8 N4 O2P -13.5452; 14.0087; 14.249
109.292; 91.673; 91.322
667.23Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518591 CIFC18 H4 Au2 F8 N4P -13.5707; 10.3087; 14.2742
107.689; 92.505; 100.205
489.99Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518592 CIFC18 H4 Au2 F8 N4P 1 21/c 17.79058; 18.7202; 6.74157
90; 103.167; 90
957.35Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518593 CIFC30 H51 Ir P2P -110.264; 16.311; 19.425
103.753; 105.008; 93.129
3027.6Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518594 CIFC31 H55 Ir O P2P 1 21/c 117.003; 20.0591; 9.4403
90; 102.986; 90
3137.41Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518595 CIFC24 H46 Cl Ir P2P 1 21/c 111.4108; 13.6574; 17.7933
90; 104.097; 90
2689.4Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518596 CIFC34 H26 F4 P2P 1 21/n 19.2062; 16.7452; 17.6319
90; 101.286; 90
2665.6Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518597 CIFC25 H22 F4 P2C 1 2 121.0973; 8.3882; 6.3567
90; 102.383; 90
1098.76Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518598 CIFC58 H26 B F21 P2P 1 21 18.4256; 21.123; 13.804
90; 95.055; 90
2447.2Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518599 CIFC59.25 H28.5 B Cl2.5 F23 P2P 1 21/c 118.8002; 17.1372; 17.8001
90; 102.564; 90
5597.6Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518604 CIFC23 H38 N2 O2 SiP 21 21 2111.9997; 12.0093; 16.8043
90; 90; 90
2421.63Xu, Xinfang; Deng, Yongming; Yim, David N.; Zavalij, Peter Y.; Doyle, Michael P.
Enantioselective cis-β-lactam synthesis by intramolecular C-H functionalization from enoldiazoacetamides and derivative donor-acceptor cyclopropenes.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 2196-2201
1518605 CIFC83 H82 F24 N12 O5 P4 Ru2P -111.2159; 12.555; 18.1382
70.206; 85.323; 67.45
2216.1Griepenburg, J. C.; Rapp, T. L.; Carroll, P. J.; Eberwine, J.; Dmochowski, I. J.
Ruthenium-Caged Antisense Morpholinos for Regulating Gene Expression in Zebrafish Embryos.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 2342-2346
1518609 CIFC35 H28 F6 N3 P S2 Se4P 1 21/n 119.6176; 7.5992; 25.2231
90; 93.7263; 90
3752.3Bedics, Matthew A.; Kearns, Hayleigh; Cox, Jordan M.; Mabbott, Sam; Ali, Fatima; Shand, Neil C.; Faulds, Karen; Benedict, Jason B.; Graham, Duncan; Detty, Michael R.
Extreme red shifted SERS nanotags
Chem. Sci., 2015, 6, 2302
1518610 CIFC20 H14P -19.6321; 11.0943; 14.7022
67.862; 79.883; 69.219
1359Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank
C‒H arylation of triphenylene, naphthalene and related arenes using Pd/C
Chem. Sci., 2015, 6, 1816
1518611 CIFC24 H16P 1 21/c 119.1157; 5.7556; 29.6669
90; 108.002; 90
3104.2Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank
C‒H arylation of triphenylene, naphthalene and related arenes using Pd/C
Chem. Sci., 2015, 6, 1816
1518612 CIFC27 H36 F2 N P PtP 1 21/n 18.7261; 31.0122; 9.6085
90; 111.319; 90
2422.29Vigalok, Arkadi
Electrophilic halogenation-reductive elimination chemistry of organopalladium and -platinum complexes.
Accounts of chemical research, 2015, 48, 238-247
1518613 CIFC22 H17 N OP 1 21/n 18.8912; 16.859; 11.238
90; 108.555; 90
1597Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping
Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.
Organic letters, 2015, 17, 334-337
1518614 CIFC22 H16 F N OP 1 21/n 18.922; 16.7585; 11.2263
90; 108.038; 90
1596.05Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping
Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.
Organic letters, 2015, 17, 334-337
1518615 CIFC52 H50 N4 Ni O2P 1 21/c 118.2078; 16.5273; 14.8317
90; 98.447; 90
4414.8Gehrold, Andreas C.; Bruhn, Torsten; Schneider, Heidi; Radius, Udo; Bringmann, Gerhard
Chiral and achiral basket-handle porphyrins: short synthesis and stereostructures of these versatile building blocks.
