Crystallography Open Database

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1556908 CIFC20 H23 N3 O3P 21 21 217.191; 13.5045; 18.6644
90; 90; 90
1812.52Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556909 CIFC20 H25 N3 O2P 1 21/n 16.8118; 17.5495; 15.1113
90; 91.427; 90
1805.9Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556910 CIFC22 H21.25 N3 O2.125P 1 21 110.18405; 9.71457; 18.82762
90; 93.0169; 90
1860.1Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556911 CIFC24 H21 F3 N2 O4 SP 21 21 2132.8358; 11.60538; 5.85758
90; 90; 90
2232.16Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556912 CIFC22 H25 N3 O2P 1 21 112.4713; 9.02632; 17.84198
90; 92.8702; 90
2005.95Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556913 CIFC20 H19 N3 OP 1 21 110.10659; 5.94958; 13.62038
90; 99.5974; 90
807.53Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556914 CIFC28 H30 N2 O2P 21 21 218.33247; 15.71709; 17.93381
90; 90; 90
2348.65Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556915 CIFC24 H24 N2 O4 SP 21 21 216.0985; 11.5023; 30.8387
90; 90; 90
2163.2Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556927 CIFC9 H19 I2 N3 PdC 1 2/c 114.7908; 7.8079; 27.592
90; 99.197; 90
3145.5Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556928 CIFC13 H21 I2 N3 PdP 1 21/c 117.5721; 12.5994; 8.4655
90; 99.55; 90
1848.27Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556929 CIFC15 H17 I2 N3 PdC 1 2/c 121.6545; 8.657; 20.1671
90; 95.408; 90
3763.8Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556930 CIFC16 H19 I2 N3 PdP -19.5333; 10.964; 11.3716
62.48; 79.571; 67.896
976.59Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556981 CIFLa3 Li6.5 Nb0.5 O12 Zr1.5I a -3 d12.913; 12.913; 12.913
90; 90; 90
2153.2Kataoka, K.
Oxide single crystals with high lithium-ion conductivity as solid electrolytes for all-solid-state lithium secondary battery applications
Journal of the Ceramic Society of Japan, 2020, 128, 7-18
1556982 CIFLa3 Li6.5 O12 Ta0.5 Zr1.5I a -3 d12.9445; 12.9445; 12.9445
90; 90; 90
2168.98Kataoka, K.
Oxide single crystals with high lithium-ion conductivity as solid electrolytes for all-solid-state lithium secondary battery applications
Journal of the Ceramic Society of Japan, 2020, 128, 7-18
1556983 CIFC23 H19.35 N5 O4.18P 21 21 217.4338; 19.1874; 28.7281
90; 90; 90
4097.64Lin, Shuang; Yu, Huimin; Yang, Beiye; Li, Fengli; Chen, Xia; Li, Huaqiang; Zhang, Sitian; Wang, Jianping; Hu, Youcai; Hu, Zhengxi; Zhang, Yonghui
Reisolation and Configurational Reinvestigation of Cottoquinazolines E-G from an Arthropod-Derived Strain of the Fungus <i>Neosartorya fischeri</i>.
Journal of natural products, 2020, 83, 169-173
1556984 CIFC25 H25 N5 O5P 6113.718; 13.718; 21.48
90; 90; 120
3500.6Lin, Shuang; Yu, Huimin; Yang, Beiye; Li, Fengli; Chen, Xia; Li, Huaqiang; Zhang, Sitian; Wang, Jianping; Hu, Youcai; Hu, Zhengxi; Zhang, Yonghui
Reisolation and Configurational Reinvestigation of Cottoquinazolines E-G from an Arthropod-Derived Strain of the Fungus <i>Neosartorya fischeri</i>.
Journal of natural products, 2020, 83, 169-173
1556985 CIFC6 H12 N4 O8 P2 S2P 1 21/c 14.6777; 8.716; 17.1651
90; 91.394; 90
699.628Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556986 CIFC6 H20 N4 O16 P4 S2P 1 21/n 111.0254; 7.0847; 13.0691
90; 96.516; 90
1014.26Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556987 CIFC3 H6 N2 O4 P SP -15.40917; 7.805; 8.856
63.995; 84.123; 83.101
333.08Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556988 CIFC3 H9 N2 O8 P2 SP -15.26221; 8.96277; 10.8217
97.609; 95.9417; 98.5964
496.242Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556989 CIFC6 H9 N4 O4 P S2P 1 21/c 113.8433; 10.0451; 8.1208
90; 95.19; 90
1124.63Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556992 CIFC18 H16 O4P b c n9.7263; 11.8883; 24.935
90; 90; 90
2883.2Liang, Kangjiang; Li, Tao; Li, Na; Zhang, Yang; Shen, Lei; Ma, Zhixian; Xia, Chengfeng
Redox-neutral photochemical Heck-type arylation of vinylphenols activated by visible light
Chemical Science, 2020, 11, 2130-2135
1556993 CIFC26 H24 N2 O2 SP -110.6565; 11.1408; 12.3
69.374; 76.912; 65.303
1236.26Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong
Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions.
Chemical science, 2020, 11, 1672-1676
1556994 CIFC28 H26 N2P 21 21 219.072; 9.846; 23.918
90; 90; 90
2136.4Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong
Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions.
