Crystallography Open Database

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7115503 CIFC36 H26 F3 N2 P PdP -19.9041; 12.3289; 13.1446
92.202; 110.621; 102.448
1455.37Anant 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 CIFC50 H38 F6 O3 P2 Pd2P -111.9714; 12.3041; 16.0441
67.975; 88.863; 86.969
2187.72Anant 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 CIFC42 H32 Cl F3 P2 PdP b c a12.1168; 23.2879; 24.9924
90; 90; 90
7052.2Anant 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 CIFC16 H12 O2P 1 21/c 114.927; 6.57; 13.515
90; 116.131; 90
1189.9Jianming 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 CIFC21 H35 Cr N2 O Si2C 1 2/m 113.073; 15.574; 12.961
90; 118.861; 90
2311.1Wen 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 CIFC21 H31 Cl Cr N2P b n a13.5642; 16.8668; 18.294
90; 90; 90
4185.4Wen 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 CIFC23 H19 Cl Cr N2P -110.747; 12.676; 16.141
90.42; 107.496; 110.92
1942.6Wen 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 CIFC27 H42 Cr N3 Si2P 1 21/n 110.5631; 19.238; 14.5072
90; 111.307; 90
2746.5Wen 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 CIFC26 H38 Cr N3 Si2P 1 21/c 19.436; 26.567; 11.327
90; 108.782; 90
2688.3Wen 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 CIFC31 H46 Cr N3C 1 2/m 115.964; 13.0182; 14.345
90; 113.436; 90
2735.3Wen 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 CIFC34 H48 Cr N4P -112.1837; 12.1849; 12.4184
106.399; 91.635; 113.395
1602.36Wen 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 CIFC28 H39 Cr N3 O2 SP b c a19.539; 9.9443; 27.28
90; 90; 90
5300.5Wen 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 CIFC32 H51 Cr N3 O2 S Si2P 1 21/n 115.985; 11.686; 19.444
90; 110.836; 90
3394.6Wen 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 CIFC44 H41 B F15 O PP 1 21 111.5255; 14.8611; 11.8913
90; 92.265; 90
2035.17Michael 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 CIFC28 H34 F3 O3 P SP 1 21/n 112.3858; 10.4816; 21.683
90; 93.545; 90
2809.6Michael 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 CIFC34 H38 F5 O3 P SP -18.2485; 9.5183; 22.078
88.372; 86.027; 73.088
1654.37Michael 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 CIFC13 H28 F3 O4 P SP 1 21/n 19.0615; 15.507; 13.509
90; 90.58; 90
1898.14Michael 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 CIFC23 H32 F3 O4 P SP 21 21 218.9375; 16.5265; 16.7035
90; 90; 90
2467.2Michael 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 CIFC13 H26 F3 O4 P SP 21 21 218.1984; 14.7753; 15.114
90; 90; 90
1830.82Michael 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 CIFC32 H26 F3 O3 P SC 1 c 110.6205; 16.669; 15.7534
90; 92.271; 90
2786.7Michael 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 CIFC32 H38 F3 O3 P SP 1 21/c 19.7033; 17.8716; 16.8564
90; 93.436; 90
2917.87Michael 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 CIFC24 H26 Br N3 O2P 21 21 2110.78; 13.453; 15.304
90; 90; 90
2219.4Yu 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 CIFC28 H35 N3 O2P 1 21 19.784; 8.872; 14.497
90; 90; 90
1258.4Yu 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 CIFC23 H13 N O2P 1 21/m 19.638; 7.105; 11.862
90; 95.858; 90
808Shivani 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 CIFC90 H122 N12 O15 SiP 1 21/n 116.9924; 27.8784; 26.0023
90; 97.315; 90
12217.6Mayumi 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 CIFC41 H40 Ga Mo N2 O5P b c n17.1431; 15.7892; 14.4285
90; 90; 90
3905.4Igor 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 CIFC44 H45 Ga Mo N2 O3P 1 21 18.82154; 38.0697; 11.69917
90; 97.2432; 90
3897.62Igor 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 CIFC104 H118 Ga2 Mo2 N4 Na2 O14P -112.162; 12.7895; 16.926
72.066; 83.271; 85.462
2485Igor 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 CIFC25 H33 B O7P -19.5236; 11.7389; 12.5461
62.68; 84.635; 81.559
1232.12Alicia 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 CIFC27 H33 B O6 S2P 1 21/c 18.1024; 13.4762; 25.6608
90; 96.518; 90
2783.78Alicia 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 CIFC22 H23 N2 O2 SP b c a12.1138; 15.4374; 22.576
90; 90; 90
4221.8Alicia 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 CIFC51 H41 F6 N6 O8 Os PP -19.349; 14.949; 20.583
106.442; 90.995; 94.554
2747.9Hai-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 CIFC43 H52 O4P -110.0808; 12.8064; 15.1154
89.88; 75.473; 75.26
1822.85Petr 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 CIFC161 H182 Cl2 O16P 1 21/c 113.22632; 25.83704; 20.88126
90; 99.786; 90