Organic letters, 2015, 17, 210-213
1518616 CIFC15 H13 N3C 1 2/c 117.719; 6.475; 22.501
90; 100.868; 90
2535.2Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui
Correction to p-Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN3 for Synthesis of 4-Aryl-NH-1,2,3-triazoles.
Organic letters, 2015, 17, 393
1518617 CIFC37 H36 Cl2 N4 O8 S2P 21 21 2112.9116; 15.1292; 18.7417
90; 90; 90
3661Liang, Kangjiang; Deng, Xu; Tong, Xiaogang; Li, Dashan; Ding, Ming; Zhou, Ankun; Xia, Chengfeng
Copper-Mediated Dimerization to Access 3a,3a'-Bispyrrolidinoindoline: Diastereoselective Synthesis of (+)-WIN 64821 and (-)-Ditryptophenaline.
Organic letters, 2015, 17, 206-209
1518618 CIFC20 H17 Br N2 OP 19.8359; 10.161; 10.307
76.557; 73.136; 64.754
884.6Fu, Niankai; Zhang, Long; Luo, Sanzhong
Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.
Organic letters, 2015, 17, 382-385
1518619 CIFC24 H20 N2 OP 21 21 2110.5861; 10.618; 17.0439
90; 90; 90
1915.79Fu, Niankai; Zhang, Long; Luo, Sanzhong
Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.
Organic letters, 2015, 17, 382-385
1518620 CIFC16 H10 B F2 N3P 1 21/n 19.559; 9.3155; 15.051
90; 102.64; 90
1307.8Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518621 CIFC16 H9 B Cl F2 N3P 1 21/n 17.7337; 19.0699; 9.655
90; 105.059; 90
1375Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518622 CIFC15 H10 B F2 N3 SP 1 21/c 17.9215; 14.0077; 25.071
90; 102.609; 90
2714.8Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518623 CIFC22 H18 B F2 N3 SP -110.092; 10.383; 10.434
65.025; 82.642; 75.499
959.2Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518624 CIFC18 H10 B F2 N3P -17.4838; 9.1552; 11.5629
79.781; 71.778; 67.825
695.26Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518625 CIFC18 H9 B Br F2 N3P -19.1788; 9.5551; 9.9844
87.602; 71.441; 65.179
749.15Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518626 CIFC24 H17 B Br F2 N3 SC 1 2/c 111.3331; 34.017; 12.736
90; 109.159; 90
4638Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518627 CIFC21 H20 Cl N O3P 1 21/c 115.6314; 21.884; 11.7948
90; 108.565; 90
3824.8Li, Lei; Zhao, Yu-Long; Wang, Qian; Lin, Tao; Liu, Qun
Base-Promoted Oxidative C-H Functionalization of α-Amino Carbonyl Compounds under Mild Metal-Free Conditions: Using Molecular Oxygen as the Oxidant.
Organic letters, 2015, 17, 370-373
1518628 CIFC11 H17 Cl F N O Pt SP 1 21/c 15.9315; 12.1005; 19.7
90; 103.067; 90
1377.34Zamora, Ana; Pérez, Sergio A; Rodríguez, Venancio; Janiak, Christoph; Yellol, Gorakh S.; Ruiz, José
Dual Antitumor and Antiangiogenic Activity of Organoplatinum(II) Complexes.
Journal of medicinal chemistry, 2015, 58, 1320-1336
1518629 CIFC31 H26 Cl F9 N O P PtP 1 21/c 117.3951; 14.9557; 11.9109
90; 98.576; 90
3064Zamora, Ana; Pérez, Sergio A; Rodríguez, Venancio; Janiak, Christoph; Yellol, Gorakh S.; Ruiz, José
Dual Antitumor and Antiangiogenic Activity of Organoplatinum(II) Complexes.
Journal of medicinal chemistry, 2015, 58, 1320-1336
1518630 CIFC34 H38 O8P 21 21 219.67492; 14.41358; 20.6293
90; 90; 90
2876.76Wu, Taizong; Wang, Qian; Jiang, Cheng; Morris-Natschke, Susan L; Cui, Hui; Wang, Yan; Yan, Yuan; Xu, Jun; Lee, Kuo-Hsiung; Gu, Qiong
neo-Clerodane Diterpenoids from Scutellaria barbata with Activity against Epstein-Barr Virus Lytic Replication.
