Crystallography Open Database

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7125142 CIFC22 H30 O2 SiP 1 21/c 111.8899; 39.592; 9.1681
90; 94.087; 90		4304.9Akram, Manjur O.; Bera, Saibal; Patil, Nitin T.
A facile strategy for accessing 3-alkynylchromones through gold-catalyzed alkynylation/cyclization of o-hydroxyarylenaminones.
Chemical communications (Cambridge, England), 2016, 52, 12306-12309
7125143 CIFC10.5 H6 Br0.5 Mn0.5 N2 O2C 1 2/m 123.4756; 12.4761; 7.29758
90; 97.067; 90		2121.11Coogan, M. P.; Platts, J. A.
Blue rhenium tricarbonyl DPPZ complexes - low energy charge-transfer absorption at tissue-penetrating wavelengths.
Chemical communications (Cambridge, England), 2016, 52, 12498-12501
7125144 CIFC7 H5 I N3 Se4P -4 21 m16.3764; 16.3764; 4.1533
90; 90; 90		1113.86Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125145 CIFC7 H5 I N3 Se4P -4 21 m16.2024; 16.2024; 4.004
90; 90; 90		1051.1Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125146 CIFC7 H5 I N3 Se4P -4 21 m16.0383; 16.0383; 3.8839
90; 90; 90		999Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125147 CIFC7 H5 I N3 Se4P -4 21 m15.9987; 15.9987; 3.87
90; 90; 90		990.6Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125148 CIFC7 H5 I N3 Se4P -4 21 m15.9908; 15.9908; 3.8382
90; 90; 90		981.4Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125149 CIFC7 H5 I N3 Se4P -4 21 m15.9014; 15.9014; 3.784
90; 90; 90		956.8Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125150 CIFC7 H5 I N3 Se4P -4 21 m15.8651; 15.8651; 3.765
90; 90; 90		947.7Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125151 CIFC7 H5 I N3 Se4P -4 21 m15.7336; 15.7336; 3.7167
90; 90; 90		920.1Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125152 CIFC7 H5 I N3 Se4P -4 21 m15.7128; 15.7128; 3.6914
90; 90; 90		911.4Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125153 CIFC7 H5 I N3 Se4P -4 21 m15.6976; 15.6976; 3.6631
90; 90; 90		902.6Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125154 CIFC7 H5 I N3 Se4P -4 21 m15.6831; 15.6831; 3.6436
90; 90; 90		896.2Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125155 CIFC7 H5 I N3 Se4P -4 21 m16.4704; 16.4704; 4.2345
90; 90; 90		1148.71Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125156 CIFC19 H18 Br N O4P 3115.6261; 15.6261; 6.58142
90; 90; 120		1391.72Donslund, Bjarke S.; Jessen, Nicolaj Inunnguaq; Jakobsen, Joakim Bøgelund; Monleón, Alicia; Nielsen, Rune Pagh; Jørgensen, Karl Anker
Enantioselective formation of cyclopropane spiroindenes from benzofulvenes by phase transfer catalysis.