7031.9Petr 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 CIFC47 H52 N0 O4P -112.3671; 12.635; 13.8467
77.854; 63.909; 80.759
1894Petr 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 CIFC43 H50 O4P -19.8496; 12.97; 14.9932
89.965; 77.36; 74.04
1793.29Petr 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 CIFC44 H52 N8 O14 Pd4P 1 21/c 17.9571; 23.6001; 13.0293
90; 92.124; 90
2445.07Marina 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 CIFC36.5 H42.5 N9.5 O9.5 Pd2C 1 c 134.577; 16.50703; 14.29901
90; 97.1631; 90
8097.66Marina 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 CIFC16 H20 N2 O2P 1 21 16.1563; 8.2068; 14.895
90; 100.888; 90
739Etienne 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 CIFC16 H19 Br N2 O2P 1 21 16.137; 8.934; 14.27
90; 99.976; 90
770.6Etienne 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 CIFC14 H16 N2 O2P 1 21 15.8127; 9.5156; 11.5873
90; 103.442; 90
623.35Etienne 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 CIFC20 H19 Br N2 O2P b c a6.56; 16.644; 33.009
90; 90; 90
3604Etienne 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 CIFC20 H12 N2P 21 21 213.88126; 11.643; 29.5312
90; 90; 90
1334.5Youhei 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 CIFC15 H13 F5 N4 O4 SP 1 21/c 19.459; 22.4257; 9.0101
90; 115.656; 90
1722.83Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115551 CIFC22 H18 Cl F6 N5 O2P b c a21.4875; 20.5465; 21.5438
90; 90; 90
9511.4Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115552 CIFC16 H20 F3 N O4C 1 2/c 121.291; 11.5227; 14.4085
90; 105.162; 90
3411.8Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115553 CIFC10 H6 F3 NP 21 21 214.7643; 12.7324; 13.8685
90; 90; 90
841.28Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115554 CIFC87 H88 F12 N4 O18 P2P 1 21/c 114.3256; 36.543; 19.3027
90; 108.61; 90
9576.6Wei-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 CIFC16 H18 N2 O3P -16.2955; 9.3559; 12.975
80.69; 89.5; 75.05
728.2Shaoxia 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 CIFC48 H102 N12 O6 Zr3P 1 21/c 123.4504; 13.3481; 20.7646
90; 103.285; 90
6325.76Adam 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 CIFC16 H18 Br N O4P 1 21 17.96; 6.2115; 17.0041
90; 98.216; 90
832.11Yi-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 CIFC168 H217 F24 N7 O40 P4P -112.6852; 17.3581; 21.7669
104.59; 100.42; 95.616
4509.7Yujuan 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 CIFC19 H17 N OP -17.5607; 9.6755; 11.352
107.554; 102.789; 103.85
729.07Anupal 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 CIFC22 H20 Eu N5 O10P -19.5509; 11.2004; 12.8518
66.27; 76.414; 80.581
1219.66Jinlei 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 CIFC275 H308 Cl6 I10 Ir4 N20 O25P -114.9997; 20.6925; 26.1024
105.607; 100.893; 99.749
7451.9Haohua Huo; Chen Fu; Chuanyong Wang; Klaus Harms; Eric Meggers
Metal-templated enantioselective enamine/H-bonding dual activation catalysis
Chem.Commun., 2014, 50, 10409
7115563 CIFC27 H31 Br2 N O4 S SiP 1 21/a 118.9903; 12.146; 26.2415
90; 108.147; 90
5751.7Tomoya Miura; Takayuki Nakamuro; Kentaro Hiraga; Masahiro Murakami
The stereoselective synthesis of alpha-amino aldols starting from terminal alkynes
Chem.Commun., 2014, 50, 10474
7115564 CIFC98 H20P 42/n c m16.8655; 16.8655; 19.6001
90; 90; 90
5575.2Venkata 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 CIFC39 H30 N O4 PP -19.6945; 11.27; 15.8376
92.446; 101.11; 113.846
1538.92Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115566 CIFC39 H23 Cl2 F3 N O4 PP 1 21/n 115.3256; 9.7698; 22.1934
90; 90.145; 90
3322.96Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115567 CIFC40 H24 N O4 PP -19.9693; 10.0382; 17.31
79.783; 89.864; 66.349
1557.1Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115568 CIFC42 H24 N O4 PP -110.2329; 10.298; 17.3524
97.558; 92.475; 116.557
1610.67Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115569 CIFC88 H100 B Cr F24 N6P 1 21/c 122.049; 17.219; 25.078
90; 114.243; 90
8682Jingmei 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 CIFC108 H100 B2 Cl4 Cr F48 N6P -113.962; 17.728; 26.214
79.116; 77.828; 70.078
5915Jingmei 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 CIFC52 H42 N4 O6P 1 21/c 17.8968; 31.81; 16.8438
90; 105.408; 90
4079Lankani 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 CIFC52 H54 N4 O6P 1 21/n 113.586; 11.951; 31.96
90; 94.14; 90
5176Lankani 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 CIFC59 H54 Cl0 Fe0 N2 O3P 1 21/c 117.8254; 10.8398; 29.3462
90; 124.42; 90
4677.6Lankani 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 CIFC4 H4 Br Cu O4 P SP 1 21/c 115.899; 7.627; 7.344
