Crystallography Open Database

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1519433 CIFC156 H132 B6 Br4 Co5 F24 N24F 41 3 234.5284; 34.5284; 34.5284
90; 90; 90
41165.1Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519434 CIFC156 H132 Co4 F48 N24 P4.96 Sb3.04C 1 2/c 143.7451; 25.115; 39.7763
90; 100.245; 90
43003.8Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519435 CIFC390 H330 Br Cl19 N60 O76 Zn10P 1 2/n 121.4814; 30.514; 34.022
90; 97.399; 90
22115Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519436 CIFC8 H20 Br4 Cl4 N2 PbP -17.792; 8.315; 16.462
97.337; 96.252; 90.184
1051.4Solis-Ibarra, D.; Smith, I. C.; Karunadasa, H. I.
Post-synthetic halide conversion and selective halogen capture in hybrid perovskites
Chem. Sci., 2015, 6, 4054
1519437 CIFC8 H20 Br4 Cl4 N2 PbP 1 21/c 15.4158; 5.4438; 35.809
90; 93.3655; 90
1053.9Solis-Ibarra, D.; Smith, I. C.; Karunadasa, H. I.
Post-synthetic halide conversion and selective halogen capture in hybrid perovskites
Chem. Sci., 2015, 6, 4054
1519438 CIFC8 H20 Br8 N2 PbP -17.9735; 8.3877; 16.775
95.611; 95.889; 90.377
1110.5Solis-Ibarra, D.; Smith, I. C.; Karunadasa, H. I.
Post-synthetic halide conversion and selective halogen capture in hybrid perovskites
Chem. Sci., 2015, 6, 4054
1519439 CIFC17 H18 F3 N SP 1 21 19.1167; 7.9295; 11.3854
90; 105.727; 90
792.25Chen, Jiean; Meng, Sixuan; Wang, Leming; Tang, Hongmei; Huang, Yong
Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst
Chem. Sci., 2015, 6, 4184
1519440 CIFC28 H27 Br O4P 21 21 218.7857; 16.2342; 17.0357
90; 90; 90
2429.8Verrier, Charlie; Melchiorre, Paolo
Diastereodivergent organocatalysis for the asymmetric synthesis of chiral annulated furans
Chem. Sci., 2015, 6, 4242
1519441 CIFC28 H28 O4C 1 2 122.183; 7.95; 15.744
90; 122.929; 90
2330.5Verrier, Charlie; Melchiorre, Paolo
Diastereodivergent organocatalysis for the asymmetric synthesis of chiral annulated furans
Chem. Sci., 2015, 6, 4242
1519442 CIFC68 H87 Cl5 Cu5 N16 O48 P2P 21 21 2116.4315; 18.87; 30.286
90; 90; 90
9390.5Marino, Nadia; Armentano, Donatella; Pardo, Emilio; Vallejo, Julia; Neve, Francesco; Di Donna, Leonardo; De Munno, Giovanni
Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion
Chem. Sci., 2015, 6, 4300
1519443 CIFC219 H238.34 Cu15 F45 N48 O117.67 P6 S15P 1 21 117.821; 49.945; 18.529
90; 108.269; 90
15661Marino, Nadia; Armentano, Donatella; Pardo, Emilio; Vallejo, Julia; Neve, Francesco; Di Donna, Leonardo; De Munno, Giovanni
Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion
Chem. Sci., 2015, 6, 4300
1519444 CIFC14 H13 N3 OP 1 21/c 113.488; 9.6611; 9.3604
90; 90.183; 90
1219.7Hean, D.; Gelbrich, T.; Griesser, U. J.; Michael, J. P.; Lemmerer, A.
Structural insights into the hexamorphic system of an isoniazid derivative
CrystEngComm, 2015, 17, 5143
1519445 CIFC14 H13 N3 OP 1 21/c 125.8998; 5.5463; 8.3187
90; 95.876; 90
1188.69Hean, D.; Gelbrich, T.; Griesser, U. J.; Michael, J. P.; Lemmerer, A.
Structural insights into the hexamorphic system of an isoniazid derivative
CrystEngComm, 2015, 17, 5143
1519446 CIFC14 H13 N3 OP 1 21/c 110.2114; 30.3315; 8.2353
90; 110.193; 90
2393.92Hean, D.; Gelbrich, T.; Griesser, U. J.; Michael, J. P.; Lemmerer, A.
Structural insights into the hexamorphic system of an isoniazid derivative
CrystEngComm, 2015, 17, 5143
1519447 CIFC14 H13 N3 OP b c a6.3542; 7.6624; 49.231
90; 90; 90
2397Hean, D.; Gelbrich, T.; Griesser, U. J.; Michael, J. P.; Lemmerer, A.
Structural insights into the hexamorphic system of an isoniazid derivative
CrystEngComm, 2015, 17, 5143
1519448 CIFC14 H13 N3 OP -19.736; 9.8752; 26.1543
92.856; 100.295; 91.291
2469.8Hean, D.; Gelbrich, T.; Griesser, U. J.; Michael, J. P.; Lemmerer, A.
Structural insights into the hexamorphic system of an isoniazid derivative
CrystEngComm, 2015, 17, 5143
1519449 CIFC14 H13 N3 OP 1 21/c 110.6217; 14.442; 8.2589
90; 109.623; 90
1193.3Hean, D.; Gelbrich, T.; Griesser, U. J.; Michael, J. P.; Lemmerer, A.
Structural insights into the hexamorphic system of an isoniazid derivative
CrystEngComm, 2015, 17, 5143
1519450 CIFC93 H80 N4 O24 S2C 1 c 143.879; 9.5887; 25.05
90; 109.94; 90
9908Ganesan, Paramaguru; Fu, Kunwu; Gao, Peng; Raabe, Ines; Schenk, Kurt; Scopelliti, Rosario; Luo, Jingshan; Wong, Lydia H.; Grätzel, Michael; Nazeeruddin, Mohammad Khaja
A simple spiro-type hole transporting material for efficient perovskite solar cells
Energy Environ. Sci., 2015, 8, 1986
1519451 CIFC84 H70.5 Cl0.5 N4 O8P -113.1111; 16.1465; 16.9214
75.2; 85.67; 75.891
3358.6Ganesan, Paramaguru; Fu, Kunwu; Gao, Peng; Raabe, Ines; Schenk, Kurt; Scopelliti, Rosario; Luo, Jingshan; Wong, Lydia H.; Grätzel, Michael; Nazeeruddin, Mohammad Khaja
A simple spiro-type hole transporting material for efficient perovskite solar cells
Energy Environ. Sci., 2015, 8, 1986
1519452 CIFC20 H18 Cl2 Cu N4 OP 1 21/c 111.3306; 14.0417; 13.3887
90; 106.842; 90
2038.79Qin, Qi-Pin; Liu, Yan-Cheng; Wang, Hai-Lu; Qin, Jiao-Lan; Cheng, Feng-Jie; Tang, Shang-Feng; Liang, Hong
Synthesis and antitumor mechanisms of a copper(ii) complex of anthracene-9-imidazoline hydrazone (9-AIH).
Metallomics : integrated biometal science, 2015, 7, 1124-1136
1519453 CIFC51 H57 N3 O6C 1 2/c 140.701; 11.574; 23.897
90; 125.863; 90
9123Bregnhøj, Mikkel; Pimenta, Frederico M.; Poronik, Yevgen M.; Gryko, Daniel T.; Ogilby, Peter R.
Subtle structural changes in octupolar merocyanine dyes influence the photosensitized production of singlet oxygen.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2015, 14, 1138-1146
1519454 CIFC54 H46 Cl2 O4 P2 PdP -19.5159; 9.961; 14.355
72.77; 70.85; 66.35
1155.9Willenbacher, Johannes; Altintas, Ozcan; Trouillet, Vanessa; Knöfel, Nicolai; Monteiro, Michael J.; Roesky, Peter W.; Barner-Kowollik, Christopher
Pd-complex driven formation of single-chain nanoparticles
Polym. Chem., 2015, 6, 4358
1519455 CIFC56 H50 Cl2 O4 P2 PdP -110.118; 14.622; 17.316
89.46; 87.53; 73.09
2448.8Willenbacher, Johannes; Altintas, Ozcan; Trouillet, Vanessa; Knöfel, Nicolai; Monteiro, Michael J.; Roesky, Peter W.; Barner-Kowollik, Christopher
Pd-complex driven formation of single-chain nanoparticles
Polym. Chem., 2015, 6, 4358
1519496 CIFC22 H20 Br NP 16.134; 7.123; 10.777
102.328; 106.299; 90.659
440.2Zhang, Zhenhua; Du, Haifeng
Cis-selective and highly enantioselective hydrogenation of 2,3,4-trisubstituted quinolines.
