Crystallography Open Database

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1542254 CIFC88.77 H103.38 Cl21.54 N12 O4.92 Pd6I 21 331.495; 31.495; 31.495
90; 90; 90		31241Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542255 CIFC88.81 H104.7 Cl21.61 N12 O5.54 Pd6I 21 331.3834; 31.3834; 31.3834
90; 90; 90		30910.1Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542256 CIFC88.28 H102.34 Cl20.56 N12 O4.89 Pd6I 21 331.4527; 31.4527; 31.4527
90; 90; 90		31115Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542257 CIFC88.82 H106.67 Cl21.63 N12 O6.52 Pd6I 21 331.493; 31.493; 31.493
90; 90; 90		31235Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542258 CIFC47.41 H49.41 Cl22.23 N6 O Pd3I -4 3 d31.3274; 31.3274; 31.3274
90; 90; 90		30744.9Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542259 CIFC88.53 H106.99 Cl21.07 N12 O6.96 Pd6I 21 331.3922; 31.3922; 31.3922
90; 90; 90		30936.1Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542260 CIFC88.34 H103.54 Cl20.68 N12 O5.43 Pd6I 21 331.3469; 31.3469; 31.3469
90; 90; 90		30802.3Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542261 CIFC88.49 H103.18 Cl20.98 N12 O5.1 Pd6I 21 331.4043; 31.4043; 31.4043
90; 90; 90		30971.9Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542262 CIFC88.52 H103.31 Cl21.04 N12 O5.14 Pd6I 21 331.4477; 31.4477; 31.4477
90; 90; 90		31100.4Kubota, Ryou; Tashiro, Shohei; Shionoya, Mitsuhiko
Chiral metal‒macrocycle frameworks: supramolecular chirality induction and helicity inversion of the helical macrocyclic structures
Chem. Sci., 2016, 7, 2217
1542263 CIFC24.5 H17 Cl N O S0.5P b c n15.9195; 13.7674; 17.3771
90; 90; 90		3808.54Xu, Bingjia; Mu, Yingxiao; Mao, Zhu; Xie, Zongliang; Wu, Haozhong; Zhang, Yi; Jin, Chongjun; Chi, Zhenguo; Liu, Siwei; Xu, Jiarui; Wu, Yuan-Chun; Lu, Po-Yen; Lien, Alan; Bryce, Martin R.
Achieving remarkable mechanochromism and white-light emission with thermally activated delayed fluorescence through the molecular heredity principle
Chem. Sci., 2016, 7, 2201
1542264 CIFC36 H24 N2 O2 S3P 1 21/n 18.1912; 20.1704; 18.0457
90; 97.807; 90		2953.87Xu, Bingjia; Mu, Yingxiao; Mao, Zhu; Xie, Zongliang; Wu, Haozhong; Zhang, Yi; Jin, Chongjun; Chi, Zhenguo; Liu, Siwei; Xu, Jiarui; Wu, Yuan-Chun; Lu, Po-Yen; Lien, Alan; Bryce, Martin R.
Achieving remarkable mechanochromism and white-light emission with thermally activated delayed fluorescence through the molecular heredity principle
Chem. Sci., 2016, 7, 2201
1542265 CIFC42 H28 N2 O2 S2P 1 21/c 119.365; 12.947; 13.257
90; 106.41; 90		3188.4Xu, Bingjia; Mu, Yingxiao; Mao, Zhu; Xie, Zongliang; Wu, Haozhong; Zhang, Yi; Jin, Chongjun; Chi, Zhenguo; Liu, Siwei; Xu, Jiarui; Wu, Yuan-Chun; Lu, Po-Yen; Lien, Alan; Bryce, Martin R.
Achieving remarkable mechanochromism and white-light emission with thermally activated delayed fluorescence through the molecular heredity principle
Chem. Sci., 2016, 7, 2201
1542266 CIFC14 H22 F12 Mg N2 O13 S4P 1 21/n 110.1949; 8.4085; 35.446
90; 96.69; 90		3017.9Terada, Shoshi; Mandai, Toshihiko; Suzuki, Soma; Tsuzuki, Seiji; Watanabe, Katsuya; Kamei, Yutaro; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Thermal and Electrochemical Stability of Tetraglyme‒Magnesium Bis(trifluoromethanesulfonyl)amide Complex: Electric Field Effect of Divalent Cation on Solvate Stability
The Journal of Physical Chemistry C, 2016, 120, 1353
1542267 CIFC15 H11 N O4 SP 21 21 216.9902; 10.327; 18.799
90; 90; 90		1357.1Lai, Bo-Nan; Qiu, Jian-Feng; Zhang, Heng-Xia; Nie, Jing; Ma, Jun-An
Stereoselective Synthesis of Fused Aziridines via One-Pot Sequential Decarboxylative Mannich Reaction and Oxidative C-H Amination of Cyclic Imines with β-Ketoacids.
Organic letters, 2016, 18, 520-523
1542268 CIFC29 H40 O10P 1 21 18.3056; 28.5217; 12.1649
90; 90.909; 90		2881.38Yu, Jin-Hai; Liu, Qun-Fang; Sheng, Li; Wang, Guo-Cai; Li, Jia; Yue, Jian-Min
Cipacinoids A-D, Four Limonoids with Spirocyclic Skeletons from Cipadessa cinerascens.
Organic letters, 2016, 18, 444-447
1542269 CIFC29 H40 O11P 1 21 18.7852; 14.5469; 11.599
90; 110.9; 90		1384.79Yu, Jin-Hai; Liu, Qun-Fang; Sheng, Li; Wang, Guo-Cai; Li, Jia; Yue, Jian-Min
Cipacinoids A-D, Four Limonoids with Spirocyclic Skeletons from Cipadessa cinerascens.
Organic letters, 2016, 18, 444-447
1542270 CIFC16 H15 N3 O3P 1 21/c 18.0689; 13.762; 14.911
90; 115.54; 90		1494Amiri, Nayereh; Rofouei, Mohammad K.; Ghasemi, Jahan B.
Multivariate optimization, preconcentration and determination of mercury ions with (1-(p-acetyl phenyl)-3-(o-methyl benzoate)) triazene in aqueous samples using ICP-AES
Anal. Methods, 2016, 8, 1111
1542271 CIFC18 H34 Cr N4P b c a11.3075; 17.5868; 20.908
90; 90; 90		4157.8Beaumier, Evan P.; Billow, Brennan S.; Singh, Amrendra K.; Biros, Shannon M.; Odom, Aaron L.
A complex with nitrogen single, double, and triple bonds to the same chromium atom: synthesis, structure, and reactivity
Chem. Sci., 2016, 7, 2532
1542272 CIFC77 H150 Cr2 K2 N12 O12P -113.565; 13.6133; 14.3228
117.74; 103.515; 90.421		2255.3Beaumier, Evan P.; Billow, Brennan S.; Singh, Amrendra K.; Biros, Shannon M.; Odom, Aaron L.
A complex with nitrogen single, double, and triple bonds to the same chromium atom: synthesis, structure, and reactivity
Chem. Sci., 2016, 7, 2532
1542273 CIFC20 H36 Cr N4 OP b c a16.6334; 14.8352; 18.1191
90; 90; 90		4471.1Beaumier, Evan P.; Billow, Brennan S.; Singh, Amrendra K.; Biros, Shannon M.; Odom, Aaron L.
A complex with nitrogen single, double, and triple bonds to the same chromium atom: synthesis, structure, and reactivity
Chem. Sci., 2016, 7, 2532
1542274 CIFC23 H42 Cr N4 OP 1 21/c 110.3071; 27.649; 18.4003
90; 99.891; 90		5165.8Beaumier, Evan P.; Billow, Brennan S.; Singh, Amrendra K.; Biros, Shannon M.; Odom, Aaron L.
A complex with nitrogen single, double, and triple bonds to the same chromium atom: synthesis, structure, and reactivity
Chem. Sci., 2016, 7, 2532
1542275 CIFC21 H22 N4 OP c c n20.862; 10.4975; 16.69
90; 90; 90		3655.1Blackham, Emma E.; Knowles, Jonathan P.; Burgess, Jonathan; Booker-Milburn, Kevin I.
Combining photochemistry and catalysis: rapid access to sp3– rich polyheterocycles from simple pyrroles
Chem. Sci., 2016, 7, 2302
1542276 CIFC25 H28 N4 O5 SP 1 c 17.4546; 18.7124; 34.4314
90; 91.776; 90		4800.6Blackham, Emma E.; Knowles, Jonathan P.; Burgess, Jonathan; Booker-Milburn, Kevin I.
Combining photochemistry and catalysis: rapid access to sp3– rich polyheterocycles from simple pyrroles
Chem. Sci., 2016, 7, 2302
1542277 CIFC25 H29 N3 O3 SP 1 21/n 113.2995; 10.5425; 16.004
90; 93.024; 90		2240.8Blackham, Emma E.; Knowles, Jonathan P.; Burgess, Jonathan; Booker-Milburn, Kevin I.
Combining photochemistry and catalysis: rapid access to sp3– rich polyheterocycles from simple pyrroles
Chem. Sci., 2016, 7, 2302
1542278 CIFC52 H68 B2 S4P 1 21/n 19.0044; 16.9419; 15.943
90; 95.155; 90		2422.29Yin, Xiaodong; Guo, Fang; Lalancette, Roger A.; Jäkle, Frieder
Luminescent Main-Chain Organoborane Polymers: Highly Robust, Electron-Deficient Poly(oligothiophene borane)s via Stille Coupling Polymerization
Macromolecules, 2016, 49, 537
1542279 CIFC42 H28 Cu La4 N6 O38 S2P -19.4008; 11.5017; 13.7959
108.56; 106.079; 97.893		1316.5Cancino, P.; Vega, A.; Santiago-Portillo, Andrea; Navalon, Sergio; Alvaro, Mercedes; Aguirre, P.; Spodine, E.; García, Hermenegildo
A novel copper(ii)‒lanthanum(iii) metal organic framework as a selective catalyst for the aerobic oxidation of benzylic hydrocarbons and cycloalkenes
Catal. Sci. Technol., 2016, 6, 3727
1542280 CIFC10 H16 N6 Na O6 VP -17.9375; 8.7365; 12.1972
102.684; 107.187; 103.796		745.41Leggett, C. J.; Parker, B. F.; Teat, S. J.; Zhang, Z.; Dau, P. D.; Lukens, W. W.; Peterson, S. M.; Cardenas, A. J. P.; Warner, M. G.; Gibson, J. K.; Arnold, J.; Rao, L.
Structural and spectroscopic studies of a rare non-oxido V(v) complex crystallized from aqueous solution
Chem. Sci., 2016, 7, 2775
1542281 CIFC5 H7 N3 Na O4 VP 1 21/c 115.0543; 5.507; 10.1794
90; 101.569; 90		826.77Leggett, C. J.; Parker, B. F.; Teat, S. J.; Zhang, Z.; Dau, P. D.; Lukens, W. W.; Peterson, S. M.; Cardenas, A. J. P.; Warner, M. G.; Gibson, J. K.; Arnold, J.; Rao, L.
Structural and spectroscopic studies of a rare non-oxido V(v) complex crystallized from aqueous solution
Chem. Sci., 2016, 7, 2775
1542282 CIFC12 H26 Ga2 O6P 1 21/c 18.15438; 8.28026; 12.8297
90; 92.0637; 90		865.7Horeglad, P.; Cybularczyk, M.; Litwińska, A.; Dąbrowska, A. M.; Dranka, M.; Żukowska, G. Z.; Urbańczyk, M.; Michalak, M.
Controlling the stereoselectivity of rac-LA polymerization by chiral recognition induced the formation of homochiral dimeric metal alkoxides
Polym. Chem., 2016, 7, 2022
1542283 CIFC12 H26 In2 O6P 16.9927; 8.3025; 8.4128
76.086; 83.924; 87.628		471.36Horeglad, P.; Cybularczyk, M.; Litwińska, A.; Dąbrowska, A. M.; Dranka, M.; Żukowska, G. Z.; Urbańczyk, M.; Michalak, M.
Controlling the stereoselectivity of rac-LA polymerization by chiral recognition induced the formation of homochiral dimeric metal alkoxides
Polym. Chem., 2016, 7, 2022
1542284 CIFC12 H26 In2 O6P 1 21/c 18.27; 8.4677; 13.1476
90; 91.014; 90		920.55Horeglad, P.; Cybularczyk, M.; Litwińska, A.; Dąbrowska, A. M.; Dranka, M.; Żukowska, G. Z.; Urbańczyk, M.; Michalak, M.
Controlling the stereoselectivity of rac-LA polymerization by chiral recognition induced the formation of homochiral dimeric metal alkoxides
Polym. Chem., 2016, 7, 2022
1542285 CIFC18 H28 Ga2 N2 O2P 1 2/n 18.0739; 8.5229; 14.463
90; 97.288; 90		987.2Horeglad, P.; Cybularczyk, M.; Litwińska, A.; Dąbrowska, A. M.; Dranka, M.; Żukowska, G. Z.; Urbańczyk, M.; Michalak, M.
Controlling the stereoselectivity of rac-LA polymerization by chiral recognition induced the formation of homochiral dimeric metal alkoxides
Polym. Chem., 2016, 7, 2022
1542286 CIFC27 H40 N4 O7P 21 21 219.9794; 14.104; 19.268
90; 90; 90		2712Almeida, Celso; Maddah, Fayrouz El; Kehraus, Stefan; Schnakenburg, Gregor; König, Gabriele M
Endolides A and B, Vasopressin and Serotonin-Receptor Interacting N-Methylated Peptides from the Sponge-Derived Fungus Stachylidium sp.
Organic letters, 2016, 18, 528-531
1542287 CIFC19 H22 O5P 1 21 19.873; 7.792; 11.34
90; 91.557; 90		872.1Shaffer, Corena V.; Cai, Shengxin; Peng, Jiangnan; Robles, Andrew J.; Hartley, Rachel M.; Powell, Douglas R.; Du, Lin; Cichewicz, Robert H.; Mooberry, Susan L.
Texas Native Plants Yield Compounds with Cytotoxic Activities against Prostate Cancer Cells.
Journal of natural products, 2016, 79, 531-540
1542288 CIFFe2 O9 Se3P 63/m7.872; 7.872; 7.3258
90; 90; 120		393.15Kovrugin, Vadim M.; Gordon, Elijah E.; Kasapbasi, Esra E.; Whangbo, Myung-Hwan; Colmont, Marie; Siidra, Oleg I.; Colis, Silviu; Krivovichev, Sergey V.; Mentré, Olivier
Bonding Scheme, Hydride Character, and Magnetic Paths of (HPO3)2‒Versus (SeO3)2‒Building Units in Solids
The Journal of Physical Chemistry C, 2016, 120, 1650
1542289 CIFFe2 H3 O9 P3P 63/m8.0195; 8.0195; 7.37
90; 90; 120		410.481Kovrugin, Vadim M.; Gordon, Elijah E.; Kasapbasi, Esra E.; Whangbo, Myung-Hwan; Colmont, Marie; Siidra, Oleg I.; Colis, Silviu; Krivovichev, Sergey V.; Mentré, Olivier
Bonding Scheme, Hydride Character, and Magnetic Paths of (HPO3)2‒Versus (SeO3)2‒Building Units in Solids
The Journal of Physical Chemistry C, 2016, 120, 1650
1542290 CIFC15 H9 Cl3 N3 O3 ReP 1 21/n 110.7568; 11.9888; 14.3677
90; 108.538; 90		1756.7Clark, Melissa L.; Rudshteyn, Benjamin; Ge, Aimin; Chabolla, Steven A.; Machan, Charles W.; Psciuk, Brian T.; Song, Jia; Canzi, Gabriele; Lian, Tianquan; Batista, Victor S.; Kubiak, Clifford P.
Orientation of Cyano-Substituted Bipyridine Re(I)fac-Tricarbonyl Electrocatalysts Bound to Conducting Au Surfaces
The Journal of Physical Chemistry C, 2016, 120, 1657
1542291 CIFC16 H8 Cl3 N4 O3 ReP 1 21/n 18.3755; 11.7615; 19.164
90; 100.728; 90		1854.8Clark, Melissa L.; Rudshteyn, Benjamin; Ge, Aimin; Chabolla, Steven A.; Machan, Charles W.; Psciuk, Brian T.; Song, Jia; Canzi, Gabriele; Lian, Tianquan; Batista, Victor S.; Kubiak, Clifford P.
Orientation of Cyano-Substituted Bipyridine Re(I)fac-Tricarbonyl Electrocatalysts Bound to Conducting Au Surfaces
The Journal of Physical Chemistry C, 2016, 120, 1657
1542292 CIFC28 H28 N2 O4P 1 21 19.0877; 15.0437; 9.2994
90; 111.757; 90		1180.78Garve, Lennart K. B.; Petzold, Martin; Jones, Peter G.; Werz, Daniel B.
[3 + 3]-Cycloaddition of Donor-Acceptor Cyclopropanes with Nitrile Imines Generated in Situ: Access to Tetrahydropyridazines.
Organic letters, 2016, 18, 564-567
1542293 CIFC24 H30 N2 O2P -18.721; 11.0214; 11.5267
101.563; 96.6362; 110.424		996.22Zhu, Zhengbo; Seidel, Daniel
An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization Step.
Organic letters, 2016, 18, 631-633
1542294 CIFC48 H66 S3 Si2P -19.8336; 14.2701; 16.3902
83.637; 85.505; 83.306		2265.2Shi, Xueliang; Quintero, Estefanía; Lee, Sangsu; Jing, Linzhi; Herng, Tun Seng; Zheng, Bin; Huang, Kuo-Wei; López Navarrete, Juan T.; Ding, Jun; Kim, Dongho; Casado, Juan; Chi, Chunyan
Benzo-thia-fused [n]thienoacenequinodimethanes with small to moderate diradical characters: the role of pro-aromaticity versus anti-aromaticity
Chem. Sci., 2016, 7, 3036
1542295 CIFC50 H66 S4 Si2P -17.4217; 19.0953; 19.1877
63.238; 89.851; 79.162		2374.2Shi, Xueliang; Quintero, Estefanía; Lee, Sangsu; Jing, Linzhi; Herng, Tun Seng; Zheng, Bin; Huang, Kuo-Wei; López Navarrete, Juan T.; Ding, Jun; Kim, Dongho; Casado, Juan; Chi, Chunyan
Benzo-thia-fused [n]thienoacenequinodimethanes with small to moderate diradical characters: the role of pro-aromaticity versus anti-aromaticity
Chem. Sci., 2016, 7, 3036
1542296 CIFC52 H66 S5 Si2P -114.9964; 18.3543; 19.3746
96.6629; 99.0302; 98.7364		5151.9Shi, Xueliang; Quintero, Estefanía; Lee, Sangsu; Jing, Linzhi; Herng, Tun Seng; Zheng, Bin; Huang, Kuo-Wei; López Navarrete, Juan T.; Ding, Jun; Kim, Dongho; Casado, Juan; Chi, Chunyan
Benzo-thia-fused [n]thienoacenequinodimethanes with small to moderate diradical characters: the role of pro-aromaticity versus anti-aromaticity
Chem. Sci., 2016, 7, 3036
1542297 CIFC54 H68 S4 Si2P 1 21/n 16.9436; 21.6735; 33.9795
90; 94.396; 90		5098.6Shi, Xueliang; Quintero, Estefanía; Lee, Sangsu; Jing, Linzhi; Herng, Tun Seng; Zheng, Bin; Huang, Kuo-Wei; López Navarrete, Juan T.; Ding, Jun; Kim, Dongho; Casado, Juan; Chi, Chunyan
Benzo-thia-fused [n]thienoacenequinodimethanes with small to moderate diradical characters: the role of pro-aromaticity versus anti-aromaticity
Chem. Sci., 2016, 7, 3036
1542298 CIFC50 H34 N2 SeP 1 21/c 110.2218; 9.8805; 20.3205
90; 117.561; 90		1819.4Xue, Jie; Li, Chen; Xin, Lijun; Duan, Lian; Qiao, Juan
High-efficiency and low efficiency roll-off near-infrared fluorescent OLEDs through triplet fusion
Chem. Sci., 2016, 7, 2888
1542299 CIFC57 H59 F6 Ir N7 PP 1 21/n 114.9598; 22.5882; 16.6294
90; 112.453; 90		5193.3Yang, Chen; Mehmood, Faisal; Lam, Tsz Lung; Chan, Sharon Lai-Fung; Wu, Yuan; Yeung, Chi-Shun; Guan, Xiangguo; Li, Kai; Chung, Clive Yik-Sham; Zhou, Cong-Ying; Zou, Taotao; Che, Chi-Ming
Stable luminescent iridium(iii) complexes with bis(N-heterocyclic carbene) ligands: photo-stability, excited state properties, visible-light-driven radical cyclization and CO2reduction, and cellular imaging
Chem. Sci., 2016, 7, 3123
1542300 CIFC42 H40 F3 Ir N6 O3 S3P b c a13.346; 19.6302; 30.1437
90; 90; 90		7897.2Yang, Chen; Mehmood, Faisal; Lam, Tsz Lung; Chan, Sharon Lai-Fung; Wu, Yuan; Yeung, Chi-Shun; Guan, Xiangguo; Li, Kai; Chung, Clive Yik-Sham; Zhou, Cong-Ying; Zou, Taotao; Che, Chi-Ming
Stable luminescent iridium(iii) complexes with bis(N-heterocyclic carbene) ligands: photo-stability, excited state properties, visible-light-driven radical cyclization and CO2reduction, and cellular imaging
Chem. Sci., 2016, 7, 3123
1542301 CIFC42 H40 F3 Ir N6 O3 S3P -115.8141; 16.3895; 18.8888
67.048; 67.5521; 82.559		4165.4Yang, Chen; Mehmood, Faisal; Lam, Tsz Lung; Chan, Sharon Lai-Fung; Wu, Yuan; Yeung, Chi-Shun; Guan, Xiangguo; Li, Kai; Chung, Clive Yik-Sham; Zhou, Cong-Ying; Zou, Taotao; Che, Chi-Ming
Stable luminescent iridium(iii) complexes with bis(N-heterocyclic carbene) ligands: photo-stability, excited state properties, visible-light-driven radical cyclization and CO2reduction, and cellular imaging
Chem. Sci., 2016, 7, 3123
1542302 CIFC44 H44 F3 Ir N6 O3 S3P -111.6716; 12.4594; 14.7489
74.683; 86.255; 83.689		2054.6Yang, Chen; Mehmood, Faisal; Lam, Tsz Lung; Chan, Sharon Lai-Fung; Wu, Yuan; Yeung, Chi-Shun; Guan, Xiangguo; Li, Kai; Chung, Clive Yik-Sham; Zhou, Cong-Ying; Zou, Taotao; Che, Chi-Ming
Stable luminescent iridium(iii) complexes with bis(N-heterocyclic carbene) ligands: photo-stability, excited state properties, visible-light-driven radical cyclization and CO2reduction, and cellular imaging
Chem. Sci., 2016, 7, 3123
1542303 CIFN O PP 1 21/c 112.2472; 4.83618; 10.8604
90; 115.803; 90		579.124Baumann, Dominik; Sedlmaier, Stefan J.; Schnick, Wolfgang
An Unprecedented AB2 Tetrahedra Network Structure Type in a High-Pressure Phase of Phosphorus Oxonitride (PON)
Angewandte Chemie International Edition, 2012, 51, 4707-4709
1542304 CIFC19 H24 N2 OP 21 21 216.955; 10.6206; 23.9572
90; 90; 90		1769.63Pan, Zhiqiang; Qin, Xu-Jie; Liu, Ya-Ping; Wu, Ting; Luo, Xiao-Dong; Xia, Chengfeng
Alstoscholarisines H-J, Indole Alkaloids from Alstonia scholaris: Structural Evaluation and Bioinspired Synthesis of Alstoscholarisine H.
