Crystallography Open Database
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Searching year of publication is 2017
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1548791 | CIF HKL Paper | C19 H14 Br F N2 O | P b c a | 13.4521; 7.181; 34.204 90; 90; 90 | 3304.1 | Kalecik, Sedanur; Yavuz, Metin; Kavraz, Fatih; Eserci, Hande; Ağar, Erbil (<i>E</i>)-2-{[(4-Anilinophenyl)imino]methyl}-4-bromo-5-fluorophenol IUCrData, 2017, 2, x171708 |
1548792 | CIF HKL Paper | C18 H18 N2 O2 | P -1 | 9.0951; 13.9582; 14.1083 61.646; 80.859; 83.665 | 1554.92 | Guerrab, Walid; Mague, Joel T.; Akrad, Rachida; Ansar, Mhammed; Taoufik, Jamal; Ramli, Youssef 5,5-Diphenyl-3-propylimidazolidine-2,4-dione IUCrData, 2017, 2, x171808 |
1548793 | CIF HKL | C15 H11 Cl F3 N O2 | P -1 | 4.5971; 6.4372; 25.237 86.984; 86.173; 78.096 | 728.56 | Atalay, Şehriman; Gerçeker, Semra; Meral, Seher; Bülbül, Hakan 2-{(<i>E</i>)-[(3-Chloro-4-methylphenyl)imino]methyl}-4-(trifluoromethoxy)phenol IUCrData, 2017, 2, x171725 |
1548794 | CIF HKL Paper | C13 H14 N2 O2 S | P -1 | 4.8078; 7.7314; 17.8011 93.412; 94.564; 103.05 | 640.5 | Missioui, Mohcine; Mague, Joel T.; El Fal, Mohammed; Taoufik, Jamal; Essassi, El Mokhtar; Ramli, Youssef Ethyl 2-[(3-methylquinoxalin-2-yl)sulfanyl]acetate IUCrData, 2017, 2, x171763 |
1548795 | CIF HKL Paper | C23 H17 F3 N2 O3 | P 1 21/c 1 | 19.817; 8.4268; 12.4459 90; 101.22; 90 | 2038.7 | Xia, Ying; Wang, Haiyan; Yu, Jianhua; Wu, Zhichao (<i>E</i>)-3-[4-(Benzo[<i>d</i>]oxazol-2-yl)styryl]-1-methylpyridin-1-ium trifluoroacetate IUCrData, 2017, 2, x171733 |
1548796 | CIF HKL Paper | O2 Te | P 21 21 21 | 4.8809; 8.5668; 4.3433 90; 90; 90 | 181.609 | Weil, Matthias Redetermination of the γ-form of tellurium dioxide IUCrData, 2017, 2 |
1548797 | CIF HKL Paper | C9 H10 Cl3 N O2 | P -1 | 6.7395; 11.3491; 16.1078 75.681; 88.031; 86.856 | 1191.69 | Suresh, S.; Pandi, P.; Kumar, R. Mohan; Chakkaravarthi, G. 4-Methylanilinium trichloroacetate IUCrData, 2017, 2, x171767 |
1548798 | CIF HKL | C22 H29 Br N4 Se2 | I 1 2/a 1 | 23.767; 5.1425; 39.806 90; 102.61; 90 | 4747.8 | Rani, Varsha; Singh, Harkesh B.; Butcher, Ray J. 3,3'-[(2-Bromo-1,3-phenylene)bis(methylene)]bis(1-butyl-2,3-dihydro-1<i>H</i>-imidazole-2-selone) IUCrData, 2017, 2, x171746 |
1548799 | CIF HKL | C12 H13 N3 O | P 1 21/c 1 | 5.7747; 6.5171; 30.234 90; 95.342; 90 | 1132.89 | El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M. 1-[5-Methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]ethanone IUCrData, 2017, 2, x171782 |
1548800 | CIF HKL | C32 H28 N8 O | P -1 | 6.6115; 15.2036; 15.3021 63.536; 83.76; 85.214 | 1367.75 | Abu El-Enin, Mohammed Abu Bakr; Abdel-Wahab, Bakr F.; Baashen, Mohammed; Ghabbour, Hazem A.; El-Hiti, Gamal A. (<i>E</i>)-1-[5-Methyl-1-(<i>p</i>-tolyl)-1<i>H</i>-1,2,3-triazol-4-yl]-3-{3-[5-methyl-1-(<i>p</i>-tolyl)-1<i>H</i>-1,2,3-triazol-4-yl]-1-phenyl-1<i>H</i>-pyrazol-4-yl}prop-2-en-1-one IUCrData, 2017, 2, x171729 |
1548801 | CIF Paper | C11 H9 N O | P 21 21 21 | 6.0506; 13.7423; 20.886 90; 90; 90 | 1736.7 | Green, Alexander R.; Owczarzak, Kendall K.; Thomas, Mallory; Olrogg, Garrett M.; Whitver, Ethan; Crescente, Joseph V.; Peters, Joshua; Doud, Cheyann M.; Storm, Mitchell M.; Fink, Kathryn D.; Bilotti, Caroline; Cardenas, Allan Jay Naphthalene-1-carbaldehyde oxime IUCrData, 2017, 2, x171720 |
1548802 | CIF HKL Paper | C18 H20 N2 O6 | P 1 21/n 1 | 4.7936; 12.9828; 14.632 90; 92.986; 90 | 909.4 | Zhang, Huihui; Wang, Haiyan; Yu, Jianhua 1,4-Bis(4-methyl-2-nitrophenoxy)butane IUCrData, 2017, 2, x171734 |
1548803 | CIF HKL Paper | C16 H21 N O | C 1 2/c 1 | 20.3655; 7.6148; 18.2999 90; 99.254; 90 | 2801 | Jebapriya, J. Christina; Reuben Jonathan, D.; Prasana, Johanan Christian; Usha, G. (2<i>E</i>)-2-[4-(Dimethylamino)benzylidene]-5-methylcyclohexanone IUCrData, 2017, 2, x171706 |
1548804 | CIF HKL Paper | C40 H28 N3 O10 P3 | C 1 2/c 1 | 32.3691; 10.7492; 13.1332 90; 125.578; 90 | 3716.6 | Hou, Guohui; Zhang, Yumeng; Zhu, Jing; Xiong, Anxian; Wei, Hongliang; Chu, Huijuan 4,4',4'',4'''-({4'λ^5^,6λ^5^,6'λ^5^-Spiro[dibenzo[<i>d</i>,<i>f</i>][1,3,2]dioxaphosphepine-6,2'-[1,3,5,2,4,6]triazatriphosphinine]-4',4',6',6'-tetrayl}tetrakis(oxy))tetrabenzaldehyde IUCrData, 2017, 2, x171712 |
1548859 | CIF | Ca Cl2 Cu3 H7.58 O6.79 | P -3 m 1 | 6.6615; 6.6615; 5.8023 90; 90; 120 | 222.985 | Crichton, Wilson A.; Müller, Harald Centennialite, CaCu3(OH)6Cl2.nH2O, n ≈ 0.7, a new kapellasite-like species, and a reassessment of calumetite Mineralogical Magazine, 2017, 81, 1105 |
1549272 | CIF | C H7.89 N O7.45 P V | P -1 | 6.3844; 7.2278; 9.2965 67.26; 72.927; 85.848 | 377.8 | C. Kouvatas; V. Alonzo; T. Bataille; L. Le Polles; C. Roiland; G. Louarn; E. Le Fur Synthesis, crystal structure of the ammonium vanadyl oxalatophosphite and its controlled conversion into catalytic vanadyl phosphates Journal of Solid State Chemistry, 2017, 253, 73-77 |
1549551 | CIF | C4 H14 Cu2 O14 P2 | C 1 2/c 1 | 16.233; 6.24; 14.955 90; 122.45; 90 | 1278.3 | Köferstein, Roberto; Arnold, Michael; Robl, Christian Synthesis, Crystal Structure, and Characterization of Two Novel One- and Two-Dimensionally Polymeric Copper(II) Phosphonoacetates Zeitschrift für anorganische und allgemeine Chemie, 2017, 643, 276 |
1549552 | CIF | C2 H12 Cu1.5 O10 P | P -1 | 6.082; 8.001; 10.836 94.98; 105.71; 109.84 | 468.08 | Köferstein, Roberto; Arnold, Michael; Robl, Christian Synthesis, Crystal Structure, and Characterization of Two Novel One- and Two-Dimensionally Polymeric Copper(II) Phosphonoacetates Zeitschrift für anorganische und allgemeine Chemie, 2017, 643, 276 |
1550125 | CIF | Cu2 S4 Sn Zn | I -4 2 m | 5.434; 5.434; 10.845 90; 90; 90 | 320.24 | Munoz, M; Vera, E; Pineda, T; Guaspud, J Synthesis and characterization by solid-state impedance spectroscopy of semiconductor Cu2ZnSnS4 material for photovoltaic technologies Journal of Physics: Conference Series, 2017, 786, 1-7 |
1551077 | CIF | Cr2 Mg2 O5 | P b a m | 9.6091; 12.4324; 2.8498 90; 90; 90 | 340.449 | Ishii, T.; Tsujino, N.; Arii, H.; Fujino, K.; Miyajima, N.; Kojitani, H.; Kunimoto, T.; Akaogi, M. A shallow origin of so-called ultrahigh-pressure chromitites, based on single-crystal X-ray structure analysis of the high-pressure Mg2Cr2O5 phase, with modified ludwigite-type structure American Mineralogist, 2017, 102, 2113-2118 |
1551161 | CIF | C18 H18 In N3 O8 | F d d d | 15.3069; 26.9467; 31.284 90; 90; 90 | 12903.7 | Carrington, Elliot J.; McAnally, Craig A.; Fletcher, Ashleigh J.; Thompson, Stephen P.; Warren, Mark; Brammer, Lee Solvent-switchable continuous-breathing behaviour in a diamoniod metal-organic framework and its influence on CO2 vs CH4 selectivity Nature Chemistry, 2017, 9, 882-889 |
1551370 | CIF | F6 K6 Mn Na3 O76 W17 | C 1 2/c 1 | 22.586; 12.292; 29.421 90; 92.34; 90 | 8161 | Roy E. Schreiber; Lothar Houben; Sharon G. Wolf; Gregory Leitus; Zhong-Ling Lang; Jorge J. Carbo; Josep M. Poblet; Ronny Neumann Real-time molecular scale observation of crystal formation Nature Chemistry, 2017, 9, 369-373 |
1551371 | CIF | Cs11 F12 K5 Mn2 Na2 O128 W34 | C m c e | 17.983; 18.413; 22.333 90; 90; 90 | 7395 | Roy E. Schreiber; Lothar Houben; Sharon G. Wolf; Gregory Leitus; Zhong-Ling Lang; Jorge J. Carbo; Josep M. Poblet; Ronny Neumann Real-time molecular scale observation of crystal formation Nature Chemistry, 2017, 9, 369-373 |
1551392 | CIF | C628.5 H496.5 B115.5 Co12 F81 N117 O54 S27 | R -3 :H | 48.517; 48.517; 64.134 90; 90; 120 | 130740 | Felix J. Rizzuto; Jonathan R. Nitschke Stereochemical plasticity modulates cooperative binding in a CoII12L6 cuboctahedron Nature Chemistry, 2017, 10, 903-908 |
1551393 | CIF | C764 H707 B264 Co12 N115 O | P -1 | 26.438; 30.374; 31.047 67.3; 84.86; 78.93 | 22569 | Felix J. Rizzuto; Jonathan R. Nitschke Stereochemical plasticity modulates cooperative binding in a CoII12L6 cuboctahedron Nature Chemistry, 2017, 10, 903-908 |
1551394 | CIF | C618 H355.5 B5.5 Co12 F133 N117 O74 S37 | P 1 21/n 1 | 40.2042; 54.2465; 40.2935 90; 90.408; 90 | 87875 | Felix J. Rizzuto; Jonathan R. Nitschke Stereochemical plasticity modulates cooperative binding in a CoII12L6 cuboctahedron Nature Chemistry, 2017, 10, 903-908 |
1551423 | CIF | C80 H104 Ag12 F12 N8 O16.8 S8 | I -4 2 m | 17.2768; 17.2768; 20.4482 90; 90; 90 | 6103.54 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551424 | CIF | C88 H128 Ag12 F12 N8 O12 S8 | I -4 2 m | 17.2793; 17.2793; 19.8246 90; 90; 90 | 5919.1 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551425 | CIF | C84 H108 Ag12 Cl12 F12 N8 O8 S8 | I -4 2 m | 17.1887; 17.1887; 20.4219 90; 90; 90 | 6033.7 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551426 | CIF | C82.4 H107.6 Ag12 F12 N9.2 O6 S8 | I -4 2 m | 17.3814; 17.3814; 20.0977 90; 90; 90 | 6071.78 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551427 | CIF | C83 H110 Ag12 F12 N8 O9 S8 | I -4 2 m | 17.27; 17.27; 20.04 90; 90; 90 | 5977 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551428 | CIF | C98 H140 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.2498; 17.2498; 21.101 90; 90; 90 | 6278.7 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551429 | CIF | C50 H75 Ag12 F18 N7 O12 S6 | P -1 | 15.4518; 15.8621; 17.9312 91.3274; 95.0852; 94.9884 | 4358.91 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551430 | CIF | C80 H104 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.34149; 17.34149; 20.1671 90; 90; 90 | 6064.8 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551431 | CIF | C80 H104 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.29649; 17.29649; 19.8753 90; 90; 90 | 5946.07 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551432 | CIF | C80 H104 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.33048; 17.33048; 20.251 90; 90; 90 | 6082.3 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551433 | CIF | C96 H136 Ag12 F12 N8 O16 S8 | I -4 2 m | 17.1785; 17.1785; 20.8487 90; 90; 90 | 6152.47 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551434 | CIF | C104 H128 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.298; 17.298; 20.5393 90; 90; 90 | 6145.79 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551435 | CIF | C94 H120 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.26652; 17.26652; 20.5352 90; 90; 90 | 6122.21 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551436 | CIF | C104 H124 Ag12 F16 N8 O8 S8 | I -4 2 m | 17.3073; 17.3073; 20.4745 90; 90; 90 | 6133 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551437 | CIF | C92 H114 Ag12 Cl2 F12 N8 O8 S8 | I -4 2 m | 17.23734; 17.23734; 20.5923 90; 90; 90 | 6118.51 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551438 | CIF | C92 H114 Ag12 Br2 F12 N8 O8 S8 | I -4 2 m | 17.2292; 17.2292; 20.5453 90; 90; 90 | 6098.8 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551439 | CIF | C92 H114 Ag12 F12 I2 N8 O8 S8 | I -4 2 m | 17.2105; 17.2105; 20.6982 90; 90; 90 | 6130.8 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551440 | CIF | C96 H124 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.2348; 17.2348; 20.8923 90; 90; 90 | 6205.8 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551441 | CIF | C96 H124 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.2529; 17.2529; 20.6795 90; 90; 90 | 6155.5 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551442 | CIF | C96 H124 Ag12 F12 N8 O8 S8 | I -4 2 m | 17.2603; 17.2603; 20.5849 90; 90; 90 | 6132.61 | Ren-Wu Huang; Yong-Sheng Wei; Xi-Yan Dong; Xiao-Hui Wu; Chen-Xia Du; Shuang-Quan Zang; Thomas C. W. Mak Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal-organic framework Nature Chemistry, 2017, 9, 689-697 |
1551483 | CIF | C336 H264 F96 Fe8 N96 Sb16 | P -1 | 25.4839; 33.5954; 37.4035 89.22; 83.44; 80.438 | 31370.6 | Ben S. Pilgrim; Derrick A. Roberts; Thorsten G. Lohr; Tanya K. Ronson; Jonathan R. Nitschke Signal transduction in a covalent post-assembly modification cascade Nature Chemistry, 2017, 9, 1276-1281 |
1551484 | CIF | C232 H194.5 F48 Fe4 N42.5 O24.5 P8 | P -1 | 22.2379; 22.4501; 30.1489 69.385; 86.301; 78.614 | 13810.4 | Ben S. Pilgrim; Derrick A. Roberts; Thorsten G. Lohr; Tanya K. Ronson; Jonathan R. Nitschke Signal transduction in a covalent post-assembly modification cascade Nature Chemistry, 2017, 9, 1276-1281 |
1551485 | CIF | C279 H244.5 As8 F48 Fe4 N37.5 O24 | C 1 2/c 1 | 53.942; 28.539; 41.2325 90; 90.231; 90 | 63475 | Ben S. Pilgrim; Derrick A. Roberts; Thorsten G. Lohr; Tanya K. Ronson; Jonathan R. Nitschke Signal transduction in a covalent post-assembly modification cascade Nature Chemistry, 2017, 9, 1276-1281 |
1551543 | CIF | C276 H174 Co6 P6 Te8 | C 1 2/c 1 | 29.47019; 17.3534; 38.00346 90; 103.98; 90 | 18859.6 | Evan S. O'Brien; M. Tuan Trinh; Rose L. Kann; Jia Chen; Giselle A. Elbaz; Amrita Masurkar; Timothy L. Atallah; Maria V. Paley; Nilam Patel; Daniel W. Paley; Ioannis Kymissis; Andrew C. Crowther; Andrew J. Millis; David R. Reichman; X.-Y. Zhu; Xavier Roy Single-crystal-to-single-crystal intercalation of a low-bandgap superatomic crystal Nature Chemistry, 2017, 9, 1170-1174 |
1551544 | CIF | C234 H126 Co6 P6 Te8 | R -3 m :H | 16.9985; 16.9985; 55.684 90; 90; 120 | 13934.2 | Evan S. O'Brien; M. Tuan Trinh; Rose L. Kann; Jia Chen; Giselle A. Elbaz; Amrita Masurkar; Timothy L. Atallah; Maria V. Paley; Nilam Patel; Daniel W. Paley; Ioannis Kymissis; Andrew C. Crowther; Andrew J. Millis; David R. Reichman; X.-Y. Zhu; Xavier Roy Single-crystal-to-single-crystal intercalation of a low-bandgap superatomic crystal Nature Chemistry, 2017, 9, 1170-1174 |
1551545 | CIF | C246 H126 Co6 N8 P6 Te8 | I 1 2/m 1 | 26.5695; 17.056; 21.1219 90; 104.26; 90 | 9276.9 | Evan S. O'Brien; M. Tuan Trinh; Rose L. Kann; Jia Chen; Giselle A. Elbaz; Amrita Masurkar; Timothy L. Atallah; Maria V. Paley; Nilam Patel; Daniel W. Paley; Ioannis Kymissis; Andrew C. Crowther; Andrew J. Millis; David R. Reichman; X.-Y. Zhu; Xavier Roy Single-crystal-to-single-crystal intercalation of a low-bandgap superatomic crystal Nature Chemistry, 2017, 9, 1170-1174 |
1551572 | CIF | C44 H58 N4 Ni2 O11 | C 1 2/c 1 | 18.321; 13.543; 18.649 90; 108.372; 90 | 4391 | LIM, Jongwan; SHIN, Yunseok; HAN, Junhee; RYU, Sanghoon; MITSUHASHI, Ryoji; MIKURIYA, Masahiro Di-μ-phenolato-μ-aqua-bridged Dinuclear Nickel(II) Complex with <i>N,N</i>′-Disalicylidene-2,2′-(ethylenedioxy)bis(ethylamine) X-ray Structure Analysis Online, 2017, 33, 5 |
1551573 | CIF | C34 H48 N4 Ni4 O10 | P 1 21/c 1 | 12.154; 11.821; 15.945 90; 112.214; 90 | 2120.8 | MIKURIYA, Masahiro; TAKEUCHI, Masahiro; YOSHIOKA, Daisuke Tetranuclear Nickel(II) Complex with an Unsymmetrical Pentadentate Schiff-base Ligand Having a Defective Double-Cubane Core X-ray Structure Analysis Online, 2017, 33, 31 |
1551574 | CIF | C30 H24 O9 | P 1 21/n 1 | 10.676; 10.017; 24.438 90; 100.89; 90 | 2566.4 | DOCHEV, Stefan; ROLLER, Alexander; MILUNOVIC, Miljan; MANOLOV, Ilia Synthesis and Crystal Structure of 4-(Bis(4-hydroxy-2-oxo-2<i>H</i>-chromen-3-yl)methyl)benzoic Acid X-ray Structure Analysis Online, 2017, 33, 53 |
1551575 | CIF | C48 H58 B F4 Fe N6 O2 | P -1 | 7.9064; 13.7091; 20.7535 90.87; 92.579; 93.419 | 2242.83 | IDE, Yuki; YAMADA, Yuya; MORI, Shigeki; IKEUE, Takahisa Crystal Structure of a Six-coordinated (2,3,7,8,12,13,17,18-Octaethylporphyrinato)iron(III) Complex with Two 4-Methylpyridine <i>N</i>-Oxides X-ray Structure Analysis Online, 2017, 33, 25 |
1551576 | CIF | C32 H30 N4 Ni O8 | C 1 2/c 1 | 17.6548; 19.0788; 9.2011 90; 103.547; 90 | 3013 | UEJI, Kan; SHINOZAKI, Satsuki; MIYAMURA, Kazuo Crystal Structure of the Bis[bis(<i>p</i>-methoxyphenyl)glyoximato]nickel(II) Complex X-ray Structure Analysis Online, 2017, 33, 71 |
1551577 | CIF | C14 H17 Cu N4 O1.5 | C 1 2/c 1 | 17.975; 18.894; 9.2081 90; 113.728; 90 | 2862.9 | MIKURIYA, Masahiro; HARA, Masashi; YOSHIOKA, Daisuke; MITSUHASHI, Ryoji Dinuclear Assembly in a Copper(II) Complex with 1,3-Bis(pyrrole-2-methylideneamino)-2-propanol X-ray Structure Analysis Online, 2017, 33, 67 |
1551578 | CIF | C72 H72 Cl7 Fe N6 O6 | P -1 | 15.2889; 15.8587; 16.2403 84.596; 63.769; 84.162 | 3508.49 | IDE, Yuki; HOSODA, Haruka; ISHIMAE, Hiroki; MORI, Shigeki; IKEUE, Takahisa Crystal Structure of a Six-coordinated [5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)porphyrinato-<i>k</i><sup>4</sup><i>N</i>]iron(III) Complex with Two 3,5-Dimethylpyridine <i>N</i>-Oxides X-ray Structure Analysis Online, 2017, 33, 49 |
1551579 | CIF | C9 H12 N2 S3 | P 1 21/c 1 | 10.178; 13.357; 8.845 90; 98.613; 90 | 1188.9 | OSMAN, Uwaisulqarni M.; TAHIR, M. Ibrahim M.; CROUSE, Karen A.; RAVOOF, Thahira Begum S. A. Crystal Structure of Methyl-<i>N</i>′-[1-(thiophen-2-yl)propylidene]hydrazinecarbodithioate X-ray Structure Analysis Online, 2017, 33, 57 |
1551580 | CIF | C13 H14 N2 Ni O4 | P 1 21/c 1 | 9.364; 17.725; 7.753 90; 105.004; 90 | 1242.9 | MIKURIYA, Masahiro; TAKEUCHI, Masahiro; YOSHIOKA, Daisuke; MITSUHASHI, Ryoji Nickel(II) Complex Derived from Unsymmetrical α-(2-Hydroxy-3-salicylideneaminopropyl)iminopropionic Acid X-ray Structure Analysis Online, 2017, 33, 45 |
