Crystallography Open Database
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Searching journal of publication like 'Chem. Commun.' volume of publication is 50
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7115503 | CIF | C36 H26 F3 N2 P Pd | P -1 | 9.9041; 12.3289; 13.1446 92.202; 110.621; 102.448 | 1455.37 | Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb [Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)] Chem.Commun., 2014, 50, 9859 |
| 7115504 | CIF | C50 H38 F6 O3 P2 Pd2 | P -1 | 11.9714; 12.3041; 16.0441 67.975; 88.863; 86.969 | 2187.72 | Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb [Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)] Chem.Commun., 2014, 50, 9859 |
| 7115505 | CIF | C42 H32 Cl F3 P2 Pd | P b c a | 12.1168; 23.2879; 24.9924 90; 90; 90 | 7052.2 | Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb [Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)] Chem.Commun., 2014, 50, 9859 |
| 7115506 | CIF | C16 H12 O2 | P 1 21/c 1 | 14.927; 6.57; 13.515 90; 116.131; 90 | 1189.9 | Jianming Liu; Xin Zhang; Lijun Shi; Muwen Liu; Yuanyuan Yue; Fuwei Li; Kelei Zhuo Base-promoted synthesis of coumarins from salicylaldehydes and aryl-substituted 1,1-dibromo-1-alkenes under transition-metal-free conditions Chem.Commun., 2014, 50, 9887 |
| 7115507 | CIF | C21 H35 Cr N2 O Si2 | C 1 2/m 1 | 13.073; 15.574; 12.961 90; 118.861; 90 | 2311.1 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115508 | CIF | C21 H31 Cl Cr N2 | P b n a | 13.5642; 16.8668; 18.294 90; 90; 90 | 4185.4 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115509 | CIF | C23 H19 Cl Cr N2 | P -1 | 10.747; 12.676; 16.141 90.42; 107.496; 110.92 | 1942.6 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115510 | CIF | C27 H42 Cr N3 Si2 | P 1 21/n 1 | 10.5631; 19.238; 14.5072 90; 111.307; 90 | 2746.5 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115511 | CIF | C26 H38 Cr N3 Si2 | P 1 21/c 1 | 9.436; 26.567; 11.327 90; 108.782; 90 | 2688.3 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115512 | CIF | C31 H46 Cr N3 | C 1 2/m 1 | 15.964; 13.0182; 14.345 90; 113.436; 90 | 2735.3 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115513 | CIF | C34 H48 Cr N4 | P -1 | 12.1837; 12.1849; 12.4184 106.399; 91.635; 113.395 | 1602.36 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115514 | CIF | C28 H39 Cr N3 O2 S | P b c a | 19.539; 9.9443; 27.28 90; 90; 90 | 5300.5 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115515 | CIF | C32 H51 Cr N3 O2 S Si2 | P 1 21/n 1 | 15.985; 11.686; 19.444 90; 110.836; 90 | 3394.6 | Wen Zhou; Brian O. Patrick; Kevin M. Smith Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity Chem.Commun., 2014, 50, 9958 |
