Crystallography Open Database

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7117480 CIFC16 H24 TiP 1 21/n 19.5686; 10.0906; 15.5541
90; 97.1528; 90		1490.11Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117481 CIFC28 H32 TiP -19.4641; 10.4852; 13.112
72.5421; 79.0295; 64.7729		1119.89Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117482 CIFC18 H24 O4 TiP -18.0338; 9.4658; 11.9668
78.479; 88.7238; 75.3323		862.25Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117483 CIFC30 H32 O4 TiC 1 2/c 134.424; 8.8424; 19.0704
90; 119.263; 90		5064.08Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117484 CIFC34 H30 N5 Nb O13P -18.934; 11.3774; 17.883
78.587; 78.363; 70.115		1657.6Willian X. C. Oliveira; Cynthia L. M. Pereira; Carlos B. Pinheiro; Joan Cano; Francesc Lloret; Miguel Julve
Relatively strong intramolecular antiferromagnetic coupling in a neutral CrIII2NbV2 heterobimetallic molecular square
Chem.Commun., 2015, 51, 11806
7117485 CIFC28 H60 Cr2 Nb2 O30 S10P -111.4285; 12.1741; 12.185
98.122; 116.838; 94.962		1475.7Willian X. C. Oliveira; Cynthia L. M. Pereira; Carlos B. Pinheiro; Joan Cano; Francesc Lloret; Miguel Julve
Relatively strong intramolecular antiferromagnetic coupling in a neutral CrIII2NbV2 heterobimetallic molecular square
Chem.Commun., 2015, 51, 11806
7117508 CIFC20 H17 N3 O0P 1 21/c 117.0546; 5.5978; 16.1901
90; 105.328; 90		1490.66R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117509 CIFC26 H21 N3P 1 21/c 113.1017; 20.7038; 7.3429
90; 105.921; 90		1915.4R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117510 CIFC30 H27 N3 O3P c a 2121.214; 8.2654; 27.017
90; 90; 90		4737.2R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117511 CIFC48 H39 N3 O3 S0C 1 2/c 114.8372; 26.503; 18.224
90; 96.42; 90		7121.3R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117512 CIFC12 H10 N2P 1 21/c 19.0822; 14.3844; 7.6234
90; 92.165; 90		995.2R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117513 CIFC32 H38 B20P -111.066; 13.248; 14.418
114.692; 103.244; 94.149		1835.3Jixi Guo; Danqing Liu; Jiahui Zhang; Jiji Zhang; Qian Miao; Zuowei Xie
o-Carborane functionalized pentacenes: synthesis, molecular packing and ambipolar organic thin-film transistors
Chem.Commun., 2015, 51, 12004
7117514 CIFC34 H42 B20C 1 2/c 120.184; 14.426; 14.526
90; 118.624; 90		3712.7Jixi Guo; Danqing Liu; Jiahui Zhang; Jiji Zhang; Qian Miao; Zuowei Xie
o-Carborane functionalized pentacenes: synthesis, molecular packing and ambipolar organic thin-film transistors
Chem.Commun., 2015, 51, 12004
7117515 CIFC38 H50 B20P 1 21/n 16.7399; 9.6832; 30.293
90; 93.691; 90		1972.9Jixi Guo; Danqing Liu; Jiahui Zhang; Jiji Zhang; Qian Miao; Zuowei Xie
o-Carborane functionalized pentacenes: synthesis, molecular packing and ambipolar organic thin-film transistors
Chem.Commun., 2015, 51, 12004
7117516 CIFC42 H21 O3 P SP 1 21 110.913; 16.97; 17.246
90; 100.936; 90		3135.8Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117517 CIFC42 H21 O3 PP 21 21 230.262; 51.48; 4.0818
90; 90; 90		6359Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117518 CIFC43 H22 Cl3 O3 P SP 1 21/n 114.036; 16.26; 16.551
90; 109.896; 90		3552Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117519 CIFC42 H23 O4 PP -320.785; 20.785; 4.1189
90; 90; 120		1541Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117520 CIFC144 H42 O6 P2R -3 :H19.058; 19.058; 20.787
90; 90; 120		6538Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117521 CIFC231 H87 Cl9 O12 P4 S4P 4131.8128; 31.8128; 16.4343
90; 90; 90		16632.4Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117522 CIFC54 H56 N26 O16P -112.0755; 12.3189; 12.3197
106.538; 97.085; 107.693		1628.94Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117523 CIFC54 H52 N28 O22P -112.5869; 16.1378; 17.8631
87.78; 89.749; 67.888		3358.8Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117524 CIFC54 H56 N26 O22 S UP -115.4905; 15.7934; 16.7184
68.423; 89.602; 83.048		3772.4Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117525 CIFC108 H112 Br2 N52 O34 UP -112.6611; 15.3936; 17.0052
90.039; 97.817; 91.364		3282.6Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117526 CIFC108 H112 Br2 N52 O34 UP -112.6458; 15.6109; 17.1344
89.597; 82.238; 84.826		3337.85Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117527 CIFC120 H136 Br2 N60 O46 U2P -113.333; 26.409; 26.515
81.73; 84.73; 84.24		9164Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117528 CIFC56 H32 N6P -19; 19.58; 23.93
77.99; 83.67; 89.86		4098.6Shipan Wang; Yuewei Zhang; Weiping Chen; Jinbei Wei; Yu Liu; Yue Wang
Achieving high power efficiency and low roll-off OLEDs based on energy transfer from thermally activated delayed excitons to fluorescent dopants
Chem.Commun., 2015, 51, 11972
7117529 CIFC26 H24 Br N O4 SP 1 21 117.678; 9.856; 20.882
90; 103.673; 90		3535.3Zhong-Hua Gao; Xiang-Yu Chen; Han-Ming Zhang; Song Ye
N-Heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals with aldimines: highly enantioselective synthesis of dihydropyridinones
Chem.Commun., 2015, 51, 12040
7117530 CIFC23 H26 Cl N O5 Pt SP -19.583; 9.8654; 14.2517
104.643; 95.718; 114.866		1149.74Oliver J. Stacey; Angelo J. Amoroso; James A. Platts; Peter N. Horton; Simon J. Coles; David Lloyd; Catrin F. Williams; Anthony J. Hayes; Jay J. Dunsford; Simon J. A. Pope
Water soluble, cyclometalated Pt(II)-Ln(III) conjugates towards novel bimodal imaging agents
Chem.Commun., 2015, 51, 12305
7117531 CIFC6 H6 Cl N O2P 1 21/c 112.132; 6.7332; 8.752
90; 91.331; 90		714.7Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117532 CIFC7 H5 Cl N2 O2P -16.037; 8.101; 9.222
70.622; 74.48; 85.612		409.9Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117533 CIFC12 H10 Cl2 N2 O4P 1 21/n 14.4859; 20.457; 14.7
90; 97.6; 90		1337.1Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117534 CIFC24 H18 Cl4 N4 O4P 1 21/c 13.9469; 27.0301; 10.9065
90; 98.544; 90		1150.65Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117535 CIFC24 H18 Cl4 N4 O4P 1 21/c 14.1263; 23.8718; 11.9867
90; 98.803; 90		1166.81Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117536 CIFC29 H21 Cl4 N5 O4 ZnP 1 21/c 114.0391; 14.1663; 15.99
90; 113.95; 90		2906.3Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117537 CIFC29 H21 Cl4 N5 O4 ZnP 1 21/c 110.7037; 17.9473; 15.8353
90; 106.927; 90		2910.2Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117538 CIFC26 H18 Ba2 F8 N2 O11P 1 21/n 17.0904; 32.27; 7.2698
90; 117.997; 90		1468.72L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117539 CIFC16 H2 Ba2 F8 O9C 1 2/c 112.5647; 7.1406; 19.823
90; 101.663; 90		1741.8L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117540 CIFC13 H6 Ca F4 N2 O7P 1 21/n 14.4398; 23.038; 14.3878
90; 96.661; 90		1461.71L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117541 CIFC13 H8 Ca F4 N2 O8P n a 2114.2384; 16.3862; 6.845
90; 90; 90		1597.03L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117542 CIFC8 Cs F4 O4I 1 2/a 19.3605; 9.6918; 11.0752
90; 108.566; 90		952.45L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117543 CIFC8 F4 O4 RbI 1 2/a 19.2821; 9.7189; 10.9837
90; 110.34; 90		929.08L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117544 CIFC11 H10 F4 N O6 SrP -16.1469; 7.0452; 16.1438
94.495; 96.741; 101.639		676.26L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117545 CIFC42 H20 F16 N2 O20 Sr3C 1 2 132.076; 6.1638; 11.5618
90; 97.569; 90		2266L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117546 CIFC13 H8 F4 N2 O8 SrP n a 2114.2686; 16.7326; 7.0181
90; 90; 90		1675.6L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117547 CIFC11 H15 F4 N O9 SrP -18.8263; 8.9293; 10.863
92.612; 93.939; 100.991		836.95L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117548 CIFC13 H8 F4 N2 O8 SrP -17.3008; 9.1264; 13.1904
101.118; 93.83; 110.526		798.95L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117549 CIFC40 H20 O4 S8P 1 21/c 13.9761; 20.6573; 9.8948
90; 96.5712; 90		807.38Jie Liu; Jieshun Cui; Filipe Vilela; Jun He; Matthias Zeller; Allen D. Hunter; Zhengtao Xu
In situ production of silver nanoparticles on an aldehyde-equipped conjugated porous polymer and subsequent heterogeneous reduction of aromatic nitro groups at room temperature
Chem.Commun., 2015, 51, 12197
7117551 CIFC40 H132 Al18 Ga2 O110.5 S8P -110.0721; 16.7628; 17.7945
90.852; 99.861; 101.175		2900.3Fairley, M.; Corum, K. W.; Johns, A.; Unruh, D. K.; Basile, M.; de Groot, J.; Mason, S. E.; Forbes, T. Z.
Isolation and characterization of the [Ga2Al18O8(OH)36(H2O)12](8+) cluster: cationic variations on the Wells-Dawson topology.
Chemical communications (Cambridge, England), 2015, 51, 12467-12469
7117555 CIFC64 H68 Cl2 N4 O P4P 1 21/c 16.515; 27.407; 16.8094
90; 97.149; 90		2978.1Iglesias, Manuel; Iturmendi, Amaia; Sanz Miguel, Pablo J.; Polo, Victor; Pérez-Torrente, Jesús J; Oro, Luis A.
Tuning PCP-Ir complexes: the impact of an N-heterocyclic olefin.