90; 100.075; 90
876.8Wei-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 CIFC74 H74 F2 O4 Yb2P 1 21/n 112.994; 12.4469; 18.4353
90; 95.132; 90
2969.68G. 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 CIFC62 H50 O YbP 1 21/n 110.272; 40.41; 11.14
90; 105.41; 90
4457.9G. 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 CIFC50 H38 B Cl2 N5 O2 PtP 1 21/c 112.2811; 12.5617; 26.9413
90; 100.943; 90
4080.69Ryo 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 CIFC11 H10 N4P 1 21/c 19.1608; 7.6873; 14.6054
90; 103.05; 90
1001.98Li Xu; Xue-Qing Mou; Zhi-Min Chen; Shao-Hua Wang
Copper-catalyzed intermolecular azidocyanation of aryl alkenes
Chem.Commun., 2014, 50, 10676
7115579 CIFC28 H22 N2P 1 21/c 112.208; 9.4997; 19.3
90; 109.62; 90
2108.3Ying 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 CIFC H Cl N OP -17.9603; 25.1844; 12.0025
90; 104.539; 90
2329.2Jun-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 CIFC24 H17 N5 O10C 1 2/c 124.48; 8.379; 11.878
90; 106.275; 90
2339Jun-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 CIFC18 H18 Br F2 N O3 S2P 21 21 2118.0666; 21.1169; 22.2584
90; 90; 90
8491.8Wenchao 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 CIFC18 H18 F2 N O SP 21 21 218.7675; 10.5238; 18.173
90; 90; 90
1676.8Wenchao 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 CIFC24 H23 F2 N O3 S2P 21 21 2110.0872; 14.0488; 16.2483
90; 90; 90
2302.6Wenchao 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 CIFC13 H8 Br N O SP 1 21 17.5255; 3.9957; 19.305
90; 95.045; 90
578.2Wenchao 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 CIFC16 H17 F2 N O SP 21 21 219.9519; 10.2705; 15.1165
90; 90; 90
1545.07Wenchao 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 CIFC31 H22 Br F2 N O3 S2P 21 21 218.5124; 14.4301; 22.503
90; 90; 90
2764.2Wenchao 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 CIFC21 H16 Br N O3 SP 1 21/n 19.876; 11.292; 16.818
90; 92.78; 90
1873.3Wenchao 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 CIFC27 H21 N O3 SC 1 c 126.342; 19.322; 18.311
90; 110.59; 90
8725Fei 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 CIFC68 H66 B F24 Ir N PP -113.42933; 18.87158; 27.7213
77.2224; 88.4024; 77.9371
6698.97Nicolas 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 CIFC28 H18 N2 S2 SeP -18.0777; 8.1703; 17.9004
83.481; 87.961; 67.919
1087.62Ann 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 CIFC12 H10 F N3 OP 1 21/c 111.785; 5.7638; 16.482
90; 102.47; 90
1093.2Komala 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 CIFC12 H9 F2 N3 OP 1 21/n 110.484; 5.4019; 19.491
90; 104.37; 90
1069.3Komala 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 CIFC12 H10 N4 O3P -16.9066; 7.942; 11.37
81.16; 87.98; 67.14
567.7Komala 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 CIFC12 H10 F N3 OP 1 n 14.5349; 11.591; 10.686
90; 98.22; 90
555.93Komala 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 CIFC12 H9 F2 N3 OP 1 21/c 13.7683; 27.238; 10.409
90; 97.29; 90
1059.8Komala 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 CIFC12 H10 N4 O3P b c a11.9799; 7.3695; 25.427
90; 90; 90
2244.8Komala 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 CIFC12 H11 F2 N3 O2P -18.9104; 9.9683; 13.1855
91.865; 92.788; 91.591
1168.65Komala 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 CIFC13 H14 N4 O4P 1 21/c 18.1756; 14.365; 11.375
90; 92.01; 90
1335.1Komala 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 CIFC13 H10 F3 N3 OP 1 21/c 114.5029; 12.713; 14.3436
90; 116.799; 90
2360.6Komala 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 CIFC46 H26 Cu F36 N4 O6P -110.3845; 10.7053; 27.4
84.153; 89.737; 64.833
2740Hyung 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 CIFC19 H19 N3 OP 1 21/c 115.709; 8.4319; 12.274
90; 96.34; 90
1615.8Zhi-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 CIFC21 H26 N6 O2 SiP 1 21/c 18.7189; 9.066; 27.8157
90; 91.003; 90
2198.37Zhi-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 CIFC18 H17 N3 O2P -18.6242; 10.2987; 10.3691
61.409; 80.7; 86.903
797.7Zhi-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 CIFC24 H25 N O6P 1 21/c 113.637; 13.749; 12.866
90; 111.745; 90
2241Thangavel 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 CIFC28 H30 N4 PdP -18.25; 14.764; 19.582
88.932; 89.487; 74.757
2300.8M. 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 CIFC15 H12 F N O3P -110.1802; 10.4053; 13.1475
90.7253; 108.201; 106.189
1262.93Aditi 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
7115612 CIFC19 H30 Cl Ir N O3 PP -18.081; 8.7266; 15.7699