| 7115516 | CIF | C44 H41 B F15 O P | P 1 21 1 | 11.5255; 14.8611; 11.8913 90; 92.265; 90 | 2035.17 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115517 | CIF | C28 H34 F3 O3 P S | P 1 21/n 1 | 12.3858; 10.4816; 21.683 90; 93.545; 90 | 2809.6 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115518 | CIF | C34 H38 F5 O3 P S | P -1 | 8.2485; 9.5183; 22.078 88.372; 86.027; 73.088 | 1654.37 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115519 | CIF | C13 H28 F3 O4 P S | P 1 21/n 1 | 9.0615; 15.507; 13.509 90; 90.58; 90 | 1898.14 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115520 | CIF | C23 H32 F3 O4 P S | P 21 21 21 | 8.9375; 16.5265; 16.7035 90; 90; 90 | 2467.2 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115521 | CIF | C13 H26 F3 O4 P S | P 21 21 21 | 8.1984; 14.7753; 15.114 90; 90; 90 | 1830.82 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115522 | CIF | C32 H26 F3 O3 P S | C 1 c 1 | 10.6205; 16.669; 15.7534 90; 92.271; 90 | 2786.7 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115523 | CIF | C32 H38 F3 O3 P S | P 1 21/c 1 | 9.7033; 17.8716; 16.8564 90; 93.436; 90 | 2917.87 | Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers Chem.Commun., 2014, 50, 10038 |
| 7115524 | CIF | C24 H26 Br N3 O2 | P 21 21 21 | 10.78; 13.453; 15.304 90; 90; 90 | 2219.4 | Yu Tan; Han-Lin Luan; Hua Lin; Xing-Wen Sun; Xiao-Di Yang; Han-Qing Dong; Guo-Qiang Lin One-pot enantioselective construction of indoloquinolizidine derivatives bearing five contiguous stereocenters using aliphatic aldehydes, nitroethylenes, and tryptamine Chem.Commun., 2014, 50, 10027 |
| 7115525 | CIF | C28 H35 N3 O2 | P 1 21 1 | 9.784; 8.872; 14.497 90; 90; 90 | 1258.4 | Yu Tan; Han-Lin Luan; Hua Lin; Xing-Wen Sun; Xiao-Di Yang; Han-Qing Dong; Guo-Qiang Lin One-pot enantioselective construction of indoloquinolizidine derivatives bearing five contiguous stereocenters using aliphatic aldehydes, nitroethylenes, and tryptamine Chem.Commun., 2014, 50, 10027 |
| 7115526 | CIF | C23 H13 N O2 | P 1 21/m 1 | 9.638; 7.105; 11.862 90; 95.858; 90 | 808 | Shivani Mahajan; Sadhika Khullar; Sanjay K. Mandal; Inder Pal Singh A one-pot, three-component reaction for the synthesis of novel 7-arylbenzo[c]acridine-5,6-diones Chem.Commun., 2014, 50, 10078 |
| 7115527 | CIF | C90 H122 N12 O15 Si | P 1 21/n 1 | 16.9924; 27.8784; 26.0023 90; 97.315; 90 | 12217.6 | Mayumi Kudo; Victor Maurizot; Hyuma Masu; Aya Tanatani; Ivan Huc Structural elucidation of foldamers with no long range conformational order Chem.Commun., 2014, 50, 10090 |
| 7115528 | CIF | C41 H40 Ga Mo N2 O5 | P b c n | 17.1431; 15.7892; 14.4285 90; 90; 90 | 3905.4 | Igor L. Fedushkin; Vladimir G. Sokolov; Alexander V. Piskunov; Valentine M. Makarov; Eugeny V. Baranov; Gleb A. Abakumov Adaptive behavior of a redox-active gallium carbenoid in complexes with molybdenum Chem.Commun., 2014, 50, 10108 |
| 7115529 | CIF | C44 H45 Ga Mo N2 O3 | P 1 21 1 | 8.82154; 38.0697; 11.69917 90; 97.2432; 90 | 3897.62 | Igor L. Fedushkin; Vladimir G. Sokolov; Alexander V. Piskunov; Valentine M. Makarov; Eugeny V. Baranov; Gleb A. Abakumov Adaptive behavior of a redox-active gallium carbenoid in complexes with molybdenum Chem.Commun., 2014, 50, 10108 |