Organic letters, 2015, 17, 2816-2819
1519497 CIFC46 H58 N4 O3P 1 21/c 117.313; 24.678; 9.5642
90; 105.015; 90
3946.8Molla, Habib Ali; Bhowmick, Rahul; Katarkar, Atul; Chaudhuri, Keya; Gangopadhyay, Sumana; Ali, Mahammad
A novel rhodamine-3,4-dihydro-2H-1,3-benzoxazine conjugate as a highly sensitive and selective chemosensor for Fe3+ions with cytoplasmic cell imaging possibilities
Anal. Methods, 2015, 7, 5149
1519498 CIFC41 H37 N OP -19.8924; 10.291; 15.6015
91.437; 94.959; 101.331
1550.05Deng, Haiqin; Hu, Rongrong; Leung, Anakin C. S.; Zhao, Engui; Lam, Jacky W. Y.; Tang, Ben Zhong
Construction of regio- and stereoregular poly(enaminone)s by multicomponent tandem polymerizations of diynes, diaroyl chloride and primary amines
Polym. Chem., 2015, 6, 4436
1519611 CIFC12 H15 F N6 O4P 437.3545; 7.3545; 27.835
90; 90; 90
1505.6Yang, Qinghua; Kang, Jinfeng; Zheng, Liyun; Wang, Xue-Jun; Wan, Na; Wu, Jie; Qiao, Yan; Niu, Pengfei; Wang, Sheng-Qi; Peng, Youmei; Wang, Qingduan; Yu, Wenquan; Chang, Junbiao
Synthesis and biological evaluation of 4-substituted fluoronucleoside analogs for the treatment of hepatitis B virus infection.
Journal of medicinal chemistry, 2015, 58, 3693-3703
1519612 CIFC24 H25 N O5P 21 21 218.713; 11.51; 20.253
90; 90; 90
2031.1Liu, Xuemei; Frydenvang, Karla; Liu, Huizhen; Zhai, Lin; Chen, Ming; Olsen, Carl Erik; Christensen, Søren Brøgger
Iminolactones from Schizophyllum commune.
Journal of natural products, 2015, 78, 1165-1168
1519613 CIFC30 H48 O4P 1 21 19.4572; 7.77569; 19.2277
90; 103.188; 90
1376.64Jiang, Kan; Chen, Lu-Lin; Wang, Shu-Fang; Wang, Yi; Li, Ya; Gao, Kun
Anti-inflammatory Terpenoids from the Leaves and Twigs of Dysoxylum gotadhora.
Journal of natural products, 2015, 78, 1037-1044
1519614 CIFC20 H28 O2P 1 21 112.4345; 6.06696; 12.7077
90; 115.588; 90
864.64Jiang, Kan; Chen, Lu-Lin; Wang, Shu-Fang; Wang, Yi; Li, Ya; Gao, Kun
Anti-inflammatory Terpenoids from the Leaves and Twigs of Dysoxylum gotadhora.
Journal of natural products, 2015, 78, 1037-1044
1519615 CIFC21 H31.5 N0.5 O2P 21 21 216.3147; 23.2682; 25.4495
90; 90; 90
3739.3Jiang, Kan; Chen, Lu-Lin; Wang, Shu-Fang; Wang, Yi; Li, Ya; Gao, Kun
Anti-inflammatory Terpenoids from the Leaves and Twigs of Dysoxylum gotadhora.
Journal of natural products, 2015, 78, 1037-1044
1519616 CIFC11 H8 I N O3P -18.2224; 9.2785; 15.4339
90.007; 90.047; 96.421
1170.09Itoh, Takahito; Tachino, Kyoko; Akira, Naoki; Uno, Takahiro; Kubo, Masataka; Tohnai, Norimitsu; Miyata, Mikiji
Twofold Helical Polymerization: Thermal Solid-State Polymerization of 7-Cyano-7-(2′-haloethoxycarbonyl)-1,4-benzoquinone Methides
Macromolecules, 2015, 48, 2935
1519617 CIFC11 H8 Cl N O3P 1 21/a 19.396; 11.516; 9.933
90; 97.59; 90
1065.4Itoh, Takahito; Tachino, Kyoko; Akira, Naoki; Uno, Takahiro; Kubo, Masataka; Tohnai, Norimitsu; Miyata, Mikiji
Twofold Helical Polymerization: Thermal Solid-State Polymerization of 7-Cyano-7-(2′-haloethoxycarbonyl)-1,4-benzoquinone Methides
Macromolecules, 2015, 48, 2935
1519618 CIFC11 H8 Br N O3P -14.108; 11.388; 11.496
93.34; 94.58; 90.96
535.05Itoh, Takahito; Tachino, Kyoko; Akira, Naoki; Uno, Takahiro; Kubo, Masataka; Tohnai, Norimitsu; Miyata, Mikiji
Twofold Helical Polymerization: Thermal Solid-State Polymerization of 7-Cyano-7-(2′-haloethoxycarbonyl)-1,4-benzoquinone Methides
Macromolecules, 2015, 48, 2935
1519619 CIFC11 H8 F N O3P 1 21/c 110.072; 5.665; 17.929
90; 103.34; 90
995.4Itoh, Takahito; Tachino, Kyoko; Akira, Naoki; Uno, Takahiro; Kubo, Masataka; Tohnai, Norimitsu; Miyata, Mikiji
Twofold Helical Polymerization: Thermal Solid-State Polymerization of 7-Cyano-7-(2′-haloethoxycarbonyl)-1,4-benzoquinone Methides
Macromolecules, 2015, 48, 2935
1519620 CIFC23 H29 N3 O6P 1 21 19.7456; 10.052; 12.315
90; 107.912; 90
1147.93Maguire, Courtney K.; Brunskill, Andrew P. J.
Assessment of the Stoichiometry of Multicomponent Crystals Using Only X-ray Powder Diffraction Data.
Molecular pharmaceutics, 2015, 12, 2061-2067
1519621 CIFC22 H27 N3 O6P 1 21 19.4995; 9.7624; 12.7614
90; 111.666; 90
1099.86Maguire, Courtney K.; Brunskill, Andrew P. J.
Assessment of the Stoichiometry of Multicomponent Crystals Using Only X-ray Powder Diffraction Data.
Molecular pharmaceutics, 2015, 12, 2061-2067
1519622 CIFC22 H18 Cl N O3 PdP 1 21/c 119.306; 4.5687; 22.128
90; 103.674; 90
1896.4Ren, Zhi; Schulz, Jonathan E.; Dong, Guangbin
Catalytic Ortho-Acetoxylation of Masked Benzyl Alcohols via an Exo-Directing Mode.
Organic letters, 2015, 17, 2696-2699
1519623 CIFC15 H10 I N O2C 1 c 124.877; 7.087; 7.92
90; 90.593; 90
1396.2Huang, Hai; Zhu, Xiaolin; He, Guangke; Liu, Qi; Fan, Junzhen; Zhu, Hongjun
Controlled Synthesis of 1,3,5-Oxadiazin-2-ones and Oxazolones through Regioselective Iodocyclization of Ynamides.
Organic letters, 2015, 17, 2510-2513
1519624 CIFC36.5 H45 N O SiP 1 21/c 117.2248; 7.9565; 45.621
90; 93.087; 90
6243.2Ma, Zhi-Xiong; Patel, Ashay; Houk, K. N.; Hsung, Richard P.