79.849; 79.048; 79.265
1061.23Xiangqing Jia; Lei Zhang; Chuan Qin; Xuebing Leng; Zheng Huang
Iridium complexes of new NCP pincer ligands: catalytic alkane dehydrogenation and alkene isomerization
Chem.Commun., 2014, 50, 11056
7115613 CIFC20 H28 Cl Ir N O PP 1 21/c 110.1303; 13.77; 15.004
90; 105.782; 90
2014.1Xiangqing Jia; Lei Zhang; Chuan Qin; Xuebing Leng; Zheng Huang
Iridium complexes of new NCP pincer ligands: catalytic alkane dehydrogenation and alkene isomerization
Chem.Commun., 2014, 50, 11056
7115614 CIFC26 H37 Cl Ir N O PP 21 21 215.6237; 16.1007; 9.9759
90; 90; 90
2509.5Xiangqing Jia; Lei Zhang; Chuan Qin; Xuebing Leng; Zheng Huang
Iridium complexes of new NCP pincer ligands: catalytic alkane dehydrogenation and alkene isomerization
Chem.Commun., 2014, 50, 11056
7115615 CIFC66 H101 N2 O5 YbP -111.4765; 14.79; 21.9149
93.494; 105.09; 110.393
3318.8Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115616 CIFC66 H101 N2 O5 YP -111.6333; 15.0256; 21.5946
94.787; 104.996; 111.655
3320.8Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115617 CIFC66 H101 N2 O5 SmP 1 21/c 113.8842; 20.6892; 22.5022
90; 91.478; 90
6461.7Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115618 CIFC70 H109 N2 Nd O6P -111.57; 13.0084; 24.217
80.278; 84.826; 74.115
3451.6Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115619 CIFC120 H106 O4P -112.656; 12.875; 16.048
72.271; 84.227; 63.603
2229.2Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115620 CIFC144 H122 O8F d d d :222.3697; 23.8656; 59.021
90; 90; 90
31509Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115621 CIFC92 H74 O4C 1 2/c 142.2144; 8.82075; 23.4233
90; 117.273; 90
7752.3Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115622 CIFC40 H54 B4 O8P 1 21/n 112.2939; 10.7476; 15.7067
90; 109.673; 90
1954.19Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115623 CIFC77 H56 Au2 F10 N2 O2P -111.9116; 12.7221; 21.939
92.367; 90.803; 102.203
3245.9Zhao Chen; Di Wu; Xie Han; Jinhua Liang; Jun Yin; Guang-Ao Yu; Sheng Hua Liu
A novel fluorene-based gold(I) complex with aggregate fluorescence change: a single-component white light-emitting
Chem.Commun., 2014, 50, 11033
7115624 CIFC22 H35 B3 N4 SP 1 21 110.765; 14.567; 14.658
90; 97.11; 90
2281Holger Braunschweig; Christian Horl
Unexpected cluster formation upon hydroboration of a neutral diborene with 9-BBN
Chem.Commun., 2014, 50, 10983
7115625 CIFC25 H43 B3 N4 S SiP 1 21/n 112.667; 14.559; 15.099
90; 94.373; 90
2776Holger Braunschweig; Christian Horl
Unexpected cluster formation upon hydroboration of a neutral diborene with 9-BBN
Chem.Commun., 2014, 50, 10983
7115626 CIFC34 H29 Cl3 N O4 S2P 1 21/c 112.6039; 13.6946; 18.7475
90; 96.73; 90
3213.6Yu Zhang; Ling Pan; Xianxiu Xu; Hongmei Luo; Qun Liu
Tandem Michael addition/imine isomerization/intramolecular [3+2] cycloaddition for the regiospecific synthesis of cyclohepta[b]pyrroles
Chem.Commun., 2014, 50, 11039
7115627 CIFC49.5 H42 Cl4.5 N1.5 O6 S3P -110.069; 13.141; 18.165
110.735; 93.826; 107.061
2109.4Yu Zhang; Ling Pan; Xianxiu Xu; Hongmei Luo; Qun Liu
Tandem Michael addition/imine isomerization/intramolecular [3+2] cycloaddition for the regiospecific synthesis of cyclohepta[b]pyrroles
Chem.Commun., 2014, 50, 11039
7115628 CIFC130 H136 Cu12 P8 S6P 42/n c m :226.081; 26.081; 19.313
90; 90; 90
13137Xiao-Xun Yang; Ibrahim Issac; Sergej Lebedkin; Michael Kuhn; Florian Weigend; Dieter Fensk; Olaf Fuhrac; Andreas Eichhofer
Red-luminescent biphosphine stabilized 'Cu12S6' cluster molecules
Chem.Commun., 2014, 50, 11043
7115629 CIFC152.5 H172 Cu12 P8 S6P -117.803; 18.522; 23.713
83.46; 80.88; 71.93
7322Xiao-Xun Yang; Ibrahim Issac; Sergej Lebedkin; Michael Kuhn; Florian Weigend; Dieter Fensk; Olaf Fuhrac; Andreas Eichhofer
Red-luminescent biphosphine stabilized 'Cu12S6' cluster molecules
Chem.Commun., 2014, 50, 11043
7115630 CIFC23 H36 O4 SiP -18.4432; 10.8187; 12.5225
82.362; 86.419; 85.558
1128.73Zhilong Li; Tsz-Fai Leung; Rongbiao Tong
Total syntheses of +/- -musellarins A-C
Chem.Commun., 2014, 50, 10990
7115631 CIFC42 H58 O2 P2P -16.5471; 10.5962; 14.3323
100.773; 101.934; 107.345
895.07Shanshan Wu; Arnold L. Rheingold; John D. Protasiewicz
Luminescent materials containing multiple benzoxaphosphole units
Chem.Commun., 2014, 50, 11036
7115632 CIFC75 H66 F12 N18 O P2 RuP b c a23.24; 13.2721; 47.443
90; 90; 90
14633.5Alexander J. Metherell; Michael D. Ward
Stepwise assembly of an adamantoid Ru4Ag6 cage by control of metal coordination geometry at specific sites
Chem.Commun., 2014, 50, 10979
7115633 CIFC288 H240 Ag6 F84 N72 P14 Ru4P 1 2/n 124.688; 30.324; 25.247