Chemical communications (Cambridge, England), 2016, 52, 12474-12477
7125157 CIFC44 H60 K2 N2 O3P 1 21/c 121.3422; 9.8659; 19.6135
90; 103.086; 90		4022.57Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125158 CIFC48 H68 Li2 N2 O4P 1 21/n 110.6922; 15.3289; 12.9982
90; 90.058; 90		2130.4Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125159 CIFC44 H60 N2 Na2 O3P 1 21/n 110.30734; 27.6447; 14.8943
90; 105.588; 90		4087.94Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125160 CIFC40 H52 N2 Na2 O2C 1 c 110.2275; 35.0736; 19.991
90; 90.758; 90		7170.4Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125161 CIFC128 H144 N8 Na8P b c n19.8237; 19.6671; 32.4878
90; 90; 90		12666.2Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125162 CIFC72 H88 K4 N4 O2P -110.4694; 16.0165; 20.7659
109.148; 102.765; 92.213		3184.74Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125168 CIFC9 H8 N2 OP 21 21 215.7785; 9.7172; 14.76
90; 90; 90		828.8Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125169 CIFC9 H7 F N2 OP 21 21 213.7769; 10.7326; 19.387
90; 90; 90		785.87Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125170 CIFC10 H10 N2 O2P 21 21 215.6704; 10.076; 16.296
90; 90; 90		931.1Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125171 CIFC10 H10 N2 OP 1 21/c 17.769; 11.243; 10.244
90; 100.15; 90		880.8Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125172 CIFC14 H24 O P2 S2P 21 21 216.4559; 12.3783; 22.5131
90; 90; 90		1799.09Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125173 CIFC16 H20 P2 S2P 1 21/c 19.3474; 7.1672; 13.3103
90; 101.49; 90		873.85Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125174 CIFC15 H18 P2 S2P b c a9.1542; 16.965; 10.682
90; 90; 90		1658.9Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125175 CIFC17 H24 O2P 1 21/n 112.7728; 8.2427; 14.1842
90; 103.024; 90		1454.93Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125176 CIFC17 H22 O2P -18.9679; 11.9038; 14.801
91.758; 94.311; 110.931		1468.8Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125177 CIFC27 H51 O Si4 SmC m c 2111.6326; 13.777; 21.1559
90; 90; 90		3390.5Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125178 CIFC32 H66 O Si6 SmP 1 21/n 111.287; 22.3415; 16.921
90; 97.974; 90		4225.7Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125179 CIFC44 H50 O2 Si2 SmI -413.1871; 13.1871; 11.4268
90; 90; 90		1987.12Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125180 CIFC54 H54 O2 Si2 SmC 1 c 117.123; 9.6421; 27.6291
90; 99.283; 90		4501.9Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125181 CIFC48 H75 N3 O9P 112.0223; 15.7744; 15.908
61.685; 76.21; 82.022		2578.18Caumes, Xavier; Baldi, Arianna; Gontard, Geoffrey; Brocorens, Patrick; Lazzaroni, Roberto; Vanthuyne, Nicolas; Troufflard, Claire; Raynal, Matthieu; Bouteiller, Laurent
Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.
Chemical communications (Cambridge, England), 2016, 52, 13369-13372
7125182 CIFC45.5 H70.75 N3.25 O9.5P 111.5502; 15.7414; 15.8302
61.491; 83.352; 79.502		2485.47Caumes, Xavier; Baldi, Arianna; Gontard, Geoffrey; Brocorens, Patrick; Lazzaroni, Roberto; Vanthuyne, Nicolas; Troufflard, Claire; Raynal, Matthieu; Bouteiller, Laurent
Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.
Chemical communications (Cambridge, England), 2016, 52, 13369-13372
7125183 CIFC62 H44 Mo4 N22 Ni S2C 1 2/c 117.6253; 13.6069; 24.0534
90; 101.343; 90		5655.9Hung, Wei-Chieh; Sigrist, Marc; Hua, Shao-An; Wu, Lai-Chin; Liu, Tsai-Jung; Jin, Bih-Yaw; Lee, Gene-Hsiang; Peng, Shie-Ming
A heteropentanuclear metal string complex [Mo<sub>2</sub>NiMo<sub>2</sub>(tpda)<sub>4</sub>(NCS)<sub>2</sub>] with two linearly aligned quadruply bonded Mo<sub>2</sub> units connected by a Ni ion and a meso configuration of the complex.
Chemical communications (Cambridge, England), 2016, 52, 12380-12382
7125184 CIFC59 H88 N5 O SmP -112.769; 13.1625; 20.932
76.406; 80.735; 63.678		3058.5Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125185 CIFC125 H187 As5 Fe N8 O2 Sm2P -113.1985; 20.5277; 24.6698
108.733; 93.697; 93.654		6291.4Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125186 CIFC125 H187 Fe N8 O2 P5 Sm2P -113.12; 20.386; 24.637
109.26; 93.54; 93.97		6181Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125187 CIFC30 H16 Br4 N2C 1 2/c 128.8213; 3.9568; 22.0852
90; 101.2; 90		2470.6Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125188 CIFC30 H16 Br4 N2C 1 2/c 128.561; 3.8983; 22.009
90; 100.956; 90		2405.8Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125189 CIFC30 H16 Br4 N2C 1 2/c 128.6436; 3.9085; 22.0408
90; 101.063; 90		2421.7Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125190 CIFC30 H16 Br4 N2C 1 2/c 128.6762; 3.9157; 22.0307
90; 101.079; 90		2427.67Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125191 CIFC30 H16 Br4 N2C 1 2/c 128.708; 3.9259; 22.0256
90; 101.117; 90		2435.8Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125192 CIFC30 H16 Br4 N2C 1 2/c 128.7391; 3.9377; 22.0251
90; 101.118; 90		2445.7Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125193 CIFC25 H18 F3 N3C 1 2/c 121.381; 12.571; 16.69
90; 117.251; 90		3988Yu, Liu-Zhu; Wei, Yin; Shi, Min
Copper-catalyzed cascade cyclization of 1,5-enynes via consecutive trifluoromethylazidation/diazidation and click reaction: self-assembly of triazole fused isoindolines.
