Crystallography Open Database
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Result: there are 1762 entries in the selection
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Searching journal of publication like 'Chemical Communications' volume of publication is 52
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7118208 | CIF | C26 H25 N O2 S | P 1 21/n 1 | 13.926; 10.6835; 14.955 90; 92.243; 90 | 2223.3 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118209 | CIF | C26 H27 N O3 S | P 1 21/n 1 | 10.4657; 19.751; 12.477 90; 114.712; 90 | 2342.9 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118210 | CIF | C24 H21 N O2 S | P 1 21/c 1 | 10.6663; 10.8826; 18.121 90; 103.78; 90 | 2042.9 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118211 | CIF | C24 H21 N O2 S | P 1 21/c 1 | 14.001; 12.335; 11.587 90; 95.497; 90 | 1991.9 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118212 | CIF | C24 H21 N O2 S | P 1 21/c 1 | 8.9249; 9.9995; 22.944 90; 107.13; 90 | 1956.8 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118213 | CIF | C54 H58 N3 P2 Rh | P 1 21/n 1 | 13.58; 21.768; 17.29 90; 111.548; 90 | 4754 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118214 | CIF | C48 H48 N3 P2 Rh | P 1 21/c 1 | 16.185; 18.144; 15.477 90; 118.406; 90 | 3998 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118215 | CIF | C72 H66 N3 P2 Rh | P 1 21/n 1 | 13.567; 28.198; 16.293 90; 109.213; 90 | 5886 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118216 | CIF | C98 H96 N6 P4 Rh2 | C 1 2/c 1 | 42.986; 17.237; 27.577 90; 119.527; 90 | 17779 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118217 | CIF | C60 H56 N3 P2 Rh | P 1 21/n 1 | 13.907; 27.103; 16.593 90; 112.133; 90 | 5793 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118218 | CIF | C36 H26 Br2 O4 | P 21 21 21 | 5.6288; 12.578; 41.669 90; 90; 90 | 2950.1 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
| 7118219 | CIF | C36 H28 O4 | P 21 21 21 | 9.263; 12.8186; 22.369 90; 90; 90 | 2656.1 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
| 7118220 | CIF | C36 H26 Br2 O4 | P 21 21 21 | 5.5911; 13.004; 40.623 90; 90; 90 | 2953.6 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
| 7118221 | CIF | C13 H11 F N2 | P -1 | 10.0641; 11.0425; 12.1824 114.924; 95.055; 111.476 | 1094.39 | Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak 'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks. Chemical communications (Cambridge, England), 2016, 52, 2141-2144 |
| 7118222 | CIF | C13 H10 F2 N2 | P 1 21/c 1 | 12.7028; 8.3775; 11.5509 90; 117.017; 90 | 1095.1 | Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak 'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks. Chemical communications (Cambridge, England), 2016, 52, 2141-2144 |
| 7118223 | CIF | C41 H33 N3 O6 | P 1 21/c 1 | 11.1829; 11.5006; 26.2259 90; 92.219; 90 | 3370.4 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
| 7118224 | CIF | C41 H33 Cd Cl0 I2 N3 O6 | R -3 :H | 54.6374; 54.6374; 8.9458 90; 90; 120 | 23127.6 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
| 7118225 | CIF | C42.17 H36 Br Cd I2 N3 O6.33 | R -3 :H | 54.5811; 54.5811; 8.9081 90; 90; 120 | 22982.7 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
| 7118226 | CIF | C42 H35 Cd I4 N3 O6 | R -3 :H | 54.772; 54.772; 8.8733 90; 90; 120 | 23053.3 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
| 7118227 | CIF | C41 H33 Cd I2 N3 O6 | R -3 :H | 54.8819; 54.8819; 8.8759 90; 90; 120 | 23152.7 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
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