| 7115530 | CIF | C104 H118 Ga2 Mo2 N4 Na2 O14 | P -1 | 12.162; 12.7895; 16.926 72.066; 83.271; 85.462 | 2485 | Igor L. Fedushkin; Vladimir G. Sokolov; Alexander V. Piskunov; Valentine M. Makarov; Eugeny V. Baranov; Gleb A. Abakumov Adaptive behavior of a redox-active gallium carbenoid in complexes with molybdenum Chem.Commun., 2014, 50, 10108 |
| 7115531 | CIF | C25 H33 B O7 | P -1 | 9.5236; 11.7389; 12.5461 62.68; 84.635; 81.559 | 1232.12 | Alicia Martos-Redruejo; Ruth Lopez-Duran; Elena Bunuel; Diego J. Cardenas Ligand-controlled divergent formation of alkenyl- or allylboronates catalyzed by Pd, and synthetic applications Chem.Commun., 2014, 50, 10094 |
| 7115532 | CIF | C27 H33 B O6 S2 | P 1 21/c 1 | 8.1024; 13.4762; 25.6608 90; 96.518; 90 | 2783.78 | Alicia Martos-Redruejo; Ruth Lopez-Duran; Elena Bunuel; Diego J. Cardenas Ligand-controlled divergent formation of alkenyl- or allylboronates catalyzed by Pd, and synthetic applications Chem.Commun., 2014, 50, 10094 |
| 7115533 | CIF | C22 H23 N2 O2 S | P b c a | 12.1138; 15.4374; 22.576 90; 90; 90 | 4221.8 | Alicia Martos-Redruejo; Ruth Lopez-Duran; Elena Bunuel; Diego J. Cardenas Ligand-controlled divergent formation of alkenyl- or allylboronates catalyzed by Pd, and synthetic applications Chem.Commun., 2014, 50, 10094 |
| 7115534 | CIF | C51 H41 F6 N6 O8 Os P | P -1 | 9.349; 14.949; 20.583 106.442; 90.995; 94.554 | 2747.9 | Hai-Jing Nie; Jiang-Yang Shao; Chang-Jiang Yao; Yu-Wu Zhong Organic-inorganic mixed-valence systems with strongly-coupled triarylamine and cyclometalated osmium Chem.Commun., 2014, 50, 10082 |
| 7115535 | CIF | C43 H52 O4 | P -1 | 10.0808; 12.8064; 15.1154 89.88; 75.473; 75.26 | 1822.85 | Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes Chem.Commun., 2014, 50, 10112 |
| 7115536 | CIF | C161 H182 Cl2 O16 | P 1 21/c 1 | 13.22632; 25.83704; 20.88126 90; 99.786; 90 | 7031.9 | Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes Chem.Commun., 2014, 50, 10112 |
| 7115537 | CIF | C47 H52 N0 O4 | P -1 | 12.3671; 12.635; 13.8467 77.854; 63.909; 80.759 | 1894 | Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes Chem.Commun., 2014, 50, 10112 |
| 7115538 | CIF | C43 H50 O4 | P -1 | 9.8496; 12.97; 14.9932 89.965; 77.36; 74.04 | 1793.29 | Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes Chem.Commun., 2014, 50, 10112 |
| 7115539 | CIF | C44 H52 N8 O14 Pd4 | P 1 21/c 1 | 7.9571; 23.6001; 13.0293 90; 92.124; 90 | 2445.07 | Marina Juribasic; Krunoslav Uzarevic; Davor Gracin; Manda Curic Mechanochemical C-H bond activation: rapid and regioselective double cyclopalladation monitored by in situ Raman spectroscopy Chem.Commun., 2014, 50, 10287 |
| 7115540 | CIF | C36.5 H42.5 N9.5 O9.5 Pd2 | C 1 c 1 | 34.577; 16.50703; 14.29901 90; 97.1631; 90 | 8097.66 | Marina Juribasic; Krunoslav Uzarevic; Davor Gracin; Manda Curic Mechanochemical C-H bond activation: rapid and regioselective double cyclopalladation monitored by in situ Raman spectroscopy Chem.Commun., 2014, 50, 10287 |
| 7115541 | CIF | C16 H20 N2 O2 | P 1 21 1 | 6.1563; 8.2068; 14.895 90; 100.888; 90 | 739 | Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach Chem.Commun., 2014, 50, 10218 |