1551581 | CIF | C21 H22 B N O | P n a 21 | 16.6818; 11.5428; 9.2234 90; 90; 90 | 1776 | SAKIYAMA, Hiroshi; ICHI, Misaki; MITSUHASHI, Ryoji; MIKURIYA, Masahiro Crystal Structure of a Tetracoordinate Organoboron Coordination Compound, Dimethylformamide-triphenylborane Complex X-ray Structure Analysis Online, 2017, 33, 29 |
1551582 | CIF | C12 H25 N O13 | P 1 | 6.914; 7.7202; 8.7383 79.467; 73.033; 67.106 | 409.71 | FUJIMOTO, Takashi; NISHIO, Toshiyuku; HOSAKA, Hiroki; MIZOGUCHI, Saori; TASHIRO, Mitsuru Crystal Structure of β-D-Fructofuranosyl-[2↔1]-6-amido-6-deoxy-α-D-glucopyranoside X-ray Structure Analysis Online, 2017, 33, 63 |
1551583 | CIF | C13.5 H16 N4 Ni O1.5 | P -1 | 9.6947; 12.0269; 13.2626 94.036; 108.801; 104.82 | 1395.3 | MIKURIYA, Masahiro; HARA, Masashi; YOSHIOKA, Daisuke Synthesis and Crystal Structure of a Nickel(II) Complex with 1,3-Bis(pyrrole-2-methylideneamino)-2-propanol X-ray Structure Analysis Online, 2017, 33, 59 |
1551584 | CIF | C21 H21 N2 O4 Pd | P 1 21/n 1 | 12.5115; 10.5337; 15.008 90; 94.0547; 90 | 1973 | AHMAD, Shahrul Nizam; BAHRON, Hadariah; TAJUDDIN, Amalina M.; YUSOF, M. Sukeri M. Crystal Structure of 2,2′-(((2,2-Dimethylpropane-1,3-diyl)bis(azanylylidene))bis(methanylylidene))bis(4-methoxyphenol)palladium(II) X-ray Structure Analysis Online, 2017, 33, 73 |
1551585 | CIF | C22 H32 N2 O2 | C 1 2/c 1 | 17.319; 9.7041; 13.352 90; 114.032; 90 | 2049.5 | MIKURIYA, Masahiro; MATSUSHIMA, Iyo; HANAMOTO, Yukiko; YOSHIOKA, Daisuke Synthesis and Crystal Structure of <i>N,N</i>′-Bis(2-hydroxy-3,5-dimethylbenzyl)-<i>N,N</i>′-dimethyl-1,2-ethanediamine X-ray Structure Analysis Online, 2017, 33, 1 |
1551586 | CIF | C9 H8 F3 N3 S | P -1 | 7.0109; 11.7862; 14.9095 111.814; 91.72; 101.036 | 1115.7 | OSMAN, Uwaisulqarni M.; FARIZAL, Azieda Syafika N.; ARSHAD, Suhana; KADIR, Maisara Abdul Crystal Structure of (<i>Z</i>)-1-[4-(Trifluoromethyl)benzylidene]thiosemicarbazide X-ray Structure Analysis Online, 2017, 33, 3 |
1551587 | CIF | C82 H100 B2 Cl2 Mg2 N4 O10 | C 1 2/c 1 | 22.7667; 19.1628; 17.3218 90; 96.15; 90 | 7513.6 | SAKIYAMA, Hiroshi; TAKAHATA, Saki; KASHIMOTO, Naoki; MITSUHASHI, Ryoji; MIKURIYA, Masahiro Crystal Structure of a Dinuclear Magnesium(II) Complex with 4-Chloro-2,6-bis[(2-hydroxyethyl)methylaminomethyl]phenolate X-ray Structure Analysis Online, 2017, 33, 75 |
1551588 | CIF | C43 H56 N4 Ni2 O11 | C 1 c 1 | 18.157; 13.1691; 18.88 90; 110.483; 90 | 4229 | LIM, Jongwan; SHIN, Yunseok; RYU, Sanghoon; MITSUHASHI, Ryoji; OMOTE, Masataka; SAKIYAMA, Hiroshi; MIKURIYA, Masahiro Ferromagnetic Dinuclear Nickel(II) Complex with a Schiff-base Having a Di-μ-phenolato-μ-methanol-bridged Core X-ray Structure Analysis Online, 2017, 33, 21 |
1551589 | CIF | C28 H26 Cl N6 O3.5 Ru | I 1 2/a 1 | 15.4085; 13.0737; 27.383 90; 98.0922; 90 | 5461.27 | TOYAMA, Mari; NAKAYASU, Toshifumi; NAGAO, Noriharu Crystal Structure of (2-Picolinato)bis(2,2′-bipyridine)ruthenium(II) Chloride X-ray Structure Analysis Online, 2017, 33, 11 |
1551590 | CIF | C20 H37 N O20 | P 21 21 21 | 8.7221; 9.697; 31.8548 90; 90; 90 | 2694.22 | FUJIMOTO, Takashi; YAMANO, Akihito; NISHIO, Toshiyuku; SAKAKI, Yohei; TASHIRO, Mitsuru Crystal Structure of β-D-Galactopyranosyl-(1\ρightarrow 6)-β-D-fructofuranosyl-(2↔1)-2-acetamido-2-deoxy-α-D-glucopyranoside X-ray Structure Analysis Online, 2017, 33, 35 |
1551591 | CIF | C8 H22 Mo2 N4 O4 S2 | C 1 2/c 1 | 13.975; 12.475; 12.158 90; 100.091; 90 | 2086.8 | MIKURIYA, Masahiro; KUSUNOKI, Koji; KOTERA, Takanori; YOSHIOKA, Daisuke; OGASAWARA, Kazuyoshi Synthesis, Crystal Structure, and DFT Calculation of a Dioxido-bridged Dinuclear Oxidomolybdenum(V) Complex with 2-(2-Aminoethyl)aminoethanethiol X-ray Structure Analysis Online, 2017, 33, 37 |
1551592 | CIF | C35 H46 B2 Cl2 Cu2 F8 N6 O5 | P 1 21/c 1 | 8.4305; 27.302; 19.131 90; 102.724; 90 | 4295.2 | UMEMOTO, Yusuke; YONEDA, Ko; YAMADA, Yasunori; KOIKAWA, Masayuki Synthesis and Crystal Structure of a Dinuclear Cu(II) Complex with <i>N,N,N</i>′,<i>N</i>′-Tetrakis(2-pyridylmethyl)-1,6-hexanediamine X-ray Structure Analysis Online, 2017, 33, 65 |
1551593 | CIF | C18 H21 Cl3 N3 O2.202 P | P 1 | 9.6898; 10.4576; 21.0199 83.6336; 89.3963; 73.819 | 2032.53 | ARIANI, Maral; POURAYOUBI, Mehrdad; DUŠEK, Michal; VAHDANI ALVIRI, Banafsheh; EIGNER, Václav; DAMODARAN, Krishnan Synthesis, Spectroscopic Study and Crystal Structure of a New Single-Enantiomer C(O)NHP(O)-based Phosphoric Triamide, CCl<sub>3</sub>C(O)NHP(O)[(R)-(+)-NHCH(CH<sub>3</sub>)(C<sub>6</sub>H<sub>5</sub>)]<sub>2</sub>·0.25H<sub>2</sub>O X-ray Structure Analysis Online, 2017, 33, 17 |
1551594 | CIF | C23 H29 N5 O5 | P -1 | 9.3554; 11.445; 11.5629 87.14; 78.807; 69.2119 | 1135.21 | GUILLON, Jean; MONTOIR, David; MARCHIVIE, Mathieu; DUFLOS, Muriel; BAZIN, Marc-Antoine Crystal Structure of <i>N</i>-(7-{[2-(Dimethylamino)ethyl]amino}-1-methyl-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-3,4,5-trimethoxybenzamide X-ray Structure Analysis Online, 2017, 33, 41 |
1551595 | CIF | C11 H14 B N O5 S | P 1 21/c 1 | 8.57927; 6.99494; 21.076 90; 99.4787; 90 | 1247.53 | TAKEYAMA, Tomoyuki; NAKAJIMA, Yuki; KATAGIRI, Kosuke; IWATSUKI, Satoshi Crystal Structure of a Methanesulfonate Salt of 3-(<i>N</i>-Methyl)quinolinium Boronic Acid X-ray Structure Analysis Online, 2017, 33, 9 |
1551596 | CIF | C23 H28 N Ni S10 | P 21 21 21 | 7.9129; 17.27; 21.673 90; 90; 90 | 2961.7 | KAKIHARA, Shunta; SAEKI, Masahiro; ICHIMURA, Shuhei; TAMAKI, Yoshinori; MIYAMURA, Kazuo Crystal Structure of Benzyldimethyl(ω-cyclohexylethyl)ammonium Bis(2-thioxo-1,3-dithiole-4,5-dithiolato)nickelate(III) X-ray Structure Analysis Online, 2017, 33, 15 |
1551826 | CIF | C194 H201 Cl8 N27 O54 Zn4 | P -1 | 20.5708; 21.4332; 24.3151 92.087; 91.4; 112.299 | 9903.7 | Jia-Cheng Chang; Shin-Han Tseng; Chien-Chen Lai; Yi-Hung Liu; Shie-Ming Peng; Sheng-Hsien Chiu Mechanically interlocked daisy-chain-like structures as multidimensional molecular muscles Nature Chemistry, 2017, 9, 128-134 |
1551827 | CIF | C55.5 H49.5 F6 N6 O6 | P -1 | 19.6706; 22.8014; 25.4507 99.269; 107.063; 106.023 | 10118.2 | Jia-Cheng Chang; Shin-Han Tseng; Chien-Chen Lai; Yi-Hung Liu; Shie-Ming Peng; Sheng-Hsien Chiu Mechanically interlocked daisy-chain-like structures as multidimensional molecular muscles Nature Chemistry, 2017, 9, 128-134 |
1551828 | CIF | C190 H147 Cl6 F18 N20 O44 Zn3 | P -1 | 12.1557; 24.1339; 39.3371 85.206; 87.55; 75.675 | 11139.3 | Jia-Cheng Chang; Shin-Han Tseng; Chien-Chen Lai; Yi-Hung Liu; Shie-Ming Peng; Sheng-Hsien Chiu Mechanically interlocked daisy-chain-like structures as multidimensional molecular muscles Nature Chemistry, 2017, 9, 128-134 |
1551829 | CIF | C124 H98 Cl4 F12 N10 O30 Zn2 | C 1 2 1 | 33.7737; 19.1957; 37.7788 90; 101.142; 90 | 24030.7 | Jia-Cheng Chang; Shin-Han Tseng; Chien-Chen Lai; Yi-Hung Liu; Shie-Ming Peng; Sheng-Hsien Chiu Mechanically interlocked daisy-chain-like structures as multidimensional molecular muscles Nature Chemistry, 2017, 9, 128-134 |
1551832 | CIF | C85.82 H25.82 B12 Cl5.46 F60 O12.99 | R -3 :H | 14.7965; 14.7965; 38.3211 90; 90; 120 | 7265.9 | Elaine A. Qian; Alex I. Wixtrom; Jonathan C. Axtell; Azin Saebi; Dahee Jung; Pavel Rehak; Yanxiao Han; Elamar Hakim Moully; Daniel Mosallaei; Sylvia Chow; Marco S. Messina; Jing Yang Wang; A. Timothy Royappa; Arnold L. Rheingold; Heather D. Maynard; Petr Kral; Alexander M. Spokoyny Atomically precise organomimetic cluster nanomolecules assembled via perfluoroaryl-thiol SNAr chemistry Nature Chemistry, 2017, 9, 333-340 |
1551833 | CIF | C156 H72 B12 F60 O12 | P -1 | 19.211; 19.674; 22.866 97.606; 114.089; 109.756 | 7048 | Elaine A. Qian; Alex I. Wixtrom; Jonathan C. Axtell; Azin Saebi; Dahee Jung; Pavel Rehak; Yanxiao Han; Elamar Hakim Moully; Daniel Mosallaei; Sylvia Chow; Marco S. Messina; Jing Yang Wang; A. Timothy Royappa; Arnold L. Rheingold; Heather D. Maynard; Petr Kral; Alexander M. Spokoyny Atomically precise organomimetic cluster nanomolecules assembled via perfluoroaryl-thiol SNAr chemistry Nature Chemistry, 2017, 9, 333-340 |
1551851 | CIF | C69 H118 N2 P4 Ti2 | P -1 | 10.838; 11.7188; 15.3855 111.957; 95.397; 103.468 | 1726.6 | Douglas P. Solowey; Manoj V. Mane,; Takashi Kurogi; Patrick J. Carroll; Brian C. Manor; Mu-Hyun Baik; Daniel J. Mindiola A new and selective cycle for dehydrogenation of linear and cyclic alkanes under mild conditions using a base metal Nature Chemistry, 2017, 9, 1126-1132 |
1551852 | CIF | C19 H15 P | P 1 21/c 1 | 10.1072; 9.2624; 15.2719 90; 93.254; 90 | 1427.4 | Douglas P. Solowey; Manoj V. Mane,; Takashi Kurogi; Patrick J. Carroll; Brian C. Manor; Mu-Hyun Baik; Daniel J. Mindiola A new and selective cycle for dehydrogenation of linear and cyclic alkanes under mild conditions using a base metal Nature Chemistry, 2017, 9, 1126-1132 |
1551886 | CIF | C31 H32 N4 Ni | P -1 | 8.4416; 10.8919; 7.2749 90.465; 113.158; 78.08 | 599.74 | Daniel R. Hummer; Bruce C. Noll; Robert M. Hazen; Robert T. Downs Crystal structure of abelsonite, the only known crystalline geoporphyrin American Mineralogist, 2017, 102, 1129-1132 |
1551889 | CIF | C29 H31 F14 N O Si | P 1 | 8.6241; 9.7969; 18.9232 80.469; 83.314; 76.243 | 1526.55 | Mattia Silvi; Charlie Verrier; Yannick P. Rey; Luca Buzzetti; Paolo Melchiorre Visible-light excitation of iminium ions enables the enantioselective catalytic beta-alkylation of enals Nature Chemistry, 2017, 9, 868-873 |
1551890 | CIF | C33 H26 O2 S | P 1 21 1 | 29.4752; 8.8183; 37.823 90; 97.4465; 90 | 9748.1 | Mattia Silvi; Charlie Verrier; Yannick P. Rey; Luca Buzzetti; Paolo Melchiorre Visible-light excitation of iminium ions enables the enantioselective catalytic beta-alkylation of enals Nature Chemistry, 2017, 9, 868-873 |
1551891 | CIF | C42 H46 B F18 N O2 Si | P 21 21 21 | 10.6934; 17.4932; 24.2485 90; 90; 90 | 4536 | Mattia Silvi; Charlie Verrier; Yannick P. Rey; Luca Buzzetti; Paolo Melchiorre Visible-light excitation of iminium ions enables the enantioselective catalytic beta-alkylation of enals Nature Chemistry, 2017, 9, 868-873 |
1551908 | CIF | C15 H13 B F2 N4 | P 1 21/c 1 | 13.747; 8.8403; 12.9567 90; 114.796; 90 | 1429.4 | Hai Qian; Morgan E. Cousins; Erik H. Horak; Audrey Wakefield; Matthew D. Liptak; Ivan Aprahamian Suppression of Kasha's rule as a mechanism for fluorescent molecular rotors and aggregation-induced emission Nature Chemistry, 2017, 9, 83-87 |
1551977 | CIF | C44 H28 Au N4 | P -1 | 6.1691; 10.6043; 12.4939 97.479; 97.453; 99.925 | 788.51 | Sebastian Preiss; Christoph Forster; Sven Otto; Matthias Bauer; Patrick Muller; Dariush Hinderberger; Haleh Hashemi Haeri; Luca Carella; Katja Heinze Structure and reactivity of a mononuclear gold(II) complex Nature Chemistry, 2017, 9, 1249-1255 |
1551978 | CIF | C88 H81 B F24 Ga N2 P2 Rh | P 1 21/n 1 | 16.1707; 13.4756; 40.4746 90; 99.5199; 90 | 8698.35 | Joseph A. B. Abdalla; Alexa Caise; Christian P. Sindlinger; Remi Tirfoin; Amber L. Thompson; Alison J. Edwards; Simon Aldridge Structural snapshots of concerted double E-H bond activation at a transition metal centre Nature Chemistry, 2017, 9, 1256-1262 |
1551979 | CIF | C87 H114 Al F37 Ga N2 O4 P2 Rh | P -1 | 15.8418; 17.8312; 19.9771 67.4818; 79.5277; 88.0398 | 5122.13 | Joseph A. B. Abdalla; Alexa Caise; Christian P. Sindlinger; Remi Tirfoin; Amber L. Thompson; Alison J. Edwards; Simon Aldridge Structural snapshots of concerted double E-H bond activation at a transition metal centre Nature Chemistry, 2017, 9, 1256-1262 |
1551980 | CIF | C71 H91 Al F36 Ga N2 O4 P2 Rh | P -1 | 11.0613; 18.6711; 20.1393 87.3183; 84.9976; 88.3665 | 4137.67 | Joseph A. B. Abdalla; Alexa Caise; Christian P. Sindlinger; Remi Tirfoin; Amber L. Thompson; Alison J. Edwards; Simon Aldridge Structural snapshots of concerted double E-H bond activation at a transition metal centre Nature Chemistry, 2017, 9, 1256-1262 |
1551981 | CIF | C72 H93 Al F36 Ga N2 O4 P2 Rh | P -1 | 18.3055; 20.3348; 22.683 95.335; 90.4516; 93.0358 | 8394.4 | Joseph A. B. Abdalla; Alexa Caise; Christian P. Sindlinger; Remi Tirfoin; Amber L. Thompson; Alison J. Edwards; Simon Aldridge Structural snapshots of concerted double E-H bond activation at a transition metal centre Nature Chemistry, 2017, 9, 1256-1262 |
1551982 | CIF | C95 H119.5 Al F36.5 Ga2 N4 O4 P Rh | P -1 | 13.5818; 19.8497; 19.8951 95.6299; 90.1027; 91.1299 | 5336.67 | Joseph A. B. Abdalla; Alexa Caise; Christian P. Sindlinger; Remi Tirfoin; Amber L. Thompson; Alison J. Edwards; Simon Aldridge Structural snapshots of concerted double E-H bond activation at a transition metal centre Nature Chemistry, 2017, 9, 1256-1262 |
1552008 | CIF | C39 H63 Th | P 1 21/n 1 | 10.7341; 19.6772; 17.8417 90; 104.847; 90 | 3642.65 | Alasdair Formanuik; Ana-Maria Ariciu; Fabrizio Ortu; Reece Beekmeyer; Andrew Kerridge; Floriana Tuna; Eric J. L. McInnes; David P. Mills Actinide covalency measured by pulsed electron paramagnetic resonance spectroscopy Nature Chemistry, 2017, 9, 578-583 |
1552009 | CIF | C39 H63 U | P 1 21/n 1 | 10.7925; 19.3497; 17.8721 90; 104.314; 90 | 3616.4 | Alasdair Formanuik; Ana-Maria Ariciu; Fabrizio Ortu; Reece Beekmeyer; Andrew Kerridge; Floriana Tuna; Eric J. L. McInnes; David P. Mills Actinide covalency measured by pulsed electron paramagnetic resonance spectroscopy Nature Chemistry, 2017, 9, 578-583 |
1552010 | CIF | C39 H63 Cl U | P 1 21/c 1 | 20.1; 21.4218; 20.1165 90; 118.596; 90 | 7605.1 | Alasdair Formanuik; Ana-Maria Ariciu; Fabrizio Ortu; Reece Beekmeyer; Andrew Kerridge; Floriana Tuna; Eric J. L. McInnes; David P. Mills Actinide covalency measured by pulsed electron paramagnetic resonance spectroscopy Nature Chemistry, 2017, 9, 578-583 |
1552051 | CIF | C34 H14 Br4 N4 | P 1 21/n 1 | 11.2408; 4.6467; 25.9293 90; 99.857; 90 | 1334.36 | Wei Liu; Xin Luo; Yang Bao; Yan Peng Liu; Guo-Hong Ning; Ibrahim Abdelwahab; Linjun Li; Chang Tai Nai; Zhi Gang Hu; Dan Zhao; Bin Liu; Su Ying Quek; Kian Ping Loh A two-dimensional conjugated aromatic polymer via C-C coupling reaction Nature Chemistry, 2017, 9, 563-570 |
1552052 | CIF | C34 H18 N4 | P 1 21/c 1 | 3.77; 16.615; 17.088 90; 95.723; 90 | 1065 | Wei Liu; Xin Luo; Yang Bao; Yan Peng Liu; Guo-Hong Ning; Ibrahim Abdelwahab; Linjun Li; Chang Tai Nai; Zhi Gang Hu; Dan Zhao; Bin Liu; Su Ying Quek; Kian Ping Loh A two-dimensional conjugated aromatic polymer via C-C coupling reaction Nature Chemistry, 2017, 9, 563-570 |
1552957 | CIF | C4 H12 K Na O10 | P 21 21 2 | 11.7721; 14.2054; 6.1836 90; 90; 90 | 1034.07 | Macdonald, Niall P.; Bunton, Grace L.; Park, Ah Young; Breadmore, Michael C.; Kilah, Nathan L. 3D Printed Micrometer-Scale Polymer Mounts for Single Crystal Analysis. Analytical chemistry, 2017, 89, 4405-4408 |
1552958 | CIF | C4 H12 K Na O10 | P 21 21 2 | 11.7708; 14.2037; 6.1841 90; 90; 90 | 1033.91 | Macdonald, Niall P.; Bunton, Grace L.; Park, Ah Young; Breadmore, Michael C.; Kilah, Nathan L. 3D Printed Micrometer-Scale Polymer Mounts for Single Crystal Analysis. Analytical chemistry, 2017, 89, 4405-4408 |
1553307 | CIF | C44.25 H74 N5 O11 | P 1 21 1 | 14.6436; 10.578; 15.5742 90; 92.794; 90 | 2409.58 | Almaliti, Jehad; Malloy, Karla L.; Glukhov, Evgenia; Spadafora, Carmenza; Gutiérrez, Marcelino; Gerwick, William H. Dudawalamides A-D, Antiparasitic Cyclic Depsipeptides from the Marine Cyanobacterium Moorea producens. Journal of natural products, 2017, 80, 1827-1836 |
1553308 | CIF | C19 H18 O2 | P 1 21/c 1 | 14.6675; 11.5099; 18.5162 90; 104.72; 90 | 3023.34 | Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence Total Synthesis of Tedarene A. Journal of natural products, 2017, 80, 1623-1630 |
1553309 | CIF | C20 H20 O2 | P 1 21/n 1 | 9.3466; 12.3756; 14.0627 90; 98.832; 90 | 1607.34 | Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence Total Synthesis of Tedarene A. Journal of natural products, 2017, 80, 1623-1630 |
1553310 | CIF | C20 H20 O2 | P 1 21 1 | 9.0364; 8.1877; 10.7482 90; 101.86; 90 | 778.25 | Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence Total Synthesis of Tedarene A. Journal of natural products, 2017, 80, 1623-1630 |
1553311 | CIF | C19 H18 O2 | P -1 | 9.7921; 11.467; 13.899 88.098; 79.234; 79.122 | 1505.6 | Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence Total Synthesis of Tedarene A. Journal of natural products, 2017, 80, 1623-1630 |
1553312 | CIF | C35 H44 O12 | P 21 21 2 | 15.7364; 19.8524; 11.454 90; 90; 90 | 3578.3 | Esposito, Mélissa; Nothias, Louis-Félix; Retailleau, Pascal; Costa, Jean; Roussi, Fanny; Neyts, Johan; Leyssen, Pieter; Touboul, David; Litaudon, Marc; Paolini, Julien Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking. Journal of natural products, 2017, 80, 2051-2059 |
1553407 | CIF | C42 H54 Cl4 N4 Ni2 O2 | P -1 | 9.7278; 10.55; 11.522 91.22; 109.68; 108.69 | 1043.6 | Zhang, Youfu; Huang, Chuanbing; Wang, Xinxin; Mahmood, Qaiser; Hao, Xiang; Hu, Xinquan; Guo, Cun-Yue; Solan, Gregory A.; Sun, Wen-Hua Highly branched unsaturated polyethylenes achievable using strained imino-cyclopenta[b]pyridyl-nickel precatalysts Polymer Chemistry, 2017, 8, 995 |