Organic letters, 2016, 18, 654-657
1542305 CIFC19 H24 N2 OP 21 21 218.0376; 12.1437; 32.747
90; 90; 90		3196.3Pan, Zhiqiang; Qin, Xu-Jie; Liu, Ya-Ping; Wu, Ting; Luo, Xiao-Dong; Xia, Chengfeng
Alstoscholarisines H-J, Indole Alkaloids from Alstonia scholaris: Structural Evaluation and Bioinspired Synthesis of Alstoscholarisine H.
Organic letters, 2016, 18, 654-657
1542306 CIFC31 H30 O9 SeP 21 21 216.22509; 17.41592; 26.9154
90; 90; 90		2918.05McDonagh, Anthony W.; Mahon, Mary F.; Murphy, Paul V.
Lewis Acid Induced Anomerization of Se-Glycosides. Application to Synthesis of α-Se-GalCer.
Organic letters, 2016, 18, 552-555
1542307 CIFC22 H18 N2 O3C 1 2/c 123.4378; 11.3628; 14.9029
90; 117.124; 90		3532.43Fox, J. C.; Gilligan, R. E.; Pitts, A. K.; Bennett, H. R.; Gaunt, M. J.
The total synthesis of K-252c (staurosporinone) via a sequential C–H functionalisation strategy
Chem. Sci., 2016, 7, 2706
1542308 CIFC14 H10 Br N O4 SP -17.608; 9.473; 9.93
99.76; 96.941; 90.08		700Maji, Arun; Bhaskararao, Bangaru; Singha, Santanu; Sunoj, Raghavan B.; Maiti, Debabrata
Directing group assisted meta-hydroxylation by C–H activation
Chem. Sci., 2016, 7, 3147
1542309 CIFC16 H12 F N O5 SP -18.087; 8.59; 11.637
87.857; 79.184; 79.188		779.9Maji, Arun; Bhaskararao, Bangaru; Singha, Santanu; Sunoj, Raghavan B.; Maiti, Debabrata
Directing group assisted meta-hydroxylation by C–H activation
Chem. Sci., 2016, 7, 3147
1542310 CIFC16 H12 Cl2 N O5 SP 21 21 215.327; 15.367; 19.69
90; 90; 90		1611.8Maji, Arun; Bhaskararao, Bangaru; Singha, Santanu; Sunoj, Raghavan B.; Maiti, Debabrata
Directing group assisted meta-hydroxylation by C‒H activation
Chem. Sci., 2016, 7, 3147
1542311 CIFC45.5 H52.5 N6 O1.5 ZnP 1 21 18.3889; 21.3112; 11.195
90; 93.127; 90		1998.43Black, Samuel P.; Wood, Daniel M.; Schwarz, Felix B.; Ronson, Tanya K.; Holstein, Julian J.; Stefankiewicz, Artur R.; Schalley, Christoph A.; Sanders, Jeremy. K. M.; Nitschke, Jonathan R.
Catenation and encapsulation induce distinct reconstitutions within a dynamic library of mixed-ligand Zn4L6cages
Chem. Sci., 2016, 7, 2614
1542312 CIFC230 H132 F24 N37 O28 P3 S2 Zn4P 1 21/c 129.307; 45.11; 26.896
90; 91.52; 90		35545Black, Samuel P.; Wood, Daniel M.; Schwarz, Felix B.; Ronson, Tanya K.; Holstein, Julian J.; Stefankiewicz, Artur R.; Schalley, Christoph A.; Sanders, Jeremy. K. M.; Nitschke, Jonathan R.
Catenation and encapsulation induce distinct reconstitutions within a dynamic library of mixed-ligand Zn4L6cages
Chem. Sci., 2016, 7, 2614
1542313 CIFC350 H327 F24 N51 O27 S8 Zn10P -3 c 135.224; 35.224; 43.354
90; 90; 120		46584Black, Samuel P.; Wood, Daniel M.; Schwarz, Felix B.; Ronson, Tanya K.; Holstein, Julian J.; Stefankiewicz, Artur R.; Schalley, Christoph A.; Sanders, Jeremy. K. M.; Nitschke, Jonathan R.
Catenation and encapsulation induce distinct reconstitutions within a dynamic library of mixed-ligand Zn4L6cages
Chem. Sci., 2016, 7, 2614
1542314 CIFC29 H38 O8P 41 21 215.0258; 15.0258; 24.0607
90; 90; 90		5432.3Chen, Chien-Chih; Tzeng, Tsai-Teng; Chen, Chin-Chu; Ni, Ching-Li; Lee, Li-Ya; Chen, Wan-Ping; Shiao, Young-Ji; Shen, Chien-Chang
Erinacine S, a Rare Sesterterpene from the Mycelia of Hericium erinaceus.
Journal of natural products, 2016, 79, 438-441
1542315 CIFC32 H30 N4 O6P 1 21/c 111.84; 10.52; 23.1
90; 96.951; 90		2856.1Ghorai, Anupam; Mondal, Jahangir; Saha, Rajat; Bhattacharya, Sumantra; Patra, Goutam K.
A highly sensitive reversible fluorescent-colorimetric azino bis-Schiff base sensor for rapid detection of Pb2+in aqueous media
Anal. Methods, 2016, 8, 2032
1542316 CIFC12 H32 Ge13.75 N2 O31 Si1.25P n m a16.8108; 19.7138; 23.9394
90; 90; 90		7933.6Liang, Jie; Xia, Wei; Sun, Junliang; Su, Jie; Dou, Maofeng; Zou, Ruqiang; Liao, Fuhui; Wang, Yingxia; Lin, Jianhua
A multi-dimensional quasi-zeolite with 12 ×10 ×7-ring channels demonstrates high thermal stability and good gas adsorption selectivity
Chem. Sci., 2016, 7, 3025
1542317 CIFC18 H18 Cl N O SP -16.3258; 8.2673; 16.726
78.52; 85.68; 79.53		842.3Wan, Jie-Ping; Zhong, Shanshan; Xie, Lili; Cao, Xiaoji; Liu, Yunyun; Wei, Li
KIO3-Catalyzed Aerobic Cross-Coupling Reactions of Enaminones and Thiophenols: Synthesis of Polyfunctionalized Alkenes by Metal-Free C-H Sulfenylation.
Organic letters, 2016, 18, 584-587
1542318 CIFC20 H32 O2P 21 21 2111.1378; 11.3745; 13.5667
90; 90; 90		1718.72Barton, Naomi A.; Marsh, Benjamin J.; Lewis, William; Narraidoo, Nathalie; Seymour, Graham B.; Fray, Rupert; Hayes, Christopher J.
Accessing low-oxidation state taxanes: is taxadiene-4(5)-epoxide on the taxol biosynthetic pathway?
Chem. Sci., 2016, 7, 3102
1542319 CIFC24 H20 La N O9C 1 c 118.4394; 13.7828; 8.116
90; 92.319; 90		2060.96Gong, Yun-Nan; Ouyang, Ting; He, Chun-Ting; Lu, Tong-Bu
Photoinduced water oxidation by an organic ligand incorporated into the framework of a stable metal‒organic framework
Chem. Sci., 2016, 7, 1070
1542320 CIFC85 H121.5 Fe2 N3.5 O6P 1 21/c 115.518; 20.0893; 26.9179
90; 104.175; 90		8136Wong, Janice L.; Higgins, Robert F.; Bhowmick, Indrani; Cao, David Xi; Szigethy, Géza; Ziller, Joseph W.; Shores, Matthew P.; Heyduk, Alan F.
Bimetallic iron‒iron and iron‒zinc complexes of the redox-active ONO pincer ligand
Chem. Sci., 2016, 7, 1594
1542321 CIFC84 H120 Fe N3 O6 ZnP 1 21/c 115.5857; 20.1236; 26.8587
90; 104.233; 90		8165.4Wong, Janice L.; Higgins, Robert F.; Bhowmick, Indrani; Cao, David Xi; Szigethy, Géza; Ziller, Joseph W.; Shores, Matthew P.; Heyduk, Alan F.
Bimetallic iron‒iron and iron‒zinc complexes of the redox-active ONO pincer ligand
Chem. Sci., 2016, 7, 1594
1542322 CIFC41.5 H54 N4 O2 ZnP 1 21 114.208; 20.222; 14.512
90; 108.954; 90		3943.4Wong, Janice L.; Higgins, Robert F.; Bhowmick, Indrani; Cao, David Xi; Szigethy, Géza; Ziller, Joseph W.; Shores, Matthew P.; Heyduk, Alan F.
Bimetallic iron‒iron and iron‒zinc complexes of the redox-active ONO pincer ligand
Chem. Sci., 2016, 7, 1594
1542323 CIFC68 H37 Co N19P n a 2118.9411; 8.6917; 33.5158
90; 90; 90		5517.7Zhang, Xuan; Wang, Zhao-Xi; Xie, Haomiao; Li, Ming-Xing; Woods, Toby J.; Dunbar, Kim R.
A cobalt(ii) spin-crossover compound with partially charged TCNQ radicals and an anomalous conducting behavior
Chem. Sci., 2016, 7, 1569
1542324 CIFC68 H37 Co N19P n a 2119.087; 8.742; 33.634
90; 90; 90		5612Zhang, Xuan; Wang, Zhao-Xi; Xie, Haomiao; Li, Ming-Xing; Woods, Toby J.; Dunbar, Kim R.
A cobalt(ii) spin-crossover compound with partially charged TCNQ radicals and an anomalous conducting behavior
Chem. Sci., 2016, 7, 1569
1542325 CIFC68 H37 Co N19P n a 2118.969; 8.681; 33.397
90; 90; 90		5499Zhang, Xuan; Wang, Zhao-Xi; Xie, Haomiao; Li, Ming-Xing; Woods, Toby J.; Dunbar, Kim R.
A cobalt(ii) spin-crossover compound with partially charged TCNQ radicals and an anomalous conducting behavior
Chem. Sci., 2016, 7, 1569
1542326 CIFC68 H37 Co N19P n a 2119.2853; 8.727; 33.589
90; 90; 90		5653.1Zhang, Xuan; Wang, Zhao-Xi; Xie, Haomiao; Li, Ming-Xing; Woods, Toby J.; Dunbar, Kim R.
A cobalt(ii) spin-crossover compound with partially charged TCNQ radicals and an anomalous conducting behavior
Chem. Sci., 2016, 7, 1569
1542327 CIFC68 H37 Co N19P n a 2118.967; 8.6864; 33.532
90; 90; 90		5524.6Zhang, Xuan; Wang, Zhao-Xi; Xie, Haomiao; Li, Ming-Xing; Woods, Toby J.; Dunbar, Kim R.
A cobalt(ii) spin-crossover compound with partially charged TCNQ radicals and an anomalous conducting behavior
Chem. Sci., 2016, 7, 1569
1542328 CIFC68 H37 Co N19P n a 2119.074; 8.705; 33.611
90; 90; 90		5581Zhang, Xuan; Wang, Zhao-Xi; Xie, Haomiao; Li, Ming-Xing; Woods, Toby J.; Dunbar, Kim R.
A cobalt(ii) spin-crossover compound with partially charged TCNQ radicals and an anomalous conducting behavior
Chem. Sci., 2016, 7, 1569
1542329 CIFC38 H52 Br2 S4P 1 21/c 122.597; 8.0328; 20.9789
90; 98.073; 90		3770.3Keerthi, Ashok; An, Cunbin; Li, Mengmeng; Marszalek, Tomasz; Ricciardulli, Antonio Gaetano; Radha, Boya; Alsewailem, Fares D.; Müllen, Klaus; Baumgarten, Martin
Dithieno[2,3-d;2′,3′-d]benzo[2,1-b;3,4-b‘]dithiophene: a novel building-block for a planar copolymer
Polym. Chem., 2016, 7, 1545
1542330 CIFC15 H9 N O3P 1 21/c 17.8507; 16.361; 9.826
90; 107.13; 90		1206.1Koleva, B. B.; Nikolova, R.; Zareva, S.; Kolev, T.; Mayer-Figge, H.; Sheldrick, W. S.
Crystal structure of 4-isonicotinoyl coumarin
X-ray Structure Analysis Online, 2010, 26, 27-28
1542331 CIFC7 H11 F6 I2 N2 PP 1 21/c 111.5373; 8.6305; 15.377
90; 107.141; 90		1463.12Mukai, Tomohiro; Nishikawa, Keiko
Halogen Bonding and Hydrogen Bonding in 4,5-Diiodo-3-methyl-1-propylimidazolium Hexafluorophosphate
X-ray Structure Analysis Online, 2010, 26, 39-40
1542332 CIFC16 H17 O4 PP 1 21 18.4621; 10.291; 8.8558
90; 105.314; 90		743.81Bigler, Raphael; Mezzetti, Antonio
Highly Enantioselective Transfer Hydrogenation of Polar Double Bonds by Macrocyclic Iron(II)/(NH)2P2Catalysts
Organic Process Research & Development, 2016, 20, 253
1542333 CIFC32 H32 O6 P2P 18.4358; 8.6021; 9.8323
104.212; 98.226; 96.026		677.2Bigler, Raphael; Mezzetti, Antonio
Highly Enantioselective Transfer Hydrogenation of Polar Double Bonds by Macrocyclic Iron(II)/(NH)2P2Catalysts
Organic Process Research & Development, 2016, 20, 253
1542334 CIFC47.5 H34.25 F12 N10.75 P2 RuP 1 21/c 120.7004; 32.7257; 14.3246
90; 107.689; 90		9245.2Poynton, Fergus E.; Hall, James P.; Keane, Páraic M.; Schwarz, Christine; Sazanovich, Igor V.; Towrie, Michael; Gunnlaugsson, Thorfinnur; Cardin, Christine J.; Cardin, David J.; Quinn, Susan J.; Long, Conor; Kelly, John M.
Direct observation by time-resolved infrared spectroscopy of the bright and the dark excited states of the [Ru(phen)2(dppz)]2+light-switch compound in solution and when bound to DNA
Chem. Sci., 2016, 7, 3075
1542335 CIFC33 H34.5 Cl2.5 Cu F6 N3 O4 PP 1 21/c 114.59; 17.504; 28.499
90; 101.456; 90		7133Lewis, J. E. M.; Bordoli, R. J.; Denis, M.; Fletcher, C. J.; Galli, M.; Neal, E. A.; Rochette, E. M.; Goldup, S. M.
High yielding synthesis of 2,2′-bipyridine macrocycles, versatile intermediates in the synthesis of rotaxanes
Chem. Sci., 2016, 7, 3154
1542336 CIFC60 H60 N4 O8P -19.688; 11.374; 13.628
100.535; 110.126; 109.435		1252.4Lewis, J. E. M.; Bordoli, R. J.; Denis, M.; Fletcher, C. J.; Galli, M.; Neal, E. A.; Rochette, E. M.; Goldup, S. M.
High yielding synthesis of 2,2′-bipyridine macrocycles, versatile intermediates in the synthesis of rotaxanes
Chem. Sci., 2016, 7, 3154
1542337 CIFC61 H75 Cl2 N5 O5P 1 21/c 110.1938; 25.558; 21.504
90; 91.243; 90		5601.2Lewis, J. E. M.; Bordoli, R. J.; Denis, M.; Fletcher, C. J.; Galli, M.; Neal, E. A.; Rochette, E. M.; Goldup, S. M.
High yielding synthesis of 2,2′-bipyridine macrocycles, versatile intermediates in the synthesis of rotaxanes
Chem. Sci., 2016, 7, 3154
1542338 CIF
HKL		C414 H324P -121.4238; 24.3862; 32.254
78.729; 76.442; 69.579		15231.9Daniel Beaudoin; Olivier Levasseur-Grenon; Thierry Maris; James D. Wuest
Building Giant Carbocycles by Reversible C-C Bond Formation
Angew. Chem. Int. Ed., 2016, 55, 894-898
1542339 CIF
HKL		C340 H338C 1 2/c 140.4249; 19.5832; 34.5941
90; 104.404; 90		26525.6Daniel Beaudoin; Olivier Levasseur-Grenon; Thierry Maris; James D. Wuest
Building Giant Carbocycles by Reversible C-C Bond Formation
Angew. Chem. Int. Ed., 2016, 55, 894-898
1542340 CIF
HKL		C388 H398P -119.769; 20.688; 21.451
99.349; 97.218; 114.704		7678.8Daniel Beaudoin; Olivier Levasseur-Grenon; Thierry Maris; James D. Wuest
Building Giant Carbocycles by Reversible C-C Bond Formation
Angew. Chem. Int. Ed., 2016, 55, 894-898
1542341 CIFC19 H16 F4 N2P 1 21/n 112.3203; 6.9979; 19.3532
90; 102.017; 90		1632Charpentier, Julie; Früh, Natalja; Foser, Simon; Togni, Antonio
Tandem Radical Fluoroalkylation-Cyclization: Synthesis of Tetrafluoro Imidazopyridines.
Organic letters, 2016, 18, 756-759
1542342 CIFC10 H12 F4 N2 OP b c a7.1579; 12.4992; 24.3054
90; 90; 90		2174.6Charpentier, Julie; Früh, Natalja; Foser, Simon; Togni, Antonio
Tandem Radical Fluoroalkylation-Cyclization: Synthesis of Tetrafluoro Imidazopyridines.
Organic letters, 2016, 18, 756-759
1542343 CIFC14 H10 F4 N2P 1 21/n 110.869; 18.902; 12.575
90; 108.712; 90		2446.9Charpentier, Julie; Früh, Natalja; Foser, Simon; Togni, Antonio
Tandem Radical Fluoroalkylation-Cyclization: Synthesis of Tetrafluoro Imidazopyridines.
Organic letters, 2016, 18, 756-759
1542344 CIFC10 H8 F4 N2 O2P 42/n20.0066; 20.0066; 5.3686
90; 90; 90		2148.86Charpentier, Julie; Früh, Natalja; Foser, Simon; Togni, Antonio
Tandem Radical Fluoroalkylation-Cyclization: Synthesis of Tetrafluoro Imidazopyridines.
Organic letters, 2016, 18, 756-759
1542345 CIFC21 H26 F3 Ir N2 O4 SiC 1 2/c 128.294; 11.04; 15.2266
90; 111.304; 90		4431.3Julián, Alejandro; Jaseer, E. A.; Garcés, Karin; Fernández-Alvarez, Francisco J.; García-Orduña, Pilar; Lahoz, Fernando J.; Oro, Luis A.
Tuning the activity and selectivity of iridium-NSiN catalyzed CO2hydrosilylation processes
Catal. Sci. Technol., 2016, 6, 4410
1542346 CIFC151 H146 Cl6 N8 O12P -114.438; 15.006; 16.156
104.214; 92.043; 94.227		3379Katoono, Ryo; Kawai, Shunsuke; Suzuki, Takanori
Dynamic helical cyclophanes with two quadruply-bridged planes arranged in an “obverse and/or reverse” relation
Chem. Sci., 2016, 7, 3240
1542347 CIFC22 H23 B F3 NP -110.2818; 13.605; 14.1948
75.66; 74.772; 86.297		1856.21Yuan, Kang; Suzuki, Naoya; Mellerup, Soren K.; Wang, Xiang; Yamaguchi, Shigehiro; Wang, Suning
Pyridyl Directed Catalyst-Free trans-Hydroboration of Internal Alkynes.
Organic letters, 2016, 18, 720-723
1542348 CIFC25 H28 B Fe NP 1 21/c 117.9223; 15.0483; 14.7492
90; 103.949; 90		3860.6Yuan, Kang; Suzuki, Naoya; Mellerup, Soren K.; Wang, Xiang; Yamaguchi, Shigehiro; Wang, Suning
Pyridyl Directed Catalyst-Free trans-Hydroboration of Internal Alkynes.