Chemical communications (Cambridge, England), 2016, 52, 13163-13166
7125194 CIFC44 H32 N12P -18.1858; 10.1508; 22.15
89.88; 83.44; 78.898		1793.9Yu, Liu-Zhu; Wei, Yin; Shi, Min
Copper-catalyzed cascade cyclization of 1,5-enynes via consecutive trifluoromethylazidation/diazidation and click reaction: self-assembly of triazole fused isoindolines.
Chemical communications (Cambridge, England), 2016, 52, 13163-13166
7125195 CIFC149 H168 Cl16 N6 PdP -112.4144; 17.9604; 33.3206
97.426; 96.076; 105.19		7033.5Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125196 CIFC142 H130 Cl2 N6 PdP 1 21/c 122.053; 39.391; 14.3467
90; 99.711; 90		12284.3Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125197 CIFC168 H166 Br4 N10 Pd2P -114.6518; 16.6609; 33.4649
97.604; 92.496; 92.487		8079.7Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125198 CIFC23 H27 N3P 1 21/c 112.0143; 8.3594; 19.0526
90; 90.316; 90		1913.47Saya, Jordy M.; Oppelaar, Barry; Cioc, Răzvan C; van der Heijden, Gydo; Vande Velde, Christophe M. L.; Orru, Romano V. A.; Ruijter, Eelco
Synthesis of polycyclic spiroindolines by highly diastereoselective interrupted Ugi cascade reactions of 3-(2-isocyanoethyl)indoles.
Chemical communications (Cambridge, England), 2016, 52, 12482-12485
7125199 CIFC9 H16 F3 Li O7 SP 1 21/n 17.0179; 13.5605; 14.8661
90; 96.427; 90		1405.86Reuter, Kirsten; Thiele, Günther; Hafner, Thomas; Uhlig, Frank; von Hänisch, Carsten
Synthesis and coordination ability of a partially silicon based crown ether.
Chemical communications (Cambridge, England), 2016, 52, 13265-13268
7125200 CIFC14 H34 Cl2 F3 Li O7 S Si4P b c a14.6745; 24.0048; 32.5952
90; 90; 90		11481.9Reuter, Kirsten; Thiele, Günther; Hafner, Thomas; Uhlig, Frank; von Hänisch, Carsten
Synthesis and coordination ability of a partially silicon based crown ether.
Chemical communications (Cambridge, England), 2016, 52, 13265-13268
7125201 CIFC25 H32 Cl N5 O4 SP 1 21 16.26161; 25.924; 8.62429
90; 102.226; 90		1368.19Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125202 CIFC12 H11 N3 O3 SP -15.8245; 7.5038; 13.8162
94.785; 94.97; 95.755		595.96Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125203 CIFC23 H28 Cl N5 O4 SP 15.94757; 9.5911; 11.4509
83.8975; 82.015; 71.9997		613.81Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125204 CIFC24 H30 Cl N5 O4 SP 1 21 16.11235; 28.1898; 7.71338
90; 92.9285; 90		1327.33Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125205 CIFC22 H27 Cl N4 O4 S2P 1 21 15.99452; 23.7139; 9.33438
90; 108.528; 90		1258.14Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125206 CIFC24 H31 N5 O4 SP 1 21 16.191; 26.0113; 8.06978
90; 102.689; 90		1267.79Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125207 CIFC24 H30 N4 O5 SP 1 21 16.06973; 23.5497; 9.2011
90; 108.609; 90		1246.45Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125208 CIFC24 H29 Cl N4 O5 SP 1 21 16.00155; 26.1427; 8.40735
90; 105.247; 90		1272.66Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125209 CIFC25 H33 N5 O4 SP 1 21 16.21672; 26.581; 7.98985
90; 99.504; 90		1302.17Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125210 CIFC20 H21 Cl N4 O3 SP 1 21 17.3493; 6.04446; 23.3114
90; 94.695; 90		1032.08Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125211 CIFC16 H26 Cu N4 O9 ZnP 1 2/n 110.95; 6.53; 13.61
90; 92.58; 90		972.2Albalad, Jorge; Aríñez-Soriano, Javier; Vidal-Gancedo, José; Lloveras, Vega; Juanhuix, Jordi; Imaz, Inhar; Aliaga-Alcalde, Núria; Maspoch, Daniel
Hetero-bimetallic paddlewheel clusters in coordination polymers formed by a water-induced single-crystal-to-single-crystal transformation.