Chemical science, 2020, 11, 1672-1676
1556995 CIFC54 H31.2 F0.8 O8 Zn2C 1 2/c 137.1066; 31.0733; 11.8903
90; 99.208; 90
13533.1Lustig, William P.; Shen, Zeqing; Teat, Simon J.; Javed, Nasir; Velasco, Ever; O'Carroll, Deirdre M.; Li, Jing
Rational design of a high-efficiency, multivariate metal‒organic framework phosphor for white LED bulbs
Chemical Science, 2020, 11, 1814-1824
1557016 CIFC22 H30 O2P 1 21/n 19.223; 6.718; 15.694
90; 90.983; 90
972.3Shu, Zhibin; Zhang, Qing; Zhang, Pan; Qin, Zhengsheng; Liu, Dan; Gao, Xiong; Guan, Bo; Qi, Haoyuan; Xiao, Mengqi; Wei, Zhongming; Dong, Huanli; Hu, Wenping
Preparing two-dimensional crystalline conjugated polymer films by synergetic polymerization and self-assembly at air/water interface
Polymer Chemistry, 2020, 11, 1572-1579
1557022 CIFC4 H18 Br5 N3 Pb S2P 1 21 110.066; 8.4068; 10.9787
90; 104.155; 90
900.8Bakthavatsalam, Rangarajan; Haris, Muhammed P. U.; Shaikh, Samir R.; Lohar, Amruta; Mohanty, Ashutosh; Moghe, Dhanashree; Sharma, Shivani; Biswas, Chinmoy; Raavi, Sai Santhosh Kumar; Gonnade, Rajesh G.; Kundu, Janardan
Ligand Structure Directed Dimensionality Reduction (2D →1D) in Lead Bromide Perovskite
The Journal of Physical Chemistry C, 2020
1557023 CIFC3 H11 Br4 N3 Pb SP 1 21/c 113.3113; 8.5838; 12.0368
90; 90.406; 90
1375.31Bakthavatsalam, Rangarajan; Haris, Muhammed P. U.; Shaikh, Samir R.; Lohar, Amruta; Mohanty, Ashutosh; Moghe, Dhanashree; Sharma, Shivani; Biswas, Chinmoy; Raavi, Sai Santhosh Kumar; Gonnade, Rajesh G.; Kundu, Janardan
Ligand Structure Directed Dimensionality Reduction (2D →1D) in Lead Bromide Perovskite
The Journal of Physical Chemistry C, 2020
1557024 CIFC38 H34 S4C 1 2/c 141.708; 5.7563; 12.67
90; 98.46; 90
3008.8Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557025 CIFC42 H42 S4P 1 21/c 123.82; 5.837; 12.5
90; 104.133; 90
1685Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557026 CIFC42 H42 S4P 1 21/c 122.15; 5.7413; 13.1188
90; 95.85; 90
1659.6Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557027 CIFC66 H30 Al3 Ba F89 O9P 1 c 128.173; 16.4313; 20.453
90; 90.107; 90
9468.1Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557028 CIFC52 H26 Al2 Ca F68 O7P 1 21 117.765; 20.654; 20.031
90; 93.018; 90
7340Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557029 CIFC36 H18 Al2 F55 In O6P -110.6319; 22.3961; 24.4869
79.144; 79.696; 77.759
5537.2Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557030 CIFC50 H22 Al2 F74 Mg N6 O8P 114.3953; 18.2606; 25.8315
73.784; 74.37; 66.821
5895.1Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557031 CIFC84 H34 Al4 F118 O12 SrP -113.8661; 20.2883; 23.0336
80.031; 85.985; 79.942
6278.6Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557032 CIFC84 H34 Al4 Ca F118 O12P -113.9542; 20.3286; 22.9128
80.085; 84.743; 80.239
6296.8Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557033 CIFC60 H26 Al3 Ca F87 O9P 1 21/c 123.429; 18.9075; 22.4874
90; 118.27; 90
8773.4Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557034 CIFC66 H30 Al3 F89 O9 SrP -113.5412; 25.3825; 27.3385
90.017; 90.111; 92.474
9387.7Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557040 CIFC17 H10 Br2 N2 OP 1 21/n 110.0349; 8.3874; 17.4347
90; 91.005; 90
1467.2Sala, Samuele; Nealon, Gareth L.; Sobolev, Alexandre N.; Fromont, Jane; Gomez, Oliver; Flematti, Gavin R.
Structure Reassignment of Echinosulfone A and the Echinosulfonic Acids A-D Supported by Single-Crystal X-ray Diffraction and Density Functional Theory Analysis.
Journal of natural products, 2020, 83, 105-110
1557041 CIFC40 H49 Br N2 OP 1 21/n 111.1088; 21.1979; 15.9518
90; 108.641; 90
3559.32Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557042 CIFC42 H44 N2 Ni O3P -110.35522; 11.18263; 16.4194
100.307; 95.6535; 99.0466
1831.63Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557043 CIFC46 H52 Au Cl N2P 1 21/c 112.2795; 16.812; 19.2885
90; 93.6946; 90
3973.7Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557044 CIFC39 H44 N2I 41/a :238.4682; 38.4682; 9.5772
90; 90; 90
14172.4Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557045 CIFC17 H14 Cl N O2P 21 21 215.3182; 10.94; 23.9705
90; 90; 90
1394.63Burg, Finn; Breitenlechner, Stefan; Jandl, Christian; Bach, Thorsten
Enantioselective oxygenation of exocyclic methylene groups by a manganese porphyrin catalyst with a chiral recognition site
Chemical Science, 2020, 11, 2121-2129
1557052 CIFC22 H28 NP -15.899; 7.547; 20.535
83.465; 84.681; 82.512
897.7Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte
Singlet oxygen stimulus for switchable functional organic cages
Chemical Science, 2020, 11, 1478-1484
1557053 CIFC28 H18 O2P 1 21/c 113.0175; 9.329; 8.3512
90; 106.37; 90
973.06Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte
Singlet oxygen stimulus for switchable functional organic cages
Chemical Science, 2020, 11, 1478-1484
1557054 CIFC20 H14 I NP c c n16.5305; 18.7386; 10.5281
90; 90; 90
3261.2Martinez, Thibaut; Alahyen, Ismail; Lemière, Gilles; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Straightforward Access to 2-Iodoindolizines via Iodine-Mediated Cyclization of 2-Pyridylallenes
Organic Process Research & Development, 2020
1557055 CIFC20 H21 B Cl2 O2C 1 2/c 127.001; 6.0841; 25.1455
90; 108.298; 90
3922Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557056 CIFC22 H27 B O2C 1 2/c 135.07; 6.2286; 20.596
90; 119.212; 90
3926.8Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557057 CIFC22 H27 B O2P c a 2125.447; 6.3811; 24.281
90; 90; 90
3942.7Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557058 CIFC36.5 H57 B Cl F4 N4 P4 RhP 31 2 113.824; 13.824; 40.089
90; 90; 120
6635Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557059 CIFC27 H42 B Cl2 F4 N2 P2 RhP 1 21 19.7105; 14.3281; 11.2851
90; 96.031; 90
1561.44Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557060 CIFC18 H19 N S SiP -18.52831; 10.39109; 11.21545
117.584; 92.3119; 95.1854
873.5Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557061 CIFC17 H13 N O SC 1 2/c 120.6204; 9.4103; 16.7239
90; 120.205; 90
2804.6Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557062 CIFC18 H15 N O SP b c a13.1964; 13.3812; 16.7048
90; 90; 90
2949.79Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557063 CIFC11 H9 N O SP 1 21/c 110.9143; 7.26579; 12.4737
90; 104.425; 90
957.99Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557064 CIFC16 H21 N S Se SiP 1 21/c 110.6588; 8.0663; 20.1272
90; 95.886; 90
1721.35Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557065 CIFC22 H23 N SP 1 21/c 113.9373; 7.7203; 17.0136
90; 105.984; 90
1759.89Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557066 CIFC21 H20 SP 1 21/n 17.5133; 25.6215; 8.2645
90; 100.591; 90
1563.83Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557067 CIFC10 H7 N SP -16.9027; 7.3743; 9.3503
68.861; 73.292; 84.246
425.18Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557068 CIFC16 H11 N O SP b c a12.2557; 9.5626; 21.5616
90; 90; 90
2526.94Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557069 CIFC17 H17 N SP 1 21/c 111.1885; 11.263; 12.1884
90; 116.756; 90
1371.48Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557075 CIFC55 H67 N3 O6 P2 RuP 1 21/n 117.5623; 13.934; 20.8795
90; 92.113; 90
5106Artús Suàrez, Lluís; Jayarathne, Upul; Balcells, David; Bernskoetter, Wesley H.; Hazari, Nilay; Jaraiz, Martín; Nova, Ainara
Rational selection of co-catalysts for the deaminative hydrogenation of amides.
