Crystallography Open Database
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Searching journal of publication like 'Chem.Commun.' volume of publication is 52
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7125247 | CIF | C16 H17 N O2 S | P 1 21 1 | 7.3082; 12.667; 7.9739 90; 102.802; 90 | 719.82 | Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B. Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions. Chemical communications (Cambridge, England), 2016, 52, 13353-13356 |
| 7125248 | CIF | C26 H36 F2 N2 O6 S2 | P -1 | 6.3281; 12.8693; 17.8671 105.544; 93.657; 100.435 | 1368.94 | Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B. Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions. Chemical communications (Cambridge, England), 2016, 52, 13353-13356 |
| 7125249 | CIF | C12 H7 N O4 Zn | P b c a | 7.1952; 19.7441; 20.4254 90; 90; 90 | 2901.7 | Zhang, Ling; Jiang, Ke; Jiang, Mengdie; Yue, Dan; Wan, Yating; Xing, Huabin; Yang, Yu; Cui, Yuanjing; Chen, Banglin; Qian, Guodong A highly stable amino-coordinated MOF for unprecedented block off N<sub>2</sub> adsorption and extraordinary CO<sub>2</sub>/N<sub>2</sub> separation. Chemical communications (Cambridge, England), 2016, 52, 13568-13571 |
| 7125250 | CIF | C21 H24 N2 O Si | P -1 | 10.08; 11.8813; 16.5509 88.653; 86.499; 89.381 | 1977.86 | Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds. Chemical communications (Cambridge, England), 2016, 52, 13151-13154 |
| 7125251 | CIF | C20 H30 N2 O Si2 | P 1 21/c 1 | 17.5738; 10.3894; 12.0069 90; 100.934; 90 | 2152.44 | Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds. Chemical communications (Cambridge, England), 2016, 52, 13151-13154 |
| 7125252 | CIF | C26 H29 N3 O3 Si | C 1 2 1 | 40.8407; 11.72; 10.659 90; 102.731; 90 | 4976.53 | Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds. Chemical communications (Cambridge, England), 2016, 52, 13151-13154 |
| 7125253 | CIF | C39 H21 Au Cl7 F2 N O4 P | P 1 21/n 1 | 8.7297; 28.9112; 15.5735 90; 103.822; 90 | 3816.7 | Hattori, Yohei; Kusamoto, Tetsuro; Sato, Tohru; Nishihara, Hiroshi Synergistic luminescence enhancement of a pyridyl-substituted triarylmethyl radical based on fluorine substitution and coordination to gold. Chemical communications (Cambridge, England), 2016, 52, 13393-13396 |
| 7125254 | CIF | C47 H43 Cl6 F6 Ir N7 O2 P | P b c a | 22.1254; 16.4448; 28.2843 90; 90; 90 | 10291.2 | Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization. Chemical communications (Cambridge, England), 2016, 52, 14165-14168 |
| 7125255 | CIF | C35.5 H30.5 Cl F6 Ir N7 O2 P | C 1 2/c 1 | 24.4157; 16.5559; 23.3462 90; 113.79; 90 | 8635.2 | Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization. Chemical communications (Cambridge, England), 2016, 52, 14165-14168 |
| 7125256 | CIF | C15 H18 O2 | P 1 21/n 1 | 6.3004; 8.2192; 25.844 90; 94.486; 90 | 1334.2 | Ma, Dengke; Fu, Chunling; Ma, Shengming Diastereoselective construction of cyclopent-2-enone-4-ols from aldehydes and 1,2-allenones catalyzed by N-heterocyclic carbene. Chemical communications (Cambridge, England), 2016, 52, 14426-14429 |
| 7125257 | CIF | C36 H28 O2 P2 Pd S | P -1 | 9.0944; 11.4218; 15.9032 95.9441; 103.474; 102.049 | 1550.8 | Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes. Chemical communications (Cambridge, England), 2016, 52, 14262-14265 |