Highly Torquoselective Electrocyclizations and Competing 1,7-Hydrogen Shifts of 1-Azatrienes with Silyl Substitution at the Allylic Carbon.
Organic letters, 2015, 150410083922001
1519625 CIFC32 H30 B NP 1 21/c 110.2671; 10.1236; 23.3329
90; 98.876; 90
2396.18Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519626 CIFC32 H32 B NP 1 21/c 110.0993; 10.2609; 23.8794
90; 97.3582; 90
2454.19Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519627 CIFC38 H34 B NP -18.8087; 11.1753; 16.1219
72.148; 78.052; 74.662
1443.04Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning
One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.
Organic letters, 2015, 17, 2486-2489
1519628 CIFC102 H70 B4 O20C 1 2/c 130.624; 56.38; 22.177
90; 93.399; 90
38223Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1519629 CIFC21 H26 N2 O2 SP 1 21/c 17.3915; 13.779; 19.135
90; 93.863; 90
1944.4Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519630 CIFC16 H14 N2 O2 SP 1 21/c 111.225; 13.361; 11.0143
90; 118.102; 90
1457.2Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519631 CIFC17 H16 N2 O2 SP 1 21/c 18.9148; 16.7339; 10.5655
90; 95.855; 90
1567.93Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar
Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.
Organic letters, 2015, 17, 2226-2229
1519632 CIFC15 H12 Mo O3P b c a16.6109; 8.7885; 17.8015
90; 90; 90
2598.75Graser, Lilian; Reich, Robert M.; Cokoja, Mirza; Pöthig, Alexander; Kühn, Fritz E.
Aryl-substituted organomolybdenum(ii) complexes as olefin epoxidation catalysts
Catal. Sci. Technol., 2015, 5, 4772
1519633 CIFC15 H7 F5 Mo O3P 1 21/n 18.1106; 14.7261; 12.4891
90; 100.409; 90
1467.12Graser, Lilian; Reich, Robert M.; Cokoja, Mirza; Pöthig, Alexander; Kühn, Fritz E.
Aryl-substituted organomolybdenum(ii) complexes as olefin epoxidation catalysts
Catal. Sci. Technol., 2015, 5, 4772
1519634 CIFC63.2 H72.55 I6 N13.06 Zn3C 1 2 135.1081; 14.6516; 31.3279
90; 101.649; 90
15782.8Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519635 CIFC60.26 H61.53 I6 N14 Zn3C 1 2 135.2721; 14.6427; 31.6037
90; 102.029; 90
15964.2Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519636 CIFC84.5 H64 I12.04 N24 S0.5 Zn6C 1 2 134.8299; 14.9133; 31.5387
90; 102.403; 90
15999.8Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519637 CIFC87.64 H68.04 I12 N24 S0.62 Zn6C 1 2 134.4391; 15.0959; 29.9556
90; 101.454; 90
15263.4Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519638 CIFC85.6 H63.3 I12 N24 O1.7 Zn6C 1 2 134.2; 15.1265; 31.003
90; 102.385; 90
15665Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519639 CIFC86.95 H64.82 I12 N24 O1.87 Zn6C 1 2 134.627; 15.0818; 31.194
90; 102.792; 90
15886Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519640 CIFC34 H50 N2 Na O4 PP 1 21/n 110.6728; 15.0865; 21.8147
90; 93.643; 90
3505.4Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519641 CIFC24 H44 N4 Na O5 PP 1 21/n 119.3693; 14.6742; 21.9183
90; 111.339; 90
5802.7Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519642 CIFC32 H54 N4 Na O6 PP 21 21 2110.4709; 17.4983; 18.6976
90; 90; 90
3425.83Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519643 CIFC38 H58 K N2 O8 PP 1 21/n 110.7457; 17.6496; 21.5074
90; 99.87; 90
4018.66Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519644 CIFC64 H92 K N4 O10 PP 1 21 113.233; 19.9093; 13.5733
90; 115.271; 90
3233.79Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519645 CIFC43 H65 Dy N2 O6P -111.0343; 12.2286; 17.5339
77.103; 85.701; 69.694
2162.9Qian, Kang; Baldoví, José J.; Jiang, Shang-Da; Gaita-Ariño, Alejandro; Zhang, Yi-Quan; Overgaard, Jacob; Wang, Bing-Wu; Coronado, Eugenio; Gao, Song
Does the thermal evolution of molecular structures critically affect the magnetic anisotropy?
Chem. Sci., 2015, 6, 4587
1519646 CIFC43 H65 Dy N2 O6P -111.0141; 12.2286; 17.5325
77.161; 85.753; 69.723
2159.67Qian, Kang; Baldoví, José J.; Jiang, Shang-Da; Gaita-Ariño, Alejandro; Zhang, Yi-Quan; Overgaard, Jacob; Wang, Bing-Wu; Coronado, Eugenio; Gao, Song
Does the thermal evolution of molecular structures critically affect the magnetic anisotropy?
Chem. Sci., 2015, 6, 4587
1519647 CIFC43 H65 Dy N2 O6P -111.087; 12.2243; 18.3363
79.664; 85.44; 68.727
2277.9Qian, Kang; Baldoví, José J.; Jiang, Shang-Da; Gaita-Ariño, Alejandro; Zhang, Yi-Quan; Overgaard, Jacob; Wang, Bing-Wu; Coronado, Eugenio; Gao, Song
Does the thermal evolution of molecular structures critically affect the magnetic anisotropy?
Chem. Sci., 2015, 6, 4587
1519649 CIF
HKL
H2 K2 O12 S2 UP n a 2113.7778; 7.2709; 11.5488
90; 90; 90
1156.92Plášil, J.; Hloušek, J.; Kasatkin, A. V.; Škoda, R.; Novák, M.; Čejka, J.
Geschieberite, K~2~(UO~2~)(SO~4~)~2~(H~2~O)~2~, a new uranyl sulfate mineral from Jáchymov
Mineralogical Magazine, 2015, 79, 205-216
1519650 CIFC52 H45 N3 O6P -111.8085; 15.4553; 25.507
73.327; 88.656; 71.56
4218.8Heinz, Luisa G.; Yushchenko, Oleksandr; Neuburger, Markus; Vauthey, Eric; Wenger, Oliver S.
Tetramethoxybenzene is a Good Building Block for Molecular Wires: Insights from Photoinduced Electron Transfer.
The journal of physical chemistry. A, 2015, 119, 5676
1519651 CIFC14 H15 F3 O4 SP 1 21/n 15.4571; 34.89; 7.6271
90; 96.378; 90
1443.2Liu, Yafei; Shao, Xinxin; Zhang, Panpan; Lu, Long; Shen, Qilong
Trifluoromethyl-substituted sulfonium ylide: rh-catalyzed carbenoid addition to trifluoromethylthioether.
Organic letters, 2015, 17, 2752-2755
1519652 CIFC47 H59 N O5P n 21 a18.4589; 58.006; 11.59672
90; 90; 90
12416.9Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519653 CIFC41 H46 O5C 1 2/c 134.9361; 10.48642; 26.842
90; 135.583; 90
6882.4Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519654 CIFC48.5 H58 O6.5P 1 21 120.7243; 10.45113; 21.5504
90; 113.543; 90
4279.1Slavík, Petr; Eigner, Václav; Lhoták, Pavel
Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.
Organic letters, 2015, 17, 2788-2791
1519655 CIFC20 H16 Br N O4C 1 c 114.0307; 8.5721; 15.203
90; 109.89; 90
1719.4Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin
Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.
Organic letters, 2015, 17, 2684-2687
1519656 CIFC25 H20 N2 O2P 1 21/c 113.373; 16.581; 8.8083
90; 93.638; 90
1949.2Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin
Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.
Organic letters, 2015, 17, 2684-2687
1519657 CIFC24 H28 Cl N O7P 1 21/n 110.5446; 9.5462; 24.575
90; 91.778; 90
2472.5Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong
Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Organic letters, 2015, 17, 2680-2683
1519658 CIFC28 H28 Br N O6P 21 21 2110.409; 15.4718; 16.588
90; 90; 90
2671.4Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong
Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Organic letters, 2015, 17, 2680-2683
1519659 CIFC20 H22 O5P 1 21 18.4907; 8.5157; 12.152
90; 109.005; 90
830.75Zhao, Qin; Chen, Guo-Dong; Feng, Xiao-Lin; Yu, Yang; He, Rong-Rong; Li, Xiao-Xia; Huang, Yan; Zhou, Wen-Xia; Guo, Liang-Dong; Zheng, Yi-Zhi; Yao, Xin-Sheng; Gao, Hao
Nodulisporiviridins A-H, Bioactive Viridins from Nodulisporium sp.