Chemical science, 2020, 11, 2225-2230
1557079 CIFC25 H23 N O3P 1 21 112.77764; 5.95718; 12.86001
90; 100.546; 90
962.352Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557080 CIFC23 H29 N O2P 21 21 2110.3193; 10.5258; 18.2046
90; 90; 90
1977.36Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557081 CIFC25 H25 N O3 SP 21 21 215.909; 12.8175; 27.4929
90; 90; 90
2082.27Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557082 CIFC24 H18 O3C 1 2/c 121.613; 12.1859; 13.5922
90; 104.043; 90
3472.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557083 CIFC26 H24 O6P 1 21/c 114.145; 7.441; 24.56
90; 96.17; 90
2570He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557084 CIFC22 H15 Cl O3P 1 21/n 116.2589; 6.7715; 16.4568
90; 106.511; 90
1737.14He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557085 CIFC25 H24 O7P 1 21/n 112.5579; 5.2167; 35.021
90; 94.917; 90
2285.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557086 CIFC25 H28 O8C 1 2/c 129.9022; 11.0935; 13.4816
90; 99.73; 90
4407.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557087 CIFC39 H34 F6 N3 O PP 1 21/c 19.3923; 29.4208; 11.9664
90; 102.511; 90
3228.14Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong
Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens
Chemical Science, 2020, 11, 2494-2503
1557088 CIFC27 H22 N2 OP 1 21/n 19.53897; 23.141; 9.5721
90; 107.33; 90
2017.04Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong
Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens
Chemical Science, 2020, 11, 2494-2503
1557089 CIFC78 H190 Dy2 K2 N6 O21 Si12C 1 2/c 125.4899; 18.8304; 25.7453
90; 103.128; 90
12034.4Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557090 CIFC42 H102 Dy K N3 O12 Si6P 1 21/n 111.0616; 27.199; 21.7721
90; 103.885; 90
6359Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557091 CIFC78 H190 K2 N6 O21 Si12 Tm2C 1 2/c 125.453; 18.757; 25.744
90; 103.142; 90
11969Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557092 CIFC42 H102 K N3 O12 Si6 TmP 21 21 2121.956; 22.554; 25.737
90; 90; 90
12745Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557093 CIFC52 H124 Gd2 K2 N4 O16 Si8P -112.6614; 15.5498; 21.205
94.4758; 94.0831; 105.746
3987.4Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557094 CIFC36 H90 Gd K N5 O6 Si6R 3 2 :H18.564; 18.564; 18.05
90; 90; 120
5387Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557095 CIFC42 H102 Er K N3 O12 Si6P 1 21/n 111.064; 27.08; 21.797
90; 103.991; 90
6337Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557096 CIFC42 H102 Ho K N3 O12 Si6P 1 21/n 111.0476; 27.157; 21.797
90; 103.905; 90
6347.9Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557097 CIFC42 H102 Gd K N3 O12 Si6P 1 21/n 111.1493; 27.059; 21.755
90; 104.007; 90
6368.1Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557098 CIFC42 H102 K N3 O12 Si6 TbP 1 21/n 111.1324; 27.081; 21.775
90; 103.924; 90
6371.8Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557099 CIFC78 H190 Gd2 K2 N6 O21 Si12C 1 2/c 125.507; 18.806; 25.726
90; 103.21; 90
12014Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557100 CIFC42 H102 K N3 O12 Si6 YP 1 21/n 111.0774; 27.0905; 21.7959
90; 104; 90
6346.5Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557101 CIFC78 H190 Ho2 K2 N6 O21 Si12C 1 2/c 125.514; 18.8; 25.712
90; 103.167; 90
12009Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557105 CIFC104 H96 B4 F16 N8 O4 Pd2I 1 2/a 128.36; 12.35285; 27.666
90; 94.6541; 90
9660.2Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E.
Conformational control of Pd2L4 assemblies with unsymmetrical ligands
Chemical Science, 2020, 11, 677-683
1557106 CIFC123 H119 B4 F16 N17 O9 Pd2C 1 2/c 123.2193; 15.8896; 38.7298
90; 112.281; 90
13222.3Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E.
Conformational control of Pd2L4 assemblies with unsymmetrical ligands
Chemical Science, 2020, 11, 677-683
1557107 CIFC16 H19 I N2P 1 21/c 16.29025; 7.62301; 32.0065
90; 90.1584; 90
1534.73Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557108 CIFC64 H87 I3 N5 O2P -114.6729; 15.6807; 16.4518
85.945; 73.88; 62.636
3222.3Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557109 CIFC17 H18 I N2P 21 21 216.9063; 7.9318; 30.157
90; 90; 90
1651.98Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557110 CIFC73 H92 N5 O2 UP -113.2857; 13.9411; 20.5686
103.573; 95.666; 116.252
3230.4Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557111 CIFC75 H88 N8 UP -113.1219; 13.5561; 20.3099
78.109; 76.264; 68.201
3230.5Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557112 CIFC76 H99 N6 O P UP 1 21/c 125.884; 13.889; 21.315
90; 110.09; 90
7197Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557113 CIFC75 H96 N6 UP 1 21/n 114.7113; 12.979; 36.748
90; 94.521; 90
6994.8Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557114 CIFC82 H101 N7 O UP -113.1812; 15.8571; 19.6743
110.71; 90.48; 105.002
3692.6Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557115 CIFC33 H26 O2P 21 21 2111.3659; 11.9259; 17.9314
90; 90; 90
2430.58Liu, Xihong; Zhang, Jingying; Bai, Lutao; Wang, Linqing; Yang, Dongxu; Wang, Rui
Catalytic asymmetric multiple dearomatizations of phenols enabled by a cascade 1,8-addition and Diels‒Alder reaction
Chemical Science, 2020, 11, 671-676
1557116 CIFC64 H88P -114.635; 18.1373; 22.0161
79.631; 75.201; 74.12
5396.2Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557117 CIFC61 H39 B F24 N7 RhP -112.9083; 14.2464; 20.148
74.898; 79.351; 89.459
3512.7Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557118 CIFC67 H62 B F24 N5 RhP -111.7452; 16.7896; 18.5777
84.062; 73.668; 70.038
3304.3Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557119 CIFC32 H16 F8P -110.7497; 11.175; 11.5688
96.962; 96.945; 116.711
1207.93Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557120 CIFC60 H51 B Cl2 F24 N5 RhC 1 c 119.4406; 17.1714; 19.516
90; 103.079; 90
6345.86Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557121 CIFC54 H37 B F24 N5 RhC 1 2/c 116.95902; 18.45666; 34.7576
90; 98.7133; 90
10753.8Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557122 CIFC68 H45 B F25 N5 O RhP -113.01044; 20.05043; 26.99316
90.7652; 97.9088; 106.636
6672.31Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557123 CIFC21 H20 O6P 21 21 218.6977; 9.9164; 20.6241
90; 90; 90
1778.83Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557124 CIFC37 H32 Br2 O9P 1 21/c 115.4799; 12.7561; 17.7032
90; 110.471; 90
3275Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557125 CIFC20 H20 O6P 1 21/c 111.1979; 12.5205; 24.904
90; 93.401; 90
3485.5Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557126 CIFC18 H16 O5P 1 21 111.2987; 10.6941; 11.9582
90; 90.723; 90
1444.79Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557127 CIFC18 H18 O7P 1 21/n 113.6526; 9.772; 24.8831
90; 101.015; 90
3258.6Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557128 CIFC27 H29 N O8P 1 21 110.1038; 12.0566; 10.4153
90; 97.827; 90
1256.95Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557129 CIFC17 H20 O6P 1 21 17.091; 16.2621; 13.2704
90; 92.494; 90
1528.82Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557130 CIFC27 H29 N O8C 1 2 126.9187; 7.6682; 12.9814
90; 108.271; 90
2544.5Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557131 CIFC6 H5 D N2P b c a6.0431; 13.3857; 14.3592
90; 90; 90
1161.53Yang, Huan; Zhang, Li; Zhou, Fei-Yu; Jiao, Lei
An umpolung approach to the hydroboration of pyridines: a novel and efficient synthesis of N-H 1,4-dihydropyridines
Chemical Science, 2020, 11, 742-747
1557132 CIFIn8 Ir1.5 S5.25P 3 1 m13.9378; 13.9378; 8.2316
90; 90; 120
1384.9Khoury, Jason F.; He, Jiangang; Pfluger, Jonathan E.; Hadar, Ido; Balasubramanian, Mahalingam; Stoumpos, Constantinos C.; Zu, Rui; Gopalan, Venkatraman; Wolverton, Chris; Kanatzidis, Mercouri G.