| 7125258 | CIF | C24 H36 O2 P2 Pd S | P -1 | 8.7065; 11.0937; 15.13 73.3056; 80.9582; 74.899 | 1346.1 | Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes. Chemical communications (Cambridge, England), 2016, 52, 14262-14265 |
| 7125259 | CIF | C28 H44 O2 P2 Pd S | P -1 | 8.6167; 11.5992; 16.4263 77.1791; 79.8629; 73.9166 | 1526.6 | Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes. Chemical communications (Cambridge, England), 2016, 52, 14262-14265 |
| 7125260 | CIF | C216 H310 Mn10 N12 O40 | P -1 | 14.9101; 17.9438; 22.3792 69.512; 75.796; 81.501 | 5424.6 | Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J. Core expansion of bis-calix[4]arene-supported clusters. Chemical communications (Cambridge, England), 2016, 52, 14246-14249 |
| 7125261 | CIF | C206 H280 Gd2 Mn8 N10 O44 | P 1 21/n 1 | 22.096; 19.157; 27.0764 90; 105.149; 90 | 11063 | Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J. Core expansion of bis-calix[4]arene-supported clusters. Chemical communications (Cambridge, England), 2016, 52, 14246-14249 |
| 7125262 | CIF | C20 H24 N2 O5 | P -1 | 8.9003; 9.3364; 11.3581 83.515; 76.869; 82.053 | 907.1 | Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E. Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents. Chemical communications (Cambridge, England), 2016, 52, 13576-13579 |
| 7125263 | CIF | C19 H21 N O6 | P -1 | 7.787; 9.08; 12.994 106.14; 91.08; 94.96 | 878.4 | Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E. Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents. Chemical communications (Cambridge, England), 2016, 52, 13576-13579 |
| 7125264 | CIF | C19 H21 N O6 | P c a 21 | 10.2; 12.903; 14.787 90; 90; 90 | 1946.1 | Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E. Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents. Chemical communications (Cambridge, England), 2016, 52, 13576-13579 |
| 7125265 | CIF | C18 H19 N O5 | P 1 21/c 1 | 7.3465; 12.3261; 18.1727 90; 95.772; 90 | 1637.3 | Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E. Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents. Chemical communications (Cambridge, England), 2016, 52, 13576-13579 |
| 7125266 | CIF | C18 H18 F N O5 | P 1 21/c 1 | 18.99; 5.418; 17.32 90; 113.9; 90 | 1629.2 | Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E. Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents. Chemical communications (Cambridge, England), 2016, 52, 13576-13579 |
| 7125267 | CIF | C25 H30 N2 O3 S | P 1 21/n 1 | 15.6911; 7.8759; 19.8219 90; 106.907; 90 | 2343.7 | Kumar, Ravi; Thorat, Shridhar H.; Reddy, Maddi Sridhar Cu-Catalyzed iminative hydroolefination of unactivated alkynes en route to 4-imino-tetrahydropyridines and 4-aminopyridines. Chemical communications (Cambridge, England), 2016, 52, 13475-13478 |
| 7125268 | CIF | C72 H110 Cl4 N7 O10 | P 1 21/n 1 | 14.6718; 22.9104; 23.5888 90; 104.564; 90 | 7674.3 | Lavendomme, Roy; Marcélis, Lionel; Wouters, Johan; Luhmer, Michel; Jabin, Ivan A nano-sized container for specific encapsulation of isolated water molecules. Chemical communications (Cambridge, England), 2016, 52, 14109-14112 |
| 7125269 | CIF | C27 H36 N3 U | P 1 21/c 1 | 14.318; 11.54; 14.975 90; 93.52; 90 | 2469.6 | Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R. Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials. Chemical communications (Cambridge, England), 2016, 52, 14373-14375 |