Organic letters, 2016, 18, 720-723
1542349 CIFC22 H26 B NP -18.7114; 9.6629; 10.9661
107.461; 90.795; 100.807		862.52Yuan, Kang; Suzuki, Naoya; Mellerup, Soren K.; Wang, Xiang; Yamaguchi, Shigehiro; Wang, Suning
Pyridyl Directed Catalyst-Free trans-Hydroboration of Internal Alkynes.
Organic letters, 2016, 18, 720-723
1542350 CIFC21 H24 B NP 1 21/c 17.5492; 15.7188; 13.8319
90; 95.749; 90		1633.1Yuan, Kang; Suzuki, Naoya; Mellerup, Soren K.; Wang, Xiang; Yamaguchi, Shigehiro; Wang, Suning
Pyridyl Directed Catalyst-Free trans-Hydroboration of Internal Alkynes.
Organic letters, 2016, 18, 720-723
1542351 CIFC18 H28 B N SiP 21 21 216.6373; 9.5044; 27.3003
90; 90; 90		1722.2Yuan, Kang; Suzuki, Naoya; Mellerup, Soren K.; Wang, Xiang; Yamaguchi, Shigehiro; Wang, Suning
Pyridyl Directed Catalyst-Free trans-Hydroboration of Internal Alkynes.
Organic letters, 2016, 18, 720-723
1542352 CIFC52 H72 N4 O19P 111.4197; 15.8645; 16.2611
66.72; 86.95; 71.548		2558.26Widlicka, Daniel W.; Murray, John C.; Coffman, Karen J.; Xiao, Chunguang; Brodney, Michael A.; Rainville, Joseph P.; Samas, Brian
Two Routes to 4-Fluorobenzisoxazol-3-one in the Synthesis of a 5-HT4Partial Agonist
Organic Process Research & Development, 2016, 20, 233
1542353 CIFC28 H41 B F4 Fe N3 O PP 1 21/c 117.888; 8.6252; 21.0338
90; 111.094; 90		3027.8Butschke, B.; Feller, M.; Diskin-Posner, Y.; Milstein, D.
Ketone hydrogenation catalyzed by a new iron(ii)‒PNN complex
Catal. Sci. Technol., 2016, 6, 4428
1542354 CIFC23 H28 Cl Co F6 N5 O3 PP 1 21/c 16.9686; 22.9724; 17.7667
90; 96.495; 90		2825.9Basu, Debashis; Mazumder, Shivnath; Niklas, Jens; Baydoun, Habib; Wanniarachchi, Dakshika; Shi, Xuetao; Staples, Richard J.; Poluektov, Oleg; Schlegel, H. Bernhard; Verani, Cláudio N.
Evaluation of the coordination preferences and catalytic pathways of heteroaxial cobalt oximes towards hydrogen generation
Chem. Sci., 2016, 7, 3264
1542355 CIFC21 H34 Cl3 Co F6 N5 O2 PI -428.715; 28.715; 7.0017
90; 90; 90		5773.3Basu, Debashis; Mazumder, Shivnath; Niklas, Jens; Baydoun, Habib; Wanniarachchi, Dakshika; Shi, Xuetao; Staples, Richard J.; Poluektov, Oleg; Schlegel, H. Bernhard; Verani, Cláudio N.
Evaluation of the coordination preferences and catalytic pathways of heteroaxial cobalt oximes towards hydrogen generation
Chem. Sci., 2016, 7, 3264
1542356 CIFC20 H30 Co N5 O2C 1 2/c 114.9757; 10.6987; 24.941
90; 98.286; 90		3954.3Basu, Debashis; Mazumder, Shivnath; Niklas, Jens; Baydoun, Habib; Wanniarachchi, Dakshika; Shi, Xuetao; Staples, Richard J.; Poluektov, Oleg; Schlegel, H. Bernhard; Verani, Cláudio N.
Evaluation of the coordination preferences and catalytic pathways of heteroaxial cobalt oximes towards hydrogen generation
Chem. Sci., 2016, 7, 3264
1542357 CIFC30 H49 Co F12 N6 O3 P2P 1 21/n 112.5242; 16.7919; 18.462
90; 91.466; 90		3881.4Basu, Debashis; Mazumder, Shivnath; Niklas, Jens; Baydoun, Habib; Wanniarachchi, Dakshika; Shi, Xuetao; Staples, Richard J.; Poluektov, Oleg; Schlegel, H. Bernhard; Verani, Cláudio N.
Evaluation of the coordination preferences and catalytic pathways of heteroaxial cobalt oximes towards hydrogen generation
Chem. Sci., 2016, 7, 3264
1542358 CIFC62 H57 Cl2 F12 Mn N15 O3 P2 Ru2P -114.6868; 15.5818; 17.997
69.889; 66.513; 67.869		3406.9Mognon, Lorenzo; Mandal, Sukanta; Castillo, Carmen E.; Fortage, Jérôme; Molton, Florian; Aromí, Guillem; Benet-Buchhlolz, Jordi; Collomb, Marie-Noëlle; Llobet, Antoni
Synthesis, structure, spectroscopy and reactivity of new heterotrinuclear water oxidation catalysts
Chem. Sci., 2016, 7, 3304
1542359 CIFC61 H50 F12 Mn N14 O5 P2 Ru2P -114.471; 15.501; 16.913
114.334; 112.431; 91.203		3122.9Mognon, Lorenzo; Mandal, Sukanta; Castillo, Carmen E.; Fortage, Jérôme; Molton, Florian; Aromí, Guillem; Benet-Buchhlolz, Jordi; Collomb, Marie-Noëlle; Llobet, Antoni
Synthesis, structure, spectroscopy and reactivity of new heterotrinuclear water oxidation catalysts
Chem. Sci., 2016, 7, 3304
1542360 CIFC16.75 H13.75 N2.25 O1.5C 1 2/c 120.3857; 5.1021; 26.5935
90; 95.583; 90		2752.9Li, Zi; Matzger, Adam J.
Influence of Coformer Stoichiometric Ratio on Pharmaceutical Cocrystal Dissolution: Three Cocrystals of Carbamazepine/4-Aminobenzoic Acid.
Molecular pharmaceutics, 2016, 13, 990-995
1542361 CIFC23 H15 N S2P 1 21/n 114.4216; 5.8914; 20.5783
90; 100.344; 90		1719.99Irgashev, Roman A.; Karmatsky, Arseny A.; Rusinov, Gennady L.; Charushin, Valery N.
Construction of Heteroacenes with Fused Thiophene and Pyrrole Rings via the Fischer Indolization Reaction.
Organic letters, 2016, 18, 804-807
1542362 CIFC25 H18 Br N O4P 1 21 110.4822; 5.9694; 17.3911
90; 106.202; 90		1044.98Möhlmann, Lennart; Chang, Geng-Hua; Madhusudhan Reddy, G.; Lee, Chia-Jui; Lin, Wenwei
Organocatalytic Enantioselective Synthesis of Tetrahydrofluoren-9-ones via Vinylogous Michael Addition/Henry Reaction Cascade of 1,3-Indandione-Derived Pronucleophiles.
Organic letters, 2016, 18, 688-691
1542363 CIFC26 H20 Br N O4P 1 21 110.763; 20.038; 11.832
90; 117.008; 90		2274Möhlmann, Lennart; Chang, Geng-Hua; Madhusudhan Reddy, G.; Lee, Chia-Jui; Lin, Wenwei
Organocatalytic Enantioselective Synthesis of Tetrahydrofluoren-9-ones via Vinylogous Michael Addition/Henry Reaction Cascade of 1,3-Indandione-Derived Pronucleophiles.
Organic letters, 2016, 18, 688-691
1542364 CIFC33 H33 N O8 SP -19.1909; 11.4084; 14.6334
86.77; 83.447; 87.553		1520.9Möhlmann, Lennart; Chang, Geng-Hua; Madhusudhan Reddy, G.; Lee, Chia-Jui; Lin, Wenwei
Organocatalytic Enantioselective Synthesis of Tetrahydrofluoren-9-ones via Vinylogous Michael Addition/Henry Reaction Cascade of 1,3-Indandione-Derived Pronucleophiles.
Organic letters, 2016, 18, 688-691
1542365 CIFC22 H17 F O3 SP -15.7185; 11.8378; 13.7061
79.111; 86.121; 80.29		897.45Xiong, Rui; Patel, Hitisha K.; Gutgesell, Lauren M.; Zhao, Jiong; Delgado-Rivera, Loruhama; Pham, Thao N. D.; Zhao, Huiping; Carlson, Kathryn; Martin, Teresa; Katzenellenbogen, John A.; Moore, Terry W.; Tonetti, Debra A.; Thatcher, Gregory R. J.
Selective Human Estrogen Receptor Partial Agonists (ShERPAs) for Tamoxifen-Resistant Breast Cancer.
Journal of medicinal chemistry, 2016, 59, 219-237
1542366 CIFC22 H36 Cl3 P RuP -17.6344; 10.5128; 15.3514
103.182; 92.237; 90.962		1198.29González-Fernández, Rebeca; González-Liste, Pedro J.; Borge, Javier; Crochet, Pascale; Cadierno, Victorio
Chlorophosphines as auxiliary ligands in ruthenium-catalyzed nitrile hydration reactions: application to the preparation of β-ketoamides
Catal. Sci. Technol., 2016, 6, 4398
1542367 CIFC24 H23 Cl2 F6 O P RuP 1 21/c 16.8231; 11.2772; 33.5183
90; 91.031; 90		2578.66González-Fernández, Rebeca; González-Liste, Pedro J.; Borge, Javier; Crochet, Pascale; Cadierno, Victorio
Chlorophosphines as auxiliary ligands in ruthenium-catalyzed nitrile hydration reactions: application to the preparation of β-ketoamides
Catal. Sci. Technol., 2016, 6, 4398
1542368 CIFC19 H12 N2 O4P -17.1803; 8.0598; 13.9214
98.659; 92.733; 108.798		750Manjappa, Kiran B.; Syu, Jia-Ru; Yang, Ding-Yah
Visible-Light-Promoted and Yb(OTf)3-Catalyzed Constructions of Coumarin-Pyrrole-(Iso)quinoline-Fused Pentacycles: Synthesis of Lamellarin Core, Lamellarin D Trimethyl Ether, and Lamellarin H.
Organic letters, 2016, 18, 332-335
1542369 CIFC25 H15 N O2P n m a23.3899; 6.7857; 11.147
90; 90; 90		1769.22Manjappa, Kiran B.; Syu, Jia-Ru; Yang, Ding-Yah
Visible-Light-Promoted and Yb(OTf)3-Catalyzed Constructions of Coumarin-Pyrrole-(Iso)quinoline-Fused Pentacycles: Synthesis of Lamellarin Core, Lamellarin D Trimethyl Ether, and Lamellarin H.
Organic letters, 2016, 18, 332-335
1542370 CIFC19 H11 N O2P 21 21 214.5729; 14.7748; 19.072
90; 90; 90		1288.6Manjappa, Kiran B.; Syu, Jia-Ru; Yang, Ding-Yah
Visible-Light-Promoted and Yb(OTf)3-Catalyzed Constructions of Coumarin-Pyrrole-(Iso)quinoline-Fused Pentacycles: Synthesis of Lamellarin Core, Lamellarin D Trimethyl Ether, and Lamellarin H.
Organic letters, 2016, 18, 332-335
1542371 CIFC25.5 H16 Cl N O2C 1 2/c 124.07; 7.6955; 22.2172
90; 117.372; 90		3654.6Manjappa, Kiran B.; Syu, Jia-Ru; Yang, Ding-Yah
Visible-Light-Promoted and Yb(OTf)3-Catalyzed Constructions of Coumarin-Pyrrole-(Iso)quinoline-Fused Pentacycles: Synthesis of Lamellarin Core, Lamellarin D Trimethyl Ether, and Lamellarin H.
Organic letters, 2016, 18, 332-335
1542372 CIFC25 H19 N3 O2P 1 21/n 110.3444; 7.3472; 25.724
90; 97.771; 90		1937.1Thikekar, Tushar Ulhas; Selvaraju, Manikandan; Sun, Chung-Ming
Skeletally Diverse Synthesis of Indole-Fused Diazocine and Diazepine Frameworks by One-Pot, Two-Component Cascade Reaction.
Organic letters, 2016, 18, 316-319
1542373 CIFC24 H18 N2 O3P n a 2110.8282; 8.7931; 19.9988
90; 90; 90		1904.15Thikekar, Tushar Ulhas; Selvaraju, Manikandan; Sun, Chung-Ming
Skeletally Diverse Synthesis of Indole-Fused Diazocine and Diazepine Frameworks by One-Pot, Two-Component Cascade Reaction.
Organic letters, 2016, 18, 316-319
1542374 CIFC23 H14 Br N3P 1 21/n 113.9894; 9.1257; 15.099
90; 108.295; 90		1830.2Thikekar, Tushar Ulhas; Selvaraju, Manikandan; Sun, Chung-Ming
Skeletally Diverse Synthesis of Indole-Fused Diazocine and Diazepine Frameworks by One-Pot, Two-Component Cascade Reaction.
Organic letters, 2016, 18, 316-319
1542375 CIFC11 H19 N O SP 1 21/c 119.131; 6.3759; 9.3218
90; 90.05; 90		1137Wei, Jianpeng; Li, Yiming; Jiang, Xuefeng
Aqueous Compatible Protocol to Both Alkyl and Aryl Thioamide Synthesis.
Organic letters, 2016, 18, 340-343
1542376 CIFC9 H8 Br N SP n m a12.7114; 7.4836; 10.6854
90; 90; 90		1016.47Wei, Jianpeng; Li, Yiming; Jiang, Xuefeng
Aqueous Compatible Protocol to Both Alkyl and Aryl Thioamide Synthesis.
Organic letters, 2016, 18, 340-343
1542377 CIFC28 H31 N5 O5P 21 21 2112.6023; 13.271; 15.6239
90; 90; 90		2613.02Yu, Guihong; Zhou, Guoliang; Zhu, Meilin; Wang, Wei; Zhu, Tianjiao; Gu, Qianqun; Li, Dehai
Neosartoryadins A and B, Fumiquinazoline Alkaloids from a Mangrove-Derived Fungus Neosartorya udagawae HDN13-313.
Organic letters, 2016, 18, 244-247
1542378 CIFC19 H18 Cl2 N2 O3 SP 1 21/c 115.0536; 11.1765; 11.8469
90; 107.065; 90		1905.44He, Qun; Wu, Liang; Kou, Xuezhen; Butt, Nicholas; Yang, Guoqiang; Zhang, Wanbin
Pd(II)-Catalyzed Asymmetric Addition of Arylboronic Acids to Isatin-Derived Ketimines.
Organic letters, 2016, 18, 288-291
1542379 CIFC25.5 H25 Cl3 N2 O3 SP 21 21 219.4307; 15.3888; 35.4348
90; 90; 90		5142.6He, Qun; Wu, Liang; Kou, Xuezhen; Butt, Nicholas; Yang, Guoqiang; Zhang, Wanbin
Pd(II)-Catalyzed Asymmetric Addition of Arylboronic Acids to Isatin-Derived Ketimines.
Organic letters, 2016, 18, 288-291
1542380 CIFC16 H20 O8C 1 2/c 118.5685; 6.67667; 13.82
90; 108.928; 90		1620.7Tortoreto, Cecilia; Achard, Thierry; Egger, Léo; Guénée, Laure; Lacour, Jérôme
Synthesis of Spiro Ketals, Orthoesters, and Orthocarbonates by CpRu-Catalyzed Decomposition of α-Diazo-β-ketoesters.
Organic letters, 2016, 18, 240-243
1542381 CIFC16 H20 O8P 1 21/n 19.60173; 12.9474; 13.2032
90; 97.478; 90		1627.43Tortoreto, Cecilia; Achard, Thierry; Egger, Léo; Guénée, Laure; Lacour, Jérôme
Synthesis of Spiro Ketals, Orthoesters, and Orthocarbonates by CpRu-Catalyzed Decomposition of α-Diazo-β-ketoesters.
Organic letters, 2016, 18, 240-243
1542382 CIFC31 H27 N O3 SeP -16.8204; 13.7059; 14.4554
72.804; 87.405; 88.793		1289.5Tang, E.; Wang, Weilin; Zhao, Yinjiao; Zhang, Meng; Dai, Xin
Catalytic and Atom-Economic Intermolecular Amidoselenenylation of Alkenes.
Organic letters, 2016, 18, 176-179
1542383 CIFC62 H71 Cl3 O8P 21 21 2110.3434; 17.047; 30.5673
90; 90; 90		5389.7Li, Chuang-Jun; Ma, Jie; Sun, Hua; Zhang, Dan; Zhang, Dong-Ming
Guajavadimer A, a Dimeric Caryophyllene-Derived Meroterpenoid with a New Carbon Skeleton from the Leaves of Psidium guajava.
Organic letters, 2016, 18, 168-171
1542384 CIFC35 H46 O6P 1 1 219.7832; 24.3518; 27.7523
90; 90; 90		6611.7Cao, Jia-Qing; Huang, Xiao-Jun; Li, Yu-Ting; Wang, Ying; Wang, Lei; Jiang, Ren-Wang; Ye, Wen-Cai
Callistrilones A and B, Triketone-Phloroglucinol-Monoterpene Hybrids with a New Skeleton from Callistemon rigidus.
Organic letters, 2016, 18, 120-123
1542385 CIFC34 H44 O7P 21 21 216.4131; 14.8983; 32.7256
90; 90; 90		3126.7Cao, Jia-Qing; Huang, Xiao-Jun; Li, Yu-Ting; Wang, Ying; Wang, Lei; Jiang, Ren-Wang; Ye, Wen-Cai
Callistrilones A and B, Triketone-Phloroglucinol-Monoterpene Hybrids with a New Skeleton from Callistemon rigidus.
Organic letters, 2016, 18, 120-123
1542386 CIFC21 H28 O4P 1 21 18.8562; 9.9924; 11.4351
90; 105.077; 90		977.11Cao, Jia-Qing; Huang, Xiao-Jun; Li, Yu-Ting; Wang, Ying; Wang, Lei; Jiang, Ren-Wang; Ye, Wen-Cai
Callistrilones A and B, Triketone-Phloroglucinol-Monoterpene Hybrids with a New Skeleton from Callistemon rigidus.
Organic letters, 2016, 18, 120-123
1542387 CIFC10 H16 N4 O5P b c n14.614; 12.706; 13.842
90; 90; 90		2570.3Zheng, Jing; Qi, Jifeng; Cui, Sunliang
Fe-Catalyzed Olefin Hydroamination with Diazo Compounds for Hydrazone Synthesis.
Organic letters, 2016, 18, 128-131
1542388 CIFC12 H14 N2 O2P 1 21/c 122.2134; 5.773; 19.6734
90; 115.56; 90		2276Zheng, Jing; Qi, Jifeng; Cui, Sunliang
Fe-Catalyzed Olefin Hydroamination with Diazo Compounds for Hydrazone Synthesis.
Organic letters, 2016, 18, 128-131
1542389 CIFC27 H21 NP 1 21/n 19.829; 17.878; 11.147
90; 102.8; 90		1910.1Xiang, Jia-Chen; Wang, Miao; Cheng, Yan; Wu, An-Xin
Molecular Iodine-Mediated Chemoselective Synthesis of Multisubstituted Pyridines through Catabolism and Reconstruction Behavior of Natural Amino Acids.
Organic letters, 2016, 18, 24-27
1542390 CIFC29 H38 O13P 1 21 19.4429; 7.8615; 37.294
90; 97.23; 90		2746.5Shi, Yi-Ming; Cai, Song-Liang; Li, Xiao-Nian; Liu, Miao; Shang, Shan-Zhai; Du, Xue; Xiao, Wei-Lie; Pu, Jian-Xin; Sun, Han-Dong
LC-UV-Guided Isolation and Structure Determination of Lancolide E: A Nortriterpenoid with a Tetracyclo[5.4.0.0(2,4).0(3,7)]undecane-Bridged System from a "Talented" Schisandra Plant.
Organic letters, 2016, 18, 100-103
1542391 CIFC18 H17 N O5P 1 21/c 121.3292; 8.2239; 18.2075
90; 91.151; 90		3193.1Dateer, Ramesh B.; Chang, Sukbok
Rh(III)-Catalyzed C-H Cyclization of Arylnitrones with Diazo Compounds: Access to N-Hydroxyindolines.
Organic letters, 2016, 18, 68-71
1542392 CIFC20 H17 N O5 SP 1 21/n 18.6285; 12.7114; 16.784
90; 101.358; 90		1804.8Dateer, Ramesh B.; Chang, Sukbok
Rh(III)-Catalyzed C-H Cyclization of Arylnitrones with Diazo Compounds: Access to N-Hydroxyindolines.
Organic letters, 2016, 18, 68-71
1542393 CIFC20 H22 Br O7 PP 1 21 15.575; 7.9619; 23.2886
90; 90.492; 90		1033.69Horwitz, Matthew A.; Zavesky, Blane P.; Martinez-Alvarado, Jesus I; Johnson, Jeffrey S.
Asymmetric Organocatalytic Reductive Coupling Reactions between Benzylidene Pyruvates and Aldehydes.
Organic letters, 2016, 18, 36-39
1542394 CIFC22 H27 N3 O SP 21 21 216.2177; 16.6885; 41.8862
90; 90; 90		4346.3Izquierdo, Cristina; Esteban, Francisco; Ruano, José Luis García; Fraile, Alberto; Alemán, José
Asymmetric Synthesis of 1,2-Diamines bearing Tetrasubstituted Centers from Nonstabilized Azomethine Ylides and N-Sulfinylketimines under Brønsted Acid Catalysis.
Organic letters, 2016, 18, 92-95
1542395 CIFC21 H25 N3 O SP 21 21 216.1444; 12.3333; 26.7768
90; 90; 90		2029.17Izquierdo, Cristina; Esteban, Francisco; Ruano, José Luis García; Fraile, Alberto; Alemán, José
Asymmetric Synthesis of 1,2-Diamines bearing Tetrasubstituted Centers from Nonstabilized Azomethine Ylides and N-Sulfinylketimines under Brønsted Acid Catalysis.
