Crystallography Open Database
Search results
Result: there are 1682 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 54
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7121236 | CIF | C24 H18 F2 N2 | P n a 21 | 14.1238; 8.54517; 15.8226 90; 90; 90 | 1909.63 | Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives. Chemical communications (Cambridge, England), 2018, 54, 2228-2231 |
| 7121237 | CIF | C47.5 H39 N | P 1 21/n 1 | 17.51974; 9.24966; 22.74222 90; 107.382; 90 | 3517.12 | Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives. Chemical communications (Cambridge, England), 2018, 54, 2228-2231 |
| 7121238 | CIF | C24 H15 F3 N2 | P 1 21/n 1 | 9.06788; 5.5036; 37.4304 90; 96.012; 90 | 1857.73 | Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives. Chemical communications (Cambridge, England), 2018, 54, 2228-2231 |
| 7121239 | CIF | C45 H27 F6 N | P 1 21/n 1 | 16.1155; 10.2929; 20.6155 90; 90.803; 90 | 3419.26 | Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives. Chemical communications (Cambridge, England), 2018, 54, 2228-2231 |
| 7121240 | CIF | C25 H19 N | P 1 21 1 | 9.652; 9.262; 10.579 90; 107.03; 90 | 904.3 | Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H. Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives. Chemical communications (Cambridge, England), 2018, 54, 2228-2231 |
| 7121241 | CIF | C8 H7 B F5 N O3 | P -1 | 6.1877; 8.3211; 11.0677 92.077; 102.377; 104.581 | 536.23 | Smirnov, Vladimir O.; Maslov, Anton S.; Kokorekin, Vladimir A.; Korlyukov, Alexander A.; Dilman, Alexander D. Photoredox generation of the trifluoromethyl radical from borate complexes via single electron reduction. Chemical communications (Cambridge, England), 2018, 54, 2236-2239 |
| 7121242 | CIF | C10 H7 B F9 N O3 | P 1 21/c 1 | 13.3594; 8.1912; 12.4704 90; 97.696; 90 | 1352.34 | Smirnov, Vladimir O.; Maslov, Anton S.; Kokorekin, Vladimir A.; Korlyukov, Alexander A.; Dilman, Alexander D. Photoredox generation of the trifluoromethyl radical from borate complexes via single electron reduction. Chemical communications (Cambridge, England), 2018, 54, 2236-2239 |
| 7121243 | CIF | C16 H24 O2 | P -1 | 6.5853; 8.4322; 11.3892 92.3437; 91.5258; 93.7139 | 630.3 | Nakanishi, Yusuke; Omachi, Haruka; Fokina, Natalie A.; Schreiner, Peter R.; Becker, Jonathan; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Shinohara, Hisanori One-dimensional hydrogen bonding networks of bis-hydroxylated diamantane formed inside double-walled carbon nanotubes. Chemical communications (Cambridge, England), 2018, 54, 3823-3826 |
| 7121244 | CIF | C15 H9 F5 O2 | P 1 21/c 1 | 10.7847; 8.7041; 28.524 90; 99.114; 90 | 2643.8 | Shen, Yi; Wu, Xin-Xing; Chen, Si; Xia, Yu; Liang, Yong-Min Synthesis of polyfluoroarene-substituted benzofuran derivatives via cooperative Pd/Cu catalysis. Chemical communications (Cambridge, England), 2018, 54, 2256-2259 |
| 7121245 | CIF | C21 H19 Cl4 N O2 | P n a 21 | 12.866; 13.4392; 11.7656 90; 90; 90 | 2034.38 | Shen, Yi; Wu, Xin-Xing; Chen, Si; Xia, Yu; Liang, Yong-Min Synthesis of polyfluoroarene-substituted benzofuran derivatives via cooperative Pd/Cu catalysis. Chemical communications (Cambridge, England), 2018, 54, 2256-2259 |
| 7121246 | CIF | C14 H16 O4 | P 1 21/n 1 | 13.2065; 6.4912; 14.9358 90; 110.261; 90 | 1201.2 | Xiao, Jian; Cong, Xiao-Wei; Yang, Gui-Zhen; Wang, Ya-Wen; Peng, Yu Stereoselective synthesis of a Podophyllum lignan core by intramolecular reductive nickel-catalysis. Chemical communications (Cambridge, England), 2018, 54, 2040-2043 |
| 7121247 | CIF | C13 H15 F O2 | P -1 | 7.467; 8.1131; 10.193 107.549; 90.344; 106.555 | 561.5 | Xiao, Jian; Cong, Xiao-Wei; Yang, Gui-Zhen; Wang, Ya-Wen; Peng, Yu Stereoselective synthesis of a Podophyllum lignan core by intramolecular reductive nickel-catalysis. Chemical communications (Cambridge, England), 2018, 54, 2040-2043 |
| 7121248 | CIF | C20 H20 O4 | P -1 | 6.4202; 8.678; 15.259 77.58; 82.191; 85.69 | 821.6 | Xiao, Jian; Cong, Xiao-Wei; Yang, Gui-Zhen; Wang, Ya-Wen; Peng, Yu Stereoselective synthesis of a Podophyllum lignan core by intramolecular reductive nickel-catalysis. Chemical communications (Cambridge, England), 2018, 54, 2040-2043 |