Chemical communications (Cambridge, England), 2015, 51, 12431-12434
7117556 CIFC41 H46 Cl2 F6 Ir N2 P3P 1 21/c 117.973; 11.5843; 19.988
90; 99.642; 90		4102.8Iglesias, Manuel; Iturmendi, Amaia; Sanz Miguel, Pablo J.; Polo, Victor; Pérez-Torrente, Jesús J; Oro, Luis A.
Tuning PCP-Ir complexes: the impact of an N-heterocyclic olefin.
Chemical communications (Cambridge, England), 2015, 51, 12431-12434
7117557 CIFC36 H40 Cl6 F6 Ir N2 O P3P 1 21/c 111.5979; 18.5435; 20.1876
90; 104; 90		4212.7Iglesias, Manuel; Iturmendi, Amaia; Sanz Miguel, Pablo J.; Polo, Victor; Pérez-Torrente, Jesús J; Oro, Luis A.
Tuning PCP-Ir complexes: the impact of an N-heterocyclic olefin.
Chemical communications (Cambridge, England), 2015, 51, 12431-12434
7117558 CIFC21 H14 Br F2 NC 1 c 111.1103; 19.8612; 8.6893
90; 119.104; 90		1675.31Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117559 CIFC22 H17 F2 NP -18.758; 9.0189; 12.1251
77.13; 80.995; 74.079		893.19Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117560 CIFC24 H16 Br3 NP -19.84; 13.6565; 15.873
102.909; 93.588; 95.664		2061.1Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117561 CIFC24 H16 F3 NP 111.219; 11.5; 14.861
72.7; 89.67; 77.32		1782.3Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117562 CIFC27 H22 F3 N O2P 1 21/n 117.8858; 5.3984; 24.0688
90; 107.814; 90		2212.5Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117563 CIFC43 H57 Au Cl3 NP 1 21/c 120.7969; 9.1006; 22.4423
90; 104.981; 90		4103.2Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117564 CIFC19 H21 Cl N4 O6P 1 21 19.96; 8.9114; 12.427
90; 105.91; 90		1060.7Xie, Ming-Sheng; Wang, Yong; Li, Jian-Ping; Du, Cong; Zhang, Yan-Yan; Hao, Er-Jun; Zhang, Yi-Ming; Qu, Gui-Rong; Guo, Hai-Ming
A straightforward entry to chiral carbocyclic nucleoside analogues via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates.
Chemical communications (Cambridge, England), 2015, 51, 12451-12454
7117565 CIFC34 H29 F3 N4 O2P -110.748; 11.799; 12.2207
76.828; 73.111; 87.926		1443.17Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117566 CIFC32 H29 B F4 N4P 1 21/c 112.7461; 9.883; 22.461
90; 106.476; 90		2713.2Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117567 CIFC24 H20 Cl N3 OP -17.956; 9.421; 13.978
107.481; 96.743; 100.43		966.2Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117568 CIFC24 H19 N3 OP 1 21/n 114.1344; 14.8496; 17.8584
90; 95.5371; 90		3730.8Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117569 CIFC40 H40 Br4 Cl2 Dy F6 N4 O8 P Zn2C 1 2/c 117.1014; 18.2552; 15.9346
90; 97.4595; 90		4932.51Oyarzabal, I.; Ruiz, J.; Ruiz, E.; Aravena, D.; Seco, J. M.; Colacio, E.
Increasing the effective energy barrier promoted by the change of a counteranion in a Zn-Dy-Zn SMM: slow relaxation via the second excited state.
Chemical communications (Cambridge, England), 2015, 51, 12353-12356
7117570 CIFC73.5 H95 Au2 Cl3 F6 N5 O4 SbP 1 21/c 117.2829; 20.6778; 21.9456
90; 90.406; 90		7842.6Gimeno, Ana; Rodríguez-Gimeno, Alejandra; Cuenca, Ana B.; Ramírez de Arellano, Carmen; Medio-Simón, Mercedes; Asensio, Gregorio
Gold(i)-catalysed cascade reactions in the synthesis of 2,3-fused indole derivatives.
Chemical communications (Cambridge, England), 2015, 51, 12384-12387
7117571 CIFC30 H28 Cl2 N4 ZnP n n a14.7556; 22.5021; 10.5208
90; 90; 90		3493.2Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117572 CIFC31 H28 Cl5 N4 ZnP n n a14.6608; 22.7977; 9.9218
90; 90; 90		3316.2Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117573 CIFC62 H60 Cl8 N8 Zn2P n n a14.6639; 22.7525; 9.8535
90; 90; 90		3287.5Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117574 CIFC32 H28 Cl4 N4 ZnP n n a14.7255; 22.4827; 10.2852
90; 90; 90		3405.1Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117575 CIFC30 H28 N4P -15.599; 7.1074; 16.1003
92.646; 98.583; 112.049		583.53Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117576 CIFC22 H22 OP 1 21/c 118.8889; 5.8024; 15.156
90; 95.856; 90		1652.44Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117577 CIFC25 H20 O3P -15.8013; 11.3046; 15.3699
110.966; 92.458; 102.961		908.83Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117578 CIFC20 H20 OP 1 21/n 16.2076; 15.3283; 16.201
90; 95.237; 90		1535.1Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117579 CIFC18 H16 OP 1 21/c 15.5946; 9.1084; 26.337
90; 90.82; 90		1341.94Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117580 CIFC9 H9 B F4 N2P 1 21/a 113.372; 6.2221; 13.8278
90; 112.232; 90		1065Leblanc, Nicolas; Sproules, Stephen; Pasquier, Claude; Auban-Senzier, Pascale; Raffy, Helene; Powell, Annie K.
Approaching the limit of Cu(II)/Cu(I) mixed valency in a Cu(I)Br2-N-methylquinoxalinium hybrid compound.
Chemical communications (Cambridge, England), 2015, 51, 12740-12743
7117581 CIFC9 H9 Br2 Cu N2C 1 2/m 115.373; 6.4099; 10.9646
90; 96.692; 90		1073.1Leblanc, Nicolas; Sproules, Stephen; Pasquier, Claude; Auban-Senzier, Pascale; Raffy, Helene; Powell, Annie K.
Approaching the limit of Cu(II)/Cu(I) mixed valency in a Cu(I)Br2-N-methylquinoxalinium hybrid compound.
Chemical communications (Cambridge, England), 2015, 51, 12740-12743
7117582 CIFC36 H108 N9 Nb9 O69.5 P5P 1 21/c 127.347; 15.4386; 24.5428
90; 91.742; 90		10357.2Son, Jung-Ho; Casey, William H.
A new Keggin-like niobium-phosphate cluster that reacts reversibly with hydrogen peroxide.
Chemical communications (Cambridge, England), 2015, 51, 12744-12747
7117583 CIFC24 H28 N2 O2P 1 21/n 111.8462; 7.6966; 22.1897
90; 94.024; 90		2018.2Rawling, M. J.; Storr, T. E.; Bawazir, W. A.; Cully, S. J.; Lewis, W.; Makki, M. S. I. T.; Strutt, I. R.; Jones, G.; Hamza, D.; Stockman, R. A.
Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.
Chemical communications (Cambridge, England), 2015, 51, 12867-12870
7117584 CIFC18 H24 N2 O2P -18.0233; 8.5269; 12.1531
107.964; 98.204; 97.133		770.22Rawling, M. J.; Storr, T. E.; Bawazir, W. A.; Cully, S. J.; Lewis, W.; Makki, M. S. I. T.; Strutt, I. R.; Jones, G.; Hamza, D.; Stockman, R. A.
Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.
Chemical communications (Cambridge, England), 2015, 51, 12867-12870
7117585 CIFC20 H21 N O3 SP 1 21/c 110.783; 12.0241; 14.0523
90; 93.965; 90		1817.6Liu, Bang; Song, Ren-Jie; Ouyang, Xuan-Hui; Li, Yang; Hu, Ming; Li, Jin-Heng
Palladium-catalyzed oxidative 6-exo-trig cyclization of 1,6-enynes: facile synthesis of bicyclo[4.1.0]heptan-5-ones.
Chemical communications (Cambridge, England), 2015, 51, 12819-12822
7117586 CIFC73 H67 N2 O PP n a 2118.9194; 14.8964; 20.0103
90; 90; 90		5639.5Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117587 CIFC88 H72 B F4 N2 PP -113.7202; 16.4329; 19.0854
74.147; 78.554; 81.404		4036.3Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117588 CIFC71 H58 F6 N2 O7 P S2P -114.4808; 14.6435; 15.4095
83.039; 84.164; 77.715		3159.5Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117589 CIFC73 H57 Fe N2 O4 PP 1 21/n 112.6626; 18.3247; 25.5405
90; 101.719; 90		5802.8Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117590 CIFC69 H57 Au2 Cl2 N2 PP 1 21/c 115.4817; 18.0766; 24.4404
90; 98.019; 90		6772.9Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117591 CIFC69 H63 B2 N2 PP 1 21/c 113.5874; 17.073; 24.447
90; 105.718; 90		5459.1Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117592 CIFC22 H25 N OP 1 21/c 112.82457; 6.61539; 20.0798
90; 93.3829; 90		1700.59Paterson, Andrew J.; St John-Campbell, Sahra; Mahon, Mary F.; Press, Neil J.; Frost, Christopher G.
Catalytic meta-selective C-H functionalization to construct quaternary carbon centres.
Chemical communications (Cambridge, England), 2015, 51, 12807-12810
7117593 CIFC222 H218 Co12 N26 O50P -117.7558; 21.8506; 21.8517
60.483; 81.896; 68.78		6870Xu, Hong; Wang, Qian; Qin, Jian-Hua; Zang, Shuang-Quan; Langley, Stuart K.; Murray, Keith S.; Moubaraki, Boujemaa; Batten, Stuart R.; Mak, Thomas C. W.
A cyclic dodecanuclear cobalt cluster based on a derivative of the rhodamine 6G dye with unusual magnetization.
Chemical communications (Cambridge, England), 2015, 51, 12716-12719
7117594 CIFC50 H62 Cl4 Cu2 N8 O21 S5P b c a18.0973; 28.4369; 28.5016
90; 90; 90		14667.8Rancan, Marzio; Armelao, Lidia
Exploiting dimensional variability in coordination polymers: solvent promotes reversible conversion between 3D and chiral 1D architectures.