Organic letters, 2016, 18, 92-95
1542396 CIFC21 H16 O3P n a 218.233; 5.5792; 34.637
90; 90; 90		1591Laha, Radha M.; Khamarui, Saikat; Manna, Saikat K.; Maiti, Dilip K.
In Situ Generated Ag(II)-Catalyzed Selective Oxo-Esterification of Alkyne with Alcohol to α-Ketoester: Photophysical Study.
Organic letters, 2016, 18, 144-147
1542397 CIFC44 H30 N8 O12 ZnP 1 21/c 113.9192; 13.7516; 21.5005
90; 103.466; 90		4002.3Lephoto, Mapudumo; Nakano, Koji; Appavoo, Divambal; Owaga, Bernard; Nozaki, Kyoko; Darkwa, James
Pyrazole Supported Zinc(II) Benzoates as Catalysts for the Ring Opening Copolymerization of Cyclohexene Oxide and Carbon Dioxide
Catalysts, 2016, 6, 17
1542398 CIFC32 H47 Br O UP 21 21 2116.436; 18.645; 19.723
90; 90; 90		6044Lichtscheidl, Alejandro; Pagano, Justin; Scott, Brian; Nelson, Andrew; Kiplinger, Jaqueline
Expanding the Chemistry of Actinide Metallocene Bromides. Synthesis, Properties and Molecular Structures of the Tetravalent and Trivalent Uranium Bromide Complexes: (C5Me4R)2UBr2, (C5Me4R)2U(O-2,6-iPr2C6H3)(Br), and [K(THF)][(C5Me4R)2UBr2] (R = Me, Et)
Inorganics, 2016, 4, 1
1542399 CIFC20 H30 Br2 UF m m 214.9546; 17.323; 8.194
90; 90; 90		2122.7Lichtscheidl, Alejandro; Pagano, Justin; Scott, Brian; Nelson, Andrew; Kiplinger, Jaqueline
Expanding the Chemistry of Actinide Metallocene Bromides. Synthesis, Properties and Molecular Structures of the Tetravalent and Trivalent Uranium Bromide Complexes: (C5Me4R)2UBr2, (C5Me4R)2U(O-2,6-iPr2C6H3)(Br), and [K(THF)][(C5Me4R)2UBr2] (R = Me, Et)
Inorganics, 2016, 4, 1
1542400 CIFC24 H38 Br2 K O UC 1 c 111.0688; 29.295; 8.7573
90; 102.609; 90		2771.2Lichtscheidl, Alejandro; Pagano, Justin; Scott, Brian; Nelson, Andrew; Kiplinger, Jaqueline
Expanding the Chemistry of Actinide Metallocene Bromides. Synthesis, Properties and Molecular Structures of the Tetravalent and Trivalent Uranium Bromide Complexes: (C5Me4R)2UBr2, (C5Me4R)2U(O-2,6-iPr2C6H3)(Br), and [K(THF)][(C5Me4R)2UBr2] (R = Me, Et)
Inorganics, 2016, 4, 1
1542401 CIFC22 H34 Br2 UP 1 21/m 18.2013; 18.6785; 8.4618
90; 118.833; 90		1135.55Lichtscheidl, Alejandro; Pagano, Justin; Scott, Brian; Nelson, Andrew; Kiplinger, Jaqueline
Expanding the Chemistry of Actinide Metallocene Bromides. Synthesis, Properties and Molecular Structures of the Tetravalent and Trivalent Uranium Bromide Complexes: (C5Me4R)2UBr2, (C5Me4R)2U(O-2,6-iPr2C6H3)(Br), and [K(THF)][(C5Me4R)2UBr2] (R = Me, Et)
Inorganics, 2016, 4, 1
1542402 CIFAg1.6 As25.48 Bi2.39 Cu10.93 Hg1.88 Pb75.54 S224 Sb69.38P 1 21/n 18.178; 28.223; 42.452
90; 93.55; 90		9779Bindi, Luca; Biagioni, Cristian; Martini, Bruno; Salvetti, Adrio
Ciriottiite, Cu(Cu,Ag)3Pb19(Sb,As)22(As2)S56, the Cu-Analogue of Sterryite from the Tavagnasco Mining District, Piedmont, Italy
Minerals, 2016, 6, 8
1542403 CIFC31 H28 Cl N5 O6 S2P 21 21 215.9591; 9.2931; 55.53
90; 90; 90		3075.2Zhang, Dan-Jie; Xie, Ming-Sheng; Qu, Gui-Rong; Gao, Yao-Wei; Guo, Hai-Ming
Synthesis of Azacyclic Nucleoside Analogues via Asymmetric [3 + 2] Cycloaddition of 9-(2-Tosylvinyl)-9H-purines.
Organic letters, 2016, 18, 820-823
1542404 CIFC12 H18 Cu N O6P -17.5973; 8.106; 12.4901
89.576; 86.095; 69.787		720.03Fernandes, Tiago A.; Santos, Carla I. M.; André, Vânia; Dias, Sara S. P.; Kirillova, Marina V.; Kirillov, Alexander M.
New aqua-soluble dicopper(ii) aminoalcoholate cores for mild and water-assisted catalytic oxidation of alkanes
Catal. Sci. Technol., 2016, 6, 4584
1542405 CIFC14 H27 Cu N2 O9P 1 21/c 19.2907; 13.3305; 15.2281
90; 107.358; 90		1800.11Fernandes, Tiago A.; Santos, Carla I. M.; André, Vânia; Dias, Sara S. P.; Kirillova, Marina V.; Kirillov, Alexander M.
New aqua-soluble dicopper(ii) aminoalcoholate cores for mild and water-assisted catalytic oxidation of alkanes
Catal. Sci. Technol., 2016, 6, 4584
1542406 CIFC62 H80 N2 O2 P2 Si2 ThP n m a19.1242; 16.7581; 18.8909
90; 90; 90		6054.3Gregson, Matthew; Lu, Erli; Tuna, Floriana; McInnes, Eric J. L.; Hennig, Christoph; Scheinost, Andreas C.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Kerridge, Andrew; Liddle, Stephen T.
Emergence of comparable covalency in isostructural cerium(iv)‒ and uranium(iv)‒carbon multiple bonds
Chem. Sci., 2016, 7, 3286
1542407 CIFC59 H82 N2 O3 P2 Si2 UP n m a18.4956; 16.94471; 18.98054
90; 90; 90		5948.55Gregson, Matthew; Lu, Erli; Tuna, Floriana; McInnes, Eric J. L.; Hennig, Christoph; Scheinost, Andreas C.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Kerridge, Andrew; Liddle, Stephen T.
Emergence of comparable covalency in isostructural cerium(iv)‒ and uranium(iv)‒carbon multiple bonds
Chem. Sci., 2016, 7, 3286
1542408 CIFC17 H16 O4P 21 21 217.47301; 12.0802; 15.6344
90; 90; 90		1411.4Weldy, N. Mace; Schafer, A. G.; Owens, C. P.; Herting, C. J.; Varela-Alvarez, A.; Chen, S.; Niemeyer, Z.; Musaev, D. G.; Sigman, M. S.; Davies, H. M. L.; Blakey, S. B.
Iridium(iii)-bis(imidazolinyl)phenyl catalysts for enantioselective C–H functionalization with ethyl diazoacetate
Chem. Sci., 2016, 7, 3142
1542409 CIFC13 H7 F3 N2 OP 1 21/c 116.4147; 4.7888; 14.7033
90; 109.132; 90		1091.9Liu, Meilin; Shu, Miaomiao; Yao, Chaochao; Yin, Guodong; Wang, Dunjia; Huang, Jinkun
Synthesis of Pyrido-Fused Quinazolinone Derivatives via Copper-Catalyzed Domino Reaction.
Organic letters, 2016, 18, 824-827
1542410 CIFC21 H15 N O6P 1 21 18.0698; 6.5112; 35.008
90; 92.98; 90		1837Joshi, Prabhakar Ramchandra; Nanubolu, Jagadeesh Babu; Menon, Rajeev S.
Oxygenative and Dehydrogenative [3 + 3] Benzannulation Reactions of α,β-Unsaturated Aldehydes and γ-Phosphonyl Crotonates Mediated by Air: Regioselective Synthesis of 4-Hydroxybiaryl-2-carboxylates.
Organic letters, 2016, 18, 752-755
1542411 CIFC21 H28 O2P 1 21 110.4012; 6.5192; 12.5869
90; 94.667; 90		850.66Jiao, Wei-Hua; Shi, Guo-Hua; Xu, Ting-Ting; Chen, Guo-Dong; Gu, Bin-Bin; Wang, Zhuo; Peng, Shuang; Wang, Shu-Ping; Li, Jia; Han, Bing-Nan; Zhang, Wei; Lin, Hou-Wen
Dysiherbols A-C and Dysideanone E, Cytotoxic and NF-κB Inhibitory Tetracyclic Meroterpenes from a Dysidea sp. Marine Sponge.
Journal of natural products, 2016, 79, 406-411
1542412 CIFC32 H25 N2P 21 21 2110.6146; 13.7299; 16.5455
90; 90; 90		2411.3Han, Ya-Ping; Song, Xian-Rong; Qiu, Yi-Feng; Zhang, Heng-Rui; Li, Lian-Hua; Jin, Dong-Po; Sun, Xiao-Qing; Liu, Xue-Yuan; Liang, Yong-Min
Lewis Acid Catalyzed [4 + 3] Cycloaddition of Propargylic Alcohols with Azides.
Organic letters, 2016, 18, 940
1542413 CIFC26 H44 O2 Si2C 1 2/c 130.17; 6.495; 13.388
90; 92.76; 90		2620Lim, Hee Nam; Dong, Guangbin
Catalytic Cage Formation via Controlled Dimerization of Norbornadienes: An Entry to Functionalized HCTDs (Heptacyclo[6.6.0.0(2,6).0(3,13).0(4,11).0(5,9).0(10,14)]tetradecanes).
Organic letters, 2016, 18, 1104
1542414 CIFC32 H36P 1 21/n 115.6222; 8.3147; 19.4923
90; 111.898; 90		2349.25Lim, Hee Nam; Dong, Guangbin
Catalytic Cage Formation via Controlled Dimerization of Norbornadienes: An Entry to Functionalized HCTDs (Heptacyclo[6.6.0.0(2,6).0(3,13).0(4,11).0(5,9).0(10,14)]tetradecanes).
Organic letters, 2016, 18, 1104
1542415 CIFC19 H19 Br2 Fe N3 NiP 1 21/c 114.1412; 9.6921; 13.6154
90; 93.23; 90		1863.13Obuah, Collins; Jordaan, Johan H. L.; Darkwa, James
(Ferrocenylpyrazolyl)nickel(ii)-catalysed ethylene oligomerisation
Catal. Sci. Technol., 2016, 6, 4814
1542416 CIFC20 H19 Br2 Fe N3 NiP 1 21/c 114.2482; 9.8031; 14.1378
90; 96.793; 90		1960.86Obuah, Collins; Jordaan, Johan H. L.; Darkwa, James
(Ferrocenylpyrazolyl)nickel(ii)-catalysed ethylene oligomerisation
Catal. Sci. Technol., 2016, 6, 4814
1542417 CIFC38 H52.2 Cu F6 N4 O6.1 S2P 1 21/c 119.9909; 37.6313; 11.8656
90; 93.9256; 90		8905.4Hoffeditz, William L.; Katz, Michael J.; Deria, Pravas; Cutsail III, George E.; Pellin, Michael J.; Farha, Omar K.; Hupp, Joseph T.
One Electron Changes Everything. A Multispecies Copper Redox Shuttle for Dye-Sensitized Solar Cells
The Journal of Physical Chemistry C, 2016, 120, 3731
1542418 CIFC24 H33 N O2 SiP 1 21/n 17.0784; 8.053; 38.854
90; 91.395; 90		2214.1Ayala, Caitlan E.; Dange, Nitin S.; Stepherson, Jacob R.; Henry, Jeffrey L.; Fronczek, Frank R.; Kartika, Rendy
Functionalization of Silyldienol Ethers at the γ-Position via 2-Silyloxypentadienyl Cations.
Organic letters, 2016, 18, 1084
1542419 CIFC24 H35 N O2 SiP 1 21/c 117.0398; 9.1263; 15.8008
90; 112.88; 90		2263.9Ayala, Caitlan E.; Dange, Nitin S.; Stepherson, Jacob R.; Henry, Jeffrey L.; Fronczek, Frank R.; Kartika, Rendy
Functionalization of Silyldienol Ethers at the γ-Position via 2-Silyloxypentadienyl Cations.
Organic letters, 2016, 18, 1084
1542420 CIFC32 H25 NP -19.465; 9.827; 14.255
98.362; 100.338; 113.651		1159.5Chand, S. Sarath; Gopalan, Greeshma; Santhini, P. V.; Preethanuj, P.; John, Jubi; Harakat, Dominique; Jaroschik, Florian; Radhakrishnan, K. V.
Lewis Acid Catalyzed Regioselective Hydroheteroarylation of Pentafulvenes.
Organic letters, 2016, 18, 964
1542421 CIFC64 H42 N12P 1 21/n 115.1361; 14.6365; 22.0466
90; 98.281; 90		4833.27Zissimou, Georgia A.; Constantinides, Christos P.; Manoli, Maria; Pieridou, Galatia K.; Hayes, Sophia C.; Koutentis, Panayiotis A.
Oxidation of Tetraphenylhexaazaanthracene: Accessing a Scissor Dimer of a 16π Biscyanine.
Organic letters, 2016, 18, 1116
1542422 CIFC18 H25 N3 Ni O3P 1 21 111.854; 6.07; 12.641
90; 104.097; 90		882.2Rettenmeier, Christoph A.; Wadepohl, Hubert; Gade, Lutz H.
Electronic structure and reactivity of nickel(i) pincer complexes: their aerobic transformation to peroxo species and site selective C–H oxygenation
Chem. Sci., 2016, 7, 3533
1542423 CIFC18 H25 N3 Ni O4P 21 21 216.25709; 16.6261; 17.4692
90; 90; 90		1817.34Rettenmeier, Christoph A.; Wadepohl, Hubert; Gade, Lutz H.
Electronic structure and reactivity of nickel(i) pincer complexes: their aerobic transformation to peroxo species and site selective C–H oxygenation
Chem. Sci., 2016, 7, 3533
1542424 CIFC28 H42 N4 Ni O5P 21 21 2111.065; 13.046; 20.098
90; 90; 90		2901Rettenmeier, Christoph A.; Wadepohl, Hubert; Gade, Lutz H.
Electronic structure and reactivity of nickel(i) pincer complexes: their aerobic transformation to peroxo species and site selective C–H oxygenation
Chem. Sci., 2016, 7, 3533
1542425 CIFC25 H25 N3 Ni O4P 21 21 216.41635; 10.31527; 32.9233
90; 90; 90		2179.07Rettenmeier, Christoph A.; Wadepohl, Hubert; Gade, Lutz H.
Electronic structure and reactivity of nickel(i) pincer complexes: their aerobic transformation to peroxo species and site selective C–H oxygenation
Chem. Sci., 2016, 7, 3533
1542426 CIFC25 H23 N3 Ni O4P 21 21 2110.1489; 12.0802; 17.62895
90; 90; 90		2161.32Rettenmeier, Christoph A.; Wadepohl, Hubert; Gade, Lutz H.
Electronic structure and reactivity of nickel(i) pincer complexes: their aerobic transformation to peroxo species and site selective C–H oxygenation
Chem. Sci., 2016, 7, 3533
1542427 CIFC31 H19 N3C 1 c 116.7003; 14.0892; 9.3429
90; 96.029; 90		2186.2Zhang, Dongdong; Cai, Minghan; Bin, Zhengyang; Zhang, Yunge; Zhang, Deqiang; Duan, Lian
Highly efficient blue thermally activated delayed fluorescent OLEDs with record-low driving voltages utilizing high triplet energy hosts with small singlet–triplet splittings
Chem. Sci., 2016, 7, 3355
1542428 CIFC31 H19 N3P 1 21/c 18.4562; 7.9666; 34.004
90; 94.974; 90		2282.1Zhang, Dongdong; Cai, Minghan; Bin, Zhengyang; Zhang, Yunge; Zhang, Deqiang; Duan, Lian
Highly efficient blue thermally activated delayed fluorescent OLEDs with record-low driving voltages utilizing high triplet energy hosts with small singlet–triplet splittings
Chem. Sci., 2016, 7, 3355
1542429 CIFC31 H19 N3P 1 21/n 19.1838; 13.264; 18.172
90; 97.142; 90		2196.4Zhang, Dongdong; Cai, Minghan; Bin, Zhengyang; Zhang, Yunge; Zhang, Deqiang; Duan, Lian
Highly efficient blue thermally activated delayed fluorescent OLEDs with record-low driving voltages utilizing high triplet energy hosts with small singlet–triplet splittings
Chem. Sci., 2016, 7, 3355
1542430 CIFC50 H32 N2P 1 21/c 112.8317; 7.8512; 17.4533
90; 90.411; 90		1758.27Chen, Ying-Hsiao; Tang, Kuo-Chun; Chen, Yi-Ting; Shen, Jiun-Yi; Wu, Yu-Sin; Liu, Shih-Hung; Lee, Chun-Shu; Chen, Chang-Hsuan; Lai, Tzu-Yu; Tung, Shih-Huang; Jeng, Ru-Jong; Hung, Wen-Yi; Jiao, Min; Wu, Chung-Chih; Chou, Pi-Tai
Insight into the mechanism and outcoupling enhancement of excimer-associated white light generation
Chem. Sci., 2016, 7, 3556
1542431 CIFC33 H27 B2 F15 N2P 1 21/n 110.3052; 33.5364; 10.5825
90; 117.953; 90		3230.6McGough, John S.; Butler, Samuel M.; Cade, Ian A.; Ingleson, Michael J.
Highly selective catalytic trans-hydroboration of alkynes mediated by borenium cations and B(C6F5)3
Chem. Sci., 2016, 7, 3384
1542432 CIFC15 H27 B N2P 1 21/c 17.3696; 11.5512; 17.0873
90; 93.641; 90		1451.67McGough, John S.; Butler, Samuel M.; Cade, Ian A.; Ingleson, Michael J.
Highly selective catalytic trans-hydroboration of alkynes mediated by borenium cations and B(C6F5)3
Chem. Sci., 2016, 7, 3384
1542433 CIFC36 H27 B2 Cl4 F15 N4P 1 21 18.8757; 20.3411; 10.7976
90; 101.728; 90		1908.7McGough, John S.; Butler, Samuel M.; Cade, Ian A.; Ingleson, Michael J.
Highly selective catalytic trans-hydroboration of alkynes mediated by borenium cations and B(C6F5)3
Chem. Sci., 2016, 7, 3384
1542434 CIFC32 H16 B Cl2 F15 N2P 1 21/c 115.2641; 10.389; 19.5887
90; 92.115; 90		3104.24McGough, John S.; Butler, Samuel M.; Cade, Ian A.; Ingleson, Michael J.
Highly selective catalytic trans-hydroboration of alkynes mediated by borenium cations and B(C6F5)3
Chem. Sci., 2016, 7, 3384
1542435 CIFC52 H48 Cu3 N6 O6C 1 2/c 118.806; 12.832; 20.966
90; 117.781; 90		4476.3Yokoyama, Takashi; Okano, Masanori; Yoshise, Masakazu; Toda, Masanori; Akashi, Haruo; Zenki, Michio
Crystal Structure of Octahedral Coordinated Trinuclear Cu(II) Complex 1,1,1-Tris(N-salicylideneaminomethyl)ethane
X-ray Structure Analysis Online, 2010, 26, 37-38
1542436 CIFC42 H53 B N2 Si ZrP -18.6885; 12.1849; 18.105
79.834; 85.356; 81.823		1864.4Wang, Min; Wang, Dongren; Widmann, Laura; Frey, Wolfgang; Buchmeiser, Michael R.
Tandem vinyl insertion-/ring-opening metathesis copolymerization with ansa-6-[2-(dimesitylboryl)-phenyl]pyrid-2-ylamido zirconium complexes: role of trialkylaluminum and MAO
Polym. Chem., 2016, 7, 1987
1542437 CIFC54 H61 B N2 Si ZrP 1 21/c 127.914; 16.0147; 10.2151
90; 95.322; 90		4546.8Wang, Min; Wang, Dongren; Widmann, Laura; Frey, Wolfgang; Buchmeiser, Michael R.
Tandem vinyl insertion-/ring-opening metathesis copolymerization with ansa-6-[2-(dimesitylboryl)-phenyl]pyrid-2-ylamido zirconium complexes: role of trialkylaluminum and MAO
Polym. Chem., 2016, 7, 1987
1542438 CIFC50 H74 B N2 O0.5 Si3 ZrP -111.1492; 11.3188; 20.2772
89.308; 82.967; 77.549		2479.64Wang, Min; Wang, Dongren; Widmann, Laura; Frey, Wolfgang; Buchmeiser, Michael R.
Tandem vinyl insertion-/ring-opening metathesis copolymerization with ansa-6-[2-(dimesitylboryl)-phenyl]pyrid-2-ylamido zirconium complexes: role of trialkylaluminum and MAO
Polym. Chem., 2016, 7, 1987
1542439 CIFC23 H29.5 O6P 21 21 2112.18; 15.448; 22.984
90; 90; 90		4325Zhao, Ximei; Xi, Xin; Hu, Zhan; Wu, Wenjun; Zhang, Jiwen
Exploration of Novel Botanical Insecticide Leads: Synthesis and Insecticidal Activity of β-Dihydroagarofuran Derivatives.
