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

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