Crystallography Open Database

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Searching year of publication is 2017

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1548791 CIF
HKL
Paper
C19 H14 Br F N2 OP b c a13.4521; 7.181; 34.204
90; 90; 90
3304.1Kalecik, 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 O2P -19.0951; 13.9582; 14.1083
61.646; 80.859; 83.665
1554.92Guerrab, 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 O2P -14.5971; 6.4372; 25.237
86.984; 86.173; 78.096
728.56Atalay, 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 SP -14.8078; 7.7314; 17.8011
93.412; 94.564; 103.05
640.5Missioui, 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 O3P 1 21/c 119.817; 8.4268; 12.4459
90; 101.22; 90
2038.7Xia, 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 TeP 21 21 214.8809; 8.5668; 4.3433
90; 90; 90
181.609Weil, Matthias
Redetermination of the γ-form of tellurium dioxide
IUCrData, 2017, 2
1548797 CIF
HKL
Paper
C9 H10 Cl3 N O2P -16.7395; 11.3491; 16.1078
75.681; 88.031; 86.856
1191.69Suresh, S.; Pandi, P.; Kumar, R. Mohan; Chakkaravarthi, G.
4-Methylanilinium trichloroacetate
IUCrData, 2017, 2, x171767
1548798 CIF
HKL
C22 H29 Br N4 Se2I 1 2/a 123.767; 5.1425; 39.806
90; 102.61; 90
4747.8Rani, 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 OP 1 21/c 15.7747; 6.5171; 30.234
90; 95.342; 90
1132.89El-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 OP -16.6115; 15.2036; 15.3021
63.536; 83.76; 85.214
1367.75Abu 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 OP 21 21 216.0506; 13.7423; 20.886
90; 90; 90
1736.7Green, 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 O6P 1 21/n 14.7936; 12.9828; 14.632
90; 92.986; 90
909.4Zhang, Huihui; Wang, Haiyan; Yu, Jianhua
1,4-Bis(4-methyl-2-nitrophenoxy)butane
IUCrData, 2017, 2, x171734
1548803 CIF
HKL
Paper
C16 H21 N OC 1 2/c 120.3655; 7.6148; 18.2999
90; 99.254; 90
2801Jebapriya, 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 P3C 1 2/c 132.3691; 10.7492; 13.1332
90; 125.578; 90
3716.6Hou, 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 CIFCa Cl2 Cu3 H7.58 O6.79P -3 m 16.6615; 6.6615; 5.8023
90; 90; 120
222.985Crichton, 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 CIFC H7.89 N O7.45 P VP -16.3844; 7.2278; 9.2965
67.26; 72.927; 85.848
377.8C. 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 CIFC4 H14 Cu2 O14 P2C 1 2/c 116.233; 6.24; 14.955
90; 122.45; 90
1278.3Köferstein, 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 CIFC2 H12 Cu1.5 O10 PP -16.082; 8.001; 10.836
94.98; 105.71; 109.84
468.08Köferstein, 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 CIFCu2 S4 Sn ZnI -4 2 m5.434; 5.434; 10.845
90; 90; 90
320.24Munoz, 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 CIFCr2 Mg2 O5P b a m9.6091; 12.4324; 2.8498
90; 90; 90
340.449Ishii, 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 CIFC18 H18 In N3 O8F d d d15.3069; 26.9467; 31.284
90; 90; 90
12903.7Carrington, 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 CIFF6 K6 Mn Na3 O76 W17C 1 2/c 122.586; 12.292; 29.421
90; 92.34; 90
8161Roy 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 CIFCs11 F12 K5 Mn2 Na2 O128 W34C m c e17.983; 18.413; 22.333
90; 90; 90
7395Roy 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 CIFC628.5 H496.5 B115.5 Co12 F81 N117 O54 S27R -3 :H48.517; 48.517; 64.134
90; 90; 120
130740Felix J. Rizzuto; Jonathan R. Nitschke
Stereochemical plasticity modulates cooperative binding in a CoII12L6 cuboctahedron
Nature Chemistry, 2017, 10, 903-908
1551393 CIFC764 H707 B264 Co12 N115 OP -126.438; 30.374; 31.047
67.3; 84.86; 78.93
22569Felix J. Rizzuto; Jonathan R. Nitschke
Stereochemical plasticity modulates cooperative binding in a CoII12L6 cuboctahedron
Nature Chemistry, 2017, 10, 903-908
1551394 CIFC618 H355.5 B5.5 Co12 F133 N117 O74 S37P 1 21/n 140.2042; 54.2465; 40.2935
90; 90.408; 90
87875Felix J. Rizzuto; Jonathan R. Nitschke
Stereochemical plasticity modulates cooperative binding in a CoII12L6 cuboctahedron
Nature Chemistry, 2017, 10, 903-908
1551423 CIFC80 H104 Ag12 F12 N8 O16.8 S8I -4 2 m17.2768; 17.2768; 20.4482
90; 90; 90
6103.54Ren-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 CIFC88 H128 Ag12 F12 N8 O12 S8I -4 2 m17.2793; 17.2793; 19.8246
90; 90; 90
5919.1Ren-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 CIFC84 H108 Ag12 Cl12 F12 N8 O8 S8I -4 2 m17.1887; 17.1887; 20.4219
90; 90; 90
6033.7Ren-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 CIFC82.4 H107.6 Ag12 F12 N9.2 O6 S8I -4 2 m17.3814; 17.3814; 20.0977
90; 90; 90
6071.78Ren-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 CIFC83 H110 Ag12 F12 N8 O9 S8I -4 2 m17.27; 17.27; 20.04
90; 90; 90
5977Ren-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 CIFC98 H140 Ag12 F12 N8 O8 S8I -4 2 m17.2498; 17.2498; 21.101
90; 90; 90
6278.7Ren-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 CIFC50 H75 Ag12 F18 N7 O12 S6P -115.4518; 15.8621; 17.9312
91.3274; 95.0852; 94.9884
4358.91Ren-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 CIFC80 H104 Ag12 F12 N8 O8 S8I -4 2 m17.34149; 17.34149; 20.1671
90; 90; 90
6064.8Ren-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 CIFC80 H104 Ag12 F12 N8 O8 S8I -4 2 m17.29649; 17.29649; 19.8753
90; 90; 90
5946.07Ren-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 CIFC80 H104 Ag12 F12 N8 O8 S8I -4 2 m17.33048; 17.33048; 20.251
90; 90; 90
6082.3Ren-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 CIFC96 H136 Ag12 F12 N8 O16 S8I -4 2 m17.1785; 17.1785; 20.8487
90; 90; 90
6152.47Ren-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 CIFC104 H128 Ag12 F12 N8 O8 S8I -4 2 m17.298; 17.298; 20.5393
90; 90; 90
6145.79Ren-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 CIFC94 H120 Ag12 F12 N8 O8 S8I -4 2 m17.26652; 17.26652; 20.5352
90; 90; 90
6122.21Ren-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 CIFC104 H124 Ag12 F16 N8 O8 S8I -4 2 m17.3073; 17.3073; 20.4745
90; 90; 90
6133Ren-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 CIFC92 H114 Ag12 Cl2 F12 N8 O8 S8I -4 2 m17.23734; 17.23734; 20.5923
90; 90; 90
6118.51Ren-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 CIFC92 H114 Ag12 Br2 F12 N8 O8 S8I -4 2 m17.2292; 17.2292; 20.5453
90; 90; 90
6098.8Ren-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 CIFC92 H114 Ag12 F12 I2 N8 O8 S8I -4 2 m17.2105; 17.2105; 20.6982
90; 90; 90
6130.8Ren-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 CIFC96 H124 Ag12 F12 N8 O8 S8I -4 2 m17.2348; 17.2348; 20.8923
90; 90; 90
6205.8Ren-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 CIFC96 H124 Ag12 F12 N8 O8 S8I -4 2 m17.2529; 17.2529; 20.6795
90; 90; 90
6155.5Ren-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 CIFC96 H124 Ag12 F12 N8 O8 S8I -4 2 m17.2603; 17.2603; 20.5849
90; 90; 90
6132.61Ren-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 CIFC336 H264 F96 Fe8 N96 Sb16P -125.4839; 33.5954; 37.4035
89.22; 83.44; 80.438
31370.6Ben 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 CIFC232 H194.5 F48 Fe4 N42.5 O24.5 P8P -122.2379; 22.4501; 30.1489
69.385; 86.301; 78.614
13810.4Ben 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 CIFC279 H244.5 As8 F48 Fe4 N37.5 O24C 1 2/c 153.942; 28.539; 41.2325
90; 90.231; 90
63475Ben 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 CIFC276 H174 Co6 P6 Te8C 1 2/c 129.47019; 17.3534; 38.00346
90; 103.98; 90
18859.6Evan 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 CIFC234 H126 Co6 P6 Te8R -3 m :H16.9985; 16.9985; 55.684
90; 90; 120
13934.2Evan 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 CIFC246 H126 Co6 N8 P6 Te8I 1 2/m 126.5695; 17.056; 21.1219
90; 104.26; 90
9276.9Evan 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 CIFC44 H58 N4 Ni2 O11C 1 2/c 118.321; 13.543; 18.649
90; 108.372; 90
4391LIM, 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 CIFC34 H48 N4 Ni4 O10P 1 21/c 112.154; 11.821; 15.945
90; 112.214; 90
2120.8MIKURIYA, 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 CIFC30 H24 O9P 1 21/n 110.676; 10.017; 24.438
90; 100.89; 90
2566.4DOCHEV, 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 CIFC48 H58 B F4 Fe N6 O2P -17.9064; 13.7091; 20.7535
90.87; 92.579; 93.419
2242.83IDE, 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 CIFC32 H30 N4 Ni O8C 1 2/c 117.6548; 19.0788; 9.2011
90; 103.547; 90
3013UEJI, 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 CIFC14 H17 Cu N4 O1.5C 1 2/c 117.975; 18.894; 9.2081
90; 113.728; 90
2862.9MIKURIYA, 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 CIFC72 H72 Cl7 Fe N6 O6P -115.2889; 15.8587; 16.2403