| 7125270 | CIF | C27 H35 Cl0 N3 Th | P -1 | 9.59; 11.143; 11.619 88.275; 77.613; 87.316 | 1211.1 | Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R. Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials. Chemical communications (Cambridge, England), 2016, 52, 14373-14375 |
| 7125271 | CIF | C111 H116 O S8 Th | P 1 21/c 1 | 14.983; 25.115; 27.353 90; 92.488; 90 | 10283 | Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R. Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials. Chemical communications (Cambridge, England), 2016, 52, 14373-14375 |
| 7125272 | CIF | C118 H124 O S8 U | P 1 21/c 1 | 15.004; 25.0884; 27.253 90; 92.527; 90 | 10248.8 | Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R. Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials. Chemical communications (Cambridge, England), 2016, 52, 14373-14375 |
| 7125273 | CIF | C180 H200 Cl18 N17 O12 P | C 1 2/c 1 | 30.3787; 19.6365; 32.742 90; 109.719; 90 | 18386 | Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H. A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes. Chemical communications (Cambridge, England), 2016, 52, 13675-13678 |
| 7125274 | CIF | C130 H130 N10 | P 43 3 2 | 36.9585; 36.9585; 36.9585 90; 90; 90 | 50483 | Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H. A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes. Chemical communications (Cambridge, England), 2016, 52, 13675-13678 |
| 7125275 | CIF | C26 H24 O3 | P 1 21/n 1 | 8.9587; 8.4815; 27.445 90; 92.802; 90 | 2082.9 | Tharra, Prabhakararao; Baire, Beeraiah Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans. Chemical communications (Cambridge, England), 2016, 52, 14290-14293 |
| 7125276 | CIF | C47 H54 N O2 S2 | P 1 21/n 1 | 16.9652; 13.3015; 18.3142 90; 108.16; 90 | 3927 | Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes. Chemical communications (Cambridge, England), 2016, 52, 14133-14136 |
| 7125277 | CIF | C50 H66 Au2 Cl3 F6 P2 Sb | P -1 | 13.279; 14.462; 15.6401 100.277; 96.426; 115.812 | 2598.8 | Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes. Chemical communications (Cambridge, England), 2016, 52, 14133-14136 |
| 7125278 | CIF | C42.5 H42 Cl F2 N O2 | P -1 | 11.0496; 12.2287; 14.2619 64.774; 82.424; 88.269 | 1727.4 | Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes. Chemical communications (Cambridge, England), 2016, 52, 14133-14136 |
| 7125279 | CIF | C36 H35 N O2 | P 1 21/n 1 | 10.8442; 13.8546; 18.575 90; 92.116; 90 | 2788.8 | Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes. Chemical communications (Cambridge, England), 2016, 52, 14133-14136 |
| 7125280 | CIF | C38 H39 N O4 | P 1 21/n 1 | 12.6921; 17.3656; 14.0302 90; 99.986; 90 | 3045.5 | Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes. Chemical communications (Cambridge, England), 2016, 52, 14133-14136 |
| 7125281 | CIF | C39 H53 Ge N2 O | P -1 | 10.7269; 11.206; 14.4819 86.134; 88.938; 81.551 | 1717.93 | Wu, Yile; Shan, Changkai; Sun, Ying; Chen, Peng; Ying, Jianxi; Zhu, Jun; Liu, Liu Leo; Zhao, Yufen Main group metal-ligand cooperation of N-heterocyclic germylene: an efficient catalyst for hydroboration of carbonyl compounds. Chemical communications (Cambridge, England), 2016, 52, 13799-13802 |
| 7125282 | CIF | C28 H24 O4 | P -1 | 5.6126; 8.3452; 12.339 88.55; 78.74; 87.54 | 566.2 | Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds. Chemical communications (Cambridge, England), 2016, 52, 13345-13348 |
| 7125283 | CIF | C28 H24 O6 | P -1 | 10.4453; 10.599; 10.8669 86.506; 84.424; 71.57 | 1135.4 | Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds. Chemical communications (Cambridge, England), 2016, 52, 13345-13348 |