1553408 | CIF | C36 H40 Cl2 N4 Ni | P 1 21/n 1 | 9.0742; 14.496; 12.391 90; 98.03; 90 | 1613.9 | Zhang, Youfu; Huang, Chuanbing; Wang, Xinxin; Mahmood, Qaiser; Hao, Xiang; Hu, Xinquan; Guo, Cun-Yue; Solan, Gregory A.; Sun, Wen-Hua Highly branched unsaturated polyethylenes achievable using strained imino-cyclopenta[b]pyridyl-nickel precatalysts Polymer Chemistry, 2017, 8, 995 |
1553409 | CIF | C17 H20 Br N O5 | P -1 | 5.2286; 8.35; 20.2441 79.956; 89.888; 81.369 | 860.17 | Xie, Tongqing; Zhang, Baicheng; Zhang, Xuepeng; Zhang, Guoqing AIE-active β-diketones containing pyridiniums: fluorogenic binding to cellulose and water-vapour-recoverable mechanochromic luminescence Materials Chemistry Frontiers, 2017, 1, 693 |
1553410 | CIF | C46 H44 Br2 N2 Ni | C 1 2/c 1 | 9.6692; 15.1682; 28.4042 90; 95.927; 90 | 4143.61 | Sui, Xuelin; Hong, Changwen; Pang, Wenmin; Chen, Changle Unsymmetrical α-diimine palladium catalysts and their properties in olefin (co)polymerization Materials Chemistry Frontiers, 2017, 1, 967 |
1553411 | CIF | C56 H49 Cl3 N2 Pd | P 1 21/n 1 | 10.7748; 24.3601; 18.0013 90; 95.951; 90 | 4699.4 | Sui, Xuelin; Hong, Changwen; Pang, Wenmin; Chen, Changle Unsymmetrical α-diimine palladium catalysts and their properties in olefin (co)polymerization Materials Chemistry Frontiers, 2017, 1, 967 |
1553412 | CIF | C47 H47 Cl N2 Pd | P -1 | 13.1491; 19.2193; 19.3227 105.127; 109.315; 96.896 | 4333 | Sui, Xuelin; Hong, Changwen; Pang, Wenmin; Chen, Changle Unsymmetrical α-diimine palladium catalysts and their properties in olefin (co)polymerization Materials Chemistry Frontiers, 2017, 1, 967 |
1553413 | CIF | C28 H20 S | I 1 2 1 | 15.4081; 6.0485; 22.1271 90; 102.299; 90 | 2014.83 | Nie, Han; Hu, Kun; Cai, Yuanjing; Peng, Qian; Zhao, Zujin; Hu, Rongrong; Chen, Junwu; Su, Shi-Jian; Qin, Anjun; Tang, Ben Zhong Tetraphenylfuran: aggregation-induced emission or aggregation-caused quenching? Materials Chemistry Frontiers, 2017, 1, 1125 |
1553414 | CIF | C28 H20 O | I 1 2/c 1 | 21.71; 8.16; 24.855 90; 113.396; 90 | 4041 | Nie, Han; Hu, Kun; Cai, Yuanjing; Peng, Qian; Zhao, Zujin; Hu, Rongrong; Chen, Junwu; Su, Shi-Jian; Qin, Anjun; Tang, Ben Zhong Tetraphenylfuran: aggregation-induced emission or aggregation-caused quenching? Materials Chemistry Frontiers, 2017, 1, 1125 |
1553415 | CIF | C40 H26 N2 O2 S2 | P -1 | 10.495; 11.772; 13.789 81.56; 71.751; 72.938 | 1543.9 | Keshav, Karunesh; Kumawat, Mukesh Kumar; Srivastava, Rohit; Ravikanth, M. Benzothiazoles-substituted tetraphenylethylenes: synthesis, structure, aggregation-induced emission and biological studies Materials Chemistry Frontiers, 2017, 1, 1207 |
1553416 | CIF | C42 H30 N2 O2 S2 | P -1 | 13.352; 16.32; 17.943 99.33; 104.402; 108.992 | 3452.4 | Keshav, Karunesh; Kumawat, Mukesh Kumar; Srivastava, Rohit; Ravikanth, M. Benzothiazoles-substituted tetraphenylethylenes: synthesis, structure, aggregation-induced emission and biological studies Materials Chemistry Frontiers, 2017, 1, 1207 |
1553417 | CIF | C78 H82 N4 O16 Zn3 | P -1 | 11.4427; 14.514; 16.196 65.694; 69.783; 73.998 | 2272.2 | King, Stephen Charles; Lin, Rui-Biao; Wang, Hailong; Arman, Hadi D.; Chen, Banglin Two-dimensional metal‒organic frameworks for selective separation of CO2/CH4 and CO2/N2 Materials Chemistry Frontiers, 2017, 1, 1514 |
1553497 | CIF | C19 H17 N O4 | P -1 | 8.125; 9.328; 11.408 90.91; 96.19; 107.69 | 817.8 | Dai, Jie; Ren, Wenlong; Chang, Wenju; Zhang, Ping; Shi, Yian An effective route to β2-amino acid derivatives via Pd-catalyzed regioselective hydrocarboxylation of 1,2-disubstituted enimides Organic Chemistry Frontiers, 2017, 4, 297 |
1553519 | CIF | C36 H32 F2 N2 O2 | P 21 21 21 | 11.5593; 14.0068; 17.8914 90; 90; 90 | 2896.78 | Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles Organic Chemistry Frontiers, 2017, 4, 57 |
1553520 | CIF | C44 H50 N2 | P 1 21/c 1 | 19.661; 10.71; 17.118 90; 97.306; 90 | 3575 | Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles Organic Chemistry Frontiers, 2017, 4, 57 |
1553521 | CIF | C16 H18 O3 S | P -1 | 6.9478; 9.1969; 11.8012 82.206; 81.643; 75.22 | 717.55 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553522 | CIF | C15 H16 O2 S | P 1 21/n 1 | 7.68603; 23.9176; 7.76261 90; 111.053; 90 | 1331.76 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553523 | CIF | C14 H11 N S | P 1 21/n 1 | 5.7042; 25.743; 7.8069 90; 94.59; 90 | 1142.71 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553524 | CIF | C15 H14 O S | P 1 21/n 1 | 5.7958; 25.4544; 8.3123 90; 93.626; 90 | 1223.85 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553525 | CIF | C15 H14 O2 S | P 1 21/n 1 | 5.611; 25.6833; 8.991 90; 98.982; 90 | 1279.8 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553526 | CIF | C14 H11 N O S | P 1 21/n 1 | 5.67633; 26.8781; 7.7875 90; 95.042; 90 | 1183.53 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553527 | CIF | C14 H8 N2 S2 | P -1 | 7.8232; 11.6428; 14.5818 84.863; 83.654; 73.557 | 1263.68 | Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang Nickel-catalyzed direct formation of the C‒S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent Organic Chemistry Frontiers, 2017, 4, 31 |
1553530 | CIF | C35 H53 N O3 | P 1 21 1 | 7.455; 11.3624; 18.4877 90; 92.585; 90 | 1564.44 | Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum Organic Chemistry Frontiers, 2017, 4, 42 |
1553531 | CIF | C30 H50 O3 | P 21 21 21 | 6.52391; 12.9427; 31.7963 90; 90; 90 | 2684.78 | Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum Organic Chemistry Frontiers, 2017, 4, 42 |
1553543 | CIF | C22 H21 N O2 | P 1 21/n 1 | 7.348; 22.781; 11.236 90; 101.092; 90 | 1845.7 | Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides Organic Chemistry Frontiers, 2017, 4, 77 |
1553544 | CIF | C15 H16 N2 O3 | P 1 21/n 1 | 9.3103; 4.8793; 30.741 90; 96.596; 90 | 1387.3 | Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides Organic Chemistry Frontiers, 2017, 4, 77 |
1553545 | CIF | C25 H21 N O2 S | R 3 c :H | 33.922; 33.922; 11.008 90; 90; 120 | 10970 | Gong, Xinxing; Li, Guangming; Wu, Jie Synthesis of polycyclic sultams via a palladium-catalyzed reaction of 1-bromo-2-(cyclopropylidenemethyl)benzenes with 2-alkynylbenzenesulfonamides Organic Chemistry Frontiers, 2017, 4, 14 |
1553547 | CIF | C18 H12 Br2 | P 1 21/n 1 | 5.3248; 17.2473; 7.6729 90; 96.167; 90 | 700.59 | Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B. Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap Organic Chemistry Frontiers, 2017, 4, 658 |
1553548 | CIF | C20 H16 Br2 | P 1 21/c 1 | 6.6723; 8.653; 15.099 90; 111.66; 90 | 810.2 | Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B. Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap Organic Chemistry Frontiers, 2017, 4, 658 |
1553549 | CIF | C28 H16 Br2 | C 1 2/c 1 | 21.802; 4.9336; 18.875 90; 90.188; 90 | 2030.2 | Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B. Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap Organic Chemistry Frontiers, 2017, 4, 658 |
1553550 | CIF | C36 H32 Br2 | P -1 | 10.0648; 11.6684; 12.2462 77.981; 86.017; 79.287 | 1381.44 | Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B. Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap Organic Chemistry Frontiers, 2017, 4, 658 |
1553551 | CIF | C34 H28 Br2 | P 1 21/n 1 | 11.131; 10.249; 11.763 90; 101.301; 90 | 1315.92 | Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B. Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap Organic Chemistry Frontiers, 2017, 4, 658 |
1553552 | CIF | C50 H38 | P -1 | 10.8252; 13.5794; 14.2122 114.377; 91.316; 95.604 | 1889.2 | Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B. Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap Organic Chemistry Frontiers, 2017, 4, 658 |
1553554 | CIF | C18 H15 I O Se | C 1 2/c 1 | 20.3; 5.882; 27.651 90; 94.075; 90 | 3293 | Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives Organic Chemistry Frontiers, 2017, 4, 277 |
1553555 | CIF | C20 H19 I O Se | P 1 2/c 1 | 19.0809; 5.7136; 17.2112 90; 100.175; 90 | 1846.87 | Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives Organic Chemistry Frontiers, 2017, 4, 277 |
1553556 | CIF | C29 H25 Cl N2 O8 S | P 1 21 1 | 11.4186; 9.7011; 13.152 90; 92.473; 90 | 1455.5 | He, Fu-Sheng; Li, Cong-Shan; Deng, Hua; Zheng, Xing; Yang, Zhong-Tao; Deng, Wei-Ping The facile and stereoselective synthesis of pyrrolidine β-amino acids via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition Organic Chemistry Frontiers, 2017, 4, 52 |
1553557 | CIF | C25 H18 O2 | P n 21 a | 14.3717; 5.917; 21.4597 90; 90; 90 | 1824.88 | Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G. Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans Organic Chemistry Frontiers, 2017, 4, 972 |
1553558 | CIF | C20 H14 O | P 21 21 21 | 7.9447; 10.3826; 17.0108 90; 90; 90 | 1403.16 | Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G. Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans Organic Chemistry Frontiers, 2017, 4, 972 |
1553559 | CIF | C27 H31 N O7 S3 | P 1 21/c 1 | 21.226; 8.2493; 16.985 90; 109.61; 90 | 2801.6 | Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes Organic Chemistry Frontiers, 2017, 4, 135 |
1553560 | CIF | C15 H21 N O3 S | C 1 2/c 1 | 25.961; 5.793; 22.2512 90; 114.088; 90 | 3055 | Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes Organic Chemistry Frontiers, 2017, 4, 135 |
1553561 | CIF | C18 H16 F3 N O2 S2 | P -1 | 6.52; 8.149; 18.175 102.278; 95.21; 97.731 | 927.9 | Chen, Min-Tao; Tang, Xiang-Ying; Shi, Min A facile approach for the trifluoromethylthiolation of methylenecyclopropanes Organic Chemistry Frontiers, 2017, 4, 86 |
1553562 | CIF | C17 H15 N O2 | P -1 | 13.451; 14.313; 15.248 86.714; 63.827; 90.014 | 2629.2 | Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles Organic Chemistry Frontiers, 2017, 4, 124 |
1553563 | CIF | C26 H20 Cl N O3 | P -1 | 7.3875; 11.6702; 13.4944 64.647; 82.911; 77.69 | 1026.5 | Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles Organic Chemistry Frontiers, 2017, 4, 124 |
1553564 | CIF | C23 H24 N2 O6 S | P -1 | 8.5455; 12.047; 12.1501 60.733; 81.883; 87.112 | 1079.97 | Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles Organic Chemistry Frontiers, 2017, 4, 124 |
1553565 | CIF | C44 H52 N4 S4 | P -1 | 9.3265; 9.7095; 23.593 78.225; 84.998; 75.52 | 2023.6 | Xia, Debin; Keerthi, Ashok; An, Cunbin; Baumgarten, Martin Synthesis of a quinoidal dithieno[2,3-d;2′,3′-d]benzo[2,1-b;3,4-b′]-dithiophene based open-shell singlet biradicaloid Organic Chemistry Frontiers, 2017, 4, 18 |
1553566 | CIF | C20 H21 N O8 | P 1 21/c 1 | 8.101; 19.041; 13.693 90; 107.19; 90 | 2017.8 | Zhang, Li; Zhang, Beichen; Jiang, Teng; Lu, Tao; Zhou, Qingfa Synthesis of tricyclic 3-hydroxyisoindolin-1-ones via triethylamine-catalyzed domino reactions of electron-deficient alkynes with phthalimidomalonate derivatives Organic Chemistry Frontiers, 2017, 4, 119 |
1553567 | CIF | C22 H16 Cl N O2 | P 1 21/n 1 | 11.366; 11.305; 14.788 90; 110.536; 90 | 1779.4 | Zhu, Chao-Qun; Deng, Zhuo-Fei; Zhang, Yahong; Wang, You-Qing Synthesis of 4-substituted 3-(2-hydroxyphenyl)-quinolines through an unexpected iron(iii) chloride promoted reaction of cyclic imine dibenzo[b,f][1,4]oxazepines with alkynes Organic Chemistry Frontiers, 2017, 4, 196 |
1553568 | CIF | C33 H30 N4 O3 | P 1 21 1 | 8.902; 13.209; 12.059 90; 99.65; 90 | 1397.9 | Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst Organic Chemistry Frontiers, 2017, 4, 101 |
1553569 | CIF | C31 H27 Br N4 O3 | P 21 21 21 | 9.662; 12.286; 24.441 90; 90; 90 | 2901 | Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst Organic Chemistry Frontiers, 2017, 4, 101 |
1553570 | CIF | C25 H23 N O3 | P 41 | 8.4091; 8.4091; 29.3175 90; 90; 90 | 2073.13 | Xu, Meng-Meng; Wang, Hai-Qing; Wan, Ying; He, Guofeng; Yan, Jingjing; Zhang, Shu; Wang, Shu-Liang; Shi, Feng Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes Organic Chemistry Frontiers, 2017, 4, 358 |
1553571 | CIF | C15 H17 Cl N2 O3 | P 21 21 21 | 7.2915; 12.7983; 15.9552 90; 90; 90 | 1488.92 | Peng, Xiao-Jiao; Ho, Yee Ann; Wang, Zhi-Peng; Shao, Pan-Lin; Zhao, Yu; He, Yun Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles Organic Chemistry Frontiers, 2017, 4, 81 |
1553572 | CIF | C15 H11 Cl F3 N3 O3 | P 21 21 21 | 7.74798; 9.1129; 21.719 90; 90; 90 | 1533.5 | Hao, Xin-Qi; Wang, Cong; Liu, Shuang-Liang; Wang, Xiao; Wang, Li; Gong, Jun-Fang; Song, Mao-Ping Cobalt(ii)/(imidazoline‒oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes Organic Chemistry Frontiers, 2017, 4, 308 |
1553573 | CIF | C14 H13 N3 O S | P -1 | 7.68; 8.494; 11.449 85.96; 77.314; 66.467 | 667.9 | Chen, Jichao; Wang, Tianyu; Wang, Tong; Lin, Aijun; Yao, Hequan; Xu, Jinyi Copper-catalyzed C5-selective thio/selenocyanation of 8-aminoquinolines Organic Chemistry Frontiers, 2017, 4, 130 |
1553574 | CIF | C19 H23 Br N O3 P | P 21 21 2 | 9.8916; 26.4389; 7.7778 90; 90; 90 | 2034.1 | Wang, Xubin; Wang, Xiaoming; Han, Zhaobin; Wang, Zheng; Ding, Kuiling Palladium-catalyzed asymmetric allylic amination: enantioselective synthesis of chiral α-methylene substituted β-aminophosphonates Organic Chemistry Frontiers, 2017, 4, 271 |
1553575 | CIF | C153.47 H187.47 Cl4.41 N2 Si8 | P 41 21 2 | 21.2715; 21.2715; 64.3247 90; 90; 90 | 29105.4 | Ushiyama, Ayako; Hiroto, Satoru; Yuasa, Junpei; Kawai, Tsuyoshi; Shinokubo, Hiroshi Synthesis of a figure-eight azahelicene dimer with high emission and CPL properties Organic Chemistry Frontiers, 2017, 4, 664 |
1553576 | CIF | C21 H21 Cl F N O2 | P 1 21/c 1 | 9.4639; 21.8249; 9.3192 90; 104.752; 90 | 1861.42 | Li, Jianxiao; Hu, Weigao; Li, Chunsheng; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng Palladium-catalyzed cascade reaction of haloalkynes with unactivated alkenes for assembly of functionalized oxetanes Organic Chemistry Frontiers, 2017, 4, 373 |
1553577 | CIF | C15 H15 Br O2 | P 1 21 1 | 7.813; 5.321; 15.394 90; 91.594; 90 | 639.7 | Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities Organic Chemistry Frontiers, 2017, 4, 1084 |
1553578 | CIF | C11 H14 Br F O2 | P 21 21 21 | 5.651; 16.364; 38.4918 90; 90; 90 | 3559 | Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities Organic Chemistry Frontiers, 2017, 4, 1084 |
1553579 | CIF | C17 H12 B F2 N5 O | C 1 2/c 1 | 10.248; 14.634; 11.146 90; 107.352; 90 | 1595.5 | Barbon, Stephanie M.; Novoa, Samantha; Bender, Desiree; Groom, Hilary; Luyt, Leonard G.; Gilroy, Joe B. Copper-assisted azide‒alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates Organic Chemistry Frontiers, 2017, 4, 178 |
1553580 | CIF | C16 H10 Br2 Cl F3 | P -1 | 7.3184; 13.4865; 17.4149 101.672; 94.139; 101.918 | 1635.33 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553581 | CIF | C20 H20 Br F3 O | P -1 | 7.8481; 10.5581; 12.2042 75.472; 72.741; 72.301 | 905.55 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553582 | CIF | C20 H20 Br F3 O2 | P -1 | 8.3533; 9.4941; 12.1934 100.216; 97.306; 100.289 | 923.7 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553583 | CIF | C18 H15 Br2 F3 | P b c a | 16.4974; 6.84171; 28.6498 90; 90; 90 | 3233.72 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553584 | CIF | C16 H11 Br2 F3 | P -1 | 7.1399; 9.7404; 22.8361 97.673; 97.146; 106.455 | 1487.32 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553585 | CIF | C17 H12 Br F3 | C 1 2/c 1 | 22.8229; 7.4881; 16.5828 90; 102.102; 90 | 2771 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553586 | CIF | C19 H17 Br Cl F3 | P 1 21/c 1 | 8.2233; 22.8182; 10.0565 90; 109.447; 90 | 1779.36 | Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V. Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes Organic Chemistry Frontiers, 2017, 4, 255 |
1553587 | CIF | C12 H11 I N2 O2 | C m c e | 6.9379; 19.798; 17.773 90; 90; 90 | 2441.2 | He, Xin; Xu, Yi-zhu; Kong, Ling-xuan; Wu, Huan-huan; Ji, De-zhong; Wang, Zhi-bin; Xu, Yun-gen; Zhu, Qi-hua Copper(i) and N-fluorobenzenesulfonimide-mediated direct regioselective halogenation of 8-amidoquinolines on the C5 position Organic Chemistry Frontiers, 2017, 4, 1046 |
1553588 | CIF | C46 H66 Cl2 | P 1 21/n 1 | 10.4263; 10.2668; 40.789 90; 90.6212; 90 | 4366 | Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R. Polymerization of acetylene: polyynes, but not carbyne Organic Chemistry Frontiers, 2017, 4, 668 |
1553589 | CIF | C47 H64 | P -1 | 10.3367; 10.4631; 19.275 88.5549; 78.0127; 88.5903 | 2038.2 | Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R. Polymerization of acetylene: polyynes, but not carbyne Organic Chemistry Frontiers, 2017, 4, 668 |
1553590 | CIF | C49 H64 | P 3 1 c | 14.154; 14.154; 12.123 90; 90; 120 | 2103.3 | Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R. Polymerization of acetylene: polyynes, but not carbyne Organic Chemistry Frontiers, 2017, 4, 668 |
1553591 | CIF | C20 H13 F7 N2 O | P 1 21/c 1 | 7.858; 26.656; 8.984 90; 90.001; 90 | 1881.8 | Xu, Jun; Qiao, Li; Ying, Beibei; Zhu, Xiaolei; Shen, Chao; Zhang, Pengfei Transition-metal-free direct perfluoroalkylation of quinoline amides at C5 position through radical cross-coupling under mild conditions Organic Chemistry Frontiers, 2017, 4, 1116 |