| 7121249 | CIF | C14 H16 O4 | P 1 21/n 1 | 5.0801; 17.337; 13.987 90; 95.513; 90 | 1226.2 | Xiao, Jian; Cong, Xiao-Wei; Yang, Gui-Zhen; Wang, Ya-Wen; Peng, Yu Stereoselective synthesis of a Podophyllum lignan core by intramolecular reductive nickel-catalysis. Chemical communications (Cambridge, England), 2018, 54, 2040-2043 |
| 7121250 | CIF | H32 Mo N3 Na2 O38 V9 | P -1 | 8.7249; 10.4654; 11.1884 69.439; 87.119; 66.575 | 872.93 | Barman, Soumitra; Das, Santu; S S, Sreejith; Garai, Somnath; Pochamoni, Ramudu; Roy, Soumyajit Selective light driven reduction of CO<sub>2</sub> to HCOOH in water using a {MoV<sub>9</sub>}<sub>n</sub> (n = 1332-3600) based soft-oxometalate (SOM). Chemical communications (Cambridge, England), 2018, 54, 2369-2372 |
| 7121251 | CIF | C47 H33 N3 S2 | P 1 21 1 | 9.99169; 14.13348; 13.64326 90; 110.211; 90 | 1808.03 | Nakagawa, Tetsuya; Miyasaka, Yosuke; Yokoyama, Yasushi Photochromism of a spiro-functionalized diarylethene derivative: multi-colour fluorescence modulation with a photon-quantitative photocyclization reactivity. Chemical communications (Cambridge, England), 2018, 54, 3207-3210 |
| 7121252 | CIF | C34 H59.7 Cl6.3 O2 P2 Si W | P 1 21/c 1 | 10.9285; 19.4442; 20.0693 90; 98.632; 90 | 4216.34 | Han, Yong-Shen; Hill, Anthony F.; Kong, Richard Y. An unusual alkylidyne homologation. Chemical communications (Cambridge, England), 2018, 54, 2292-2295 |
| 7121253 | CIF | C27 H49 Cl6 O P2 W | P 21 21 21 | 12.31677; 14.9414; 18.7844 90; 90; 90 | 3456.89 | Han, Yong-Shen; Hill, Anthony F.; Kong, Richard Y. An unusual alkylidyne homologation. Chemical communications (Cambridge, England), 2018, 54, 2292-2295 |
| 7121254 | CIF | C32 H59 Cl3 P2 W | P b c a | 14.7156; 23.4584; 23.8845 90; 90; 90 | 8245 | Han, Yong-Shen; Hill, Anthony F.; Kong, Richard Y. An unusual alkylidyne homologation. Chemical communications (Cambridge, England), 2018, 54, 2292-2295 |
| 7121255 | CIF | C27 H49 Cl6.43 O0.58 P2 W | P 21 21 21 | 12.31677; 14.9414; 18.7844 90; 90; 90 | 3456.89 | Han, Yong-Shen; Hill, Anthony F.; Kong, Richard Y. An unusual alkylidyne homologation. Chemical communications (Cambridge, England), 2018, 54, 2292-2295 |
| 7121256 | CIF | C32 H30 F N3 O3 S | P 1 21 1 | 9.27904; 18.37857; 16.77742 90; 104.276; 90 | 2772.8 | Yu, Lemao; Zhong, Yuan; Yu, Jicong; Gan, Lu; Cai, Zhengjun; Wang, Rui; Jiang, Xianxing Highly diastereoselective oxa-[3+3] cyclization with C,N-cyclic azomethine imines via the copper-catalyzed aerobic oxygenated C[double bond, length as m-dash]C bond of indoles. Chemical communications (Cambridge, England), 2018, 54, 2353-2356 |
| 7121257 | CIF | C32 H30 Cl N3 O3 S | P 1 21 1 | 8.6912; 27.8849; 11.428 90; 94.876; 90 | 2759.6 | Yu, Lemao; Zhong, Yuan; Yu, Jicong; Gan, Lu; Cai, Zhengjun; Wang, Rui; Jiang, Xianxing Highly diastereoselective oxa-[3+3] cyclization with C,N-cyclic azomethine imines via the copper-catalyzed aerobic oxygenated C[double bond, length as m-dash]C bond of indoles. Chemical communications (Cambridge, England), 2018, 54, 2353-2356 |
| 7121258 | CIF | C25 H24 F N3 O2 S | P 1 21/c 1 | 8.9433; 19.2152; 13.0237 90; 96.049; 90 | 2225.63 | Yu, Lemao; Zhong, Yuan; Yu, Jicong; Gan, Lu; Cai, Zhengjun; Wang, Rui; Jiang, Xianxing Highly diastereoselective oxa-[3+3] cyclization with C,N-cyclic azomethine imines via the copper-catalyzed aerobic oxygenated C[double bond, length as m-dash]C bond of indoles. Chemical communications (Cambridge, England), 2018, 54, 2353-2356 |
| 7121259 | CIF | C36 H62 N2 O6 W2 | C 1 2/c 1 | 18.8904; 16.4256; 13.4978 90; 106.813; 90 | 4009.2 | Ikeda, Hideaki; Nishi, Kohei; Tsurugi, Hayato; Mashima, Kazushi Metathesis cleavage of an N[double bond, length as m-dash]N bond in benzo[c]cinnolines and azobenzenes by triply-bonded ditungsten complexes. Chemical communications (Cambridge, England), 2018, 54, 3709-3711 |
| 7121260 | CIF | C56 H80 F12 N12 O12 S4 W4 | P 1 21/c 1 | 14.2203; 11.6883; 22.162 90; 98.946; 90 | 3638.8 | Ikeda, Hideaki; Nishi, Kohei; Tsurugi, Hayato; Mashima, Kazushi Metathesis cleavage of an N[double bond, length as m-dash]N bond in benzo[c]cinnolines and azobenzenes by triply-bonded ditungsten complexes. Chemical communications (Cambridge, England), 2018, 54, 3709-3711 |
| 7121261 | CIF | C35 H39 N O3 S Si | P 21 21 21 | 8.4929; 9.8371; 39.949 90; 90; 90 | 3337.6 | Zhu, Chao-Ze; Feng, Jian-Jun; Zhang, Junliang Divergent synthesis of functionalized pyrrolidines and γ-amino ketones via rhodium-catalyzed switchable reactions of vinyl aziridines and silyl enol ethers. Chemical communications (Cambridge, England), 2018, 54, 2401-2404 |