Chemical communications (Cambridge, England), 2016, 52, 13397-13400
7125212 CIFC32 H48 Cu3 N8 O26 ZnP 1 21/c 111.56; 16.83; 12.92
90; 110.97; 90		2347.2Albalad, Jorge; Aríñez-Soriano, Javier; Vidal-Gancedo, José; Lloveras, Vega; Juanhuix, Jordi; Imaz, Inhar; Aliaga-Alcalde, Núria; Maspoch, Daniel
Hetero-bimetallic paddlewheel clusters in coordination polymers formed by a water-induced single-crystal-to-single-crystal transformation.
Chemical communications (Cambridge, England), 2016, 52, 13397-13400
7125213 CIFC12 H14 N2 O7P 21 21 215.8274; 9.9168; 23.1227
90; 90; 90		1336.24Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125214 CIFC18 H20 N4 O8P 1 2 18.934; 5.1587; 43.225
90; 93; 90		1989.4Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125215 CIFC24 H28 N4 O14P 15.0886; 7.2518; 17.1681
93.324; 93.952; 97.338		625.42Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125216 CIFC24 H26 N6 O9P 1 21 15.074; 29.696; 8.498
90; 103.16; 90		1246.8Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125217 CIFC13 H18 N2 O8P 15.0892; 7.5329; 19.7851
84.757; 85.752; 81.727		746.03Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125218 CIFC7 H7 N2 O3P b c a7.2149; 12.4451; 15.6775
90; 90; 90		1407.69Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125219 CIFC4 H13 B F3 NP b c m5.577; 11.436; 11.447
90; 90; 90		730.1Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125220 CIFC6 H24 B11 F2 NP 1 21 110.452; 13.828; 10.773
90; 90.102; 90		1557Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125221 CIFC6 H22 B11 F2 I2 NP -112.4538; 13.5015; 13.544
60.759; 72.3; 86.331		1883.28Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125222 CIFC20 H23 N O3 SP 21 21 218.3041; 10.2744; 22.465
90; 90; 90		1916.7Huang, Wei; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diastereoselective synthesis of 2-methoxyimidoyloxiranes via dimethyl phosphite-mediated coupling of α-keto N-sulfinyl imidates with aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 13592-13595
7125223 CIFC28 H26 O4P 1 2/c 131.22; 10.5893; 13.5925
90; 89.984; 90		4493.7Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125224 CIFC25 H26 O4P 1 21 18.8392; 12.746; 9.5979
90; 99.664; 90		1066Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125225 CIFC24 H24 O5P 1 21/c 112.7888; 15.597; 11.0139
90; 110.204; 90		2061.73Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125226 CIFC16 H52 B20 Co N2 S4P n a 2136.4636; 9.9056; 9.921
90; 90; 90		3583.4Tu, Deshuang; Shao, Dong; Yan, Hong; Lu, Changsheng
A carborane-incorporated mononuclear Co(ii) complex showing zero-field slow magnetic relaxation.
Chemical communications (Cambridge, England), 2016, 52, 14326-14329
7125227 CIFC26 H46 Cl2 N4 SnC 1 c 110.291; 21.844; 12.742
90; 106.679; 90		2743.8Bertermann, Rüdiger; Braunschweig, Holger; Celik, Mehmet Ali; Dellermann, Theresa; Kelch, Hauke
Cyclisation of biscarbenoids - a novel mode of cyclobutadiene stabilisation.