| 7115542 | CIF | C16 H19 Br N2 O2 | P 1 21 1 | 6.137; 8.934; 14.27 90; 99.976; 90 | 770.6 | Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach Chem.Commun., 2014, 50, 10218 |
| 7115543 | CIF | C14 H16 N2 O2 | P 1 21 1 | 5.8127; 9.5156; 11.5873 90; 103.442; 90 | 623.35 | Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach Chem.Commun., 2014, 50, 10218 |
| 7115544 | CIF | C20 H19 Br N2 O2 | P b c a | 6.56; 16.644; 33.009 90; 90; 90 | 3604 | Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach Chem.Commun., 2014, 50, 10218 |
| 7115549 | CIF | C20 H12 N2 | P 21 21 21 | 3.88126; 11.643; 29.5312 90; 90; 90 | 1334.5 | Youhei Takeda; Masato Okazaki; Satoshi Minakata Oxidative skeletal rearrangement of 1,1'-binaphthalene-2,2'-diamines (BINAMs) via C-C bond cleavage and nitrogen migration: a versatile synthesis of U-shaped azaacenes Chem.Commun., 2014, 50, 10291 |
| 7115550 | CIF | C15 H13 F5 N4 O4 S | P 1 21/c 1 | 9.459; 22.4257; 9.0101 90; 115.656; 90 | 1722.83 | Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media Chem.Commun., 2014, 50, 10237 |
| 7115551 | CIF | C22 H18 Cl F6 N5 O2 | P b c a | 21.4875; 20.5465; 21.5438 90; 90; 90 | 9511.4 | Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media Chem.Commun., 2014, 50, 10237 |
| 7115552 | CIF | C16 H20 F3 N O4 | C 1 2/c 1 | 21.291; 11.5227; 14.4085 90; 105.162; 90 | 3411.8 | Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media Chem.Commun., 2014, 50, 10237 |
| 7115553 | CIF | C10 H6 F3 N | P 21 21 21 | 4.7643; 12.7324; 13.8685 90; 90; 90 | 841.28 | Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media Chem.Commun., 2014, 50, 10237 |
| 7115554 | CIF | C87 H88 F12 N4 O18 P2 | P 1 21/c 1 | 14.3256; 36.543; 19.3027 90; 108.61; 90 | 9576.6 | Wei-Bo Hu; Hong-Mei Yang; Wen-Jing Hu; Ming-Liang Ma; Xiao-Li Zhao; Xian-Qiang Mi; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen A pillar[5]arene and crown ether fused bicyclic host: synthesis, guest discrimination and simultaneous binding of two guests with different shapes, sizes and electronic constitutions Chem.Commun., 2014, 50, 10460 |
| 7115555 | CIF | C16 H18 N2 O3 | P -1 | 6.2955; 9.3559; 12.975 80.69; 89.5; 75.05 | 728.2 | Shaoxia Lin; Ling Li; Fushun Liang; Qun Liu DABCO-catalyzed ring opening of activated cyclopropanes and recyclization leading to gamma-lactams with an all-carbon quaternary center Chem.Commun., 2014, 50, 10491 |
| 7115557 | CIF | C48 H102 N12 O6 Zr3 | P 1 21/c 1 | 23.4504; 13.3481; 20.7646 90; 103.285; 90 | 6325.76 | Adam C. Lamb; Zheng Lu; Zi-Ling Xue Reactions of zirconium amide amidinates with dioxygen. Observation of an unusual peroxo intermediate in the formation of oxo compounds Chem.Commun., 2014, 50, 10517 |
| 7115558 | CIF | C16 H18 Br N O4 | P 1 21 1 | 7.96; 6.2115; 17.0041 90; 98.216; 90 | 832.11 | Yi-ning Xuan; Zhen-yu Chen; Ming Yan An organocatalytic cascade reaction of 2-nitrocyclohexanone and alpha,beta-unsaturated aldehydes with unusual regioselectivity Chem.Commun., 2014, 50, 10471 |