90; 102.819; 90
18430Alexander J. Metherell; Michael D. Ward
Stepwise assembly of an adamantoid Ru4Ag6 cage by control of metal coordination geometry at specific sites
Chem.Commun., 2014, 50, 10979
7115634 CIFC51 H34 N5 PtP -19.5314; 12.4762; 16.9813
111.157; 97.191; 90.47
1865.3Abraham B. Alemayehu; Hugo Vazquez-Lima; Christine M. Beavers; Kevin J. Gagnon; Jesper Bendix; Abhik Ghosh
Platinum corroles
Chem.Commun., 2014, 50, 11093
7115635 CIFC56.23 H45.24 Cl0.31 N4.96 PtP -110.4746; 11.6239; 18.2464
87.752; 83.482; 77.657
2156Abraham B. Alemayehu; Hugo Vazquez-Lima; Christine M. Beavers; Kevin J. Gagnon; Jesper Bendix; Abhik Ghosh
Platinum corroles
Chem.Commun., 2014, 50, 11093
7115636 CIFC54 H40 N5 PtP -19.5493; 12.9707; 17.3628
106.105; 96.859; 93.679
2040.7Abraham B. Alemayehu; Hugo Vazquez-Lima; Christine M. Beavers; Kevin J. Gagnon; Jesper Bendix; Abhik Ghosh
Platinum corroles
Chem.Commun., 2014, 50, 11093
7115638 CIFC24 H18 Ba2 N2 O13P -17.8709; 8.8711; 19.835
100.55; 92.53; 92.59
1358.2Chan Song; Guan-Yao Wang; Ya-Ling Wang; De-Ming Kong; Yong-Jian Wang; Yue Li; Wen-Juan Ruan
A barium based coordination polymer for the activity assay of deoxyribonuclease I
Chem.Commun., 2014, 50, 11177
7115639 CIFC32 H32 F6 N2 O4 P2 RuP -112.66; 13.268; 13.386
119.526; 92.516; 115.846
1662Yusuke Kita; Takafumi Higuchi; Kazushi Mashima
Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt
Chem.Commun., 2014, 50, 11211
7115640 CIFC20 H22 N2 O5P -112.199; 12.84; 14.621
100.605; 114.357; 104.026
1916.8Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115641 CIFC20 H22 N2 O5P 1 21/c 115.2319; 7.8737; 15.4675
90; 90.233; 90
1855Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115642 CIFC20 H22 N2 O5P 1 21/c 19.6837; 9.5017; 20.5631
90; 92.044; 90
1890.8Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115643 CIFC20 H22 N2 O6P 1 21/c 19.3854; 18.319; 11.434
90; 109.579; 90
1852.2Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115644 CIFC20 H22 N2 O6P 1 21/c 19.6391; 27.15; 8.0064
90; 111.845; 90
1944.8Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115645 CIFC20 H22 N2 O6P 1 21/c 111.626; 10.168; 15.862
90; 97.357; 90
1859.7Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115647 CIFC118.79 H92.79 Cl26.38 N18 Zn2P 1 21/n 118.058; 17.549; 21.217
90; 100.9; 90
6602Huimin Ding; Xiangshi Meng; Xu Cui; Yihui Yang; Tailin Zhou; Caixing Wang; Matthias Zeller; Cheng Wang
Highly-efficient synthesis of covalent porphyrinic cages via DABCO-templated imine condensation reactions
Chem.Commun., 2014, 50, 11162
7115648 CIFC56.5 H70 Fe2 N6P 1 21/n 115.9655; 14.7809; 21.7126
90; 104.422; 90
4962.4Richard A. Lewis; K. Cory MacLeod; Brandon Q. Mercado; Patrick L. Holland
Geometric and redox flexibility of pyridine as a redox-active ligand that can reversibly accept one or two electrons
Chem.Commun., 2014, 50, 11114
7115649 CIFC145 H183 Fe4 N17 O3P c a 2127.6897; 11.5655; 42.052
90; 90; 90
13467Richard A. Lewis; K. Cory MacLeod; Brandon Q. Mercado; Patrick L. Holland
Geometric and redox flexibility of pyridine as a redox-active ligand that can reversibly accept one or two electrons
Chem.Commun., 2014, 50, 11114
7115650 CIFC12 H18 Al3 Cl12 DyP -19.5626; 9.6465; 17.8181
93.3339; 97.4937; 119.608
1402.42Shan-Shan Liu; Joseph W. Ziller; Yi-Quan Zhang; Bing-Wu Wang; William J. Evans; Song Gao
A half-sandwich organometallic single-ion magnet with hexamethylbenzene coordinated to the Dy(III) ion
Chem.Commun., 2014, 50, 11418
7115651 CIFC12 H18 Al3 Cl12 TbP -19.5934; 9.6912; 17.8558
93.2661; 97.3859; 119.652
1416.64Shan-Shan Liu; Joseph W. Ziller; Yi-Quan Zhang; Bing-Wu Wang; William J. Evans; Song Gao
A half-sandwich organometallic single-ion magnet with hexamethylbenzene coordinated to the Dy(III) ion
Chem.Commun., 2014, 50, 11418
7115652 CIFC23 H24 N2 O10 SeP -110.0929; 11.5641; 11.7886
67.928; 77.776; 67.513
1174.4Mohammad S. Afzal; Jean-Philippe Pitteloud; Daniela Buccella
Enhanced ratiometric fluorescent indicators for magnesium based on azoles of the heavier chalcogens
Chem.Commun., 2014, 50, 11358
7115653 CIFC23 H24 N2 O10 SP -110.094; 11.5565; 11.7894
67.376; 77.489; 67.165
1166.3Mohammad S. Afzal; Jean-Philippe Pitteloud; Daniela Buccella
Enhanced ratiometric fluorescent indicators for magnesium based on azoles of the heavier chalcogens
Chem.Commun., 2014, 50, 11358
7115654 CIFC35 H53 Cl N2 Si ZnP 1 21/n 111.089; 17.537; 17.947
90; 98.91; 90
3448Sebastian Schafer; Ralf Koppe; Michael T. Gamer; Peter W. Roesky
Zinc-silylene complexes
Chem.Commun., 2014, 50, 11401
7115655 CIFC54 H66 Cl2 N4 Si2 Zn2P 1 21/n 112.479; 14.937; 14.85