Chemical communications (Cambridge, England), 2015, 51, 12947-12949
7117595 CIFC9 H16 Cl Cu0.5 N O6 S2P 31 2 110.7197; 10.7197; 23.0839
90; 90; 120		2297.2Rancan, Marzio; Armelao, Lidia
Exploiting dimensional variability in coordination polymers: solvent promotes reversible conversion between 3D and chiral 1D architectures.
Chemical communications (Cambridge, England), 2015, 51, 12947-12949
7117596 CIFC9 H16 Cl Cu0.5 N O6 S2P 32 2 110.7314; 10.7314; 23.1419
90; 90; 120		2308.04Rancan, Marzio; Armelao, Lidia
Exploiting dimensional variability in coordination polymers: solvent promotes reversible conversion between 3D and chiral 1D architectures.
Chemical communications (Cambridge, England), 2015, 51, 12947-12949
7117597 CIFC16 H12 O3P 1 21/n 16.0914; 8.5177; 23.947
90; 90.598; 90		1242.4Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π+2π]-cycloadditions of tert-butyl propiolates with aldehydes and ketones to form 4H-1,3-dioxine derivatives.
Chemical communications (Cambridge, England), 2015, 51, 13004-13007
7117598 CIFC21 H18 F N O2C 1 2/c 140.945; 4.8118; 18.994
90; 114.23; 90		3412.5Zhou, Peng; Hao, Wen-Juan; Zhang, Jin-Peng; Jiang, Bo; Li, Guigen; Tu, Shu-Jiang
Cascade bicyclizations of o-alkynyl aldehydes with thiazolium salts: a new access toward poly-functionalized indeno[2,1-b]pyrroles.
Chemical communications (Cambridge, England), 2015, 51, 13012-13015
7117599 CIFC24 H18 Cu N6 O7I 1 2/a 116.6086; 7.1589; 19.141
90; 102.179; 90		2224.6Larragy, Ruth; Fitzgerald, Jenny; Prisecaru, Andreea; McKee, Vickie; Leonard, Paul; Kellett, Andrew
Protein engineering with artificial chemical nucleases.
Chemical communications (Cambridge, England), 2015, 51, 12908-12911
7117600 CIFC41 H56 B2 Cl4 Fe2 N2 O4P 1 21/c 19.156; 10.84; 22.94
90; 100.259; 90		2240Braunschweig, Holger; Ewing, William C.; Ferkinghoff, Katharina; Hermann, Alexander; Kramer, Thomas; Shang, Rong; Siedler, Eva; Werner, Christine
Activation of boryl-, borylene and metalloborylene complexes by isonitriles.
Chemical communications (Cambridge, England), 2015, 51, 13032-13035
7117601 CIFC21 H31 B Mn N3 O2P 1 21/c 19.5331; 12.839; 18.276
90; 97.456; 90		2217.99Braunschweig, Holger; Ewing, William C.; Ferkinghoff, Katharina; Hermann, Alexander; Kramer, Thomas; Shang, Rong; Siedler, Eva; Werner, Christine
Activation of boryl-, borylene and metalloborylene complexes by isonitriles.
Chemical communications (Cambridge, England), 2015, 51, 13032-13035
7117602 CIFC38 H48 B Cr Fe N3 O7P 1 21 110.8; 18.449; 19.691
90; 96.23; 90		3900Braunschweig, Holger; Ewing, William C.; Ferkinghoff, Katharina; Hermann, Alexander; Kramer, Thomas; Shang, Rong; Siedler, Eva; Werner, Christine
Activation of boryl-, borylene and metalloborylene complexes by isonitriles.
Chemical communications (Cambridge, England), 2015, 51, 13032-13035
7117603 CIFC14 H19 Cd N3 O2 SP b c a13.9096; 10.5234; 22.6923
90; 90; 90		3321.61Roy, Sumit; Dey, Arka; Ray, Partha Pratim; Ortega-Castro, Joaquín; Frontera, Antonio; Chattopadhyay, Shouvik
Application of a novel 2D cadmium(ii)-MOF in the formation of a photo-switch with a substantial on-off ratio.
Chemical communications (Cambridge, England), 2015, 51, 12974-12976
7117604 CIFC58 H44 F20 Ir2 N12 O P2P -19.382; 13.771; 14.966
63; 76.75; 82.82		1676.5Li, Guangfu; Ren, Xinyao; Shan, Guogang; Che, Weilong; Zhu, Dongxia; Yan, Likai; Su, Zhongmin; Bryce, Martin R.
New AIE-active dinuclear Ir(iii) complexes with reversible piezochromic phosphorescence behaviour.
Chemical communications (Cambridge, England), 2015, 51, 13036-13039
7117605 CIFC40 H49 Cu N3 O2P 1 21/c 114.9821; 27.9247; 18.0471
90; 107.42; 90		7204.1Doistau, Benjamin; Cantin, Jean-Louis; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Mechanical switching of magnetic interaction by tweezers-type complex.
Chemical communications (Cambridge, England), 2015, 51, 12916-12919
7117606 CIFC91 H99 Cu2 N7 O10P b c n11.3594; 40.7108; 19.0962
90; 90; 90		8831Doistau, Benjamin; Cantin, Jean-Louis; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Mechanical switching of magnetic interaction by tweezers-type complex.
Chemical communications (Cambridge, England), 2015, 51, 12916-12919
7117607 CIFC94 H101 Cl11 Cu2 N7 O4 ZnC 1 2/c 169.071; 14.7327; 19.7966
90; 98.123; 90		19943Doistau, Benjamin; Cantin, Jean-Louis; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Mechanical switching of magnetic interaction by tweezers-type complex.
Chemical communications (Cambridge, England), 2015, 51, 12916-12919
7117611 CIFC12 H9 F6 N O4P 1 21/c 113.0242; 13.3563; 8.2205
90; 100.66; 90		1405.32Sarkar, Satavisha; Khan, Abu T.
Beyond conventional routes, an unprecedented metal-free chemoselective synthesis of anthranilate esters via a multicomponent reaction (MCR) strategy.
Chemical communications (Cambridge, England), 2015, 51, 12673-12676
7117612 CIFC15 H20 N2 O3P 1 21/c 14.8164; 12.3382; 24.0676
90; 94.39; 90		1426.04Sarkar, Satavisha; Khan, Abu T.
Beyond conventional routes, an unprecedented metal-free chemoselective synthesis of anthranilate esters via a multicomponent reaction (MCR) strategy.
Chemical communications (Cambridge, England), 2015, 51, 12673-12676
7117613 CIFC8 H25 Ag6 Cl N16 O7I 41/a m d29.5862; 29.5862; 3.4563
90; 90; 90		3025.4Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117614 CIFC8 H13 Ag6 Cl N16 OP -4 n 219.3474; 19.3474; 3.5013
90; 90; 90		1310.61Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117615 CIFC12 H29 Ag6 Cl N12 O7I 41/a m d29.415; 29.415; 3.525
90; 90; 90		3050Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117616 CIFC12 H17 Ag6 Cl N12 OI -4 2 d28.708; 28.708; 3.5249
90; 90; 90		2905Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117617 CIFC8 H25 Ag6 Br N16 O7I 41/a m d29.6337; 29.6337; 3.4913
90; 90; 90		3065.9Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117618 CIFC8 H13 Ag6 Br N16 OP -4 n 219.455; 19.455; 3.5339
90; 90; 90		1337.6Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117619 CIFC12 H29 Ag6 Br N12 O7I 41/a m d29.419; 29.419; 3.5564
90; 90; 90		3078Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117620 CIFC12 H17 Ag6 Br N12 OI -4 2 d28.503; 28.503; 3.5383
90; 90; 90		2874.6Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117621 CIFC40 H36 F4 Ir N7 OP -111.9138; 12.3154; 14.3549
99.444; 98.544; 116.93		1791.9Feng, Yansong; Li, Ping; Zhuang, Xuming; Ye, Kaiqi; Peng, Tai; Liu, Yu; Wang, Yue
A novel bipolar phosphorescent host for highly efficient deep-red OLEDs at a wide luminance range of 1000-10 000 cd m(-2).
Chemical communications (Cambridge, England), 2015, 51, 12544-12547
7117622 CIFC29 H37 N3 O3P 113.8032; 14.0849; 14.8146
89.715; 77.329; 77.339		2738.9Wu, Xiaowei; Zhang, Dengyou; Zhou, Shengbin; Gao, Feng; Liu, Hong
Site-specific indolation of proline-based peptides via copper(ii)-catalyzed oxidative coupling of tertiary amine N-oxides.
Chemical communications (Cambridge, England), 2015, 51, 12571-12573
7117623 CIFC28 H27 N O5 SP 1 21/n 110.29; 16.124; 15.403
90; 106.6; 90		2449.1Gao, Zhenzhen; Wang, Chang; Yuan, Chunhao; Zhou, Leijie; Xiao, Yumei; Guo, Hongchao
Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates: synthesis of trans-2,3-disubstitued indolines.
Chemical communications (Cambridge, England), 2015, 51, 12653-12656
7117624 CIFC26 H20 N2 O4P -17.361; 8.3907; 16.3626
80.826; 89.447; 85.419		994.5Zou, Lin; Wang, Xiao-Ye; Zhang, Xiao-Xiao; Dai, Ya-Zhong; Wu, Yun-Dong; Wang, Jie-Yu; Pei, Jian
Toward electron-deficient pyrene derivatives: construction of pyrene tetracarboxylic diimide containing five-membered imide rings.
Chemical communications (Cambridge, England), 2015, 51, 12585-12588
7117625 CIFC20 H36 N4 P2P n m a9.2644; 14.3849; 17.7198
90; 90; 90		2361.5Su, Jing; Wang, Bingqiang; Liu, Dongling; Du, Libo; Liu, Yang; Su, Jihu; Zheng, Wenjun
A 1,2,4-diazaphospholyl radical and its nitrogen-phosphorus coupled dimer: synthesis, X-ray structural characterization, EPR analysis, and computational studies.
Chemical communications (Cambridge, England), 2015, 51, 12680-12683
7117626 CIFC27 H21 B0 Cl Co F0 N4 O2P b c m8.6043; 16.622; 21.331
90; 90; 90		3050.8Das, Biswanath; Orthaber, Andreas; Ott, Sascha; Thapper, Anders
Water oxidation catalysed by a mononuclear Co(II) polypyridine complex; possible reaction intermediates and the role of the chloride ligand.