| 7121262 | CIF | C34 H35 I N2 O5 S2 | P -1 | 12.2348; 13.7713; 21.3593 74.8147; 78.2115; 80.192 | 3373.8 | Moriyama, Katsuhiko; Hamada, Tsukasa; Ishida, Kazuma; Togo, Hideo 1,3-Iodo-amination of 2-methyl indoles via C<sub>sp<sup>2</sup></sub>-C<sub>sp<sup>3</sup></sub> dual functionalization with iodine reagent. Chemical communications (Cambridge, England), 2018, 54, 4258-4261 |
| 7121263 | CIF | C28 H29 I N2 O5 S2 | P 1 21/c 1 | 11.244; 10.311; 24.381 90; 100.978; 90 | 2774.9 | Moriyama, Katsuhiko; Hamada, Tsukasa; Ishida, Kazuma; Togo, Hideo 1,3-Iodo-amination of 2-methyl indoles via C<sub>sp<sup>2</sup></sub>-C<sub>sp<sup>3</sup></sub> dual functionalization with iodine reagent. Chemical communications (Cambridge, England), 2018, 54, 4258-4261 |
| 7121264 | CIF | C30 H35 N5 O8 S | P 1 21/n 1 | 15.023; 12.3995; 17.7457 90; 112.661; 90 | 3050.4 | Moriyama, Katsuhiko; Hamada, Tsukasa; Ishida, Kazuma; Togo, Hideo 1,3-Iodo-amination of 2-methyl indoles via C<sub>sp<sup>2</sup></sub>-C<sub>sp<sup>3</sup></sub> dual functionalization with iodine reagent. Chemical communications (Cambridge, England), 2018, 54, 4258-4261 |
| 7121266 | CIF | C58 H32 F12 | P 1 21/c 1 | 13.8363; 19.0251; 10.7855 90; 97.886; 90 | 2812.29 | Jiang, Chuanling; Bang, Yawen; Wang, Xinhao; Lu, Xuefeng; Lim, Zhenglong; Wei, Haipeng; El-Hankari, Samir; Wu, Jishan; Zeng, Zebing Tetrabenzo-Chichibabin's hydrocarbons: substituent effects and unusual thermochromic and thermomagnetic behaviours. Chemical communications (Cambridge, England), 2018, 54, 2389-2392 |
| 7121267 | CIF | C64 H56 Cl4 O8 | P -1 | 10.826; 11.158; 12.125 89.92; 87.592; 72.944 | 1398.9 | Jiang, Chuanling; Bang, Yawen; Wang, Xinhao; Lu, Xuefeng; Lim, Zhenglong; Wei, Haipeng; El-Hankari, Samir; Wu, Jishan; Zeng, Zebing Tetrabenzo-Chichibabin's hydrocarbons: substituent effects and unusual thermochromic and thermomagnetic behaviours. Chemical communications (Cambridge, England), 2018, 54, 2389-2392 |
| 7121268 | CIF | C68 H64 Cl4 O12 | P -1 | 7.3362; 12.952; 16.918 106.135; 94.598; 100.939 | 1501 | Jiang, Chuanling; Bang, Yawen; Wang, Xinhao; Lu, Xuefeng; Lim, Zhenglong; Wei, Haipeng; El-Hankari, Samir; Wu, Jishan; Zeng, Zebing Tetrabenzo-Chichibabin's hydrocarbons: substituent effects and unusual thermochromic and thermomagnetic behaviours. Chemical communications (Cambridge, England), 2018, 54, 2389-2392 |
| 7121269 | CIF | C69 H64 N4 | P -1 | 12.4719; 16.0534; 17.5659 95.63; 96.899; 112.346 | 3189.5 | Jiang, Chuanling; Bang, Yawen; Wang, Xinhao; Lu, Xuefeng; Lim, Zhenglong; Wei, Haipeng; El-Hankari, Samir; Wu, Jishan; Zeng, Zebing Tetrabenzo-Chichibabin's hydrocarbons: substituent effects and unusual thermochromic and thermomagnetic behaviours. Chemical communications (Cambridge, England), 2018, 54, 2389-2392 |
| 7121270 | CIF | C12 H6 F I N4 O2 | P 1 21/c 1 | 16.618; 9.329; 8.15 90; 90.387; 90 | 1263.5 | Tu, Daoquan; Luo, Jun; Jiang, Chao Copper-mediated domino C-H iodination and nitration of indoles. Chemical communications (Cambridge, England), 2018, 54, 2514-2517 |
| 7121271 | CIF | C23 H21 Br N2 O | P 21 21 21 | 5.955; 18.08; 18.63 90; 90; 90 | 2005.8 | Wei, Liang; Zhu, Qiao; Song, Zhi-Min; Liu, Kang; Wang, Chun-Jiang Catalytic asymmetric inverse electron demand Diels-Alder reaction of fulvenes with azoalkenes. Chemical communications (Cambridge, England), 2018, 54, 2506-2509 |
| 7121273 | CIF | C12 H12 N2 O | P 1 21/n 1 | 10.4481; 7.0131; 13.7142 90; 99.787; 90 | 990.3 | Yuan, Zaifeng; Li, Na; Zhu, Chunyu; Xia, Chengfeng Copper-catalyzed synthesis of α-amino nitriles through methyl transfer from DMF to aromatic amines. Chemical communications (Cambridge, England), 2018, 54, 2854-2857 |
| 7121274 | CIF | C26 H24 O4 | P 21 21 21 | 7.4823; 13.0258; 21.7018 90; 90; 90 | 2115.12 | Chen, Song; Wu, Liang; Shao, Qihang; Yang, Guoqiang; Zhang, Wanbin Pd(ii)-Catalyzed asymmetric 1,6-conjugate addition of arylboronic acids to Meldrum's acid-derived dienes. Chemical communications (Cambridge, England), 2018, 54, 2522-2525 |
| 7121275 | CIF | C45 H35 Cl N6 Ni O | P -1 | 15.2703; 15.9604; 16.2276 81.48; 83.595; 67.656 | 3611.1 | Fu, Xinliang; Meng, Yankui; Li, Xiaofang; Stępień, Marcin; Chmielewski, Piotr J. Extension of antiaromatic norcorrole by cycloaddition. Chemical communications (Cambridge, England), 2018, 54, 2510-2513 |