90; 104.21; 90
2683.3Sebastian Schafer; Ralf Koppe; Michael T. Gamer; Peter W. Roesky
Zinc-silylene complexes
Chem.Commun., 2014, 50, 11401
7115656 CIFC34 H56 Cl2 N4 Si2 ZnP 1 21/c 111.432; 23.618; 16.42
90; 105.97; 90
4262.3Sebastian Schafer; Ralf Koppe; Michael T. Gamer; Peter W. Roesky
Zinc-silylene complexes
Chem.Commun., 2014, 50, 11401
7115657 CIFC14 H26 B7 N2P -19.6172; 9.7108; 10.0025
96.336; 109.264; 102.874
842.34Marc-Andre Legare; Marc-Andre Courtemanche; Frederic-Georges Fontaine
Lewis base activation of borane-dimethylsulfide into strongly reducing ion pairs for the transformation of carbon dioxide to methoxyboranes
Chem.Commun., 2014, 50, 11362
7115658 CIFC35 H42 N5 O P ZnP 1 21/c 110.6521; 14.2354; 21.9063
90; 95.875; 90
3304.4Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115659 CIFC31 H46 N5 P ZnP 1 21/n 113.017; 17.0162; 14.0147
90; 90.091; 90
3104.3Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115660 CIFC33 H37 Cl K0 Li0 N5 O P ZnP 1 21/n 114.4797; 10.8889; 20.9293
90; 100.088; 90
3248.9Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115661 CIFC37 H48 N5 O P Si ZnP -19.9691; 11.3621; 17.9387
102.22; 98.414; 109.478
1819.61Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115662 CIFC35 H47 N6 P Si2 ZnP 1 21/c 118.0474; 12.0098; 17.5841
90; 102.768; 90
3717Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115663 CIFC10 H15 N O5P 21 21 215.598; 13.2848; 14.6114
90; 90; 90
1086.63William P. Unsworth; Nicola Clark; Thomas O. Ronson; Kiri Stevens; Amber L. Thompson; Scott G. Lamont; Jeremy Robertson
Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans
Chem.Commun., 2014, 50, 11393
7115664 CIFC10 H15 N O5P 21 21 215.8112; 7.6935; 23.7155
90; 90; 90
1060.28William P. Unsworth; Nicola Clark; Thomas O. Ronson; Kiri Stevens; Amber L. Thompson; Scott G. Lamont; Jeremy Robertson
Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans
Chem.Commun., 2014, 50, 11393
7115665 CIFC10 H15 N O5P 21 21 215.7625; 8.6145; 21.3435
90; 90; 90
1059.51William P. Unsworth; Nicola Clark; Thomas O. Ronson; Kiri Stevens; Amber L. Thompson; Scott G. Lamont; Jeremy Robertson
Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans
Chem.Commun., 2014, 50, 11393
7115666 CIFC36.5 H31 Cl O2P -19.1923; 9.5033; 17.017
75.35; 77.27; 84.99
1402.1Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115667 CIFC88 H92 O4P -110.871; 11.053; 15.84
81.772; 77.584; 68.14
1720.9Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115668 CIFC44 H40 O4P 21 21 219.6016; 14.338; 24.574
90; 90; 90
3383Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115669 CIFC60 H56 OP -19.6111; 9.8047; 12.6063
75.516; 79.934; 88.667
1132.2Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115670 CIFC6 H18 S Si2C 1 2/c 118.407; 5.7619; 11.61
90; 113.848; 90
1126.2Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115671 CIFC64 H82 Cl10 Cu2 O4 P2 S8 Sn6P -112.6985; 13.1259; 15.4384
115.138; 101.519; 101.37
2164.23Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115672 CIFC84 H118 Cl2 Cu2 O8 P2 S14 Sn10P -112.4911; 15.09; 15.4207
91.029; 102.416; 101.294
2778.2Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115673 CIFC84 H118 Ag2 Cl2 O8 P2 S14 Sn10P -112.528; 15.2617; 15.4195
91.365; 102.845; 100.328
2821.6Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115674 CIFC63.5 H127 Ag10 Cl7 N20 S20 Sn10I 41/a :230.8293; 30.8293; 54.2835
90; 90; 90
51593.5Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115675 CIFC48 H52 Au2 O2 P2 S4 Sn2P 1 21/c 114.5079; 12.1592; 15.0025
90; 103.39; 90
2574.57Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115676 CIFC53 H66 Au2 Cl10 N4 P2 S4 Sn2P -18.522; 12.3547; 17.3906
77.566; 83.985; 71.477
1694.12Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115677 CIFC164.5 H217 Au6 B2 Cl F8 N12 O6P -118.436; 18.589; 30.244
99.0625; 91.888; 117.078
9048.7Alba Collado; Adrian Gomez-Suarez; Paul B. Webb; Hedi Kruger; Michael Buhl; David B. Cordes; Alexandra M. Z. Slawin; Steven P. Nolan
Trapping atmospheric CO2 with gold
Chem.Commun., 2014, 50, 11321
7115678 CIFC31 H24 Cl O PP -110.1588; 13.9351; 18.4004
78.641; 75.556; 73.465
2395.8Anup Bhunia; Trinadh Kaicharla; Digvijay Porwal; Rajesh G. Gonnade; Akkattu T. Biju
Multicomponent reactions involving phosphines, arynes and aldehydes
Chem.Commun., 2014, 50, 11389
7115679 CIFC32 H25 As Cl F3 O4 SP 1 21/c 19.6419; 14.7407; 20.9802
90; 91.849; 90
2980.33Anup Bhunia; Trinadh Kaicharla; Digvijay Porwal; Rajesh G. Gonnade; Akkattu T. Biju
Multicomponent reactions involving phosphines, arynes and aldehydes
Chem.Commun., 2014, 50, 11389