1553592 | CIF | C44 H58 N2 Se2 Si4 | P 1 21/n 1 | 14.2771; 14.228; 22.6224 90; 99.427; 90 | 4533.33 | Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C. Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Organic Chemistry Frontiers, 2017, 4, 682 |
1553593 | CIF | C44 H58 N2 S2 Si4 | P 1 21/n 1 | 14.2494; 14.1245; 22.4876 90; 98.8; 90 | 4472.7 | Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C. Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Organic Chemistry Frontiers, 2017, 4, 682 |
1553594 | CIF | C32 H22 Br8 N2 | P -1 | 10.8503; 12.4427; 12.9897 100.306; 91.28; 108.652 | 1628.82 | Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C. Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Organic Chemistry Frontiers, 2017, 4, 682 |
1553595 | CIF | C50 H52 N14 O4 | P 1 21/c 1 | 9.842; 21.609; 25.234 90; 91.32; 90 | 5365.2 | Zhang, Qian; Wang, Mei-Xiang Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule Organic Chemistry Frontiers, 2017, 4, 283 |
1553596 | CIF | C54.83 H62.12 Cl1.76 N16.83 O2 | C 1 2/c 1 | 28.402; 9.816; 18.722 90; 90.7; 90 | 5219.2 | Zhang, Qian; Wang, Mei-Xiang Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule Organic Chemistry Frontiers, 2017, 4, 283 |
1553597 | CIF | C54 H60 N16 O2 | P -1 | 9.6636; 15.1098; 18.1939 69.768; 84.466; 84.513 | 2475.53 | Zhang, Qian; Wang, Mei-Xiang Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule Organic Chemistry Frontiers, 2017, 4, 283 |
1553598 | CIF | C40 H24 S2 | P -1 | 7.5051; 8.6296; 11.6509 73.729; 77.669; 77.532 | 697.78 | Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices Organic Chemistry Frontiers, 2017, 4, 675 |
1553599 | CIF | C46 H32 | P n a 21 | 16.8864; 7.4906; 24.7447 90; 90; 90 | 3129.94 | Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices Organic Chemistry Frontiers, 2017, 4, 675 |
1553600 | CIF | C44 H28 | P -1 | 7.597; 8.9994; 11.0344 78.931; 75.805; 83.409 | 715.94 | Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices Organic Chemistry Frontiers, 2017, 4, 675 |
1553601 | CIF | C26 H22 N4 O5 S | C 1 2/c 1 | 26.478; 8.1615; 23.0582 90; 96.411; 90 | 4951.7 | Chen, Dianpeng; Xing, Gangdong; Yao, Jinzhong; Zhou, Hongwei Applicable β-sulfonium carbanions: facile construction of thiophene derivatives Organic Chemistry Frontiers, 2017, 4, 1042 |
1553602 | CIF | C12 H9 N O S3 | P b c n | 7.9629; 16.9905; 18.7808 90; 90; 90 | 2540.92 | Chen, Qiao; Lei, Yingjie; Wang, Yanfang; Wang, Chao; Wang, Yanan; Xu, Zhaoqing; Wang, Huan; Wang, Rui Direct thiocyanation of ketene dithioacetals under transition-metal-free conditions Organic Chemistry Frontiers, 2017, 4, 369 |
1553603 | CIF | C71 H46 B F24 Ir N O P | P 21 21 21 | 12.2302; 15.3106; 36.571 90; 90; 90 | 6848 | Wang, Qian; Zhang, Zongpeng; Chen, Caiyou; Yang, Hailong; Han, Zhengyu; Dong, Xiu-Qin; Zhang, Xumu Iridium catalysts with modular axial-unfixed biphenyl phosphine‒oxazoline ligands: asymmetric hydrogenation of α,β-unsaturated carboxylic acids Organic Chemistry Frontiers, 2017, 4, 627 |
1553604 | CIF | C26 H16 Cu N4 O8 | P 1 21/c 1 | 11.1134; 21.1702; 9.8578 90; 101.189; 90 | 2275.19 | Baur, Andreas; Bustin, Katelyn A.; Aguilera, Ellen; Petersen, Jeffrey L.; Hoover, Jessica M. Copper and silver benzoate and aryl complexes and their implications for oxidative decarboxylative coupling reactions Organic Chemistry Frontiers, 2017, 4, 519 |
1553605 | CIF | C16 H11 N O3 | P 1 21/c 1 | 8.269; 9.296; 16.904 90; 93.281; 90 | 1297.3 | Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones Organic Chemistry Frontiers, 2017, 4, 292 |
1553606 | CIF | C22 H15 N O2 | P b c a | 8.874; 13.733; 27.215 90; 90; 90 | 3317 | Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones Organic Chemistry Frontiers, 2017, 4, 292 |
1553607 | CIF | C19 H12 N2 O4 | P -1 | 8.066; 8.242; 12.157 92.727; 102.604; 98.233 | 778 | Li, Yingying; Gao, Mingchun; Liu, Bingxin; Xu, Bin Copper nitrate-mediated chemo- and regioselective annulation from two different alkynes: a direct route to isoxazoles Organic Chemistry Frontiers, 2017, 4, 445 |
1553608 | CIF | C H F N O | P -1 | 9.4574; 9.9936; 14.0156 89.023; 76.071; 71.074 | 1213.5 | Xu, Jian; Song, Qiuling Synthesis of fully-substituted 1,2,3-triazoles via copper(i)-catalyzed three-component coupling of sulfoximines, alkynes and azides Organic Chemistry Frontiers, 2017, 4, 938 |
1553609 | CIF | C41 H40 O11 | P -1 | 9.7469; 13.1171; 17.5212 70.806; 75.292; 73.524 | 1996.5 | Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng Total synthesis of I3,II8-biapigenin and ridiculuflavone A Organic Chemistry Frontiers, 2017, 4, 578 |
1553610 | CIF | C43 H46 O11 | P -1 | 15.1534; 15.8118; 17.7296 68.774; 76.898; 79.352 | 3832 | Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng Total synthesis of I3,II8-biapigenin and ridiculuflavone A Organic Chemistry Frontiers, 2017, 4, 578 |
1553611 | CIF | C31 H23 Cl0 N O4 | P 21 21 21 | 9.9046; 10.4946; 23.736 90; 90; 90 | 2467.2 | Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins Organic Chemistry Frontiers, 2017, 4, 560 |
1553612 | CIF | C30 H21 N O3 | P 1 21/n 1 | 9.263; 16.211; 15.413 90; 91.21; 90 | 2313.9 | Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins Organic Chemistry Frontiers, 2017, 4, 560 |
1553613 | CIF | C38.5 H33 Cl O3 | P -1 | 12.3342; 12.422; 20.4886 94.35; 97.642; 100.981 | 3037.8 | Zhang, Yuexia; Wu, Xingxing; Hao, Lin; Wong, Zeng Rong; Lauw, Sherman J. L.; Yang, Song; Webster, Richard D.; Chi, Yonggui Robin Trimerization of enones under air enabled by NHC/NaOtBu via a SET radical pathway Organic Chemistry Frontiers, 2017, 4, 467 |
1553614 | CIF | C13 H12 N2 O | P n a 21 | 9.077; 10.4; 11.75 90; 90; 90 | 1109.2 | Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming A copper-catalyzed arylation/nucleophilic addition/fragmentation/C‒S bond formation cascade: synthesis of bis(arylthio)imines Organic Chemistry Frontiers, 2017, 4, 510 |
1553615 | CIF | C23 H19 N O2 S2 | P 21 21 21 | 8.189; 14.782; 17.421 90; 90; 90 | 2108.8 | Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming A copper-catalyzed arylation/nucleophilic addition/fragmentation/C‒S bond formation cascade: synthesis of bis(arylthio)imines Organic Chemistry Frontiers, 2017, 4, 510 |
1553616 | CIF | C22 H24 S4 Si2 | P 1 21/c 1 | 10.5479; 16.6; 13.9079 90; 92.242; 90 | 2433.3 | Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi Organic Chemistry Frontiers, 2017, 4, 1019 |
1553617 | CIF | C44 H72 Li4 O4 S4 Si4 | I 41/a :2 | 20.763; 20.763; 13.7545 90; 90; 90 | 5929.6 | Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi Organic Chemistry Frontiers, 2017, 4, 1019 |
1553618 | CIF | C17 H17 N O4 | P -1 | 5.7832; 10.4921; 12.3215 90.576; 97.913; 93.157 | 739.28 | Chen, Hui; Lin, Cong; Xiong, Chunhua; Liu, Zhanxiang; Zhang, Yuhong One-pot synthesis of fluorescent 2,4-dialkenylindoles by rhodium-catalyzed dual C‒H functionalization Organic Chemistry Frontiers, 2017, 4, 455 |
1553619 | CIF | C21 H17 F O | P 1 21/c 1 | 13.585; 12.569; 9.741 90; 106.741; 90 | 1592.8 | Cao, Tongxiang; Chen, Kai; Zhu, Shifa An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes Organic Chemistry Frontiers, 2017, 4, 450 |
1553620 | CIF | C23 H26 O | P 1 21/c 1 | 12.3103; 20.299; 6.9248 90; 95.884; 90 | 1721.3 | Cao, Tongxiang; Chen, Kai; Zhu, Shifa An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes Organic Chemistry Frontiers, 2017, 4, 450 |
1553621 | CIF | C60 H28 F20 N6 O2 | P -1 | 12.4994; 13.1859; 16.0253 102.651; 95.439; 92.29 | 2560.5 | Almeida, José; Aguiar, António; Leite, Andreia; Silva, André M. N.; Cunha-Silva, Luís; de Castro, Baltazar; Rangel, Maria; Barone, Giampaolo; Tomé, Augusto C.; Silva, Ana M. G. 1,3-Dipolar cycloadditions with meso-tetraarylchlorins ‒ site selectivity and mixed bisadducts Organic Chemistry Frontiers, 2017, 4, 534 |
1553622 | CIF | C23 H30 N4 O2 Si | P b c a | 15.6516; 14.7041; 20.8303 90; 90; 90 | 4793.9 | Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S. Regioselective Zn(OAc)2-catalyzed azide‒alkyne cycloaddition in water: the green click-chemistry Organic Chemistry Frontiers, 2017, 4, 978 |
1553623 | CIF | C20 H21 N5 O2 Si | P -1 | 9.4684; 10.4692; 12.771 96.2634; 95.7478; 113.644 | 1138.27 | Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S. Regioselective Zn(OAc)2-catalyzed azide‒alkyne cycloaddition in water: the green click-chemistry Organic Chemistry Frontiers, 2017, 4, 978 |
1553624 | CIF | C14 H8 Br3 N3 | P 1 21/n 1 | 16.2913; 10.0932; 19.7897 90; 112.895; 90 | 2997.7 | Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S. Regioselective Zn(OAc)2-catalyzed azide‒alkyne cycloaddition in water: the green click-chemistry Organic Chemistry Frontiers, 2017, 4, 978 |
1553625 | CIF | C21 H34 N4 O2 Si | P b c a | 8.9462; 11.9145; 43.549 90; 90; 90 | 4641.9 | Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S. Regioselective Zn(OAc)2-catalyzed azide‒alkyne cycloaddition in water: the green click-chemistry Organic Chemistry Frontiers, 2017, 4, 978 |
1553626 | CIF | C25 H20 O4 | P 1 21/c 1 | 11.9761; 15.4866; 11.0055 90; 106.167; 90 | 1960.46 | Mao, Wenbin; Zhu, Chen Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids Organic Chemistry Frontiers, 2017, 4, 1029 |
1553627 | CIF | C35 H18 Fe O4 | P -1 | 8.8576; 9.515; 15.8743 79.571; 74.479; 86.413 | 1267.66 | Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian From tetrabenzoheptafulvalene to sp2 carbon nano-rings Organic Chemistry Frontiers, 2017, 4, 699 |
1553628 | CIF | C32 H18 O | P 1 21/n 1 | 12.737; 10.827; 15.738 90; 105.708; 90 | 2089.3 | Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian From tetrabenzoheptafulvalene to sp2 carbon nano-rings Organic Chemistry Frontiers, 2017, 4, 699 |
1553629 | CIF | C51 H29 Cl3 O4 | P 21 21 21 | 10.5417; 14.8356; 24.1274 90; 90; 90 | 3773.3 | Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian From tetrabenzoheptafulvalene to sp2 carbon nano-rings Organic Chemistry Frontiers, 2017, 4, 699 |
1553630 | CIF | C51 H30 Cl2 O | P 1 21/n 1 | 12.3541; 20.5251; 15.593 90; 111.562; 90 | 3677.21 | Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian From tetrabenzoheptafulvalene to sp2 carbon nano-rings Organic Chemistry Frontiers, 2017, 4, 699 |
1553631 | CIF | C51 H30 Cl2 | P 1 21/n 1 | 12.2233; 20.4397; 15.612 90; 111.759; 90 | 3622.59 | Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian From tetrabenzoheptafulvalene to sp2 carbon nano-rings Organic Chemistry Frontiers, 2017, 4, 699 |
1553632 | CIF | C20 H19 Br N2 O5 S | P 21 21 21 | 8.8208; 12.857; 18.1141 90; 90; 90 | 2054.3 | Yu, Lu; Cheng, Yuyu; Qi, Fei; Li, Rou; Li, Pengfei Organocatalytic regioselective, diastereoselective, and enantioselective annulation of cyclic 1-azadienes with γ-nitro ketones via 3,4-cyclization Organic Chemistry Frontiers, 2017, 4, 1336 |
1553633 | CIF | C29 H25 N3 | P -1 | 5.768; 9.924; 20.463 100.063; 91.086; 92.46 | 1151.8 | Zhao, Fen; Liu, Yaowen; Yang, Shu; Xie, Kai; Jiang, Yubo Pd-catalyzed selective N(3)-ortho C‒H arylation of 1,4-disubstituted 1,2,3-triazoles Organic Chemistry Frontiers, 2017, 4, 1112 |
1553634 | CIF | C21 H15 Br2 N O2 | P 1 21/n 1 | 16.003; 7.036; 16.456 90; 101.876; 90 | 1813.2 | Qiu, Guanyinsheng; Li, Yuewen; Ma, Lele; Zhou, Hongwei KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide Organic Chemistry Frontiers, 2017, 4, 1069 |
1553635 | CIF | C33 H31 N O3 | P 1 21/n 1 | 15.552; 9.109; 20 90; 111.508; 90 | 2636 | Liu, Feng; Tian, Jiaxin; Liu, Yong; Tao, Chuangan; Zhu, Hao; Zhang, Aina; Xu, Dongfang; Zhao, Baoguo Decarboxylative Umpolung of conjugated enals to β-carbanions for intramolecular nucleophilic addition to an aldehyde Organic Chemistry Frontiers, 2017, 4, 1586 |
1553636 | CIF | C25 H20 N2 O2 S | P 21 21 21 | 7.7445; 13.971; 19.15 90; 90; 90 | 2072 | Lin, Ye; Liu, Lei; Du, Da-Ming Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis of pyrrolidinyl spirooxindoles Organic Chemistry Frontiers, 2017, 4, 1229 |
1553637 | CIF | C16 H21 N3 O5 | P 21 21 21 | 8.4855; 15.887; 25.5299 90; 90; 90 | 3441.7 | Deng, Tao; Thota, Ganesh Kumar; Li, Yi; Kang, Qiang Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex Organic Chemistry Frontiers, 2017, 4, 573 |
1553638 | CIF | C36 H40 N2 O4 | P 1 21/c 1 | 11.882; 6.1567; 22.083 90; 99.617; 90 | 1592.8 | Purc, Anna; Koszarna, Beata; Iachina, Irina; Friese, Daniel H.; Tasior, Mariusz; Sobczyk, Krzysztof; Pędziński, Tomasz; Brewer, Jonathan; Gryko, Daniel T. The impact of interplay between electronic and steric effects on the synthesis and the linear and non-linear optical properties of diketopyrrolopyrrole bearing benzofuran moieties Organic Chemistry Frontiers, 2017, 4, 724 |
1553639 | CIF | C32 H38 N2 O2 S3 | P 1 21/c 1 | 20.477; 5.2589; 28.0402 90; 101.007; 90 | 2964 | Chen, Wangqiao; Nakano, Masahiro; Takimiya, Kazuo; Zhang, Qichun Selective thionation of naphtho[2,3-b]thiophene diimide: tuning of the optoelectronic properties and packing structure Organic Chemistry Frontiers, 2017, 4, 704 |
1553643 | CIF | C27 H33 B2 F11 Fe N6 | F -4 3 c | 29.3374; 29.3374; 29.3374 90; 90; 90 | 25250.2 | Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers. Chemical science, 2017, 8, 2448-2456 |
1553644 | CIF | C26 H31.5 B2 F10 Fe N6.5 | P -1 | 11.4603; 14.9231; 18.6992 110.254; 106.434; 91.133 | 2853 | Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers. Chemical science, 2017, 8, 2448-2456 |
1553645 | CIF | C25 H30 B2 F10 N6 Zn | P 1 c 1 | 13.6092; 14.5112; 14.1222 90; 90.875; 90 | 2788.61 | Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers. Chemical science, 2017, 8, 2448-2456 |
1553646 | CIF | C24 H27 B2 F11 Fe N6 | P 3 | 16.8376; 16.8376; 7.8829 90; 90; 120 | 1935.43 | Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers. Chemical science, 2017, 8, 2448-2456 |
1553647 | CIF | C27 H33 B2 F11 N6 Zn | F -4 3 c | 29.282; 29.282; 29.282 90; 90; 90 | 25107.4 | Thorarinsdottir, Agnes E.; Gaudette, Alexandra I.; Harris, T. David Spin-crossover and high-spin iron(ii) complexes as chemical shift <sup>19</sup>F magnetic resonance thermometers. Chemical science, 2017, 8, 2448-2456 |
1553648 | CIF | C8 H8 F6 N4 Ni Si Xe0.34 | P 4/m m m | 7.0187; 7.0187; 7.5098 90; 90; 90 | 369.95 | Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K. Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks. Chemical science, 2017, 8, 2373-2380 |
1553649 | CIF | C8 H8 F6 N4 Ni Si | P 4/m m m | 7.00122; 7.00122; 7.49794 90; 90; 90 | 367.527 | Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K. Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks. Chemical science, 2017, 8, 2373-2380 |
1553650 | CIF | C8 H8 F6 N4 Ni Si | P 4/m m m | 6.99732; 6.99732; 7.49177 90; 90; 90 | 366.816 | Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K. Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks. Chemical science, 2017, 8, 2373-2380 |
1553651 | CIF | C8 H8 F6 Fe N4 O Si | P 4/m m m | 7.1831; 7.1831; 7.5839 90; 90; 90 | 391.31 | Elsaidi, Sameh K.; Mohamed, Mona H.; Simon, Cory M.; Braun, Efrem; Pham, Tony; Forrest, Katherine A.; Xu, Wenqian; Banerjee, Debasis; Space, Brian; Zaworotko, Michael J.; Thallapally, Praveen K. Effect of ring rotation upon gas adsorption in SIFSIX-3-M (M = Fe, Ni) pillared square grid networks. Chemical science, 2017, 8, 2373-2380 |
1553652 | CIF | C6 H8 Bi I4 N | P 1 21/c 1 | 7.7618; 14.0412; 13.1959 90; 92.959; 90 | 1436.24 | Li, Tianyue; Hu, Yue; Morrison, Carole A.; Wu, Wenjun; Han, Hongwei; Robertson, Neil Lead-free pseudo-three-dimensional organic‒inorganic iodobismuthates for photovoltaic applications Sustainable Energy & Fuels, 2017, 1, 308 |
1553653 | CIF | C5 H6 Bi I4 N | P 1 21/c 1 | 12.6997; 28.3198; 7.716 90; 95.288; 90 | 2763.27 | Li, Tianyue; Hu, Yue; Morrison, Carole A.; Wu, Wenjun; Han, Hongwei; Robertson, Neil Lead-free pseudo-three-dimensional organic‒inorganic iodobismuthates for photovoltaic applications Sustainable Energy & Fuels, 2017, 1, 308 |
1553654 | CIF | C42 H42 I2 N2 | P 61 2 2 | 15.6598; 15.6598; 34.08 90; 90; 120 | 7237.7 | Samanta, Soham; Halder, Senjuti; Dey, Poulomi; Manna, Utsab; Ramesh, Aiyagari; Das, Gopal A ratiometric fluorogenic probe for the real-time detection of SO<sub>3</sub><sup>2-</sup> in aqueous medium: application in a cellulose paper based device and potential to sense SO<sub>3</sub><sup>2-</sup> in mitochondria. The Analyst, 2017, 143, 250-257 |
1553662 | CIF | C46 H38 N6 O4 S2 | P 1 21/c 1 | 16.2355; 14.4863; 17.7924 90; 106.064; 90 | 4021.2 | Zhao, Xueqian; Ge, Congwu; Yang, Xiaodi; Gao, Xike Dithieno[3,2-a:3′,2′-j][5,6,11,12]chrysene diimides and their molecular energy level regulation Materials Chemistry Frontiers, 2017, 1, 1635 |
1553663 | CIF | C26 H18 S2 | P 1 21/c 1 | 5.641; 9.315; 19.216 90; 103.97; 90 | 979.9 | Zhang, Jibo; Ma, Suqian; Fang, Honghua; Xu, Bin; Sun, Hongbo; Chan, Im; Tian, Wenjing Insights into the origin of aggregation enhanced emission of 9,10-distyrylanthracene derivatives Materials Chemistry Frontiers, 2017, 1, 1422 |