| 7121276 | CIF | C30 H21 B F2 N6 | P 1 21/n 1 | 11.0347; 13.6496; 17.0188 90; 106.691; 90 | 2455.36 | Zhang, Huaxing; Chen, Xingyu; Lan, Jingbo; Liu, Yanhong; Zhou, Fulin; Wu, Di; You, Jingsong Silver-mediated direct C-H amination of BODIPYs for screening endoplasmic reticulum-targeting reagents. Chemical communications (Cambridge, England), 2018, 54, 3219-3222 |
| 7121277 | CIF | C20 H20 B F2 N3 O | P 1 21/c 1 | 15.2429; 8.7432; 15.0494 90; 115.235; 90 | 1814.25 | Zhang, Huaxing; Chen, Xingyu; Lan, Jingbo; Liu, Yanhong; Zhou, Fulin; Wu, Di; You, Jingsong Silver-mediated direct C-H amination of BODIPYs for screening endoplasmic reticulum-targeting reagents. Chemical communications (Cambridge, England), 2018, 54, 3219-3222 |
| 7121278 | CIF | C27 H52 Br N3 Ni O0 P2 | P 1 21/c 1 | 18.6867; 10.6672; 15.862 90; 93.817; 90 | 3154.8 | Yao, Changguang; Wang, Xiufang; Huang, Kuo-Wei Nitrogen atom transfer mediated by a new PN<sup>3</sup>P-pincer nickel core via a putative nitrido nickel intermediate. Chemical communications (Cambridge, England), 2018, 54, 3940-3943 |
| 7121279 | CIF | C28 H52 N4 Ni O0 P2 | P 1 21/c 1 | 18.4429; 10.992; 15.5534 90; 93.613; 90 | 3146.79 | Yao, Changguang; Wang, Xiufang; Huang, Kuo-Wei Nitrogen atom transfer mediated by a new PN<sup>3</sup>P-pincer nickel core via a putative nitrido nickel intermediate. Chemical communications (Cambridge, England), 2018, 54, 3940-3943 |
| 7121280 | CIF | C27 H52 N6 Ni P2 | P 1 21/c 1 | 17.9904; 11.7439; 14.8246 90; 94.373; 90 | 3123 | Yao, Changguang; Wang, Xiufang; Huang, Kuo-Wei Nitrogen atom transfer mediated by a new PN<sup>3</sup>P-pincer nickel core via a putative nitrido nickel intermediate. Chemical communications (Cambridge, England), 2018, 54, 3940-3943 |
| 7121281 | CIF | C39 H64 N5 Ni P2 | P 1 21/c 1 | 8.5405; 23.6154; 41.0704 90; 90.8; 90 | 8282.6 | Yao, Changguang; Wang, Xiufang; Huang, Kuo-Wei Nitrogen atom transfer mediated by a new PN<sup>3</sup>P-pincer nickel core via a putative nitrido nickel intermediate. Chemical communications (Cambridge, England), 2018, 54, 3940-3943 |
| 7121282 | CIF | C32 H61 N5 Ni P2 | P -1 | 10.089; 11.3946; 17.0248 88.997; 83.173; 67.559 | 1795.31 | Yao, Changguang; Wang, Xiufang; Huang, Kuo-Wei Nitrogen atom transfer mediated by a new PN<sup>3</sup>P-pincer nickel core via a putative nitrido nickel intermediate. Chemical communications (Cambridge, England), 2018, 54, 3940-3943 |
| 7121283 | CIF | C27 H52 I N3 Ni P2 | P 1 21/c 1 | 18.2867; 11.3201; 15.4141 90; 94.71; 90 | 3180.1 | Yao, Changguang; Wang, Xiufang; Huang, Kuo-Wei Nitrogen atom transfer mediated by a new PN<sup>3</sup>P-pincer nickel core via a putative nitrido nickel intermediate. Chemical communications (Cambridge, England), 2018, 54, 3940-3943 |
| 7121284 | CIF | C24 H24 Br N O4 | P -1 | 9.1087; 9.6236; 13.9209 106.948; 95.031; 99.718 | 1138.3 | Cao, Bo; Wei, Yin; Shi, Min An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes. Chemical communications (Cambridge, England), 2018, 54, 2870-2873 |
| 7121285 | CIF | C22 H21 N O4 | P c a 21 | 17.5019; 8.4032; 12.4676 90; 90; 90 | 1833.63 | Cao, Bo; Wei, Yin; Shi, Min An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes. Chemical communications (Cambridge, England), 2018, 54, 2870-2873 |
| 7121286 | CIF | C24 H24 Br N O4 | P 1 21/c 1 | 11.8749; 13.1162; 14.6639 90; 106.809; 90 | 2186.4 | Cao, Bo; Wei, Yin; Shi, Min An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes. Chemical communications (Cambridge, England), 2018, 54, 2870-2873 |
| 7121287 | CIF | C28 H22 Br Cl N2 O2 | C 1 2/c 1 | 32.328; 10.078; 15.161 90; 109.44; 90 | 4658 | Cao, Bo; Wei, Yin; Shi, Min An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes. Chemical communications (Cambridge, England), 2018, 54, 2870-2873 |
| 7121288 | CIF | C20 H21 N O2 | P 1 21 1 | 14.0718; 7.9328; 14.6162 90; 92.868; 90 | 1629.54 | Cao, Bo; Wei, Yin; Shi, Min An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes. Chemical communications (Cambridge, England), 2018, 54, 2870-2873 |