Chemical communications (Cambridge, England), 2016, 52, 13249-13252
7125228 CIFC92 H56 N8 Zn2P 1 2/c 110.8018; 17.3515; 26.7953
90; 97.145; 90		4983.2Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125229 CIFC53 H38 N4 NiP 1 2/n 110.7748; 11.5828; 35.9716
90; 93.971; 90		4478.6Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125230 CIFC46 H28 N4 NiP c a 2118.03; 11.0785; 16.251
90; 90; 90		3246.1Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125231 CIFC46 H30 N4C 1 2/c 126.2435; 13.5308; 9.407
90; 99.357; 90		3295.9Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125232 CIFC136 H110 Ag4 F12 N16 O15 S4 Zn4P 1 21/n 19.4384; 34.9486; 20.3325
90; 101.347; 90		6575.8Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125233 CIFC63 H40 Ag3 F9 N8 O9 S3 Zn2P 1 21/n 111.3487; 18.6122; 33.9443
90; 95.1; 90		7141.5Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125234 CIFC216 H172 Ag4 F12 N16 O17 S4 Zn4P -115.4217; 16.4469; 22.1055
69.989; 69.909; 73.752		4863.4Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125235 CIFC17 H16 N2 O3P 1 21/n 18.5064; 17.8133; 9.4824
90; 99.126; 90		1418.7Zhou, Tao; Li, Bin; Wang, Baiquan
Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles.
Chemical communications (Cambridge, England), 2016, 52, 14117-14120
7125236 CIFC21 H20 N2 O4P -19.2814; 10.273; 11.8447
79.305; 79.574; 83.084		1087Zhou, Tao; Li, Bin; Wang, Baiquan
Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles.
Chemical communications (Cambridge, England), 2016, 52, 14117-14120
7125237 CIFC16 H16 O4 S4P -17.6541; 9.3183; 12.9177
106.268; 100.626; 91.743		865.98Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125238 CIFC32 H30 O8 S8C 1 2/c 117.3602; 9.8696; 20.8727
90; 96.315; 90		3554.6Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125239 CIFC68 H102 Au2 Cl8 O8 S8P -19.062; 10.7865; 22.897
84.698; 80.375; 70.592		2079.6Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125240 CIFC60 H60 Cl2 Cu N12 O14C 1 2/c 136.068; 14.096; 16.023
90; 109.397; 90		7684Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125241 CIFC60 H60 B2 Cu F8 N12 O6C 1 2/c 135.729; 13.9528; 15.8889
90; 109.211; 90		7479.8Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125242 CIFC60 H60 Cu N14 O12C 1 2/c 135.509; 14.304; 15.395
90; 108.369; 90		7421Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125243 CIFC264 H300 Cl6 Cu6 N54 O48P -124.331; 24.388; 24.415
118.745; 91.861; 118.748		10460Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125244 CIFC264 H290 Br12 Cu6 N48 O24C 1 2/c 134.915; 33.412; 34.291
90; 90.352; 90		40002Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125245 CIFC14 H20 F N O2 SP 1 21/c 17.9327; 9.5312; 19.6547
90; 100.885; 90		1459.32Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125246 CIFC16 H18 F N O2 SP 21 21 218.2947; 9.5293; 18.8749
90; 90; 90		1491.92Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125247 CIFC16 H17 N O2 SP 1 21 17.3082; 12.667; 7.9739
90; 102.802; 90		719.82Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125248 CIFC26 H36 F2 N2 O6 S2P -16.3281; 12.8693; 17.8671
105.544; 93.657; 100.435		1368.94Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125249 CIFC12 H7 N O4 ZnP b c a7.1952; 19.7441; 20.4254
90; 90; 90		2901.7Zhang, Ling; Jiang, Ke; Jiang, Mengdie; Yue, Dan; Wan, Yating; Xing, Huabin; Yang, Yu; Cui, Yuanjing; Chen, Banglin; Qian, Guodong
A highly stable amino-coordinated MOF for unprecedented block off N<sub>2</sub> adsorption and extraordinary CO<sub>2</sub>/N<sub>2</sub> separation.