1553664 | CIF | C19 H15 B F2 N2 | P -1 | 6.418; 8.632; 14.198 74.951; 81.658; 86.211 | 751.2 | Yamaguchi, Madoka; Ito, Shunichiro; Hirose, Amane; Tanaka, Kazuo; Chujo, Yoshiki Control of aggregation-induced emission versus fluorescence aggregation-caused quenching by bond existence at a single site in boron pyridinoiminate complexes Materials Chemistry Frontiers, 2017, 1, 1573 |
1553665 | CIF | C19 H13 B F2 N2 | P 1 21/n 1 | 9.2376; 11.5433; 13.4497 90; 98.264; 90 | 1419.3 | Yamaguchi, Madoka; Ito, Shunichiro; Hirose, Amane; Tanaka, Kazuo; Chujo, Yoshiki Control of aggregation-induced emission versus fluorescence aggregation-caused quenching by bond existence at a single site in boron pyridinoiminate complexes Materials Chemistry Frontiers, 2017, 1, 1573 |
1553666 | CIF | C20 H14 Hg I2 N2 S2 | P -1 | 10.2226; 10.3008; 12.2126 74.477; 67.707; 71.185 | 1110.69 | Gabr, Moustafa T.; Christopher Pigge, F. A turn-on AIE active fluorescent sensor for Hg2+ by combination of 1,1-bis(2-pyridyl)ethylene and thiophene/bithiophene fragments Materials Chemistry Frontiers, 2017, 1, 1654 |
1553667 | CIF | C18 H16 Cl4 N4 O2 | R 3 :H | 14.7047; 14.7047; 23.9058 90; 90; 120 | 4476.6 | Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties Materials Chemistry Frontiers, 2017, 1, 1041 |
1553668 | CIF | C27 H30 N4 O3 | P 1 21/c 1 | 9.8325; 11.2257; 22.882 90; 98.783; 90 | 2496 | Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties Materials Chemistry Frontiers, 2017, 1, 1041 |
1553669 | CIF | C18 H18 F2 N2.67 O2 | R -3 :H | 14.4761; 14.4761; 40.5191 90; 90; 120 | 7353.5 | Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties Materials Chemistry Frontiers, 2017, 1, 1041 |
1553670 | CIF | C30 H34 N4 O6 | P 21 21 21 | 6.29545; 15.9502; 28.8235 90; 90; 90 | 2894.27 | Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties Materials Chemistry Frontiers, 2017, 1, 1041 |
1553671 | CIF | C39 H54 N4 O3 | P -1 | 12.9272; 13.0256; 23.4928 82.005; 79.707; 86.311 | 3851.2 | Zhang, Xiaohong; Shi, Jun; Shen, Guangyu; Gou, Fei; Cheng, Jinghui; Zhou, Xiangge; Xiang, Haifeng Non-conjugated fluorescent molecular cages of salicylaldehyde-based tri-Schiff bases: AIE, enantiomers, mechanochromism, anion hosts/probes, and cell imaging properties Materials Chemistry Frontiers, 2017, 1, 1041 |
1553672 | CIF | C21 H23 N O2 | P 1 21/c 1 | 15.43; 10.791; 10.129 90; 101.94; 90 | 1650 | Wang, Fang; DeRosa, Christopher A.; Daly, Margaret L.; Song, Daniel; Fraser, Cassandra L. Multi-stimuli responsive luminescent azepane-substituted β-diketones and difluoroboron complexes. Materials chemistry frontiers, 2017, 1, 1866-1874 |
1553673 | CIF | C42 H29 N O2 | P -1 | 9.4456; 9.9577; 16.2906 102.183; 93.914; 93.086 | 1490.57 | Peng, Zhixing; Huang, Kai; Tao, Yuhan; Li, Xihui; Zhang, Lianpeng; Lu, Ping; Wang, Yanguang Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence Materials Chemistry Frontiers, 2017, 1, 1858 |
1553674 | CIF | C42 H29 N O2 | P -1 | 9.4088; 11.452; 15.1598 90.309; 105.929; 93.468 | 1567.45 | Peng, Zhixing; Huang, Kai; Tao, Yuhan; Li, Xihui; Zhang, Lianpeng; Lu, Ping; Wang, Yanguang Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence Materials Chemistry Frontiers, 2017, 1, 1858 |
1553675 | CIF | C42 H29 N O2 | P 1 21/c 1 | 18.2932; 19.3313; 9.1613 90; 103.67; 90 | 3148 | Peng, Zhixing; Huang, Kai; Tao, Yuhan; Li, Xihui; Zhang, Lianpeng; Lu, Ping; Wang, Yanguang Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence Materials Chemistry Frontiers, 2017, 1, 1858 |
1553676 | CIF | C37 H43 Cu2 I2 N5 O2 S3 | P -1 | 9.102; 14.511; 17.16 66.114; 88.537; 80.515 | 2041.9 | Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules Materials Chemistry Frontiers, 2017, 1, 1764 |
1553677 | CIF | C34 H27 Cu2 I2 N3 O S3 | P -1 | 9.4203; 14.3226; 17.3309 65.977; 77.856; 79.467 | 2075.6 | Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules Materials Chemistry Frontiers, 2017, 1, 1764 |
1553678 | CIF | C30 H34 Cu2 I2 N4 O S3 | P -1 | 9.174; 14.442; 17.023 113.404; 90.013; 99.203 | 2038 | Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules Materials Chemistry Frontiers, 2017, 1, 1764 |
1553679 | CIF | C31 H33 Cu2 I2 N5 S3 | P -1 | 8.962; 14.515; 16.577 112.653; 91.205; 98.338 | 1962 | Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules Materials Chemistry Frontiers, 2017, 1, 1764 |
1553680 | CIF | C31 H39 Cu2 I2 N3 O2 S5 | P -1 | 9.353; 14.189; 17.257 113.336; 94.402; 100.137 | 2043 | Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules Materials Chemistry Frontiers, 2017, 1, 1764 |
1553681 | CIF | C35 H45 Cu2 I2 N5 O2 S3 | P -1 | 9.252; 14.347; 17.158 113.914; 91.45; 99.705 | 2041.1 | Yang, Xin-Yu; Yuan, Shuai; Qin, Jun-Sheng; Lollar, Christina; Alsalme, Ali; Zhou, Hong-Cai A flexible thioether-based MOF as a crystalline sponge for structural characterization of liquid organic molecules Materials Chemistry Frontiers, 2017, 1, 1764 |
1553682 | CIF | C17 H16 I N O2 | P 21 21 21 | 6.1493; 12.443; 19.762 90; 90; 90 | 1512.1 | Butler, Tristan; Wang, Fang; Sabat, Michal; Fraser, Cassandra L. Controlling solid-state optical properties of stimuli responsive dimethylamino-substituted dibenzoylmethane materials Materials Chemistry Frontiers, 2017, 1, 1804 |
1553683 | CIF | C9 H4 N2 O4 Y0.33 | P 3 1 c | 12.8501; 12.8501; 15.709 90; 90; 120 | 2246.4 | Liu, Kang; Li, Xu; Ma, Dingxuan; Han, Yi; Li, Baiyan; Shi, Zhan; Li, Zhenjiang; Wang, Lei A microporous yttrium metal‒organic framework of an unusual nia topology for high adsorption selectivity of C2H2and CO2over CH4at room temperature Materials Chemistry Frontiers, 2017, 1, 1982 |
1553684 | CIF | C22 H24 N3 Ni0.5 | P -1 | 8.3884; 8.4668; 14.2802 95.006; 94.479; 113.925 | 916.34 | Yoshida, Takuya; Shinokubo, Hiroshi Direct amination of the antiaromatic NiII norcorrole Materials Chemistry Frontiers, 2017, 1, 1853 |
1553685 | CIF | C37 H24 N2 O3 | P 1 21/n 1 | 24.2035; 9.4392; 24.306 90; 109.203; 90 | 5244 | Gan, Shifeng; Zhou, Jian; Smith, Trevor A.; Su, Huifang; Luo, Wenwen; Hong, Yuning; Zhao, Zujin; Tang, Ben Zhong New AIEgens with delayed fluorescence for fluorescence imaging and fluorescence lifetime imaging of living cells Materials Chemistry Frontiers, 2017, 1, 2554 |
1553686 | CIF | C25 H17 N O2 | P 1 21/c 1 | 8.4792; 29.902; 7.9399 90; 117.656; 90 | 1783.1 | Gan, Shifeng; Zhou, Jian; Smith, Trevor A.; Su, Huifang; Luo, Wenwen; Hong, Yuning; Zhao, Zujin; Tang, Ben Zhong New AIEgens with delayed fluorescence for fluorescence imaging and fluorescence lifetime imaging of living cells Materials Chemistry Frontiers, 2017, 1, 2554 |
1553687 | CIF | C29 H23 N3 O2 | P 1 21/n 1 | 7.3698; 10.7294; 27.0518 90; 90.5158; 90 | 2138.99 | Tokuo, Kokichi; Sakai, Hayato; Sakanoue, Tomo; Takenobu, Taishi; Araki, Yasuyuki; Wada, Takehiko; Hasobe, Taku Control of the electrochemical and photophysical properties of N-substituted benzo[ghi]perylene derivatives Materials Chemistry Frontiers, 2017, 1, 2299 |
1553688 | CIF | C27 H18 Cu2 O11 | P 63/m m c | 18.4455; 18.4455; 26.4268 90; 90; 120 | 7786.7 | Chen, Fengli; Bai, Dongjie; Wang, Yao; Jiang, Donghao; He, Yabing A family of ssa-type copper-based MOFs constructed from unsymmetrical diisophthalates: synthesis, characterization and selective gas adsorption Materials Chemistry Frontiers, 2017, 1, 2283 |
1553689 | CIF | C28 H20 Cu2 O11 | P 63/m m c | 18.2664; 18.2664; 26.5488 90; 90; 120 | 7671.5 | Chen, Fengli; Bai, Dongjie; Wang, Yao; Jiang, Donghao; He, Yabing A family of ssa-type copper-based MOFs constructed from unsymmetrical diisophthalates: synthesis, characterization and selective gas adsorption Materials Chemistry Frontiers, 2017, 1, 2283 |
1553690 | CIF | C38 H48 Cu2 N4 O16 | P 63/m m c | 18.315; 18.315; 26.7665 90; 90; 120 | 7775.6 | Chen, Fengli; Bai, Dongjie; Wang, Yao; Jiang, Donghao; He, Yabing A family of ssa-type copper-based MOFs constructed from unsymmetrical diisophthalates: synthesis, characterization and selective gas adsorption Materials Chemistry Frontiers, 2017, 1, 2283 |
1553691 | CIF | C48 H30 N4 | P n n a | 14.768; 15.377; 16.689 90; 90; 90 | 3790 | Zhang, Yahui; Kong, Lingwei; Mao, Huiling; Pan, Xiaoling; Shi, Jianbing; Tong, Bin; Dong, Yuping Light/temperature-enhanced emission characteristics of malononitrile-containing hexaphenyl-1,3-butadiene derivatives: the hotter, the brighter Materials Chemistry Frontiers, 2017, 1, 2569 |
1553692 | CIF | C23.5 H20 B0.5 | C 1 2/c 1 | 10.3419; 16.4056; 20.936 90; 100.537; 90 | 3492.2 | Chi, Weijie; Yin, Wenting; Qi, Qingkai; Qiao, Qinglong; Lin, Yuyan; Zhu, Zhuohui; Vijayan, Sindhu; Hashimoto, Michinao; Udayakumar, Gayathri; Xu, Zhaochao; Liu, Xiaogang Ground-state conformers enable bright single-fluorophore ratiometric thermometers with positive temperature coefficients Materials Chemistry Frontiers, 2017, 1, 2383 |
1553693 | CIF | C29 H34 B Br2 N | P -1 | 7.9955; 11.139; 14.735 87.095; 78.445; 81.208 | 1270.3 | Matsumoto, Takuya; Takamine, Hirofumi; Tanaka, Kazuo; Chujo, Yoshiki Design of bond-cleavage-induced intramolecular charge transfer emission with dibenzoboroles and their application to ratiometric sensors for discriminating chain lengths of alkanes Materials Chemistry Frontiers, 2017, 1, 2368 |
1553694 | CIF | C38 H27 Br2 N O2 | C 1 2/c 1 | 19.61; 15.469; 20.516 90; 107.135; 90 | 5947.2 | Gopikrishna, Peddaboodi; Raman Adil, Laxmi; Iyer, Parameswar Krishnan Bridge-driven aggregation control in dibenzofulvene‒naphthalimide based donor‒bridge‒acceptor systems: enabling fluorescence enhancement, blue to red emission and solvatochromism Materials Chemistry Frontiers, 2017, 1, 2590 |
1553695 | CIF | C38 H29 N O2 | P 1 21/c 1 | 11.2762; 13.9376; 17.8045 90; 101.143; 90 | 2745.5 | Gopikrishna, Peddaboodi; Raman Adil, Laxmi; Iyer, Parameswar Krishnan Bridge-driven aggregation control in dibenzofulvene‒naphthalimide based donor‒bridge‒acceptor systems: enabling fluorescence enhancement, blue to red emission and solvatochromism Materials Chemistry Frontiers, 2017, 1, 2590 |
1553724 | CIF | C22 H23 Cl N2 O0 Ru | P -1 | 10.445; 14.347; 14.407 82.53; 85.3; 74.55 | 2060.7 | Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie Ruthenium-catalyzed meta-selective C‒H sulfonation of azoarenes with arylsulfonyl chlorides Organic Chemistry Frontiers, 2017, 4, 1145 |
1553725 | CIF | C18 H13 Cl N2 O2 S | C 1 2/c 1 | 34.644; 7.0976; 13.544 90; 98.63; 90 | 3292.6 | Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie Ruthenium-catalyzed meta-selective C‒H sulfonation of azoarenes with arylsulfonyl chlorides Organic Chemistry Frontiers, 2017, 4, 1145 |
1553726 | CIF | C16 H15 N O7 | P 21 21 21 | 11.4884; 11.9792; 20.8251 90; 90; 90 | 2866 | Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun Asymmetric total synthesis of (−)-δ-lycorane Organic Chemistry Frontiers, 2017, 4, 1149 |
1553727 | CIF | C60 H46 N4.5 | P -1 | 13.8813; 14.4392; 23.5317 95.8618; 105.365; 91.4814 | 4517.3 | Kimura, Yosuke; Kawajiri, Ikumi; Ueki, Masanori; Morimoto, Takayuki; Nishida, Jun-ichi; Ikeda, Hiroshi; Tanaka, Mirai; Kawase, Takeshi A new fluorophore displaying remarkable solvatofluorochromism and solid-state light emission, and serving as a turn-on fluorescent sensor for cyanide ions Organic Chemistry Frontiers, 2017, 4, 743 |
1553728 | CIF | C11 H16 F3 N O2 S2 | C 1 2 1 | 11.5; 10.46; 11.413 90; 95.06; 90 | 1367.5 | Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers, 2017, 4, 1051 |
1553729 | CIF | C19 H10 F4 O2 S | P 21 21 21 | 6.6977; 8.1914; 30.513 90; 90; 90 | 1674.1 | Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers, 2017, 4, 1051 |
1553730 | CIF | C15 H15 F3 O5 S | P 21 21 21 | 7.5426; 13.2312; 15.9887 90; 90; 90 | 1595.6 | Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers, 2017, 4, 1051 |
1553731 | CIF | C17 H11 F3 N2 O S | P 21 21 21 | 8.5502; 11.0835; 16.8212 90; 90; 90 | 1594.1 | Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers, 2017, 4, 1051 |
1553732 | CIF | C11 H14 Cl2 F3 N O2 S2 | P 1 21 1 | 7.7869; 10.8732; 8.8809 90; 95.062; 90 | 749 | Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers, 2017, 4, 1051 |
1553733 | CIF | C13 H20 F3 N O4 S2 | P 1 21 1 | 12.4266; 8.8229; 15.107 90; 105.7; 90 | 1594.5 | Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers, 2017, 4, 1051 |
1553734 | CIF | C101 H110 N4 Ni P Pt0.5 | P -1 | 15.566; 15.831; 17.7553 80.813; 89.907; 88.251 | 4317.2 | Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro meso-to-meso PtII-bridged NiII-porphyrin dimers Organic Chemistry Frontiers, 2017, 4, 767 |
1553735 | CIF | C162 H174 Cl10 N8 Ni2 Pt | P -1 | 16.142; 21.227; 22.446 106.1; 92.132; 93.364 | 7365 | Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro meso-to-meso PtII-bridged NiII-porphyrin dimers Organic Chemistry Frontiers, 2017, 4, 767 |
1553736 | CIF | C76 H38 Br N O8 | P 1 21/n 1 | 13.8397; 24.2642; 16.7166 90; 109.444; 90 | 5293.4 | Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R Organic Chemistry Frontiers, 2017, 4, 750 |
1553737 | CIF | C76 H39 N O9 | P n a 21 | 21.489; 10.179; 22.215 90; 90; 90 | 4859.2 | Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R Organic Chemistry Frontiers, 2017, 4, 750 |
1553738 | CIF | C17 H13 Br N2 O4 S | P 1 21/c 1 | 17.5147; 7.024; 15.73 90; 114.033; 90 | 1767.4 | Pal, Kuntal; Volla, Chandra M. R. Rhodium-catalyzed denitrogenative transannulation of 1,2,3-triazolyl-carbamates: efficient access to 4-aminooxazolidinones Organic Chemistry Frontiers, 2017, 4, 1380 |
1553739 | CIF | C15 H9 F N2 | P b c a | 25.513; 13.881; 6.794 90; 90; 90 | 2406 | Panaka, Sangeetha; Trivedi, Rajiv; Sony, T.; Prabhakar, S.; Raju Chowhan, L. Silver(i) catalyzed intramolecular cyclization of N-(2-(alk-1-yn-1-yl))-1H-tetrazoles leading to the formation of N-cyano-2-substituted indoles under ambient conditions Org. Chem. Front., 2017, 4, 1574 |
1553740 | CIF | C16 H13 N2 | P b c a | 25.555; 14.1257; 6.8724 90; 90; 90 | 2480.8 | Panaka, Sangeetha; Trivedi, Rajiv; Sony, T.; Prabhakar, S.; Raju Chowhan, L. Silver(i) catalyzed intramolecular cyclization of N-(2-(alk-1-yn-1-yl))-1H-tetrazoles leading to the formation of N-cyano-2-substituted indoles under ambient conditions Org. Chem. Front., 2017, 4, 1574 |
1553741 | CIF | C19 H22 O3 | C 1 2/c 1 | 28.543; 7.309; 16.361 90; 105.04; 90 | 3296.3 | Chang, Wenju; Dai, Jie; Li, Jingfu; Shi, Yuan; Ren, Wenlong; Shi, Yian A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid Organic Chemistry Frontiers, 2017, 4, 1074 |
1553742 | CIF | C11 H8 N O2 S | P 1 21/c 1 | 5.69674; 8.92923; 19.6982 90; 94.927; 90 | 998.3 | Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties Organic Chemistry Frontiers, 2017, 4, 861 |
1553743 | CIF | C67.5 H66 Cl3 N O2 S | P -1 | 14.0225; 15.4902; 15.6494 109.303; 105.791; 106.459 | 2814.2 | Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties Organic Chemistry Frontiers, 2017, 4, 861 |
1553744 | CIF | C84 H108 Si4 | P -1 | 8.2685; 13.793; 17.645 72.588; 88.716; 77.009 | 1868.8 | Bettinger, Holger F.; Einholz, Ralf; Göttler, Andreas; Junge, Marc; Sättele, Marie-Sophie; Schnepf, Andreas; Schrenk, Claudio; Schundelmeier, Simon; Speiser, Bernd 6,6′,11,11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1,4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization Organic Chemistry Frontiers, 2017, 4, 853 |
1553745 | CIF | C14 H14 N2 O2 S | P -1 | 6.121; 8.835; 13.265 83.14; 79.6; 72.93 | 672.8 | Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis Organic Chemistry Frontiers, 2017, 4, 1266 |
1553746 | CIF | C15 H17 N3 O4 S | P 1 21 1 | 8.6132; 7.4744; 12.867 90; 109.429; 90 | 781.2 | Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis Organic Chemistry Frontiers, 2017, 4, 1266 |
1553747 | CIF | C30 H24 | C 1 c 1 | 21.7066; 21.7067; 20.1949 90; 122.509; 90 | 8024.4 | Takai, Atsuro; Freas, Dylan J.; Suzuki, Toshikane; Sugimoto, Manabu; Labuta, Jan; Haruki, Rie; Kumai, Reiji; Adachi, Shin-ichi; Sakai, Hayato; Hasobe, Taku; Matsushita, Yoshitaka; Takeuchi, Masayuki The effect of a highly twisted CC double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states Organic Chemistry Frontiers, 2017, 4, 650 |
1553748 | CIF | C15 H13 N O4 S2 | P -1 | 7.6834; 8.0281; 12.554 85.471; 73.42; 74.044 | 713.6 | Zhou, Kaida; Xia, Hongguang; Wu, Jie Generation of benzosultams via a radical process with the insertion of sulfur dioxide Organic Chemistry Frontiers, 2017, 4, 1121 |
1553749 | CIF | C15 H13 N O4 S2 | P 1 21/c 1 | 8.151; 8.239; 22.94 90; 100.06; 90 | 1517 | Zhou, Kaida; Xia, Hongguang; Wu, Jie Generation of benzosultams via a radical process with the insertion of sulfur dioxide Organic Chemistry Frontiers, 2017, 4, 1121 |
1553750 | CIF | C26 H31 N3 O6 | P 1 | 9.0047; 9.2247; 9.4826 109.875; 108.593; 107.103 | 626.45 | Guo, Jing; Lin, Zi-Hui; Chen, Kai-Bin; Xie, Ying; Chan, Albert S. C.; Weng, Jiang; Lu, Gui Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids Organic Chemistry Frontiers, 2017, 4, 1400 |
1553751 | CIF | C54 H48 O8 | P -1 | 8.9558; 9.4432; 13.6247 92.926; 95.287; 111 | 1066.8 | Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems Organic Chemistry Frontiers, 2017, 4, 828 |