Journal of natural products, 2015, 78, 500-509
1518631 CIFC26 H36 O7P 21 21 219.60332; 9.87431; 26.75
90; 90; 90
2536.6Wu, Taizong; Wang, Qian; Jiang, Cheng; Morris-Natschke, Susan L; Cui, Hui; Wang, Yan; Yan, Yuan; Xu, Jun; Lee, Kuo-Hsiung; Gu, Qiong
neo-Clerodane Diterpenoids from Scutellaria barbata with Activity against Epstein-Barr Virus Lytic Replication.
Journal of natural products, 2015, 78, 500-509
1518632 CIFC15 H22 O3P 21 21 2110.8914; 10.9342; 11.4227
90; 90; 90
1360.32Del Valle, Paulina; Figueroa, Mario; Mata, Rachel
Phytotoxic Eremophilane Sesquiterpenes from the Coprophilous Fungus Penicillium sp. G1-a14.
Journal of natural products, 2015, 78, 339-342
1518633 CIFC24 H17 N OP 1 21/n 19.5489; 9.6991; 19.1473
90; 97.465; 90
1758.31Li, Ziyuan; Huang, Xiaoqiang; Chen, Feng; Zhang, Chun; Wang, Xiaoyang; Jiao, Ning
Cu-Catalyzed Concise Synthesis of Pyridines and 2-(1H)-Pyridones from Acetaldehydes and Simple Nitrogen Donors.
Organic letters, 2015, 17, 584-587
1518634 CIFC20 H22 B F3 K N OP 21 21 216.3906; 7.7434; 38.9797
90; 90; 90
1928.91Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.
Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 940-943
1518635 CIFC26 H29 B F4 N2 O2P 21 21 218.447; 16.3195; 17.2927
90; 90; 90
2383.8Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.
Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 940-943
1518636 CIFC46 H44 B3 N3 O7P 1 21/c 116.559; 16.774; 15.989
90; 115.658; 90
4003.2Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518637 CIFC27 H24 B3 N3 O12R -3 :H19.9798; 19.9798; 12.6217
90; 90; 120
4363.46Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518638 CIFC37 H33 B3 Cl3 N3 O7P 1 21/c 113.0661; 12.1247; 22.3242
90; 98.251; 90
3500Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518639 CIFC33 H40 B N O4 SiP 1 21/c 113.3949; 14.3478; 15.283
90; 92.281; 90
2934.9Kubota, Koji; Iwamoto, Hiroaki; Yamamoto, Eiji; Ito, Hajime
Silicon-tethered strategy for copper(i)-catalyzed stereo- and regioselective alkylboration of alkynes.
Organic letters, 2015, 17, 620-623
1518640 CIFC20 H22 N2 O5P -19.272; 15.087; 26.669
75.828; 88.836; 88.885
3616Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She
Synthetic Study toward the Misassigned (±)-Tronoharine.
Organic letters, 2015, 17, 720-723
1518641 CIFC18 H18 N2 O3P 1 21/n 18.2569; 11.5402; 15.727
90; 102.251; 90
1464.4Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She
Synthetic Study toward the Misassigned (±)-Tronoharine.
Organic letters, 2015, 17, 720-723
1518642 CIFC13 H12 O3P -19.562; 10.2591; 10.618
87.713; 85.512; 88.206
1037.16Kratochvíl, Jiří; Novák, Zdeněk; Ghavre, Mukund; Nováková, Lucie; Růžička, Aleš; Kuneš, Jiří; Pour, Milan
Fully Substituted Pyranones via Quasi-Heterogeneous Genuinely Ligand-Free Migita-Stille Coupling of Iodoacrylates.
Organic letters, 2015, 17, 520-523
1518643 CIFC21 H18 N2 OP 21 21 218.964; 12.046; 16.315
90; 90; 90
1761.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518644 CIFC23 H20 N2 OP -16.345; 11.725; 13.3
67.812; 80.532; 84.005
902.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518645 CIFC24 H35 N3 O2P 1 21 112.8948; 9.7854; 18.3889
90; 94.667; 90
2312.6Li, Xun; Taechalertpaisarn, Jaru; Xin, Dongyue; Burgess, Kevin
Protein-Protein Interface Mimicry by an Oxazoline Piperidine-2,4-dione.