| 7115559 | CIF | C168 H217 F24 N7 O40 P4 | P -1 | 12.6852; 17.3581; 21.7669 104.59; 100.42; 95.616 | 4509.7 | Yujuan Zhou; Zhengtao Li; Xiaodong Chi; Connor Thompson; Yong Yao Formation of a [2]pseudorotaxane based on a pillar[5]arene and a rigid guest in solution and in the solid state Chem.Commun., 2014, 50, 10482 |
| 7115560 | CIF | C19 H17 N O | P -1 | 7.5607; 9.6755; 11.352 107.554; 102.789; 103.85 | 729.07 | Anupal Gogoi; Anju Modi; Srimanta Guin; Saroj Kumar Rout; Debapratim Das; Bhisma K. Patel A metal free domino synthesis of 3-aroylindoles via two sp3 C-H activation Chem.Commun., 2014, 50, 10445 |
| 7115561 | CIF | C22 H20 Eu N5 O10 | P -1 | 9.5509; 11.2004; 12.8518 66.27; 76.414; 80.581 | 1219.66 | Jinlei Chen; Fei-Yan Yi; Hong Yu; Shihui Jiao; Guangsheng Pang; Zhong-Ming Sun Fast response and highly selective sensing of amine vapors using a luminescent coordination polymer Chem.Commun., 2014, 50, 10506 |
| 7115562 | CIF | C275 H308 Cl6 I10 Ir4 N20 O25 | P -1 | 14.9997; 20.6925; 26.1024 105.607; 100.893; 99.749 | 7451.9 | Haohua Huo; Chen Fu; Chuanyong Wang; Klaus Harms; Eric Meggers Metal-templated enantioselective enamine/H-bonding dual activation catalysis Chem.Commun., 2014, 50, 10409 |
| 7115563 | CIF | C27 H31 Br2 N O4 S Si | P 1 21/a 1 | 18.9903; 12.146; 26.2415 90; 108.147; 90 | 5751.7 | Tomoya Miura; Takayuki Nakamuro; Kentaro Hiraga; Masahiro Murakami The stereoselective synthesis of alpha-amino aldols starting from terminal alkynes Chem.Commun., 2014, 50, 10474 |
| 7115564 | CIF | C98 H20 | P 42/n c m | 16.8655; 16.8655; 19.6001 90; 90; 90 | 5575.2 | Venkata S. Pavan K. Neti; Maira R. Ceron; A. Duarte-Ruiz; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen High-yield, regiospecific bis-functionalization of C70 using a Diels-Alder reaction in molten anthracene Chem.Commun., 2014, 50, 10584 |
| 7115565 | CIF | C39 H30 N O4 P | P -1 | 9.6945; 11.27; 15.8376 92.446; 101.11; 113.846 | 1538.92 | Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates Chem.Commun., 2014, 50, 10580 |
| 7115566 | CIF | C39 H23 Cl2 F3 N O4 P | P 1 21/n 1 | 15.3256; 9.7698; 22.1934 90; 90.145; 90 | 3322.96 | Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates Chem.Commun., 2014, 50, 10580 |
| 7115567 | CIF | C40 H24 N O4 P | P -1 | 9.9693; 10.0382; 17.31 79.783; 89.864; 66.349 | 1557.1 | Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates Chem.Commun., 2014, 50, 10580 |
| 7115568 | CIF | C42 H24 N O4 P | P -1 | 10.2329; 10.298; 17.3524 97.558; 92.475; 116.557 | 1610.67 | Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates Chem.Commun., 2014, 50, 10580 |
| 7115569 | CIF | C88 H100 B Cr F24 N6 | P 1 21/c 1 | 22.049; 17.219; 25.078 90; 114.243; 90 | 8682 | Jingmei Shen; Glenn P. A. Yap; William E. Barker IV; William E. Geiger; Klaus H. Theopold An electron transfer series of octahedral chromium complexes containing a redox non-innocent alpha-diimine ligand Chem.Commun., 2014, 50, 10626 |