1553752 | CIF | C66 H72 O6 | P 1 21/n 1 | 11.8673; 14.8352; 15.9367 90; 102.976; 90 | 2734.08 | Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems Organic Chemistry Frontiers, 2017, 4, 828 |
1553753 | CIF | C41 H27 O | C 1 2/c 1 | 23.6823; 14.1831; 19.4393 90; 101.921; 90 | 6388.6 | Ip, Ho-Wang; Chow, Hak-Fun; Kuck, Dietmar Electronic and steric effects on the three-fold Scholl-type cycloheptatriene ring formation around a tribenzotriquinacene core Organic Chemistry Frontiers, 2017, 4, 817 |
1553754 | CIF | C18 H16 N2 O2 | P 1 21/c 1 | 12.4244; 8.0614; 14.7164 90; 100.607; 90 | 1448.78 | Selvaraju, Manikandan; Wang, Ying-Lien; Sun, Chung-Ming Ruthenium(ii)-catalyzed C‒H alkenylation/annulation cascade for the rapid synthesis of benzoimidazoisoindoles Organic Chemistry Frontiers, 2017, 4, 1358 |
1553755 | CIF | C7.75 H7.75 F7.75 N7.75 O7.75 S7.75 | P 21 21 21 | 8.086; 14.196; 23.304 90; 90; 90 | 2675 | Pouambeka, Tony Wheellyam; Zhang, Ge; Zheng, Guang-Fan; Xu, Guo-Xing; Zhang, Qian; Xiong, Tao; Zhang, Qian Copper-catalyzed oxidative amidation of α,β-unsaturated ketones via selective C‒H or C‒C bond cleavage Organic Chemistry Frontiers, 2017, 4, 1420 |
1553756 | CIF | C27 H21 N O2 S2 | P 21 21 21 | 5.9608; 18.7773; 20.3817 90; 90; 90 | 2281.3 | Shi, Qing; Li, Pinhua; Zhang, Yan; Wang, Lei Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions Organic Chemistry Frontiers, 2017, 4, 1322 |
1553757 | CIF | C16 H12 Cl N O | P 1 21/c 1 | 9.0611; 7.1551; 20.5051 90; 93.684; 90 | 1326.66 | Zhang, Zhiguo; Zhang, Yongchao; Huang, Guoqing; Zhang, Guisheng Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles Organic Chemistry Frontiers, 2017, 4, 1372 |
1553758 | CIF | C17 H18 Br F3 N2 O6 | P 21 21 21 | 8.3955; 14.09; 16.7651 90; 90; 90 | 1983.19 | Liu, Qiang; Zhao, Kun; Zhi, Ying; Raabe, Gerhard; Enders, Dieter Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines Organic Chemistry Frontiers, 2017, 4, 1416 |
1553759 | CIF | C23 H22 Br Cl2 N3 O5 | P 1 21/n 1 | 9.593; 15.307; 16.705 90; 93.785; 90 | 2447.6 | Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes Organic Chemistry Frontiers, 2017, 4, 1289 |
1553760 | CIF | C20 H17 Br Cl3 N3 O3 | P -1 | 6.299; 11.774; 14.904 99.608; 94.163; 96.363 | 1078 | Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes Organic Chemistry Frontiers, 2017, 4, 1289 |
1553761 | CIF | C17 H16 O | P 21 21 21 | 7.738; 11.656; 14.0895 90; 90; 90 | 1270.79 | Zhang, Bo-Sheng; Hua, Hui-Liang; Gao, Lu-Yao; Liu, Ce; Qiu, Yi-Feng; Zhou, Ping-Xin; Zhou, Zhao-Zhao; Zhao, Jia-Hui; Liang, Yong-Min Palladium-catalyzed arene C‒H activation/ketone C‒H functionalization reaction: route to spirodihydroindenones Organic Chemistry Frontiers, 2017, 4, 1376 |
1553762 | CIF | C4 H3.167 N0.167 O0.333 S0.167 | C 1 2/c 1 | 16.382; 18.322; 14.538 90; 120.472; 90 | 3760.9 | Zhang, Pengbo; Gao, Yuzhen; Chen, Su; Tang, Guo; Zhao, Yufen Direct synthesis of 2-sulfonated 9H-pyrrolo[1,2-a]indoles via NaI-catalyzed cascade radical addition/cyclization/isomerization Organic Chemistry Frontiers, 2017, 4, 1350 |
1553763 | CIF | C14 H12 N2 O3 | P -1 | 7.1026; 7.8866; 11.4159 92.777; 92.263; 114.968 | 577.75 | Hong, Longcheng; Ahles, Sebastian; Strauss, Marcel A.; Logemann, Christian; Wegner, Hermann A. Synthesis of 2,3-diaza-anthraquinones via the bidentate Lewis acid catalysed inverse electron-demand Diels‒Alder (IEDDA) reaction Organic Chemistry Frontiers, 2017, 4, 871 |
1553764 | CIF | C25 H22 F I2 N O2 S | P -1 | 8.7048; 10.5461; 13.9946 82.33; 79.359; 79.1 | 1233.4 | Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines Organic Chemistry Frontiers, 2017, 4, 1294 |
1553765 | CIF | C25 H24 Cl N O2 S | P 1 21/c 1 | 13.2671; 18.296; 19.283 90; 108.684; 90 | 4434 | Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines Organic Chemistry Frontiers, 2017, 4, 1294 |
1553766 | CIF | C18 H17 N S3 | P -1 | 12.112; 13.064; 13.586 113.51; 114.37; 96.715 | 1690.6 | Schneeweis, Arno; Neidlinger, Andreas; Reiss, Guido J.; Frank, Walter; Heinze, Katja; Müller, Thomas J. J. Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine Organic Chemistry Frontiers, 2017, 4, 839 |
1553767 | CIF | C26 H20 F3 N O | P -1 | 9.3089; 10.692; 10.826 98.78; 90.325; 108.111 | 1010.5 | An, Yuanyuan; Zhang, Jun; Xia, Hongguang; Wu, Jie Radical cyclization of benzene-tethered 1,7-enynes with aryldiazonium tetrafluoroborates: a facile route to benzo[j]phenanthridines Organic Chemistry Frontiers, 2017, 4, 1318 |
1553768 | CIF | C22 H26 F2 N2 O2 | P 1 21/c 1 | 8.7598; 25.852; 8.8958 90; 96.431; 90 | 2001.9 | Liu, Kai; Sui, Lin-Chao; Jin, Qiao; Li, Deng-Yuan; Liu, Pei-Nian CuBr-mediated radical cascade difluoroacetamidation of acrylamides using α,α-difluoro-α-(TMS)-acetamides Organic Chemistry Frontiers, 2017, 4, 1606 |
1553769 | CIF | C16 H11 F N2 O | P 1 21/c 1 | 21.229; 3.919; 15.628 90; 105.861; 90 | 1250.7 | Ding, Junshuai; Zhang, Yingchao; Li, Jizhen Nickel-catalyzed selective C-5 fluorination of 8-aminoquinolines with NFSI Organic Chemistry Frontiers, 2017, 4, 1528 |
1553770 | CIF | C20 H12 Cl3 N O0 | P 1 21/n 1 | 11.93574; 7.18231; 19.3705 90; 94.7142; 90 | 1654.94 | Li, Jianxiao; An, Yanni; Li, Jiawei; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng Palladium-catalyzed C‒S bond activation and functionalization of 3-sulfenylindoles and related electron-rich heteroarenes Organic Chemistry Frontiers, 2017, 4, 1590 |
1553771 | CIF | C34 H52 Cl4 N16 O2 | P -1 | 9.8942; 11.644; 20.487 87.078; 78.302; 68.651 | 2152 | Liang, Dong-Dong; Wang, Mei-Xiang Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines Organic Chemistry Frontiers, 2017, 4, 1425 |
1553772 | CIF | C5.33 H10 Cl0.67 Co0.33 N2.67 O4 | P 1 21/c 1 | 11.9766; 19.3355; 12.7804 90; 114.734; 90 | 2688.09 | Liang, Dong-Dong; Wang, Mei-Xiang Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines Organic Chemistry Frontiers, 2017, 4, 1425 |
1553773 | CIF | C27 H41 N16 O3.5 S1.5 | P -1 | 13.18; 19.895; 20.59 108.27; 107.63; 90.48 | 4854 | Liang, Dong-Dong; Wang, Mei-Xiang Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines Organic Chemistry Frontiers, 2017, 4, 1425 |
1553774 | CIF | C20 H23 B F2 N2 O2 | P -1 | 9.003; 10.762; 11.631 73.19; 69.99; 72.45 | 987.6 | Kubota, Yasuhiro; Tsukamoto, Masahiro; Ohnishi, Katsuhiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki Synthesis and fluorescence properties of novel squarylium‒boron complexes Organic Chemistry Frontiers, 2017, 4, 1522 |
1553775 | CIF | C21 H17 Cl F3 N3 | P 1 21 1 | 8.6045; 11.4959; 10.3691 90; 114.544; 90 | 933 | Xie, En; Rahman, Abdul; Lin, Xufeng Asymmetric synthesis of CF3- and indole-containing tetrahydro-β-carbolines via chiral spirocyclic phosphoric acid-catalyzed aza-Friedel‒Crafts reaction Organic Chemistry Frontiers, 2017, 4, 1407 |
1553776 | CIF | C22 H17 I N2 | P 1 21/n 1 | 10.326; 9.584; 19.601 90; 104.43; 90 | 1878.6 | Liu, Cheng-Kou; Yang, Zhao; Zeng, Yu; Guo, Kai; Fang, Zheng; Li, Bo Sodium nitrite-promoted aerobic oxidative coupling of aryl methyl ketones with ammonium under metal-free conditions: a facile access to polysubstitution imidazoles Organic Chemistry Frontiers, 2017, 4, 1508 |
1553777 | CIF | C10 H12 O2 S | P 21 21 21 | 5.7817; 8.2558; 19.972 90; 90; 90 | 953.3 | Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides Organic Chemistry Frontiers, 2017, 4, 1601 |
1553778 | CIF | C17 H19 N O2 S | P 1 21 1 | 11.3637; 6.0455; 11.3636 90; 98.45; 90 | 772.2 | Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides Organic Chemistry Frontiers, 2017, 4, 1601 |
1553779 | CIF | C21 H16 N2 O3 | P c a 21 | 11.0348; 21.2718; 7.2221 90; 90; 90 | 1695.2 | Tang, Hai-Tao; Zeng, Jia-Hao; Chen, Jun-Jia; Zhou, Yun-Bing; Li, Ren-Hao; Zhan, Zhuang-Ping Synthesis of pyrazolo[5,1-a]isoquinolines through copper-catalyzed regioselective bicyclization of N-propargylic sulfonylhydrazones Organic Chemistry Frontiers, 2017, 4, 1513 |
1553780 | CIF | C19 H11 Cl F3 N O | C 1 2/c 1 | 17.5265; 18.9585; 11.1154 90; 120.995; 90 | 3166 | Mishra, Kalpana; Singh, Jay Bahadur; Gupta, Tanu; Singh, Radhey M. TBAB-catalyzed cascade reactions: facile synthesis of 1-trifluoromethyl-3-alkylidene-1,3-dihydrofuro[3,4-b]quinolines via 5-exo-dig cyclization of o-arylalkynylquinoline aldehydes Organic Chemistry Frontiers, 2017, 4, 1926 |
1553781 | CIF | C2 H4 N4 O | P n m a | 5.0951; 6.0539; 14.8931 90; 90; 90 | 459.38 | Wan, Huabin; Li, Hongmin; Xu, Jian; Wu, Zhuang; Liu, Qifan; Chu, Xianxu; Abe, Manabu; Bégué, Didier; Zeng, Xiaoqing N-Methylcarbamoyl azide: spectroscopy, X-ray structure and decomposition via methylcarbamoyl nitrene Organic Chemistry Frontiers, 2017, 4, 1839 |
1553782 | CIF | C21 H18 F2 O4 | P n a 21 | 12.326; 11.032; 13.445 90; 90; 90 | 1828.3 | Li, Yuewen; Lu, Yiye; Mao, Runyu; Li, Zhiming; Wu, Jie A photoinduced reaction of perfluoroalkyl halides with 1,3-diarylprop-2-yn-1-ones catalyzed by DABSO Organic Chemistry Frontiers, 2017, 4, 1745 |
1553783 | CIF | C22 H18 Br4 N2 | P b c a | 10.7971; 15.2395; 26.1285 90; 90; 90 | 4299.2 | Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives Organic Chemistry Frontiers, 2017, 4, 1785 |
1553784 | CIF | C18 H26 Br2 N2 | P 1 21/c 1 | 6.6642; 19.8278; 14.8224 90; 101.924; 90 | 1916.3 | Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives Organic Chemistry Frontiers, 2017, 4, 1785 |
1553785 | CIF | C26 H25 F3 N O S | P 21 21 2 | 23.66; 10.2673; 10.5398 90; 90; 90 | 2560.4 | Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2017, 4, 1772 |
1553786 | CIF | C27 H23 Cl F3 N O3 | P 21 21 21 | 8.5817; 10.4128; 27.6259 90; 90; 90 | 2468.64 | Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2017, 4, 1772 |
1553787 | CIF | C15 H16 F3 N O2 S | P 21 21 21 | 6.2282; 7.0351; 36.2461 90; 90; 90 | 1588.16 | Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter Organic Chemistry Frontiers, 2017, 4, 1772 |
1553788 | CIF | C28 H21 N2 O2 P | P 1 21/c 1 | 12.9056; 8.981; 20.4045 90; 106.848; 90 | 2263.48 | Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides Organic Chemistry Frontiers, 2017, 4, 1981 |
1553789 | CIF | C28 H21 N2 O2 P | P 1 21/n 1 | 14.3374; 9.71; 18.7718 90; 105.341; 90 | 2520.22 | Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides Organic Chemistry Frontiers, 2017, 4, 1981 |
1553790 | CIF | C29 H23 N2 O3 P | P -1 | 9.5853; 9.8739; 14.7007 103.11; 94.035; 114.371 | 1213.1 | Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides Organic Chemistry Frontiers, 2017, 4, 1981 |
1553791 | CIF | C28 H21 N2 O2 P | P 1 21/c 1 | 11.9961; 8.631; 21.6563 90; 95.014; 90 | 2233.68 | Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides Organic Chemistry Frontiers, 2017, 4, 1981 |
1553792 | CIF | C33 H27 O2 P | P 21 21 21 | 9.0757; 10.4623; 26.2445 90; 90; 90 | 2491.99 | Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides Organic Chemistry Frontiers, 2017, 4, 1854 |
1553793 | CIF | C32 H25 O P | P 1 21/c 1 | 12.3885; 18.8197; 10.4583 90; 103.828; 90 | 2367.66 | Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides Organic Chemistry Frontiers, 2017, 4, 1854 |
1553794 | CIF | C28 H33 B O4 | P -1 | 10.0442; 10.4197; 11.9542 84.471; 84.954; 75.059 | 1200.58 | Hsieh, Jen-Chieh; Hong, Ya-Chun; Yang, Chun-Ming; Mannathan, Subramaniyan; Cheng, Chien-Hong Nickel-catalyzed highly chemo- and stereoselective borylative cyclization of 1,6-enynes with bis(pinacolato)diboron Organic Chemistry Frontiers, 2017, 4, 1615 |
1553795 | CIF | C19 H19 Br O6 | P 21 21 2 | 22.0623; 14.5144; 5.67392 90; 90; 90 | 1816.91 | Hao, Xiaoyu; Lin, Lili; Tan, Fei; Ge, Shulin; Liu, Xiaohua; Feng, Xiaoming Asymmetric synthesis of chromans via the Friedel‒Crafts alkylation‒hemiketalization catalysed by an N,N′-dioxide scandium(iii) complex Organic Chemistry Frontiers, 2017, 4, 1647 |
1553796 | CIF | C21 H18 Br N O3 | P 1 21 1 | 10.4368; 6.0294; 15.7294 90; 107.537; 90 | 943.81 | De Munck, Lode; Sukowski, Verena; Vila, Carlos; Muñoz, M. Carmen; Pedro, José R. Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines Organic Chemistry Frontiers, 2017, 4, 1624 |
1553797 | CIF | C20 H13 F N2 O | P 1 21/n 1 | 9.17425; 7.88736; 21.7312 90; 99.3556; 90 | 1551.57 | Ren, Xuhong; Wang, Qiyang; Yu, Wenjia; Zhan, Xiaoyu; Yao, Yishan; Qin, Bingjie; Dong, Mingxin; He, Xinhua Photoredox catalytic intramolecular imine C‒H bond functionalization using ligand free Cu(ii) salts Organic Chemistry Frontiers, 2017, 4, 2022 |
1553798 | CIF | C7 H9 N7 O9 | C 1 c 1 | 7.6272; 13.3952; 11.846 90; 90.87; 90 | 1210.1 | Hou, Tianjiao; Zhang, Jian; Wang, Chenjiao; Luo, Jun A facile method to construct a 2,4,9-triazaadamantane skeleton and synthesize nitramine derivatives Organic Chemistry Frontiers, 2017, 4, 1819 |
1553799 | CIF | C21 H40 O3 Si | P 1 21/c 1 | 15.7593; 6.7689; 21.0839 90; 104.622; 90 | 2176.24 | Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis Gold(i)-catalyzed access to neomerane skeletons Organic Chemistry Frontiers, 2017, 4, 1906 |
1553800 | CIF | C22 H26 N4 O6 | P -1 | 8.7959; 10.4916; 13.2932 70.468; 74.252; 71.371 | 1076.8 | Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis Gold(i)-catalyzed access to neomerane skeletons Organic Chemistry Frontiers, 2017, 4, 1906 |
1553801 | CIF | C22 H26 N4 O6 | P 1 21/n 1 | 15.8792; 7.383; 18.5839 90; 94.011; 90 | 2173.37 | Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis Gold(i)-catalyzed access to neomerane skeletons Organic Chemistry Frontiers, 2017, 4, 1906 |
1553802 | CIF | C22 H26 N4 O6 | P 1 21/c 1 | 19.2372; 19.7853; 12.577 90; 107.983; 90 | 4553.1 | Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis Gold(i)-catalyzed access to neomerane skeletons Organic Chemistry Frontiers, 2017, 4, 1906 |
1553803 | CIF | C21 H38 O3 Si | P 1 21/n 1 | 15.0743; 6.8149; 21.2545 90; 92.709; 90 | 2181.03 | Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis Gold(i)-catalyzed access to neomerane skeletons Organic Chemistry Frontiers, 2017, 4, 1906 |
1553804 | CIF | C28 H29 I O4 S | P 1 21/n 1 | 12.0087; 17.7464; 12.6045 90; 103.892; 90 | 2607.6 | Miao, Maozhong; Xu, Huaping; Luo, Yi; Jin, Mengchao; Chen, Zhengkai; Xu, Jianfeng; Ren, Hongjun A modular approach to highly functionalized 3-sulfonylfurans via conjugate addition of 3-cyclopropylideneprop-2-en-1-ones with sodium sulfinates and sequential 5-endo-trig iodocyclization Organic Chemistry Frontiers, 2017, 4, 1824 |
1553805 | CIF | C22 H20 O3 | P -1 | 9.8395; 10.7013; 10.8636 114.335; 94.477; 116.312 | 885.4 | Shi, Xiaonan; He, Yan; Zhang, Xinying; Fan, Xuesen Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones Organic Chemistry Frontiers, 2017, 4, 1967 |
1553806 | CIF | C22 H19 N O5 S | P 21 21 21 | 8.8173; 14.3926; 15.3659 90; 90; 90 | 1949.99 | Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin Ni(ii)-Catalyzed enantioselective Mukaiyama‒Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters Organic Chemistry Frontiers, 2017, 4, 1858 |
1553807 | CIF | C21 H23 N O5 S | P 1 21 1 | 8.2203; 9.1263; 13.0906 90; 102.302; 90 | 959.52 | Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin Ni(ii)-Catalyzed enantioselective Mukaiyama‒Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters Organic Chemistry Frontiers, 2017, 4, 1858 |
1553808 | CIF | C62 H102 Cl8 N26 O21 Zn2 | C 1 2/c 1 | 29.3492; 12.5025; 25.3876 90; 113.65; 90 | 8533.3 | Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 1799 |
1553809 | CIF | C60 H68 Cl8 N26 O28 Zn2 | C 1 2/c 1 | 27.52; 17.25; 18.358 90; 94.006; 90 | 8694 | Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 1799 |
1553810 | CIF | C58 H94 Cl6 N26 O22 Zn2 | P -1 | 12.2894; 12.4667; 14.986 73.289; 84.747; 62.451 | 1947.4 | Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 1799 |
1553811 | CIF | C60 H112 Cl10 N26 O28 Zn2 | P -1 | 12.298; 12.903; 15.662 75.259; 70.211; 76.684 | 2233 | Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 1799 |
1553812 | CIF | C62 H108 Cl10 N26 O28 Zn2 | P -1 | 12.315; 12.875; 15.525 75.131; 70.361; 77.82 | 2219.6 | Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 1799 |
1553813 | CIF | C21 H21 Br N2 O2 | P -1 | 5.095; 12.261; 17 73.395; 81.56; 78.69 | 993 | Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines Organic Chemistry Frontiers, 2017, 4, 1833 |
1553814 | CIF | C22 H26 N2 O4 | P -1 | 6.1408; 10.54; 16.567 87.399; 81.181; 79.922 | 1043.1 | Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines Organic Chemistry Frontiers, 2017, 4, 1833 |
1553815 | CIF | C23 H23 Cl O7 | P 21 21 21 | 6.82668; 9.4989; 34.5079 90; 90; 90 | 2237.7 | Yao, Qian; Lin, Lili; Zhang, Hang; Yu, Han; Xiong, Qian; Liu, Xiaohua; Feng, Xiaoming The asymmetric synthesis of multisubstituted diquinanes via the domino reaction of electron-deficient enynes Organic Chemistry Frontiers, 2017, 4, 2012 |
1553816 | CIF | C19 H17 N O3 S | P 1 21/n 1 | 7.8333; 8.7742; 23.1441 90; 95.475; 90 | 1583.46 | De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M. TBAF catalyzed one-pot synthesis of allenyl-indoles Organic Chemistry Frontiers, 2017, 4, 1849 |
1553817 | CIF | C20 H16 F3 N O3 S | P 1 | 8.5679; 12.3701; 18.181 83.843; 89.595; 80.871 | 1891.4 | De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M. TBAF catalyzed one-pot synthesis of allenyl-indoles Organic Chemistry Frontiers, 2017, 4, 1849 |