Journal of agricultural and food chemistry, 2016, 64, 1503-1508
1542440 CIFC25 H38 O6P 21 21 218.313; 16.817; 17.345
90; 90; 90		2424.8Zhao, Ximei; Xi, Xin; Hu, Zhan; Wu, Wenjun; Zhang, Jiwen
Exploration of Novel Botanical Insecticide Leads: Synthesis and Insecticidal Activity of β-Dihydroagarofuran Derivatives.
Journal of agricultural and food chemistry, 2016, 64, 1503-1508
1542441 CIFC21 H26 O3 SeP 1 21/c 17.494; 15.0837; 17.3328
90; 100.884; 90		1924Tang, E.; Zhao, Yinjiao; Li, Wen; Wang, Weilin; Zhang, Meng; Dai, Xin
Catalytic Selenium-Promoted Intermolecular Friedel-Crafts Alkylation with Simple Alkenes.
Organic letters, 2016, 18, 912
1542442 CIFC18 H20 OP -17.3183; 10.0305; 10.947
69.766; 77.72; 85.037		736.66Tang, E.; Zhao, Yinjiao; Li, Wen; Wang, Weilin; Zhang, Meng; Dai, Xin
Catalytic Selenium-Promoted Intermolecular Friedel-Crafts Alkylation with Simple Alkenes.
Organic letters, 2016, 18, 912
1542443 CIFC19 H11 F3 N2 O2P -17.5256; 7.9629; 13.641
103.84; 91.68; 98.51		783.2Li, Ting; Wang, Zhiqiang; Xu, Kun; Liu, Wenmin; Zhang, Xu; Mao, Wutao; Guo, Yongming; Ge, Xiaolin; Pan, Fei
Rhodium-Catalyzed/Copper-Mediated Tandem C(sp(2))-H Alkynylation and Annulation: Synthesis of 11-Acylated Imidazo[1,2-a:3,4-a']dipyridin-5-ium-4-olates from 2H-[1,2'-Bipyridin]-2-ones and Propargyl Alcohols.
Organic letters, 2016, 18, 1064
1542444 CIFC18 H12 N2 O2P b c a16.336; 7.549; 21.555
90; 90; 90		2658Li, Ting; Wang, Zhiqiang; Xu, Kun; Liu, Wenmin; Zhang, Xu; Mao, Wutao; Guo, Yongming; Ge, Xiaolin; Pan, Fei
Rhodium-Catalyzed/Copper-Mediated Tandem C(sp(2))-H Alkynylation and Annulation: Synthesis of 11-Acylated Imidazo[1,2-a:3,4-a']dipyridin-5-ium-4-olates from 2H-[1,2'-Bipyridin]-2-ones and Propargyl Alcohols.
Organic letters, 2016, 18, 1064
1542445 CIFC28 H37.68 N O4.34P 21 21 218.823; 9.7832; 28.016
90; 90; 90		2418.3Yan, Bing-Chao; Wang, Wei-Guang; Hu, Dong-Bao; Sun, Xiang; Kong, Ling-Mei; Li, Xiao-Nian; Du, Xue; Luo, Shi-Hong; Liu, Yan; Li, Yan; Sun, Han-Dong; Pu, Jian-Xin
Phomopchalasins A and B, Two Cytochalasans with Polycyclic-Fused Skeletons from the Endophytic Fungus Phomopsis sp. shj2.
Organic letters, 2016, 18, 1108
1542446 CIFC31 H43 N O7P 1 21 19.7486; 14.4556; 10.3782
90; 102.099; 90		1430.03Yan, Bing-Chao; Wang, Wei-Guang; Hu, Dong-Bao; Sun, Xiang; Kong, Ling-Mei; Li, Xiao-Nian; Du, Xue; Luo, Shi-Hong; Liu, Yan; Li, Yan; Sun, Han-Dong; Pu, Jian-Xin
Phomopchalasins A and B, Two Cytochalasans with Polycyclic-Fused Skeletons from the Endophytic Fungus Phomopsis sp. shj2.
Organic letters, 2016, 18, 1108
1542447 CIFC49 H60 Cl N7 O6 S3P 1 21/c 112.9375; 11.6146; 32.205
90; 94.227; 90		4826.1Vastl, Julian; Kartika, Rendy; Park, Kichul; Cho, Art E.; Spiegel, David A.
Peptidines: glycine-amidine-based oligomers for solution- and solid-phase synthesis
Chem. Sci., 2016, 7, 3317
1542448 CIFC34 H34 Br Dy N13 O6.5P -110.5922; 12.3446; 15.3053
107.337; 90.559; 90.554		1910.1Wu, Jianfeng; Jung, Julie; Zhang, Peng; Zhang, Haixia; Tang, Jinkui; Le Guennic, Boris
Cis‒trans isomerism modulates the magnetic relaxation of dysprosium single-molecule magnets
Chem. Sci., 2016, 7, 3632
1542449 CIFC32 H30 Dy N13 O9C 1 2/c 130.25; 17.599; 20.537
90; 129.531; 90		8433Wu, Jianfeng; Jung, Julie; Zhang, Peng; Zhang, Haixia; Tang, Jinkui; Le Guennic, Boris
Cis‒trans isomerism modulates the magnetic relaxation of dysprosium single-molecule magnets
Chem. Sci., 2016, 7, 3632
1542450 CIFC33 H34 Dy F3 N12 O11 SC 1 2/c 120.791; 18.7611; 13.6144
90; 129.032; 90		4125.1Wu, Jianfeng; Jung, Julie; Zhang, Peng; Zhang, Haixia; Tang, Jinkui; Le Guennic, Boris
Cis‒trans isomerism modulates the magnetic relaxation of dysprosium single-molecule magnets
Chem. Sci., 2016, 7, 3632
1542451 CIFC26 H20 Cl O PC 1 2/c 116.6184; 10.9196; 23.5465
90; 100.366; 90		4203.2Sabounchei, Seyyed Javad; Nemattalab, Hassan; Khavasi, Hamid Reza
Crystal Structure of 4'-Chlorobenzoylmethylenetriphenylphosphorane ylide, C~26~H~20~Cl~O~P
X-ray Structure Analysis Online, 2010, 26, 35-36
1542452 CIF
HKL
Paper		C16 H21 F N2 O3 SP 1 21/c 111.5613; 16.4245; 8.873
90; 107.768; 90		1604.5Efimov, Ilya; Slepukhin, Pavel; Beliaev, Nikolai; Bakulev, Vasiliy
(<i>E</i>)-<i>N</i>-[Cyclopentyl(morpholin-4-yl)methylidene]-4-fluorobenzenesulfonamide
IUCrData, 2016, 1, x160013
1542453 CIF
HKL		C12 H11 N SF d d 217.743; 37.3075; 6.142
90; 90; 90		4065.7Mdluli, Velabo; Golen, James A.; Manke, David R.
2-(Phenylsulfanyl)aniline
IUCrData, 2016, 1, x152489
1542454 CIF
HKL
Paper		C6 H6 Br NP 1 21/m 16.1889; 6.614; 7.835
90; 93.503; 90		320.11Roy, Mrittika; Golen, James A.; Manke, David R.
2-Bromo-5-methylpyridine
IUCrData, 2016, 1, x160090
1542455 CIF
HKL
Paper		C10 H10 N4 OP b c a10.2208; 10.8693; 18.1059
90; 90; 90		2011.44Cunha, Anna C.; Jordão, Alessandro K.; de Souza, Maria C. B. V.; Ferreira, Vitor F.; de Almeida, Maria C. B.; Wardell, James L.; Tiekink, Edward R. T.
1-Anilino-5-methyl-1<i>H</i>-1,2,3-triazole-4-carbaldehyde
IUCrData, 2016, 1, x160038
1542456 CIF
HKL
Paper		C35 H32 Au2 Fe O P2 SP 1 21/n 113.7434; 12.6277; 18.763
90; 98.352; 90		3221.7Itai, Takuma; Kojima, Tatsuhiro; Konno, Takumi
μ-Sulfido-bis{[1,1'-bis(diphenylphosphanyl)ferrocene-κ^2^<i>P</i>,<i>P</i>']gold} methanol monosolvate
IUCrData, 2016, 1, x152492
1542457 CIF
HKL
Paper		C52 H36 Cd N10 O4P -19.2984; 9.3261; 12.5747
107.16; 103.719; 96.55		992.1Guo, Lei-Qun; Jiang, Yin-Hua
Bis(acetato-κ<i>O</i>)bis{2-[4-(pyridin-2-yl)phenyl]-1<i>H</i>-imidazo[4,5-<i>f</i>][1,10]phenanthroline-κ^2^<i>N</i>,<i>N</i>'}cadmium(II)
IUCrData, 2016, 1, x160063
1542458 CIF
HKL
Paper		C34 H40 B N3 O2P 1 21/c 114.3033; 10.3598; 20.2825
90; 105.468; 90		2896.6Tiritiris, Ioannis; Kantlehner, Willi
2-Dimethylamino-1-(2-ethoxy-2-oxoethyl)-3-methyl-4,5-dihydroimidazolium tetraphenylborate
IUCrData, 2016, 1, x160109
1542459 CIF
HKL		C17 H19 CoP 1 21/n 18.0307; 14.4939; 22.2528
90; 98.814; 90		2559.55Jungk, Phillip; Spannenberg, Anke; Hapke, Marko
Crystal structure of (η^2^,η^2^-cycloocta-1,5-diene)(η^5^-indenyl)cobalt(I)
IUCrData, 2016, 1, x160027
1542460 CIF
HKL		C8 H12 N4 O2P 1 21/c 110.5015; 23.561; 7.7533
90; 96.604; 90		1905.6Beliaev, Nikolai; Slepukhin, Pavel
Crystal structure of dimethyl[(<i>E</i>)-2-(1-methyl-5-nitro-1<i>H</i>-imidazol-4-yl)ethenyl]amine
IUCrData, 2016, 1, x152488
1542461 CIF
HKL
Paper		C23 H30 Cl N O4P -19.205; 9.688; 12.943
104.871; 91.465; 100.983		1091.8Sheshadri, S. N.; Nagendra, P.; Siddaraju, B. P.; Byrappa, K.; Lokanath, N. K.; Madan Kumar, S.
Tramadolium 2-chlorobenzoate
IUCrData, 2016, 1, x160014
1542462 CIF
HKL
Paper		C11 H13 Cl OP 1 21/c 15.2434; 25.902; 7.7027
90; 104.756; 90		1011.64Bechmann, Nicole; Kniess, Torsten; Pietzsch, Jens; König, Jonas; Köckerling, Martin
5-Chloro-1-phenylpentan-1-one
IUCrData, 2016, 1, x160055
1542463 CIF
HKL
Paper		C48 H40 Mo4 O16 P4P b c n16.1061; 19.891; 15.254
90; 90; 90		4886.9Mota Merelo de Aguiar, Sara Raquel; Stöger, Berthold; Weil, Matthias; Kirchner, Karl
Tetrakis(μ~2~-diphenylphosphinato-κ^2^<i>O</i>,<i>O</i>')tetra-μ~3~-oxido-tetraoxidohexamolybdenum(V)
IUCrData, 2016, 1, x160036
1542464 CIF
HKL
Paper		C23 H25 Cd N3 S4P 1 21/n 18.9361; 14.832; 18.968
90; 101.613; 90		2462.6Ehsan, Muhammad Ali; Mazhar, Muhammad; Tiekink, Edward R. T.
Bis(<i>N</i>-benzyl-<i>N</i>-methyldithiocarbamato-κ^2^<i>S</i>,<i>S</i>')(pyridine-κ<i>N</i>)cadmium(II)
IUCrData, 2016, 1, x152429
1542465 CIF
HKL		C18 H17 Cl N2 OP -111.0767; 12.067; 12.16
90.825; 102.561; 95.142		1579.1Adam, Farook; Ameram, Nadiah; Samshuddin, Seranthimata; Brighten Antony, Moonnanjilikkal; Ali Khan, Musthakeem
1-[5-(2-Chlorophenyl)-3-(4-methylphenyl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl]ethan-1-one
IUCrData, 2016, 1, x152460
1542466 CIF
Paper		C20 H19 N O3 PtP 1 21/c 113.225; 15.0844; 8.4294
90; 93.951; 90		1677.59Bui, Thi Yen Hang; Nguyen Thi Thanh, Chi; Van Meervelt, Luc
{4,5-Dimethoxy-2-[(2,3-η)-2-prop-2-en-1-yl]phenyl-κ<i>C</i>^1^}(8-hydroxyquinolinato-κ<i>N</i>,<i>O</i>)platinum(II)
IUCrData, 2016, 1, x152428
1542467 CIF
HKL
Paper		C10 H15 N O4P 1 21/c 17.328; 17.0138; 8.9223
90; 107.818; 90		1059.05Baul, Tushar S. Basu; Chaurasiya, Anurag; Tiekink, Edward R. T.
3-[(2-Hydroxybenzyl)azaniumyl]propanoate monohydrate
IUCrData, 2016, 1, x152453
1542468 CIF
HKL
Paper		C24 H30 N4 O4P 1 21/n 18.1476; 17.6289; 8.8692
90; 114.835; 90		1156.1Alshawi, Jasim; Yousif, Muoayed; Timco, Grigore; Zangana, Karzan H.; Winpenny, Richard; Al-Jeboori, Mohamad J.
Diethyl 2,2'-({[1,4-phenylenebis(azanediyl)]bis(methylene)}bis(1<i>H</i>-pyrrole-2,1-diyl))diacetate
IUCrData, 2016, 1, x160046
1542469 CIF
HKL
Paper		C40 H52 Li2 N2 O4 S2P -19.654; 9.9211; 11.2854
73.537; 88.138; 72.42		986.5Mdluli, Velabo; Golen, James A.; Manke, David R.
Bis[μ-2-(phenylsulfanyl)anilido-κ^2^<i>N</i>:<i>N</i>]bis[bis(tetrahydrofuran-κ<i>O</i>)lithium]
IUCrData, 2016, 1, x160130
1542470 CIF
Paper		C12 H13 Cl Fe OP 1 21/n 16.0366; 7.6215; 23.0837
90; 91.737; 90		1061.55McAdam, C. John; Simpson, Jim
2-Chloro-1-ferrocenylethanol
IUCrData, 2016, 1, x160102
1542471 CIF
HKL
Paper		C18 H26 N2 O2P -18.1839; 9.1461; 11.7669
106.557; 97.687; 96.63		825.65Abdelhamida, Antar A.; Mohamed, Shaaban K.; Simpson, Jim
3,3'-[(Cyclohexane-1,4-diyl)bis(azanediyl)]bis(cyclohex-2-en-1-one)
IUCrData, 2016, 1, x152175
1542472 CIF
HKL		C16 H20 N2 O8P -15.4194; 9.0619; 9.4607
81.285; 82.771; 77.208		445.8Wang, Yi; Stoeckli-Evans, Helen
Tetraethyl pyrazine-2,3,5,6-tetracarboxylate
IUCrData, 2016, 1, x152174
1542473 CIF
HKL		C10 H14 N8 O6.5C 1 2/c 121.494; 6.43; 19.193
90; 99.98; 90		2612.5Krueger, Martin; Albat, Martin; Pieper, Florian; Stock, Norbert
Dimethylammonium 2-amino-5-nitroterephthalate hemihydrate
IUCrData, 2016, 1, x160048
1542474 CIF
HKL
Paper		C10 H24 N6 O6 SP 1 21/c 19.7194; 9.4737; 17.9416
90; 105.386; 90		1592.83Tiritiris, Ioannis; Kantlehner, Willi
Morpholine-4-carboxamidinium sulfate
IUCrData, 2016, 1, x160069
1542475 CIF
HKL
Paper		C26 H45 Br2 N6 O1.5P 1 21/c 112.1957; 7.9654; 30.4821
90; 97.934; 90		2932.8Tiritiris, Ioannis; Kantlehner, Willi
<i>N</i>-Benzyl-<i>N</i>-[2-(<i>N</i>-benzyl-<i>N</i>',<i>N</i>',<i>N</i>'',<i>N</i>''-tetramethylguanidiniumyl)ethyl]-<i>N</i>',<i>N</i>',<i>N</i>'',<i>N</i>''-tetramethylguanidinium dibromide 1.5-hydrate
IUCrData, 2016, 1, x160047
1542476 CIF
HKL
Paper		C16 H19 Cl2 N O2 PtP 1 21/n 115.1282; 7.25666; 16.3038
90; 108.013; 90		1702.11Bui, Thi Yen Hang; Nguyen Thi Thanh, Chi; Van Meervelt, Luc
<i>trans</i>-Dichlorido{3,4-dimethoxy-2-[(2,3-η)-prop-2-en-1-yl]benzene}(pyridine-κ<i>N</i>)platinum(II)
IUCrData, 2016, 1, x152176
1542477 CIF
HKL
Paper		C13 H15 Cl4 N3P -17.0474; 9.7775; 12.8695
71.744; 89.177; 72.582		800.44Klass, Michaela; Näther, Christian; Tuczek, Felix
6-Methyl-2-[(6-methylpyridin-2-yl)amino]pyridinium chloride chloroform monosolvate
IUCrData, 2016, 1, x152467
1542478 CIF
HKL
Paper		Ba5.78 Cl2 F12 Pb1.22P -610.5878; 10.5878; 4.1528
90; 90; 120		403.17Weil, Matthias
The solid solution Ba~5.78~Pb~1.22~F~12~Cl~2~
IUCrData, 2016, 1, x152427
1542479 CIF
HKL
Paper		C17 H19 N O3P 1 21/c 113.669; 10.817; 10.9271
90; 109.365; 90		1524.25Laus, Gerhard; Kahlenberg, Volker; Nerdinger, Sven; Richter, Frank; Schottenberger, Herwig
<i>tert</i>-Butyl 3-(3-methyl-1-oxidopyridin-1-ium-2-yl)benzoate
IUCrData, 2016, 1, x152490
1542480 CIF
HKL
Paper		C15 H13 N2 PP 1 21/n 110.2774; 7.4256; 17.4094
90; 92.472; 90		1327.38Duan, Lian; Ma, Fengle; Zheng, Wenjun
1-Methyl-3,5-diphenyl-1<i>H</i>-1,2,4-diazaphosphole
IUCrData, 2016, 1, x160083
1542481 CIF
HKL
Paper		C14 H15 Br I N O2P -17.3066; 7.9672; 12.8467
72.994; 86.5; 87.152		713.42Barnes, Paul; Storey, John M. D.; Harrison, William T. A.
Ethyl 2-(5-bromo-2-iodoanilino)cyclopent-1-ene-1-carboxylate
IUCrData, 2016, 1, x152178
1542482 CIF
HKL		C18 H12 Na2 O6 S2P 1 21/c 117.662; 8.2854; 5.9719
90; 91.38; 90		873.7Albat, Martin; Stock, Norbert
Polymeric structure of disodium <i>p</i>-terphenyl-4,4''-disulfonate [Na~2~(O~3~S-C~6~H~4~-C~6~H~4~-C~6~H~4~-SO~3~]
IUCrData, 2016, 1, x160039
1542483 CIF
HKL
Paper		C10 H10 Cl2 N4 OP 1 21/c 112.1802; 7.3646; 13.9001
90; 112.276; 90		1153.82Cunha, Anna C.; Jordão, Alessandro K.; de Souza, Maria C. B. V.; Ferreira, Vitor F.; de Almeida, Maria C. B.; Wardell, James L.; Tiekink, Edward R. T.
[1-(2,5-Dichloroanilino)-5-methyl-1<i>H</i>-1,2,3-triazol-4-yl]methanol
IUCrData, 2016, 1, x152447
1542484 CIF
HKL		C14 H28 N2 O8 S2P 15.0283; 5.058; 20.8394
86.645; 83.338; 68.908		491.08Nageshwari, M.; Kumaresan, S.; Caroline, M. Lydia; Mani, G.; Kumari, C. Rathika Thaya; Sudha, S.; Jayaprakash, P.
<small>L</small>-Methionine–succinic acid (2/1)
IUCrData, 2016, 1, x152459
1542485 CIF
HKL
Paper		C36 H40 S4C 1 2/c 111.2972; 13.0708; 21.3833
90; 98.4; 90		3123.7Sohr, Barbara; Glöcklhofer, Florian; Stöger, Berthold; Weil, Matthias; Fröhlich, Johannes
<i>cis</i>,<i>trans</i>,<i>cis</i>-1,2,3,4-Tetrakis[2-(ethylsulfanyl)phenyl]cyclobutane
IUCrData, 2016, 1, x152426
1542486 CIF
Paper		C21 H22 Br N O4C 1 c 116.0067; 8.9455; 16.1617
90; 128.853; 90		1802.17Abdelhamid, Antar A.; Mohamed, Shaaban K.; Simpson, Jim
9-(5-Bromo-2-hydroxyphenyl)-10-(2-hydroxyethyl)-3,4,6,7-tetrahydroacridine-1,8(2<i>H</i>,5<i>H</i>,9<i>H</i>,10<i>H</i>)-dione
IUCrData, 2016, 1, x152425
1542487 CIF
HKL
Paper		C15 H16 Br N O2 S2P 1 21/n 17.8958; 8.0536; 25.2735
90; 97.909; 90		1591.84Vinduvahini, M.; Anitha, B. R.; Kumar, K. Mahesh; Kotresh, O.; Devarajegowda, H. C.