Journal of natural products, 2015, 78, 1221-1230
1519660 CIFC19 H20 O7P 1 21 17.2425; 8.2512; 13.6931
90; 96.661; 90
812.77Zhao, Qin; Chen, Guo-Dong; Feng, Xiao-Lin; Yu, Yang; He, Rong-Rong; Li, Xiao-Xia; Huang, Yan; Zhou, Wen-Xia; Guo, Liang-Dong; Zheng, Yi-Zhi; Yao, Xin-Sheng; Gao, Hao
Nodulisporiviridins A-H, Bioactive Viridins from Nodulisporium sp.
Journal of natural products, 2015, 78, 1221-1230
1519661 CIFLi0.9 S2 TiR -3 m :H3.53131; 3.53131; 18.609
90; 90; 120
200.967Wiedemann, Dennis; Islam, Mazharul M.; Nakhal, Suliman; Senyshyn, Anatoliy; Bredow, Thomas; Lerch, Martin
Lithium Diffusion Pathways in 3R-LixTiS2: A Combined Neutron Diffraction and Computational Study
The Journal of Physical Chemistry C, 2015, 119, 11370
1519662 CIFLi0.7 S2 TiR -3 m :H3.49902; 3.49902; 18.6498
90; 90; 120
197.741Wiedemann, Dennis; Islam, Mazharul M.; Nakhal, Suliman; Senyshyn, Anatoliy; Bredow, Thomas; Lerch, Martin
Lithium Diffusion Pathways in 3R-LixTiS2: A Combined Neutron Diffraction and Computational Study
The Journal of Physical Chemistry C, 2015, 119, 11370
1519663 CIFLi0.9 S2 TiR -3 m :H3.52138; 3.52138; 18.5588
90; 90; 120
199.3Wiedemann, Dennis; Islam, Mazharul M.; Nakhal, Suliman; Senyshyn, Anatoliy; Bredow, Thomas; Lerch, Martin
Lithium Diffusion Pathways in 3R-LixTiS2: A Combined Neutron Diffraction and Computational Study
The Journal of Physical Chemistry C, 2015, 119, 11370
1519664 CIFLi0.7 S2 TiR -3 m :H3.49658; 3.49658; 18.6529
90; 90; 120
197.499Wiedemann, Dennis; Islam, Mazharul M.; Nakhal, Suliman; Senyshyn, Anatoliy; Bredow, Thomas; Lerch, Martin
Lithium Diffusion Pathways in 3R-LixTiS2: A Combined Neutron Diffraction and Computational Study
The Journal of Physical Chemistry C, 2015, 119, 11370
1519665 CIFC66 H66 Co3 N10 O24 S2P -18.066; 11.397; 19.555
74.776; 80.442; 85.17
1708.9Datta, Amitabha; Massera, Chiara; Clegg, Jack K.; Aromí, Guillem; Aguilà, David; Huang, Jui-Hsien; Chuang, Sheng-Jie
Discrete and polymeric complexes formed from cobalt(ii), 4,4′-bipyridine and 2-sulfoterephthalate: synthetic, crystallographic and magnetic studies
CrystEngComm, 2015, 17, 4502
1519666 CIFC26 H26 Co3 N2 O20 S2C 1 2/c 125.2378; 8.6872; 18.8139
90; 130.447; 90
3139.1Datta, Amitabha; Massera, Chiara; Clegg, Jack K.; Aromí, Guillem; Aguilà, David; Huang, Jui-Hsien; Chuang, Sheng-Jie
Discrete and polymeric complexes formed from cobalt(ii), 4,4′-bipyridine and 2-sulfoterephthalate: synthetic, crystallographic and magnetic studies
CrystEngComm, 2015, 17, 4502
1519667 CIFC56 H74 Co3 N8 O32 S2P 1 21/n 17.6877; 24.3258; 18.1655
90; 94.185; 90
3388.1Datta, Amitabha; Massera, Chiara; Clegg, Jack K.; Aromí, Guillem; Aguilà, David; Huang, Jui-Hsien; Chuang, Sheng-Jie
Discrete and polymeric complexes formed from cobalt(ii), 4,4′-bipyridine and 2-sulfoterephthalate: synthetic, crystallographic and magnetic studies
CrystEngComm, 2015, 17, 4502
1519668 CIFC36 H26 Co N4 O14 S2P -19.4916; 9.5694; 10.5062
105.776; 109.863; 94.71
847.49Datta, Amitabha; Massera, Chiara; Clegg, Jack K.; Aromí, Guillem; Aguilà, David; Huang, Jui-Hsien; Chuang, Sheng-Jie
Discrete and polymeric complexes formed from cobalt(ii), 4,4′-bipyridine and 2-sulfoterephthalate: synthetic, crystallographic and magnetic studies
CrystEngComm, 2015, 17, 4502
1519669 CIFC56 H56 Co2 N8 O22 S2P 1 21/n 110.118; 13.926; 19.699
90; 90.537; 90
2775.5Datta, Amitabha; Massera, Chiara; Clegg, Jack K.; Aromí, Guillem; Aguilà, David; Huang, Jui-Hsien; Chuang, Sheng-Jie
Discrete and polymeric complexes formed from cobalt(ii), 4,4′-bipyridine and 2-sulfoterephthalate: synthetic, crystallographic and magnetic studies
CrystEngComm, 2015, 17, 4502
1519670 CIFC7 H6 I N OC 1 2/c 110.5832; 15.6631; 9.8457
90; 96.447; 90
1621.76Kratzer, Philipp; Ramming, Bastian; Römisch, Steven; Maas, Gerhard
The iodine‒oxygen halogen bond: solid-state structures of 3-iodopropiolamides
CrystEngComm, 2015, 17, 4486
1519671 CIFC7 H8 I N OC 1 2/c 110.344; 15.8341; 10.4832
90; 95.996; 90
1707.63Kratzer, Philipp; Ramming, Bastian; Römisch, Steven; Maas, Gerhard
The iodine‒oxygen halogen bond: solid-state structures of 3-iodopropiolamides
CrystEngComm, 2015, 17, 4486
1519672 CIFC8 H10 I N OP 1 21/c 19.1784; 8.6829; 11.5199
90; 92.699; 90
917.06Kratzer, Philipp; Ramming, Bastian; Römisch, Steven; Maas, Gerhard
The iodine‒oxygen halogen bond: solid-state structures of 3-iodopropiolamides
CrystEngComm, 2015, 17, 4486
1519673 CIFC7 H8 I N O2P 1 21/c 18.7638; 8.591; 11.4989
90; 101.488; 90
848.41Kratzer, Philipp; Ramming, Bastian; Römisch, Steven; Maas, Gerhard
The iodine‒oxygen halogen bond: solid-state structures of 3-iodopropiolamides
CrystEngComm, 2015, 17, 4486
1519674 CIFC5 H5 I N2 OP 1 21/c 110.812; 8.1725; 9.279
90; 102.202; 90
801.38Kratzer, Philipp; Ramming, Bastian; Römisch, Steven; Maas, Gerhard
The iodine‒oxygen halogen bond: solid-state structures of 3-iodopropiolamides
CrystEngComm, 2015, 17, 4486
1519675 CIFC4 H4 I N OP c a 2116.1674; 4.1334; 9.0094
90; 90; 90
602.07Kratzer, Philipp; Ramming, Bastian; Römisch, Steven; Maas, Gerhard
The iodine‒oxygen halogen bond: solid-state structures of 3-iodopropiolamides
CrystEngComm, 2015, 17, 4486
1519676 CIFC33 H21 N9P 1 21/n 18.3311; 19.4283; 16.2362
90; 103.855; 90
2551.52Laramée-Milette, Baptiste; Lussier, Félix; Ciofini, Ilaria; Hanan, Garry S.