Organic letters, 2015, 17, 632-635
1518646 CIFC34 H56 N2 O7 Si2P 21 21 219.052; 19.871; 22.2031
90; 90; 90
3993.72Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518647 CIFC33 H44 N2 O7 SiP 1 21 118.0919; 10.7097; 18.935
90; 107.979; 90
3489.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518648 CIFC22 H28 N2 O7P 21 21 2111.0538; 12.5835; 15.8359
90; 90; 90
2202.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518649 CIFC17 H17 N O3P 1 21/c 18.9854; 18.5028; 9.4678
90; 109.249; 90
1486.07Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518650 CIFC25 H22 Cl N O4P -18.5929; 9.9207; 13.6227
73.585; 78.745; 86.593
1092.53Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518651 CIFC31 H27 N3 O2P 1 21 17.6192; 12.0803; 14.0233
90; 102.158; 90
1261.8Pertejo, Pablo; Corres, Nazaret; Torroba, Tomás; García-Valverde, María
Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones.
Organic letters, 2015, 17, 612-615
1518652 CIFC30 H38 N2 O7P 1 21 111.3323; 8.5548; 14.1288
90; 92.453; 90
1368.47Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518653 CIFC32 H40 N2 O7P 1 21 113.4499; 7.46; 14.9726
90; 104.948; 90
1451.46Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518654 CIFC42 H59 F3 O10P 1 21 113.4566; 8.18811; 19.1862
90; 100.629; 90
2077.74Inahashi, Yuki; Iwatsuki, Masato; Ishiyama, Aki; Matsumoto, Atsuko; Hirose, Tomoyasu; Oshita, Jun; Sunazuka, Toshiaki; Panbangred, Watanalai; Takahashi, Yoko; Kaiser, Marcel; Otoguro, Kazuhiko; O̅mura, Satoshi
Actinoallolides A-E, New Anti-trypanosomal Macrolides, Produced by an Endophytic Actinomycete, Actinoallomurus fulvus MK10-036.
Organic letters, 2015, 17, 864-867
1518655 CIFC13 H10 N2 O2 SP 1 21/c 111.9124; 7.5041; 14.67
90; 111.533; 90
1219.9Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518656 CIFC13 H10 N4 OP -16.9373; 8.2261; 9.7516
85.814; 78.171; 89.197
543.22Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518657 CIFC14 H11 N5P -17.9667; 8.6666; 9.6847
109.198; 107.554; 92.006
595.36Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518658 CIFC16 H19 N O4P 1 21 18.2102; 6.2167; 14.102
90; 90.69; 90
719.7Lou, Yan-Peng; Zheng, Chang-Wu; Pan, Ren-Ming; Jin, Qiao-Wen; Zhao, Gang; Li, Zhong
Enantioselective Direct Mannich Reactions of Cyclic β-Ketoesters Catalyzed by Chiral Phosphine via a Novel Dual-Reagent Catalysis.
Organic letters, 2015, 17, 688-691
1518659 CIFC25 H23 Br O S2 SeP 1 21/c 19.5704; 11.7332; 21.056
90; 97.692; 90
2343.1Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518660 CIFC20 H21 F O2 S2P 1 21/c 110.5963; 16.7072; 10.9555
90; 95.184; 90
1931.57Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518661 CIFC64 H48 S4P 1 21/n 120.159; 5.0166; 25.728
90; 109.164; 90
2457.7Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518662 CIFC65 H50 S4P 1 21/n 120.1; 5.1652; 25.159
90; 109.501; 90
2462.2Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518663 CIFC68 H56 Cl2 S4P 1 21/c 17.6706; 17.4871; 20.506
90; 100.272; 90
2706.5Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518664 CIFC66 H52 S4P 1 21/n 121.43; 5.2798; 24.95
90; 111.599; 90
2624.8Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518665 CIFC66 H52 S4P 1 21/n 120.0834; 5.2324; 24.6005
90; 109.019; 90
2444.01Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518666 CIFC8 H16 F7 O6 P2 S2 SbP 1 21/n 114.5029; 8.9034; 14.9927
90; 97.26; 90
1920.41Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518667 CIFC43 H71 F9 N3 O9 P3 S3 Sb4P -111.4789; 11.9874; 26.0864
91.82; 97.564; 112.074
3284.57Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518668 CIFC29 H61.5 F12 N0.5 O12 P4 S4 Sb4P 1 21/c 123.986; 21.83; 22.193
90; 106.57; 90
11138Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518669 CIFC31 H41 F6 N2 O6 S2 SbP 1 21/c 112.3127; 17.4575; 17.0214
90; 91.03; 90
3658.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518670 CIFC4 H9 F4 O3 P SP 1 21/m 110.2147; 8.6511; 11.0323
90; 94.5503; 90
971.83Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518671 CIFC14 H30 F6 O6 P2 S2P 1 21/n 113.4271; 11.8532; 15.7504
90; 110.993; 90
2340.4Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518672 CIFC27 H24 Cl5 F6 N5 O P2 RuP -111.1445; 12.0548; 14.8726
67.197; 84.942; 67.025
1691.09Walden, Andrew G.; Miller, Alexander J. M.