Chemical communications (Cambridge, England), 2015, 51, 13074-13077
7117627 CIFC27 H29 Cl3 N2 O7P 21 21 2111.0927; 15.2908; 17.2201
90; 90; 90		2920.8Zhou, Rui; Wu, Qinjie; Guo, Mingrui; Huang, Wei; He, Xianghong; Yang, Lei; Peng, Fu; He, Gu; Han, Bo
Organocatalytic cascade reaction for the asymmetric synthesis of novel chroman-fused spirooxindoles that potently inhibit cancer cell proliferation.
Chemical communications (Cambridge, England), 2015, 51, 13113-13116
7117628 CIFC17 H13 F3 N2 O2 SC 1 2/c 117.549; 11.355; 18.82
90; 111.289; 90		3494.3Duan, Yaya; Zhou, Bin; Lin, Jin-Hong; Xiao, Ji-Chang
Diastereoselective Johnson-Corey-Chaykovsky trifluoroethylidenation.
Chemical communications (Cambridge, England), 2015, 51, 13127-13130
7117629 CIFC9 H6 F3 N O3P 21 21 214.8359; 6.4223; 30.645
90; 90; 90		951.8Duan, Yaya; Zhou, Bin; Lin, Jin-Hong; Xiao, Ji-Chang
Diastereoselective Johnson-Corey-Chaykovsky trifluoroethylidenation.
Chemical communications (Cambridge, England), 2015, 51, 13127-13130
7117633 CIFC52 H54 S2 Si2P 1 21/c 117.7574; 14.7085; 17.0416
90; 90.251; 90		4451Xueliang Shi; Sangsu Lee; Minjung Son; Bin Zheng; Jingjing Chang; Linzhi Jing; Kuo-Wei Huang; Dongho Kim; Chunyan Chi
Pro-aromatic bisphenaleno-thieno[3,2-b]thiophene versus anti-aromatic bisindeno-thieno[3,2-b]thiophene: different ground-state properties and applications in field-effect transistors
Chem.Commun., 2015, 51, 13178
7117634 CIFC70 H68 N16 O8 ZnP -114.4171; 16.6908; 17.855
63.51; 76.303; 74.915		3676.5Lucas Kocher; Stephanie Durot; Valerie Heitz
Control of the cavity size of flexible covalent cages by silver coordination to the peripheral binding sites
Chem.Commun., 2015, 51, 13181
7117635 CIFC13 H15 F3 N4P 1 21/n 111.3589; 8.1467; 15.8924
90; 99.885; 90		1448.81Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117636 CIFC24 H22 F3 N O2C 1 2/c 133.4249; 6.2204; 20.9937
90; 96.885; 90		4333.5Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117637 CIFC21 H19 F3 N2P -19.987; 10.061; 10.168
71.21; 75.39; 79.84		930.9Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117638 CIFC14 H10 F3 N OP 1 21 19.2351; 5.3558; 12.9094
90; 104.113; 90		619.24Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117639 CIFC15 H10 F3 N OP 1 21/c 113.226; 13.605; 7.27
90; 92.84; 90		1306.6Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117640 CIFC11 H17 N O5 PbR -3 :H14.4445; 14.4445; 34.0453
90; 90; 120		6151.7Saet Byeol Kim; Dong Woo Lee; Suk-Kyu Chang; Kang Min Ok
Pb3[C6(CH3)3(CO2)3H6]2[DMF]3: first layered Pb-Kemp's triacid complex
Chem.Commun., 2015, 51, 13166
7117641 CIFC36 H30 Ho N O11I m a 221.403; 34.255; 8.023
90; 90; 90		5882Gerard Tobin; Steve Comby; Nianyong Zhu; Rodolphe Clerac; Thorfinnur Gunnlaugsson; Wolfgang Schmitt
Towards multifunctional lanthanide-based metal-organic frameworks
Chem.Commun., 2015, 51, 13313
7117642 CIFC6 H14 O9C 1 2/c 17.3942; 9.2111; 14.029
90; 93.117; 90		954.1Nipuni-Dhanesh; H. Gamage; Benedikt Stiasny; Jorg Stierstorfer; Philip D. Martin; Thomas M. Klapotke; Charles H. Winter
Less sensitive oxygen-rich organic peroxides containing geminal hydroperoxy groups
Chem.Commun., 2015, 51, 13298
7117643 CIFC4 H5 O4P 1 21/c 19.776; 6.0458; 8.133
90; 100.964; 90		471.9Nipuni-Dhanesh; H. Gamage; Benedikt Stiasny; Jorg Stierstorfer; Philip D. Martin; Thomas M. Klapotke; Charles H. Winter
Less sensitive oxygen-rich organic peroxides containing geminal hydroperoxy groups
Chem.Commun., 2015, 51, 13298
7117644 CIFC16 H12 F3 N O2P -18.1909; 9.5693; 10.5301
75.88; 72.823; 67.507		720.5Haiqing Luo; Guojiao Wu; Shuai Xu; Kang Wang; Chaoqiang Wu; Yan Zhang; Jianbo Wang
Palladium-catalyzed cross-coupling of aryl fluorides with N-tosylhydrazones via C-F bond activation
Chem.Commun., 2015, 51, 13321
7117645 CIFC15 H10 F3 N O2P 21 21 215.8037; 15.049; 15.033
90; 90; 90		1313Haiqing Luo; Guojiao Wu; Shuai Xu; Kang Wang; Chaoqiang Wu; Yan Zhang; Jianbo Wang
Palladium-catalyzed cross-coupling of aryl fluorides with N-tosylhydrazones via C-F bond activation
Chem.Commun., 2015, 51, 13321
7117646 CIFC76 H180 K2 Mn2 O18 Si12P -112.5416; 16.0775; 27.2358
87.785; 85.0576; 79.8209		5383.7C.-Y. Lin; J. C. Fettinger; N. F. Chilton; A. Formanuik; F. Grandjean; G. J. Long; P. P. Power
Salts of the two-coordinate homoleptic manganese(I) dialkyl anion [Mn{C(SiMe3)3}2]^-^ with quenched orbital magnetism
Chem.Commun., 2015, 51, 13275
7117647 CIFC40 H94 K Mn O10 Si6I 1 2/a 118.4983; 14.4287; 21.2812
90; 90.821; 90		5679.5C.-Y. Lin; J. C. Fettinger; N. F. Chilton; A. Formanuik; F. Grandjean; G. J. Long; P. P. Power
Salts of the two-coordinate homoleptic manganese(I) dialkyl anion [Mn{C(SiMe3)3}2]^-^ with quenched orbital magnetism
Chem.Commun., 2015, 51, 13275
7117648 CIFC19 H21 B2 Cu F8 N4P 1 21/c 114.516; 9.366; 15.706
90; 97.731; 90		2115.9Hiroaki Kotani; Tomomi Yagi; Tomoya Ishizuka; Takahiko Kojima
Enhancement of 4-electron O2 reduction by a Cu(II)-pyridylamine complex via protonation of a pendant pyridine in the second coordination sphere in water
Chem.Commun., 2015, 51, 13385
7117650 CIFC51 H47 K2 N18 Ni2 O12P 1 21/n 112.536; 28.635; 15.794
90; 91.53; 90		5668Jesus Ferrando-Soria; Oscar Fabelo; Maria Castellano; Joan Cano; Stephen Fordham; Hong-Cai Zhou
Multielectron oxidation in a ferromagnetically coupled dinickel(II) triple mesocate
Chem.Commun., 2015, 51, 13381
7117653 CIFC39 H74 N6 O10P 19.7972; 10.4809; 12.3285
107.162; 102.474; 101.595		1132.47Mothukuri Ganesh Kumar; Sushil N. Benke; K. Muruga Poopathi Raja; Hosahudya N. Gopi
Engineering polypeptide folding through trans double bonds: transformation of miniature beta-meanders to hybrid helices
Chem.Commun., 2015, 51, 13397
7117654 CIFC49 H76 N6 O9P 1 21 19.286; 20.892; 27.661
90; 98.639; 90		5305Mothukuri Ganesh Kumar; Sushil N. Benke; K. Muruga Poopathi Raja; Hosahudya N. Gopi
Engineering polypeptide folding through trans double bonds: transformation of miniature beta-meanders to hybrid helices
Chem.Commun., 2015, 51, 13397
7117655 CIFC49 H72 N6 O9C 1 2 135.352; 10.43; 17.876
90; 107.549; 90		6285Mothukuri Ganesh Kumar; Sushil N. Benke; K. Muruga Poopathi Raja; Hosahudya N. Gopi
Engineering polypeptide folding through trans double bonds: transformation of miniature beta-meanders to hybrid helices
Chem.Commun., 2015, 51, 13397
7117656 CIFC27 H26 B Cl2 F2 N3P 1 21/c 119.318; 7.0637; 19.042
90; 101.007; 90		2550.6Sisi Wang; Hui Liu; John Mack; Jiangwei Tian; Bin Zou; Hua Lu; Zhifang Li; Jianxiong Jiang; Zhen Shen
A BODIPY-based 'turn-on' fluorescent probe for hypoxic cell imaging
Chem.Commun., 2015, 51, 13389
7117657 CIFC34 H11 B F20 SP 1 21/c 113.4674; 13.8265; 17.2405
90; 94.8693; 90		3198.72Yoshiaki Shoji; Naoki Tanaka; Daisuke Hashizume; Takanori Fukushima
The molecular and electronic structures of a thioaroyl cation formed by borinium ion-mediated C[double bond, length as m-dash]S double bond cleavage of CS2
Chem.Commun., 2015, 51, 13342
7117658 CIFC34 H11 B F20 SP 1 21/c 113.4674; 13.8265; 17.2405
90; 94.8693; 90		3198.72Yoshiaki Shoji; Naoki Tanaka; Daisuke Hashizume; Takanori Fukushima
The molecular and electronic structures of a thioaroyl cation formed by borinium ion-mediated C[double bond, length as m-dash]S double bond cleavage of CS2
Chem.Commun., 2015, 51, 13342
7117659 CIFC162 H162 Au13 F18 N4 O2 P13C 1 2/c 125.72; 21.2708; 31.007
90; 96.865; 90		16842Mizuho Sugiuchi; Yukatsu Shichibu; Takayuki Nakanishi; Yasuchika Hasegawa; Katsuaki Konishi
Cluster-pi electronic interaction in a superatomic Au13 cluster bearing sigma-bonded acetylide ligands
Chem.Commun., 2015, 51, 13519
7117660 CIFC21 H22 Cl2 Mn4 P4C 1 2/c 140.9164; 9.3302; 27.2353
90; 116.922; 90		9270.5Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117661 CIFC20 H20 Br Cu Mn4 P4C 1 c 114.1032; 12.6047; 12.7139
90; 101.172; 90		2217.28Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117662 CIFC22 H24 Cl5 Cu Mn4 P4C 1 2/c 123.8316; 12.8659; 18.4127
90; 93.404; 90		5635.6Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117663 CIFC28 H27 Cl2 Mn5 O2 P4P 1 21/n 111.9099; 14.821; 17.9552