Chemical communications (Cambridge, England), 2016, 52, 13568-13571
7125250 CIFC21 H24 N2 O SiP -110.08; 11.8813; 16.5509
88.653; 86.499; 89.381		1977.86Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125251 CIFC20 H30 N2 O Si2P 1 21/c 117.5738; 10.3894; 12.0069
90; 100.934; 90		2152.44Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125252 CIFC26 H29 N3 O3 SiC 1 2 140.8407; 11.72; 10.659
90; 102.731; 90		4976.53Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125253 CIFC39 H21 Au Cl7 F2 N O4 PP 1 21/n 18.7297; 28.9112; 15.5735
90; 103.822; 90		3816.7Hattori, Yohei; Kusamoto, Tetsuro; Sato, Tohru; Nishihara, Hiroshi
Synergistic luminescence enhancement of a pyridyl-substituted triarylmethyl radical based on fluorine substitution and coordination to gold.
Chemical communications (Cambridge, England), 2016, 52, 13393-13396
7125254 CIFC47 H43 Cl6 F6 Ir N7 O2 PP b c a22.1254; 16.4448; 28.2843
90; 90; 90		10291.2Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José
Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization.
Chemical communications (Cambridge, England), 2016, 52, 14165-14168
7125255 CIFC35.5 H30.5 Cl F6 Ir N7 O2 PC 1 2/c 124.4157; 16.5559; 23.3462
90; 113.79; 90		8635.2Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José
Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization.
Chemical communications (Cambridge, England), 2016, 52, 14165-14168
7125256 CIFC15 H18 O2P 1 21/n 16.3004; 8.2192; 25.844
90; 94.486; 90		1334.2Ma, Dengke; Fu, Chunling; Ma, Shengming
Diastereoselective construction of cyclopent-2-enone-4-ols from aldehydes and 1,2-allenones catalyzed by N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2016, 52, 14426-14429
7125257 CIFC36 H28 O2 P2 Pd SP -19.0944; 11.4218; 15.9032
95.9441; 103.474; 102.049		1550.8Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125258 CIFC24 H36 O2 P2 Pd SP -18.7065; 11.0937; 15.13
73.3056; 80.9582; 74.899		1346.1Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125259 CIFC28 H44 O2 P2 Pd SP -18.6167; 11.5992; 16.4263
77.1791; 79.8629; 73.9166		1526.6Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125260 CIFC216 H310 Mn10 N12 O40P -114.9101; 17.9438; 22.3792
69.512; 75.796; 81.501		5424.6Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J.
Core expansion of bis-calix[4]arene-supported clusters.
Chemical communications (Cambridge, England), 2016, 52, 14246-14249
7125261 CIFC206 H280 Gd2 Mn8 N10 O44P 1 21/n 122.096; 19.157; 27.0764
90; 105.149; 90		11063Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J.
Core expansion of bis-calix[4]arene-supported clusters.
Chemical communications (Cambridge, England), 2016, 52, 14246-14249
7125262 CIFC20 H24 N2 O5P -18.9003; 9.3364; 11.3581
83.515; 76.869; 82.053		907.1Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125263 CIFC19 H21 N O6P -17.787; 9.08; 12.994
106.14; 91.08; 94.96		878.4Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125264 CIFC19 H21 N O6P c a 2110.2; 12.903; 14.787
90; 90; 90		1946.1Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125265 CIFC18 H19 N O5P 1 21/c 17.3465; 12.3261; 18.1727
90; 95.772; 90		1637.3Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125266 CIFC18 H18 F N O5P 1 21/c 118.99; 5.418; 17.32
90; 113.9; 90		1629.2Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125267 CIFC25 H30 N2 O3 SP 1 21/n 115.6911; 7.8759; 19.8219
90; 106.907; 90		2343.7Kumar, Ravi; Thorat, Shridhar H.; Reddy, Maddi Sridhar
Cu-Catalyzed iminative hydroolefination of unactivated alkynes en route to 4-imino-tetrahydropyridines and 4-aminopyridines.
Chemical communications (Cambridge, England), 2016, 52, 13475-13478
7125268 CIFC72 H110 Cl4 N7 O10P 1 21/n 114.6718; 22.9104; 23.5888
90; 104.564; 90		7674.3Lavendomme, Roy; Marcélis, Lionel; Wouters, Johan; Luhmer, Michel; Jabin, Ivan
A nano-sized container for specific encapsulation of isolated water molecules.