Ir6In32S21, a polar, metal-rich semiconducting subchalcogenide
Chemical Science, 2020, 11, 870-878
1557138 CIFC19 H30 O3P 1 21 18.4484; 22.6578; 17.8169
90; 90.006; 90
3410.55Chen, He-Ping; Zhao, Zhen-Zhu; Cheng, Gui-Guang; Zhao, Kuan; Han, Kai-Yue; Zhou, Lin; Feng, Tao; Li, Zheng-Hui; Liu, Ji-Kai
Immunosuppressive Nor-isopimarane Diterpenes from Cultures of the Fungicolous Fungus <i>Xylaria longipes</i> HFG1018.
Journal of natural products, 2020
1557139 CIFC19 H30 O3P 21 21 216.8215; 10.0565; 24.1425
90; 90; 90
1656.2Chen, He-Ping; Zhao, Zhen-Zhu; Cheng, Gui-Guang; Zhao, Kuan; Han, Kai-Yue; Zhou, Lin; Feng, Tao; Li, Zheng-Hui; Liu, Ji-Kai
Immunosuppressive Nor-isopimarane Diterpenes from Cultures of the Fungicolous Fungus <i>Xylaria longipes</i> HFG1018.
Journal of natural products, 2020
1557140 CIFC19 H30 O2C 1 2 121.2462; 8.9711; 8.8437
90; 98.376; 90
1667.65Chen, He-Ping; Zhao, Zhen-Zhu; Cheng, Gui-Guang; Zhao, Kuan; Han, Kai-Yue; Zhou, Lin; Feng, Tao; Li, Zheng-Hui; Liu, Ji-Kai
Immunosuppressive Nor-isopimarane Diterpenes from Cultures of the Fungicolous Fungus <i>Xylaria longipes</i> HFG1018.
Journal of natural products, 2020
1557141 CIFC68 H50 N2 O4P 1 21 113.949; 15.719; 15.272
90; 107.438; 90
3194.7Chen, Michelle; Powers-Riggs, Natalia E.; Coleman, Adam F.; Young, Ryan M.; Wasielewski, Michael R.
Singlet Fission in Quaterrylenediimide Thin Films
The Journal of Physical Chemistry C, 2020
1557142 CIFC18 H20 Cl N3 O PdP -17.5074; 11.2005; 11.2581
70.42; 78.131; 84.462
872.46Czyz, Milena L.; Weragoda, Geethika K.; Horngren, Tyra H.; Connell, Timothy U.; Gomez, Daniel; O'Hair, Richard A. J.; Polyzos, Anastasios
Photoexcited Pd(ii) auxiliaries enable light-induced control in C(sp3)‒H bond functionalisation
Chemical Science, 2020, 11, 2455-2463
1557143 CIFC23 H24 N O4 PP 1 21/c 114.1914; 9.0659; 16.0033
90; 101.488; 90
2017.7Hirai, Yuichi; Wrona-Piotrowicz, Anna; Zakrzewski, Janusz; Brosseau, Arnaud; Guillot, Régis; Métivier, Rémi; Allain, Clémence
Mechanofluorochromism of pyrene-derived amidophosphonates.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 229-234
1557144 CIFC25 H28 N O4 PC 1 2/c 126.8408; 9.9974; 17.4578
90; 110.506; 90
4387.8Hirai, Yuichi; Wrona-Piotrowicz, Anna; Zakrzewski, Janusz; Brosseau, Arnaud; Guillot, Régis; Métivier, Rémi; Allain, Clémence
Mechanofluorochromism of pyrene-derived amidophosphonates.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 229-234
1557145 CIFC28 H26 N O4 PP -19.7414; 10.2898; 13.4571
110.284; 109.513; 90.732
1179.9Hirai, Yuichi; Wrona-Piotrowicz, Anna; Zakrzewski, Janusz; Brosseau, Arnaud; Guillot, Régis; Métivier, Rémi; Allain, Clémence
Mechanofluorochromism of pyrene-derived amidophosphonates.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 229-234
1557149 CIFC30 H32 N4 O3P 1 21/n 112.2782; 11.9261; 18.859
90; 103.754; 90
2682.4Wang, Shuo; Ren, Jia-Shu; Shan, Lian-Yun; Sun, Xiao-Yan; Di, Bin; Gu, Ning; Chen, Jin-Long
Triplexed Tracking Labile Sulfur-Containing Species on a Single-Molecule "Nezha" Sensor.