90; 106.097; 90		3045.13Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117664 CIFC36 H34 Cl4 Mn6 O4 P4P -110.5319; 10.8158; 18.0191
77.832; 80.265; 85.858		1976.14Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117665 CIFC85 H76 Cl6 Mn14 O12 P8P -110.3548; 10.5563; 20.4728
79.072; 82.668; 83.529		2170.28Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117666 CIFC50 H44 Cl4 Mn8 O8 P4C 1 2/c 129.4777; 11.0635; 21.2608
90; 132.06; 90		5147.9Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117667 CIFC20 H16 Br N O6 SP 21 21 218.30101; 10.28989; 23.4389
90; 90; 90		2002.07Lewis S. Aitken; Lisa E. Hammond; Rajkumar Sundaram; Kenneth Shankland; Geoffrey D. Brown; Alexander J. A. Cobb
Asymmetric cyclopropanation of conjugated cyanosulfones using a novel cupreine organocatalyst: rapid access to delta^3^-amino acids
Chem.Commun., 2015, 51, 13558
7117668 CIFC18 H26 B F4 N RuP n a 2116.1385; 14.1014; 8.2801
90; 90; 90		1884.35Andrey I. Konovalov; Evgeniya O. Gorbacheva; Fedor M. Miloserdov; Vladimir V. Grushin
Ruthenium-catalyzed nucleophilic fluorination of halobenzenes
Chem.Commun., 2015, 51, 13527
7117669 CIFC12 H11 N O2P 1 21 17.7718; 5.5207; 11.7443
90; 91.969; 90		503.6Dipak Kumar Tiwari; Jaya Pogula; B. Sridhar; Dharmendra Kumar Tiwari; Pravin R. Likhar
Nano-copper catalysed highly regioselective synthesis of 2,4-disubstituted pyrroles from terminal alkynes and isocyanides
Chem.Commun., 2015, 51, 13646
7117670 CIFC20 H20 Br N O3P 1 21 15.3126; 9.6321; 18.149
90; 92.117; 90		928.1Francesco Berti; Federico Malossi; Fabio Marchetti; Mauro Pineschi
A highly enantioselective Mannich reaction of aldehydes with cyclic N-acyliminium ions by synergistic catalysis
Chem.Commun., 2015, 51, 13694
7117671 CIFC8 H8 F6 N4 Ni O2 SiP 4/m m m7.0148; 7.0148; 7.5655
90; 90; 90		372.28Osama Shekhah; Youssef Belmabkhout; Karim Adil; Prashant M. Bhatt; Amy J. Cairns; Mohamed Eddaoudi
A facile solvent-free synthesis route for the assembly of a highly CO2 selective and H2S tolerant NiSIFSIX metal-organic framework
Chem.Commun., 2015, 51, 13595
7117672 CIFC18 H16 Cl2 Hg N2 S2C 1 2/c 126.6229; 10.0005; 13.9461
90; 93.414; 90		3706.45Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117673 CIFC19 H19 Ag F3 N2 O3 S3C 1 2/c 123.7546; 9.6388; 18.5295
90; 93.688; 90		4233.84Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117674 CIFC20 H19 Cl2 N3 S2 ZnP 1 21/c 18.5494; 18.8079; 13.9638
90; 99.017; 90		2217.58Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117675 CIFC18 H12 Hg I2 N2 S2C 1 2/c 126.4973; 10.4756; 14.4782
90; 94.642; 90		4005.6Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117676 CIFC28 H22 Br F3 O4P 1 21 110.6758; 9.3185; 25.405
90; 99.557; 90		2492.3Bjarke S. Donslund; Alicia Monleon; Jesper Larsen; Lise Ibsen; Karl Anker Jorgensen
The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks
Chem.Commun., 2015, 51, 13666
7117677 CIFC24 H22 Br F3 O3P 21 21 219.671; 10.892; 21.822
90; 90; 90		2298.7Bjarke S. Donslund; Alicia Monleon; Jesper Larsen; Lise Ibsen; Karl Anker Jorgensen
The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks
Chem.Commun., 2015, 51, 13666
7117678 CIFC27 H27 N O5 SP -19.687; 10.731; 12.624
99.142; 109.67; 102.46		1168Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117679 CIFC28 H26 F3 N O7 S2P 1 21/n 110.689; 16.049; 16.697
90; 103.962; 90		2780Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117680 CIFC23 H27 N O5 SP 21 21 217.466; 13.997; 20.362
90; 90; 90		2128Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117681 CIFC17 H21 N O5 SP 1 21/n 113.648; 8.763; 14.28
90; 91.288; 90		1707.4Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117682 CIFC23 H27 N O6 SP 1 21/c 18.2174; 25.204; 10.5671
90; 95.161; 90		2179.7Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117683 CIFC27 H29 N O4 SP -18.05; 16.385; 18.274
94.603; 93.801; 94.487		2388.8Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117684 CIFC42 H46 N2 O2P 1 21/n 111.2948; 16.3779; 19.5856
90; 103.789; 90		3518.6Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117685 CIFC36 H34 N2 O2P b c a15.3406; 16.1078; 22.8598
90; 90; 90		5648.7Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117686 CIFC36 H36 N2 O2C 1 c 122.1106; 8.5517; 15.1278
90; 93.349; 90		2855.5Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117687 CIFC43 H51 B Cl2 F4 N2 OP 21 21 2112.1048; 16.0393; 21.3761
90; 90; 90		4150.22Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117688 CIFC43 H48 Cl0.5 N3.5 O2.5P -113.2188; 16.6509; 19.82
68.92; 86.793; 67.534		3744.8Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117689 CIFC32 H23 N3 O2C 1 2/c 133.04; 21.838; 7.2037
90; 95.946; 90		5169.7Rui Chen; Ru-Qiang Lu; Ke Shi; Fan Wu; Hong-Xun Fang; Zhe-Xuan Niu; Xiao-Yun Yan; Ming Luo; Xin-Chang Wang; Chi-Yuan Yang; Xiao-Ye Wang; Binbin Xu; Haiping Xia; Jian Pei; Xiao-Yu Cao
Corannulene derivatives with low LUMO levels and dense convex-concave packing for n-channel organic field-effect transistors
Chem.Commun., 2015, 51, 13768
7117690 CIFC30 H19 N3 O2I 1 2/a 17.2119; 21.7175; 31.966
90; 95.488; 90		4983.7Rui Chen; Ru-Qiang Lu; Ke Shi; Fan Wu; Hong-Xun Fang; Zhe-Xuan Niu; Xiao-Yun Yan; Ming Luo; Xin-Chang Wang; Chi-Yuan Yang; Xiao-Ye Wang; Binbin Xu; Haiping Xia; Jian Pei; Xiao-Yu Cao
Corannulene derivatives with low LUMO levels and dense convex-concave packing for n-channel organic field-effect transistors
Chem.Commun., 2015, 51, 13768
7117691 CIFC96 H86 F4 N2 Sn2P -110.1387; 14.5652; 15.407
109.721; 103.913; 101.78		1974.97C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117692 CIFC94 H86 N2 Sn2P -110.3114; 12.6833; 14.8438
101.757; 90.344; 99.28		1874.19C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117693 CIFC72 H66 Cl2 N2 Sb2P -110.5945; 12.3644; 12.5871
98.608; 105.285; 100.205		1531.5C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117694 CIFC48 H43 Cl4 F2 N Sb2P 1 21/n 116.2248; 10.8555; 26.4376
90; 106.24; 90		4470.6C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117695 CIFC74 H70 Bi Cl7 N2 SnP -110.519; 14.7566; 22.9059
75.62; 86.231; 80.569		3396.4C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117696 CIFC84 H76 Bi Cl3 F2 N2 SnP n a 2121.3654; 31.1166; 10.7124
90; 90; 90		7121.8C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117697 CIFC26 H36 N2 S4P -14.5302; 10.3934; 14.1186
81.405; 86.591; 82.721		651.44Te-Fang Yang; Sheng-Han Huang; Yi-Pang Chiu; Bo-Hsiang Chen; Yu-Wei Shih; Yu-Chang Chang; Jie-Yi Yao; Yao-Jen Lee; Ming-Yu Kuo
Pyromellitic dithioimides: thionation improves air-stability and electron mobility of N-type organic field-effect transistors
Chem.Commun., 2015, 51, 13772
7117698 CIFC19 H19 N O4 S2P -18.0274; 8.1297; 14.6961
76.433; 74.709; 85.528		899.17Sridhar Undeela; Srinivas Thadkapally; Jagadeesh Babu Nanubolu; Kiran Kumar Singarapu; Rajeev S. Menon
Catalyst-controlled divergence in cycloisomerisation reactions of N-propargyl-N-vinyl sulfonamides: gold-catalysed synthesis of 2-sulfonylmethyl pyrroles and dihydropyridines
Chem.Commun., 2015, 51, 13748
7117699 CIFC22 H14 N2P -15.8666; 11.4535; 12.2113
83.981; 81.526; 76.578		787.26Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117700 CIFC22 H15 N O2P 1 21/c 110.0557; 10.3647; 15.6302
90; 97.658; 90		1614.5Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117701 CIFC16 H10 N2P 1 21/n 111.476; 6.7685; 15.8831
90; 106.572; 90		1182.5Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117702 CIFC24 H16 N2 OP 1 21/c 113.1944; 9.7945; 14.6162
90; 100.206; 90		1859Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117703 CIFC94 H116 N8 O17P 1 21 118.7521; 23.0271; 25.3314
90; 89.8645; 90		10938.2Hanna Jedrzejewska; Marcin Kwit; Agnieszka Szumna
Switching of inherent chirality driven by self-assembly
Chem.Commun., 2015, 51, 13799
7117704 CIFFe11 H78 Na27 O258 Sb6 W60P -117.5189; 24.8676; 25.0737
60.828; 74.889; 72.982		9028.7Xiaoqiang Du; Yong Ding; Fangyuan Song; Baochun Ma; Junwei Zhao; Jie Song
Efficient photocatalytic water oxidation catalyzed by polyoxometalate [Fe11(H2O)14(OH)2(W3O10)2(alpha-SbW9O33)6]^27-^ based on abundant metals
Chem.Commun., 2015, 51, 13925
7117705 CIFC50 H70 F12 N4 O2.93 P2P 1 21/c 115.137; 14.675; 13.735