Chemical communications (Cambridge, England), 2016, 52, 14109-14112
7125269 CIFC27 H36 N3 UP 1 21/c 114.318; 11.54; 14.975
90; 93.52; 90		2469.6Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125270 CIFC27 H35 Cl0 N3 ThP -19.59; 11.143; 11.619
88.275; 77.613; 87.316		1211.1Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125271 CIFC111 H116 O S8 ThP 1 21/c 114.983; 25.115; 27.353
90; 92.488; 90		10283Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125272 CIFC118 H124 O S8 UP 1 21/c 115.004; 25.0884; 27.253
90; 92.527; 90		10248.8Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125273 CIFC180 H200 Cl18 N17 O12 PC 1 2/c 130.3787; 19.6365; 32.742
90; 109.719; 90		18386Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H.
A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes.
Chemical communications (Cambridge, England), 2016, 52, 13675-13678
7125274 CIFC130 H130 N10P 43 3 236.9585; 36.9585; 36.9585
90; 90; 90		50483Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H.
A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes.
Chemical communications (Cambridge, England), 2016, 52, 13675-13678
7125275 CIFC26 H24 O3P 1 21/n 18.9587; 8.4815; 27.445
90; 92.802; 90		2082.9Tharra, Prabhakararao; Baire, Beeraiah
Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans.
Chemical communications (Cambridge, England), 2016, 52, 14290-14293
7125276 CIFC47 H54 N O2 S2P 1 21/n 116.9652; 13.3015; 18.3142
90; 108.16; 90		3927Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125277 CIFC50 H66 Au2 Cl3 F6 P2 SbP -113.279; 14.462; 15.6401
100.277; 96.426; 115.812		2598.8Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125278 CIFC42.5 H42 Cl F2 N O2P -111.0496; 12.2287; 14.2619
64.774; 82.424; 88.269		1727.4Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125279 CIFC36 H35 N O2P 1 21/n 110.8442; 13.8546; 18.575
90; 92.116; 90		2788.8Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125280 CIFC38 H39 N O4P 1 21/n 112.6921; 17.3656; 14.0302
90; 99.986; 90		3045.5Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125281 CIFC39 H53 Ge N2 OP -110.7269; 11.206; 14.4819
86.134; 88.938; 81.551		1717.93Wu, Yile; Shan, Changkai; Sun, Ying; Chen, Peng; Ying, Jianxi; Zhu, Jun; Liu, Liu Leo; Zhao, Yufen
Main group metal-ligand cooperation of N-heterocyclic germylene: an efficient catalyst for hydroboration of carbonyl compounds.
Chemical communications (Cambridge, England), 2016, 52, 13799-13802
7125282 CIFC28 H24 O4P -15.6126; 8.3452; 12.339
88.55; 78.74; 87.54		566.2Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125283 CIFC28 H24 O6P -110.4453; 10.599; 10.8669
86.506; 84.424; 71.57		1135.4Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125284 CIFC26 H20 O3P 1 21/c 110.2062; 19.416; 10.5696
90; 109.487; 90		1974.5Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125285 CIFC30 H30 O6 Te3P 1 21/n 115.5616; 24.9422; 15.8574
90; 104.681; 90		5954Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125286 CIFC30 H32 O6 Te2P 1 21/n 18.3225; 15.076; 23.2305
90; 95.2; 90		2902.7Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125287 CIFC30 H36 Br6 O9 Te3P -110.889; 10.89; 18.299
86.12; 86.29; 71.19		2047.2Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125288 CIFC23 H27 N3 O2P -18.2014; 10.9469; 12.241
99.951; 94.49; 103.679		1043.58El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125289 CIFC26 H31 N3 O2P -19.3834; 11.8498; 22.2318
87.603; 82.452; 71.9		2329.3El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125290 CIFC25 H27 N4 O5 PC 1 2/c 129.5009; 7.6614; 21.6674
90; 92.924; 90		4890.85El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125291 CIFC24 H24 Cu4 I4 N4 O16 Zr3I 4/m m m17.5411; 17.5411; 34.6975
90; 90; 90		10676.1Tan, Yan-Xi; Yang, Xue; Li, Bei-Bei; Yuan, Daqiang
Rational design of a flu-type heterometallic cluster-based Zr-MOF.