Analytical chemistry, 2020
1557155 CIFC116 H154 Cl N9 O9 Ti2P 1 21/n 126.5998; 13.18144; 32.7719
90; 104.629; 90
11118.1Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557156 CIFC30 H44 Cl2 O2 TiP 1 21 111.0509; 9.6943; 14.8668
90; 108.131; 90
1513.61Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557157 CIFC220 H283 Cl6 N15 O20 Ti6P -117.651; 18.2749; 19.8507
67.4531; 68.6833; 73.3966
5428.93Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557158 CIFC125 H172.5 Cl N8.5 O9 Ti2P -117.4371; 17.7765; 21.1345
100.63; 93.526; 104.426
6195.8Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557159 CIFC120 H164 Cl2 N6 O8 Ti2P -112.5697; 18.1183; 27.5282
104.559; 98.781; 102.093
5792.04Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557160 CIFC108 H140 Cl N7 O9 Ti2P -113.9465; 17.4744; 23.5392
85.6028; 74.2347; 74.5316
5320.83Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557161 CIFC130.71 H174.42 Cl N2.85 O11.43 Ti2P -116.3253; 17.3213; 23.5069
102.481; 91.495; 101.593
6340.9Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557162 CIFC113 H149.5 Cl N7.5 O9 Ti2P 1 21/n 126.6007; 13.18235; 32.7812
90; 104.622; 90
11122.7Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557163 CIFC49 H61 Cl N2 O4 TiP -112.14575; 18.0271; 21.0909
95.2564; 105.355; 90.2869
4432.27Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557164 CIFC54 H72 Cl2 N2 O4 TiC 1 2/c 143.9803; 12.41683; 19.4608
90; 94.9954; 90
10587.1Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557165 CIFC100 H102 Au4 P2 Ru2 S8P 1 21/c 113.9904; 14.295; 48.384
90; 94.664; 90
9644.4Sun, Yongnan; Pei, Wei; Xie, Mingcai; Xu, Shun; Zhou, Si; Zhao, Jijun; Xiao, Kang; Zhu, Yan
Excitonic Au4Ru2(PPh3)2(SC2H4Ph)8 cluster for light-driven dinitrogen fixation
Chemical Science, 2020, 11, 2440-2447
1557169 CIFC23 H22 O5P 1 21/c 116.4615; 7.573; 16.0803
90; 111.302; 90
1867.7Maeda, Gasper; van der Wal, Jelle; Gupta, Arvind Kumar; Munissi, Joan J. E.; Orthaber, Andreas; Sunnerhagen, Per; Nyandoro, Stephen S.; Erdélyi, Máté
Oxygenated Cyclohexene Derivatives and Other Constituents from the Roots of <i>Monanthotaxis trichocarpa</i>.
Journal of natural products, 2020
1557170 CIFC22 H21 Cl O6P 1 21 15.933; 13.4485; 12.3282
90; 96.291; 90
977.74Maeda, Gasper; van der Wal, Jelle; Gupta, Arvind Kumar; Munissi, Joan J. E.; Orthaber, Andreas; Sunnerhagen, Per; Nyandoro, Stephen S.; Erdélyi, Máté
Oxygenated Cyclohexene Derivatives and Other Constituents from the Roots of <i>Monanthotaxis trichocarpa</i>.
Journal of natural products, 2020
1557171 CIFC37 H53 F N2 O2 ZnP 1 21/n 122.1881; 11.5778; 29.7479
90; 106.38; 90
7331.75Jiang, Jinxing; Cui, Yaqin; Lu, Yaguang; Zhang, Bin; Pan, Xiaobo; Wu, Jincai
Weak Lewis Pairs as Catalysts for Highly Isoselective Ring-Opening Polymerization of Epimerically Labile rac-O-Carboxyanhydride of Mandelic Acid
Macromolecules, 2020
1557172 CIFC36 H51 F N2 O2 ZnP 1 21/c 115.3766; 17.6353; 13.571
90; 105.2; 90
3551.32Jiang, Jinxing; Cui, Yaqin; Lu, Yaguang; Zhang, Bin; Pan, Xiaobo; Wu, Jincai
Weak Lewis Pairs as Catalysts for Highly Isoselective Ring-Opening Polymerization of Epimerically Labile rac-O-Carboxyanhydride of Mandelic Acid
Macromolecules, 2020
1557173 CIFC54.28 H49.13 Ir O0.28 P3P 1 21/c 117.31801; 12.99024; 19.71788
90; 94.4442; 90
4422.5Tickner, Ben J.; Semenova, Olga; Iali, Wissam; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.
Optimisation of pyruvate hyperpolarisation using SABRE by tuning the active magnetisation transfer catalyst.
Catalysis science & technology, 2020, 10, 1343-1355
1557174 CIFC57 H68 Cl2 Ir2 N4 O S2P 1 21/c 112.9317; 16.6; 25.5365
90; 90.2757; 90
5481.76Tickner, Ben J.; Semenova, Olga; Iali, Wissam; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.
Optimisation of pyruvate hyperpolarisation using SABRE by tuning the active magnetisation transfer catalyst.
Catalysis science & technology, 2020, 10, 1343-1355
1557175 CIF
HKL
Paper
C16 H21 N3 O4P -18.127; 8.411; 12.536
105.36; 96.52; 94.77
815.2Yoo, Miri; Koh, Dongsoo
Diethyl 4-(1<i>H</i>-imidazol-2-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
IUCrData, 2020, 5, x200034
1557176 CIF
HKL
Paper
C25 H22 N2 O2 SeP 1 21/c 113.209; 6.343; 27.08
90; 103.356; 90
2207.5Morris, LaQuze L.; Alvarado, Clarisa A.; Goncalves, Julia M.; Singh, Ravi P.; Lovely, Carl J.; Yousufuddin, Muhammed
[4-(4-Methoxyphenyl)-8-oxo-3-(phenylselanyl)spiro[4.5]deca-3,6,9-trien-2-yl]methylcyanamide
IUCrData, 2020, 5, x200078
1557177 CIF
HKL
Paper
C40 H74 Co N8 S4P -17.484; 8.587; 18.523
83.782; 81.868; 71.189
1113Giltzau, Niels Ole; Köckerling, Martin
Bis(1-dodecyl-4-aza-1-azoniabicyclo[2.2.2]octane)tetraisothiocyanatocobalt(II)
IUCrData, 2020, 5, x200023
1557178 CIF
HKL
Paper
C18 H17 F O5P 1 21/c 115.5801; 8.3414; 12.1298
90; 97.086; 90
1564.35Yoo, Miri; Koh, Dongsoo
(<i>E</i>)-1-(4-Fluoro-2-hydroxyphenyl)-3-(2,3,4-trimethoxyphenyl)prop-2-en-1-one
IUCrData, 2020, 5, x200071
1557183 CIFC26 H28 N4 O5P 4111.7728; 11.7728; 17.1159
90; 90; 90
2372.2Yang, Yaxi; Zhang, Rukang; Li, Zhaojun; Mei, Lianghe; Wan, Shili; Ding, Hong; Chen, Zhifeng; Xing, Jing; Feng, Huijin; Han, Jie; Jiang, Hualiang; Zheng, Mingyue; Luo, Cheng; Zhou, Bing
Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors.
Journal of medicinal chemistry, 2020
1557184 CIFC13 H15 N3 O5P 21 21 218.4194; 8.5433; 19.1641
90; 90; 90
1378.46Yang, Yaxi; Zhang, Rukang; Li, Zhaojun; Mei, Lianghe; Wan, Shili; Ding, Hong; Chen, Zhifeng; Xing, Jing; Feng, Huijin; Han, Jie; Jiang, Hualiang; Zheng, Mingyue; Luo, Cheng; Zhou, Bing
Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors.