| 7121291 | CIF | C21 H27 I N2 O4 S | P 1 21/c 1 | 7.9761; 18.633; 15.9637 90; 90.406; 90 | 2372.44 | Wang, Kang-Nan; Chao, Xi-Juan; Liu, Bing; Zhou, Dan-Jie; He, Liang; Zheng, Xiao-Hui; Cao, Qian; Tan, Cai-Ping; Zhang, Chen; Mao, Zong-Wan Red fluorescent probes for real-time imaging of the cell cycle by dynamic monitoring of the nucleolus and chromosome. Chemical communications (Cambridge, England), 2018, 54, 2635-2638 |
| 7121292 | CIF | C20 H8 O6 | I 41 m d | 10.781; 10.781; 12.687 90; 90; 90 | 1474.6 | Shuku, Yoshiaki; Mizuno, Asato; Ushiroguchi, Ryo; Hyun, Chang Seok; Ryu, Young Jun; An, Byeong-Kwan; Kwon, Ji Eon; Park, Soo Young; Tsuchiizu, Masahisa; Awaga, Kunio An exotic band structure of a supramolecular honeycomb lattice formed by a pancake π-π interaction between triradical trianions of triptycene tribenzoquinone. Chemical communications (Cambridge, England), 2018, 54, 3815-3818 |
| 7121293 | CIF | C20 H8 O6 Rb3 | P 6/m | 11.6406; 11.6406; 8.6575 90; 90; 120 | 1016 | Shuku, Yoshiaki; Mizuno, Asato; Ushiroguchi, Ryo; Hyun, Chang Seok; Ryu, Young Jun; An, Byeong-Kwan; Kwon, Ji Eon; Park, Soo Young; Tsuchiizu, Masahisa; Awaga, Kunio An exotic band structure of a supramolecular honeycomb lattice formed by a pancake π-π interaction between triradical trianions of triptycene tribenzoquinone. Chemical communications (Cambridge, England), 2018, 54, 3815-3818 |
| 7121294 | CIF | C22 H17 Li3 N O9 | P -1 | 9.739; 10.881; 11.611 116.488; 92.9867; 110.107 | 1002.8 | Shuku, Yoshiaki; Mizuno, Asato; Ushiroguchi, Ryo; Hyun, Chang Seok; Ryu, Young Jun; An, Byeong-Kwan; Kwon, Ji Eon; Park, Soo Young; Tsuchiizu, Masahisa; Awaga, Kunio An exotic band structure of a supramolecular honeycomb lattice formed by a pancake π-π interaction between triradical trianions of triptycene tribenzoquinone. Chemical communications (Cambridge, England), 2018, 54, 3815-3818 |
| 7121295 | CIF | C14 H9 Br Cl N3 | P 21 21 21 | 7.656; 9.85; 18.33 90; 90; 90 | 1382.3 | Kumar, Navaneet; Ansari, Mohd Yeshab; Kant, Ruchir; Kumar, Atul Copper-catalyzed decarboxylative regioselective synthesis of 1,5-disubstituted 1,2,3-triazoles. Chemical communications (Cambridge, England), 2018, 54, 2627-2630 |
| 7121296 | CIF | C24 H32 Br N O3 | P 1 21/c 1 | 18.98; 10.7749; 11.4258 90; 93.315; 90 | 2332.8 | Zubillaga, A.; Ferreira, P.; Parola, A. J.; Gago, S.; Basílio, N pH-Gated photoresponsive shuttling in a water-soluble pseudorotaxane. Chemical communications (Cambridge, England), 2018, 54, 2743-2746 |
| 7121297 | CIF | C56 H98 Cl5 Gd5 Mn2 N4 O36 | C 1 2/c 1 | 26.495; 13.471; 23.632 90; 91.092; 90 | 8433 | Huang, Wei; Huang, Shuaidan; Zhang, Ming; Chen, Yancong; Zhuang, Gui-Lin; Li, Yao; Tong, Ming-Liang; Yong, Juan; Li, Yujie; Wu, Dayu Multifunctional luminescent magnetic cryocooler in a Gd<sub>5</sub>Mn<sub>2</sub> pyramidal complex. Chemical communications (Cambridge, England), 2018, 54, 4104-4107 |
| 7121298 | CIF | C86 H102 O72 P2 Zr12 | P -1 | 12.2903; 16.666; 19.138 72.79; 80.54; 74.886 | 3598.8 | Bezrukov, Andrey A.; Törnroos, Karl W; Le Roux, Erwan; Dietzel, Pascal D. C. Incorporation of an intact dimeric Zr<sub>12</sub> oxo cluster from a molecular precursor in a new zirconium metal-organic framework. Chemical communications (Cambridge, England), 2018, 54, 2735-2738 |
| 7121299 | CIF | C58 H100.97 O76.48 Zr12 | P 1 21/c 1 | 20.287; 12.5914; 20.241 90; 100.188; 90 | 5088.9 | Bezrukov, Andrey A.; Törnroos, Karl W; Le Roux, Erwan; Dietzel, Pascal D. C. Incorporation of an intact dimeric Zr<sub>12</sub> oxo cluster from a molecular precursor in a new zirconium metal-organic framework. Chemical communications (Cambridge, England), 2018, 54, 2735-2738 |
| 7121300 | CIF | C30 H25 N3 O4 S | P 1 21 1 | 8.6468; 10.3139; 14.8549 90; 98.238; 90 | 1311.12 | Nakamura, Shuichi; Furukawa, Takashi; Hatanaka, Tsubasa; Funahashi, Yasuhiro Enantioselective aza-Friedel-Crafts reaction of cyclic ketimines with indoles using chiral imidazoline-phosphoric acid catalysts. Chemical communications (Cambridge, England), 2018, 54, 3811-3814 |
| 7121301 | CIF | C173 H163 Cl8 F12 N4 O18 P10 Pd4 S2 | P 1 21/n 1 | 14.8431; 26.413; 22.3504 90; 93.09; 90 | 8749.8 | Frieiro-Gomis, Pablo; Lucio-Martínez, Fátima; Munín-Cruz, Paula; Ortigueira, Juan M.; Pereira, M. Teresa; Polo-Ces, Paula; Vázquez-García, Digna; Vila, José M The chelate-to-bridging shift of phosphane dipalladacycles: convenient synthesis of double A-frame tetranuclear complexes. Chemical communications (Cambridge, England), 2018, 54, 2662-2665 |