84.596; 63.769; 84.162
3508.49IDE, 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 CIFC9 H12 N2 S3P 1 21/c 110.178; 13.357; 8.845
90; 98.613; 90
1188.9OSMAN, 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 CIFC13 H14 N2 Ni O4P 1 21/c 19.364; 17.725; 7.753
90; 105.004; 90
1242.9MIKURIYA, 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 CIFC21 H22 B N OP n a 2116.6818; 11.5428; 9.2234
90; 90; 90
1776SAKIYAMA, 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 CIFC12 H25 N O13P 16.914; 7.7202; 8.7383
79.467; 73.033; 67.106
409.71FUJIMOTO, 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 CIFC13.5 H16 N4 Ni O1.5P -19.6947; 12.0269; 13.2626
94.036; 108.801; 104.82
1395.3MIKURIYA, 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 CIFC21 H21 N2 O4 PdP 1 21/n 112.5115; 10.5337; 15.008
90; 94.0547; 90
1973AHMAD, 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 CIFC22 H32 N2 O2C 1 2/c 117.319; 9.7041; 13.352
90; 114.032; 90
2049.5MIKURIYA, 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 CIFC9 H8 F3 N3 SP -17.0109; 11.7862; 14.9095
111.814; 91.72; 101.036
1115.7OSMAN, 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 CIFC82 H100 B2 Cl2 Mg2 N4 O10C 1 2/c 122.7667; 19.1628; 17.3218
90; 96.15; 90
7513.6SAKIYAMA, 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 CIFC43 H56 N4 Ni2 O11C 1 c 118.157; 13.1691; 18.88
90; 110.483; 90
4229LIM, 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 CIFC28 H26 Cl N6 O3.5 RuI 1 2/a 115.4085; 13.0737; 27.383
90; 98.0922; 90
5461.27TOYAMA, 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 CIFC20 H37 N O20P 21 21 218.7221; 9.697; 31.8548
90; 90; 90
2694.22FUJIMOTO, 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 CIFC8 H22 Mo2 N4 O4 S2C 1 2/c 113.975; 12.475; 12.158
90; 100.091; 90
2086.8MIKURIYA, 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 CIFC35 H46 B2 Cl2 Cu2 F8 N6 O5P 1 21/c 18.4305; 27.302; 19.131
90; 102.724; 90
4295.2UMEMOTO, 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 CIFC18 H21 Cl3 N3 O2.202 PP 19.6898; 10.4576; 21.0199
83.6336; 89.3963; 73.819
2032.53ARIANI, 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 CIFC23 H29 N5 O5P -19.3554; 11.445; 11.5629
87.14; 78.807; 69.2119
1135.21GUILLON, 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 CIFC11 H14 B N O5 SP 1 21/c 18.57927; 6.99494; 21.076
90; 99.4787; 90
1247.53TAKEYAMA, 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 CIFC23 H28 N Ni S10P 21 21 217.9129; 17.27; 21.673
90; 90; 90
2961.7KAKIHARA, 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 CIFC194 H201 Cl8 N27 O54 Zn4P -120.5708; 21.4332; 24.3151
92.087; 91.4; 112.299
9903.7Jia-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 CIFC55.5 H49.5 F6 N6 O6P -119.6706; 22.8014; 25.4507
99.269; 107.063; 106.023
10118.2Jia-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 CIFC190 H147 Cl6 F18 N20 O44 Zn3P -112.1557; 24.1339; 39.3371
85.206; 87.55; 75.675
11139.3Jia-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 CIFC124 H98 Cl4 F12 N10 O30 Zn2C 1 2 133.7737; 19.1957; 37.7788
90; 101.142; 90
24030.7Jia-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 CIFC85.82 H25.82 B12 Cl5.46 F60 O12.99R -3 :H14.7965; 14.7965; 38.3211
90; 90; 120
7265.9Elaine 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 CIFC156 H72 B12 F60 O12P -119.211; 19.674; 22.866
97.606; 114.089; 109.756
7048Elaine 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 CIFC69 H118 N2 P4 Ti2P -110.838; 11.7188; 15.3855
111.957; 95.397; 103.468
1726.6Douglas 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 CIFC19 H15 PP 1 21/c 110.1072; 9.2624; 15.2719
90; 93.254; 90
1427.4Douglas 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 CIFC31 H32 N4 NiP -18.4416; 10.8919; 7.2749
90.465; 113.158; 78.08
599.74Daniel 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 CIFC29 H31 F14 N O SiP 18.6241; 9.7969; 18.9232
80.469; 83.314; 76.243
1526.55Mattia 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 CIFC33 H26 O2 SP 1 21 129.4752; 8.8183; 37.823
90; 97.4465; 90
9748.1Mattia 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 CIFC42 H46 B F18 N O2 SiP 21 21 2110.6934; 17.4932; 24.2485
90; 90; 90
4536Mattia 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 CIFC15 H13 B F2 N4P 1 21/c 113.747; 8.8403; 12.9567
90; 114.796; 90
1429.4Hai 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 CIFC44 H28 Au N4P -16.1691; 10.6043; 12.4939
97.479; 97.453; 99.925
788.51Sebastian 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 CIFC88 H81 B F24 Ga N2 P2 RhP 1 21/n 116.1707; 13.4756; 40.4746
90; 99.5199; 90
8698.35Joseph 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 CIFC87 H114 Al F37 Ga N2 O4 P2 RhP -115.8418; 17.8312; 19.9771
67.4818; 79.5277; 88.0398
5122.13Joseph 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 CIFC71 H91 Al F36 Ga N2 O4 P2 RhP -111.0613; 18.6711; 20.1393
87.3183; 84.9976; 88.3665
4137.67Joseph 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 CIFC72 H93 Al F36 Ga N2 O4 P2 RhP -118.3055; 20.3348; 22.683
95.335; 90.4516; 93.0358
8394.4Joseph 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 CIFC95 H119.5 Al F36.5 Ga2 N4 O4 P RhP -113.5818; 19.8497; 19.8951
95.6299; 90.1027; 91.1299
5336.67Joseph 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 CIFC39 H63 ThP 1 21/n 110.7341; 19.6772; 17.8417
90; 104.847; 90
3642.65Alasdair 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 CIFC39 H63 UP 1 21/n 110.7925; 19.3497; 17.8721
90; 104.314; 90
3616.4Alasdair 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 CIFC39 H63 Cl UP 1 21/c 120.1; 21.4218; 20.1165
90; 118.596; 90
7605.1Alasdair 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 CIFC34 H14 Br4 N4P 1 21/n 111.2408; 4.6467; 25.9293
90; 99.857; 90
1334.36Wei 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 CIFC34 H18 N4P 1 21/c 13.77; 16.615; 17.088
90; 95.723; 90
1065Wei 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 CIFC4 H12 K Na O10P 21 21 211.7721; 14.2054; 6.1836
90; 90; 90
1034.07Macdonald, 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 CIFC4 H12 K Na O10P 21 21 211.7708; 14.2037; 6.1841
90; 90; 90
1033.91Macdonald, 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 CIFC44.25 H74 N5 O11P 1 21 114.6436; 10.578; 15.5742
90; 92.794; 90
2409.58Almaliti, 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 CIFC19 H18 O2P 1 21/c 114.6675; 11.5099; 18.5162
90; 104.72; 90
3023.34Maurent, 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 CIFC20 H20 O2P 1 21/n 19.3466; 12.3756; 14.0627
90; 98.832; 90
1607.34Maurent, 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 CIFC20 H20 O2P 1 21 19.0364; 8.1877; 10.7482
90; 101.86; 90
778.25Maurent, 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 CIFC19 H18 O2P -19.7921; 11.467; 13.899
88.098; 79.234; 79.122
1505.6Maurent, 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 CIFC35 H44 O12P 21 21 215.7364; 19.8524; 11.454
90; 90; 90
3578.3Esposito, 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 CIFC42 H54 Cl4 N4 Ni2 O2P -19.7278; 10.55; 11.522
91.22; 109.68; 108.69
1043.6Zhang, 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 CIFC36 H40 Cl2 N4 NiP 1 21/n 19.0742; 14.496; 12.391
90; 98.03; 90
1613.9Zhang, 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 CIFC17 H20 Br N O5P -15.2286; 8.35; 20.2441
79.956; 89.888; 81.369
860.17Xie, 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 CIFC46 H44 Br2 N2 NiC 1 2/c 19.6692; 15.1682; 28.4042
90; 95.927; 90
4143.61Sui, 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 CIFC56 H49 Cl3 N2 PdP 1 21/n 110.7748; 24.3601; 18.0013
90; 95.951; 90
4699.4Sui, 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 CIFC47 H47 Cl N2 PdP -113.1491; 19.2193; 19.3227
105.127; 109.315; 96.896
4333Sui, 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 CIFC28 H20 SI 1 2 115.4081; 6.0485; 22.1271
90; 102.299; 90
2014.83Nie, 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 CIFC28 H20 OI 1 2/c 121.71; 8.16; 24.855
90; 113.396; 90
4041Nie, 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 CIFC40 H26 N2 O2 S2P -110.495; 11.772; 13.789
81.56; 71.751; 72.938
1543.9Keshav, 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 CIFC42 H30 N2 O2 S2P -113.352; 16.32; 17.943
99.33; 104.402; 108.992
3452.4Keshav, 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 CIFC78 H82 N4 O16 Zn3P -111.4427; 14.514; 16.196
65.694; 69.783; 73.998
2272.2King, 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 CIFC19 H17 N O4P -18.125; 9.328; 11.408
90.91; 96.19; 107.69