Journal of medicinal chemistry, 2020
1557185 CIFC25 H23 F4 N5 O5P 110.1492; 10.1392; 25.2626
96.515; 96.515; 107.35
2435.42Yang, Yaxi; Zhang, Rukang; Li, Zhaojun; Mei, Lianghe; Wan, Shili; Ding, Hong; Chen, Zhifeng; Xing, Jing; Feng, Huijin; Han, Jie; Jiang, Hualiang; Zheng, Mingyue; Luo, Cheng; Zhou, Bing
Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors.
Journal of medicinal chemistry, 2020
1557186 CIFC15 H14 N4 O2P 21 21 215.8178; 16.9835; 28.2863
90; 90; 90
2794.9Yang, Yaxi; Zhang, Rukang; Li, Zhaojun; Mei, Lianghe; Wan, Shili; Ding, Hong; Chen, Zhifeng; Xing, Jing; Feng, Huijin; Han, Jie; Jiang, Hualiang; Zheng, Mingyue; Luo, Cheng; Zhou, Bing
Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors.
Journal of medicinal chemistry, 2020
1557187 CIFC15 H16 O6P 1 21/c 16.20271; 12.9748; 17.3444
90; 96.612; 90
1386.57Liu, Tingting; Wu, Haibo; Zhang, Jing; Deng, Wenjie; Yang, Luowenlei
Modified Eremophilanes from Parasenecio hastatus and Their Neuroprotective Activities
Journal of Natural Products, 2020
1557188 CIFC16 H18 O3P 1 21 18.7529; 5.1376; 14.4614
90; 104.921; 90
628.39Liu, Tingting; Wu, Haibo; Zhang, Jing; Deng, Wenjie; Yang, Luowenlei
Modified Eremophilanes from Parasenecio hastatus and Their Neuroprotective Activities
Journal of Natural Products, 2020
1557189 CIFC22 H12 F6 N2 O3P 1 21/n 110.7749; 15.2475; 12.314
90; 108.515; 90
1918.4Malla, Javid Ahmad; Umesh, Rintu M.; Vijay, Amal; Mukherjee, Arnab; Lahiri, Mayurika; Talukdar, Pinaki
Apoptosis-inducing activity of a fluorescent barrel-rosette M+/Cl− channel
Chemical Science, 2020, 11, 2420-2428
1557193 CIFC20 H14P 1 21/c 114.0565; 5.9201; 7.8474
90; 92.837; 90
652.23Shibuya, Yusuke; Aonuma, Kazuhiro; Kimura, Tomohiro; Kaneko, Takuro; Fujiwara, Wataru; Yamaguchi, Yuji; Kumaki, Daisuke; Tokito, Shizuo; Katagiri, Hiroshi
Linear Biazulene Isomers: Effects of Molecular and Packing Structure on Optoelectronic and Charge-Transport Properties
The Journal of Physical Chemistry C, 2020
1557194 CIFC20 H14P 1 21/c 113.5349; 6.0042; 8.1543
90; 94.232; 90
660.86Shibuya, Yusuke; Aonuma, Kazuhiro; Kimura, Tomohiro; Kaneko, Takuro; Fujiwara, Wataru; Yamaguchi, Yuji; Kumaki, Daisuke; Tokito, Shizuo; Katagiri, Hiroshi
Linear Biazulene Isomers: Effects of Molecular and Packing Structure on Optoelectronic and Charge-Transport Properties
The Journal of Physical Chemistry C, 2020
1557195 CIFC20 H14P -15.9457; 7.8815; 14.0822
86.684; 87.09; 88.848
657.85Shibuya, Yusuke; Aonuma, Kazuhiro; Kimura, Tomohiro; Kaneko, Takuro; Fujiwara, Wataru; Yamaguchi, Yuji; Kumaki, Daisuke; Tokito, Shizuo; Katagiri, Hiroshi
Linear Biazulene Isomers: Effects of Molecular and Packing Structure on Optoelectronic and Charge-Transport Properties
The Journal of Physical Chemistry C, 2020
1557196 CIFC20 H14P -16.087; 7.5639; 14.4293
97.942; 95.597; 90.921
654.54Shibuya, Yusuke; Aonuma, Kazuhiro; Kimura, Tomohiro; Kaneko, Takuro; Fujiwara, Wataru; Yamaguchi, Yuji; Kumaki, Daisuke; Tokito, Shizuo; Katagiri, Hiroshi
Linear Biazulene Isomers: Effects of Molecular and Packing Structure on Optoelectronic and Charge-Transport Properties
The Journal of Physical Chemistry C, 2020
1557197 CIFC58 H62 N6 O13 Zn2P 1 21/c 115.21; 16.731; 23.716
90; 104.529; 90
5842Fu, Guorui; He, Yani; Li, Wentao; Miao, Tiezheng; Lü, Xingqiang; He, Hongshan; Liu, Li; Wong, Wai-Yeung
Efficient white polymer light-emitting diodes (WPLEDs) based on covalent-grafting of [Zn2(MP)3(OAc)] into PVK
Chemical Science, 2020, 11, 2640-2646
1557201 CIFC23 H28 O8P 1 21 15.996; 12.4304; 14.2341
90; 94.361; 90
1057.83Wang, Rong; Fan, Run-Zhu; Ni, Fu-Qiang; Sang, Jun; Xie, Xing-Lin; Luo, Si-Yuan; Tang, Gui-Hua; Yin, Sheng
19-nor-, 20-nor-, and tetranor-Halimane-Type Furanoditerpenoids from Croton crassifolius
Journal of Natural Products, 2020
1557202 CIFC21 H26 O5P 16.3062; 7.6848; 9.7183
87.904; 80.198; 87.694
463.505Wang, Rong; Fan, Run-Zhu; Ni, Fu-Qiang; Sang, Jun; Xie, Xing-Lin; Luo, Si-Yuan; Tang, Gui-Hua; Yin, Sheng
19-nor-, 20-nor-, and tetranor-Halimane-Type Furanoditerpenoids from Croton crassifolius
Journal of Natural Products, 2020
1557203 CIFC21 H26 O6P 21 21 218.0315; 8.3527; 27.8078
90; 90; 90
1865.48Wang, Rong; Fan, Run-Zhu; Ni, Fu-Qiang; Sang, Jun; Xie, Xing-Lin; Luo, Si-Yuan; Tang, Gui-Hua; Yin, Sheng
19-nor-, 20-nor-, and tetranor-Halimane-Type Furanoditerpenoids from Croton crassifolius
Journal of Natural Products, 2020
1557204 CIFC24 H26 O10P 21 21 217.77753; 10.89287; 25.97545
90; 90; 90
2200.63Wang, Rong; Fan, Run-Zhu; Ni, Fu-Qiang; Sang, Jun; Xie, Xing-Lin; Luo, Si-Yuan; Tang, Gui-Hua; Yin, Sheng
19-nor-, 20-nor-, and tetranor-Halimane-Type Furanoditerpenoids from Croton crassifolius
Journal of Natural Products, 2020
1557205 CIFC23 H28 O8P 21 21 217.9019; 10.2955; 25.9952
90; 90; 90
2114.81Wang, Rong; Fan, Run-Zhu; Ni, Fu-Qiang; Sang, Jun; Xie, Xing-Lin; Luo, Si-Yuan; Tang, Gui-Hua; Yin, Sheng
19-nor-, 20-nor-, and tetranor-Halimane-Type Furanoditerpenoids from Croton crassifolius
Journal of Natural Products, 2020
1557206 CIFC20 H30 N2 O2P 1 21/c 111.012; 16.138; 11.225
90; 96.899; 90
1980Chen, Hang; Ye, Hebo; Hai, Yu; Zhang, Ling; You, Lei
n →π* interactions as a versatile tool for controlling dynamic imine chemistry in both organic and aqueous media
Chemical Science, 2020, 11, 2707-2715
1557207 CIFC19 H29 N3 O2I 1 2/a 117.03; 10.58; 22.26
90; 103.23; 90
3904Chen, Hang; Ye, Hebo; Hai, Yu; Zhang, Ling; You, Lei
n →π* interactions as a versatile tool for controlling dynamic imine chemistry in both organic and aqueous media
Chemical Science, 2020, 11, 2707-2715
1557208 CIF
HKL
Paper
C20 H24 N2 O6 S2C 1 2/c 129.1537; 8.8739; 19.9919
90; 123.621; 90
4306.9Narvekar, Kedar U.; Srinivasan, Bikshandarkoil R.