A family of Ru(ii) complexes built on a novel sexipyridine building block: synthesis, photophysical properties and the rare structural characterization of a triruthenium species.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11551-11561
1519677 CIFC99 H78 B6 F24 N24 Ru3P 1 21/c 122.8909; 13.6566; 35.3984
90; 91.874; 90
11060Laramée-Milette, Baptiste; Lussier, Félix; Ciofini, Ilaria; Hanan, Garry S.
A family of Ru(ii) complexes built on a novel sexipyridine building block: synthesis, photophysical properties and the rare structural characterization of a triruthenium species.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11551-11561
1519678 CIFC6 H24 Cd Cl2 N36 O8P -3 c 111.9445; 11.9445; 13.2162
90; 90; 120
1633Wang, Kun; Zeng, Dihao; Zhang, Jian-Guo; Cui, Yan; Zhang, Tong-Lai; Li, Zhi-Min; Jin, Xin
Controllable explosion: fine-tuning the sensitivity of high-energy complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12497-12501
1519679 CIFC6 H24 Cl2 N36 O8 ZnP -311.8398; 11.8398; 6.57
90; 90; 120
797.6Wang, Kun; Zeng, Dihao; Zhang, Jian-Guo; Cui, Yan; Zhang, Tong-Lai; Li, Zhi-Min; Jin, Xin
Controllable explosion: fine-tuning the sensitivity of high-energy complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12497-12501
1519680 CIFC49 H42 Au2 Cl2 N2 O4 P4 S2C 1 2/c 125.848; 11.2564; 20.6909
90; 122.413; 90
5082.2Vidal, C.; Merz, L.; García-Álvarez, J.
Deep eutectic solvents: biorenewable reaction media for Au( <scp>i</scp> )-catalysed cycloisomerisations and one-pot tandem cycloisomerisation/Diels–Alder reactions
Green Chemistry, 2015, 17, 3870-3878
1519685 CIFC32 H48 O5P 1 21 110.7801; 12.9089; 23.4459
90; 101.782; 90
3193.97Xu, Wen-Jun; Zhu, Meng-Di; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jun; Kong, Ling-Yi
Hypermongones A-J, Rare Methylated Polycyclic Polyprenylated Acylphloroglucinols from the Flowers of Hypericum monogynum.
Journal of natural products, 2015, 78, 1093-1100
1519686 CIFC43 H59 Cl3 N4 O7P 6525.987; 25.987; 12.7789
90; 90; 120
7473.7Lim, Kuan-Hon; Raja, Vijay J.; Bradshaw, Tracey D.; Lim, Siew-Huah; Low, Yun-Yee; Kam, Toh-Seok
Ibogan, tacaman, and cytotoxic bisindole alkaloids from tabernaemontana. Cononusine, an iboga alkaloid with unusual incorporation of a pyrrolidone moiety.
Journal of natural products, 2015, 78, 1129-1138
1519687 CIFC59 H41 Eu F18 O8 P2 Ru2C 1 2/c 119.8829; 17.3599; 17.7114
90; 93.9113; 90
6099.1Hasegawa, Yasuchika; Sato, Nao; Hirai, Yuichi; Nakanishi, Takayuki; Kitagawa, Yuichi; Kobayashi, Atsushi; Kato, Masako; Seki, Tomohiro; Ito, Hajime; Fushimi, Koji
Enhanced electric dipole transition in lanthanide complex with organometallic ruthenocene units.
The journal of physical chemistry. A, 2015, 119, 4825-4833
1519688 CIFC49 H31 Eu F18 O8 P2 RuP -113.2288; 15.9521; 25.7223
89.205; 78.7105; 85.587
5307.3Hasegawa, Yasuchika; Sato, Nao; Hirai, Yuichi; Nakanishi, Takayuki; Kitagawa, Yuichi; Kobayashi, Atsushi; Kato, Masako; Seki, Tomohiro; Ito, Hajime; Fushimi, Koji
Enhanced electric dipole transition in lanthanide complex with organometallic ruthenocene units.
The journal of physical chemistry. A, 2015, 119, 4825-4833
1519689 CIFC28 H21 NP 1 21/n 111.152; 12.874; 13.332
90; 90.179; 90
1914.1Sasaki, Shunsuke; Hattori, Kengo; Igawa, Kazunobu; Konishi, Gen-Ichi
Directional Control of π-Conjugation Enabled by Distortion of the Donor Plane in Diarylaminoanthracenes: A Photophysical Study.
The journal of physical chemistry. A, 2015, 119, 4898-4906
1519690 CIFC26 H19 NP 1 21/c 112.939; 8.692; 16.454
90; 105.933; 90
1779.4Sasaki, Shunsuke; Hattori, Kengo; Igawa, Kazunobu; Konishi, Gen-Ichi
Directional Control of π-Conjugation Enabled by Distortion of the Donor Plane in Diarylaminoanthracenes: A Photophysical Study.
The journal of physical chemistry. A, 2015, 119, 4898-4906
1519691 CIFC28 H52 N2 ZrP -19.7837; 17.3161; 17.4313
80.898; 88.203; 89.242
2914.4Zhang, Chunming; Pan, Heqi; Klosin, Jerzy; Tu, Siyu; Jaganathan, Arvind; Fontaine, Philip P.
Synthetic Optimization and Scale-Up of Imino‒Amido Hafnium and Zirconium Olefin Polymerization Catalysts
Organic Process Research & Development, 2015, 19, 1383
1519692 CIFC25 H23 N5 O3P n a 2114.8632; 7.9124; 18.9392
90; 90; 90
2227.32Kiang, Y.-H.; Bercot, Eric A.; Wu, Qiong; Liu, Jodi; Milburn, Robert R.; Cohen, Dawn E.; Borths, Christopher J.; Saw, Robert E.; Staples, Richard J.; Davis, Carl; Thiel, Oliver R.
Selection of a Suitable Physical Form and Development of a Crystallization Process for a PDE10A Inhibitor Exhibiting Enantiotropic Polymorphism
Organic Process Research & Development, 2015, 19, 1849
1519693 CIFC25 H23 N5 O3P 1 21/c 118.0735; 12.3153; 9.8022
90; 91.823; 90
2180.7Kiang, Y.-H.; Bercot, Eric A.; Wu, Qiong; Liu, Jodi; Milburn, Robert R.; Cohen, Dawn E.; Borths, Christopher J.; Saw, Robert E.; Staples, Richard J.; Davis, Carl; Thiel, Oliver R.
Selection of a Suitable Physical Form and Development of a Crystallization Process for a PDE10A Inhibitor Exhibiting Enantiotropic Polymorphism
Organic Process Research & Development, 2015, 19, 1849
1519694 CIFC14 H11 N O4 SP 1 21/c 15.7372; 21.0648; 10.9631
90; 94.428; 90
1321Singh, Rahul; Allam, Bharat Kumar; Singh, Neetu; Kumari, Kumkum; Singh, Satish Kumar; Singh, Krishna Nand
A Direct Metal-Free Decarboxylative Sulfono Functionalization (DSF) of Cinnamic Acids to α,β-Unsaturated Phenyl Sulfones.
Organic letters, 2015, 17, 2656-2659
1519695 CIFC23 H22 O2P 21 21 218.099; 13.445; 16.407
90; 90; 90
1786.6Mitra, Nirmal K.; Meudom, Rolande; Gorden, John D.; Merner, Bradley L.
A non-cross-coupling approach to arene-bridged macrocycles: synthesis, structure, and direct, regioselective functionalization of a cycloparaphenylene fragment.