(6-Bromo-2-oxo-2<i>H</i>-chromen-4-yl)methyl diethylcarbamodithioate
IUCrData, 2016, 1, x160015
1542488 CIF
HKL
Paper		C6 H16 Cl2 N2 O2 S2 ZnP -16.907; 10.32; 10.707
68.331; 81.936; 71.917		673.9Kuwamura, Naoto; Laskar, Payel; Konno, Takumi
(Acetato-κ<i>O</i>){2-[(2-aminoethyl-κ<i>N</i>)disulfanyl]ethanaminium}dichloridozinc(II)
IUCrData, 2016, 1, x160105
1542489 CIF
HKL
Paper		C14 H13 N O2 S2P -16.9841; 8.3241; 13.116
89.276; 75.614; 72.095		701.2El Ajlaoui, Rahhal; Rakib, El Mostapha; Mojahidi, Souad; Saadi, Mohamed; El Ammari, Lahcen
(<i>Z</i>)-3-Allyl-5-(3-methoxybenzylidene)-2-sulfanylidene-1,3-thiazolidin-4-one
IUCrData, 2016, 1, x160052
1542490 CIF
HKL
Paper		C24 H24 Cl N O4P -17.621; 10.753; 13.138
92.102; 93.806; 91.275		1073.2Ahamed, F. M. Mashood; Padusha, M. Syed Ali; Gunasekaran, B.
Diethyl 4-(3-chlorophenyl)-2-methyl-6-phenyl-1,4-dihydropyridine-3,5-dicarboxylate
IUCrData, 2016, 1, x160155
1542491 CIF
HKL
Paper		C12 H11 Cl Fe OP 1 21 17.4235; 9.6339; 7.5209
90; 99.728; 90		530.14McAdam, C. John; Simpson, Jim
2-Chloro-1-ferrocenylethanone
IUCrData, 2016, 1, x152177
1542492 CIF
HKL
Paper		C25 H20 O12P b c a20.944; 9.316; 24.309
90; 90; 90		4743Moriguchi, Tetsuji; Sakao, Kozue; Hou, De-Xing; Yoza, Kenji
3,5,7-Triacetoxy-2-(3,4-diacetoxyphenyl)-4<i>H</i>-1-benzopyran-4-one
IUCrData, 2016, 1, x160028
1542493 CIF
HKL
Paper		C50 H68 N2 O4 S4P 1 21/c 120.7072; 20.4462; 12.8292
90; 107.294; 90		5186.1Omran, Omran A.; Mague, Joel T.; Mohamed, Shaaban K.; Akkurt, Mehmet; Mohamed, Alaa F.
<i>N</i>,<i>N</i>,<i>N</i>-Triethylethanaminium 5,11,17,23-tetra-<i>tert</i>-butyl-25-cyanomethoxy-26,28-dihydroxy-27-oxido-2,8,14,20-tetrathiacalix[4]arene: a molecular salt
IUCrData, 2016, 1, x160115
1542494 CIF
HKL
Paper		C27 H44 N4 P2 RuP -110.922; 11.661; 13.641
86.619; 79.75; 62.441		1515.1Ren, Lili; Zheng, Wenjun
(η^4^-Bicyclo[2.2.1]hepta-2,5-diene)bis(η^2^-3,5-di-<i>tert</i>-butyl-1,2,4-diazaphospholido)ruthenium
IUCrData, 2016, 1, x160110
1542495 CIF
HKL
Paper		C8 H5 Br N O2.5C 1 2/c 17.4556; 12.9055; 16.334
90; 95.063; 90		1565.5Turbitt, John R.; Golen, James A.; Manke, David R.
6-Bromo-1<i>H</i>-indole-2,3-dione hemihydrate
IUCrData, 2016, 1, x152434
1542496 CIF
HKL
Paper		C12 H16 N2 O2 SP 21 21 217.351; 12.452; 13.423
90; 90; 90		1228.7Jamaludin, Nazzatush Shimar; Halim, Siti Nadiah Abdul; Tiekink, Edward R. T.
3-(2-Hydroxyethyl)-3-methyl-1-(4-methylbenzoyl)thiourea
IUCrData, 2016, 1, x152457
1542497 CIF
HKL
Paper		C20 H24 O4 S2P 1 21/n 112.1691; 13.1263; 12.275
90; 99.818; 90		1932Moriguchi, Tetsuji; Miyamoto, Daisuke; Jalli, Ventakaprasad; Yoza, Kenji; Tsuge, Akihiko
<i>syn</i>-6,15-Dihydroxy-2,11-dithia[3.3]metacyclophane ethyl acetate monosolvate
IUCrData, 2016, 1, x160082
1542498 CIFC24 H33 N O SiP 1 21/c 17.1879; 34.402; 17.855
90; 91.042; 90		4414.4Shaikh, Aslam C.; Shinde, Dinesh R.; Patil, Nitin T.
Gold vs Rhodium Catalysis: Tuning Reactivity through Catalyst Control in the C-H Alkynylation of Isoquinolones.
Organic letters, 2016, 18, 1056
1542499 CIFC21 H27 Br N O SiP -18.162; 11.461; 12.471
82.763; 71.881; 79.447		1087Shaikh, Aslam C.; Shinde, Dinesh R.; Patil, Nitin T.
Gold vs Rhodium Catalysis: Tuning Reactivity through Catalyst Control in the C-H Alkynylation of Isoquinolones.
Organic letters, 2016, 18, 1056
1542500 CIFC16 H14 Br NC 1 2/c 116.1198; 12.3819; 15.1359
90; 116.573; 90		2701.9Jhang, Yuan-Ye; Fan-Chiang, Tai-Ting; Huang, Jun-Min; Hsieh, Jen-Chieh
Copper-Catalyzed Annulation: A Method for the Systematic Synthesis of Phenanthridinium Bromide.
Organic letters, 2016, 18, 1154
1542501 CIFC17 H20 Br N OP 21 21 217.4548; 10.863; 19.6508
90; 90; 90		1591.35Jhang, Yuan-Ye; Fan-Chiang, Tai-Ting; Huang, Jun-Min; Hsieh, Jen-Chieh
Copper-Catalyzed Annulation: A Method for the Systematic Synthesis of Phenanthridinium Bromide.
Organic letters, 2016, 18, 1154
1542502 CIF
HKL		C11 H10 O3P 1 21/c 112.209; 20.3796; 7.4335
90; 95.98; 90		1839.5Ramprasad, N.; Gowda, Ramakrishna; Gowda, K. V. Arjuna; Basanagouda, Mahantesha
2-(5-Methyl-1-benzofuran-3-yl)acetic acid
IUCrData, 2016, 1, x160170
1542503 CIF
HKL
Paper		C18 H20 N2 O5P 1 21/c 122.135; 8.468; 8.6198
90; 93.287; 90		1613Moriguchi, Tetsuji; Kamoto, Ryota; Jalli, Venkataprasad; Tsuge, Akihiko
2,5-Bis(3,4-dimethoxyphenyl)-1,3,4-oxadiazole
IUCrData, 2016, 1, x160167
1542504 CIF
HKL		C11 H10 N2 O3P 21 21 215.1565; 12.4881; 15.1083
90; 90; 90		972.9Limbach, Daniel; Stengelin, Elena; Schollmeyer, Dieter; Detert, Heiner
1-Ethyl-3-nitroquinolin-4(1<i>H</i>)-one
IUCrData, 2016, 1, x160125
1542505 CIF
HKL
Paper		C26 H30 O8P 21 21 218.877; 14.533; 17.748
90; 90; 90		2289.7Bauri, A. K.; Foro, Sabine; Nhu, Quynh Nguyen Do
Limonin isolated from the seeds of <i>Citrus limetta</i> (Indian sweet lemon)
IUCrData, 2016, 1, x160172
1542506 CIF
HKL
Paper		C18 H21 N O2 S2P 1 21/c 111.6767; 16.2058; 9.1417
90; 99.486; 90		1706.23Ravi, A. J.; Kumar, K. Mahesh; Devarajegowda, H. C.
(7,8-Dimethyl-2-oxo-2<i>H</i>-chromen-4-yl)methyl piperidine-1-carbodithioate
IUCrData, 2016, 1, x160171
1542507 CIF
HKL		C11 H12 Br N3 OP 1 21/c 15.4965; 11.9528; 17.7702
90; 95.354; 90		1162.38Jiang, Xian-Wu; Zhang, Heng-Qiang; Sun, Zhuo-Dong; Shan, Yong-Kui
6<i>H</i>-Dipyrido[1,2-<i>a</i>:2',1'-<i>d</i>][1,3,5]triazin-5-ium bromide monohydrate
IUCrData, 2016, 1, x160180
1542508 CIF
HKL
Paper		C13 H19 Cl3 N2P 1 21/c 110.9608; 9.5199; 14.0262
90; 95.398; 90		1457.1Bhat, Muzzaffar Ahmad; Srivastava, Sanjay K.; Sharma, Pooja; Chopra, Ambika; Butcher, Ray J.
4-(3-Chlorophenyl)-1-(3-chloropropyl)piperazin-1-ium chloride redetermined at 100K
IUCrData, 2016, 1, x160168
1542509 CIF
HKL
Paper		C17 H19 N O3 S2P -16.9573; 7.9838; 15.6037
75.485; 87.122; 75.763		813.22Anitha, B. R.; Roopashree, K. R.; Kumar, K. Mahesh; Ravi, A. J.; Devarajegowda, H. C.
(5,7-Dimethyl-2-oxo-2<i>H</i>-chromen-4-yl)methyl morpholine-4-carbodithioate
IUCrData, 2016, 1, x160169
1542510 CIF
HKL
Paper		C62 H74 B2 N4 OP -114.1885; 17.5801; 22.2543
72.911; 86.243; 80.123		5226.6Tiritiris, Ioannis; Kantlehner, Willi
<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>',<i>N</i>''-Pentamethyl-<i>N</i>''-[2-(trimethylazaniumyl)ethyl]guanidinium bis(tetraphenylborate) acetone monosolvate
IUCrData, 2016, 1, x160231
1542511 CIF
HKL
Paper		C19 H19 Fe N OP -17.344; 14.831; 15.267
79.094; 79.627; 87.508		1606.1Khelef, Abdelhamid; Mahboub, Mohammed Sadok; Lanez, Touhami
<i>N</i>-Ferrocenymethyl-<i>N</i>-phenylacetamide
IUCrData, 2016, 1, x160203
1542512 CIF
HKL
Paper		C8 H4 I N O2P 1 21/c 17.6138; 13.9658; 7.3866
90; 91.249; 90		785.25Golen, James A.; Manke, David R.
4-Iodo-1<i>H</i>-indole-2,3-dione
IUCrData, 2016, 1, x160215
1542513 CIF
HKL
Paper		C12 H14 Ag N3 O3 SP 1 21/n 111.1568; 9.7852; 12.5715
90; 107.055; 90		1312.09Rietzler, Barbara; Laus, Gerhard; Kahlenberg, Volker; Schottenberger, Herwig
<i>catena</i>-Poly[silver(I)-μ-[1-(pyridin-2-ylmethyl-κ<i>N</i>)-3-(3-sulfonatopropyl)imidazolin-2-ylidene]-κ<i>C</i>^2^]
IUCrData, 2016, 1, x160245
1542514 CIF
HKL
Paper		C23 H33 N OP 1 21 16.588; 16.582; 19.448
90; 95.051; 90		2116.3Zhang, Fangqin; Zhang, Yongbin; Liu, Diansheng
2,4-Di-<i>tert</i>-butyl-6-({[(<i>R</i>)-1-phenylethyl]amino}methyl)phenol
IUCrData, 2016, 1, x160205
1542515 CIF
HKL
Paper		C38 H30 N4 O12 Pt S2P 1 21/n 16.9957; 12.0819; 20.904
90; 97.296; 90		1752.5Liu, Jing; Zhu, Long-Guan
Bis(1,10-phenanthroline-κ^2^<i>N</i>,<i>N</i>')platinum(II) bis(3-carboxybenzenesulfonate) dihydrate
IUCrData, 2016, 1, x160211
1542516 CIF
HKL		C18 H20 N2 O3 S2P 1 21/c 16.24258; 11.4063; 26.2386
90; 90.1171; 90		1868.31Islam, M. A. A. A. A.; Sheikh, M. C.; Mahmud, A. A.; Miyatake, R.; Zangrando, E.
Benzyl 3-(3,4,5-trimethoxybenzylidene)dithiocarbazate
IUCrData, 2016, 1, x160190
1542517 CIF
HKL
Paper		C8 H4 F N O2P 21 21 214.988; 5.5522; 24.2578
90; 90; 90		671.8Golen, James A.; Manke, David R.
6-Fluoro-1<i>H</i>-indole-2,3-dione
IUCrData, 2016, 1, x160165
1542518 CIF
HKL
Paper		C60 H64 B2 N4P 1 21/n 113.8527; 10.4892; 16.7462
90; 103.034; 90		2370.6Tiritiris, Ioannis; Kress, Ralf; Kantlehner, Willi
<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>',<i>N</i>'',<i>N</i>'',<i>N</i>''',<i>N</i>'''-Octamethyl(but-2-yne)bisamidinium bis(tetraphenylborate)
IUCrData, 2016, 1, x160166
1542519 CIF
HKL
Paper		C8 H4 Br N O2P n a 2125.1411; 5.6851; 5.1593
90; 90; 90		737.42Gurung, Sita; Golen, James A.; Manke, David R.
5-Bromo-1<i>H</i>-indole-2,3-dione
IUCrData, 2016, 1, x160177
1542520 CIF
HKL
Paper		C64 H78 B2 N4 O2P -111.4419; 14.1461; 18.8503
110.635; 101.824; 97.8879		2720.7Tiritiris, Ioannis; Kantlehner, Willi
<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-Tetramethyl-<i>N</i>''-[2-(trimethylazaniumyl)ethyl]guanidinium bis(tetraphenylborate) acetone disolvate
IUCrData, 2016, 1, x160129
1542521 CIFC21 H24 O3P 1 21 18.8945; 21.16; 9.0481
90; 91.63; 90		1702.23Hammer, Niels; Leth, Lars A.; Stiller, Julian; Jensen, Magnus E.; Jørgensen, Karl Anker
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes
Chem. Sci., 2016, 7, 3649
1542522 CIFC18 H20 O3P 1 21 17.503; 10.304; 10.253
90; 92.82; 90		791.7Hammer, Niels; Leth, Lars A.; Stiller, Julian; Jensen, Magnus E.; Jørgensen, Karl Anker
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes
Chem. Sci., 2016, 7, 3649
1542523 CIFC22 H28 O3P 21 21 217.5376; 10.5784; 23.8774
90; 90; 90		1903.9Hammer, Niels; Leth, Lars A.; Stiller, Julian; Jensen, Magnus E.; Jørgensen, Karl Anker
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes
Chem. Sci., 2016, 7, 3649
1542524 CIFC15 H13 Br O2P 21 21 216.1506; 7.564; 28.362
90; 90; 90		1319.5Hammer, Niels; Leth, Lars A.; Stiller, Julian; Jensen, Magnus E.; Jørgensen, Karl Anker
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes
Chem. Sci., 2016, 7, 3649
1542525 CIFC20 H24 O3P 21 21 218.6911; 9.1112; 21.5901
90; 90; 90		1709.64Hammer, Niels; Leth, Lars A.; Stiller, Julian; Jensen, Magnus E.; Jørgensen, Karl Anker
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes
Chem. Sci., 2016, 7, 3649
1542526 CIFC12 H10 O2P 21 21 217.0175; 11.1406; 11.9874
90; 90; 90		937.16Hammer, Niels; Leth, Lars A.; Stiller, Julian; Jensen, Magnus E.; Jørgensen, Karl Anker
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes
Chem. Sci., 2016, 7, 3649
1542527 CIFC72 H45 Ir N3P a -322.825; 22.825; 22.825
90; 90; 90		11891Pan, Long; Xu, Meng-Ying; Feng, Li-Juan; Chen, Qi; He, Yu-Jian; Han, Bao-Hang
Conjugated microporous polycarbazole containing tris(2-phenylpyridine)iridium(iii) complexes: phosphorescence, porosity, and heterogeneous organic photocatalysis
Polym. Chem., 2016, 7, 2299
1542528 CIF
HKL		C14 H10 Cl N3 OP -16.8759; 8.2563; 12.0403
109.156; 103.979; 91.485		622.41Bittencourt, Viviane C. D.; Almeida, Roberta M. F. C.; Bortoluzzi, Adailton J.; Gervini, Vanessa C.; de Oliveira, Adriano Bof
(3<i>E</i>)-5-Chloro-3-(2-phenylhydrazinylidene)-1<i>H</i>-indol-2(3<i>H</i>)-one
IUCrData, 2016, 1, x160258
1542529 CIF
HKL
Paper		C8 H4 Br N O2P 1 21/c 13.832; 13.072; 15.004
90; 91.917; 90		751.2Golen, James A.; Manke, David R.
7-Bromo-1<i>H</i>-indole-2,3-dione
IUCrData, 2016, 1, x160268
1542530 CIF
HKL		C15 H22 N4 O16P -19.4495; 10.0608; 12.3484
109.133; 91.964; 106.201		1054.79Bengiat, Ravell; Klein, Asne; Gil, Maayan; Bogoslavsky, Benny; Cohen, Shmuel; Yardeni, Guy; Zilbermann, Israel; Almog, Joseph
5-[2,4-Dihydroxy-5-(5-hydroxy-2,4,6-trioxo-3,5-dihydro-1<i>H</i>-pyrimidin-5-yl)-3-methoxyphenyl]-5-hydroxy-3,5-dihydro-1<i>H</i>-pyrimidine-2,4,6-trione pentahydrate
IUCrData, 2016, 1, x160261
1542531 CIF
HKL
Paper		C26 H30 Cl4 N6 Ni2 O2P b c a11.913; 11.445; 20.7458
90; 90; 90		2828.6Glazier, Brian M.; Golen, James A.; Manke, David R.
Di-μ-chlorido-bis[(2,2'-bipyridine-κ^2^<i>N</i>,<i>N</i>')chlorido(<i>N</i>,<i>N</i>-dimethylformamide-κ<i>O</i>)nickel(II)]
IUCrData, 2016, 1, x160259
1542532 CIF
HKL
Paper		C8 H4 Br N O2P 1 21/c 17.3655; 13.689; 7.2866
90; 93.378; 90		733.4Huang, Haobo; Golen, James A.; Manke, David R.
4-Bromo-1<i>H</i>-indole-2,3-dione
IUCrData, 2016, 1, x160007
1542533 CIFC28 H32 O4 S2P -16.0485; 6.9813; 15.2806
94.625; 94.955; 95.942		636.76Wang, Xiao-Ye; Zhang, Meng-Wen; Zhuang, Fang-Dong; Wang, Jie-Yu; Pei, Jian
Lactone-fused electron-deficient building blocks for n-type polymer field-effect transistors: synthesis, properties, and impact of alkyl substitution positions
Polym. Chem., 2016, 7, 2264
1542534 CIFC19 H18 N2 O3P c a 2118.7959; 22.7469; 8.0182
90; 90; 90		3428.17Kischkewitz, Marvin; Daniliuc, Constantin-Gabriel; Studer, Armido
3-Alkylperoxy-3-cyano-oxindoles from 2-Cyano-2-diazo-N-phenyl-acetamides via Cyclizing Carbene Insertion and Subsequent Radical Oxidation.
Organic letters, 2016, 18, 1206
1542535 CIFC11 H10 F N O3 SP 1 21/c 15.1196; 11.2852; 18.9656
90; 97.224; 90		1087.05Lorion, Mélanie M; Duarte, Filipe J. S.; Calhorda, Maria José; Oble, Julie; Poli, Giovanni
Opening the Way to Catalytic Aminopalladation/Proxicyclic Dehydropalladation: Access to Methylidene γ-Lactams.
Organic letters, 2016, 18, 1020
1542536 CIFC22 H16 F6 N4 O6 S2 ZnC 1 2/c 19.92044; 14.02733; 18.6185
90; 101.515; 90		2538.75Comerford, James W.; Hart, Sam J.; North, Michael; Whitwood, Adrian C.
Homogeneous and silica-supported zinc complexes for the synthesis of propylene carbonate from propane-1,2-diol and carbon dioxide
Catal. Sci. Technol., 2016, 6, 4824
1542537 CIFC26 H16 F6 N4 O6 S2 ZnC 1 2/c 19.75476; 14.26536; 19.5942
90; 95.2384; 90		2715.25Comerford, James W.; Hart, Sam J.; North, Michael; Whitwood, Adrian C.
Homogeneous and silica-supported zinc complexes for the synthesis of propylene carbonate from propane-1,2-diol and carbon dioxide
Catal. Sci. Technol., 2016, 6, 4824
1542538 CIFC24 H32 F6 N8 O6 S2 ZnP 18.3731; 8.6907; 11.7281
68.851; 81.968; 82.401		785.04Comerford, James W.; Hart, Sam J.; North, Michael; Whitwood, Adrian C.
Homogeneous and silica-supported zinc complexes for the synthesis of propylene carbonate from propane-1,2-diol and carbon dioxide
Catal. Sci. Technol., 2016, 6, 4824
1542539 CIFC26 H27 N O7 SP 1 21 111.1671; 7.62443; 14.6056
90; 94.1026; 90		1240.37Liao, Yuting; Liu, Xiaohua; Zhang, Yu; Xu, Yali; Xia, Yong; Lin, Lili; Feng, Xiaoming
Asymmetric [3 + 2] cycloaddition of donor–acceptor aziridines with aldehydes via carbon–carbon bond cleavage
Chem. Sci., 2016, 7, 3775
1542540 CIF
HKL
Paper		C4 H26 B12 Cs N OP 21 21 218.9771; 12.868; 14.5449
90; 90; 90		1680.19Tiritiris, Ioannis; Schleid, Thomas
Caesium tetramethylammonium dodecahydrido-<i>closo</i>-dodecaborate monohydrate
IUCrData, 2016, 1, x160291
1542541 CIF
HKL
Paper		C22 H22 N2 O4 SP 1 21/n 15.6473; 26.7798; 13.3219
90; 99.743; 90		1985.66Mague, Joel T.; Mohamed, Shaaban K.; Akkurt, Mehmet; Bakhite, Etify A.; Albayati, Mustafa R.
