Crystallography Open Database
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Searching journal of publication like 'Chemical science' volume of publication is 11
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1557531 | CIF | C21 Al F36 N O10 W | P 4/n :2 | 13.699; 13.699; 9.5293 90; 90; 90 | 1788.29 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557532 | CIF | C30 Al2 F55 Mo O12 | P a -3 | 17.285; 17.285; 17.285 90; 90; 90 | 5164.3 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557533 | CIF | C22 Al F36 Mo O10 | P 4/n :2 | 13.759; 13.759; 9.5821 90; 90; 90 | 1813.99 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557534 | CIF | C30 Al2 F55 O12 W | P a -3 | 17.3168; 17.3168; 17.3168 90; 90; 90 | 5192.82 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557535 | CIF | C21 Al F36 Mo N O10 | P 4/n :2 | 13.7152; 13.7152; 9.5418 90; 90; 90 | 1794.88 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557536 | CIF | C36 Al2 F73 O12 W | P -1 | 11.5888; 11.5986; 12.7755 82.965; 67.136; 87.863 | 1570.27 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557537 | CIF | C32 Al2 Cl3 F55 O14 W2 | P -1 | 11.3269; 12.2795; 23.4349 76.883; 86.161; 66.485 | 2909.8 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557538 | CIF | C46 Al2 F72 I3 Mo3 O22 | P 1 21/n 1 | 13.9703; 28.8124; 20.6169 90; 90.443; 90 | 8298.4 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557539 | CIF | C30 Al2 F55 I O12 W | P -1 | 10.5119; 12.5617; 21.1226 85.595; 76.545; 78.485 | 2656.7 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557540 | CIF | C68 Al4 F128 O26 W2 | P -1 | 15.848; 17.229; 22.395 94.072; 102.24; 101.653 | 5811.1 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557541 | CIF | C22 Al F36 I O10 W | P 1 21/c 1 | 16.438; 28.3511; 17.5878 90; 110.764; 90 | 7664.2 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557542 | CIF | C96 Al6 F165 I6 Mo6 O42 | P -1 | 13.385; 21.4285; 31.305 85.822; 81.782; 83.84 | 8820.3 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
| 1557543 | CIF | C57 H88 N2 O | P 1 21/n 1 | 16.2198; 10.77; 28.9971 90; 96.1; 90 | 5036.7 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557544 | CIF | C71 H94 Mg2 N8 | P 1 21/c 1 | 12.8246; 21.5786; 24.2161 90; 103.493; 90 | 6516.52 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557545 | CIF | C49 H60 Mg2 N6 | P 1 21/c 1 | 12.4858; 12.0704; 31.1338 90; 92.762; 90 | 4686.68 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557546 | CIF | C137.5 H189.63 I0.04 Mg2 N4 O0.13 | P 1 21/n 1 | 18.2067; 26.3297; 25.8355 90; 105.806; 90 | 11916.7 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557547 | CIF | C117 H144 Mg4 N12 O4 | P -1 | 15.1058; 19.0783; 20.0582 85.762; 88.909; 66.998 | 5306.17 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557548 | CIF | C70 H86 Mg2 N8 | C 1 2/c 1 | 18.7699; 15.7829; 22.8274 90; 109.172; 90 | 6387.4 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557549 | CIF | C57 H76 Mg2 N6 | P 1 21/c 1 | 18.7194; 11.3129; 26.0645 90; 103.791; 90 | 5360.57 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557550 | CIF | C57 H87 I Mg N2 O | P -1 | 10.437; 14.8235; 18.7188 84.547; 75.886; 71.426 | 2661.85 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557551 | CIF | C151 H208 Mg4 N12 O6 | P -1 | 17.919; 19.6004; 20.9467 79.292; 75.685; 86.86 | 7004 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557552 | CIF | C134 H184 Mg4 N12 O12 | P 1 21/c 1 | 15.48; 15.114; 27.505 90; 103.08; 90 | 6268 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
| 1557570 | CIF | C20 H18 N2 O5 | P -1 | 8.27; 9.1848; 12.4194 71.619; 82.065; 79.191 | 876.19 | Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R. Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction Chemical Science, 2020, 11, 3569-3573 |
| 1557571 | CIF | C44 H44 N4 O11 | P 21 21 21 | 10.9162; 11.3807; 31.809 90; 90; 90 | 3951.8 | Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R. Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction Chemical Science, 2020, 11, 3569-3573 |
| 1557572 | CIF | C8 H8 O5 | P 1 21 1 | 9.2321; 18.768; 18.876 90; 93.72; 90 | 3263.7 | Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R. Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction Chemical Science, 2020, 11, 3569-3573 |
| 1557580 | CIF | C15 H12 N4 O3 S | P 21 21 21 | 6.4901; 13.5853; 17.2054 90; 90; 90 | 1517 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
| 1557581 | CIF | C25 H21 Cl N2 O3 | P 21 21 21 | 6.2023; 15.1707; 23.3424 90; 90; 90 | 2196.36 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
| 1557582 | CIF | C18 H14 Br2 N4 O3 | P 1 21 1 | 7.6364; 11.6851; 11.5473 90; 104.259; 90 | 998.65 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