817.8Dai, 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 CIFC36 H32 F2 N2 O2P 21 21 2111.5593; 14.0068; 17.8914
90; 90; 90
2896.78Zhu, 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 CIFC44 H50 N2P 1 21/c 119.661; 10.71; 17.118
90; 97.306; 90
3575Zhu, 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 CIFC16 H18 O3 SP -16.9478; 9.1969; 11.8012
82.206; 81.643; 75.22
717.55Wang, 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 CIFC15 H16 O2 SP 1 21/n 17.68603; 23.9176; 7.76261
90; 111.053; 90
1331.76Wang, 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 CIFC14 H11 N SP 1 21/n 15.7042; 25.743; 7.8069
90; 94.59; 90
1142.71Wang, 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 CIFC15 H14 O SP 1 21/n 15.7958; 25.4544; 8.3123
90; 93.626; 90
1223.85Wang, 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 CIFC15 H14 O2 SP 1 21/n 15.611; 25.6833; 8.991
90; 98.982; 90
1279.8Wang, 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 CIFC14 H11 N O SP 1 21/n 15.67633; 26.8781; 7.7875
90; 95.042; 90
1183.53Wang, 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 CIFC14 H8 N2 S2P -17.8232; 11.6428; 14.5818
84.863; 83.654; 73.557
1263.68Wang, 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 CIFC35 H53 N O3P 1 21 17.455; 11.3624; 18.4877
90; 92.585; 90
1564.44Li, 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 CIFC30 H50 O3P 21 21 216.52391; 12.9427; 31.7963
90; 90; 90
2684.78Li, 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 CIFC22 H21 N O2P 1 21/n 17.348; 22.781; 11.236
90; 101.092; 90
1845.7Yu, 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 CIFC15 H16 N2 O3P 1 21/n 19.3103; 4.8793; 30.741
90; 96.596; 90
1387.3Yu, 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 CIFC25 H21 N O2 SR 3 c :H33.922; 33.922; 11.008
90; 90; 120
10970Gong, 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 CIFC18 H12 Br2P 1 21/n 15.3248; 17.2473; 7.6729
90; 96.167; 90
700.59Wilbuer, 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 CIFC20 H16 Br2P 1 21/c 16.6723; 8.653; 15.099
90; 111.66; 90
810.2Wilbuer, 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 CIFC28 H16 Br2C 1 2/c 121.802; 4.9336; 18.875
90; 90.188; 90
2030.2Wilbuer, 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 CIFC36 H32 Br2P -110.0648; 11.6684; 12.2462
77.981; 86.017; 79.287
1381.44Wilbuer, 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 CIFC34 H28 Br2P 1 21/n 111.131; 10.249; 11.763
90; 101.301; 90
1315.92Wilbuer, 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 CIFC50 H38P -110.8252; 13.5794; 14.2122
114.377; 91.316; 95.604
1889.2Wilbuer, 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 CIFC18 H15 I O SeC 1 2/c 120.3; 5.882; 27.651
90; 94.075; 90
3293Pistoia, 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 CIFC20 H19 I O SeP 1 2/c 119.0809; 5.7136; 17.2112
90; 100.175; 90
1846.87Pistoia, 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 CIFC29 H25 Cl N2 O8 SP 1 21 111.4186; 9.7011; 13.152
90; 92.473; 90
1455.5He, 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 CIFC25 H18 O2P n 21 a14.3717; 5.917; 21.4597
90; 90; 90
1824.88Sreenivasulu, 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 CIFC20 H14 OP 21 21 217.9447; 10.3826; 17.0108
90; 90; 90
1403.16Sreenivasulu, 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 CIFC27 H31 N O7 S3P 1 21/c 121.226; 8.2493; 16.985
90; 109.61; 90
2801.6Chen, 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 CIFC15 H21 N O3 SC 1 2/c 125.961; 5.793; 22.2512
90; 114.088; 90
3055Chen, 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 CIFC18 H16 F3 N O2 S2P -16.52; 8.149; 18.175
102.278; 95.21; 97.731
927.9Chen, Min-Tao; Tang, Xiang-Ying; Shi, Min
A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
Organic Chemistry Frontiers, 2017, 4, 86
1553562 CIFC17 H15 N O2P -113.451; 14.313; 15.248
86.714; 63.827; 90.014
2629.2Rajaguru, 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 CIFC26 H20 Cl N O3P -17.3875; 11.6702; 13.4944
64.647; 82.911; 77.69
1026.5Rajaguru, 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 CIFC23 H24 N2 O6 SP -18.5455; 12.047; 12.1501
60.733; 81.883; 87.112
1079.97Rajaguru, 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 CIFC44 H52 N4 S4P -19.3265; 9.7095; 23.593
78.225; 84.998; 75.52
2023.6Xia, 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 CIFC20 H21 N O8P 1 21/c 18.101; 19.041; 13.693
90; 107.19; 90
2017.8Zhang, 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 CIFC22 H16 Cl N O2P 1 21/n 111.366; 11.305; 14.788
90; 110.536; 90
1779.4Zhu, 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 CIFC33 H30 N4 O3P 1 21 18.902; 13.209; 12.059
90; 99.65; 90
1397.9Cheng, 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 CIFC31 H27 Br N4 O3P 21 21 219.662; 12.286; 24.441
90; 90; 90
2901Cheng, 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 CIFC25 H23 N O3P 418.4091; 8.4091; 29.3175
90; 90; 90
2073.13Xu, 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 CIFC15 H17 Cl N2 O3P 21 21 217.2915; 12.7983; 15.9552
90; 90; 90
1488.92Peng, 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 CIFC15 H11 Cl F3 N3 O3P 21 21 217.74798; 9.1129; 21.719
90; 90; 90
1533.5Hao, 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 CIFC14 H13 N3 O SP -17.68; 8.494; 11.449
85.96; 77.314; 66.467
667.9Chen, 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 CIFC19 H23 Br N O3 PP 21 21 29.8916; 26.4389; 7.7778
90; 90; 90
2034.1Wang, 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 CIFC153.47 H187.47 Cl4.41 N2 Si8P 41 21 221.2715; 21.2715; 64.3247
90; 90; 90
29105.4Ushiyama, 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 CIFC21 H21 Cl F N O2P 1 21/c 19.4639; 21.8249; 9.3192
90; 104.752; 90
1861.42Li, 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 CIFC15 H15 Br O2P 1 21 17.813; 5.321; 15.394
90; 91.594; 90
639.7Li, 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 CIFC11 H14 Br F O2P 21 21 215.651; 16.364; 38.4918
90; 90; 90
3559Li, 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 CIFC17 H12 B F2 N5 OC 1 2/c 110.248; 14.634; 11.146
90; 107.352; 90
1595.5Barbon, 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 CIFC16 H10 Br2 Cl F3P -17.3184; 13.4865; 17.4149
101.672; 94.139; 101.918
1635.33Kazakova, 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 CIFC20 H20 Br F3 OP -17.8481; 10.5581; 12.2042
75.472; 72.741; 72.301
905.55Kazakova, 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 CIFC20 H20 Br F3 O2P -18.3533; 9.4941; 12.1934
100.216; 97.306; 100.289
923.7Kazakova, 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 CIFC18 H15 Br2 F3P b c a16.4974; 6.84171; 28.6498
90; 90; 90
3233.72Kazakova, 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 CIFC16 H11 Br2 F3P -17.1399; 9.7404; 22.8361
97.673; 97.146; 106.455
1487.32Kazakova, 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 CIFC17 H12 Br F3C 1 2/c 122.8229; 7.4881; 16.5828
90; 102.102; 90
2771Kazakova, 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 CIFC19 H17 Br Cl F3P 1 21/c 18.2233; 22.8182; 10.0565
90; 109.447; 90
1779.36Kazakova, 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 CIFC12 H11 I N2 O2C m c e6.9379; 19.798; 17.773
90; 90; 90
2441.2He, 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 CIFC46 H66 Cl2P 1 21/n 110.4263; 10.2668; 40.789
90; 90.6212; 90
4366Prenzel, 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 CIFC47 H64P -110.3367; 10.4631; 19.275
88.5549; 78.0127; 88.5903
2038.2Prenzel, 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 CIFC49 H64P 3 1 c14.154; 14.154; 12.123
90; 90; 120
2103.3Prenzel, 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 CIFC20 H13 F7 N2 OP 1 21/c 17.858; 26.656; 8.984
90; 90.001; 90
1881.8Xu, 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 CIFC44 H58 N2 Se2 Si4P 1 21/n 114.2771; 14.228; 22.6224
90; 99.427; 90
4533.33Xiong, 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 CIFC44 H58 N2 S2 Si4P 1 21/n 114.2494; 14.1245; 22.4876
90; 98.8; 90
4472.7Xiong, 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 CIFC32 H22 Br8 N2P -110.8503; 12.4427; 12.9897
100.306; 91.28; 108.652
1628.82Xiong, 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 CIFC50 H52 N14 O4P 1 21/c 19.842; 21.609; 25.234
90; 91.32; 90
5365.2Zhang, 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 CIFC54.83 H62.12 Cl1.76 N16.83 O2C 1 2/c 128.402; 9.816; 18.722
90; 90.7; 90
5219.2Zhang, 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 CIFC54 H60 N16 O2P -19.6636; 15.1098; 18.1939
69.768; 84.466; 84.513
2475.53Zhang, 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 CIFC40 H24 S2P -17.5051; 8.6296; 11.6509