Diethyl 3-amino-6-methyl-4-[(<i>E</i>)-2-phenylethenyl]thieno[2,3-<i>b</i>]pyridine-2,5-dicarboxylate
IUCrData, 2016, 1, x160270
1542542 CIF
HKL
Paper		C16 H22 N2 O7P 16.778; 6.953; 9.458
109.182; 93.369; 98.437		413.7Numata, Takashi; Ikenomoto, Shun; Akitsu, Takashiro
4,4'-(1,2-Diazaniumylethane-1,2-diyl)dibenzoate trihydrate
IUCrData, 2016, 1, x160252
1542543 CIFC9 H6.2 N6 O0.1R -3 m :H12.657; 12.657; 9.296
90; 90; 120		1289.7Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542544 CIFC12 H17 F9 N6 O7P b c n12.335; 21.047; 7.89
90; 90; 90		2048.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542545 CIFC14 H3.5 F10.5 N7P 41 3 215.8427; 15.8427; 15.8427
90; 90; 90		3976.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542546 CIFC32 H50 Cu Na O8 S2P 1 21/c 110.5883; 21.967; 14.4286
90; 95.682; 90		3339.5Johnson, Miles W.; Hannoun, Kareem I.; Tan, Yichen; Fu, Gregory C.; Peters, Jonas C.
A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide.
Chemical science, 2016, 7, 4091-4100
1542547 CIFC18 H16 B2 F8 N4P -17.547; 7.886; 8.992
66.005; 85.305; 83.508		485.4Leblanc, Nicolas; Sproules, Stephen; Fink, Karin; Sanguinet, Lionel; Alévêque, Olivier; Levillain, Eric; Rosa, Patrick; Powell, Annie K.
A fascinating multifaceted redox-active chelating ligand: introducing the N,N′-dimethyl-3,3′-biquinoxalinium “methylbiquinoxen” platform
Chem. Sci., 2016, 7, 3820
1542548 CIFC18 H17 B F4 N4P 1 21/n 17.133; 20.036; 11.526
90; 99.454; 90		1624.9Leblanc, Nicolas; Sproules, Stephen; Fink, Karin; Sanguinet, Lionel; Alévêque, Olivier; Levillain, Eric; Rosa, Patrick; Powell, Annie K.
A fascinating multifaceted redox-active chelating ligand: introducing the N,N′-dimethyl-3,3′-biquinoxalinium “methylbiquinoxen” platform
Chem. Sci., 2016, 7, 3820
1542549 CIFC18 H16 Cd Cl2 N4P -17.4683; 10.4739; 11.3249
80.15; 82.274; 81.982		858.7Leblanc, Nicolas; Sproules, Stephen; Fink, Karin; Sanguinet, Lionel; Alévêque, Olivier; Levillain, Eric; Rosa, Patrick; Powell, Annie K.
A fascinating multifaceted redox-active chelating ligand: introducing the N,N′-dimethyl-3,3′-biquinoxalinium “methylbiquinoxen” platform
Chem. Sci., 2016, 7, 3820
1542550 CIFC40 H44 Fe N6 O6P 1 21/c 112.5879; 20.8699; 13.6448
90; 93.531; 90		3577.8Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542551 CIFC44 H38 Cl6 N6 O6P -110.1932; 12.318; 19.654
72.773; 77.793; 81.49		2294.1Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542552 CIFC62.5 H99 Cl N6 O11 P2P 1 21/n 119.5077; 15.3419; 22.1726
90; 95.401; 90		6606.47Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542553 CIFC46.5 H64.5 Cl1.5 N5 O8 PP -19.9599; 14.6932; 16.4802
81.05; 75.273; 88.017		2304.1Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542554 CIFC119 H151 Cl9 N14 O20 P2P -116.0755; 18.9299; 24.4976
93.415; 96.103; 111.261		6869.2Deliomeroglu, Murat K.; Lynch, Vincent M.; Sessler, Jonathan L.
Non-cyclic formylated dipyrromethanes as phosphate anion receptors
Chem. Sci., 2016, 7, 3843
1542555 CIFC69 H62.5 Cl6 I6 N12 Zn3C 1 2/c 135.7365; 15.061; 30.9345
90; 104.141; 90		16145.3Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto
Structure determination of microbial metabolites by the crystalline sponge method
Chem. Sci., 2016, 7, 3910
1542556 CIFC132.77 H131.15 I12 N24 O15.14 Zn6C 1 2 136.3783; 14.6755; 31.2278
90; 103.184; 90		16232.2Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto
Structure determination of microbial metabolites by the crystalline sponge method
Chem. Sci., 2016, 7, 3910
1542557 CIFC134.29 H138.92 I12 N24 O8.41 Zn6C 1 2 134.7707; 14.8406; 31.2152
90; 102.601; 90		15719.6Inokuma, Yasuhide; Ukegawa, Tomoya; Hoshino, Manabu; Fujita, Makoto
Structure determination of microbial metabolites by the crystalline sponge method
Chem. Sci., 2016, 7, 3910
1542558 CIFC68 H74 N Ni O3 P3 S3 Si3P b c a27.4702; 17.1432; 27.9778
90; 90; 90		13175.5Chiou, Tzung-Wen; Tseng, Yen-Ming; Lu, Tsai-Te; Weng, Tsu-Chien; Sokaras, Dimosthenes; Ho, Wei-Chieh; Kuo, Ting-Shen; Jang, Ling-Yun; Lee, Jyh-Fu; Liaw, Wen-Feng
[NiIII(OMe)]-mediated reductive activation of CO2affording a Ni(κ1-OCO) complex
Chem. Sci., 2016, 7, 3640
1542559 CIFC68 H74 N2 Ni O2 P3 S3 Si3P b c a27.5733; 17.0409; 27.8585
90; 90; 90		13090Chiou, Tzung-Wen; Tseng, Yen-Ming; Lu, Tsai-Te; Weng, Tsu-Chien; Sokaras, Dimosthenes; Ho, Wei-Chieh; Kuo, Ting-Shen; Jang, Ling-Yun; Lee, Jyh-Fu; Liaw, Wen-Feng
[NiIII(OMe)]-mediated reductive activation of CO2affording a Ni(κ1-OCO) complex
Chem. Sci., 2016, 7, 3640
1542560 CIFC67 H78 N3 Ni O P3 S3 Si3P 1 21/n 114.316; 26.0756; 18.0992
90; 97.069; 90		6705Chiou, Tzung-Wen; Tseng, Yen-Ming; Lu, Tsai-Te; Weng, Tsu-Chien; Sokaras, Dimosthenes; Ho, Wei-Chieh; Kuo, Ting-Shen; Jang, Ling-Yun; Lee, Jyh-Fu; Liaw, Wen-Feng
[NiIII(OMe)]-mediated reductive activation of CO2affording a Ni(κ1-OCO) complex
Chem. Sci., 2016, 7, 3640
1542561 CIFC50 H68 O4P -19.1934; 13.5122; 18.2252
76.83; 75.995; 86.625		2138.9Wang, Can; Xu, Bingjia; Li, Mengshu; Chi, Zhenguo; Xie, Yujun; Li, Qianqian; Li, Zhen
A stable tetraphenylethene derivative: aggregation-induced emission, different crystalline polymorphs, and totally different mechanoluminescence properties
Mater. Horiz., 2016, 3, 220
1542562 CIFC17 H21.3 N O4.15P 21 21 219.7421; 9.7391; 16.0471
90; 90; 90		1522.54Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542563 CIFC16 H22 N O4.5P 21 21 218.0372; 15.6818; 22.5648
90; 90; 90		2844.02Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542564 CIFC23 H30.01 N2 O4P 1 21 19.4965; 11.4906; 9.9133
90; 95.247; 90		1077.21Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542565 CIFC23 H30 N2 O4P 1 21 19.6195; 11.6392; 9.6441
90; 94.229; 90		1076.85Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542566 CIFC18 H27 N O5P 21 21 217.9947; 8.6002; 24.7362
90; 90; 90		1700.76Zhan, Guanqun; Zhou, Junfei; Liu, Rong; Liu, Tingting; Guo, Guoli; Wang, Jianping; Xiang, Ming; Xue, Yongbo; Luo, Zengwei; Zhang, Yonghui; Yao, Guangmin
Galanthamine, Plicamine, and Secoplicamine Alkaloids from Zephyranthes candida and Their Anti-acetylcholinesterase and Anti-inflammatory Activities.
Journal of natural products, 2016, 79, 760-766
1542567 CIFC21 H17 N3 OC 1 2/c 117.9422; 9.9101; 19.1301
90; 99.879; 90		3351.1Chen, Zhengkai; Li, Hongli; Dong, Weipeng; Miao, Maozhong; Ren, Hongjun
I2-Catalyzed Oxidative Coupling Reactions of Hydrazones and Amines and the Application in the Synthesis of 1,3,5-Trisubstituted 1,2,4-Triazoles.
Organic letters, 2016, 18, 1334-1337
1542568 CIFC38 H30 N4 S3P b c n29.6046; 11.8388; 17.1781
90; 90; 90		6020.6Zhang, Jing; Gu, Peiyang; Long, Guankui; Ganguly, Rakesh; Li, Yongxin; Aratani, Naoki; Yamada, Hiroko; Zhang, Qichun
Switching charge-transfer characteristics from p-type to n-type through molecular “doping” (co-crystallization)
Chem. Sci., 2016, 7, 3851
1542569 CIFC88 H64 N12 S6P -110.6919; 11.6399; 14.4791
90.178; 104.4; 95.311		1737.22Zhang, Jing; Gu, Peiyang; Long, Guankui; Ganguly, Rakesh; Li, Yongxin; Aratani, Naoki; Yamada, Hiroko; Zhang, Qichun
Switching charge-transfer characteristics from p-type to n-type through molecular “doping” (co-crystallization)
Chem. Sci., 2016, 7, 3851
1542570 CIFC13 H10 Cl N O2P 17.02512; 8.17982; 10.0807
104.135; 104.019; 91.6954		542.58Sanchez-Diez, Eduardo; Vesga, Diana L.; Reyes, Efraim; Uria, Uxue; Carrillo, Luisa; Vicario, Jose L.
Organocatalytically Generated Donor-Acceptor Cyclopropanes in Domino Reactions. One-Step Enantioselective Synthesis of Pyrrolo[1,2-a]quinolines.
Organic letters, 2016, 18, 1270-1273
1542571 CIFC8 H11 N O4 SP -16.4922; 8.38; 9.896
74.212; 73.241; 80.346		493.74Mommer, Stefan; Truong, Khai-Nghi; Keul, Helmut; Möller, Martin
An epoxy thiolactone on stage: four component reactions, synthesis of poly(thioether urethane)s and the respective hydrogels
Polym. Chem., 2016, 7, 2291
1542572 CIFC23 H18 O3P 1 c 15.82646; 9.44106; 15.616
90; 100.11; 90		845.67Han, Ting; Deng, Haiqin; Yu, Chris Y. Y.; Gui, Chen; Song, Zhegang; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Tang, Ben Zhong
Functional isocoumarin-containing polymers synthesized by rhodium-catalyzed oxidative polycoupling of aryl diacid and internal diyne
Polym. Chem., 2016, 7, 2501
1542573 CIFC26 H19 N3 O2P 1 21/c 110.0072; 23.043; 9.4047
90; 110.772; 90		2027.7Cai, Qun; Li, Deng-Kui; Zhou, Rong-Rong; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Catalyzed Multicomponent Tandem Cyclizations: Access to Polyfunctional Dihydroindolizino[8,7-b]indoles.
Organic letters, 2016, 18, 1342-1345
1542574 CIFC28 H22 Cl3 N3 O3P 1 21/c 112.2576; 19.07; 11.4688
90; 97.837; 90		2655.8Cai, Qun; Li, Deng-Kui; Zhou, Rong-Rong; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Catalyzed Multicomponent Tandem Cyclizations: Access to Polyfunctional Dihydroindolizino[8,7-b]indoles.
Organic letters, 2016, 18, 1342-1345
1542575 CIFC21 H15 Br N4P b c a13.3161; 7.7509; 33.992
90; 90; 90		3508.4Cai, Qun; Li, Deng-Kui; Zhou, Rong-Rong; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Catalyzed Multicomponent Tandem Cyclizations: Access to Polyfunctional Dihydroindolizino[8,7-b]indoles.
Organic letters, 2016, 18, 1342-1345
1542576 CIFC14 H16 O4P 21 21 217.2935; 8.8494; 19.329
90; 90; 90		1247.55Sun, Wang-Bin; Wang, Xuan; Sun, Bing-Feng; Zou, Jian-Ping; Lin, Guo-Qiang
Catalytic Asymmetric Total Synthesis of Hedyosumins A, B, and C.
Organic letters, 2016, 18, 1219-1221
1542577 CIFC14 H16 O4P 21 21 215.5435; 7.7426; 27.879
90; 90; 90		1196.6Sun, Wang-Bin; Wang, Xuan; Sun, Bing-Feng; Zou, Jian-Ping; Lin, Guo-Qiang
Catalytic Asymmetric Total Synthesis of Hedyosumins A, B, and C.
Organic letters, 2016, 18, 1219-1221
1542578 CIFC16 H11 F3 Mo O3P -17.1145; 7.6417; 15.3159
93.275; 97.569; 113.744		749.96Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542579 CIFC16 H11 F3 Mo O3P 1 21/c 17.2471; 31.8822; 6.7406
90; 104.266; 90		1509.41Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542580 CIFC16 H11 F3 Mo O3P 1 21/c 18.9791; 12.3295; 13.7453
90; 100.651; 90		1495.49Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542581 CIFC17 H10 F6 Mo O3P -18.4202; 10.2245; 10.5319
101.377; 102.663; 103.044		832.29Reich, Robert M.; Kaposi, Marlene; Pöthig, Alexander; Kühn, Fritz E.
Kinetic studies of fluorinated aryl molybdenum(ii) tricarbonyl precursors in epoxidation catalysis
Catal. Sci. Technol., 2016, 6, 4970
1542582 CIFC32 H33 N3 Ni O3P 1 21 111.0798; 21.9977; 11.88015
90; 102.003; 90		2832.25Miles, Jennifer A.; Yeo, David J.; Rowell, Philip; Rodriguez-Marin, Silvia; Pask, Christopher M.; Warriner, Stuart L.; Edwards, Thomas A.; Wilson, Andrew J.
Hydrocarbon constrained peptides ‒ understanding preorganisation and binding affinity
Chem. Sci., 2016, 7, 3694
1542583 CIFC16 H11 Fe3 N O7 S2P -17.7263; 11.203; 11.9
94.504; 108.019; 93.687		972.2Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542584 CIFC40 H35 Fe3 N O5 P2 S2P -111.3103; 12.9416; 15.479
105.449; 100.216; 110.921		1944.2Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542585 CIFC20.2 H22.23 B F4 Fe3 N4.6 O6.72 S2P -110.4593; 11.6085; 12.256
76.988; 85.341; 81.75		1433.02Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542586 CIFC80 H75 B F24 Fe3 N O4 P4 S2P -113.352; 13.623; 24.074
92.828; 94.41; 99.584		4296Lunsford, Allen M.; Beto, Christopher C.; Ding, Shengda; Erdem, Özlen F.; Wang, Ning; Bhuvanesh, Nattamai; Hall, Michael B.; Darensbourg, Marcetta Y.
Cyanide-bridged iron complexes as biomimetics of tri-iron arrangements in maturases of the H cluster of the di-iron hydrogenase
Chem. Sci., 2016, 7, 3710
1542587 CIFC25 H23 N5 O8P -17.856; 11.799; 14.315
66.98; 77.401; 74.377		1166.6Biswas, Arnab; Dubey, Mrigendra; Mukhopadhyay, Sujay; Kumar, Ashish; Pandey, Daya Shankar
Anion triggered metallogels: demetalation and crystal growth inside the gel matrix and improvement in viscoelastic properties using Au-NPs.
Soft matter, 2016, 12, 2997-3003
1542588 CIFO4 Ru Sr2I 4/m m m3.871; 3.871; 12.702
90; 90; 90		190.335Miwa, K.; Kagomiya, I.; Ohsato, H.; Sakai, H.; Maeda, Y.
Electrical properties of the Sr2 Ru1-x Tix O4 solid solutions
Journal of the European Ceramic Society, 2007, 27, 4287-4290
1542589 CIFC25 H25 N OP 1 21/c 111.1357; 10.6585; 17.1362
90; 90.608; 90		2033.8Wang, Nan-Nan; Huang, Lei-Rong; Hao, Wen-Juan; Zhang, Tian-Shu; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Synergistic Rhodium/Copper Catalysis: Synthesis of 1,3-Enynes and N-Aryl Enaminones.
Organic letters, 2016, 18, 1298-1301
1542590 CIFC26 H21 Cl OP 1 21 113.2144; 5.6194; 14.8801
90; 111.914; 90		1025.11Wang, Nan-Nan; Huang, Lei-Rong; Hao, Wen-Juan; Zhang, Tian-Shu; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Synergistic Rhodium/Copper Catalysis: Synthesis of 1,3-Enynes and N-Aryl Enaminones.
Organic letters, 2016, 18, 1298-1301
1542591 CIFC79.27 H80.86 N5.59 ZnP -110.0013; 14.5831; 24.366
75.428; 87.017; 71.26		3255.5Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542592 CIFC64.5 H68 Cl7.5 N5 Ni O2P b c n11.0983; 34.992; 32.965
90; 90; 90		12802Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542593 CIFC69 H77 N5 Ni O2P -114.734; 20.554; 20.788
90.073; 103.209; 109.518		5756Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542594 CIFC74 H77 N4 Ni O PP 1 21/n 112.3714; 28.233; 41.36
90; 96.168; 90		14363Fukui, Norihito; Lee, Seung-Kyu; Kato, Kenichi; Shimizu, Daiki; Tanaka, Takayuki; Lee, Sangsu; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro
Regioselective phenylene-fusion reactions of Ni(ii)-porphyrins controlled by an electron-withdrawing meso-substituent
Chem. Sci., 2016, 7, 4059
1542595 CIFC44 H36 Br N O P2 PdP -111.12; 12.074; 15.487
69.218; 72.309; 70.811		1794.3Wu, Jiang; Liu, Yafei; Lu, Changhui; Shen, Qilong
Palladium-catalyzed difluoromethylthiolation of heteroaryl bromides, iodides, triflates and aryl iodides
Chem. Sci., 2016, 7, 3757
1542596 CIFC18 H27 Cl N2 O12 SP 1 21 17.2371; 9.8802; 15.9674
90; 97.002; 90		1133.2Liang, Yong; Suzol, Sazzad H.; Wen, Zhiwei; Artiles, Alain G.; Mathivathanan, Logesh; Raptis, Raphael G.; Wnuk, Stanislaw F.
Uracil Nucleosides with Reactive Group at C5 Position: 5-(1-Halo-2-sulfonylvinyl)uridine Analogues.
Organic letters, 2016, 18, 1418-1421
1542597 CIFC23 H24 N2 O4 S2P 1 21/n 18.2793; 22.107; 12.8092
90; 105.304; 90		2261.3Liang, Yong; Suzol, Sazzad H.; Wen, Zhiwei; Artiles, Alain G.; Mathivathanan, Logesh; Raptis, Raphael G.; Wnuk, Stanislaw F.
Uracil Nucleosides with Reactive Group at C5 Position: 5-(1-Halo-2-sulfonylvinyl)uridine Analogues.
Organic letters, 2016, 18, 1418-1421
1542598 CIFC41 H32 N2 OP 1 21/c 117.751; 6.9635; 26.097
90; 107.904; 90		3069.6Jiang, Pingping; Xu, Yongbao; Sun, Fuxing; Liu, Xufei; Li, Feng; Yu, Renfu; Li, Yang; Wang, Qifeng
Pd(II)-Catalyzed ortho-C-H Olefination/Dearomatization of N-Aryl Ureas: An Approach to Imine Derivatives.
Organic letters, 2016, 18, 1426-1429
1542599 CIFC37 H30 N2 OP 1 21/n 120.5458; 14.0737; 20.9813
90; 108.671; 90		5747.6Jiang, Pingping; Xu, Yongbao; Sun, Fuxing; Liu, Xufei; Li, Feng; Yu, Renfu; Li, Yang; Wang, Qifeng
Pd(II)-Catalyzed ortho-C-H Olefination/Dearomatization of N-Aryl Ureas: An Approach to Imine Derivatives.
Organic letters, 2016, 18, 1426-1429
1542600 CIFC41 H32 N2 OP 1 21/c 119.0371; 9.7457; 18.7726
90; 114.993; 90		3156.7Jiang, Pingping; Xu, Yongbao; Sun, Fuxing; Liu, Xufei; Li, Feng; Yu, Renfu; Li, Yang; Wang, Qifeng
Pd(II)-Catalyzed ortho-C-H Olefination/Dearomatization of N-Aryl Ureas: An Approach to Imine Derivatives.
Organic letters, 2016, 18, 1426-1429
1542601 CIF
HKL
Paper		C14 H8 Cl F3 N2 OP -16.4998; 7.4286; 14.8289
84.859; 86.707; 83.313		707.47Maheswari, R.; Manjula, J.; Gunasekaran, B.
(<i>E</i>)-4-Chloro-<i>N</i>'-(2,4,5-trifluorobenzylidene)benzohydrazide
IUCrData, 2016, 1, x160304
1542602 CIF
HKL
Paper		C12 H11 F3 N2 O3P 1 21/c 19.9339; 10.6614; 12.6802
90; 105.863; 90		1291.8Avezov, Kuvondik G.; Umarov, Bako B.; Talipov, Samat A.; Kunafiev, Rishad J.; Ibragimov, Bakhtiyar T.
(5-Hydroxy-3-methyl-5-trifluoromethyl-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)(2-hydroxyphenyl)methanone
IUCrData, 2016, 1, x160316
1542603 CIFC13 H9 N5 O2P 1 21/c 13.8512; 19.078; 21.23
90; 91.015; 90		1559.6Kaloo, Masood Ayoub; Sunder Raman, Ramya; Sankar, Jeyaraman
Novel structurally tuned DAMN receptor for "in situ" diagnosis of bicarbonate in environmental waters.