Benzene-1,2-diaminium bis(4-methylbenzene-1-sulfonate)
IUCrData, 2020, 5, x200100
1557209 CIF
HKL
Paper
Br Cs F4I m m m5.5075; 6.789; 12.2572
90; 90; 90
458.3Malin, Artem V.; Ivlev, Sergei I.; Ostvald, Roman V.; Kraus, Florian
Redetermination of the crystal structure of caesium tetrafluoridobromate(III) from single-crystal X-ray diffraction data
IUCrData, 2020, 5, x200114
1557210 CIF
HKL
Paper
C19 H13 I O2P 1 21/n 17.0481; 18.2185; 12.6391
90; 104.947; 90
1568.02Dean, Raven; Miller, Chelsea N.; Zingales, Sarah K.; Padgett, Clifford W.
3-(4-Iodophenyl)-2,3-dihydro-1<i>H</i>-benzo[<i>f</i>]chromen-1-one
IUCrData, 2020, 5, x200110
1557213 CIFC29 H21 NP 1 21/c 116.841; 5.9463; 21.001
90; 96.31; 90
2090.3Li, Ye-Xin; Chen, You-Gui; Yu, Zhen-Feng; Yang, Xiao-Feng; Nie, Yong; Cui, Yu; Sun, Guo-Xin
Polymorph-Dependent Multicolor-Switchable Mechanofluorochromism of 1-(9-Anthryl)vinyl-3-(3-pyridyl)vinylbenzene: Molecular Conformation versus Intermolecular Interaction
The Journal of Physical Chemistry C, 2020
1557214 CIFC29 H21 NP 4/n :227.4933; 27.4933; 5.8624
90; 90; 90
4431.3Li, Ye-Xin; Chen, You-Gui; Yu, Zhen-Feng; Yang, Xiao-Feng; Nie, Yong; Cui, Yu; Sun, Guo-Xin
Polymorph-Dependent Multicolor-Switchable Mechanofluorochromism of 1-(9-Anthryl)vinyl-3-(3-pyridyl)vinylbenzene: Molecular Conformation versus Intermolecular Interaction
The Journal of Physical Chemistry C, 2020
1557215 CIFC29 H21 NP 1 21/c 15.5332; 11.857; 31.179
90; 90.172; 90
2045.6Li, Ye-Xin; Chen, You-Gui; Yu, Zhen-Feng; Yang, Xiao-Feng; Nie, Yong; Cui, Yu; Sun, Guo-Xin
Polymorph-Dependent Multicolor-Switchable Mechanofluorochromism of 1-(9-Anthryl)vinyl-3-(3-pyridyl)vinylbenzene: Molecular Conformation versus Intermolecular Interaction
The Journal of Physical Chemistry C, 2020
1557220 CIFS8F d d d :210.331; 12.6786; 24.3519
90; 90; 90
3189.7MIKURIYA, Masahiro; TANIGUCHI, Kazuki; KOYAMA, Yoshiki; WATANABE, Hiroaki; YOSHIOKA, Daisuke; MITSUHASHI, Ryoji; ASATO, Eiji
Crystal Structure of S<sub>8</sub> Molecule from Thiourea
X-ray Structure Analysis Online, 2020, 36, 1-2
1557221 CIFC398.15 H435.65 B16 Co8 F64 N74.85 O39.35C 1 2/c 132.77108; 30.00687; 40.3365
90; 96.1279; 90
39438.6Mozaceanu,; Taylor,; Piper,; Argent,; Ward,
Catalysis of an Aldol Condensation Using a Coordination Cage
Chemistry, 2020, 2, 22-32
1557222 CIFC20 H12 Cu N2 O4P 1 21/c 15.6674; 10.9072; 14.5876
90; 93.491; 90
900.07He, Tengjiao; Xiao, Yonghou; Zhao, Qidong; Zhou, Mengxue; He, Gaohong
Ultramicroporous Metal‒Organic Framework Qc-5-Cu for Highly Selective Adsorption of CO2 from C2H4 Stream
Industrial & Engineering Chemistry Research, 2020
1557223 CIFC55.6 H49 Br2 Cl2 Cu F6 N2 O1.9 P3P -110.93; 14.2927; 19.2894
70.366; 86.491; 73.206
2715Nohara, Isaak; Keller, Aramis; Tarassenko, Nikolai; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Heteroleptic [Cu(P^P)(N^N)][PF6] Compounds with Isomeric Dibromo-1,10-Phenanthroline Ligands
Inorganics, 2020, 8, 4
1557224 CIFC49 H36 Br2 Cl2 Cu F6 N2 O P3P -112.4032; 18.9805; 22.0591
70.33; 77.791; 87.292
4777.9Nohara, Isaak; Keller, Aramis; Tarassenko, Nikolai; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Heteroleptic [Cu(P^P)(N^N)][PF6] Compounds with Isomeric Dibromo-1,10-Phenanthroline Ligands
Inorganics, 2020, 8, 4
1557225 CIFC50 H39 Br2 Cu F6 N2 O1.5 P3P -115.1949; 18.5322; 18.5423
107.867; 104.444; 101.088
4603.2Nohara, Isaak; Keller, Aramis; Tarassenko, Nikolai; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Heteroleptic [Cu(P^P)(N^N)][PF6] Compounds with Isomeric Dibromo-1,10-Phenanthroline Ligands
Inorganics, 2020, 8, 4
1557226 CIFC54.9 H47.2 Br2 Cl2.2 Cu F6 N2 O1.7 P3P -110.1768; 13.7504; 20.1505
90.204; 98.12; 99.535
2751.9Nohara, Isaak; Keller, Aramis; Tarassenko, Nikolai; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Heteroleptic [Cu(P^P)(N^N)][PF6] Compounds with Isomeric Dibromo-1,10-Phenanthroline Ligands
Inorganics, 2020, 8, 4
1557227 CIFC52.1 H40.2 Br2 Cl2.2 Cu F6 N2 O P3C 1 2/m 133.3182; 14.105; 11.8205
90; 102.059; 90
5432.5Nohara, Isaak; Keller, Aramis; Tarassenko, Nikolai; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Heteroleptic [Cu(P^P)(N^N)][PF6] Compounds with Isomeric Dibromo-1,10-Phenanthroline Ligands
Inorganics, 2020, 8, 4
1557228 CIFC101 H48 F40 N12 Ni O7P n a 2127.571; 19.7599; 19.1951
90; 90; 90
10457.5Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557229 CIFC89.5 H19 Cl Cu F40 N8 Ni O3C 1 2/c 147.886; 13.8742; 28.061
90; 119.602; 90