| 7121302 | CIF | C176 H172 Cl2 F12 N4 O20 P10 Pd4 | P -1 | 16.4987; 16.5332; 17.1548 82.897; 71.882; 75.24 | 4295.6 | Frieiro-Gomis, Pablo; Lucio-Martínez, Fátima; Munín-Cruz, Paula; Ortigueira, Juan M.; Pereira, M. Teresa; Polo-Ces, Paula; Vázquez-García, Digna; Vila, José M The chelate-to-bridging shift of phosphane dipalladacycles: convenient synthesis of double A-frame tetranuclear complexes. Chemical communications (Cambridge, England), 2018, 54, 2662-2665 |
| 7121303 | CIF | C85 H80 Br F6 N2 O8 P5 Pd2 | P -1 | 16.498; 16.561; 17.1294 83.263; 71.977; 75.228 | 4299.7 | Frieiro-Gomis, Pablo; Lucio-Martínez, Fátima; Munín-Cruz, Paula; Ortigueira, Juan M.; Pereira, M. Teresa; Polo-Ces, Paula; Vázquez-García, Digna; Vila, José M The chelate-to-bridging shift of phosphane dipalladacycles: convenient synthesis of double A-frame tetranuclear complexes. Chemical communications (Cambridge, England), 2018, 54, 2662-2665 |
| 7121304 | CIF | C30 H40 Br2 N2 O8 | P 1 21 1 | 5.8799; 29.0285; 9.8495 90; 101.082; 90 | 1649.81 | Martínez-Pardo, Pablo; Blay, Gonzalo; Muñoz, M Carmen; Pedro, José R; Sanz-Marco, Amparo; Vila, Carlos Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis. Chemical communications (Cambridge, England), 2018, 54, 2862-2865 |
| 7121305 | CIF | C55 H76 As2 Sn | P -1 | 12.7953; 12.9297; 16.8382 75.874; 77.693; 69.763 | 2509.21 | Izod, Keith; Evans, Peter; Waddell, Paul G. A diarsagermylene and a diarsastannylene stabilised by areneGe/Sn interactions. Chemical communications (Cambridge, England), 2018, 54, 2526-2529 |
| 7121306 | CIF | C55 H76 As2 Ge | P -1 | 12.6717; 12.8423; 16.8971 77.0882; 78.4162; 71.263 | 2513.24 | Izod, Keith; Evans, Peter; Waddell, Paul G. A diarsagermylene and a diarsastannylene stabilised by areneGe/Sn interactions. Chemical communications (Cambridge, England), 2018, 54, 2526-2529 |
| 7121307 | CIF | C72.01 H116.97 As2 Li2 O6 | P -1 | 11.4059; 17.5174; 19.381 68.376; 80.7734; 89.4407 | 3548.12 | Izod, Keith; Evans, Peter; Waddell, Paul G. A diarsagermylene and a diarsastannylene stabilised by areneGe/Sn interactions. Chemical communications (Cambridge, England), 2018, 54, 2526-2529 |
| 7121308 | CIF | C30 H50 Ni P2 S | P 1 21/n 1 | 9.911; 16.711; 18.048 90; 92.402; 90 | 2986.5 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121309 | CIF | C37.5 H65 B Br Cl3 Ni O2 P2 S | P 21 21 21 | 8.752; 21.67; 22.43 90; 90; 90 | 4254 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121310 | CIF | C76 H104 Ni2 O2 P4 S2 | C 1 2/c 1 | 48.534; 12.095; 26.019 90; 110.276; 90 | 14327 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121311 | CIF | C41 H66 B Br Cl2 Ni O2 P2 S | P 1 21/c 1 | 23.717; 11.746; 16.282 90; 105.722; 90 | 4366.1 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121312 | CIF | C37 H59 I Ni P2 S | P -1 | 8.481; 11.052; 21.03 96.001; 91.24; 101.865 | 1917 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121313 | CIF | C38.98 H61.83 Ni P2 S Si | P -1 | 10.9627; 15.9681; 35.1062 82.137; 82.667; 83.181 | 6005.73 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121314 | CIF | C35 H55 I Ni P2 S | P -1 | 12.354; 16.268; 20.938 75.82; 88.78; 78.187 | 3992 | Terada, Misaki; Nishii, Yuji; Miura, Masahiro Synthesis, crystal structure and reactivity of η<sup>2</sup>-thiophyne Ni complexes. Chemical communications (Cambridge, England), 2018, 54, 2918-2921 |
| 7121315 | CIF | C24 H18 N P Se | P -1 | 9.689; 9.904; 11.312 95.848; 101.924; 111.026 | 972.8 | Jiang, He; Jia, Linlin; Li, Yuanyuan; Liu, Sirui; Chen, Runfeng; Jin, Lu; Jin, Jibiao; Zheng, Chao; Fan, Quli; Huang, Wei Selenide-containing organic resonance molecules as turn-on fluorescent probes for the selective detection of hypochlorous acid. Chemical communications (Cambridge, England), 2018, 54, 2926-2929 |
| 7121316 | CIF | C30 H25 N2 P Se | P 1 21/n 1 | 11.612; 17.433; 12.594 90; 103.247; 90 | 2481.6 | Jiang, He; Jia, Linlin; Li, Yuanyuan; Liu, Sirui; Chen, Runfeng; Jin, Lu; Jin, Jibiao; Zheng, Chao; Fan, Quli; Huang, Wei Selenide-containing organic resonance molecules as turn-on fluorescent probes for the selective detection of hypochlorous acid. Chemical communications (Cambridge, England), 2018, 54, 2926-2929 |