| 7125284 | CIF | C26 H20 O3 | P 1 21/c 1 | 10.2062; 19.416; 10.5696 90; 109.487; 90 | 1974.5 | Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds. Chemical communications (Cambridge, England), 2016, 52, 13345-13348 |
| 7125285 | CIF | C30 H30 O6 Te3 | P 1 21/n 1 | 15.5616; 24.9422; 15.8574 90; 104.681; 90 | 5954 | Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine. Chemical communications (Cambridge, England), 2016, 52, 14486-14489 |
| 7125286 | CIF | C30 H32 O6 Te2 | P 1 21/n 1 | 8.3225; 15.076; 23.2305 90; 95.2; 90 | 2902.7 | Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine. Chemical communications (Cambridge, England), 2016, 52, 14486-14489 |
| 7125287 | CIF | C30 H36 Br6 O9 Te3 | P -1 | 10.889; 10.89; 18.299 86.12; 86.29; 71.19 | 2047.2 | Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine. Chemical communications (Cambridge, England), 2016, 52, 14486-14489 |
| 7125288 | CIF | C23 H27 N3 O2 | P -1 | 8.2014; 10.9469; 12.241 99.951; 94.49; 103.679 | 1043.58 | El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles. Chemical communications (Cambridge, England), 2016, 52, 14490-14493 |
| 7125289 | CIF | C26 H31 N3 O2 | P -1 | 9.3834; 11.8498; 22.2318 87.603; 82.452; 71.9 | 2329.3 | El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles. Chemical communications (Cambridge, England), 2016, 52, 14490-14493 |
| 7125290 | CIF | C25 H27 N4 O5 P | C 1 2/c 1 | 29.5009; 7.6614; 21.6674 90; 92.924; 90 | 4890.85 | El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles. Chemical communications (Cambridge, England), 2016, 52, 14490-14493 |
| 7125291 | CIF | C24 H24 Cu4 I4 N4 O16 Zr3 | I 4/m m m | 17.5411; 17.5411; 34.6975 90; 90; 90 | 10676.1 | Tan, Yan-Xi; Yang, Xue; Li, Bei-Bei; Yuan, Daqiang Rational design of a flu-type heterometallic cluster-based Zr-MOF. Chemical communications (Cambridge, England), 2016, 52, 13671-13674 |
| 7125292 | CIF | C20 H18 Br N O5 S | P -1 | 7.88851; 8.9545; 14.9033 92.1745; 99.8465; 107.839 | 982.77 | Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives. Chemical communications (Cambridge, England), 2016, 52, 13916-13919 |
| 7125293 | CIF | C25 H26 N2 O6 S | P -1 | 8.3702; 12.3731; 13.2427 108.688; 105.715; 98.948 | 1205.6 | Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives. Chemical communications (Cambridge, England), 2016, 52, 13916-13919 |
| 7125294 | CIF | C21 H23 Br F3 N O6 | P 21 21 21 | 8.6647; 15.3884; 17.0772 90; 90; 90 | 2277 | Zhi, Ying; Zhao, Kun; Liu, Qiang; Wang, Ai; Enders, Dieter Asymmetric synthesis of functionalized trifluoromethyl-substituted pyrrolidines via an organocatalytic domino Michael/Mannich [3+2] cycloaddition. Chemical communications (Cambridge, England), 2016, 52, 14011-14014 |
| 7125295 | CIF | C26 H19 N O | P 1 21/c 1 | 27.556; 7.4414; 19.1328 90; 109.435; 90 | 3699.7 | Bagle, Pradip N.; Mane, Manoj V.; Vanka, K.; Shinde, Dinesh R.; Shaikh, Samir R.; Gonnade, Rajesh G.; Patil, Nitin T. Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides. Chemical communications (Cambridge, England), 2016, 52, 14462-14465 |
| 7125296 | CIF | C56 H46 Br Cl2 F4 O3 P3 Pd S | P -1 | 12.108; 12.5; 18.24 76.07; 74.442; 82.349 | 2574.3 | Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W. A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane. Chemical communications (Cambridge, England), 2016, 52, 13967-13970 |