16210Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557230 CIFC89 H22 F40 N8 O3P -111.6188; 14.403; 26.7956
82.937; 77.65; 70.954
4133.7Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557231 CIFC97 H32 F40 N12 Ni O3P -114.057; 14.08; 24.646
92.257; 101.581; 108.23
4511.4Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557232 CIFC89 H18 Cu F40 N8 Ni O3P -114.0363; 14.1385; 24.8547
91.904; 101.174; 107.743
4586.3Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion
Chemical Science, 2020, 11, 2790-2795
1557233 CIFS8 V7P 32 2 16.689; 6.689; 17.403
90; 90; 120
674.3Bindi,; Zaccarini,; Ifandi,; Tsikouras,; Stanley,; Garuti,; Mauro,
Grammatikopoulosite, NiVP, a New Phosphide from the Chromitite of the Othrys Ophiolite, Greece
Minerals, 2020, 10, 131
1557234 CIFC61 H90 Au2 Cl2 F12 N2 P2 Sb2P 1 21/n 110.4398; 18.5854; 16.9617
90; 94.354; 90
3281.5Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557235 CIFC34 H50 Au Cl2 F6 N O P SbP 1 21/c 110.9121; 17.7644; 19.509
90; 104.904; 90
3654.5Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557236 CIFC33 H48 Au Cl2 F6 N O2 P SbP 1 21 114.8546; 12.2517; 20.5946
90; 99.848; 90
3692.9Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557237 CIFC21 H20 N4 O5P 1 21/c 115.4212; 13.4652; 9.4134
90; 102.515; 90
1908.2Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557238 CIFC29 H36 Au B10 Cl2 F6 P2 SbP 1 n 110.0221; 13.3021; 14.7578
90; 95.633; 90
1957.94Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557239 CIFC38 H47 Au F6 N2 O2 P SbP 1 21/c 110.7728; 11.143; 30.591
90; 98.974; 90
3627.2Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier
Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes
Chemical Science, 2020, 11, 2750-2758
1557240 CIFC10 H16 Br4 SeC 1 2/c 120.9331; 6.0827; 15.253
90; 132.9; 90
1422.72Potapov, Vladimir A.; Musalov, Maxim V.; Kurkutov, Evgeny O.; Yakimov, Vladimir A.; Khabibulina, Alfiya G.; Musalova, Maria V.; Amosova, Svetlana V.; Borodina, Tatyana N.; Albanov, Alexander I.
Remarkable Alkene-to-Alkene and Alkene-to-Alkyne Transfer Reactions of Selenium Dibromide and PhSeBr. Stereoselective Addition of Selenium Dihalides to Cycloalkenes.
Molecules (Basel, Switzerland), 2020, 25, 194
1557241 CIFC10 H16 Cl4 SeC 1 2/c 120.6655; 6.0655; 14.7555
90; 133.69; 90
1337.4Potapov, Vladimir A.; Musalov, Maxim V.; Kurkutov, Evgeny O.; Yakimov, Vladimir A.; Khabibulina, Alfiya G.; Musalova, Maria V.; Amosova, Svetlana V.; Borodina, Tatyana N.; Albanov, Alexander I.
Remarkable Alkene-to-Alkene and Alkene-to-Alkyne Transfer Reactions of Selenium Dibromide and PhSeBr. Stereoselective Addition of Selenium Dihalides to Cycloalkenes.
Molecules (Basel, Switzerland), 2020, 25, 194
1557242 CIFC23 H19 Co N2 O7 SP -19.1273; 12.0439; 12.0526
62.4993; 75.9211; 79.9212
1136.88Chhetri, Pradhumna Mahat; Wu, Ming-Hao; Hsieh, Chou-Ting; Yang, Xiang-Kai; Wu, Chen-Ming; Yang, En-Che; Wang, Chih-Chieh; Chen, Jhy-Der
A Pair of Co<sup>II</sup> Supramolecular Isomers Based on Flexible Bis-Pyridyl-Bis-Amide and Angular Dicarboxylate Ligands.
Molecules (Basel, Switzerland), 2020, 25, 201
1557243 CIFC23.5 H22 Co N2 O8 SP -19.2206; 11.0642; 13.345
96.611; 109.696; 103.697
1216.7Chhetri, Pradhumna Mahat; Wu, Ming-Hao; Hsieh, Chou-Ting; Yang, Xiang-Kai; Wu, Chen-Ming; Yang, En-Che; Wang, Chih-Chieh; Chen, Jhy-Der
A Pair of Co<sup>II</sup> Supramolecular Isomers Based on Flexible Bis-Pyridyl-Bis-Amide and Angular Dicarboxylate Ligands.
Molecules (Basel, Switzerland), 2020, 25, 201
1557252 CIF
HKL
Paper
C29 H23 Cl N2 OP 1 21/n 19.0627; 10.7595; 24.4636
90; 100.599; 90
2344.7Shraddha, K. N.; Devika, S.; Begum, Noor Shahina
4-Chloro-2-[1-(4-ethylphenyl)-4,5-diphenyl-1<i>H</i>-imidazol-2-yl]phenol
IUCrData, 2020, 5, x191690
1557253 CIFC54 H99 Am Br3 O3 P3P c a 2128.768; 11.456; 18.185
90; 90; 90
5993Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557254 CIFC54 H99 Br3 Nd O3 P3P c a 2128.7058; 11.4228; 18.1359
90; 90; 90
5946.8Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557255 CIFC54 H99 Br3 Ce O3 P3P c a 2128.92; 11.434; 18.209
90; 90; 90
6021.2Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557256 CIFC54 H99 Br3 La O3 P3P c a 2128.879; 11.4223; 18.2083
90; 90; 90
6006.3Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782
1557257 CIFC54 H99 Br3 O3 P3 PrP c a 2128.7155; 11.4126; 18.1299
90; 90; 90
5941.5Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E.
Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes
Chemical Science, 2020, 11, 2770-2782

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