| 7121317 | CIF | C30 H21 N2 P Se | P -1 | 9.5713; 11.6043; 12.0406 72.019; 68.768; 73.861 | 1164.7 | Jiang, He; Jia, Linlin; Li, Yuanyuan; Liu, Sirui; Chen, Runfeng; Jin, Lu; Jin, Jibiao; Zheng, Chao; Fan, Quli; Huang, Wei Selenide-containing organic resonance molecules as turn-on fluorescent probes for the selective detection of hypochlorous acid. Chemical communications (Cambridge, England), 2018, 54, 2926-2929 |
| 7121318 | CIF | C18 H23 N | P -1 | 8.5072; 9.2974; 9.7885 88.049; 78.84; 70.388 | 715.11 | Li, Rui-Qi; He, Yu; Ding, Yao; Ang, Chee-Kiat; Tian, Jie-Sheng; Loh, Teck-Peng Formal synthesis of chelamidine alkaloids and their derivatives. Chemical communications (Cambridge, England), 2018, 54, 3150-3153 |
| 7121319 | CIF | C23 H29 Br N5 O6 | P 1 21/n 1 | 10.716; 18.53; 13.213 90; 91.445; 90 | 2622.8 | Santhini, P. V.; Smrithy, A. S.; Irfana Jesin, C. P.; Varughese, Sunil; John, Jubi; Radhakrishnan, K. V. Accessing highly functionalized cyclopentanoids via a cascade palladation approach: unprecedented benzylic C-H activation towards cyclopentenoindanes. Chemical communications (Cambridge, England), 2018, 54, 2982-2985 |
| 7121320 | CIF | C24 H32 N2 O6 | P 1 21/c 1 | 13.677; 17.67; 10.71 90; 106.085; 90 | 2487 | Santhini, P. V.; Smrithy, A. S.; Irfana Jesin, C. P.; Varughese, Sunil; John, Jubi; Radhakrishnan, K. V. Accessing highly functionalized cyclopentanoids via a cascade palladation approach: unprecedented benzylic C-H activation towards cyclopentenoindanes. Chemical communications (Cambridge, England), 2018, 54, 2982-2985 |
| 7121321 | CIF | C36 H52 N2 P Sb | P -1 | 9.5816; 11.7784; 16.7485 88.332; 80.966; 70.456 | 1758.61 | Balmer, Markus; Gottschling, Hannah; von Hänisch, Carsten Phosphaalkene-substituted organo-group 15 compounds: synthesis and characterisation of (NHC)P-EtBu<sub>2</sub> (E = P, As, Sb and Bi). Chemical communications (Cambridge, England), 2018, 54, 2659-2661 |
| 7121322 | CIF | C29 H44 Bi N2 P | P -1 | 8.5219; 10.0762; 37.319 85.58; 87.36; 68.332 | 2968.7 | Balmer, Markus; Gottschling, Hannah; von Hänisch, Carsten Phosphaalkene-substituted organo-group 15 compounds: synthesis and characterisation of (NHC)P-EtBu<sub>2</sub> (E = P, As, Sb and Bi). Chemical communications (Cambridge, England), 2018, 54, 2659-2661 |
| 7121323 | CIF | C29 H44 N2 P2 | P 1 21/n 1 | 9.7612; 24.4504; 14.3595 90; 94.6105; 90 | 3416 | Balmer, Markus; Gottschling, Hannah; von Hänisch, Carsten Phosphaalkene-substituted organo-group 15 compounds: synthesis and characterisation of (NHC)P-EtBu<sub>2</sub> (E = P, As, Sb and Bi). Chemical communications (Cambridge, England), 2018, 54, 2659-2661 |
| 7121324 | CIF | C36 H52 As N2 P | P -1 | 9.4313; 11.7613; 16.5108 88.7; 82.678; 71.476 | 1722.09 | Balmer, Markus; Gottschling, Hannah; von Hänisch, Carsten Phosphaalkene-substituted organo-group 15 compounds: synthesis and characterisation of (NHC)P-EtBu<sub>2</sub> (E = P, As, Sb and Bi). Chemical communications (Cambridge, England), 2018, 54, 2659-2661 |
| 7121325 | CIF | C22 H23 F12 N7 Ni P2 | C 1 2/c 1 | 37.426; 8.0756; 23.616 90; 128.46; 90 | 5589.1 | Su, Xiaojun; McCardle, Kaitlin M.; Panetier, Julien A.; Jurss, Jonah W. Electrocatalytic CO<sub>2</sub> reduction with nickel complexes supported by tunable bipyridyl-N-heterocyclic carbene donors: understanding redox-active macrocycles. Chemical communications (Cambridge, England), 2018, 54, 3351-3354 |
| 7121326 | CIF | C19 H16 Cl2 N6 Ni O8 | C 1 2/m 1 | 13.978; 12.184; 13.374 90; 109.402; 90 | 2148 | Su, Xiaojun; McCardle, Kaitlin M.; Panetier, Julien A.; Jurss, Jonah W. Electrocatalytic CO<sub>2</sub> reduction with nickel complexes supported by tunable bipyridyl-N-heterocyclic carbene donors: understanding redox-active macrocycles. Chemical communications (Cambridge, England), 2018, 54, 3351-3354 |
| 7121327 | CIF | C22 H21 F12 N7 Ni P2 | P -1 | 9.9845; 12.1671; 12.4094 69.474; 70.998; 83.804 | 1334.85 | Su, Xiaojun; McCardle, Kaitlin M.; Panetier, Julien A.; Jurss, Jonah W. Electrocatalytic CO<sub>2</sub> reduction with nickel complexes supported by tunable bipyridyl-N-heterocyclic carbene donors: understanding redox-active macrocycles. Chemical communications (Cambridge, England), 2018, 54, 3351-3354 |