Rapid water oxidation electrocatalysis by a ruthenium complex of the tripodal ligand tris(2-pyridyl)phosphine oxide
Chem. Sci., 2015, 6, 2405
1518673 CIFC33 H48 N2 O9 SP 1 21 113.6507; 10.3032; 13.9805
90; 109.803; 90
1850.02Shen, Hongyun; Shen, Chao; Chen, Chao; Wang, Anming; Zhang, Pengfei
Novel glycosyl pyridyl-triazole@palladium nanoparticles: efficient and recoverable catalysts for C‒C cross-coupling reactions
Catal. Sci. Technol., 2015, 5, 2065
1518674 CIFC75 H71 Cl2 N3 PdP -112.3155; 15.9288; 19.2346
79.609; 87.992; 81.295
3668.5Maluenda, Irene; Chen, Ming-Tsz; Guest, Daniel; Mark Roe, S.; Turner, Michael L.; Navarro, Oscar
Room temperature, solventless telomerization of isoprene with alcohols using (N-heterocyclic carbene)‒palladium catalysts
Catal. Sci. Technol., 2015, 5, 1447
1518675 CIFC27 H39 Cl2 N3 PdC 1 2/c 135.0018; 11.2158; 15.2054
90; 111.789; 90
5542.8Maluenda, Irene; Chen, Ming-Tsz; Guest, Daniel; Mark Roe, S.; Turner, Michael L.; Navarro, Oscar
Room temperature, solventless telomerization of isoprene with alcohols using (N-heterocyclic carbene)‒palladium catalysts
Catal. Sci. Technol., 2015, 5, 1447
1518676 CIFC17 H25 N O2 SiP 1 21/n 17.8451; 10.8055; 41.681
90; 92.188; 90
3530.7Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518677 CIFC19 H19 Cl2 N O SP 1 21/c 19.4678; 22.465; 8.4857
90; 94.892; 90
1798.3Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518680 CIFC21 H31 Ni O3 P SP 1 21/n 19.5684; 16.352; 13.9609
90; 95.255; 90
2175.18Chen, Min; Zou, Wenping; Cai, Zhengguo; Chen, Changle
Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts
Polym. Chem., 2015, 6, 2669
1518681 CIFC46 H39 B F15 Ni O3 P SP n a 2124.5629; 15.6599; 11.5597
90; 90; 90
4446.47Chen, Min; Zou, Wenping; Cai, Zhengguo; Chen, Changle
Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts
Polym. Chem., 2015, 6, 2669
1518682 CIFH18 N8 Ni O6F m -3 m10.8738; 10.8738; 10.8738
90; 90; 90
1285.71Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518683 CIFH12 N2 Ni O12P -15.7531; 7.6604; 11.4876
106.347; 98.45; 101.538
464.73Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518684 CIFH12 N2 Ni O12P -15.8056; 7.7023; 11.6864
105.841; 98.451; 102.203
479.59Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518685 CIFC52 H48 N4 O4P n a 2118.809; 10.08; 20.725
90; 90; 90
3929Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518686 CIFC62 H66 Cl6 N4 O12P -19.8315; 14.743; 21.249
101.193; 91.334; 94.028
3011.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518687 CIFC63 H70 N4 O16P -111.12; 14.029; 20.02
108.726; 98.537; 94.981
2894.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518711 CIFC15 H22 O5P 1 21/c 113.3435; 7.2491; 15.3576
90; 92.261; 90
1484.36Peng, Jin-Bao; Qi, Yue; Jing, Ze-Ran; Wang, Shao-Hua; Tu, Yong-Qiang; Zhu, Dao-Yong; Zhang, Fu-Min
Efficient Oxa-Diels‒Alder/Semipinacol Rearrangement/Aldol Cascade Reaction: Short Approach to Polycyclic Architectures
Organic Letters, 2015, 150209135056006
1518712 CIFC21 H28 O3P 21 21 216.0078; 15.1366; 20.0221
90; 90; 90
1820.76Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518713 CIFC23 H27 F3 O3P 21 21 216.2097; 14.9142; 23.193
90; 90; 90
2147.97Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518714 CIFC14 H26 Cl3 N4 O P RuP 1 21/n 16.9163; 23.66; 11.8396
90; 97.078; 90
1922.7Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518715 CIFC15 H23 Cl2 N4 O P RuP -110.5379; 12.8283; 13.7451
100.766; 97.279; 91.491
1808.34Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518716 CIFC42 H55 Cl2 N5 O10C 1 2 125.187; 8.1556; 21.154
90; 99.308; 90
4288.1Rose, Tristan E.; Lawson, Kenneth V.; Harran, Patrick. G.