73.729; 77.669; 77.532
697.78Lo, 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 CIFC46 H32P n a 2116.8864; 7.4906; 24.7447
90; 90; 90
3129.94Lo, 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 CIFC44 H28P -17.597; 8.9994; 11.0344
78.931; 75.805; 83.409
715.94Lo, 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 CIFC26 H22 N4 O5 SC 1 2/c 126.478; 8.1615; 23.0582
90; 96.411; 90
4951.7Chen, Dianpeng; Xing, Gangdong; Yao, Jinzhong; Zhou, Hongwei
Applicable β-sulfonium carbanions: facile construction of thiophene derivatives
Organic Chemistry Frontiers, 2017, 4, 1042
1553602 CIFC12 H9 N O S3P b c n7.9629; 16.9905; 18.7808
90; 90; 90
2540.92Chen, 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 CIFC71 H46 B F24 Ir N O PP 21 21 2112.2302; 15.3106; 36.571
90; 90; 90
6848Wang, 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 CIFC26 H16 Cu N4 O8P 1 21/c 111.1134; 21.1702; 9.8578
90; 101.189; 90
2275.19Baur, 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 CIFC16 H11 N O3P 1 21/c 18.269; 9.296; 16.904
90; 93.281; 90
1297.3Fang, 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 CIFC22 H15 N O2P b c a8.874; 13.733; 27.215
90; 90; 90
3317Fang, 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 CIFC19 H12 N2 O4P -18.066; 8.242; 12.157
92.727; 102.604; 98.233
778Li, 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 CIFC H F N OP -19.4574; 9.9936; 14.0156
89.023; 76.071; 71.074
1213.5Xu, 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 CIFC41 H40 O11P -19.7469; 13.1171; 17.5212
70.806; 75.292; 73.524
1996.5Lu, 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 CIFC43 H46 O11P -115.1534; 15.8118; 17.7296
68.774; 76.898; 79.352
3832Lu, 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 CIFC31 H23 Cl0 N O4P 21 21 219.9046; 10.4946; 23.736
90; 90; 90
2467.2Xu, 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 CIFC30 H21 N O3P 1 21/n 19.263; 16.211; 15.413
90; 91.21; 90
2313.9Xu, 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 CIFC38.5 H33 Cl O3P -112.3342; 12.422; 20.4886
94.35; 97.642; 100.981
3037.8Zhang, 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 CIFC13 H12 N2 OP n a 219.077; 10.4; 11.75
90; 90; 90
1109.2Guo, 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 CIFC23 H19 N O2 S2P 21 21 218.189; 14.782; 17.421
90; 90; 90
2108.8Guo, 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 CIFC22 H24 S4 Si2P 1 21/c 110.5479; 16.6; 13.9079
90; 92.242; 90
2433.3Li, 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 CIFC44 H72 Li4 O4 S4 Si4I 41/a :220.763; 20.763; 13.7545
90; 90; 90
5929.6Li, 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 CIFC17 H17 N O4P -15.7832; 10.4921; 12.3215
90.576; 97.913; 93.157
739.28Chen, 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 CIFC21 H17 F OP 1 21/c 113.585; 12.569; 9.741
90; 106.741; 90
1592.8Cao, 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 CIFC23 H26 OP 1 21/c 112.3103; 20.299; 6.9248
90; 95.884; 90
1721.3Cao, 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 CIFC60 H28 F20 N6 O2P -112.4994; 13.1859; 16.0253
102.651; 95.439; 92.29
2560.5Almeida, 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 CIFC23 H30 N4 O2 SiP b c a15.6516; 14.7041; 20.8303
90; 90; 90
4793.9Morozova, 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 CIFC20 H21 N5 O2 SiP -19.4684; 10.4692; 12.771
96.2634; 95.7478; 113.644
1138.27Morozova, 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 CIFC14 H8 Br3 N3P 1 21/n 116.2913; 10.0932; 19.7897
90; 112.895; 90
2997.7Morozova, 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 CIFC21 H34 N4 O2 SiP b c a8.9462; 11.9145; 43.549
90; 90; 90
4641.9Morozova, 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 CIFC25 H20 O4P 1 21/c 111.9761; 15.4866; 11.0055
90; 106.167; 90
1960.46Mao, 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 CIFC35 H18 Fe O4P -18.8576; 9.515; 15.8743
79.571; 74.479; 86.413
1267.66Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553628 CIFC32 H18 OP 1 21/n 112.737; 10.827; 15.738
90; 105.708; 90
2089.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553629 CIFC51 H29 Cl3 O4P 21 21 2110.5417; 14.8356; 24.1274
90; 90; 90
3773.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553630 CIFC51 H30 Cl2 OP 1 21/n 112.3541; 20.5251; 15.593
90; 111.562; 90
3677.21Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553631 CIFC51 H30 Cl2P 1 21/n 112.2233; 20.4397; 15.612
90; 111.759; 90
3622.59Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553632 CIFC20 H19 Br N2 O5 SP 21 21 218.8208; 12.857; 18.1141
90; 90; 90
2054.3Yu, 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 CIFC29 H25 N3P -15.768; 9.924; 20.463
100.063; 91.086; 92.46
1151.8Zhao, 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 CIFC21 H15 Br2 N O2P 1 21/n 116.003; 7.036; 16.456
90; 101.876; 90
1813.2Qiu, Guanyinsheng; Li, Yuewen; Ma, Lele; Zhou, Hongwei
KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide
Organic Chemistry Frontiers, 2017, 4, 1069
1553635 CIFC33 H31 N O3P 1 21/n 115.552; 9.109; 20
90; 111.508; 90
2636Liu, 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 CIFC25 H20 N2 O2 SP 21 21 217.7445; 13.971; 19.15
90; 90; 90
2072Lin, 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 CIFC16 H21 N3 O5P 21 21 218.4855; 15.887; 25.5299
90; 90; 90
3441.7Deng, 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 CIFC36 H40 N2 O4P 1 21/c 111.882; 6.1567; 22.083
90; 99.617; 90
1592.8Purc, 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 CIFC32 H38 N2 O2 S3P 1 21/c 120.477; 5.2589; 28.0402
90; 101.007; 90
2964Chen, 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 CIFC27 H33 B2 F11 Fe N6F -4 3 c29.3374; 29.3374; 29.3374
90; 90; 90
25250.2Thorarinsdottir, 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 CIFC26 H31.5 B2 F10 Fe N6.5P -111.4603; 14.9231; 18.6992
110.254; 106.434; 91.133
2853Thorarinsdottir, 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 CIFC25 H30 B2 F10 N6 ZnP 1 c 113.6092; 14.5112; 14.1222
90; 90.875; 90
2788.61Thorarinsdottir, 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 CIFC24 H27 B2 F11 Fe N6P 316.8376; 16.8376; 7.8829
90; 90; 120
1935.43Thorarinsdottir, 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 CIFC27 H33 B2 F11 N6 ZnF -4 3 c29.282; 29.282; 29.282
90; 90; 90
25107.4Thorarinsdottir, 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 CIFC8 H8 F6 N4 Ni Si Xe0.34P 4/m m m7.0187; 7.0187; 7.5098
90; 90; 90
369.95Elsaidi, 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 CIFC8 H8 F6 N4 Ni SiP 4/m m m7.00122; 7.00122; 7.49794
90; 90; 90
367.527Elsaidi, 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 CIFC8 H8 F6 N4 Ni SiP 4/m m m6.99732; 6.99732; 7.49177
90; 90; 90
366.816Elsaidi, 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 CIFC8 H8 F6 Fe N4 O SiP 4/m m m7.1831; 7.1831; 7.5839
90; 90; 90
391.31Elsaidi, 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 CIFC6 H8 Bi I4 NP 1 21/c 17.7618; 14.0412; 13.1959
90; 92.959; 90
1436.24Li, 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 CIFC5 H6 Bi I4 NP 1 21/c 112.6997; 28.3198; 7.716
90; 95.288; 90
2763.27Li, 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 CIFC42 H42 I2 N2P 61 2 215.6598; 15.6598; 34.08
90; 90; 120
7237.7Samanta, 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 CIFC46 H38 N6 O4 S2P 1 21/c 116.2355; 14.4863; 17.7924
90; 106.064; 90
4021.2Zhao, 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 CIFC26 H18 S2P 1 21/c 15.641; 9.315; 19.216
90; 103.97; 90
979.9Zhang, 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 CIFC19 H15 B F2 N2P -16.418; 8.632; 14.198
74.951; 81.658; 86.211
751.2Yamaguchi, 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 CIFC19 H13 B F2 N2P 1 21/n 19.2376; 11.5433; 13.4497
90; 98.264; 90
1419.3Yamaguchi, 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 CIFC20 H14 Hg I2 N2 S2P -110.2226; 10.3008; 12.2126
74.477; 67.707; 71.185
1110.69Gabr, 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 CIFC18 H16 Cl4 N4 O2R 3 :H14.7047; 14.7047; 23.9058
90; 90; 120
4476.6Zhang, 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 CIFC27 H30 N4 O3P 1 21/c 19.8325; 11.2257; 22.882
90; 98.783; 90
2496Zhang, 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 CIFC18 H18 F2 N2.67 O2R -3 :H14.4761; 14.4761; 40.5191
90; 90; 120
7353.5Zhang, 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 CIFC30 H34 N4 O6P 21 21 216.29545; 15.9502; 28.8235
90; 90; 90
2894.27Zhang, 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 CIFC39 H54 N4 O3P -112.9272; 13.0256; 23.4928
82.005; 79.707; 86.311