| 7121328 | CIF | C19 H22 N2 O3 S | P 21 21 21 | 9.389; 12.021; 17.402 90; 90; 90 | 1964.1 | Feng, Jie; Ma, Peng-Ju; Zeng, Yong-Ming; Xu, Yan-Jun; Lu, Chong-Dao Construction of α-methoxyimidoyl ketonitrones via phosphite-mediated addition of α-keto N-tert-butanesulfinyl imidates to nitrosoarenes. Chemical communications (Cambridge, England), 2018, 54, 2882-2885 |
| 7121329 | CIF | C19 H21 F N2 O3 S | P 1 | 11.4001; 12.5665; 14.19 76.975; 89.282; 79.014 | 1943.3 | Feng, Jie; Ma, Peng-Ju; Zeng, Yong-Ming; Xu, Yan-Jun; Lu, Chong-Dao Construction of α-methoxyimidoyl ketonitrones via phosphite-mediated addition of α-keto N-tert-butanesulfinyl imidates to nitrosoarenes. Chemical communications (Cambridge, England), 2018, 54, 2882-2885 |
| 7121330 | CIF | C16 H16 N2 O2 S | P 21 21 21 | 7.8609; 10.9333; 17.847 90; 90; 90 | 1533.9 | Feng, Jie; Ma, Peng-Ju; Zeng, Yong-Ming; Xu, Yan-Jun; Lu, Chong-Dao Construction of α-methoxyimidoyl ketonitrones via phosphite-mediated addition of α-keto N-tert-butanesulfinyl imidates to nitrosoarenes. Chemical communications (Cambridge, England), 2018, 54, 2882-2885 |
| 7121331 | CIF | C19 H22 N2 O3 S | P 1 21/n 1 | 11.0074; 11.0674; 15.1861 90; 91.889; 90 | 1849.02 | Feng, Jie; Ma, Peng-Ju; Zeng, Yong-Ming; Xu, Yan-Jun; Lu, Chong-Dao Construction of α-methoxyimidoyl ketonitrones via phosphite-mediated addition of α-keto N-tert-butanesulfinyl imidates to nitrosoarenes. Chemical communications (Cambridge, England), 2018, 54, 2882-2885 |
| 7121332 | CIF | C20 H26 N2 O3 S | P 1 21 1 | 9.546; 8.931; 12.96 90; 107.93; 90 | 1051 | Feng, Jie; Ma, Peng-Ju; Zeng, Yong-Ming; Xu, Yan-Jun; Lu, Chong-Dao Construction of α-methoxyimidoyl ketonitrones via phosphite-mediated addition of α-keto N-tert-butanesulfinyl imidates to nitrosoarenes. Chemical communications (Cambridge, England), 2018, 54, 2882-2885 |
| 7121333 | CIF | C21 H26 N2 O3 S | P 43 | 11.1348; 11.1348; 16.3745 90; 90; 90 | 2030.17 | Feng, Jie; Ma, Peng-Ju; Zeng, Yong-Ming; Xu, Yan-Jun; Lu, Chong-Dao Construction of α-methoxyimidoyl ketonitrones via phosphite-mediated addition of α-keto N-tert-butanesulfinyl imidates to nitrosoarenes. Chemical communications (Cambridge, England), 2018, 54, 2882-2885 |
| 7121334 | CIF | C7 H4 Br N | C 1 m 1 | 9.531; 8.5593; 4.1352 90; 90.295; 90 | 337.34 | Alimi, Lukman O.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J. Hand-twistable plastically deformable crystals of a rigid small organic molecule. Chemical communications (Cambridge, England), 2018, 54, 2994-2997 |
| 7121335 | CIF | C7 H4 Br N | C 1 m 1 | 9.509; 8.535; 4.127 90; 90.311; 90 | 334.9 | Alimi, Lukman O.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J. Hand-twistable plastically deformable crystals of a rigid small organic molecule. Chemical communications (Cambridge, England), 2018, 54, 2994-2997 |
| 7121336 | CIF | C33 H45.5 N7.5 O11.5 Zn | R -3 :H | 47.432; 47.432; 13.658 90; 90; 120 | 26611 | Zhou, Yue; Yao, Shuo; Ma, Yali; Li, Guanghua; Huo, Qisheng; Liu, Yunling An anionic single-walled metal-organic nanotube with an armchair (3,3) topology as an extremely smart adsorbent for the effective and selective adsorption of cationic carcinogenic dyes. Chemical communications (Cambridge, England), 2018, 54, 3006-3009 |
| 7121342 | CIF | C13 H15 Cl N4 O3 Pt | P 1 21/c 1 | 7.4875; 15.363; 13.1787 90; 93.153; 90 | 1513.7 | Zhou, Wen; Almeqdadi, Mohammad; Xifaras, Michael E.; Riddell, Imogen A.; Yilmaz, Ömer H; Lippard, Stephen J. The effect of geometric isomerism on the anticancer activity of the monofunctional platinum complex trans-[Pt(NH<sub>3</sub>)<sub>2</sub>(phenanthridine)Cl]NO<sub>3</sub>. Chemical communications (Cambridge, England), 2018, 54, 2788-2791 |
| 7121343 | CIF | C2.12 H1.75 N0.12 O0.25 S0.12 | P -1 | 7.8523; 9.176; 10.4482 90.106; 92.683; 94.315 | 749.85 | Sun, Jianfeng; Li, Peng; Guo, Lei; Yu, Fang; He, Yu-Peng; Chu, Lingling Catalytic, metal-free sulfonylcyanation of alkenes via visible light organophotoredox catalysis. Chemical communications (Cambridge, England), 2018, 54, 3162-3165 |
| 7121344 | CIF | C23 H20 N2 | P 1 21/c 1 | 19.4749; 10.8598; 8.3747 90; 97.699; 90 | 1755.2 | Zhang, Xi; Wang, Tong-Lin; Huo, Cong-De; Wang, Xi-Cun; Quan, Zheng-Jun Base-controlled chemoselectivity reaction of vinylanilines with isothiocyanates for synthesis of quinolino-2-thione and 2-aminoquinoline derivatives. Chemical communications (Cambridge, England), 2018, 54, 3114-3117 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!