Crystallography Open Database

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7125247 CIFC16 H17 N O2 SP 1 21 17.3082; 12.667; 7.9739
90; 102.802; 90
719.82Okoromoba, 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 CIFC26 H36 F2 N2 O6 S2P -16.3281; 12.8693; 17.8671
105.544; 93.657; 100.435
1368.94Okoromoba, 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 CIFC12 H7 N O4 ZnP b c a7.1952; 19.7441; 20.4254
90; 90; 90
2901.7Zhang, 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 CIFC21 H24 N2 O SiP -110.08; 11.8813; 16.5509
88.653; 86.499; 89.381
1977.86Pan, 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 CIFC20 H30 N2 O Si2P 1 21/c 117.5738; 10.3894; 12.0069
90; 100.934; 90
2152.44Pan, 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 CIFC26 H29 N3 O3 SiC 1 2 140.8407; 11.72; 10.659
90; 102.731; 90
4976.53Pan, 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 CIFC39 H21 Au Cl7 F2 N O4 PP 1 21/n 18.7297; 28.9112; 15.5735
90; 103.822; 90
3816.7Hattori, 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 CIFC47 H43 Cl6 F6 Ir N7 O2 PP b c a22.1254; 16.4448; 28.2843
90; 90; 90
10291.2Yellol, 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 CIFC35.5 H30.5 Cl F6 Ir N7 O2 PC 1 2/c 124.4157; 16.5559; 23.3462
90; 113.79; 90
8635.2Yellol, 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 CIFC15 H18 O2P 1 21/n 16.3004; 8.2192; 25.844
90; 94.486; 90
1334.2Ma, 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 CIFC36 H28 O2 P2 Pd SP -19.0944; 11.4218; 15.9032
95.9441; 103.474; 102.049
1550.8Ma, 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 CIFC24 H36 O2 P2 Pd SP -18.7065; 11.0937; 15.13
73.3056; 80.9582; 74.899
1346.1Ma, 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 CIFC28 H44 O2 P2 Pd SP -18.6167; 11.5992; 16.4263
77.1791; 79.8629; 73.9166
1526.6Ma, 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 CIFC216 H310 Mn10 N12 O40P -114.9101; 17.9438; 22.3792
69.512; 75.796; 81.501
5424.6Coletta, 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 CIFC206 H280 Gd2 Mn8 N10 O44P 1 21/n 122.096; 19.157; 27.0764
90; 105.149; 90
11063Coletta, 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 CIFC20 H24 N2 O5P -18.9003; 9.3364; 11.3581
83.515; 76.869; 82.053
907.1Mallo, 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 CIFC19 H21 N O6P -17.787; 9.08; 12.994
106.14; 91.08; 94.96
878.4Mallo, 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 CIFC19 H21 N O6P c a 2110.2; 12.903; 14.787
90; 90; 90
1946.1Mallo, 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 CIFC18 H19 N O5P 1 21/c 17.3465; 12.3261; 18.1727
90; 95.772; 90
1637.3Mallo, 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 CIFC18 H18 F N O5P 1 21/c 118.99; 5.418; 17.32
90; 113.9; 90
1629.2Mallo, 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 CIFC25 H30 N2 O3 SP 1 21/n 115.6911; 7.8759; 19.8219
90; 106.907; 90
2343.7Kumar, 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 CIFC72 H110 Cl4 N7 O10P 1 21/n 114.6718; 22.9104; 23.5888
90; 104.564; 90
7674.3Lavendomme, 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 CIFC27 H36 N3 UP 1 21/c 114.318; 11.54; 14.975
90; 93.52; 90
2469.6Behrle, 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 CIFC27 H35 Cl0 N3 ThP -19.59; 11.143; 11.619
88.275; 77.613; 87.316
1211.1Behrle, 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 CIFC111 H116 O S8 ThP 1 21/c 114.983; 25.115; 27.353
90; 92.488; 90
10283Behrle, 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 CIFC118 H124 O S8 UP 1 21/c 115.004; 25.0884; 27.253
90; 92.527; 90
10248.8Behrle, 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 CIFC180 H200 Cl18 N17 O12 PC 1 2/c 130.3787; 19.6365; 32.742
90; 109.719; 90
18386Qiao, 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 CIFC130 H130 N10P 43 3 236.9585; 36.9585; 36.9585
90; 90; 90
50483Qiao, 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 CIFC26 H24 O3P 1 21/n 18.9587; 8.4815; 27.445
90; 92.802; 90
2082.9Tharra, 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 CIFC47 H54 N O2 S2P 1 21/n 116.9652; 13.3015; 18.3142
90; 108.16; 90
3927Ruch, 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 CIFC50 H66 Au2 Cl3 F6 P2 SbP -113.279; 14.462; 15.6401
100.277; 96.426; 115.812
2598.8Ruch, 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 CIFC42.5 H42 Cl F2 N O2P -111.0496; 12.2287; 14.2619
64.774; 82.424; 88.269
1727.4Ruch, 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 CIFC36 H35 N O2P 1 21/n 110.8442; 13.8546; 18.575
90; 92.116; 90
2788.8Ruch, 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 CIFC38 H39 N O4P 1 21/n 112.6921; 17.3656; 14.0302
90; 99.986; 90
3045.5Ruch, 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 CIFC39 H53 Ge N2 OP -110.7269; 11.206; 14.4819
86.134; 88.938; 81.551
1717.93Wu, 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 CIFC28 H24 O4P -15.6126; 8.3452; 12.339
88.55; 78.74; 87.54
566.2Zhou, 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 CIFC28 H24 O6P -110.4453; 10.599; 10.8669
86.506; 84.424; 71.57
1135.4Zhou, 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 CIFC26 H20 O3P 1 21/c 110.2062; 19.416; 10.5696
90; 109.487; 90
1974.5Zhou, 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 CIFC30 H30 O6 Te3P 1 21/n 115.5616; 24.9422; 15.8574
90; 104.681; 90
5954Wang, 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 CIFC30 H32 O6 Te2P 1 21/n 18.3225; 15.076; 23.2305
90; 95.2; 90
2902.7Wang, 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 CIFC30 H36 Br6 O9 Te3P -110.889; 10.89; 18.299
86.12; 86.29; 71.19
2047.2Wang, 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 CIFC23 H27 N3 O2P -18.2014; 10.9469; 12.241
99.951; 94.49; 103.679
1043.58El 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 CIFC26 H31 N3 O2P -19.3834; 11.8498; 22.2318
87.603; 82.452; 71.9
2329.3El 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 CIFC25 H27 N4 O5 PC 1 2/c 129.5009; 7.6614; 21.6674
90; 92.924; 90
4890.85El 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 CIFC24 H24 Cu4 I4 N4 O16 Zr3I 4/m m m17.5411; 17.5411; 34.6975
90; 90; 90
10676.1Tan, 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 CIFC20 H18 Br N O5 SP -17.88851; 8.9545; 14.9033
92.1745; 99.8465; 107.839
982.77Modak, 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 CIFC25 H26 N2 O6 SP -18.3702; 12.3731; 13.2427
108.688; 105.715; 98.948
1205.6Modak, 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 CIFC21 H23 Br F3 N O6P 21 21 218.6647; 15.3884; 17.0772
90; 90; 90
2277Zhi, 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 CIFC26 H19 N OP 1 21/c 127.556; 7.4414; 19.1328
90; 109.435; 90
3699.7Bagle, 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 CIFC56 H46 Br Cl2 F4 O3 P3 Pd SP -112.108; 12.5; 18.24
76.07; 74.442; 82.349
2574.3Firth, 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

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