7115680 CIFC31 H23 Cl2 O1.25 PP 1 21/c 114.2166; 28.5677; 12.5338
90; 97.179; 90
5050.5Anup Bhunia; Trinadh Kaicharla; Digvijay Porwal; Rajesh G. Gonnade; Akkattu T. Biju
Multicomponent reactions involving phosphines, arynes and aldehydes
Chem.Commun., 2014, 50, 11389
7115681 CIFC17.85 H111 Br N O41.69I m m a21.0197; 25.2728; 12.0096
90; 90; 90
6379.8S. Muromachi; K. A. Udachin; K. Shin; S. Alavi; I. L. Moudrakovski; R. Ohmura; J. A. Ripmeester
Guest-induced symmetry lowering of an ionic clathrate material for carbon capture
Chem.Commun., 2014, 50, 11476
7115682 CIFC130 H97 Co6.5 Mo24 N26 O88 P2P 1 21/c 129.607; 26.66; 24.133
90; 108.178; 90
18098C. Zhang; X. Lin; Z. Zhang; L.-S. Long; C. Wang; W. Lin
A hybrid polyoxometalate-organic molecular catalyst for visible light driven water oxidation
Chem.Commun., 2014, 50, 11591
7115683 CIFC44 H44 B2 F4 N6 O2P -111.4702; 13.147; 14.9642
113.625; 95.348; 105.167
1944.7Yafei Wang; Long Chen; Reda M. El-Shishtawy; Saadullah G. Aziz; Klaus Mullen
Synthesis and optophysical properties of dimeric aza-BODIPY dyes with a push-pull benzodipyrrolidone core
Chem.Commun., 2014, 50, 11540
7115684 CIFC46 H46 B2 Cl4 F6 N6 O2P 1 21/c 14.7273; 19.711; 25.1808
90; 97.316; 90
2327.2Yafei Wang; Long Chen; Reda M. El-Shishtawy; Saadullah G. Aziz; Klaus Mullen
Synthesis and optophysical properties of dimeric aza-BODIPY dyes with a push-pull benzodipyrrolidone core
Chem.Commun., 2014, 50, 11540
7115685 CIFC36 H27.5 N0.5 O4P 1 21 111.7738; 12.39402; 19.49664
90; 106.917; 90
2721.92Weiliang Chen; Xuan Fu; Lili Lin; Xiao Yuan; Weiwei Luo; Juhua Feng; Xiaohua Liu; Xiaoming Feng
An asymmetric [3+2] cycloaddition of alkynes with oxiranes by selective C-C bond cleavage of epoxides: highly efficient synthesis of chiral furan derivatives
Chem.Commun., 2014, 50, 11480
7115686 CIFC60 H80 N2 O4P -19.93781; 15.1528; 17.8125
69.7564; 88.9555; 87.1772
2513.57Kamil Kotwica; Piotr Bujak; Damian Wamil; Mariusz Materna; Lukasz Skorka; Piotr A. Gunka; Robert Nowakowski; Barbara Golec; Beata Luszczynska; Malgorzata Zagorska; Adam Pron
Indanthrone dye revisited after sixty years
Chem.Commun., 2014, 50, 11543
7115687 CIFC26 H39 Ni O2 P3P 1 21/n 111.4995; 14.7887; 16.1942
90; 98.174; 90
2726.1Yeong-Eun Kim; Jin Kim; Yunho Lee
Formation of a nickel carbon dioxide adduct and its transformation mediated by a Lewis acid
Chem.Commun., 2014, 50, 11458
7115688 CIFC65 H63 B F15 Ni O2 P3P -113.7796; 15.3191; 15.8751
97.002; 95.9; 111.372
3057.8Yeong-Eun Kim; Jin Kim; Yunho Lee
Formation of a nickel carbon dioxide adduct and its transformation mediated by a Lewis acid
Chem.Commun., 2014, 50, 11458
7115689 CIFC50 H78 N2 Ni2 P6I b c a18.508; 19.9088; 28.5632
90; 90; 90
10524.7Yeong-Eun Kim; Jin Kim; Yunho Lee
Formation of a nickel carbon dioxide adduct and its transformation mediated by a Lewis acid
Chem.Commun., 2014, 50, 11458
7115690 CIFC180 H132 K2 O26 Yb2P -114.1075; 14.4693; 17.9695
102.772; 90.083; 91.038
3576.6Brodie L. Reid; Stefano Stagni; Joanna M. Malicka; Massimo Cocchi; Garry S. Hanan; Mark I. Ogden; Massimiliano Massi
Lanthanoid beta-triketonates: a new class of highly efficient NIR emitters for bright NIR-OLEDs
Chem.Commun., 2014, 50, 11580
7115691 CIFC35 H76 Cl N13 O9 P4 Ru2P -114.5313; 17.5256; 18.3097
66.927; 73.12; 76.513
4067.1Manuel Serrano-Ruiz; Silvia Imberti; Leonardo Bernasconi; Nazira Jadagayeva; Franco Scalambra; Antonio Romerosa
Study of the interaction of water with the aqua-soluble dimeric complex [RuCp(PTA)2-mu-CN-1 kappa C:2 kappa^2^ N-RuCp(PTA)2](CF3SO3) (PTA = 1,3,5-triaza-7-phosphaadamantane) by neutron and X-ray diffraction in solution
Chem.Commun., 2014, 50, 11587
7115692 CIFC186 H102 In9 N30 O72 Ru2P 3 2 115.778; 15.778; 28.032
90; 90; 120
6043.5Lei Wang; Weiting Yang; Yangxue Li; Zhigang Xie; Wei Zhu; Zhong-Ming Sun
Dynamically controlled one-pot synthesis of heterogeneous core-shell MOF single crystals using guest molecules
Chem.Commun., 2014, 50, 11653
7115693 CIFC14 H6 In N2 O8R -3 c :H15.7069; 15.7069; 52.887
90; 90; 120
11300Lei Wang; Weiting Yang; Yangxue Li; Zhigang Xie; Wei Zhu; Zhong-Ming Sun
Dynamically controlled one-pot synthesis of heterogeneous core-shell MOF single crystals using guest molecules
Chem.Commun., 2014, 50, 11653
7115694 CIFC21.5 H19 Cl N2 O2 SP n n a14.6631; 22.9825; 13.3003
90; 90; 90
4482.13Wenyan Hao; Jiangbo Zeng; Mingzhong Cai
The copper(I)-catalyzed tandem reaction of o-alkynylphenyl isothiocyanates with isocyanides: a rapid synthesis of 5H-benzo[d]imidazo[5,1-b][1,3]thiazines
Chem.Commun., 2014, 50, 11686
7115695 CIFC194 H156 N O24 Sc3P -117.8883; 18.2158; 28.6383