Large ring-forming alkylations provide facile access to composite macrocycles
Chem. Sci., 2015, 6, 2219
1518717 CIFC18 H27 B Br N O5 SP -19.483; 13.115; 17.336
90.88; 99.38; 91.32
2126.3Carrillo, Josué Ayuso; Ingleson, Michael J.; Turner, Michael L.
Thienyl MIDA Boronate Esters as Highly Effective Monomers for Suzuki‒Miyaura Polymerization Reactions
Macromolecules, 2015, 48, 979
1518718 CIFC18 H26 O4 SiP b c a16.759; 7.4334; 30.141
90; 90; 90
3754.9Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518719 CIFC18 H26 O4 SiP -16.1239; 16.8945; 17.8873
91.468; 95.3024; 90.184
1842.1Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518720 CIFC166 H366 Ag62 F6 Mo38 N2 O129 S42P -118.4308; 19.5522; 35.0688
93.065; 95.734; 112.904
11523.9Huang, Ren-Wu; Xu, Qing-Qing; Lu, Hong-Lin; Guo, Xiao-Kang; Zang, Shuang-Quan; Gao, Guang-Gang; Tang, Ming-Sheng; Mak, Thomas C. W.
Self-assembly of an unprecedented polyoxomolybdate anion [Mo20O66](12-) in a giant peanut-like 62-core silver-thiolate nanocluster.
Nanoscale, 2015, 7, 7151-7154
1518723 CIFC32 H28 O4 SiP -17.0418; 10.4998; 17.4226
93.591; 96.204; 103.663
1239.21Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518724 CIFC31 H28 O4 SiP 1 21/n 114.0146; 10.5314; 16.6752
90; 100.775; 90
2417.8Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518725 CIFC18 H12 F N O3P 1 21/c 13.798; 11.416; 31.2
90; 90.82; 90
1353Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518726 CIFC22 H16 F4 O3P -17.668; 11.45; 11.497
97.96; 98.584; 103.944
952.6Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518727 CIFC53 H53 F3 N4 O3 P2 SC 1 c 124.05898; 12.60445; 17.26646
90; 109.899; 90
4923.42Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518728 CIFC67 H72 Cl Ir N4 P2P -111.53121; 15.09347; 16.48026
91.4726; 100.955; 90.9436
2814.45Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518729 CIFC54 H52 Cl Ir N4 O2 P2R -330.1754; 30.1754; 27.5094
90; 90; 120
21692.9Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518730 CIFC71.5 H80 Cl2 Ir2 N4 P2P -113.28816; 15.4534; 18.6095
66.4438; 87.7181; 64.8361
3131.28Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518731 CIFC55.5 H62 Au2 Cl3 Ir N4 P2P 1 21/c 112.88426; 13.46559; 30.9781
90; 99.5872; 90
5299.46Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518732 CIFC48.63 H73.25 Cl3.25 N6 O10P 21 21 2110.3987; 18.7734; 27.849
90; 90; 90
5436.7Pettit, George R.; Smith, Thomas H.; Arce, Pablo M.; Flahive, Erik J.; Anderson, Collin R.; Chapuis, Jean-Charles; Xu, Jun-Ping; Groy, Thomas L.; Belcher, Paul E.; Macdonald, Christian B.
Antineoplastic agents. 599. Total synthesis of dolastatin 16.
Journal of natural products, 2015, 78, 476-485
1518733 CIFC20 H22 O7P c a 2128.5983; 8.3343; 7.7428
90; 90; 90
1845.47Kim, Hiyoung; Yang, Inho; Ryu, Shin-Young; Won, Dong Hwan; Giri, Awadut G.; Wang, Weihong; Choi, Hyukjae; Chin, Jungwook; Hahn, Dongyup; Kim, Eunhee; Han, Chulkyeong; Lee, Jihye; Nam, Sang-Jip; Ho, Won-Kyung; Kang, Heonjoong
Acredinones A and B, Voltage-Dependent Potassium Channel Inhibitors from the Sponge-Derived Fungus Acremonium sp. F9A015.