| 7115570 | CIF | C108 H100 B2 Cl4 Cr F48 N6 | P -1 | 13.962; 17.728; 26.214 79.116; 77.828; 70.078 | 5915 | Jingmei Shen; Glenn P. A. Yap; William E. Barker IV; William E. Geiger; Klaus H. Theopold An electron transfer series of octahedral chromium complexes containing a redox non-innocent alpha-diimine ligand Chem.Commun., 2014, 50, 10626 |
| 7115571 | CIF | C52 H42 N4 O6 | P 1 21/c 1 | 7.8968; 31.81; 16.8438 90; 105.408; 90 | 4079 | Lankani P. Wijesinghe; Buddhie S. Lankage; Gearoid M. O Maille; Sarath D. Perera; Deanne Nolan; Longsheng Wang; Sylvia M. Draper Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes Chem.Commun., 2014, 50, 10637 |
| 7115572 | CIF | C52 H54 N4 O6 | P 1 21/n 1 | 13.586; 11.951; 31.96 90; 94.14; 90 | 5176 | Lankani P. Wijesinghe; Buddhie S. Lankage; Gearoid M. O Maille; Sarath D. Perera; Deanne Nolan; Longsheng Wang; Sylvia M. Draper Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes Chem.Commun., 2014, 50, 10637 |
| 7115573 | CIF | C59 H54 Cl0 Fe0 N2 O3 | P 1 21/c 1 | 17.8254; 10.8398; 29.3462 90; 124.42; 90 | 4677.6 | Lankani P. Wijesinghe; Buddhie S. Lankage; Gearoid M. O Maille; Sarath D. Perera; Deanne Nolan; Longsheng Wang; Sylvia M. Draper Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes Chem.Commun., 2014, 50, 10637 |
| 7115574 | CIF | C4 H4 Br Cu O4 P S | P 1 21/c 1 | 15.899; 7.627; 7.344 90; 100.075; 90 | 876.8 | Wei-Xuan Nie; Song-Song Bao; Dai Zeng; Li-Rong Guo; Li-Min Zheng Exfoliated layered copper phosphonate showing enhanced adsorption capability towards Pb ions Chem.Commun., 2014, 50, 10622 |
| 7115575 | CIF | C74 H74 F2 O4 Yb2 | P 1 21/n 1 | 12.994; 12.4469; 18.4353 90; 95.132; 90 | 2969.68 | G. B. Deacon; F. Jaroschik; P. C. Junk; R. P. Kelly A divalent heteroleptic lanthanoid fluoride complex stabilised by the tetraphenylcyclopentadienyl ligand, arising from C-F activation of pentafluorobenzene Chem.Commun., 2014, 50, 10655 |
| 7115576 | CIF | C62 H50 O Yb | P 1 21/n 1 | 10.272; 40.41; 11.14 90; 105.41; 90 | 4457.9 | G. B. Deacon; F. Jaroschik; P. C. Junk; R. P. Kelly A divalent heteroleptic lanthanoid fluoride complex stabilised by the tetraphenylcyclopentadienyl ligand, arising from C-F activation of pentafluorobenzene Chem.Commun., 2014, 50, 10655 |
| 7115577 | CIF | C50 H38 B Cl2 N5 O2 Pt | P 1 21/c 1 | 12.2811; 12.5617; 26.9413 90; 100.943; 90 | 4080.69 | Ryo Sekiya; Yusuke Tsutsui; Wookjin Choi; Tsuneaki Sakurai; Shu Seki; Yuya Bandoa; Hiromitsu Maeda Ion-based assemblies of planar anion complexes and cationic PtII complexes Chem.Commun., 2014, 50, 10615 |
| 7115578 | CIF | C11 H10 N4 | P 1 21/c 1 | 9.1608; 7.6873; 14.6054 90; 103.05; 90 | 1001.98 | Li Xu; Xue-Qing Mou; Zhi-Min Chen; Shao-Hua Wang Copper-catalyzed intermolecular azidocyanation of aryl alkenes Chem.Commun., 2014, 50, 10676 |
| 7115579 | CIF | C28 H22 N2 | P 1 21/c 1 | 12.208; 9.4997; 19.3 90; 109.62; 90 | 2108.3 | Ying Xie; Tengfei Chen; Shaomin Fu; Xing-Shu Li; Yuanfu Deng; Huanfeng Jiang; Wei Zeng Pd-Catalyzed [3+2] cycloaddition of ketoimines with alkynes via directed sp3 C-H bond activation Chem.Commun., 2014, 50, 10699 |