90; 114.58; 90		2774.6Saioa Cobo; Frederic Lafolet; Eric Saint-Aman; Christian Philouze; Christophe Bucher; Serena Silvi; Alberto Credi; Guy Royal
Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen
Chem.Commun., 2015, 51, 13886
7117706 CIFC39 H32 Br2 Fe N2P 1 21/n 113.1652; 12.2178; 20.8109
90; 107.514; 90		3192.3C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117707 CIFC47 H55 Fe N2 Na O3P 1 21/n 121.2714; 16.1257; 24.0679
90; 99.18; 90		8149.9C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117708 CIFC67.63 H55.63 Fe3 N4 O0.63P 21 21 225.8932; 14.78371; 13.25563
90; 90; 90		5074.22C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117709 CIFC274 H230 Fe4 N16 O3P n a 2126.9704; 17.93806; 21.5915
90; 90; 90		10445.9C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117710 CIFC44 H44P -110.4488; 12.4887; 13.5525
71.996; 79.884; 82.754		1650.87C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117711 CIFC58 H47 Fe N2P -110.1232; 14.1732; 15.1866
103.795; 93.762; 92.887		2106.63C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117712 CIFC36 H34 N2 O2P 1 21/c 18.9045; 8.871; 17.5783
90; 96.259; 90		1380.3C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117713 CIFC17 H17 N O3P -16.0589; 8.071; 15.6647
100.41; 96.485; 93.141		746.38Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117714 CIFC12 H12 Cl3 N O3P -18.6581; 11.8588; 14.7395
101.56; 104.761; 90.004		1431.65Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117715 CIFC15 H16 Cl3 N O3P -16.0347; 11.3911; 13.0283
67.611; 89.839; 85.877		825.64Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117716 CIFC15 H19 N O4P c a 2111.5083; 13.3657; 9.5834
90; 90; 90		1474.08Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117717 CIFC14 H20 O2 S2P 21 21 2110.1194; 11.6313; 12.1672
90; 90; 90		1432.1Amol P. Jadhav; V. U. Bhaskara Rao; Pradeep Singh; R. G. Gonnade; Ravi P. Singh
Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans
Chem.Commun., 2015, 51, 13941
7117718 CIFC13 H18 O2 S2P 21 21 216.6349; 8.9609; 21.6859
90; 90; 90		1289.33Amol P. Jadhav; V. U. Bhaskara Rao; Pradeep Singh; R. G. Gonnade; Ravi P. Singh
Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans
Chem.Commun., 2015, 51, 13941
7117719 CIFC105 H113 F27 N4 O18 P4.5P -114.1777; 20.5414; 24.643
71.116; 78.71; 76.663		6549.9Wei-Bo Hu; Wen-Jing Hu; Xiao-Li Zhao; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen
A [2]rota[2]catenane, constructed from a pillar[5]arene-crown ether fused double-cavity macrocycle: synthesis and structural characterization
Chem.Commun., 2015, 51, 13882
7117720 CIFC166 H205 F30 N8 O26 P5P -120.5486; 21.3959; 24.984
65.622; 74.313; 66.014		9071.3Wei-Bo Hu; Wen-Jing Hu; Xiao-Li Zhao; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen
A [2]rota[2]catenane, constructed from a pillar[5]arene-crown ether fused double-cavity macrocycle: synthesis and structural characterization
Chem.Commun., 2015, 51, 13882
7117721 CIFC199 H189 N23 O53 Zn11P 1 2/c 122.018; 20.783; 37.062
90; 94.845; 90		16899S. A. Sapchenko; D. N. Dybtsev; D. G. Samsonenko; R. V. Belosludov; V. R. Belosludov; Y. Kawazoe; M. Schroder; V. P. Fedin
Selective gas adsorption in microporous metal-organic frameworks incorporating urotropine basic sites: an experimental and theoretical study
Chem.Commun., 2015, 51, 13918
7117722 CIFC17 H15 N O2 SP 21 21 216.2454; 7.9709; 30.185
90; 90; 90		1502.7Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117723 CIFC30 H27.5 N O5.25 SC 1 2/c 141.536; 9.8916; 25.763
90; 93.59; 90		10564Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117724 CIFC24 H23 N O5 SP -111.0389; 13.5784; 24.5769
87.24; 84.094; 69.682		3436Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117725 CIFC25 H25 N O5 SC 1 c 18.4273; 18.696; 14.628
90; 96.208; 90		2291.2Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117726 CIFC24 H23 N O5 SP b c a12.5654; 18.5476; 18.7414
90; 90; 90		4367.8Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117727 CIFC25 H26 N2 O4 SP 1 21/n 112.5847; 17.5982; 20.1268
90; 92.772; 90		4452.2Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117728 CIFC31 H29 N2 O6 S2P 1 21/c 118.1593; 10.1358; 15.6691
90; 91.647; 90		2882.8Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117729 CIFC94.5 H81.75 Eu F9 N23.25 O27 S3P -115.608; 15.7058; 22.744
88.97; 80.503; 77.211		5361.5Eoin P. McCarney; Joseph P. Byrne; Brendan Twamley; Miguel Martinez-Calvo; Gavin Ryan; Matthias E. Mobius; Thorfinnur Gunnlaugsson
Self-assembly formation of a healable lanthanide luminescent supramolecular metallogel from 2,6-bis(1,2,3-triazol-4-yl)pyridine (btp) ligands
Chem.Commun., 2015, 51, 14123
7117730 CIFC34 H33 Cl2 F6 Ir N7 PP b c a10.918; 16.0878; 39.16
90; 90; 90		6878.3Kamrul Hasan; Amlan K. Pal; Thomas Auvray; Eli Zysman-Colman; Garry S. Hanan
Blue-green emissive cationic iridium(III) complexes using partially saturated strongly-donating guanidyl-pyridine/-pyrazine ancillary ligands
Chem.Commun., 2015, 51, 14060
7117731 CIFC96 H122.5 Cl10.5 Mg2 N13 O2.5P 1 21/c 113.281; 26.435; 28.814
90; 94.579; 90		10084Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117732 CIFC177 H219 Cl3 Mg4 N26P -113.848; 16.029; 19.255
96.237; 97.714; 105.938		4025Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117733 CIFC96 H121 Cl6 Mg2 N14 O2P 1 21/n 114.137; 26.982; 25.473
90; 105.387; 90		9368Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117734 CIFC92 H121 Cl4 Mg2 N9 O4P -113.267; 18.521; 20.98
86.112; 73.433; 69.33		4620Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117735 CIFC4 H9 B11 Cs F9 O9 S3P 1 21/c 112.5292; 18.424; 10.6894
90; 106.109; 90		2370.6Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117736 CIFC2 H5.94 B11 Br5.06 Cs F3 O3 SP b c n11.355; 27.735; 13.353
90; 90; 90		4205.3Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117737 CIFC8 H16 B11 Cl10 F3 O3 S SiP 1 21/n 116.213; 21.072; 17.832
90; 102.362; 90		5951Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117738 CIFC38 H61 B11 Cl11 F5 O7 P4 Pd2 SP 1 21/n 114.477; 35.02; 26.24
90; 92.565; 90		13290Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117739 CIFC17 H27 B11 Cl10 F4 O3 S SiP 1 21/c 19.327; 20.08; 20.281
90; 94.518; 90		3786.5Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117740 CIFC27 H21 B11 Cl10 F4 O3 SP b c a12.5691; 22.529; 27.755
90; 90; 90		7859.4Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117741 CIFC26 H36 B11 Br Cl10 F4 O5 P2 Pd SP 1 21/n 114.099; 12.676; 28.345
90; 102.072; 90		4954Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117742 CIFC20 H31 B11 Cl10 F4 O5 P2 Pd SP -112.224; 13.31; 14.337
72.268; 74.431; 78.566		2123Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117743 CIFC19 H31 B11 Cl11 F O2 P2 PdP -19.1582; 12.0726; 20.864
76.534; 88.597; 78.715		2199.5Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117744 CIFC3 H B11 Cl9 Cs F6 O6 S2P b c a17.7687; 15.7898; 18.9559
90; 90; 90		5318.3Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117745 CIFC34 H45 B2 F N12 O UP -110.4532; 11.0258; 18.1147
102.153; 98.067; 96.74		1997.41Christopher L. Clark; Jill J. Lockhart; Phillip E. Fanwick; Suzanne C. Bart
Synthesis of low-valent uranium fluorides by C-F bond activation
Chem.Commun., 2015, 51, 14084
7117746 CIFC30 H43 B2 F2 N12 UP 1 21/n 111.784; 22.3831; 17.0603
90; 93.165; 90		4493Christopher L. Clark; Jill J. Lockhart; Phillip E. Fanwick; Suzanne C. Bart
Synthesis of low-valent uranium fluorides by C-F bond activation
Chem.Commun., 2015, 51, 14084
7117747 CIFC7 H14 Cl3 N O4P 1 21/n 112.6911; 12.471; 14.9357
90; 91.68; 90		2362.87A. J. K. Roth; M. Tretbar; C. B. W. Stark
Mimicking the active site of aldehyde dehydrogenases: stabilization of carbonyl hydrates through hydrogen bonds
Chem.Commun., 2015, 51, 14175
7117748 CIFC7 H8 Cl3 N O3P 1 21/c 16.1594; 12.8396; 13.3985
90; 101.56; 90		1038.12A. J. K. Roth; M. Tretbar; C. B. W. Stark
Mimicking the active site of aldehyde dehydrogenases: stabilization of carbonyl hydrates through hydrogen bonds
Chem.Commun., 2015, 51, 14175
7117749 CIFC6 H6 S0.95 Se0.05P b c n13.8535; 11.4448; 7.1913