3851.2Zhang, 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 CIFC21 H23 N O2P 1 21/c 115.43; 10.791; 10.129
90; 101.94; 90
1650Wang, 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 CIFC42 H29 N O2P -19.4456; 9.9577; 16.2906
102.183; 93.914; 93.086
1490.57Peng, 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 CIFC42 H29 N O2P -19.4088; 11.452; 15.1598
90.309; 105.929; 93.468
1567.45Peng, 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 CIFC42 H29 N O2P 1 21/c 118.2932; 19.3313; 9.1613
90; 103.67; 90
3148Peng, 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 CIFC37 H43 Cu2 I2 N5 O2 S3P -19.102; 14.511; 17.16
66.114; 88.537; 80.515
2041.9Yang, 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 CIFC34 H27 Cu2 I2 N3 O S3P -19.4203; 14.3226; 17.3309
65.977; 77.856; 79.467
2075.6Yang, 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 CIFC30 H34 Cu2 I2 N4 O S3P -19.174; 14.442; 17.023
113.404; 90.013; 99.203
2038Yang, 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 CIFC31 H33 Cu2 I2 N5 S3P -18.962; 14.515; 16.577
112.653; 91.205; 98.338
1962Yang, 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 CIFC31 H39 Cu2 I2 N3 O2 S5P -19.353; 14.189; 17.257
113.336; 94.402; 100.137
2043Yang, 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 CIFC35 H45 Cu2 I2 N5 O2 S3P -19.252; 14.347; 17.158
113.914; 91.45; 99.705
2041.1Yang, 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 CIFC17 H16 I N O2P 21 21 216.1493; 12.443; 19.762
90; 90; 90
1512.1Butler, 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 CIFC9 H4 N2 O4 Y0.33P 3 1 c12.8501; 12.8501; 15.709
90; 90; 120
2246.4Liu, 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 CIFC22 H24 N3 Ni0.5P -18.3884; 8.4668; 14.2802
95.006; 94.479; 113.925
916.34Yoshida, Takuya; Shinokubo, Hiroshi
Direct amination of the antiaromatic NiII norcorrole
Materials Chemistry Frontiers, 2017, 1, 1853
1553685 CIFC37 H24 N2 O3P 1 21/n 124.2035; 9.4392; 24.306
90; 109.203; 90
5244Gan, 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 CIFC25 H17 N O2P 1 21/c 18.4792; 29.902; 7.9399
90; 117.656; 90
1783.1Gan, 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 CIFC29 H23 N3 O2P 1 21/n 17.3698; 10.7294; 27.0518
90; 90.5158; 90
2138.99Tokuo, 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 CIFC27 H18 Cu2 O11P 63/m m c18.4455; 18.4455; 26.4268
90; 90; 120
7786.7Chen, 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 CIFC28 H20 Cu2 O11P 63/m m c18.2664; 18.2664; 26.5488
90; 90; 120
7671.5Chen, 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 CIFC38 H48 Cu2 N4 O16P 63/m m c18.315; 18.315; 26.7665
90; 90; 120
7775.6Chen, 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 CIFC48 H30 N4P n n a14.768; 15.377; 16.689
90; 90; 90
3790Zhang, 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 CIFC23.5 H20 B0.5C 1 2/c 110.3419; 16.4056; 20.936
90; 100.537; 90
3492.2Chi, 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 CIFC29 H34 B Br2 NP -17.9955; 11.139; 14.735
87.095; 78.445; 81.208
1270.3Matsumoto, 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 CIFC38 H27 Br2 N O2C 1 2/c 119.61; 15.469; 20.516
90; 107.135; 90
5947.2Gopikrishna, 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 CIFC38 H29 N O2P 1 21/c 111.2762; 13.9376; 17.8045
90; 101.143; 90
2745.5Gopikrishna, 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 CIFC22 H23 Cl N2 O0 RuP -110.445; 14.347; 14.407
82.53; 85.3; 74.55
2060.7Li, 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 CIFC18 H13 Cl N2 O2 SC 1 2/c 134.644; 7.0976; 13.544
90; 98.63; 90
3292.6Li, 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 CIFC16 H15 N O7P 21 21 2111.4884; 11.9792; 20.8251
90; 90; 90
2866Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun
Asymmetric total synthesis of (−)-δ-lycorane
Organic Chemistry Frontiers, 2017, 4, 1149
1553727 CIFC60 H46 N4.5P -113.8813; 14.4392; 23.5317
95.8618; 105.365; 91.4814
4517.3Kimura, 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 CIFC11 H16 F3 N O2 S2C 1 2 111.5; 10.46; 11.413
90; 95.06; 90
1367.5Zhang, 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 CIFC19 H10 F4 O2 SP 21 21 216.6977; 8.1914; 30.513
90; 90; 90
1674.1Zhang, 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 CIFC15 H15 F3 O5 SP 21 21 217.5426; 13.2312; 15.9887
90; 90; 90
1595.6Zhang, 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 CIFC17 H11 F3 N2 O SP 21 21 218.5502; 11.0835; 16.8212
90; 90; 90
1594.1Zhang, 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 CIFC11 H14 Cl2 F3 N O2 S2P 1 21 17.7869; 10.8732; 8.8809
90; 95.062; 90
749Zhang, 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 CIFC13 H20 F3 N O4 S2P 1 21 112.4266; 8.8229; 15.107
90; 105.7; 90
1594.5Zhang, 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 CIFC101 H110 N4 Ni P Pt0.5P -115.566; 15.831; 17.7553
80.813; 89.907; 88.251
4317.2Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro
meso-to-meso PtII-bridged NiII-porphyrin dimers
Organic Chemistry Frontiers, 2017, 4, 767
1553735 CIFC162 H174 Cl10 N8 Ni2 PtP -116.142; 21.227; 22.446
106.1; 92.132; 93.364
7365Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro
meso-to-meso PtII-bridged NiII-porphyrin dimers
Organic Chemistry Frontiers, 2017, 4, 767
1553736 CIFC76 H38 Br N O8P 1 21/n 113.8397; 24.2642; 16.7166
90; 109.444; 90
5293.4Xu, 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 CIFC76 H39 N O9P n a 2121.489; 10.179; 22.215
90; 90; 90
4859.2Xu, 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 CIFC17 H13 Br N2 O4 SP 1 21/c 117.5147; 7.024; 15.73
90; 114.033; 90
1767.4Pal, 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 CIFC15 H9 F N2P b c a25.513; 13.881; 6.794
90; 90; 90
2406Panaka, 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 CIFC16 H13 N2P b c a25.555; 14.1257; 6.8724
90; 90; 90
2480.8Panaka, 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 CIFC19 H22 O3C 1 2/c 128.543; 7.309; 16.361
90; 105.04; 90
3296.3Chang, 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 CIFC11 H8 N O2 SP 1 21/c 15.69674; 8.92923; 19.6982
90; 94.927; 90
998.3Ammon, 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 CIFC67.5 H66 Cl3 N O2 SP -114.0225; 15.4902; 15.6494
109.303; 105.791; 106.459
2814.2Ammon, 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 CIFC84 H108 Si4P -18.2685; 13.793; 17.645
72.588; 88.716; 77.009
1868.8Bettinger, 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 CIFC14 H14 N2 O2 SP -16.121; 8.835; 13.265
83.14; 79.6; 72.93
672.8Wang, 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 CIFC15 H17 N3 O4 SP 1 21 18.6132; 7.4744; 12.867
90; 109.429; 90
781.2Wang, 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 CIFC30 H24C 1 c 121.7066; 21.7067; 20.1949
90; 122.509; 90
8024.4Takai, 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 CC double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states
Organic Chemistry Frontiers, 2017, 4, 650
1553748 CIFC15 H13 N O4 S2P -17.6834; 8.0281; 12.554
85.471; 73.42; 74.044
713.6Zhou, 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 CIFC15 H13 N O4 S2P 1 21/c 18.151; 8.239; 22.94
90; 100.06; 90
1517Zhou, 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 CIFC26 H31 N3 O6P 19.0047; 9.2247; 9.4826
109.875; 108.593; 107.103
626.45Guo, 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 CIFC54 H48 O8P -18.9558; 9.4432; 13.6247
92.926; 95.287; 111
1066.8Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi
Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems
Organic Chemistry Frontiers, 2017, 4, 828
1553752 CIFC66 H72 O6P 1 21/n 111.8673; 14.8352; 15.9367
90; 102.976; 90
2734.08Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi
Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems
Organic Chemistry Frontiers, 2017, 4, 828
1553753 CIFC41 H27 OC 1 2/c 123.6823; 14.1831; 19.4393
90; 101.921; 90
6388.6Ip, 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 CIFC18 H16 N2 O2P 1 21/c 112.4244; 8.0614; 14.7164
90; 100.607; 90
1448.78Selvaraju, 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 CIFC7.75 H7.75 F7.75 N7.75 O7.75 S7.75P 21 21 218.086; 14.196; 23.304
90; 90; 90
2675Pouambeka, 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 CIFC27 H21 N O2 S2P 21 21 215.9608; 18.7773; 20.3817
90; 90; 90
2281.3Shi, 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 CIFC16 H12 Cl N OP 1 21/c 19.0611; 7.1551; 20.5051
90; 93.684; 90
1326.66Zhang, Zhiguo; Zhang, Yongchao; Huang, Guoqing; Zhang, Guisheng
Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 1372
1553758 CIFC17 H18 Br F3 N2 O6P 21 21 218.3955; 14.09; 16.7651