| 7115580 | CIF | C H Cl N O | P -1 | 7.9603; 25.1844; 12.0025 90; 104.539; 90 | 2329.2 | Jun-Hui Xu; Jian-Ping Wei; Zheng Hao; Qing-Guo Ma; Xin-Hua Peng Highly double selective nitration of nitrostilbenes over zeolite Chem.Commun., 2014, 50, 10710 |
| 7115581 | CIF | C24 H17 N5 O10 | C 1 2/c 1 | 24.48; 8.379; 11.878 90; 106.275; 90 | 2339 | Jun-Hui Xu; Jian-Ping Wei; Zheng Hao; Qing-Guo Ma; Xin-Hua Peng Highly double selective nitration of nitrostilbenes over zeolite Chem.Commun., 2014, 50, 10710 |
| 7115586 | CIF | C18 H18 Br F2 N O3 S2 | P 21 21 21 | 18.0666; 21.1169; 22.2584 90; 90; 90 | 8491.8 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115587 | CIF | C18 H18 F2 N O S | P 21 21 21 | 8.7675; 10.5238; 18.173 90; 90; 90 | 1676.8 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115588 | CIF | C24 H23 F2 N O3 S2 | P 21 21 21 | 10.0872; 14.0488; 16.2483 90; 90; 90 | 2302.6 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115589 | CIF | C13 H8 Br N O S | P 1 21 1 | 7.5255; 3.9957; 19.305 90; 95.045; 90 | 578.2 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115590 | CIF | C16 H17 F2 N O S | P 21 21 21 | 9.9519; 10.2705; 15.1165 90; 90; 90 | 1545.07 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115591 | CIF | C31 H22 Br F2 N O3 S2 | P 21 21 21 | 8.5124; 14.4301; 22.503 90; 90; 90 | 2764.2 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115592 | CIF | C21 H16 Br N O3 S | P 1 21/n 1 | 9.876; 11.292; 16.818 90; 92.78; 90 | 1873.3 | Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines Chem.Commun., 2014, 50, 10596 |
| 7115593 | CIF | C27 H21 N O3 S | C 1 c 1 | 26.342; 19.322; 18.311 90; 110.59; 90 | 8725 | Fei Pan; Shuang Liu; Chao Shu; Rong-Kun Lin; Yong-Fei Yu; Jin-Mei Zhou; Long-Wu Ye Gold-catalyzed intermolecular oxidation of o-alkynylbiaryls: an easy and practical access to functionalized fluorenes Chem.Commun., 2014, 50, 10726 |
| 7115594 | CIF | C68 H66 B F24 Ir N P | P -1 | 13.42933; 18.87158; 27.7213 77.2224; 88.4024; 77.9371 | 6698.97 | Nicolas Humbert; Devendra J. Vyas; Celine Besnard; Clement Mazet An air-stable cationic iridium hydride as a highly active and general catalyst for the isomerization of terminal epoxides Chem.Commun., 2014, 50, 10592 |
| 7115595 | CIF | C28 H18 N2 S2 Se | P -1 | 8.0777; 8.1703; 17.9004 83.481; 87.961; 67.919 | 1087.62 | Ann Christin Jahnke; Mariana Spulber; Markus Neuburger; Cornelia G. Palivan; Oliver S. Wenger Electronic coupling mediated by furan, thiophene, selenophene and tellurophene in a homologous series of organic mixed valence compounds Chem.Commun., 2014, 50, 10883 |
| 7115596 | CIF | C12 H10 F N3 O | P 1 21/c 1 | 11.785; 5.7638; 16.482 90; 102.47; 90 | 1093.2 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115597 | CIF | C12 H9 F2 N3 O | P 1 21/n 1 | 10.484; 5.4019; 19.491 90; 104.37; 90 | 1069.3 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115598 | CIF | C12 H10 N4 O3 | P -1 | 6.9066; 7.942; 11.37 81.16; 87.98; 67.14 | 567.7 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115599 | CIF | C12 H10 F N3 O | P 1 n 1 | 4.5349; 11.591; 10.686 90; 