1553818 | CIF | C15 H10 I2 O4 | P 1 21/c 1 | 14.884; 4.3831; 27.39 90; 117.921; 90 | 1578.9 | Tang, Yang; Yu, Qiong; Ma, Shengming Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C‒C bond cleavage Organic Chemistry Frontiers, 2017, 4, 1762 |
1553819 | CIF | C25 H26 F3 N O5 | P 1 21/n 1 | 14.9433; 9.3141; 17.6377 90; 102.36; 90 | 2397.98 | Tang, Yang; Yu, Qiong; Ma, Shengming Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C‒C bond cleavage Organic Chemistry Frontiers, 2017, 4, 1762 |
1553820 | CIF | C21 H24 F3 N O4 | P 1 21/c 1 | 15.6855; 9.6366; 13.4345 90; 96.4; 90 | 2018.03 | Tang, Yang; Yu, Qiong; Ma, Shengming Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C‒C bond cleavage Organic Chemistry Frontiers, 2017, 4, 1762 |
1553821 | CIF | C19 H21 F3 O5 | P -1 | 8.577; 11.253; 11.3999 83.261; 69.715; 68.411 | 959.58 | Tang, Yang; Yu, Qiong; Ma, Shengming Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C‒C bond cleavage Organic Chemistry Frontiers, 2017, 4, 1762 |
1553822 | CIF | C19 H15 N3 O4 | P c a 21 | 16.2553; 8.3116; 24.8996 90; 90; 90 | 3364.12 | Krylov, Igor B.; Paveliev, Stanislav A.; Shelimov, Boris N.; Lokshin, Boris V.; Garbuzova, Irina A.; Tafeenko, Viktor A.; Chernyshev, Vladimir V.; Budnikov, Alexander S.; Nikishin, Gennady I.; Terent'ev, Alexander O. Selective cross-dehydrogenative C‒O coupling of N-hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis Organic Chemistry Frontiers, 2017, 4, 1947 |
1553823 | CIF | C24 H21 F2 O3 P | C 1 2/c 1 | 25.317; 8.8649; 22.042 90; 120.571; 90 | 4259.3 | Zhang, Pengbo; Ying, Jianxi; Tang, Guo; Zhao, Yufen Phosphinodifluoroalkylation of alkynes using P(O)H compounds and ethyl difluoroiodoacetate Organic Chemistry Frontiers, 2017, 4, 2054 |
1553824 | CIF | C26 H28 N2 O5 | P 1 21/n 1 | 7.75; 20.882; 14.5149 90; 93.914; 90 | 2343.5 | Yang, Minghua; Zhang, Shusheng; Zhang, Xiang; Wang, Haoyang; Zhang, Fang; Hou, Yuting; Su, Yue; Guo, Yinlong An unexpected acid-catalyzed decomposition reaction of cilnidipine and pranidipine to the decarboxylative bridged tricyclic products via cascade rearrangements Organic Chemistry Frontiers, 2017, 4, 2163 |
1553825 | CIF | C18 H22 O5 | I 1 2/a 1 | 9.6871; 14.029; 23.8866 90; 90.258; 90 | 3246.2 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553826 | CIF | C20 H26 O6 | P 1 21/c 1 | 10.2811; 28.3515; 12.9191 90; 103.741; 90 | 3657.9 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553827 | CIF | C27 H33 N O7 S | C 1 2/c 1 | 22.151; 9.8005; 26.0531 90; 117.401; 90 | 5021.3 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553828 | CIF | C18 H22 O6 | P -1 | 8.9279; 10.0249; 10.8557 115.731; 104.925; 90.322 | 838 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553829 | CIF | C19 H23 O6 | P 1 21/n 1 | 5.9908; 12.2284; 23.731 90; 90; 90 | 1738.5 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553830 | CIF | C27 H33 N O7 S | C 1 2/c 1 | 13.7047; 15.4463; 24.0895 90; 97.806; 90 | 5052.2 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553831 | CIF | C19 H24 O5 | P -1 | 8.981; 10.331; 10.885 66.11; 71.31; 87.32 | 870.7 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553832 | CIF | C25 H29 N O7 S | P -1 | 9.88; 10.9717; 12.836 85.382; 71.391; 65.05 | 1193.2 | Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters Organic Chemistry Frontiers, 2017, 4, 2109 |
1553833 | CIF | C23 H19 Cl F3 N O5 | P -1 | 7.3052; 10.5757; 14.449 88.853; 83.694; 77.708 | 1084.1 | Sun, Yao-Liang; Wei, Yin; Shi, Min Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides Organic Chemistry Frontiers, 2017, 4, 2392 |
1553834 | CIF | C19 H23 Cl F3 N O4 | P 1 21/n 1 | 11.287; 12.727; 14.808 90; 103.68; 90 | 2066.8 | Sun, Yao-Liang; Wei, Yin; Shi, Min Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides Organic Chemistry Frontiers, 2017, 4, 2392 |
1553835 | CIF | C21 H17 Cl F3 N O3 | C 1 2/c 1 | 21.872; 7.604; 24.313 90; 110.597; 90 | 3785.1 | Sun, Yao-Liang; Wei, Yin; Shi, Min Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides Organic Chemistry Frontiers, 2017, 4, 2392 |
1553836 | CIF | C16 H15 N O | P 1 21 1 | 6.9086; 9.5831; 19.453 90; 96.737; 90 | 1279 | Zhang, Wei; Yu, Wenlong; Yan, Qiangqiang; Liu, Zhanxiang; Zhang, Yuhong Synthesis of substituted oxazoles via Pd-catalyzed tandem oxidative cyclization Organic Chemistry Frontiers, 2017, 4, 2428 |
1553837 | CIF | C25 H29 N O5 S | P 1 21/c 1 | 11.7381; 13.2058; 14.4879 90; 98.487; 90 | 2221.19 | Lv, Leiyang; Lu, Shenglin; Chen, Yuanjin; Li, Zhiping Diastereoselective building up polycyclic tetrahydrofurans via tandem annulation of 1,n-enynes with aliphatic acids Organic Chemistry Frontiers, 2017, 4, 2147 |
1553838 | CIF | C29 H25 N O7 S | P 21 21 21 | 8.0159; 15.545; 21.174 90; 90; 90 | 2638.4 | Li, Shoulei; Zhang, Enge; Feng, Junjun; Li, Xin An enantioselective conjugate addition reaction of 3-substituted benzothiophen-2-ones and 2-phthalimidoacrylates Organic Chemistry Frontiers, 2017, 4, 2301 |
1553839 | CIF | C15 H17 F N2 O2 | P -1 | 9.5214; 9.6784; 9.8861 114.205; 92.568; 116.743 | 712.04 | Yang, Zi; Lin, Xing; Wang, Lianhui; Cui, Xiuling Facile synthesis of 1-aminoindoles via Rh(iii)-catalysed intramolecular three-component annulation Organic Chemistry Frontiers, 2017, 4, 2179 |
1553840 | CIF | C23 H22 Br N O4 S | P 1 21/n 1 | 10.723; 9.856; 20.94 90; 100.205; 90 | 2178 | Wang, Weiyi; He, Qiuqin; Fan, Renhua PhI(OAc)2-mediated dialkoxylation of 4-aminostyrenes through a dearomatization process under metal-free conditions Organic Chemistry Frontiers, 2017, 4, 2156 |
1553841 | CIF | C17 H21 N O4 S | P 1 21/n 1 | 13.746; 8.2548; 15.646 90; 104.468; 90 | 1719.1 | Wang, Weiyi; He, Qiuqin; Fan, Renhua PhI(OAc)2-mediated dialkoxylation of 4-aminostyrenes through a dearomatization process under metal-free conditions Organic Chemistry Frontiers, 2017, 4, 2156 |
1553842 | CIF | C40 H48 Cl2 N2 O2 Pd | P 1 21/n 1 | 11.7394; 19.838; 16.5546 90; 94.489; 90 | 3843.5 | Chen, Fu-Min; Huang, Fei-Dong; Yao, Xue-Yi; Li, Tian; Liu, Feng-Shou Direct C‒H heteroarylation by an acenaphthyl-based α-diimine palladium complex: improvement of the reaction efficiency for bi(hetero)aryls under aerobic conditions Organic Chemistry Frontiers, 2017, 4, 2336 |
1553843 | CIF | C16 H15 N O4 | P 21 21 21 | 7.973; 12.9128; 14.3781 90; 90; 90 | 1480.28 | Wu, Qiuju; Li, Chengcheng; Wang, Weihong; Wang, Hongling; Pan, Dingwu; Zheng, Pengcheng NHC-catalyzed enantioselective synthesis of dihydropyran-4-carbonitriles bearing all-carbon quaternary centers Organic Chemistry Frontiers, 2017, 4, 2323 |
1553844 | CIF | C20 H21 N O2 | P 1 21/n 1 | 11.831; 8.4718; 16.4581 90; 90.759; 90 | 1649.45 | Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming Asymmetric SN2′-type C‒H functionalization of arenes with propargylic alcohols Organic Chemistry Frontiers, 2017, 4, 2002 |
1553845 | CIF | C24 H27 N O | P -1 | 8.316; 10.229; 13.179 69.905; 82.818; 72.23 | 1002.3 | Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming Asymmetric SN2′-type C‒H functionalization of arenes with propargylic alcohols Organic Chemistry Frontiers, 2017, 4, 2002 |
1553846 | CIF | C17 H22 I N O2 | P 1 21/n 1 | 11.781; 12.2621; 12.7517 90; 110.261; 90 | 1728.1 | Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming Asymmetric SN2′-type C‒H functionalization of arenes with propargylic alcohols Organic Chemistry Frontiers, 2017, 4, 2002 |
1553847 | CIF | C8 H6 Br F3 O S | P 1 21/c 1 | 20.993; 3.9406; 12.147 90; 95.906; 90 | 999.5 | Zhang, Yunxiao; Wu, Dongping; Weng, Zhiqiang Synthesis of 1,2,2-trifluorovinyl sulphides and selenides from trifluorovinylation of organic thiocyanates and selenocyanates Organic Chemistry Frontiers, 2017, 4, 2226 |
1553848 | CIF | C26 H20 Br N O4 S | P -1 | 9.3385; 11.1134; 11.912 69.983; 88.735; 69.443 | 1080.8 | Jin, Hongxing; Li, Erqing; Huang, You Divergent synthesis of hydropyridine derivatives via nitrogen-containing Lewis base mediated regioselective [4 + 2] cyclizations Organic Chemistry Frontiers, 2017, 4, 2216 |
1553849 | CIF | C26 H20 Br N O4 S | C 1 2/c 1 | 27.96; 10.908; 16.954 90; 121.023; 90 | 4431 | Jin, Hongxing; Li, Erqing; Huang, You Divergent synthesis of hydropyridine derivatives via nitrogen-containing Lewis base mediated regioselective [4 + 2] cyclizations Organic Chemistry Frontiers, 2017, 4, 2216 |
1553850 | CIF | C18 H16 O4 S | P 21 21 21 | 9.7797; 10.9021; 14.8619 90; 90; 90 | 1584.6 | Zhao, Wei-Wei; Liu, Yan-Kai Enantio- and diastereoselective synthesis of tetrahydrofuro[2,3-b]furan-2(3H)-one derivatives and related oxygen heterocycles via an asymmetric organocatalytic cascade process Organic Chemistry Frontiers, 2017, 4, 2358 |
1553851 | CIF | C100 H96 Cl6 N6 O10 | P -1 | 9.8074; 13.2321; 17.7176 100.836; 99.601; 93.264 | 2217.36 | Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang Novel, linear oligoisoindole compounds with a conjugated electronic structure Organic Chemistry Frontiers, 2017, 4, 2364 |
1553852 | CIF | C88 H122 N2 O4 S2 | P 1 | 8.9041; 14.0916; 16.2768 104.121; 91.824; 94.954 | 1970.23 | Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang Novel, linear oligoisoindole compounds with a conjugated electronic structure Organic Chemistry Frontiers, 2017, 4, 2364 |
1553853 | CIF | C202 H249 Cl14 N9 O15 | P -1 | 18.0089; 19.4187; 29.7417 90.357; 95.539; 107.328 | 9875.8 | Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang Novel, linear oligoisoindole compounds with a conjugated electronic structure Organic Chemistry Frontiers, 2017, 4, 2364 |
1553854 | CIF | C132 H154 Cl12 N6 O8 | P 1 21/c 1 | 9.9153; 27.367; 23.7531 90; 93.29; 90 | 6434.8 | Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang Novel, linear oligoisoindole compounds with a conjugated electronic structure Organic Chemistry Frontiers, 2017, 4, 2364 |
1553855 | CIF | C18 H16 Cl N O4 S | P 21 21 21 | 5.1621; 16.3247; 20.251 90; 90; 90 | 1706.5 | Deng, Hua; He, Fu-Sheng; Li, Cong-Shan; Yang, Wu-Lin; Deng, Wei-Ping Enantioselective construction of tricyclic pyrrolidine-fused benzo[b]thiophene 1,1-dioxide derivatives via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition Organic Chemistry Frontiers, 2017, 4, 2343 |
1553866 | CIF | C31 H36 N2 O4 | P -1 | 8.4885; 10.6796; 16.8127 74.369; 82.265; 75.011 | 1414.37 | Wu, Jia-Le; Wang, Jing-Yi; Wu, Ping; Mei, Guang-Jian; Shi, Feng Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols Organic Chemistry Frontiers, 2017, 4, 2465 |
1553867 | CIF | C23 H20 N O2 | P 61 | 18.5578; 18.5578; 9.8682 90; 90; 120 | 2943.2 | Wu, Jia-Le; Wang, Jing-Yi; Wu, Ping; Mei, Guang-Jian; Shi, Feng Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols Organic Chemistry Frontiers, 2017, 4, 2465 |
1553868 | CIF | C17 H22 N2 O2 | P 1 21/n 1 | 6.0777; 22.245; 11.8606 90; 96.163; 90 | 1594.3 | Liu, Xueke; Qian, Ping; Wang, Yi; Pan, Yi Metal-free sequential decarbonylative annulation of N-cyanamides for the construction of 2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ones Organic Chemistry Frontiers, 2017, 4, 2370 |
1553869 | CIF | C20 H22 N2 O | C 1 2/c 1 | 21.107; 7.3437; 21.914 90; 101.993; 90 | 3322.6 | Liu, Xueke; Qian, Ping; Wang, Yi; Pan, Yi Metal-free sequential decarbonylative annulation of N-cyanamides for the construction of 2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ones Organic Chemistry Frontiers, 2017, 4, 2370 |
1553870 | CIF | C31 H38 O9 | P 1 21 1 | 7.9044; 11.5678; 15.8146 90; 98.267; 90 | 1431.01 | Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence Organic Chemistry Frontiers, 2017, 4, 2417 |
1553871 | CIF | C31 H38 O9 | P 21 21 21 | 14.6815; 17.2043; 23.1115 90; 90; 90 | 5837.62 | Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence Organic Chemistry Frontiers, 2017, 4, 2417 |
1553875 | CIF | C25 H24 Br2 N2 O3 S | P -1 | 8.4549; 13.872; 14.009 117.552; 101.368; 92.964 | 1408.7 | Jiang, Bo; Shi, Min Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene Organic Chemistry Frontiers, 2017, 4, 2459 |
1553876 | CIF | C44 H45 Br2 N3 O6 S2 | P 1 21/c 1 | 13.823; 11.5473; 30.267 90; 98.559; 90 | 4777.4 | Jiang, Bo; Shi, Min Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene Organic Chemistry Frontiers, 2017, 4, 2459 |
1553877 | CIF | C43 H38 Br N3 O4 S2 | P -1 | 11.936; 13.1209; 13.8558 89.702; 84.883; 66.69 | 1983.8 | Jiang, Bo; Shi, Min Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene Organic Chemistry Frontiers, 2017, 4, 2459 |
1553878 | CIF | C31 H26 N2 O2 S | P -1 | 10.688; 10.745; 11.245 103.535; 94.412; 96.045 | 1241.6 | Jiang, Bo; Shi, Min Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene Organic Chemistry Frontiers, 2017, 4, 2459 |
1553879 | CIF | C25 H21 Br N2 O2 S | C 1 2/c 1 | 24.816; 10.401; 16.9512 90; 96.192; 90 | 4349.8 | Jiang, Bo; Shi, Min Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene Organic Chemistry Frontiers, 2017, 4, 2459 |
1553881 | CIF | C72 H112 Cl2 N28 O26 | C 1 2/c 1 | 24.1839; 31.5567; 12.6112 90; 104.99; 90 | 9296.9 | Xiao, Zhi-You; Lin, Rui-Lian; Tao, Zhu; Liu, Qing-Yun; Liu, Jing-Xin; Xiao, Xin Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and α,α′,δ,δ′-tetramethylcucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 2422 |
1553882 | CIF | C108 H176 Cl6 N52 O50 Sr2 | P -1 | 12.8381; 15.6916; 22.2878 92.995; 98.521; 106.862 | 4227.9 | Xiao, Zhi-You; Lin, Rui-Lian; Tao, Zhu; Liu, Qing-Yun; Liu, Jing-Xin; Xiao, Xin Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and α,α′,δ,δ′-tetramethylcucurbit[6]uril Organic Chemistry Frontiers, 2017, 4, 2422 |
1554091 | CIF | C42 H36 N2 O2 | P 42/n :2 | 23.1475; 23.1475; 12.6145 90; 90; 90 | 6758.9 | Mallia, Ajith R.; Hariharan, Mahesh Self-Assembled Donor‒Acceptor Trefoils: Long-Lived Charge Separated State through Aggregation The Journal of Physical Chemistry C, 2017, 121, 4778 |
1554092 | CIF | C28 H28 N2 O4 | P 1 21 1 | 11.584; 12.031; 18.156 90; 96.06; 90 | 2516.2 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554093 | CIF | C26 H24 N2 O4 | P 21 21 21 | 9.65062; 11.62065; 19.4417 90; 90; 90 | 2180.32 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554094 | CIF | C26 H24 N2 O4 | P 21 21 21 | 9.754; 11.691; 19.628 90; 90; 90 | 2238.3 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554095 | CIF | C26 H23 Br N2 O4 | P 1 21/c 1 | 16.479; 9.0821; 15.44 90; 101.98; 90 | 2260.5 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554096 | CIF | C26 H23 Br N2 O4 | P 41 21 2 | 11.3983; 11.3983; 36.807 90; 90; 90 | 4782 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554097 | CIF | C28 H27 Br N2 O4 | P 1 21 1 | 11.4; 19.6; 11.58 90; 91.95; 90 | 2586 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554098 | CIF | C26 H23 Br N2 O4 | P 1 21/c 1 | 10.863; 11.675; 19.581 90; 77.94; 90 | 2428.6 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554099 | CIF | C26 H23 Br N2 O4 | P 43 21 2 | 11.3202; 11.3202; 36.3968 90; 90; 90 | 4664.14 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554100 | CIF | C28 H27 Br N2 O4 | P 1 21 1 | 11.4015; 19.6478; 11.6171 90; 91.917; 90 | 2600.9 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554101 | CIF | C28 H27 Br N2 O4 | P 1 21/c 1 | 11.401; 11.654; 19.628 90; 96.697; 90 | 2590 | Zhu, Qiuhua; Dai, Chenshu; Huang, Cuihong; Zheng, Sichao; Tian, Yuanxin Racemates Have Much Higher Solid-State Fluorescence Efficiency than Their Levo- and Dextrorotary Enantiomers The Journal of Physical Chemistry C, 2017, 121, 25503 |
1554168 | CIF | C41 H46 Br2 Cl2 N2 Ni | P -1 | 16.4259; 17.1593; 17.2162 76.75; 69.223; 75.674 | 4342 | Zhong, Liu; Li, Guiliang; Liang, Guodong; Gao, Haiyang; Wu, Qing Enhancing Thermal Stability and Living Fashion in α-Diimine‒Nickel-Catalyzed (Co)polymerization of Ethylene and Polar Monomer by Increasing the Steric Bulk of Ligand Backbone Macromolecules, 2017, 50, 2675 |
1554169 | CIF | C48 H60 Br2 N2 Ni | R -3 :H | 26.8702; 26.8702; 35.7526 90; 90; 120 | 22355.3 | Zhong, Liu; Li, Guiliang; Liang, Guodong; Gao, Haiyang; Wu, Qing Enhancing Thermal Stability and Living Fashion in α-Diimine‒Nickel-Catalyzed (Co)polymerization of Ethylene and Polar Monomer by Increasing the Steric Bulk of Ligand Backbone Macromolecules, 2017, 50, 2675 |
1554170 | CIF | C48 H54 N2 O2 Y2 | P 1 21/c 1 | 9.447; 15.805; 13.524 90; 100.792; 90 | 1983.6 | Pahl, Philipp; Schwarzenböck, Christina; Herz, Fabian A. D.; Soller, Benedikt S.; Jandl, Christian; Rieger, Bernhard Core-First Synthesis of Three-Armed Star-Shaped Polymers by Rare Earth Metal-Mediated Group Transfer Polymerization Macromolecules, 2017, 50, 6569 |
1554171 | CIF | C76 H86 N3 O3 Y3 | P -1 | 7.9941; 19.5986; 23.2344 78.1666; 89.6646; 88.2859 | 3561.3 | Pahl, Philipp; Schwarzenböck, Christina; Herz, Fabian A. D.; Soller, Benedikt S.; Jandl, Christian; Rieger, Bernhard Core-First Synthesis of Three-Armed Star-Shaped Polymers by Rare Earth Metal-Mediated Group Transfer Polymerization Macromolecules, 2017, 50, 6569 |