| 1557583 | CIF | C19 H15 F N4 O3 | P 21 21 21 | 10.3148; 11.9114; 14.6673 90; 90; 90 | 1802.08 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
| 1557584 | CIF | C25 H21 Cl N2 O3 | P 21 21 21 | 6.6447; 14.3101; 22.5008 90; 90; 90 | 2139.5 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
| 1557585 | CIF | C37 H61 Eu N8 O15 | F d d d :2 | 18.1194; 20.3557; 43.9834 90; 90; 90 | 16222.5 | Hewitt, Sarah H.; Macey, Georgina; Mailhot, Romain; Elsegood, Mark R. J.; Duarte, Fernanda; Kenwright, Alan M.; Butler, Stephen J. Tuning the anion binding properties of lanthanide receptors to discriminate nucleoside phosphates in a sensing array Chemical Science, 2020, 11, 3619-3628 |
| 1557586 | CIF | C22 H18 Br Cl0 N O2 | P 21 21 21 | 5.8675; 12.4208; 24.4967 90; 90; 90 | 1785.3 | Shen, Bin; He, Qianwen; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming A chiral cobalt(ii) complex catalyzed enantioselective aza-Piancatelli rearrangement/Diels‒Alder cascade reaction Chemical Science, 2020, 11, 3862-3867 |
| 1557587 | CIF | C11 H10 Br N O | P -1 | 6.732; 7.228; 12.0162 80.831; 86.517; 62.902 | 513.81 | Ikeda, Hideaki; Nishi, Kohei; Tsurugi, Hayato; Mashima, Kazushi Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine Chemical Science, 2020, 11, 3604-3609 |
| 1557598 | CIF | C18 H18 F3 N O4 | P 21 21 21 | 10.186; 11.3558; 15.5296 90; 90; 90 | 1796.31 | Zhang, Shuyue; Greenhalgh, Mark D.; Slawin, Alexandra M. Z.; Smith, Andrew D. Tandem sequential catalytic enantioselective synthesis of highly-functionalised tetrahydroindolizine derivatives Chemical Science, 2020, 11, 3885-3892 |
| 1557603 | CIF | C21 H18 N2 O2 S | C 1 2/c 1 | 17.4822; 9.78677; 20.9912 90; 103.576; 90 | 3491.13 | Li, Guofeng; Zhao, Man; Xie, Junqiu; Yao, Ying; Mou, Lingyun; Zhang, Xiaowei; Guo, Xiaomin; Sun, Wangsheng; Wang, Zheng; Xu, Jiecheng; Xue, Jianzhong; Hu, Tao; Zhang, Ming; Li, Min; Hong, Liang Efficient synthesis of cyclic amidine-based fluorophores via 6π-electrocyclic ring closure Chemical Science, 2020, 11, 3586-3591 |
| 1557604 | CIF | C20 H44 Cl2 N2 O2 P2 U | P 1 21/c 1 | 12.7105; 28.115; 8.1727 90; 105.391; 90 | 2815.8 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557605 | CIF | C18 H40 Cl2 N2 O2 P2 U | P 1 21/c 1 | 14.48; 14.59; 12.5668 90; 102.29; 90 | 2594.1 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557606 | CIF | C40 H88 Cl4 N4 O4 P4 Pd2 U2 | P c c n | 16.3226; 22.813; 14.7718 90; 90; 90 | 5500.5 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557607 | CIF | C44 H96 Cl4 N4 O6 P4 Pt3 U2 | C 1 2/c 1 | 12.663; 21.4809; 23.0838 90; 99.354; 90 | 6195.6 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557608 | CIF | C22 H48 Cl2 N2 Ni O3 P2 U | P 1 21/n 1 | 11.3508; 12.914; 20.597 90; 95.165; 90 | 3006.9 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557609 | CIF | C44 H96 Cl4 N4 Ni2 O5 P4 U2 | P 1 21/n 1 | 14.5223; 15.8953; 27.339 90; 103.728; 90 | 6130.6 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557610 | CIF | C40 H63 Cl2 N2 O3 P3 Pd U | P -1 | 12.208; 12.209; 17.048 108.557; 90.701; 108.839 | 2261 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
| 1557613 | CIF | C22 H28 O5 S | P -1 | 7.3975; 10.7485; 13.1441 92.571; 96.25; 97.449 | 1028.29 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
| 1557614 | CIF | C15 H22 O3 | P 1 21/n 1 | 7.6688; 22.4305; 15.4747 90; 101.329; 90 | 2610.02 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro–Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
| 1557615 | CIF | C12 H20 O2 | P 1 21/c 1 | 7.1285; 11.9273; 13.4833 90; 104.629; 90 | 1109.24 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
| 1557616 | CIF | C15 H20 O3 | P -1 | 7.2165; 8.3504; 11.317 82.649; 76.258; 68.964 | 617.61 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
| 1557617 | CIF | C23 H28 N2 O3 S | P 1 21/c 1 | 10.3539; 19.9619; 11.8443 90; 113.384; 90 | 2246.95 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
| 1557618 | CIF | C22 H30 N2 O4 S | P 1 21/n 1 | 9.961; 17.5295; 13.2899 90; 101.667; 90 | 2272.62 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
| 1557625 | CIF | C48 H55 Au F6 N4 O11 S2 | P 21 21 21 | 9.1199; 23.4191; 23.6083 90; 90; 90 | 5042.3 | Reid, Jolene P.; Hu, Mingyou; Ito, Susumu; Huang, Banruo; Hong, Cynthia M.; Xiang, Hengye; Sigman, Matthew S.; Toste, F. Dean Strategies for remote enantiocontrol in chiral gold(iii) complexes applied to catalytic enantioselective γ,δ-Diels‒Alder reactions Chemical Science, 2020, 11, 6450-6456 |
| 1557626 | CIF | C21 H9 N3 O6 Ti | P a -3 | 20.9953; 20.9953; 20.9953 90; 90; 90 | 9254.8 | Cao, Jing; Ma, Wenjie; Lyu, Kangjie; Zhuang, Lin; Cong, Hengjiang; Deng, Hexiang Twist and sliding dynamics between interpenetrated frames in Ti-MOF revealing high proton conductivity Chemical Science, 2020, 11, 3978-3985 |
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