Crystallography Open Database
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Searching journal of publication like 'Chem. Commun.'
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1572878 | CIF | C24 H18 N2 O3 | P 21 21 21 | 8.6718; 9.0165; 24.3506 90; 90; 90 | 1903.96 | Weng, Rui; Zhou, Yuqiao; Zhang, Yaqin; Feng, Xiaoming; Liu, Xiaohua Catalytic asymmetric Michael and Nef-type sequential reaction of nitroolefin with azlactone to construct oxazole-fused succinimide. Chemical communications (Cambridge, England), 2024, 60, 13384-13387 |
| 1572879 | CIF | C24 H15 Cl O4 | P 1 21/n 1 | 11.941; 8.391; 19.4783 90; 107.214; 90 | 1864.24 | Dey, Sovan; Das, Arindam; Yadav, Ram Naresh; Boruah, Palash Jyoti; Sarkar, Koushik; Paul, Amit Kumar; Hossain, Md Firoj Electron donor-acceptor complex enabled photocascade strategy for the synthesis of <i>trans</i>-dihydrofuro[3,2-<i>c</i>]chromen-4-one scaffolds <i>via</i> radical conjugate addition of pyridinium ylide. Chemical communications (Cambridge, England), 2024, 60, 14384-14387 |
| 1572880 | CIF | C26 H20 Br N O4 | P -1 | 5.0399; 14.26675; 15.137 82.4456; 83.3581; 85.9012 | 1069.96 | Dey, Sovan; Das, Arindam; Yadav, Ram Naresh; Boruah, Palash Jyoti; Sarkar, Koushik; Paul, Amit Kumar; Hossain, Md Firoj Electron donor-acceptor complex enabled photocascade strategy for the synthesis of <i>trans</i>-dihydrofuro[3,2-<i>c</i>]chromen-4-one scaffolds <i>via</i> radical conjugate addition of pyridinium ylide. Chemical communications (Cambridge, England), 2024, 60, 14384-14387 |
| 1573283 | CIF | C35 H21 N3 O | P 1 21/n 1 | 15.5452; 4.78961; 32.495 90; 103.488; 90 | 2352.7 | Singh, Hemant K.; Bodzioch, Agnieszka; Pietrzak, Anna; Kaszyński, Piotr π-Curved Blatter radicals: Blatter helicenes. Chemical communications (Cambridge, England), 2025, 61, 496-499 |
| 1573284 | CIF | C27 H16 N3 O | R -3 :H | 43.189; 43.189; 5.1711 90; 90; 120 | 8353.3 | Singh, Hemant K.; Bodzioch, Agnieszka; Pietrzak, Anna; Kaszyński, Piotr π-Curved Blatter radicals: Blatter helicenes. Chemical communications (Cambridge, England), 2025, 61, 496-499 |
| 1573285 | CIF | C35 H20 N3 O | P 1 21/c 1 | 21.3059; 11.4684; 9.6844 90; 94.685; 90 | 2358.42 | Singh, Hemant K.; Bodzioch, Agnieszka; Pietrzak, Anna; Kaszyński, Piotr π-Curved Blatter radicals: Blatter helicenes. Chemical communications (Cambridge, England), 2025, 61, 496-499 |
| 1573583 | CIF | C49 H69 Mg N4 P Si | P -1 | 10.9738; 12.7041; 18.1148 85.417; 85.746; 80.856 | 2480.5 | Nath, Priyanku; Sagar, Shweta; Ray, Aranya; Karmakar, Himadri; Sarkar, Alok; Chandrasekhar, Vadapalli; Panda, Tarun K. Crafting tailored, well-defined block copolymers of cyclic esters with an organomagnesium initiator. Chemical communications (Cambridge, England), 2025, 61, 2341-2344 |
| 1573616 | CIF | C2 H5 Cu I N | P 62 2 2 | 17.5937; 17.5937; 7.3368 90; 90; 120 | 1966.76 | Panda, Sankalpa N.; Pradhan, Prabhanjan; Nath, Satyapriya; Mohapatra, Jeebanjyoti; Patra, Biplab K.; Biswal, Bishnu P. Inducing piezoelectric behavior in a copper iodide cubane cluster-based metal-organic framework <i>via</i> linker engineering. Chemical communications (Cambridge, England), 2025, 61, 2536-2539 |