Journal of natural products, 2015, 78, 363-367
1518734 CIFC20 H18 O2P 1 21/c 18.7862; 16.6613; 11.1995
90; 112.702; 90
1512.47Sun, Qiu; Yao, Chang Jiang; König, Burkhard
A triphenylphosphine mediated photo-rearrangement and methanol addition of aryl chalcones to 1-propanones.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2015, 14, 948-952
1518735 CIFC46 H34 N4 O4P b c a10.981; 16.009; 19.987
90; 90; 90
3513.6Nielsen, Christian Benedikt Orea; Sørensen, Henning Osholm; Kongsted, Jacob
Comparison between Theoretically and Experimentally Determined Electronic Properties: Applications to Two-Photon Singlet Oxygen Sensitizers.
The journal of physical chemistry. A, 2015, 119, 1906-1916
1518736 CIFC55 H48 N2 O3P -110.069; 13.876; 16.5
109.803; 94.46; 103.692
2075.7Nielsen, Christian Benedikt Orea; Sørensen, Henning Osholm; Kongsted, Jacob
Comparison between Theoretically and Experimentally Determined Electronic Properties: Applications to Two-Photon Singlet Oxygen Sensitizers.
The journal of physical chemistry. A, 2015, 119, 1906-1916
1518737 CIFC55 H44 N2 O2P -18.5037; 9.8109; 13.1211
92.898; 97.615; 107.974
1027.2Nielsen, Christian Benedikt Orea; Sørensen, Henning Osholm; Kongsted, Jacob
Comparison between Theoretically and Experimentally Determined Electronic Properties: Applications to Two-Photon Singlet Oxygen Sensitizers.
The journal of physical chemistry. A, 2015, 119, 1906-1916
1518738 CIFC19.5 H18.5 As3 Cl6.5 S6P n m a20.703; 9.885; 14.702
90; 90; 90
3008.8Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518739 CIFC24 H24 Cl3 S6 Sb3R -3 c :H14.2066; 14.2066; 33.41
90; 90; 120
5839.7Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518740 CIFC36 H42 As3 Cl3 S6P -110.0055; 12.424; 16.522
81.285; 88.456; 84.579
2020.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518741 CIFC30 H42 As3 Cl3 S6R -3 :H16.413; 16.413; 23.8
90; 90; 120
5552.4Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518742 CIFC24 H30 Cl3 S6 Sb3P 1 21/n 116.0971; 11.4604; 16.3368
90; 91.867; 90
3012.2Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518743 CIFC30 H42 Cl3 S6 Sb3R -3 :H16.458; 16.458; 23.9449
90; 90; 120
5616.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518744 CIFC32 H30 N8 O5 Zn4P 42/m c m11.5382; 11.5382; 25.813
90; 90; 90
3436.5Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518745 CIFC34 H32 N8 O5 Zn4P 42/m c m11.517; 11.517; 34.474
90; 90; 90
4573Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518747 CIFC14 H9 Cl N4 O2P -111.31; 13.792; 13.982
93.902; 90.56; 112.233
2012.7Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518748 CIFC15 H11 Br N4 O2P b c a10.784; 9.6655; 28.858
90; 90; 90
3007.9Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518753 CIFC37 H31 Cu F12 N4P -112.1667; 12.1867; 13.5954
81.549; 77.873; 65.444
1788.5Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions
Chem. Sci., 2015, 6, 2474
1518754 CIFC16 H6 F12 N2I 41/a :236.71; 36.71; 4.9148
90; 90; 90
6623.3Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions
Chem. Sci., 2015, 6, 2474
1518755 CIFC18 H27 Au B Cl N2 O2P 1 21/n 111.295; 10.512; 16.9583
90; 102.328; 90
1967.1Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518756 CIFC53 H79 Au B Cl N4 O4P 1 21/c 115.396; 14.4925; 24.966
90; 100.935; 90
5469.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518757 CIFC19 H27 B F3 Li N2 O5 SP -15.9513; 10.9562; 17.3953
96.176; 93.242; 97.646
1114.73Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518758 CIFC26 H39 B Cl N2 O2 RhP 1 21/c 116.46; 13.8072; 11.9483
90; 104.628; 90
2627.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518759 CIFC33 H47 B Cl Ir N2 O2C 1 2/c 135.4699; 10.667; 18.1337
90; 115.404; 90
6197.6Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518760 CIFC193.98 H267.94 N41 O29 Ru2C 1 2/c 129.8268; 17.7117; 38.0786
90; 96.79; 90
19975.2Anderson, Bryce L.; Maher, Andrew G.; Nava, Matthew; Lopez, Nazario; Cummins, Christopher C.; Nocera, Daniel G.