Chemical communications (Cambridge, England), 2016, 52, 13671-13674
7125292 CIFC20 H18 Br N O5 SP -17.88851; 8.9545; 14.9033
92.1745; 99.8465; 107.839		982.77Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata
Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives.
Chemical communications (Cambridge, England), 2016, 52, 13916-13919
7125293 CIFC25 H26 N2 O6 SP -18.3702; 12.3731; 13.2427
108.688; 105.715; 98.948		1205.6Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata
Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives.
Chemical communications (Cambridge, England), 2016, 52, 13916-13919
7125294 CIFC21 H23 Br F3 N O6P 21 21 218.6647; 15.3884; 17.0772
90; 90; 90		2277Zhi, Ying; Zhao, Kun; Liu, Qiang; Wang, Ai; Enders, Dieter
Asymmetric synthesis of functionalized trifluoromethyl-substituted pyrrolidines via an organocatalytic domino Michael/Mannich [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2016, 52, 14011-14014
7125295 CIFC26 H19 N OP 1 21/c 127.556; 7.4414; 19.1328
90; 109.435; 90		3699.7Bagle, Pradip N.; Mane, Manoj V.; Vanka, K.; Shinde, Dinesh R.; Shaikh, Samir R.; Gonnade, Rajesh G.; Patil, Nitin T.
Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides.
Chemical communications (Cambridge, England), 2016, 52, 14462-14465
7125296 CIFC56 H46 Br Cl2 F4 O3 P3 Pd SP -112.108; 12.5; 18.24
76.07; 74.442; 82.349		2574.3Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125297 CIFC63 H53 Br F2 P3 PdP -112.225; 12.671; 19.4112
98.543; 90.489; 118.142		2611.3Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125298 CIFC57.5 H47 Br Cl3 F4 O4 P3 Pd SP 1 21/c 114.2329; 20.4798; 19.1729
90; 96.688; 90		5550.6Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125299 CIFC22 H54 N8 Ni2 O10.01 P2P -110.3977; 14.1488; 22.4532
90.093; 90.531; 90.097		3303.05Neri, Gaia; Forster, Mark; Walsh, James J.; Robertson, C. M.; Whittles, T. J.; Farràs, Pau; Cowan, Alexander J.
Photochemical CO<sub>2</sub> reduction in water using a co-immobilised nickel catalyst and a visible light sensitiser.
Chemical communications (Cambridge, England), 2016, 52, 14200-14203
7125300 CIFC15 H10 N2P b c a13.936; 7.077; 22.807
90; 90; 90		2249.3Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125301 CIFC19 H16 N2 O2 SP 1 21/c 19.3811; 20.8484; 8.6963
90; 99.098; 90		1679.43Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125302 CIFC16 H12 N2 O2 SP 1 21/c 19.0829; 10.2351; 15.664
90; 97.384; 90		1444.1Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125303 CIFC45 H21 Dy F18 N2 O6P 21 21 2111.111; 17.6697; 22.6965
90; 90; 90		4456Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125304 CIFC45 H21 Dy F18 N2 O6P 21 21 2111.1191; 17.6604; 22.693
90; 90; 90		4456.2Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125305 CIFC48 H28 Dy F18 N2 O6P -113.216; 13.9132; 14.5959
67.984; 72.454; 84.724		2371.71Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125306 CIFC28 H19 N OP 1 21 113.0425; 10.2377; 16.1011
90; 109.601; 90		2025.32Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M
Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation.
Chemical communications (Cambridge, England), 2016, 52, 14121-14124
7125307 CIFC32 H21 N OP 1 21 17.6244; 7.9489; 18.4283
90; 93.193; 90		1115.12Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M
Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation.
Chemical communications (Cambridge, England), 2016, 52, 14121-14124
7125308 CIFC22 H25 N O5P 1 21/n 16.2373; 36.3214; 8.6667
90; 94.598; 90		1957.1Fuentes de Arriba, Angel L.; Urbitsch, Felix; Dixon, Darren J.
Umpolung synthesis of branched α-functionalized amines from imines via photocatalytic three-component reductive coupling reactions.
Chemical communications (Cambridge, England), 2016, 52, 14434-14437

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