| 1573791 | CIF | C30 H25 N O2 Si | P 1 21/n 1 | 8; 21.9129; 14.2074 90; 105.405; 90 | 2401.12 | Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence. Chemical communications (Cambridge, England), 2025, 61, 4662-4665 |
| 1573792 | CIF | C54 H36 B Cl2 F4 N O | P n a 21 | 15.799; 10.5487; 24.3174 90; 90; 90 | 4052.7 | Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence. Chemical communications (Cambridge, England), 2025, 61, 4662-4665 |
| 1573793 | CIF | C29 H23 N O Si | P 1 21/c 1 | 7.7962; 22.1366; 13.7791 90; 105.129; 90 | 2295.6 | Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence. Chemical communications (Cambridge, England), 2025, 61, 4662-4665 |
| 1573794 | CIF | C80 H55.93 B2 Br0.07 N2 O0 | P 1 21/c 1 | 25.5585; 9.9428; 24.0807 90; 91.408; 90 | 6117.6 | Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence. Chemical communications (Cambridge, England), 2025, 61, 4662-4665 |
| 1573795 | CIF | C44.66667 H33 N O2 Pt | P -1 | 12.7645; 18.0822; 22.7774 89.964; 81.068; 85.594 | 5177.8 | Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence. Chemical communications (Cambridge, England), 2025, 61, 4662-4665 |
| 1573796 | CIF | C21 H21 N O2 | P b c a | 9.3805; 17.9125; 20.6371 90; 90; 90 | 3467.61 | Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones. Chemical communications (Cambridge, England), 2025, 61, 3720-3723 |
| 1573797 | CIF | C18 H16 Cl N O2 | P 1 21 1 | 9.7449; 12.6197; 12.8104 90; 91.761; 90 | 1574.65 | Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones. Chemical communications (Cambridge, England), 2025, 61, 3720-3723 |
| 1573798 | CIF | C21 H19 F2 N O2 | I 1 a 1 | 9.7705; 13.1781; 14.487 90; 103.85; 90 | 1811.07 | Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones. Chemical communications (Cambridge, England), 2025, 61, 3720-3723 |
| 1573799 | CIF | C18 H16 F N O2 | P 1 21/n 1 | 8.35635; 20.16774; 9.47069 90; 111.53; 90 | 1484.72 | Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones. Chemical communications (Cambridge, England), 2025, 61, 3720-3723 |
| 1573800 | CIF | C21 H19 Br2 N O2 | I 1 2/a 1 | 16.9874; 9.81932; 24.6758 90; 109.044; 90 | 3890.77 | Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones. Chemical communications (Cambridge, England), 2025, 61, 3720-3723 |
| 1575107 | CIF | C36 H30 Cl5 In S2 | I 1 2 1 | 9.5069; 14.7416; 12.734 90; 90.609; 90 | 1784.53 | Qin, Ying; Tang, Yali; Pan, Yue Xiao; Chen, Yingnuo; Xiao, Hongping; Zou, Jun Tailoring the properties of Sb<sup>3+</sup>-doped in-based organic-inorganic hybrid metal halides through A-site cation engineering. Chemical communications (Cambridge, England), 2025, 61, 12518-12521 |
| 1575108 | CIF | C26 H35 Cl6 In N2 S3 | C 1 2 1 | 14.2222; 9.351; 12.4182 90; 93.818; 90 | 1647.85 | Qin, Ying; Tang, Yali; Pan, Yue Xiao; Chen, Yingnuo; Xiao, Hongping; Zou, Jun Tailoring the properties of Sb<sup>3+</sup>-doped in-based organic-inorganic hybrid metal halides through A-site cation engineering. Chemical communications (Cambridge, England), 2025, 61, 12518-12521 |
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