Ultrafast Photoinduced Electron Transfer from Peroxide Dianion.
The journal of physical chemistry. B, 2015, 119, 7422-7429
1518761 CIFC25 H23 F12 Fe2 O10P -19.507; 11.729; 16.605
102.703; 96.771; 112.595
1625Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518762 CIFC35 H25 F24 Fe3 O14P 1 21 19.7834; 20.8414; 12.0955
90; 102.57; 90
2407.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518763 CIFC35 H25 F24 Fe3 O14P 1 21 19.7979; 20.819; 12.0998
90; 102.659; 90
2408.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518764 CIFC35 H19 F30 Fe3 O14C 1 2/c 120.934; 13.481; 17.739
90; 92.848; 90
5000Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518765 CIFC25 H23 F12 Fe Mn O10P -19.464; 11.8255; 16.508
102.022; 97.859; 112.682
1618.3Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518766 CIFC35 H25 F24 Fe Ni2 O14P 1 21 19.7682; 20.7583; 12.0575
90; 103.126; 90
2381Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518767 CIFC16 H11 Br N6 O3P 1 21/c 117.554; 6.445; 15.846
90; 111.672; 90
1666Okamoto, Noriko; Sueda, Takuya; Minami, Hideki; Miwa, Yoshihisa; Yanada, Reiko
Regioselective Iodoazidation of Alkynes: Synthesis of α,α-Diazidoketones
Organic Letters, 2015, 150226085504000
1518768 CIFC15 H18 Cl2 N4 O3 PtP 1 21/c 119.113; 8.7386; 12.407
90; 107.31; 90
1978.4Tabatabaei Rezaei, Seyed Jamal; Amani, Vahid; Nabid, Mohammad Reza; Safari, Nasser; Niknejad, Hassan
Folate-decorated polymeric Pt(ii) prodrug micelles for targeted intracellular delivery and cytosolic glutathione-triggered release of platinum anticancer drugs
Polym. Chem., 2015, 6, 2844
1518769 CIFC25 H33 N3 O4P 21 21 216.0367; 19.1261; 20.5025
90; 90; 90
2367.2Meng, Ling-Hong; Du, Feng-Yu; Li, Xiao-Ming; Pedpradab, Patchara; Xu, Gang-Ming; Wang, Bin-Gui
Rubrumazines A-C, Indolediketopiperazines of the Isoechinulin Class from Eurotium rubrum MA-150, a Fungus Obtained from Marine Mangrove-Derived Rhizospheric Soil.
Journal of natural products, 2015, 78, 909-913
1518770 CIFC20 H16 Cl4 N2P b c a11.2813; 14.1148; 24.5832
90; 90; 90
3914.5Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518771 CIFC18 H26 Cl2 N2P -19.3474; 9.8657; 12.3923
66.695; 69.579; 62.115
908.59Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518772 CIFC28 H23 Br Cl3 N O2P 21 21 219.6557; 10.7366; 25.0366
90; 90; 90
2595.53Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518773 CIFC26 H21 N O2 SP 21 21 217.3516; 9.5635; 29.4896
90; 90; 90
2073.33Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518774 CIFC17 H24 O6C 1 2 119.391; 6.455; 15.383
90; 115.322; 90
1740Gao, Chun; Han, Li; Zheng, Dan; Jin, Hongwei; Gai, Chunyan; Wang, Jianbin; Zhang, Hao; Zhang, Liangren; Fu, Hongzheng
Dimeric Abietane Diterpenoids and Sesquiterpenoid Lactones from Teucrium viscidum.
Journal of natural products, 2015, 78, 630-638
1518775 CIFC20 H28 O4P 21 21 2110.734; 12.344; 13.282
90; 90; 90
1759.9Gao, Chun; Han, Li; Zheng, Dan; Jin, Hongwei; Gai, Chunyan; Wang, Jianbin; Zhang, Hao; Zhang, Liangren; Fu, Hongzheng
Dimeric Abietane Diterpenoids and Sesquiterpenoid Lactones from Teucrium viscidum.
Journal of natural products, 2015, 78, 630-638

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