98.22; 90 | 555.93 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115600 | CIF | C12 H9 F2 N3 O | P 1 21/c 1 | 3.7683; 27.238; 10.409 90; 97.29; 90 | 1059.8 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115601 | CIF | C12 H10 N4 O3 | P b c a | 11.9799; 7.3695; 25.427 90; 90; 90 | 2244.8 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115602 | CIF | C12 H11 F2 N3 O2 | P -1 | 8.9104; 9.9683; 13.1855 91.865; 92.788; 91.591 | 1168.65 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115603 | CIF | C13 H14 N4 O4 | P 1 21/c 1 | 8.1756; 14.365; 11.375 90; 92.01; 90 | 1335.1 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115604 | CIF | C13 H10 F3 N3 O | P 1 21/c 1 | 14.5029; 12.713; 14.3436 90; 116.799; 90 | 2360.6 | Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli Chem.Commun., 2014, 50, 10819 |
| 7115605 | CIF | C46 H26 Cu F36 N4 O6 | P -1 | 10.3845; 10.7053; 27.4 84.153; 89.737; 64.833 | 2740 | Hyung Joon Jeon; Ryotaro Matsuda; Prakash Kanoo; Hiroshi Kajiro; Liangchun Li; Hiroshi Sato; Yongtai Zheng; Susumu Kitagawa The densely fluorinated nanospace of a porous coordination polymer composed of perfluorobutyl-functionalized ligands Chem.Commun., 2014, 50, 10861 |
| 7115606 | CIF | C19 H19 N3 O | P 1 21/c 1 | 15.709; 8.4319; 12.274 90; 96.34; 90 | 1615.8 | Zhi-Min Chen; Zhen Zhang; Yong-Qiang Tu; Ming-Hui Xu; Fu-Min Zhang; Chen-Chen Li; Shao-Hua Wang A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers Chem.Commun., 2014, 50, 10805 |
| 7115607 | CIF | C21 H26 N6 O2 Si | P 1 21/c 1 | 8.7189; 9.066; 27.8157 90; 91.003; 90 | 2198.37 | Zhi-Min Chen; Zhen Zhang; Yong-Qiang Tu; Ming-Hui Xu; Fu-Min Zhang; Chen-Chen Li; Shao-Hua Wang A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers Chem.Commun., 2014, 50, 10805 |
| 7115608 | CIF | C18 H17 N3 O2 | P -1 | 8.6242; 10.2987; 10.3691 61.409; 80.7; 86.903 | 797.7 | Zhi-Min Chen; Zhen Zhang; Yong-Qiang Tu; Ming-Hui Xu; Fu-Min Zhang; Chen-Chen Li; Shao-Hua Wang A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers Chem.Commun., 2014, 50, 10805 |
| 7115609 | CIF | C24 H25 N O6 | P 1 21/c 1 | 13.637; 13.749; 12.866 90; 111.745; 90 | 2241 | Thangavel Selvia; Kannupal Srinivasan Synthesis of 2,4,5-trisubstituted oxazoles through tin(IV) chloride-mediated reaction of trans-2-aryl-3-nitro-cyclopropane-1,1-dicarboxylates with nitriles Chem.Commun., 2014, 50, 10845 |
| 7115610 | CIF | C28 H30 N4 Pd | P -1 | 8.25; 14.764; 19.582 88.932; 89.487; 74.757 | 2300.8 | M. G. Derry Holaday; Gourav Tarafdar; B. Adinarayana; M. L. P. Reddy; A. Srinivasan Chemodosimetric cyanide sensing in a 5,15-porphodimethene Pd(II) complex Chem.Commun., 2014, 50, 10584 |
| 7115611 | CIF | C15 H12 F N O3 | P -1 | 10.1802; 10.4053; 13.1475 90.7253; 108.201; 106.189 | 1262.93 | Aditi P. Chavannavar; Allen G. Oliver; Brandon L. Ashfeld An umpolung approach toward N-aryl nitrone construction: a phosphine-mediated addition of 1,2-dicarbonyls to nitroso electrophiles Chem.Commun., 2014, 50, 10853 |
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