1555980 | CIF | C26 H27 N7 O2 | P 1 21 1 | 11.8603; 9.4892; 12.0188 90; 118.477; 90 | 1188.99 | Shiomi, Noriyuki; Yamamoto, Keisuke; Nagasaki, Kazuma; Hatanaka, Tsubasa; Funahashi, Yasuhiro; Nakamura, Shuichi Enantioselective Oxidative Ring-Opening Reaction of Aziridines with α-Nitroesters Using Cinchona Alkaloid Amide/Nickel(II) Catalysts. Organic letters, 2017, 19, 74-77 |
1555992 | CIF | C26 H24 N2 O2 | P -1 | 8.1158; 9.2869; 14.1457 86.852; 84.763; 70.523 | 1000.62 | Fan, Ling; Liu, Meilin; Ye, Yu; Yin, Guodong Synthesis of 6-Substituted 6H-Indolo[2,3-b]quinolines from Isoindigos. Organic letters, 2017, 19, 186-189 |
1555993 | CIF | C21 H13 F N2 | P 43 | 11.1632; 11.1632; 12.0079 90; 90; 90 | 1496.4 | Fan, Ling; Liu, Meilin; Ye, Yu; Yin, Guodong Synthesis of 6-Substituted 6H-Indolo[2,3-b]quinolines from Isoindigos. Organic letters, 2017, 19, 186-189 |
1555994 | CIF | C19 H27 Br N O2 Si | P 21 21 21 | 10.5667; 11.1762; 18.221 90; 90; 90 | 2151.8 | Alicea-Matías, Eyleen; Soderquist, John A. Asymmetric Propargylboration of Aldimines and Ketimines with the Borabicyclo[3.3.2]decanes: Novel Entries to Allenyl Carbinamines, Amino Acids, and Their α-Methyl Counterparts. Organic letters, 2017, 19, 336-339 |
1555996 | CIF | C21 H22 Br N O2 | P 1 21 1 | 6.0625; 19.5089; 16.3468 90; 96.885; 90 | 1919.44 | Wu, Chun-Yan; Yu, Yue-Na; Xu, Ming-Hua Construction of Chiral Tricyclic Indoles through a Rhodium-Catalyzed Asymmetric Arylation Protocol. Organic letters, 2017, 19, 384-387 |
1555997 | CIF | C21 H15 N3 O2 | P -1 | 7.1592; 9.8482; 12.3493 81.6372; 83.2218; 80.227 | 845.03 | Ramakrishna, Isai; Bhajammanavar, Vinod; Mallik, Sumitava; Baidya, Mahiuddin Advanced Nitroso Aldol Reaction: Metal-Free Cross-Coupling of Anilines with Silyl Enol Ethers en Route to α-Amino Ketones. Organic letters, 2017, 19, 516-519 |
1555998 | CIF | C20 H12 F3 N3 | P 1 21/c 1 | 11.696; 9.0705; 15.811 90; 102.782; 90 | 1635.8 | Ramakrishna, Isai; Bhajammanavar, Vinod; Mallik, Sumitava; Baidya, Mahiuddin Advanced Nitroso Aldol Reaction: Metal-Free Cross-Coupling of Anilines with Silyl Enol Ethers en Route to α-Amino Ketones. Organic letters, 2017, 19, 516-519 |
1555999 | CIF | C17 H17 N O3 | P -1 | 8.4056; 9.8583; 10.2022 69.4122; 78.7895; 71.4852 | 747.18 | Ramakrishna, Isai; Bhajammanavar, Vinod; Mallik, Sumitava; Baidya, Mahiuddin Advanced Nitroso Aldol Reaction: Metal-Free Cross-Coupling of Anilines with Silyl Enol Ethers en Route to α-Amino Ketones. Organic letters, 2017, 19, 516-519 |
1556000 | CIF | C19 H24 N2 O2 S | P 1 21 1 | 11.0611; 6.743; 13.0444 90; 102.392; 90 | 950.25 | Ma, Peng-Ju; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun Diastereoselective Electrophilic α-Hydroxyamination of N-tert-Butanesulfinyl Imidates. Organic letters, 2017, 19, 670-673 |
1556001 | CIF | C30 H30 N2 O3 | R -3 :H | 26.495; 26.495; 25.84 90; 90; 120 | 15709 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556002 | CIF | C29 H28 N2 O3 | P 1 21/c 1 | 12.7136; 19.6481; 10.0368 90; 104.806; 90 | 2423.9 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556003 | CIF | C29 H28 N2 O3 | P 1 21/c 1 | 8.088; 29.039; 10.3957 90; 98.253; 90 | 2416.3 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556004 | CIF | C28 H26 N2 O3 | P -1 | 9.715; 11.622; 13.28 64.317; 86.248; 74.246 | 1298.2 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556005 | CIF | C26 H30 N2 O3 | P 1 21/c 1 | 11.5919; 14.5845; 13.8674 90; 97.872; 90 | 2322.4 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556006 | CIF | C34 H36 Cl2 N2 O5 | P 1 21/c 1 | 10.3241; 23.365; 13.7004 90; 99.642; 90 | 3258.2 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556007 | CIF | C33 H34 N2 O5 | P 1 21/c 1 | 13.9135; 11.8443; 18.4125 90; 108.518; 90 | 2877.2 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556008 | CIF | C29.5 H29 Cl N2 O3 S | P 32 2 1 | 18.4813; 18.4813; 16.4257 90; 90; 120 | 4858.7 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556009 | CIF | C26 H30 N2 O3 | P 1 21/n 1 | 9.5688; 10.3956; 23.8948 90; 96.847; 90 | 2359.9 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556010 | CIF | C24 H24 N2 O2 | P 1 21/c 1 | 10.9969; 11.8906; 15.8497 90; 106.796; 90 | 1984.1 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556011 | CIF | C33 H34 N2 O5 | P 1 21/c 1 | 16.2583; 8.9359; 19.545 90; 95.231; 90 | 2827.7 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556012 | CIF | C26 H30 N2 O3 | P 1 21/c 1 | 15.2433; 10.1136; 14.943 90; 94.937; 90 | 2295.1 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556013 | CIF | C29 H28 N2 O3 | P 1 21/c 1 | 7.8226; 30.639; 10.1141 90; 98.682; 90 | 2396.3 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556014 | CIF | C29 H28 N2 O3 S | P 1 21/c 1 | 8.6571; 29.45; 10.2183 90; 98.7924; 90 | 2574.56 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556015 | CIF | C26 H30 N2 O3 | C 1 2/c 1 | 17.3068; 12.0144; 22.5999 90; 96.044; 90 | 4673.1 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556016 | CIF | C29 H28 N2 O3 | C 1 2 1 | 22.49; 5.1816; 20.19 90; 90.78; 90 | 2352.6 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556017 | CIF | C29 H28 N2 O3 S | P 1 21/n 1 | 19.7344; 12.7882; 20.279 90; 97.031; 90 | 5079.3 | Halli, Juliette; Bolte, Michael; Bats, Jan; Manolikakes, Georg Modular Two-Step Approach for the Stereodivergent Synthesis of 1,3-Diamines with Three Continuous Stereocenters. Organic letters, 2017, 19, 674-677 |
1556018 | CIF | C23 H17 Cl O3 | C 1 2 1 | 20.5553; 9.5675; 22.2196 90; 115.687; 90 | 3937.9 | Infante, Rebeca; Martin-Alvarez, Jose M; Andrés, Celia; Nieto, Javier Dimethylzinc-Mediated Addition of Phenylacetylene to α-Diketones Catalyzed by Chiral Perhydro-1,3-benzoxazines. Organic letters, 2017, 19, 1516-1519 |
1556019 | CIF | C16 H11 F N2 O | P 21 21 21 | 8.4334; 9.1934; 16.9142 90; 90; 90 | 1311.4 | Jin, Yushu; Chen, Ming; Ge, Shaozhong; Hartwig, John F. Palladium-Catalyzed, Enantioselective α-Arylation of α-Fluorooxindoles. Organic letters, 2017, 19, 1390-1393 |
1556020 | CIF | C15 H12 N2 O | P 1 21/n 1 | 16.4017; 7.1335; 20.0858 90; 95.665; 90 | 2338.6 | Yin, Kun; Zhang, Ronghua Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature. Organic letters, 2017, 19, 1530-1533 |
1556021 | CIF | C16 H14 N2 O | P n a 21 | 9.9288; 26.7988; 4.7384 90; 90; 90 | 1260.79 | Yin, Kun; Zhang, Ronghua Transition-Metal-Free Direct C-H Arylation of Quinoxalin-2(1H)-ones with Diaryliodonium Salts at Room Temperature. Organic letters, 2017, 19, 1530-1533 |
1556022 | CIF | C17 H13 N O | P 1 21/c 1 | 4.0198; 13.908; 23.21 90; 94.2; 90 | 1294.1 | Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines. Organic letters, 2017, 19, 1550-1553 |
1556023 | CIF | C11 H13 N S2 | P 1 21 1 | 9.9321; 22.705; 19.824 90; 98.538; 90 | 4420.9 | Wu, Xia; Geng, Xiao; Zhao, Peng; Zhang, Jingjing; Gong, Xingxing; Wu, Yan-Dong; Wu, An-Xin I<sub>2</sub>-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines. Organic letters, 2017, 19, 1550-1553 |
1556024 | CIF | C43 H30 N2 O2 | P -1 | 10.4789; 12.074; 12.5011 92.552; 94.697; 98.319 | 1557.2 | Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions. Organic letters, 2017, 19, 1658-1661 |
1556025 | CIF | C42 H28 N2 O2 | P b c a | 18.5446; 17.7946; 18.9442 90; 90; 90 | 6251.5 | Feng, Yadong; Tian, Nian; Li, Yudong; Jia, Chunqi; Li, Xuening; Wang, Lianhui; Cui, Xiuling Construction of Fused Polyheterocycles through Sequential [4 + 2] and [3 + 2] Cycloadditions. Organic letters, 2017, 19, 1658-1661 |
1556026 | CIF | C47 H36 Cl2 N4 O S Zn | P -1 | 11.0032; 12.6313; 14.724 98.868; 96.16; 102.84 | 1950 | Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality. Organic letters, 2017, 19, 1722-1725 |
1556027 | CIF | C51 H37 N5 O S Zn | P 1 | 10.6689; 10.8762; 18.2817 83.457; 84.152; 77.519 | 2051.2 | Gholami, Hadi; Zhang, Jun; Anyika, Mercy; Borhan, Babak Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality. Organic letters, 2017, 19, 1722-1725 |
1556028 | CIF | C32 H27 Br O2 | P 1 21 1 | 9.624; 31.096; 13.229 90; 91.141; 90 | 3958 | Perveen, Saima; Zhao, Zhifei; Zhang, Guoxiang; Liu, Jian; Anwar, Muhammad; Fang, Xinqiang Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis. Organic letters, 2017, 19, 2470-2473 |
1556029 | CIF | C94 H64 O2 | P -1 | 9.9734; 11.3386; 15.3837 79.9686; 85.4756; 79.5603 | 1682.69 | Vadehra, Geeta S.; Jiang, Xing; Dotson, Jordan J.; Chu, Gong M.; Garcia-Garibay, Miguel A High-Yielding and Divergent Paradigm for the Synthesis of D<sub>2h</sub>-Symmetric Octakis-Substituted Pentiptycenequinones. Organic letters, 2017, 19, 1838-1841 |
1556030 | CIF | C24 H26 N2 O6 | P 1 21 1 | 11.0167; 8.4713; 13.145 90; 112.969; 90 | 1129.5 | Ran, Guang-Yao; Gong, Ming; Yue, Jing-Fei; Yang, Xing-Xing; Zhou, Su-Lan; Du, Wei; Chen, Ying-Chun Asymmetric Cascade Assembly of 1,2-Diaza-1,3-dienes and α,β-Unsaturated Aldehydes via Dienamine Activation. Organic letters, 2017, 19, 1874-1877 |
1556031 | CIF | C14 H9 N O3 S | P 1 21/c 1 | 12.0277; 13.0209; 8.1447 90; 106.121; 90 | 1225.4 | Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation. Organic letters, 2017, 19, 2042-2045 |
1556032 | CIF | C14 H13 N O3 S | P 21 21 21 | 7.4865; 10.7242; 32.3467 90; 90; 90 | 2597.01 | Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation. Organic letters, 2017, 19, 2042-2045 |
1556033 | CIF | C14 H12 N O3 S | P 21 21 21 | 9.4952; 13.78766; 23.3234 90; 90; 90 | 3053.42 | Jeran, Marko; Cotman, Andrej Emanuel; Stephan, Michel; Mohar, Barbara Stereopure Functionalized Benzosultams via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation. Organic letters, 2017, 19, 2042-2045 |
1556034 | CIF | C24 H24 N2 O3 Se | P 1 21/c 1 | 9.4838; 10.5004; 21.1264 90; 90.868; 90 | 2103.6 | Foley, Christopher; Shaw, Arthur; Hulme, Christopher Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles. Organic letters, 2017, 19, 2238-2241 |
1556035 | CIF | C14 H16 N4 O | P 1 21/m 1 | 7.7378; 6.7075; 12.6395 90; 102.323; 90 | 640.89 | Foley, Christopher; Shaw, Arthur; Hulme, Christopher Oxidative Deaminations and Deisatinylations of Ugi-Azide and Ugi-3CR Products: A Two-Step MCR-Oxidation Protocol toward Functionalized α-Ketoamides and α-Ketotetrazoles. Organic letters, 2017, 19, 2238-2241 |
1556036 | CIF | C28 H44 Cl2 N8 Ni O2 | I m -3 m | 17.0714; 17.0714; 17.0714 90; 90; 90 | 4975.2 | Zhang, Xingjie; Xia, Aiyou; Chen, Haoyi; Liu, Yuanhong General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)<sub>2</sub>: Key Roles of DMAP. Organic letters, 2017, 19, 2118-2121 |
1556037 | CIF | C23 H18 O2 | P 1 21 1 | 6.0965; 7.8294; 17.9271 90; 96.951; 90 | 849.41 | Zhang, Jingfang; Tang, Yuhai; Wei, Wen; Wu, Yong; Li, Yang; Zhang, Junjie; Zheng, Yuansuo; Xu, Silong Organocatalytic Cloke-Wilson Rearrangement: DABCO-Catalyzed Ring Expansion of Cyclopropyl Ketones to 2,3-Dihydrofurans. Organic letters, 2017, 19, 3043-3046 |
1556038 | CIF | C26 H34 O4 Si | P 21 21 21 | 9.47; 15.075; 17.824 90; 90; 90 | 2544.6 | Han, Man-Yi; Xie, Xiaoyu; Zhou, Di; Li, Pinhua; Wang, Lei Organocatalyzed Direct Aldol Reaction of Silyl Glyoxylates for the Synthesis of α-Hydroxysilanes. Organic letters, 2017, 19, 2282-2285 |
1556039 | CIF | C16 H13 Br F3 N O3 | P 21 21 21 | 5.8132; 8.851; 31.166 90; 90; 90 | 1603.6 | Wang, Pei; Li, Hong-Feng; Zhao, Jia-Zhen; Du, Zhi-Hong; Da, Chao-Shan Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones. Organic letters, 2017, 19, 2634-2637 |
1556040 | CIF | C22 H26 O4 S | P b c a | 5.5413; 15.8031; 45.3572 90; 90; 90 | 3971.92 | Zhurakovskyi, Oleksandr; Ellis, Sam R.; Thompson, Amber L.; Robertson, Jeremy Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland-Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl. Organic letters, 2017, 19, 2174-2177 |
1556041 | CIF | C19 H37 Br Cu N3 P2 | I 41 c d | 31.5316; 31.5316; 18.8701 90; 90; 90 | 18761.4 | Mastalir, Matthias; Pittenauer, Ernst; Stöger, Berthold; Allmaier, Günter; Kirchner, Karl Three Different Reactions, One Catalyst: A Cu(I) PNP Pincer Complex as Catalyst for C-C and C-N Cross-Couplings. Organic letters, 2017, 19, 2178-2181 |
1556042 | CIF | C27 H22 O S | P 21 21 21 | 5.3756; 8.23448; 44.3104 90; 90; 90 | 1961.41 | Wang, Zhaobin; Sun, Jianwei Enantioselective [4 + 2] Cycloaddition of o-Quinone Methides and Vinyl Sulfides: Indirect Access to Generally Substituted Chiral Chromanes. Organic letters, 2017, 19, 2334-2337 |
1556043 | CIF | C11 H10 F7 N3 O2 | P 1 21/c 1 | 16.1302; 7.5328; 12.1195 90; 90.161; 90 | 1472.6 | Wang, Rui; Guan, Wei; Han, Zheng-Bo; Liang, Fushun; Suga, Takeo; Bi, Xihe; Nishide, Hiroyuki Ambient-Light-Promoted Three-Component Annulation: Synthesis of Perfluoroalkylated Pyrimidines. Organic letters, 2017, 19, 2358-2361 |
1556044 | CIF | C25 H31 N O7 Si | P -1 | 9.5604; 11.3393; 12.5938 64.094; 79.058; 86.136 | 1205.56 | Parsons, Philip J.; Jones, Daniel R.; Walsh, Lee J.; Allen, Lewis A. T.; Onwubiko, Ada; Preece, Lewis; Board, Johnathan; White, Andrew J. P. An Approach to the Core of Lactonamycin. Organic letters, 2017, 19, 2533-2535 |
1556045 | CIF | C19 H20 O3 | C 1 2 1 | 17.9303; 6.8625; 13.4226 90; 99.456; 90 | 1629.16 | Iwamoto, Hiroaki; Akiyama, Sota; Hayama, Keiichi; Ito, Hajime Copper(I)-Catalyzed Stereo- and Chemoselective Borylative Radical Cyclization of Alkyl Halides Bearing an Alkene Moiety. Organic letters, 2017, 19, 2614-2617 |
1556046 | CIF | C12 H6 O S2 | P b c a | 5.541; 15.387; 22.574 90; 90; 90 | 1925 | Mitsudo, Koichi; Kurimoto, Yuji; Mandai, Hiroki; Suga, Seiji Synthesis of 3-Benzo[b]thienyl 3-Thienyl Ether via an Addition-Elimination Reaction and Its Transformation to an Oxygen-Fused Dithiophene Skeleton: Synthesis and Properties of Benzodithienofuran and Its π-Extended Derivatives. Organic letters, 2017, 19, 2821-2824 |
1556047 | CIF | C19 H26 Cl N2 O Rh | P b c a | 8.0471; 16.3426; 29.6614 90; 90; 90 | 3900.8 | Long, Zhen; Yang, Yudong; You, Jingsong Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles. Organic letters, 2017, 19, 2781-2784 |
1556048 | CIF | C22 H24 Cl N2 O Rh | P 1 21/n 1 | 7.58618; 16.9757; 15.6843 90; 93.0656; 90 | 2016.94 | Long, Zhen; Yang, Yudong; You, Jingsong Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2H-Indazoles. Organic letters, 2017, 19, 2781-2784 |
1556049 | CIF | C116 H112 Cl2 N10 Ni | P -1 | 12.6554; 19.7134; 21.0374 72.334; 80.809; 82.734 | 4919.7 | Yin, Bangshao; Kim, Taeyeon; Zhou, Mingbo; Huang, Weiming; Kim, Dongho; Song, Jianxin Porphyrin-Azobenzene-Bodipy Triads: Syntheses, Structures, and Photophysical Properties. Organic letters, 2017, 19, 2654-2657 |
1556050 | CIF | C27 H23 N O3 S | P 21 21 21 | 11.4379; 12.8956; 15.0848 90; 90; 90 | 2225 | Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations. Organic letters, 2017, 19, 3111-3114 |
1556051 | CIF | C33 H26 Cl N O4 S | P 21 21 21 | 8.9355; 14.869; 20.8047 90; 90; 90 | 2764.2 | Wang, Zhen; Xu, Huacheng; Su, Qin; Hu, Ping; Shao, Pan-Lin; He, Yun; Lu, Yixin Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations. Organic letters, 2017, 19, 3111-3114 |
1556052 | CIF | C204 H280 N24 O20 S12 | P 1 21/n 1 | 22.6919; 27.504; 32.801 90; 93.8825; 90 | 20425 | Cholewiak, Agnieszka; Tycz, Agnieszka; Jurczak, Janusz 8-Propyldithieno[3,2-b:2',3'-e]pyridine-3,5-diamine (DITIPIRAM) Derivatives as Neutral Receptors Tailored for Binding of Carboxylates. Organic letters, 2017, 19, 3001-3004 |
1556053 | CIF | C22 H22 Cl N O6 | C 1 2 1 | 21.5482; 6.1634; 16.9021 90; 111.981; 90 | 2081.59 | Drelich, Piotr; Moczulski, Marek; Albrecht, Łukasz d<sup>0</sup>a<sup>3</sup> Synthon Equivalents for the Stereocontrolled Synthesis of Functionalized 1,4-Amino Alcohol Precursors. Organic letters, 2017, 19, 3143-3146 |
1556054 | CIF | C19 H18 N2 O2 S | P 1 21/n 1 | 7.8427; 22.614; 18.528 90; 93.229; 90 | 3280.8 | Wang, Xingyong; Liu, Chulong; Zeng, Xiaobao; Wang, Xuesong; Wang, Xinyan; Hu, Yuefei Ruthenium-Catalyzed Synthesis of Fused Tricyclic 1H-2,3-Dihydropyrimido[1,2-a]quinolines in One Step. Organic letters, 2017, 19, 3378-3381 |
1556055 | CIF | C19 H19 Cl N6 O | C 1 2 1 | 20.4899; 9.7314; 10.0601 90; 101.493; 90 | 1965.72 | Li, Dan; Wang, Kezhou; Wang, Linqing; Wang, Yuan; Wang, Pengxin; Liu, Xin; Yang, Dongxu; Wang, Rui Magnesium Catalysis Mediated Tetrazoles in Desymmetrization Reaction of Aziridines. Organic letters, 2017, 19, 3211-3214 |
1556056 | CIF | C17.5 H14 N2 O1.5 | P 21 21 21 | 7.1969; 9.884; 38.6328 90; 90; 90 | 2748.11 | Mei, Guang-Jian; Bian, Chen-Yu; Li, Guo-Hao; Xu, Shao-Li; Zheng, Wen-Qin; Shi, Feng Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization. Organic letters, 2017, 19, 3219-3222 |
1556057 | CIF | C14 H10 N2 O2 | P b c a | 8.0739; 10.2485; 27.568 90; 90; 90 | 2281.1 | Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O. Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers. Organic letters, 2017, 19, 3512-3515 |
1556058 | CIF | C18 H18 N2 O3 | C 1 2/c 1 | 34.507; 7.3494; 13.4613 90; 110.662; 90 | 3194.3 | Jones, D. Heulyn; Kay, Steven T.; McLellan, Jayde A.; Kennedy, Alan R.; Tomkinson, Nicholas C. O. Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers. Organic letters, 2017, 19, 3512-3515 |
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