90; 90; 90		1140.2Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117750 CIFC6 H6 S0.91 Se0.09P b c n13.856; 11.425; 7.1934
90; 90; 90		1138.7Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117751 CIFC6 H6 S0.75 Se0.25P n a b7.2109; 11.3897; 13.9705
90; 90; 90		1147.4Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117752 CIFC6 H6 SeP n a b7.329; 11.226; 14.422
90; 90; 90		1186.6Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117753 CIFC6 H6 SP n a b7.1905; 11.4643; 13.815
90; 90; 90		1138.8Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117754 CIFC6 H6 S0.57 Se0.43P n a b7.2621; 11.371; 14.155
90; 90; 90		1168.9Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117755 CIFC25 H28 N2 O3 SC 1 2/c 110.9399; 21.02; 20.547
90; 98.769; 90		4669.7Dongari Yadagiri; Pazhamalai Anbarasan
An iodine(III) mediated oxidative rearrangement of enamines: efficient synthesis of alpha-amino ketones
Chem.Commun., 2015, 51, 14203
7117756 CIFC54 H18 N0 O41 Zn9I 2 323.503; 23.503; 23.503
90; 90; 90		12983Yun-Wu Li; Jian Xu; Da-Cheng Li; Jian-Min Dou; Hui Yan; Tong-Liang Hu; Xian-He Bu
Two microporous MOFs constructed from different metal cluster SBUs for selective gas adsorption
Chem.Commun., 2015, 51, 14211
7117757 CIFC15 H20 Cd N2 O7P 1 21/n 110.099; 14.363; 12.975
90; 105.69; 90		1811.9Yun-Wu Li; Jian Xu; Da-Cheng Li; Jian-Min Dou; Hui Yan; Tong-Liang Hu; Xian-He Bu
Two microporous MOFs constructed from different metal cluster SBUs for selective gas adsorption
Chem.Commun., 2015, 51, 14211
7117758 CIFC30 H26 N2 SC 1 2/c 119.059; 5.647; 42.733
90; 93.669; 90		4590Alok Ranjan; Anupam Mandal; Swapnil G. Yerande; Dattatraya H. Dethe
An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates
Chem.Commun., 2015, 51, 14215
7117759 CIFC30 H23 Br N2 O SP 19.724; 11.581; 11.774
75.443; 87.986; 89.04		1282.5Alok Ranjan; Anupam Mandal; Swapnil G. Yerande; Dattatraya H. Dethe
An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates
Chem.Commun., 2015, 51, 14215
7117760 CIFC88 H88 Cl2 F36 N13 O2 S6C 1 2/c 120.3759; 35.024; 16.9047
90; 98.951; 90		11917Hennie Valkenier; Christopher M. Dias; Kathryn L. Porter Goff; Ondrej Jurcek; Rakesh Puttreddy; Kari Rissanen; Anthony P. Davis
Sterically geared tris-thioureas; transmembrane chloride transporters with unusual activity and accessibility
Chem.Commun., 2015, 51, 14235
7117761 CIFC25 H19 N O3P 21 21 214.11501; 10.0552; 45.8911
90; 90; 90		1898.85Zhong-Jian Cai; Chao Yang; Shun-Yi Wang; Shun-Jun Ji
Palladium-catalyzed highly regioselective 6-exo-dig cyclization and alkenylation of ortho-ethynylanilides: the synthesis of polyene-substituted benzo[d][1,3]oxazines
Chem.Commun., 2015, 51, 14267
7117762 CIFC110 H56 Br2I 41/a c d39.709; 39.709; 39.724
90; 90; 90		62637Melanie Kitchin; Kristina Konstas; Christopher J. Sumby; Milena L. Czyz; Peter Valente; Matthew R. Hill; Anastasios Polyzos; Christian J. Doonan
Continuous flow synthesis of a carbon-based molecular cage macrocycle via a three-fold homocoupling reaction
Chem.Commun., 2015, 51, 14231
7117763 CIFC21 H20 Br2 O4 SP 1 21 110.927; 19.507; 19.81
90; 105.742; 90		4064.2Nagamoto, Midori; Nishimura, Takahiro
Stereoselective hydroacylation of bicyclic alkenes with 2-hydroxybenzaldehydes catalyzed by hydroxoiridium/diene complexes.
Chemical communications (Cambridge, England), 2015, 51, 13791-13794
7117766 CIFC168 H162 Ag3 F18 N18 P3R -335.4661; 35.4661; 26.194
90; 90; 120		28534Mejuto, Carmen; Guisado-Barrios, Gregorio; Gusev, Dmitry; Peris, Eduardo
First homoleptic MIC and heteroleptic NHC-MIC coordination cages from 1,3,5-triphenylbenzene-bridged tris-MIC and tris-NHC ligands.
Chemical communications (Cambridge, England), 2015, 51, 13914-13917
7117767 CIFC31 H25 N O2 SP 1 21/c 113.1; 16.35; 13.048
90; 117.404; 90		2481.1Pi, Rui; Zhou, Ming-Bo; Yang, Yuan; Gao, Cai; Song, Ren-Jie; Li, Jin-Heng
Rhodium(iii)-catalyzed oxidative bicyclization of 4-arylbut-3-yn-1-amines with internal alkynes through C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 13550-13553
7117768 CIFC26 H23 N O2 SP 21 21 219.311; 10.003; 23.556
90; 90; 90		2194Pi, Rui; Zhou, Ming-Bo; Yang, Yuan; Gao, Cai; Song, Ren-Jie; Li, Jin-Heng
Rhodium(iii)-catalyzed oxidative bicyclization of 4-arylbut-3-yn-1-amines with internal alkynes through C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 13550-13553
7117769 CIFC34 H30 Br2 N2 O4 S2P b c a9.5442; 15.093; 45.323
90; 90; 90		6528.8Pi, Rui; Zhou, Ming-Bo; Yang, Yuan; Gao, Cai; Song, Ren-Jie; Li, Jin-Heng
Rhodium(iii)-catalyzed oxidative bicyclization of 4-arylbut-3-yn-1-amines with internal alkynes through C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 13550-13553
7117772 CIFC16 H21 Br Co N O4C 1 m 18.2934; 13.814; 7.8377
90; 92.388; 90		897.1Jeremy Demarteau; Anthony Kermagoret; Ian German; Daniela Cordella; Koen Robeyns; Julien De Winter; Pascal Gerbaux; Christine Jerome; Antoine Debuigne; Christophe Detrembleur
Halomethyl-cobalt(bis-acetylacetonate) for the controlled synthesis of functional polymers
Chem.Commun., 2015, 51, 14334
7117773 CIFC16 H21 Cl Co N O4C 1 m 18.1891; 13.7998; 7.73787
90; 91.89; 90		873.97Jeremy Demarteau; Anthony Kermagoret; Ian German; Daniela Cordella; Koen Robeyns; Julien De Winter; Pascal Gerbaux; Christine Jerome; Antoine Debuigne; Christophe Detrembleur
Halomethyl-cobalt(bis-acetylacetonate) for the controlled synthesis of functional polymers
Chem.Commun., 2015, 51, 14334
7117774 CIFC10 H10 Cu2 I2 N6 O4P 1 n 14.1982; 14.3433; 13.6017
90; 94.707; 90		816.28P. Amo-Ochoa; K. Hassanein; C. J. Gomez-Garcia; S. Benmansour; J. Perles; O. Castillo; J. I. Martinez; P. Oconf; F. Zamora
Reversible stimulus-responsive Cu(I) iodide pyridine coordination polymer
Chem.Commun., 2015, 51, 14306
7117775 CIFC5 H5 Cu I N3 O2P 1 21/n 14.2284; 14.3638; 13.684
90; 95.241; 90		827.64P. Amo-Ochoa; K. Hassanein; C. J. Gomez-Garcia; S. Benmansour; J. Perles; O. Castillo; J. I. Martinez; P. Oconf; F. Zamora
Reversible stimulus-responsive Cu(I) iodide pyridine coordination polymer
Chem.Commun., 2015, 51, 14306
7117776 CIFC5 H5 Cu I N3 O2P 1 21/c 14.0708; 7.5386; 28.2779
90; 90.88; 90		867.69P. Amo-Ochoa; K. Hassanein; C. J. Gomez-Garcia; S. Benmansour; J. Perles; O. Castillo; J. I. Martinez; P. Oconf; F. Zamora
Reversible stimulus-responsive Cu(I) iodide pyridine coordination polymer
Chem.Commun., 2015, 51, 14306
7117777 CIFC18 H15 N OP 1 21/c 112.7421; 7.5139; 14.7733
90; 106.877; 90		1353.52Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117778 CIFC30 H21 N OP b c a11.1528; 12.1629; 32.522
90; 90; 90		4411.6Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117779 CIFC32 H25 N OP 1 21/c 117.0755; 11.3454; 12.5168
90; 103.806; 90		2354.8Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117780 CIFC32 H23 N OP -19.948; 10.1669; 12.7171
88.203; 70.071; 73.961		1159.31Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117781 CIFC18 H18 Au2 N8 S4C 1 2/c 117.112; 12.896; 11.447
90; 90.276; 90		2526.1Ryan J. Roberts; Debbie Le; Daniel B. Leznoff
Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour
Chem.Commun., 2015, 51, 14299
7117782 CIFC18 H24 Au2 N6 S4P 1 21/c 19.6338; 22.019; 11.351
90; 91.513; 90		2407Ryan J. Roberts; Debbie Le; Daniel B. Leznoff
Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour
Chem.Commun., 2015, 51, 14299
7117783 CIFC18 H32 Au2 N8 O S4P 1 21/c 110.5756; 23.18; 11.6908
90; 99.794; 90		2824.1Ryan J. Roberts; Debbie Le; Daniel B. Leznoff
Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour
Chem.Commun., 2015, 51, 14299
7117784 CIFC22 H20 N2P 1 21 110.8234; 6.6783; 12.8182
90; 108.899; 90		876.58Tsuneomi Kawasaki; Naoya Takamatsu; Shohei Aiba; Yuji Tokunaga
Spontaneous formation and amplification of an enantioenriched alpha-amino nitrile: a chiral precursor for Strecker amino acid synthesis
Chem.Commun., 2015, 51, 14377
7117785 CIFC32 H30 F N O5P 1 21 111.665; 18.047; 13.71
90; 106.488; 90		2767.5Junjun Feng; Xin Li; Jin-Pei Cheng
An asymmetric allylic alkylation reaction of 3-alkylidene oxindoles
Chem.Commun., 2015, 51, 14342
7117786 CIFC20 H34 B2 N2P 1 21/n 110.4675; 14.4066; 13.3847