90; 90; 90
1983.19Liu, 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 CIFC23 H22 Br Cl2 N3 O5P 1 21/n 19.593; 15.307; 16.705
90; 93.785; 90
2447.6Chen, 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 CIFC20 H17 Br Cl3 N3 O3P -16.299; 11.774; 14.904
99.608; 94.163; 96.363
1078Chen, 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 CIFC17 H16 OP 21 21 217.738; 11.656; 14.0895
90; 90; 90
1270.79Zhang, 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 CIFC4 H3.167 N0.167 O0.333 S0.167C 1 2/c 116.382; 18.322; 14.538
90; 120.472; 90
3760.9Zhang, 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 CIFC14 H12 N2 O3P -17.1026; 7.8866; 11.4159
92.777; 92.263; 114.968
577.75Hong, 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 CIFC25 H22 F I2 N O2 SP -18.7048; 10.5461; 13.9946
82.33; 79.359; 79.1
1233.4Wang, 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 CIFC25 H24 Cl N O2 SP 1 21/c 113.2671; 18.296; 19.283
90; 108.684; 90
4434Wang, 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 CIFC18 H17 N S3P -112.112; 13.064; 13.586
113.51; 114.37; 96.715
1690.6Schneeweis, 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 CIFC26 H20 F3 N OP -19.3089; 10.692; 10.826
98.78; 90.325; 108.111
1010.5An, 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 CIFC22 H26 F2 N2 O2P 1 21/c 18.7598; 25.852; 8.8958
90; 96.431; 90
2001.9Liu, 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 CIFC16 H11 F N2 OP 1 21/c 121.229; 3.919; 15.628
90; 105.861; 90
1250.7Ding, Junshuai; Zhang, Yingchao; Li, Jizhen
Nickel-catalyzed selective C-5 fluorination of 8-aminoquinolines with NFSI
Organic Chemistry Frontiers, 2017, 4, 1528
1553770 CIFC20 H12 Cl3 N O0P 1 21/n 111.93574; 7.18231; 19.3705
90; 94.7142; 90
1654.94Li, 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 CIFC34 H52 Cl4 N16 O2P -19.8942; 11.644; 20.487
87.078; 78.302; 68.651
2152Liang, 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 CIFC5.33 H10 Cl0.67 Co0.33 N2.67 O4P 1 21/c 111.9766; 19.3355; 12.7804
90; 114.734; 90
2688.09Liang, 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 CIFC27 H41 N16 O3.5 S1.5P -113.18; 19.895; 20.59
108.27; 107.63; 90.48
4854Liang, 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 CIFC20 H23 B F2 N2 O2P -19.003; 10.762; 11.631
73.19; 69.99; 72.45
987.6Kubota, 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 CIFC21 H17 Cl F3 N3P 1 21 18.6045; 11.4959; 10.3691
90; 114.544; 90
933Xie, 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 CIFC22 H17 I N2P 1 21/n 110.326; 9.584; 19.601
90; 104.43; 90
1878.6Liu, 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 CIFC10 H12 O2 SP 21 21 215.7817; 8.2558; 19.972
90; 90; 90
953.3Meng, 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 CIFC17 H19 N O2 SP 1 21 111.3637; 6.0455; 11.3636
90; 98.45; 90
772.2Meng, 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 CIFC21 H16 N2 O3P c a 2111.0348; 21.2718; 7.2221
90; 90; 90
1695.2Tang, 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 CIFC19 H11 Cl F3 N OC 1 2/c 117.5265; 18.9585; 11.1154
90; 120.995; 90
3166Mishra, 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 CIFC2 H4 N4 OP n m a5.0951; 6.0539; 14.8931
90; 90; 90
459.38Wan, 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 CIFC21 H18 F2 O4P n a 2112.326; 11.032; 13.445
90; 90; 90
1828.3Li, 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 CIFC22 H18 Br4 N2P b c a10.7971; 15.2395; 26.1285
90; 90; 90
4299.2Huang, 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 CIFC18 H26 Br2 N2P 1 21/c 16.6642; 19.8278; 14.8224
90; 101.924; 90
1916.3Huang, 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 CIFC26 H25 F3 N O SP 21 21 223.66; 10.2673; 10.5398
90; 90; 90
2560.4Liu, 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 CIFC27 H23 Cl F3 N O3P 21 21 218.5817; 10.4128; 27.6259
90; 90; 90
2468.64Liu, 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 CIFC15 H16 F3 N O2 SP 21 21 216.2282; 7.0351; 36.2461
90; 90; 90
1588.16Liu, 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 CIFC28 H21 N2 O2 PP 1 21/c 112.9056; 8.981; 20.4045
90; 106.848; 90
2263.48Qiao, 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 CIFC28 H21 N2 O2 PP 1 21/n 114.3374; 9.71; 18.7718
90; 105.341; 90
2520.22Qiao, 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 CIFC29 H23 N2 O3 PP -19.5853; 9.8739; 14.7007
103.11; 94.035; 114.371
1213.1Qiao, 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 CIFC28 H21 N2 O2 PP 1 21/c 111.9961; 8.631; 21.6563
90; 95.014; 90
2233.68Qiao, 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 CIFC33 H27 O2 PP 21 21 219.0757; 10.4623; 26.2445
90; 90; 90
2491.99Li, 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 CIFC32 H25 O PP 1 21/c 112.3885; 18.8197; 10.4583
90; 103.828; 90
2367.66Li, 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 CIFC28 H33 B O4P -110.0442; 10.4197; 11.9542
84.471; 84.954; 75.059
1200.58Hsieh, 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 CIFC19 H19 Br O6P 21 21 222.0623; 14.5144; 5.67392
90; 90; 90
1816.91Hao, 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 CIFC21 H18 Br N O3P 1 21 110.4368; 6.0294; 15.7294
90; 107.537; 90
943.81De 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 CIFC20 H13 F N2 OP 1 21/n 19.17425; 7.88736; 21.7312
90; 99.3556; 90
1551.57Ren, 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 CIFC7 H9 N7 O9C 1 c 17.6272; 13.3952; 11.846
90; 90.87; 90
1210.1Hou, 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 CIFC21 H40 O3 SiP 1 21/c 115.7593; 6.7689; 21.0839
90; 104.622; 90
2176.24Tugny, 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 CIFC22 H26 N4 O6P -18.7959; 10.4916; 13.2932
70.468; 74.252; 71.371
1076.8Tugny, 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 CIFC22 H26 N4 O6P 1 21/n 115.8792; 7.383; 18.5839
90; 94.011; 90
2173.37Tugny, 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 CIFC22 H26 N4 O6P 1 21/c 119.2372; 19.7853; 12.577
90; 107.983; 90
4553.1Tugny, 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 CIFC21 H38 O3 SiP 1 21/n 115.0743; 6.8149; 21.2545
90; 92.709; 90
2181.03Tugny, 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 CIFC28 H29 I O4 SP 1 21/n 112.0087; 17.7464; 12.6045
90; 103.892; 90
2607.6Miao, 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 CIFC22 H20 O3P -19.8395; 10.7013; 10.8636
114.335; 94.477; 116.312
885.4Shi, 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 CIFC22 H19 N O5 SP 21 21 218.8173; 14.3926; 15.3659
90; 90; 90
1949.99Xie, 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 CIFC21 H23 N O5 SP 1 21 18.2203; 9.1263; 13.0906
90; 102.302; 90
959.52Xie, 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 CIFC62 H102 Cl8 N26 O21 Zn2C 1 2/c 129.3492; 12.5025; 25.3876
90; 113.65; 90
8533.3Qu, 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 CIFC60 H68 Cl8 N26 O28 Zn2C 1 2/c 127.52; 17.25; 18.358
90; 94.006; 90
8694Qu, 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 CIFC58 H94 Cl6 N26 O22 Zn2P -112.2894; 12.4667; 14.986
73.289; 84.747; 62.451
1947.4Qu, 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 CIFC60 H112 Cl10 N26 O28 Zn2P -112.298; 12.903; 15.662
75.259; 70.211; 76.684
2233Qu, 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 CIFC62 H108 Cl10 N26 O28 Zn2P -112.315; 12.875; 15.525
75.131; 70.361; 77.82
2219.6Qu, 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 CIFC21 H21 Br N2 O2P -15.095; 12.261; 17
73.395; 81.56; 78.69
993Yan, 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 CIFC22 H26 N2 O4P -16.1408; 10.54; 16.567
87.399; 81.181; 79.922
1043.1Yan, 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 CIFC23 H23 Cl O7P 21 21 216.82668; 9.4989; 34.5079
90; 90; 90
2237.7Yao, 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 CIFC19 H17 N O3 SP 1 21/n 17.8333; 8.7742; 23.1441
90; 95.475; 90
1583.46De 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 CIFC20 H16 F3 N O3 SP 18.5679; 12.3701; 18.181
83.843; 89.595; 80.871
1891.4De 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 CIFC15 H10 I2 O4P 1 21/c 114.884; 4.3831; 27.39
90; 117.921; 90
1578.9Tang, 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 CIFC25 H26 F3 N O5P 1 21/n 114.9433; 9.3141; 17.6377
90; 102.36; 90
2397.98Tang, 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 CIFC21 H24 F3 N O4P 1 21/c 115.6855; 9.6366; 13.4345
90; 96.4; 90
2018.03Tang, 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 CIFC19 H21 F3 O5P -18.577; 11.253; 11.3999
83.261; 69.715; 68.411
959.58Tang, 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 CIFC19 H15 N3 O4P c a 2116.2553; 8.3116; 24.8996