| 7125297 | CIF | C63 H53 Br F2 P3 Pd | P -1 | 12.225; 12.671; 19.4112 98.543; 90.489; 118.142 | 2611.3 | Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W. A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane. Chemical communications (Cambridge, England), 2016, 52, 13967-13970 |
| 7125298 | CIF | C57.5 H47 Br Cl3 F4 O4 P3 Pd S | P 1 21/c 1 | 14.2329; 20.4798; 19.1729 90; 96.688; 90 | 5550.6 | Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W. A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane. Chemical communications (Cambridge, England), 2016, 52, 13967-13970 |
| 7125299 | CIF | C22 H54 N8 Ni2 O10.01 P2 | P -1 | 10.3977; 14.1488; 22.4532 90.093; 90.531; 90.097 | 3303.05 | Neri, Gaia; Forster, Mark; Walsh, James J.; Robertson, C. M.; Whittles, T. J.; Farràs, Pau; Cowan, Alexander J. Photochemical CO<sub>2</sub> reduction in water using a co-immobilised nickel catalyst and a visible light sensitiser. Chemical communications (Cambridge, England), 2016, 52, 14200-14203 |
| 7125300 | CIF | C15 H10 N2 | P b c a | 13.936; 7.077; 22.807 90; 90; 90 | 2249.3 | Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates. Chemical communications (Cambridge, England), 2016, 52, 14404-14407 |
| 7125301 | CIF | C19 H16 N2 O2 S | P 1 21/c 1 | 9.3811; 20.8484; 8.6963 90; 99.098; 90 | 1679.43 | Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates. Chemical communications (Cambridge, England), 2016, 52, 14404-14407 |
| 7125302 | CIF | C16 H12 N2 O2 S | P 1 21/c 1 | 9.0829; 10.2351; 15.664 90; 97.384; 90 | 1444.1 | Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates. Chemical communications (Cambridge, England), 2016, 52, 14404-14407 |
| 7125303 | CIF | C45 H21 Dy F18 N2 O6 | P 21 21 21 | 11.111; 17.6697; 22.6965 90; 90; 90 | 4456 | Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B. Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets. Chemical communications (Cambridge, England), 2016, 52, 14474-14477 |
| 7125304 | CIF | C45 H21 Dy F18 N2 O6 | P 21 21 21 | 11.1191; 17.6604; 22.693 90; 90; 90 | 4456.2 | Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B. Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets. Chemical communications (Cambridge, England), 2016, 52, 14474-14477 |
| 7125305 | CIF | C48 H28 Dy F18 N2 O6 | P -1 | 13.216; 13.9132; 14.5959 67.984; 72.454; 84.724 | 2371.71 | Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B. Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets. Chemical communications (Cambridge, England), 2016, 52, 14474-14477 |
| 7125306 | CIF | C28 H19 N O | P 1 21 1 | 13.0425; 10.2377; 16.1011 90; 109.601; 90 | 2025.32 | Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation. Chemical communications (Cambridge, England), 2016, 52, 14121-14124 |
| 7125307 | CIF | C32 H21 N O | P 1 21 1 | 7.6244; 7.9489; 18.4283 90; 93.193; 90 | 1115.12 | Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation. Chemical communications (Cambridge, England), 2016, 52, 14121-14124 |
| 7125308 | CIF | C22 H25 N O5 | P 1 21/n 1 | 6.2373; 36.3214; 8.6667 90; 94.598; 90 | 1957.1 | Fuentes de Arriba, Angel L.; Urbitsch, Felix; Dixon, Darren J. Umpolung synthesis of branched α-functionalized amines from imines via photocatalytic three-component reductive coupling reactions. Chemical communications (Cambridge, England), 2016, 52, 14434-14437 |
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