90; 112.212; 90		1868.64Jeffrey M. Farrell; Douglas W. Stephan
Synthesis of a diboryl-N-heterocycle and its conversion to a bidentate cationic Lewis acid
Chem.Commun., 2015, 51, 14322
7117787 CIFC20 H33 B2 I N2P 1 21/n 114.5093; 7.7961; 18.6255
90; 106.364; 90		2021.5Jeffrey M. Farrell; Douglas W. Stephan
Synthesis of a diboryl-N-heterocycle and its conversion to a bidentate cationic Lewis acid
Chem.Commun., 2015, 51, 14322
7117788 CIFC44 H32 B3 F20 N2P b c a17.2516; 17.706; 27.4233
90; 90; 90		8376.6Jeffrey M. Farrell; Douglas W. Stephan
Synthesis of a diboryl-N-heterocycle and its conversion to a bidentate cationic Lewis acid
Chem.Commun., 2015, 51, 14322
7117789 CIFC40 H30 B2 F8 N2 O2P b c a12.1706; 19.581; 27.574
90; 90; 90		6571.2Yuto Sakano; Ryo Katoono; Kenshu Fujiwara; Takanori Suzuki
Two-way chromic interconversion of the 2,2'-biphenol-6,6'-diyl dication with 5H,10H-dioxapyrene or 9H,10H-4,5-dihydroxyphenanthrene
Chem.Commun., 2015, 51, 14303
7117790 CIFC40 H28 N2 O2P 1 21/c 19.176; 8.514; 18.197
90; 104.035; 90		1379.2Yuto Sakano; Ryo Katoono; Kenshu Fujiwara; Takanori Suzuki
Two-way chromic interconversion of the 2,2'-biphenol-6,6'-diyl dication with 5H,10H-dioxapyrene or 9H,10H-4,5-dihydroxyphenanthrene
Chem.Commun., 2015, 51, 14303
7117791 CIFC44 H38 B2 F8 N2 O4P 1 21/c 120.444; 13.566; 28.627
90; 90.776; 90		7939Yuto Sakano; Ryo Katoono; Kenshu Fujiwara; Takanori Suzuki
Two-way chromic interconversion of the 2,2'-biphenol-6,6'-diyl dication with 5H,10H-dioxapyrene or 9H,10H-4,5-dihydroxyphenanthrene
Chem.Commun., 2015, 51, 14303
7117795 CIFC13 H17 Br O5P n a 2114.3578; 11.7005; 8.2619
90; 90; 90		1387.9Jola Pospech; Alastair J. J. Lennox; Matthias Beller
Rhodium-catalysed alkoxylation/acetalization of diazo compounds: one-step synthesis of highly functionalised quaternary carbon centres
Chem.Commun., 2015, 51, 14505
7117796 CIFC20 H22 O7P 1 21/n 19.7096; 7.1009; 26.6401
90; 100.031; 90		1808.68Jola Pospech; Alastair J. J. Lennox; Matthias Beller
Rhodium-catalysed alkoxylation/acetalization of diazo compounds: one-step synthesis of highly functionalised quaternary carbon centres
Chem.Commun., 2015, 51, 14505
7117797 CIFC12 H15 Br O5P 1 21/c 112.7047; 8.5755; 13.6576
90; 115.546; 90		1342.52Jola Pospech; Alastair J. J. Lennox; Matthias Beller
Rhodium-catalysed alkoxylation/acetalization of diazo compounds: one-step synthesis of highly functionalised quaternary carbon centres
Chem.Commun., 2015, 51, 14505
7117798 CIFC25 H18 OP 1 21 18.2582; 6.2091; 17.8371
90; 103.148; 90		890.64Beom Shin Cho; Young Keun Chung
Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: tandem C(sp3)-H and C(sp2)-H activation reactions of 3-alkylbenzofurans
Chem.Commun., 2015, 51, 14543
7117799 CIFC19 H25 N O4P 21 21 215.8467; 17.0069; 17.374
90; 90; 90		1727.57Jorge M. M. Verkade; Peter J. L. M. Quaedflieg; Gerard K. M. Verzijl; Laurent Lefort; Floris L. van Delft; Johannes G. de Vries; Floris P. J. T. Rutjes
Enantio- and diastereoselective synthesis of upsilon-amino alcohol
Chem.Commun., 2015, 51, 14462
7117800 CIFC75 H84 F12 Fe2 N17 O16 S4P 1 21/n 116.179; 15.362; 17.899
90; 90.91; 90		4448Sujoy Rana; Aniruddha Dey; Debabrata Maiti
Mechanistic elucidation of C-H oxidation by electron rich non-heme iron(IV)-oxo at room temperature
Chem.Commun., 2015, 51, 14469
7117801 CIFC149 H135 Cl3 N12 O Zn2P -112.1388; 21.415; 25.499
83.635; 80.874; 83.613		6474.6Tuan Anh Pham; Fei Song; Mariza N. Alberti; Manh-Thuong Nguyen; Nils Trapp; Carlo Thilgen; Francois Diederich; Meike Stohr
Heat-induced formation of one-dimensional coordination polymers on Au(111): an STM study
Chem.Commun., 2015, 51, 14473
7117802 CIFC23 H18 N4 O SP 1 21/c 17.387; 32.39; 8.251
90; 92.434; 90		1972Masood Ayoub Kaloo; Jeyaraman Sankar
Reusable and specific proton transfer signalling by inorganic cyanide in solution and solid phase
Chem.Commun., 2015, 51, 14528
7117803 CIFC47 H36 B N OC 1 2/c 119.192; 10.293; 35.255
90; 96.3; 90		6922Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117804 CIFC50 H42 B N OP -112.592; 15.365; 20.175
103.7; 92.293; 94.425		3774Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117805 CIFC51 H46 B N OP 1 21/n 113.873; 17.556; 16.244
90; 102.03; 90		3869Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117806 CIFC48 H46 B N OP 1 21/c 110.604; 32.49; 11.704
90; 114.4; 90		3672Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117807 CIFC152 H120 Cd8 N4 O54P 1 21 117.656; 16.2741; 26.219
90; 90.609; 90		7533.2Yun-Hu Han; Yue-Cheng Liu; Xiu-Shuang Xing; Chong-Bin Tian; Ping Lin; Shao-Wu Du
Chiral template induced homochiral MOFs built from achiral components: SHG enhancement and enantioselective sensing of chiral alkamines by ion-exchange
Chem.Commun., 2015, 51, 14481
7117808 CIFC152 H120 Cd8 N4 O54P 1 21 117.745; 16.263; 26.25
90; 90.775; 90		7575Yun-Hu Han; Yue-Cheng Liu; Xiu-Shuang Xing; Chong-Bin Tian; Ping Lin; Shao-Wu Du
Chiral template induced homochiral MOFs built from achiral components: SHG enhancement and enantioselective sensing of chiral alkamines by ion-exchange
Chem.Commun., 2015, 51, 14481
7117809 CIFC74.1 H109.2 Mg2 N6P 1 21/c 118.9579; 19.7413; 18.7107
90; 99.765; 90		6901.1Catherine Weetman; Michael S. Hill; Mary F. Mahon
Magnesium-catalysed hydroboration of isonitriles
Chem.Commun., 2015, 51, 14477
7117810 CIFC24 H15 Co6 N13 O12P 21 317.4611; 17.4611; 17.4611
90; 90; 90		5323.72Ya-Dong Yu; Chan Luo; Bao-Yu Liu; Xiao-Chun Huang; Dan Li
Spontaneous symmetry breaking of Co(II) metal-organic frameworks from achiral precursors via asymmetrical crystallization
Chem.Commun., 2015, 51, 14489
7117811 CIFC24 H15 Co6 N13 O12P 21 317.4882; 17.4882; 17.4882
90; 90; 90		5348.54Ya-Dong Yu; Chan Luo; Bao-Yu Liu; Xiao-Chun Huang; Dan Li
Spontaneous symmetry breaking of Co(II) metal-organic frameworks from achiral precursors via asymmetrical crystallization
Chem.Commun., 2015, 51, 14489
7117812 CIFC24 H14 Co6 N12 O13P 21 317.5279; 17.5279; 17.5279
90; 90; 90		5385Ya-Dong Yu; Chan Luo; Bao-Yu Liu; Xiao-Chun Huang; Dan Li
Spontaneous symmetry breaking of Co(II) metal-organic frameworks from achiral precursors via asymmetrical crystallization
Chem.Commun., 2015, 51, 14489
7117813 CIFC33 H25 N O3P 1 21/n 115.116; 11.464; 15.484
90; 105.324; 90		2587.8Rong Zhou; Kai Zhang; Yusong Chen; Qiang Meng; Yiyi Liu; Ruifeng Li; Zhengjie He
P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans
Chem.Commun., 2015, 51, 14663
7117814 CIFC31 H22 Br N O3P 1 21/n 115.016; 11.906; 15.221
90; 100.25; 90		2677.8Rong Zhou; Kai Zhang; Yusong Chen; Qiang Meng; Yiyi Liu; Ruifeng Li; Zhengjie He
P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans
Chem.Commun., 2015, 51, 14663
7117815 CIFC27 H19 N3 O3C 1 2/c 121.917; 9.529; 23.123
90; 115.112; 90		4373Rong Zhou; Kai Zhang; Yusong Chen; Qiang Meng; Yiyi Liu; Ruifeng Li; Zhengjie He
P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans
Chem.Commun., 2015, 51, 14663
7117816 CIFC25 H55 B2 O7 P2 RhP 1 21/n 110.9348; 25.1626; 12.1658
90; 93.209; 90		3342.1Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117817 CIFC24 H57 B O3 P3 RhP 1 21 110.8214; 13.3028; 11.7681
90; 113.017; 90		1559.21Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117818 CIFC25 H47 B N O3 P2 RhP 19.0037; 11.2268; 15.1421
83.982; 80.95; 82.455		1492.9Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117819 CIFC81 H181 B4 O8 P8 Rh4 S4C 1 2/c 140.16; 15.9681; 20.1668
90; 118.333; 90		11383.3Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117820 CIFC17 H20 O5P b c a14.3785; 10.3694; 19.867
90; 90; 90		2962.1Dong Chen; Hao-Miao Liu; Ming-Ming Li; Yong-Min Yan; Wen-Dan Xu; Xiao-Nian Li; Yong-Xian Cheng; Hong-Bo Qin
Concise synthesis of (+/-)-Lingzhiol via epoxy-arene cyclization
Chem.Commun., 2015, 51, 14594
7117821 CIFC20 H17 Cl O4P 1 21 19.7149; 5.7291; 15.133
90; 91.157; 90		842.1Qijian Ni; Jiawen Xiong; Xiaoxiao Song; Gerhard Raabe; Dieter Enders
NHC-catalyzed activation of alpha,beta-unsaturated N-acyltriazoles: an easy access to dihydropyranones
Chem.Commun., 2015, 51, 14628

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