72.268; 88.036; 63.205
7875.6Min-Yen Ku; Shing-Jong Huang; Shou-Ling Huang; Yi-Hung Liu; Chien-Chen Lai; Shie-Ming Peng; Sheng-Hsien Chiu
Hemicarceplex formation allows ready identification of the isomers of the metallofullerene Sc3N@C80 using 1H and 13C NMR spectroscopy
Chem.Commun., 2014, 50, 11709
7115696 CIFC68 H40 Cu2 N8 O17 Zn4I b c a28.1305; 26.1877; 28.1745
90; 90; 90
20755.4Alexandre Burgun; Rachel S. Crees; Marcus L. Cole; Christian J. Doonan; Christopher J. Sumby
A 3-D diamondoid MOF catalyst based on in situ generated [Cu(L)2] N-heterocyclic carbene (NHC) linkers: hydroboration of CO2
Chem.Commun., 2014, 50, 11760
7115697 CIFC27 H30.88 Cl2 N4.5 O1.25 P PdC 1 2/c 117.6807; 21.7456; 15.1674
90; 103.312; 90
5674.8Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115698 CIFC52 H56 Cl2 N8 O2 P2 Pd2P 1 21/c 113.5981; 17.4517; 10.9141
90; 100.235; 90
2548.8Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115699 CIFC26 H28 N4 O PP 1 21/c 118.7336; 10.702; 11.7743
90; 94.201; 90
2354.3Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115700 CIFC26 H30 Cl2 N4 O2 P PdP -18.972; 9.771; 16.661
101.704; 100.03; 94.767
1397.7Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115701 CIFC154 H148 B4 N6 O3 Si2P 1 21/n 111.8934; 26.2175; 20.3647
90; 101.101; 90
6231.2Shannon A. Couchman; Trevor K. Thompson; David J. D. Wilson; Jason L. Dutton; Caleb D. Martin
Investigating the ring expansion reaction of pentaphenylborole and an azide
Chem.Commun., 2014, 50, 11724
7115702 CIFC23 H19 N3 O5 SP -18.6842; 10.9725; 11.2956
100.974; 95.529; 99.687
1032.37Xianyu Meng; Peiqiu Liao; Jianquan Liu; Xihe Bi
Silver-catalyzed cyclization of 2-pyridyl alkynyl carbinols with isocyanides: divergent synthesis of indolizines and pyrroles
Chem.Commun., 2014, 50, 11837
7115703 CIFC H Br N O SP 17.1457; 9.8623; 11.5311
96.212; 94.459; 97.061
798.31Xianyu Meng; Peiqiu Liao; Jianquan Liu; Xihe Bi
Silver-catalyzed cyclization of 2-pyridyl alkynyl carbinols with isocyanides: divergent synthesis of indolizines and pyrroles
Chem.Commun., 2014, 50, 11837
7115704 CIFC17 H13 N3 OP 1 21/c 117.916; 4.643; 20.248
90; 124.13; 90
1394.2Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115705 CIFC11 H12 N2 O2P -17.423; 8.934; 9.001
118.77; 97.71; 93.62
512.87Sascha Wiechmann; Tyll Freese; Martin H. H. Drafz; Eike G. Hubner; Jan C. Namyslo; Martin Nieger; Andreas Schmidt
Sydnone anions and abnormal N-heterocyclic carbenes of O-ethylsydnones. Characterizations, calculations and catalyses
Chem.Commun., 2014, 50, 11822
7115706 CIFC44 H35 Br N2 O2 P2 PdP 1 21/c 111.8099; 17.9947; 17.1796
90; 100.544; 90
3589.3Sascha Wiechmann; Tyll Freese; Martin H. H. Drafz; Eike G. Hubner; Jan C. Namyslo; Martin Nieger; Andreas Schmidt
Sydnone anions and abnormal N-heterocyclic carbenes of O-ethylsydnones. Characterizations, calculations and catalyses
Chem.Commun., 2014, 50, 11822
7115707 CIFC27 H36 Br N O3P -17.548; 8.2091; 20.886
92.198; 95.579; 101.425
1260.3Peiyi Wang; Yuan Lin; Mark Smith; Sheng Feng; Baoan Song; Song Yang; Jun Hu
Host-guest interaction manipulated self-assembly of pyridinium-tailored naphthalene
Chem.Commun., 2014, 50, 11950
7115708 CIFC180 H270 Ag55 Mo6 O60R -3 :H22.261; 22.261; 47.421
90; 90; 120
20351.2Kun Zhou; Yun Geng; Li-Kai Yan; Xin-Long Wang; Xian-Chun Liu; Guo-Gang Shan; Kui-Zhan Shao; Zhong-Min Su; Ying-Ning Yu
An ultrastable {Ag55Mo6} nanocluster with a Ag-centered multishell structure
Chem.Commun., 2014, 50, 11934
7115709 CIFC34 H38 N4 O6 S2C 1 2/c 122.6373; 9.557; 16.0764
90; 105.708; 90
3348.15Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115710 CIFC36 H40 N6 O6P b c a15.1665; 17.7506; 24.997
90; 90; 90
6729.6Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115711 CIFC36 H40 N6 O6P 1 21/c 18.387; 14.2432; 14.6816
90; 104.354; 90
1699.08Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115712 CIFC33 H27 Br N2 O2P 21 21 218.9032; 11.1649; 27.772
90; 90; 90
2760.6Yan Liu; Hong-Hao Zhang; Yu-Chen Zhang; Yan Jiang; Feng Shi; Shu-Jiang Tu
Organocatalytic enantioselective and (Z)-selective allylation of 3-indolylmethanol via hydrogen-bond activation
Chem.Commun., 2014, 50, 12054
7115713 CIFC26 H20P 1 21 19.8251; 9.502; 10.709
90; 107.096; 90
955.6Guo-Feng Zhang; Ze-Qiang Chen; Matthew P. Aldred; Zhe Hu; Tao Chen; Zhenli Huang; Xianggao Meng; Ming-Qiang Zhu
Direct validation of the restriction of intramolecular rotation hypothesis via the synthesis of novel ortho-methyl substituted tetraphenylethenes and their application in cell imaging
Chem.Commun., 2014, 50, 12058

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