90; 90; 90
3364.12Krylov, 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 CIFC24 H21 F2 O3 PC 1 2/c 125.317; 8.8649; 22.042
90; 120.571; 90
4259.3Zhang, 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 CIFC26 H28 N2 O5P 1 21/n 17.75; 20.882; 14.5149
90; 93.914; 90
2343.5Yang, 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 CIFC18 H22 O5I 1 2/a 19.6871; 14.029; 23.8866
90; 90.258; 90
3246.2Sun, 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 CIFC20 H26 O6P 1 21/c 110.2811; 28.3515; 12.9191
90; 103.741; 90
3657.9Sun, 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 CIFC27 H33 N O7 SC 1 2/c 122.151; 9.8005; 26.0531
90; 117.401; 90
5021.3Sun, 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 CIFC18 H22 O6P -18.9279; 10.0249; 10.8557
115.731; 104.925; 90.322
838Sun, 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 CIFC19 H23 O6P 1 21/n 15.9908; 12.2284; 23.731
90; 90; 90
1738.5Sun, 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 CIFC27 H33 N O7 SC 1 2/c 113.7047; 15.4463; 24.0895
90; 97.806; 90
5052.2Sun, 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 CIFC19 H24 O5P -18.981; 10.331; 10.885
66.11; 71.31; 87.32
870.7Sun, 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 CIFC25 H29 N O7 SP -19.88; 10.9717; 12.836
85.382; 71.391; 65.05
1193.2Sun, 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 CIFC23 H19 Cl F3 N O5P -17.3052; 10.5757; 14.449
88.853; 83.694; 77.708
1084.1Sun, 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 CIFC19 H23 Cl F3 N O4P 1 21/n 111.287; 12.727; 14.808
90; 103.68; 90
2066.8Sun, 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 CIFC21 H17 Cl F3 N O3C 1 2/c 121.872; 7.604; 24.313
90; 110.597; 90
3785.1Sun, 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 CIFC16 H15 N OP 1 21 16.9086; 9.5831; 19.453
90; 96.737; 90
1279Zhang, 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 CIFC25 H29 N O5 SP 1 21/c 111.7381; 13.2058; 14.4879
90; 98.487; 90
2221.19Lv, 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 CIFC29 H25 N O7 SP 21 21 218.0159; 15.545; 21.174
90; 90; 90
2638.4Li, 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 CIFC15 H17 F N2 O2P -19.5214; 9.6784; 9.8861
114.205; 92.568; 116.743
712.04Yang, 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 CIFC23 H22 Br N O4 SP 1 21/n 110.723; 9.856; 20.94
90; 100.205; 90
2178Wang, 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 CIFC17 H21 N O4 SP 1 21/n 113.746; 8.2548; 15.646
90; 104.468; 90
1719.1Wang, 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 CIFC40 H48 Cl2 N2 O2 PdP 1 21/n 111.7394; 19.838; 16.5546
90; 94.489; 90
3843.5Chen, 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 CIFC16 H15 N O4P 21 21 217.973; 12.9128; 14.3781
90; 90; 90
1480.28Wu, 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 CIFC20 H21 N O2P 1 21/n 111.831; 8.4718; 16.4581
90; 90.759; 90
1649.45Wu, 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 CIFC24 H27 N OP -18.316; 10.229; 13.179
69.905; 82.818; 72.23
1002.3Wu, 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 CIFC17 H22 I N O2P 1 21/n 111.781; 12.2621; 12.7517
90; 110.261; 90
1728.1Wu, 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 CIFC8 H6 Br F3 O SP 1 21/c 120.993; 3.9406; 12.147
90; 95.906; 90
999.5Zhang, 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 CIFC26 H20 Br N O4 SP -19.3385; 11.1134; 11.912
69.983; 88.735; 69.443
1080.8Jin, 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 CIFC26 H20 Br N O4 SC 1 2/c 127.96; 10.908; 16.954
90; 121.023; 90
4431Jin, 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 CIFC18 H16 O4 SP 21 21 219.7797; 10.9021; 14.8619
90; 90; 90
1584.6Zhao, 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 CIFC100 H96 Cl6 N6 O10P -19.8074; 13.2321; 17.7176
100.836; 99.601; 93.264
2217.36Zhang, 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 CIFC88 H122 N2 O4 S2P 18.9041; 14.0916; 16.2768
104.121; 91.824; 94.954
1970.23Zhang, 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 CIFC202 H249 Cl14 N9 O15P -118.0089; 19.4187; 29.7417
90.357; 95.539; 107.328
9875.8Zhang, 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 CIFC132 H154 Cl12 N6 O8P 1 21/c 19.9153; 27.367; 23.7531
90; 93.29; 90
6434.8Zhang, 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 CIFC18 H16 Cl N O4 SP 21 21 215.1621; 16.3247; 20.251
90; 90; 90
1706.5Deng, 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 CIFC31 H36 N2 O4P -18.4885; 10.6796; 16.8127
74.369; 82.265; 75.011
1414.37Wu, 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 CIFC23 H20 N O2P 6118.5578; 18.5578; 9.8682
90; 90; 120
2943.2Wu, 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 CIFC17 H22 N2 O2P 1 21/n 16.0777; 22.245; 11.8606
90; 96.163; 90
1594.3Liu, 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 CIFC20 H22 N2 OC 1 2/c 121.107; 7.3437; 21.914
90; 101.993; 90
3322.6Liu, 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 CIFC31 H38 O9P 1 21 17.9044; 11.5678; 15.8146
90; 98.267; 90
1431.01Luo, 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 CIFC31 H38 O9P 21 21 2114.6815; 17.2043; 23.1115
90; 90; 90
5837.62Luo, 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 CIFC25 H24 Br2 N2 O3 SP -18.4549; 13.872; 14.009
117.552; 101.368; 92.964
1408.7Jiang, 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 CIFC44 H45 Br2 N3 O6 S2P 1 21/c 113.823; 11.5473; 30.267
90; 98.559; 90
4777.4Jiang, 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 CIFC43 H38 Br N3 O4 S2P -111.936; 13.1209; 13.8558
89.702; 84.883; 66.69
1983.8Jiang, 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 CIFC31 H26 N2 O2 SP -110.688; 10.745; 11.245
103.535; 94.412; 96.045
1241.6Jiang, 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 CIFC25 H21 Br N2 O2 SC 1 2/c 124.816; 10.401; 16.9512
90; 96.192; 90
4349.8Jiang, 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 CIFC72 H112 Cl2 N28 O26C 1 2/c 124.1839; 31.5567; 12.6112
90; 104.99; 90
9296.9Xiao, 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 CIFC108 H176 Cl6 N52 O50 Sr2P -112.8381; 15.6916; 22.2878
92.995; 98.521; 106.862
4227.9Xiao, 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 CIFC42 H36 N2 O2P 42/n :223.1475; 23.1475; 12.6145
90; 90; 90
6758.9Mallia, 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 CIFC28 H28 N2 O4P 1 21 111.584; 12.031; 18.156
90; 96.06; 90
2516.2Zhu, 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 CIFC26 H24 N2 O4P 21 21 219.65062; 11.62065; 19.4417
90; 90; 90
2180.32Zhu, 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 CIFC26 H24 N2 O4P 21 21 219.754; 11.691; 19.628
90; 90; 90
2238.3Zhu, 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 CIFC26 H23 Br N2 O4P 1 21/c 116.479; 9.0821; 15.44
90; 101.98; 90
2260.5Zhu, 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 CIFC26 H23 Br N2 O4P 41 21 211.3983; 11.3983; 36.807
90; 90; 90
4782Zhu, 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 CIFC28 H27 Br N2 O4P 1 21 111.4; 19.6; 11.58
90; 91.95; 90
2586Zhu, 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 CIFC26 H23 Br N2 O4P 1 21/c 110.863; 11.675; 19.581
90; 77.94; 90
2428.6Zhu, 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 CIFC26 H23 Br N2 O4P 43 21 211.3202; 11.3202; 36.3968
90; 90; 90
4664.14Zhu, 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 CIFC28 H27 Br N2 O4P 1 21 111.4015; 19.6478; 11.6171
90; 91.917; 90
2600.9Zhu, 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 CIFC28 H27 Br N2 O4P 1 21/c 111.401; 11.654; 19.628
90; 96.697; 90
2590Zhu, 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 CIFC41 H46 Br2 Cl2 N2 NiP -116.4259; 17.1593; 17.2162
76.75; 69.223; 75.674
4342Zhong, 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 CIFC48 H60 Br2 N2 NiR -3 :H26.8702; 26.8702; 35.7526
90; 90; 120
22355.3Zhong, 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 CIFC48 H54 N2 O2 Y2P 1 21/c 19.447; 15.805; 13.524
90; 100.792; 90
1983.6Pahl, 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 CIFC76 H86 N3 O3 Y3P -17.9941; 19.5986; 23.2344
78.1666; 89.6646; 88.2859
3561.3Pahl, 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 CIFC26 H27 N7 O2P 1 21 111.8603; 9.4892; 12.0188
90; 118.477; 90
1188.99Shiomi, 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 CIFC26 H24 N2 O2P -18.1158; 9.2869; 14.1457
86.852; 84.763; 70.523
1000.62Fan, 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 CIFC21 H13 F N2P 4311.1632; 11.1632; 12.0079
90; 90; 90
1496.4Fan, 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 CIFC19 H27 Br N O2 SiP 21 21 2110.5667; 11.1762; 18.221