Organic letters, 2015, 17, 2700-2703
1519696 CIFC13 H13 F OP 21 21 216.1061; 18.8064; 27.8827
90; 90; 90
3201.88Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519697 CIFC9 H10 Br F OP 1 21 18.013; 5.1662; 10.972
90; 93.376; 90
453.4Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519698 CIFC10 H13 F OP 21 21 215.5342; 11.1421; 14.6505
90; 90; 90
903.39Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519699 CIFC40 H46 Cl8 Co5 N18P -111.5936; 11.9201; 12.1223
63.593; 88.025; 67.331
1365.41Yao, Peng-Fei; Li, Hai-Ye; Huang, Fu-Ping; Yu, Qing; Qin, Xao-Huan; Tang, Jie; Tao, Ye; Bian, He-Dong
A series of multidimensional MOFs incorporating a new N-heterocyclic building block: 5,5′-di(pyridin-4-yl)-3,3′-bi(1,2,4-triazole)
RSC Advances, 2015, 5, 48596-48606
1519700 CIFC30.5 H18 Co3 N8 O8.5P -19.2529; 10.6355; 11.0493
63.622; 86.489; 74.907
938.7Yao, Peng-Fei; Li, Hai-Ye; Huang, Fu-Ping; Yu, Qing; Qin, Xao-Huan; Tang, Jie; Tao, Ye; Bian, He-Dong
A series of multidimensional MOFs incorporating a new N-heterocyclic building block: 5,5′-di(pyridin-4-yl)-3,3′-bi(1,2,4-triazole)
RSC Advances, 2015, 5, 48596-48606
1519701 CIFC28 H22 Co N16 O2P 1 21/n 19.2567; 15.269; 10.2578
90; 96.72; 90
1439.9Yao, Peng-Fei; Li, Hai-Ye; Huang, Fu-Ping; Yu, Qing; Qin, Xao-Huan; Tang, Jie; Tao, Ye; Bian, He-Dong
A series of multidimensional MOFs incorporating a new N-heterocyclic building block: 5,5′-di(pyridin-4-yl)-3,3′-bi(1,2,4-triazole)
RSC Advances, 2015, 5, 48596-48606
1519702 CIFC28 H22 N16 Ni O2P 1 21/n 19.1787; 15.2181; 10.3355
90; 96.657; 90
1434Yao, Peng-Fei; Li, Hai-Ye; Huang, Fu-Ping; Yu, Qing; Qin, Xao-Huan; Tang, Jie; Tao, Ye; Bian, He-Dong
A series of multidimensional MOFs incorporating a new N-heterocyclic building block: 5,5′-di(pyridin-4-yl)-3,3′-bi(1,2,4-triazole)
RSC Advances, 2015, 5, 48596-48606
1519703 CIFC14 H8 Cu2 N8 OP b c n14.6978; 19.3933; 10.356
90; 90; 90
2951.9Yao, Peng-Fei; Li, Hai-Ye; Huang, Fu-Ping; Yu, Qing; Qin, Xao-Huan; Tang, Jie; Tao, Ye; Bian, He-Dong
A series of multidimensional MOFs incorporating a new N-heterocyclic building block: 5,5′-di(pyridin-4-yl)-3,3′-bi(1,2,4-triazole)
RSC Advances, 2015, 5, 48596-48606
1519704 CIFC14 H16 Mn N8 O4I 41/a c d19.1314; 19.1314; 20.6667
90; 90; 90
7564.2Yao, Peng-Fei; Li, Hai-Ye; Huang, Fu-Ping; Yu, Qing; Qin, Xao-Huan; Tang, Jie; Tao, Ye; Bian, He-Dong
A series of multidimensional MOFs incorporating a new N-heterocyclic building block: 5,5′-di(pyridin-4-yl)-3,3′-bi(1,2,4-triazole)
RSC Advances, 2015, 5, 48596-48606
1519705 CIFC104 H154 I4 O P8 Pd4P 1 21/c 116.2343; 15.9423; 20.8753
90; 94.704; 90
5384.6Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519706 CIFC25 H36 Br P2 PdP 1 21/n 112.5686; 13.9781; 14.9939
90; 97.33; 90
2612.7Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519707 CIFC25 H37 Br P2 PdP 1 21/n 111.2438; 13.7677; 17.4246
90; 106.978; 90
2579.8Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519708 CIFC25 H36 Cl P2 PdP 1 21/n 111.6639; 13.5934; 16.568
90; 105.116; 90
2536Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519709 CIFC29 H47 P3 PdP 1 21/n 110.3086; 24.0617; 12.5709
90; 107.577; 90
2972.5Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519710 CIFC26 H40 Cl2 P2 PdC 1 2/c 113.0569; 16.808; 31.261
90; 93.209; 90
6849.8Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519711 CIFC26 H39 Cl P2 PdP 1 21/c 111.2685; 20.7303; 23.1605
90; 99.234; 90
5340.2Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519712 CIFC25 H37 I P2 PdC 1 2/c 129.176; 12.515; 22.247
90; 105.315; 90
7835Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519713 CIFC51 H78 Br4 Cl2 P4 Pd2P 1 21/n 110.3876; 16.2993; 17.0895
90; 103.477; 90
2813.8Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519714 CIFC56 H33 D6 N O5P -112.741; 16.6787; 20.596
102.918; 90.565; 106.517
4077.3Hwang, Jungwun; Dial, Brent E.; Li, Ping; Kozik, Michael E.; Smith, Mark D.; Shimizu, Ken D.
How important are dispersion interactions to the strength of aromatic stacking interactions in solution?
Chem. Sci., 2015, 6, 4358
1519715 CIFC42 H29 N O4P 21 21 218.0214; 18.267; 21.084
90; 90; 90
3089.4Hwang, Jungwun; Dial, Brent E.; Li, Ping; Kozik, Michael E.; Smith, Mark D.; Shimizu, Ken D.
How important are dispersion interactions to the strength of aromatic stacking interactions in solution?
Chem. Sci., 2015, 6, 4358
1519716 CIFC54 H36 N O4P -19.7344; 12.477; 16.268
91.644; 99.097; 94.093
1944.4Hwang, Jungwun; Dial, Brent E.; Li, Ping; Kozik, Michael E.; Smith, Mark D.; Shimizu, Ken D.
How important are dispersion interactions to the strength of aromatic stacking interactions in solution?
Chem. Sci., 2015, 6, 4358
1519717 CIFC78 H76 B F24 P Ru S Si2P -113.1832; 16.891; 20.072
67.256; 76.552; 73.916
3920.8Stahl, Timo; Hrobárik, Peter; Königs, C. David F.; Ohki, Yasuhiro; Tatsumi, Kazuyuki; Kemper, Sebastian; Kaupp, Martin; Klare, Hendrik F. T.; Oestreich, Martin
Mechanism of the cooperative Si‒H bond activation at Ru‒S bonds
Chem. Sci., 2015, 6, 4324
1519718 CIFC66 H64 B F24 P Ru S SiP 1 21/n 113.56; 27.705; 18.609
90; 102.006; 90
6838Stahl, Timo; Hrobárik, Peter; Königs, C. David F.; Ohki, Yasuhiro; Tatsumi, Kazuyuki; Kemper, Sebastian; Kaupp, Martin; Klare, Hendrik F. T.; Oestreich, Martin
Mechanism of the cooperative Si‒H bond activation at Ru‒S bonds
Chem. Sci., 2015, 6, 4324
1519719 CIFC46 H38 B F24 O P SiP 1 21/c 116.929; 18.161; 16.113
90; 97.045; 90
4916.5Stahl, Timo; Hrobárik, Peter; Königs, C. David F.; Ohki, Yasuhiro; Tatsumi, Kazuyuki; Kemper, Sebastian; Kaupp, Martin; Klare, Hendrik F. T.; Oestreich, Martin
Mechanism of the cooperative Si‒H bond activation at Ru‒S bonds
Chem. Sci., 2015, 6, 4324
1519720 CIFC104 H154 I4 O P8 Pd4P 1 21/c 116.2343; 15.9423; 20.8753
90; 94.704; 90
5384.6Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519721 CIFC25 H36 Br P2 PdP 1 21/n 112.5686; 13.9781; 14.9939
90; 97.33; 90
2612.7Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519722 CIFC25 H37 Br P2 PdP 1 21/n 111.2438; 13.7677; 17.4246
90; 106.978; 90
2579.8Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519723 CIFC25 H36 Cl P2 PdP 1 21/n 111.6639; 13.5934; 16.568
90; 105.116; 90
2536Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519724 CIFC29 H47 P3 PdP 1 21/n 110.3086; 24.0617; 12.5709
90; 107.577; 90
2972.5Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519725 CIFC26 H40 Cl2 P2 PdC 1 2/c 113.0569; 16.808; 31.261
90; 93.209; 90
6849.8Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519726 CIFC26 H39 Cl P2 PdP 1 21/c 111.2685; 20.7303; 23.1605
90; 99.234; 90
5340.2Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519727 CIFC25 H37 I P2 PdC 1 2/c 129.176; 12.515; 22.247
90; 105.315; 90
7835Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519728 CIFC51 H78 Br4 Cl2 P4 Pd2P 1 21/n 110.3876; 16.2993; 17.0895
90; 103.477; 90
2813.8Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519755 CIFC15 H16 O4P 1 21/c 17.4665; 21.583; 8.4033
90; 107.586; 90
1290.9Zhang, Xuxue; Dai, Wenpeng; Wu, Wei; Cao, Song
Copper-Catalyzed Coupling Cyclization of gem-Difluoroalkenes with Activated Methylene Carbonyl Compounds: Facile Domino Access to Polysubstituted Furans.
Organic letters, 2015, 17, 2708-2711
1519756 CIFC30 H42 O5P 1 21 17.3312; 12.6193; 14.4778
90; 98.847; 90
1323.47Zhao, Qian-Qian; Song, Qiu-Yan; Jiang, Kan; Li, Guang-Da; Wei, Wen-Jun; Li, Ya; Gao, Kun
Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis.
Organic letters, 2015, 17, 2760-2763
1519757 CIFC10 H7 Br Cl2 N2 OP b c a12.6226; 12.3709; 14.1124
90; 90; 90
2203.7Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519758 CIFC12 H12 Br2 N2 OP 1 21/c 17.3945; 20.124; 17.43
90; 91.44; 90
2592.9Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519759 CIFC11 H10 Br2 N2P 1 21/c 114.9133; 10.5056; 7.3297
90; 103.561; 90
1116.35Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519760 CIFC11 H7 Cl2 F3 N2 O1.5P 1 21/c 17.501; 40.025; 16.7795
90; 94.664; 90
5021Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519761 CIFC11 H9 Br2 F N2P b c a14.443; 7.5861; 21.306
90; 90; 90
2334.4Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519762 CIFC19 H16 Cl2 N O P PdP 21 21 219.394; 10.5702; 19.7348
90; 90; 90
1959.6Menendez-Rodriguez, Lucia; Tomás-Mendivil, Eder; Francos, Javier; Najera, Carmen; Crochet, Pascale; Cadierno, Victorio
Palladium(II) complexes with a phosphino-oxime ligand: Synthesis, structure and applications to the catalytic rearrangement and dehydration of aldoximes
Catal. Sci. Technol., 2015
1519763 CIFC38 H32 Cl2 N2 O2 P2 PdF 2 d d10.2329; 21.5082; 31.0365
90; 90; 90
6830.9Menendez-Rodriguez, Lucia; Tomás-Mendivil, Eder; Francos, Javier; Najera, Carmen; Crochet, Pascale; Cadierno, Victorio
Palladium(II) complexes with a phosphino-oxime ligand: Synthesis, structure and applications to the catalytic rearrangement and dehydration of aldoximes
Catal. Sci. Technol., 2015
1519764 CIFC15 H22 N2 O5P 21 21 2110.7542; 11.2346; 13.4066
90; 90; 90
1619.77Wang, Chao; Zhang, Li; Chen, Changpeng; Han, Jian; Yao, Yingming; Zhao, Yingsheng
Oxalyl amide assisted palladium-catalyzed synthesis of pyrrolidones via carbonylation of γ-C(sp3)‒H bonds of aliphatic amine substrates
Chem. Sci., 2015, 6, 4610
1519847 CIFC9 H19 N O3P 1 21/c 116.8512; 11.1738; 11.0083
90; 104.138; 90
2010McNally, Joshua S.; Noll, Bruce; Orme, Christopher J.; Wilson, Aaron D.
Density Functional Theory Analysis of the Impact of Steric Interaction on the Function of Switchable Polarity Solvents.
The journal of physical chemistry. B, 2015, 119, 6766
1519848 CIFC12 H14 O3P 1 21/c 18.8887; 18.4179; 6.9957
90; 115.638; 90
1032.52Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519849 CIFC12 H14 O3P 1 21/c 110.7308; 8.7467; 12.089
90; 109.485; 90
1069.68Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519850 CIFC22 H16 Br N O2P 1 21/c 15.7399; 15.532; 20.365
90; 96.93; 90
1802.3Dhanasekaran, Sivasankaran; Kayet, Anirban; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama-Mannich Lactamization/Alkylations: Application in the Synthesis of (±)-Homolaudanosine.
Organic letters, 2015, 17, 2780-2783
1519851 CIFC16 H12 N4P 1 21/c 14.8624; 11.167; 23.437
90; 94.33; 90
1269Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Consecutive Cycloaddition/SNAr/Reduction/Cyclization/Oxidation Sequences: A Copper-Catalyzed Multicomponent Synthesis of Fused N-Heterocycles.
Organic letters, 2015, 17, 2820-2823
1519852 CIFC40 H46 N2P 1 21/c 110.701; 27.6694; 11.1215
90; 98.764; 90
3254.52Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519853 CIFC46 H51 I6 N2P 1 21/c 115.047; 24.399; 13.754
90; 108.9; 90
4777.3Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519854 CIFC46 H58 N2P 1 21/n 113.312; 18.813; 15.401
90; 97.762; 90
3821.7Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519855 CIFC86 H108 N4C 1 2/c 130.6695; 12.1512; 23.0584
90; 119.572; 90
7473.9Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519923 CIFC21 H34 O3P 1 21 16.1791; 23.0423; 6.9392
90; 110.037; 90
928.21Hosseini, Abolfazl; Seidel, Daniel; Miska, Andreas; Schreiner, Peter R.
Fluoride-assisted activation of calcium carbide: a simple method for the ethynylation of aldehydes and ketones.
Organic letters, 2015, 17, 2808-2811
1519924 CIFC25 H21 Fe N3P 1 21/c 110.9392; 8.3314; 22.5089
90; 102.759; 90
2000.78Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu
Cu/Pd-Catalyzed, Three-Component Click Reaction of Azide, Alkyne, and Aryl Halide: One-Pot Strategy toward Trisubstituted Triazoles.
Organic letters, 2015, 17, 2860-2863
1519925 CIFC80 H56 Co7 F18 N16 O18 SiP a -324.5063; 24.5063; 24.5063
90; 90; 90
14717.5Chen, Kai-Jie; Perry IV, John J.; Scott, Hayley S.; Yang, Qing-Yuan; Zaworotko, Michael J.
Double-walled pyr topology networks from a novel fluoride-bridged heptanuclear metal cluster
Chem. Sci., 2015, 6, 4784
1519926 CIFC54 H62 Co N2 O4P -110.6748; 11.9906; 19.6875
101.316; 101.953; 103.763
2313.24Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519927 CIFC54 H62 Co N2 O4P -110.7956; 12.0991; 19.834
102.162; 101.446; 104.036
2370.3Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519928 CIFC54 H62 Co N2 O4P -19.8997; 10.812; 12.1278
104.002; 102.27; 101.408
1187.5Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519929 CIFC82 H94 Co N2 O4P 1 21/n 116.5308; 11.7257; 18.9821
90; 107.445; 90
3510.2Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519930 CIFC18 H26 Sn0.5P b c m10.9013; 12.0601; 25.222
90; 90; 90
3315.96Sindlinger, Christian P.; Stasch, Andreas; Bettinger, Holger F.; Wesemann, Lars
A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination
Chem. Sci., 2015, 6, 4737
1519931 CIFC89 H134 N2 Sn2P -112.7122; 15.3521; 22.5773
84.881; 89.932; 82.556
4351.4Sindlinger, Christian P.; Stasch, Andreas; Bettinger, Holger F.; Wesemann, Lars
A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination
Chem. Sci., 2015, 6, 4737
1519932 CIFC48.5 H70 SnP 1 21/c 115.9849; 15.9056; 17.7408
90; 100.754; 90
4431.37Sindlinger, Christian P.; Stasch, Andreas; Bettinger, Holger F.; Wesemann, Lars
A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination
Chem. Sci., 2015, 6, 4737
1519944 CIFC35 H36 Cl2 F12 N2 O6C 1 2/c 129.3901; 13.5696; 21.1866
90; 105.652; 90
8136.1Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519945 CIFC33 H42 N4 O9P 1 21/n 110.4318; 18.5656; 17.6555
90; 90.817; 90
3419.04Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519946 CIFC32 H32 F12 N2 O9P 1 21/c 111.9175; 19.021; 17.226
90; 108.787; 90
3696.8Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519947 CIFC45 H38 Cl2 N4 O4P -19.5715; 18.5858; 23.8686
67.485; 81.597; 88.411
3878.5Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519998 CIFC20 H30 N0 O5P 21 21 217.0685; 15.143; 17.388
90; 90; 90
1861.2Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1519999 CIFC20 H28 O5P 1 21 19.4777; 7.3392; 13.4089
90; 91.432; 90
932.41Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1520000 CIFC29 H36 O8P 1 21/c 113.2416; 13.1779; 15.2428
90; 109.387; 90
2509Fukaya, Keisuke; Kodama, Keisuke; Tanaka, Yuta; Yamazaki, Hirohisa; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis.