90; 90; 90
2151.8Alicea-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 CIFC21 H22 Br N O2P 1 21 16.0625; 19.5089; 16.3468
90; 96.885; 90
1919.44Wu, 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 CIFC21 H15 N3 O2P -17.1592; 9.8482; 12.3493
81.6372; 83.2218; 80.227
845.03Ramakrishna, 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 CIFC20 H12 F3 N3P 1 21/c 111.696; 9.0705; 15.811
90; 102.782; 90
1635.8Ramakrishna, 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 CIFC17 H17 N O3P -18.4056; 9.8583; 10.2022
69.4122; 78.7895; 71.4852
747.18Ramakrishna, 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 CIFC19 H24 N2 O2 SP 1 21 111.0611; 6.743; 13.0444
90; 102.392; 90
950.25Ma, 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 CIFC30 H30 N2 O3R -3 :H26.495; 26.495; 25.84
90; 90; 120
15709Halli, 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 CIFC29 H28 N2 O3P 1 21/c 112.7136; 19.6481; 10.0368
90; 104.806; 90
2423.9Halli, 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 CIFC29 H28 N2 O3P 1 21/c 18.088; 29.039; 10.3957
90; 98.253; 90
2416.3Halli, 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 CIFC28 H26 N2 O3P -19.715; 11.622; 13.28
64.317; 86.248; 74.246
1298.2Halli, 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 CIFC26 H30 N2 O3P 1 21/c 111.5919; 14.5845; 13.8674
90; 97.872; 90
2322.4Halli, 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 CIFC34 H36 Cl2 N2 O5P 1 21/c 110.3241; 23.365; 13.7004
90; 99.642; 90
3258.2Halli, 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 CIFC33 H34 N2 O5P 1 21/c 113.9135; 11.8443; 18.4125
90; 108.518; 90
2877.2Halli, 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 CIFC29.5 H29 Cl N2 O3 SP 32 2 118.4813; 18.4813; 16.4257
90; 90; 120
4858.7Halli, 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 CIFC26 H30 N2 O3P 1 21/n 19.5688; 10.3956; 23.8948
90; 96.847; 90
2359.9Halli, 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 CIFC24 H24 N2 O2P 1 21/c 110.9969; 11.8906; 15.8497
90; 106.796; 90
1984.1Halli, 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 CIFC33 H34 N2 O5P 1 21/c 116.2583; 8.9359; 19.545
90; 95.231; 90
2827.7Halli, 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 CIFC26 H30 N2 O3P 1 21/c 115.2433; 10.1136; 14.943
90; 94.937; 90
2295.1Halli, 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 CIFC29 H28 N2 O3P 1 21/c 17.8226; 30.639; 10.1141
90; 98.682; 90
2396.3Halli, 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 CIFC29 H28 N2 O3 SP 1 21/c 18.6571; 29.45; 10.2183
90; 98.7924; 90
2574.56Halli, 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 CIFC26 H30 N2 O3C 1 2/c 117.3068; 12.0144; 22.5999
90; 96.044; 90
4673.1Halli, 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 CIFC29 H28 N2 O3C 1 2 122.49; 5.1816; 20.19
90; 90.78; 90
2352.6Halli, 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 CIFC29 H28 N2 O3 SP 1 21/n 119.7344; 12.7882; 20.279
90; 97.031; 90
5079.3Halli, 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 CIFC23 H17 Cl O3C 1 2 120.5553; 9.5675; 22.2196
90; 115.687; 90
3937.9Infante, 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 CIFC16 H11 F N2 OP 21 21 218.4334; 9.1934; 16.9142
90; 90; 90
1311.4Jin, Yushu; Chen, Ming; Ge, Shaozhong; Hartwig, John F.
Palladium-Catalyzed, Enantioselective α-Arylation of α-Fluorooxindoles.
Organic letters, 2017, 19, 1390-1393
1556020 CIFC15 H12 N2 OP 1 21/n 116.4017; 7.1335; 20.0858
90; 95.665; 90
2338.6Yin, 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 CIFC16 H14 N2 OP n a 219.9288; 26.7988; 4.7384
90; 90; 90
1260.79Yin, 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 CIFC17 H13 N OP 1 21/c 14.0198; 13.908; 23.21
90; 94.2; 90
1294.1Wu, 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 CIFC11 H13 N S2P 1 21 19.9321; 22.705; 19.824
90; 98.538; 90
4420.9Wu, 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 CIFC43 H30 N2 O2P -110.4789; 12.074; 12.5011
92.552; 94.697; 98.319
1557.2Feng, 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 CIFC42 H28 N2 O2P b c a18.5446; 17.7946; 18.9442
90; 90; 90
6251.5Feng, 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 CIFC47 H36 Cl2 N4 O S ZnP -111.0032; 12.6313; 14.724
98.868; 96.16; 102.84
1950Gholami, 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 CIFC51 H37 N5 O S ZnP 110.6689; 10.8762; 18.2817
83.457; 84.152; 77.519
2051.2Gholami, 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 CIFC32 H27 Br O2P 1 21 19.624; 31.096; 13.229
90; 91.141; 90
3958Perveen, 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 CIFC94 H64 O2P -19.9734; 11.3386; 15.3837
79.9686; 85.4756; 79.5603
1682.69Vadehra, 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 CIFC24 H26 N2 O6P 1 21 111.0167; 8.4713; 13.145
90; 112.969; 90
1129.5Ran, 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 CIFC14 H9 N O3 SP 1 21/c 112.0277; 13.0209; 8.1447
90; 106.121; 90
1225.4Jeran, 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 CIFC14 H13 N O3 SP 21 21 217.4865; 10.7242; 32.3467
90; 90; 90
2597.01Jeran, 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 CIFC14 H12 N O3 SP 21 21 219.4952; 13.78766; 23.3234
90; 90; 90
3053.42Jeran, 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 CIFC24 H24 N2 O3 SeP 1 21/c 19.4838; 10.5004; 21.1264
90; 90.868; 90
2103.6Foley, 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 CIFC14 H16 N4 OP 1 21/m 17.7378; 6.7075; 12.6395
90; 102.323; 90
640.89Foley, 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 CIFC28 H44 Cl2 N8 Ni O2I m -3 m17.0714; 17.0714; 17.0714
90; 90; 90
4975.2Zhang, 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 CIFC23 H18 O2P 1 21 16.0965; 7.8294; 17.9271
90; 96.951; 90
849.41Zhang, 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 CIFC26 H34 O4 SiP 21 21 219.47; 15.075; 17.824
90; 90; 90
2544.6Han, 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 CIFC16 H13 Br F3 N O3P 21 21 215.8132; 8.851; 31.166
90; 90; 90
1603.6Wang, 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 CIFC22 H26 O4 SP b c a5.5413; 15.8031; 45.3572
90; 90; 90
3971.92Zhurakovskyi, 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 CIFC19 H37 Br Cu N3 P2I 41 c d31.5316; 31.5316; 18.8701
90; 90; 90
18761.4Mastalir, 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 CIFC27 H22 O SP 21 21 215.3756; 8.23448; 44.3104
90; 90; 90
1961.41Wang, 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 CIFC11 H10 F7 N3 O2P 1 21/c 116.1302; 7.5328; 12.1195
90; 90.161; 90
1472.6Wang, 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 CIFC25 H31 N O7 SiP -19.5604; 11.3393; 12.5938
64.094; 79.058; 86.136
1205.56Parsons, 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 CIFC19 H20 O3C 1 2 117.9303; 6.8625; 13.4226
90; 99.456; 90
1629.16Iwamoto, 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 CIFC12 H6 O S2P b c a5.541; 15.387; 22.574
90; 90; 90
1925Mitsudo, 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 CIFC19 H26 Cl N2 O RhP b c a8.0471; 16.3426; 29.6614
90; 90; 90
3900.8Long, 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 CIFC22 H24 Cl N2 O RhP 1 21/n 17.58618; 16.9757; 15.6843
90; 93.0656; 90
2016.94Long, 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 CIFC116 H112 Cl2 N10 NiP -112.6554; 19.7134; 21.0374
72.334; 80.809; 82.734
4919.7Yin, 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 CIFC27 H23 N O3 SP 21 21 2111.4379; 12.8956; 15.0848
90; 90; 90
2225Wang, 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 CIFC33 H26 Cl N O4 SP 21 21 218.9355; 14.869; 20.8047
90; 90; 90
2764.2Wang, 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 CIFC204 H280 N24 O20 S12P 1 21/n 122.6919; 27.504; 32.801
90; 93.8825; 90
20425Cholewiak, 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 CIFC22 H22 Cl N O6C 1 2 121.5482; 6.1634; 16.9021
90; 111.981; 90
2081.59Drelich, 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 CIFC19 H18 N2 O2 SP 1 21/n 17.8427; 22.614; 18.528
90; 93.229; 90
3280.8Wang, 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 CIFC19 H19 Cl N6 OC 1 2 120.4899; 9.7314; 10.0601
90; 101.493; 90
1965.72Li, 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 CIFC17.5 H14 N2 O1.5P 21 21 217.1969; 9.884; 38.6328
90; 90; 90
2748.11Mei, 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 CIFC14 H10 N2 O2P b c a8.0739; 10.2485; 27.568
90; 90; 90
2281.1Jones, 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 CIFC18 H18 N2 O3C 1 2/c 134.507; 7.3494; 13.4613
90; 110.662; 90
3194.3Jones, 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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