Organic letters, 2015, 17, 2574-2577
1520001 CIFC54 H46 Co N2 P3P 1 21/n 114.376; 14.699; 21.34
90; 107.79; 90
4293.8Scheuermann, Margaret L.; Johnson, Elizabeth J.; Chirik, Paul J.
Alkene isomerization-hydroboration promoted by phosphine-ligated cobalt catalysts.
Organic letters, 2015, 17, 2716-2719
1520002 CIFC29 H38 O8P 1 21/n 19.3612; 19.6336; 14.1965
90; 101.762; 90
2554.4Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520003 CIF
Paper
C42 H50 O10P -19.6397; 13.6008; 15.0461
83.6966; 77.488; 77.9768
1879.2Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520004 CIFC30.25 H41 O8P -111.3343; 15.4666; 16.487
85.1124; 78.3773; 78.5231
2771.3Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520005 CIFC15 H21 N O2P 1 21/c 18.5353; 10.6984; 15.609
90; 104.429; 90
1380.4Zhou, Wei; Ni, Shengyang; Mei, Haibo; Han, Jianlin; Pan, Yi
Hydroxyalkylation-initiated radical cyclization of N-allylbenzamide for direct construction of isoquinolinone.
Organic letters, 2015, 17, 2724-2727
1520006 CIFBi9 O7.5 S6R -3 m :H4.0685; 4.0685; 31.029
90; 90; 120
444.8Meng, Sha; Zhang, Xian; Zhang, Ganghua; Wang, Yaoming; Zhang, Hui; Huang, Fuqiang
Synthesis, Crystal Structure, and Photoelectric Properties of a New Layered Bismuth Oxysulfide.
Inorganic chemistry, 2015, 54, 5768-5773
1520007 CIFC62 H132 Cu2 Gd2 N2 O26P 1 21/n 113.447; 22.2429; 14.1737
90; 103.936; 90
4114.6Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520008 CIFC64 H122 Cu2 Dy2 N4 O22P -111.1732; 13.2788; 15.503
102.315; 97.228; 110.072
2060.47Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520009 CIFC64 H124 Co2 Dy2 N4 O22P -111.3913; 13.3809; 15.4188
103.07; 98.378; 109.653
2092.03Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520010 CIFC64 H122 Co2 Gd2 N3 O22P 1 21/c 115.7469; 13.0245; 21.9609
90; 110.893; 90
4207.93Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520011 CIFC62 H120 Dy2 Mg2 N2 O22P 1 21/c 115.4531; 19.5753; 14.0907
90; 109.082; 90
4028.21Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520012 CIFC64 H125 Gd2 Mg2 N3 O22P 1 21/c 115.7351; 13.1771; 21.9189
90; 109.951; 90
4272Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520013 CIFC62 H122 Er2 Mg2 N2 O22P -112.9581; 14.1259; 14.2362
98.689; 107.817; 116.987
2077.6Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520014 CIFC62 H122 N2 Ni2 O22 Y2C 1 2/c 120.8134; 21.3724; 18.3457
90; 101.401; 90
7999.7Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520015 CIFC62 H122 Er2 N2 Ni2 O22C 1 2/c 120.7791; 21.3052; 18.3054
90; 101.596; 90
7938.45Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520016 CIFC62 H122 Dy2 N2 Ni2 O22C 1 2/c 120.6807; 21.2712; 18.2888
90; 101.566; 90
7881.9Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520017 CIFC66 H128 Gd2 N4 Ni2 O22P 1 21/c 115.9042; 12.969; 21.7691
90; 111.352; 90
4181.9Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520018 CIFC68 H120 Mn2 N5 O22 Y2P -113.1987; 13.575; 14.1952
71.486; 64.349; 81.392
2173.9Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520019 CIFC68 H122 Dy2 Mn2 N5 O22P -113.2219; 13.5495; 14.156
71.5364; 64.2521; 81.4352
2166.48Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520020 CIFC62 H123.33 Gd2 Mn2 N2 O22.67P -112.9744; 13.147; 13.1693
86.455; 77.91; 66.666
2016.3Moreno Pineda, Eufemio; Chilton, Nicholas F.; Tuna, Floriana; Winpenny, Richard E. P.; McInnes, Eric J. L.
Systematic Study of a Family of Butterfly-Like {M <sub>2</sub> Ln <sub>2</sub> } Molecular Magnets (M = Mg <sup>II</sup> , Mn <sup>III</sup> , Co <sup>II</sup> , Ni <sup>II</sup> , and Cu <sup>II</sup> ; Ln = Y <sup>III</sup> , Gd <sup>III</sup> , Tb <sup>III</sup> , Dy <sup>III</sup> , Ho <sup>III</sup> , and Er <sup>III</sup> )
Inorganic Chemistry, 2015, 54, 5930-5941
1520021 CIFC30 H34 Cu F6 N2 O2P 1 21/n 18.3007; 17.9066; 19.9819
90; 98.904; 90
2934.3Chiang, Linus; Herasymchuk, Khrystyna; Thomas, Fabrice; Storr, Tim
Influence of Electron-Withdrawing Substituents on the Electronic Structure of Oxidized Ni and Cu Salen Complexes.
Inorganic chemistry, 2015, 54, 5970-5980
1520022 CIFC12 H13 Cl O2P 21 21 215.8119; 10.51; 18.411
90; 90; 90
1124.6Sai, Masahiro; Yamamoto, Hisashi
Chiral Brønsted Acid as a True Catalyst: Asymmetric Mukaiyama Aldol and Hosomi-Sakurai Allylation Reactions.
Journal of the American Chemical Society, 2015, 137, 7091-7094
1520023 CIFC58 H75 B P Pt SP -19.553; 13.221; 20.742
101.583; 90.792; 97.863
2539.9Cowie, Bradley E.; Emslie, David J. H.
Bis-hydrocarbyl Platinum(II) Ambiphilic Ligand Complexes: Alkyl‒Aryl Exchange between Platinum and Boron
Organometallics, 2015, 34, 2737
1520024 CIFC53 H63 B Cl2 P Pt SP -113.306; 14.095; 14.176
97.362; 105.671; 107.033
2384.7Cowie, Bradley E.; Emslie, David J. H.
Bis-hydrocarbyl Platinum(II) Ambiphilic Ligand Complexes: Alkyl‒Aryl Exchange between Platinum and Boron
Organometallics, 2015, 34, 2737
1520025 CIFC70 H75 B Cl3 O3 P2 Pt SP -19.592; 12.7606; 26.7696
97.074; 93.659; 102.019
3166.8Cowie, Bradley E.; Emslie, David J. H.
Bis-hydrocarbyl Platinum(II) Ambiphilic Ligand Complexes: Alkyl‒Aryl Exchange between Platinum and Boron
Organometallics, 2015, 34, 2737

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