The Analyst, 2016, 141, 2367-2370
1542604 CIFC14 H23 O5 RhP 1 21/n 17.2023; 13.3209; 16.1663
90; 93.426; 90		1548.24Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542605 CIFC20 H24 Cl4 F6 Rh2R -328.1638; 28.1638; 8.1635
90; 90; 120		5607.8Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542606 CIFC24 H38 Cl4 Rh2P -18.2993; 8.9088; 9.3961
102.335; 106.607; 94.5603		643Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C‒H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542607 CIFC10 H5 I O2P -17.7536; 8.2731; 14.2858
73.2168; 78.223; 85.339		858.63Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542608 CIFC11 H7 I O3P 1 21/c 18.1168; 7.9198; 15.1553
90; 93.0671; 90		972.84Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542609 CIFC12 H9 I O3P 1 21/c 117.2465; 16.7627; 7.5137
90; 91.9216; 90		2170.97Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542610 CIFC10 H4 I N O4P 1 21/c 17.7794; 9.0897; 13.9834
90; 99.5625; 90		975.06Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542611 CIFC10 H4 Br I O2P 21 21 215.0752; 6.1752; 30.9217
90; 90; 90		969.1Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542612 CIFC10 H3 Br2 I O2P -17.1805; 8.2069; 10.2503
67.006; 88.761; 69.374		515.67Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542613 CIFC10 H5 I O2P 1 21/c 114.1706; 4.1298; 15.9165
90; 106.661; 90		892.36Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542614 CIFC10 H4 I2 O2P 1 21/n 113.9652; 4.4527; 16.4351
90; 102.327; 90		998.42Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542615 CIFC10 H5 Br O2P 1 21/c 17.7808; 8.1027; 12.8379
90; 94.413; 90		806.97Jardim, Guilherme A. M.; da Silva Júnior, Eufrânio N.; Bower, John F.
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
Chem. Sci., 2016, 7, 3780
1542616 CIFC57 H38 Cl3P 1 21/c 19.65924; 9.12014; 50.6162
90; 91.6555; 90		4457.1Zhang, Yun; Zhao, Engui; Deng, Haiqin; Lam, Jacky W. Y.; Tang, Ben Zhong
Development of a transition metal-free polymerization route to functional conjugated polydiynes from a haloalkyne-based organic reaction
Polym. Chem., 2016, 7, 2492
1542617 CIFC9 H10 N3 O5C 1 2 115.791; 5.0056; 16.133
90; 122.52; 90		1075.3Dixit, Manish Kumar; Pandey, Vinay Kumar; Dubey, Mrigendra
Alkali base triggered intramolecular charge transfer metallogels based on symmetrical A-π-D-chiral-D-π-A type ligands.
Soft matter, 2016, 12, 3622-3630
1542618 CIFC27 H32 O8P 1 21 17.5013; 11.6919; 14.619
90; 103.882; 90		1244.7Wang, Guo-Cai; Yu, Jin-Hai; Shen, Yu; Leng, Ying; Zhang, Hua; Yue, Jian-Min
Limonoids and Triterpenoids as 11β-HSD1 Inhibitors from Walsura robusta.
Journal of natural products, 2016, 79, 899-906
1542619 CIFC27 H34 O8P 1 21 17.4553; 12.0869; 28.1295
90; 90.18; 90		2534.78Wang, Guo-Cai; Yu, Jin-Hai; Shen, Yu; Leng, Ying; Zhang, Hua; Yue, Jian-Min
Limonoids and Triterpenoids as 11β-HSD1 Inhibitors from Walsura robusta.
Journal of natural products, 2016, 79, 899-906
1542620 CIFC27 H43 O5.5C 1 2 111.4484; 18.1806; 25.8417
90; 98.082; 90		5325.2Liu, Zhaoming; Chen, Yan; Chen, Senhua; Liu, Yayue; Lu, Yongjun; Chen, Dongni; Lin, Yongcheng; Huang, Xishan; She, Zhigang
Aspterpenacids A and B, Two Sesterterpenoids from a Mangrove Endophytic Fungus Aspergillus terreus H010.
Organic letters, 2016, 18, 1406-1409
1542621 CIFC26 H28 N3 O7.5P -110.42; 11.567; 12.233
60.629; 74.155; 87.858		1227.9Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542622 CIFC14 H9 Cl N4 O7P 1 21/n 18.8587; 18.447; 9.759
90; 110.87; 90		1490.1Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542623 CIFC33 H34 F N3 O7P -18.201; 11.187; 17.705
91.352; 103.004; 105.472		1519.3Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542624 CIFC30 H29 N3 O5P -110.485; 10.4852; 13.306
79.14; 67.26; 76.51		1304Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542625 CIFC23 H16 N2 OC 1 c 15.5058; 26.046; 11.867
90; 97.83; 90		1685.9Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542626 CIFC29 H27 N3 O5P 1 21/c 113.4022; 10.939; 16.5069
90; 91.481; 90		2419.2Yang, Changjiang; Chen, Xiangyu; Tang, Tong; He, Zhengjie
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides.
Organic letters, 2016, 18, 1486-1489
1542627 CIFC23 H25 N2 O6 ReP -19.569; 9.937; 12.748
89.068; 68.454; 84.701		1122.4Li, Dan; Chen, Yuanyuan; Wang, Xia; Deuther-Conrad, Winnie; Chen, Xin; Jia, Bing; Dong, Chengyan; Steinbach, Jörg; Brust, Peter; Liu, Boli; Jia, Hongmei
(99m)Tc-Cyclopentadienyl Tricarbonyl Chelate-Labeled Compounds as Selective Sigma-2 Receptor Ligands for Tumor Imaging.
Journal of medicinal chemistry, 2016, 59, 934-946
1542628 CIFC63 H39 B F24 N3 P PdP -112.7129; 13.3917; 17.6166
93.824; 90.923; 93.204		2987.2Ojwach, Stephen O.; Ogweno, Aloice O.; Akerman, Matthew P.
(Pyridyl)benzoazole palladium(ii) complexes as homogeneous catalysts in hydrogenation of alkenes and alkynes
Catal. Sci. Technol., 2016, 6, 5069
1542629 CIFC16 H12 N2 O2P 1 21/c 19.0373; 6.9446; 20.7426
90; 100.138; 90		1281.49Dhanasekaran, Sivasankaran; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Approach to Isoindolinones, Isoquinolinones, and THIQs via Lewis Acid-Catalyzed Domino Strecker-Lactamization/Alkylations.
Organic letters, 2016, 18, 634-637
1542630 CIFC19 H20 N2 O3P 1 21/n 18.4076; 9.6355; 20.2875
90; 98.838; 90		1624.01Dhanasekaran, Sivasankaran; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Approach to Isoindolinones, Isoquinolinones, and THIQs via Lewis Acid-Catalyzed Domino Strecker-Lactamization/Alkylations.
Organic letters, 2016, 18, 634-637
1542631 CIFC17 H22 N2 O5P b c a8.5688; 19.141; 21.222
90; 90; 90		3480.7Izumi, Sanae; Kobayashi, Yusuke; Takemoto, Yoshiji
Catalytic Asymmetric Synthesis of anti-α,β-Diamino Acid Derivatives.
Organic letters, 2016, 18, 696-699
1542632 CIFC19 H15 Br O4P 1 21 110.8044; 6.7767; 12.3031
90; 113.354; 90		827Sun, Xue-Li; Chen, Ying-Han; Zhu, Dan-Yang; Zhang, Yan; Liu, Yan-Kai
Substrate-Controlled, One-Pot Synthesis: Access to Chiral Chroman-2-one and Polycyclic Derivatives.
Organic letters, 2016, 18, 864-867
1542633 CIFC23 H28 O5P 1 21 17.1955; 19.2595; 7.6395
90; 101.353; 90		1037.98Wang, Peng; Li, Rui-Jun; Liu, Rui-Huan; Jian, Kai-Li; Yang, Ming-Hua; Yang, Lei; Kong, Ling-Yi; Luo, Jun
Sarglaperoxides A and B, Sesquiterpene-Normonoterpene Conjugates with a Peroxide Bridge from the Seeds of Sarcandra glabra.
Organic letters, 2016, 18, 832-835
1542634 CIFC15 H25 N O2P 1 21/c 110.6087; 12.4575; 10.8471
90; 104.219; 90		1389.6Song, Dengpeng; Wang, Zhengshen; Mei, Ruoming; Zhang, Weiwei; Ma, Donghui; Xu, Dengyu; Xie, Xingang; She, Xuegong
Short and Scalable Total Synthesis of Myrioneuron Alkaloids (±)-α,β-Myrifabral A and B.
Organic letters, 2016, 18, 669-671
1542635 CIFC31 H31 N3 O3P -110.139; 11.268; 11.71
92.64; 97.053; 92.437		1324.7Tian, Yaming; Tian, Lumin; Li, Chunju; Jia, Xueshun; Li, Jian
Temperature-Dependent Double Isocyanide Insertion Reaction To Construct a Polycyclic Skeleton.
Organic letters, 2016, 18, 840-843
1542636 CIFC30 H29 N3 O3P 1 21/c 111.499; 25.987; 18.929
90; 115.027; 90		5125Tian, Yaming; Tian, Lumin; Li, Chunju; Jia, Xueshun; Li, Jian
Temperature-Dependent Double Isocyanide Insertion Reaction To Construct a Polycyclic Skeleton.
Organic letters, 2016, 18, 840-843
1542637 CIFC33 H26 Br N3 OP -17.873; 11.346; 15.84
80.449; 77.035; 74.443		1319.9Tian, Yaming; Tian, Lumin; Li, Chunju; Jia, Xueshun; Li, Jian
Temperature-Dependent Double Isocyanide Insertion Reaction To Construct a Polycyclic Skeleton.
Organic letters, 2016, 18, 840-843
1542638 CIFC16 H11 N OP 1 21/c 19.9587; 12.7222; 9.7025
90; 94.493; 90		1225.5Zhang, Lianpeng; Peng, Zhixing; Wen, Qiaodong; Li, Xihui; Lu, Ping; Wang, Yanguang
Copper-Catalyzed Preparation of 2-Aryl-3-cyanobenzofurans with Bright Blue Photoluminescence.
Organic letters, 2016, 18, 728-731
1542639 CIFC16 H28 F N O5P 21 21 2132.528; 6.026; 9.305
90; 90; 90		1823.9Hu, Xiang-Guo; Lawer, Aggie; Peterson, Matthew B.; Iranmanesh, Hasti; Ball, Graham E.; Hunter, Luke
Diastereoselective Synthesis and Conformational Analysis of (2R)- and (2S)-Fluorostatines: An Approach Based on Organocatalytic Fluorination of a Chiral Aldehyde.
Organic letters, 2016, 18, 662-665
1542640 CIFC28 H22 N2 O5 SP -18.28533; 11.53237; 14.1641
111.2; 94.4487; 93.4599		1252.27Wang, Kai-Kai; Jin, Tian; Huang, Xin; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation.
Organic letters, 2016, 18, 872-875
1542641 CIFC26 H21 N O4 SP 1 21/n 115.5173; 9.24556; 15.6647
90; 90.404; 90		2247.3Wang, Kai-Kai; Jin, Tian; Huang, Xin; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation.
Organic letters, 2016, 18, 872-875
1542642 CIFC28 H24 N2 O5 SP 21 21 218.797; 12.2522; 22.914
90; 90; 90		2469.7Wang, Kai-Kai; Jin, Tian; Huang, Xin; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
α-Regioselective Asymmetric [3 + 2] Annulations of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes and Mechanism Elucidation.
Organic letters, 2016, 18, 872-875
1542643 CIFC24 H21 B F2 N2P n a 2116.262; 8.2789; 15.194
90; 90; 90		2045.6Zhou, Xin; Wu, Qinghua; Yu, Yang; Yu, Changjiang; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Metal-Free Direct α-Selective Arylation of Boron Dipyrromethenes via Base-Mediated C-H Functionalization.
Organic letters, 2016, 18, 736-739
1542644 CIFC25 H23 B F2 N2 OP n a 2117.9538; 8.2467; 14.4494
90; 90; 90		2139.4Zhou, Xin; Wu, Qinghua; Yu, Yang; Yu, Changjiang; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Metal-Free Direct α-Selective Arylation of Boron Dipyrromethenes via Base-Mediated C-H Functionalization.
Organic letters, 2016, 18, 736-739
1542645 CIFC30 H25 B F2 N2P -113.143; 13.3965; 15.473
67.831; 78.64; 87.648		2471.8Zhou, Xin; Wu, Qinghua; Yu, Yang; Yu, Changjiang; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Metal-Free Direct α-Selective Arylation of Boron Dipyrromethenes via Base-Mediated C-H Functionalization.
Organic letters, 2016, 18, 736-739
1542646 CIFC43 H28 N4P 1 21/n 111.523; 16.7116; 17.0577
90; 106.759; 90		3145.2Huang, Jau-Jiun; Hung, Yu-Hsiang; Ting, Pei-Ling; Tsai, Yu-Ning; Gao, Huan-Jie; Chiu, Tien-Lung; Lee, Jiun-Haw; Chen, Chi-Lin; Chou, Pi-Tai; Leung, Man-Kit
Orthogonally Substituted Benzimidazole-Carbazole Benzene As Universal Hosts for Phosphorescent Organic Light-Emitting Diodes.
Organic letters, 2016, 18, 672-675
1542647 CIFC31 H23 N3 O0.5P 1 21/n 19.8285; 13.81; 17.3341
90; 91.02; 90		2352.41Huang, Jau-Jiun; Hung, Yu-Hsiang; Ting, Pei-Ling; Tsai, Yu-Ning; Gao, Huan-Jie; Chiu, Tien-Lung; Lee, Jiun-Haw; Chen, Chi-Lin; Chou, Pi-Tai; Leung, Man-Kit
Orthogonally Substituted Benzimidazole-Carbazole Benzene As Universal Hosts for Phosphorescent Organic Light-Emitting Diodes.
Organic letters, 2016, 18, 672-675
1542648 CIFC16 H8 Ag Br F8 N2P 1 21/n 16.8291; 15.1012; 16.8892
90; 100.705; 90		1711.4Kaplan, Peter T.; Vicic, David A.
Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks.
Organic letters, 2016, 18, 884-886
1542649 CIFC16 H8 Br Cu F8 N2P 1 21/c 16.598; 17.1674; 14.6901
90; 95.676; 90		1655.8Kaplan, Peter T.; Vicic, David A.
Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks.
Organic letters, 2016, 18, 884-886
1542650 CIFC10 H4 Br F8 N O2P -16.1276; 8.3737; 12.5585
108.992; 90.118; 90.223		609.3Kaplan, Peter T.; Vicic, David A.
Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks.
Organic letters, 2016, 18, 884-886
1542651 CIFC11 H4 Br F8 NP 1 21/c 15.9092; 15.55; 13.5414
90; 91.044; 90		1244.09Kaplan, Peter T.; Vicic, David A.
Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks.
Organic letters, 2016, 18, 884-886
1542652 CIFC12 H4 Br F12 N O2P -16.0576; 8.4076; 15.1254
73.883; 89.304; 89.536		739.99Kaplan, Peter T.; Vicic, David A.
Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks.
Organic letters, 2016, 18, 884-886
1542653 CIFC13 H4 Br F12 NP -15.9088; 8.397; 15.6935
105.477; 90.42; 91.565		750.05Kaplan, Peter T.; Vicic, David A.
Versatile Route to Arylated Fluoroalkyl Bromide Building Blocks.
Organic letters, 2016, 18, 884-886
1542654 CIFC17 H15 N O4P 21 21 215.9263; 14.358; 17.7263
90; 90; 90		1508.33Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo
Anti-Selective Asymmetric Nitro-Michael Reaction of Furanones: Diastereocontrol by Catalyst.
Organic letters, 2016, 18, 646-649
1542655 CIFC24 H26 N4 O4P -19.715; 10.003; 13.038
105.483; 98.771; 111.44		1091.5Zhao, Hong-Wu; Li, Bo; Pang, Hai-Liang; Tian, Ting; Chen, Xiao-Qin; Song, Xiu-Qing; Meng, Wei; Yang, Zhao; Zhao, Yu-Di; Liu, Yue-Yang
Diastereoselective 1,3-Dipolar Cycloadditions of N,N'-Cyclic Azomethine Imines with Iminooxindoles for Access to Oxindole Spiro-N,N-bicyclic Heterocycles.
Organic letters, 2016, 18, 848-851
1542656 CIFC20 H11 Cl6 O2 P S2P 1 21/n 111.338; 11.077; 18.981
90; 106.186; 90		2289.4Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542657 CIFC18 H9 O3 P SP 1 21/n 18.3936; 15.6127; 10.697
90; 100.496; 90		1378.35Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542658 CIFC18 H9 P S3P -13.9829; 10.6559; 17.2702
86.043; 89.121; 81.767		723.68Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542659 CIFC18 H9 O2 P SP c c n16.762; 22.071; 7.4782
90; 90; 90		2766.6Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542660 CIFC21 H16 F2 N O4 P SP 1 21/c 111.099; 11.479; 14.854
90; 95.89; 90		1882.5Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542661 CIFC18 H9 O P S3P 1 21/n 19.166; 10.699; 15.212
90; 101.527; 90		1461.7Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542662 CIFC18 H9 O P S2P b c a8.0119; 20.775; 34.265
90; 90; 90		5703.3Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542663 CIFC30 H28 N O3 PP 1 21/c 18.675; 19.74; 15.454
90; 106.49; 90		2538Jiang, Jin; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diethyl Phosphite Initiated Coupling of α-Ketoesters with Imines for Synthesis of α-Phosphonyloxy-β-amino Acid Derivatives and Aziridine-2-carboxylates.
Organic letters, 2016, 18, 880-883
1542664 CIFC29 H36 N O9 P SP 1 21/a 116.58; 10.731; 17.82
90; 104.369; 90		3071Jiang, Jin; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diethyl Phosphite Initiated Coupling of α-Ketoesters with Imines for Synthesis of α-Phosphonyloxy-β-amino Acid Derivatives and Aziridine-2-carboxylates.
Organic letters, 2016, 18, 880-883
1542665 CIFC19 H26 Cl3 N2 RhP 1 21/c 111.0944; 14.838; 13.848
90; 105.603; 90		2195.6Qi, Zisong; Yu, Songjie; Li, Xingwei
Rh(III)-Catalyzed Synthesis of N-Unprotected Indoles from Imidamides and Diazo Ketoesters via C-H Activation and C-C/C-N Bond Cleavage.
Organic letters, 2016, 18, 700-703
1542666 CIFC17 H13 Br N2 O2P 1 21/c 14.4677; 16.8234; 20.1968
90; 92.566; 90		1516.51Ma, Haichao; Li, Dianjun; Yu, Wei
Synthesis of Quinoxaline Derivatives via Tandem Oxidative Azidation/Cyclization Reaction of N-Arylenamines.
Organic letters, 2016, 18, 868-871
1542667 CIFC26 H34 O8P 21 21 217.8754; 9.4243; 32.1424
90; 90; 90		2385.61Wan, Luo-Sheng; Shao, Li-Dong; Fu, Liangbing; Xu, Jun; Zhu, Guo-Lei; Peng, Xing-Rong; Li, Xiao-Nian; Li, Yan; Qiu, Ming-Hua
One-Step Semisynthesis of a Segetane Diterpenoid from a Jatrophane Precursor via a Diels-Alder Reaction.
Organic letters, 2016, 18, 496-499
1542668 CIFC42 H32 SP -18.317; 16.04; 23.373
108.62; 98.945; 90.295		2913.9Bhanuchandra, M.; Yorimitsu, Hideki; Osuka, Atsuhiro
Synthesis of Spirocyclic Diarylfluorenes by One-Pot Twofold SNAr Reactions of Diaryl Sulfones with Diarylmethanes.
Organic letters, 2016, 18, 384-387
1542669 CIFC26 H15 F3 SP -17.4947; 10.4244; 12.3741
83; 82.694; 81.603		943.36Bhanuchandra, M.; Yorimitsu, Hideki; Osuka, Atsuhiro
Synthesis of Spirocyclic Diarylfluorenes by One-Pot Twofold SNAr Reactions of Diaryl Sulfones with Diarylmethanes.
Organic letters, 2016, 18, 384-387
1542670 CIFC24 H32 N2 O3 SP 1 21 116.9083; 5.97938; 23.1232
90; 103.885; 90		2269.47Yoshizaki, Soichi; Nakamura, Yu; Masutomi, Koji; Yoshida, Tomoka; Noguchi, Keiichi; Shibata, Yu; Tanaka, Ken
Rhodium-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of 1,6-Enynes with Cyclopropylideneacetamides.
Organic letters, 2016, 18, 388-391
1542671 CIFC28 H20 N2 O6 SP b c a13.7519; 14.9993; 22.6562
90; 90; 90		4673.27Kumar, N. N. Bhuvan; Kutateladze, Andrei G.
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications.
Organic letters, 2016, 18, 460-463
1542672 CIFC17 H14 N2 O4P 1 21/n 19.1645; 8.7385; 18.3694
90; 104.426; 90		1424.71Kumar, N. N. Bhuvan; Kutateladze, Andrei G.
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications.
Organic letters, 2016, 18, 460-463
1542673 CIFC19 H13 Cl N2 O3C 1 2/c 117.6228; 12.8352; 14.1014
90; 91.786; 90		3188.08Kumar, N. N. Bhuvan; Kutateladze, Andrei G.
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications.
Organic letters, 2016, 18, 460-463
1542674 CIFC36 H50 S4 Si2P -112.2329; 17.7221; 19.3408
69.034; 72.015; 72.867		3643.1Chang, Shao-Ling; Lu, Chih-Wen; Lai, Yu-Ying; Hsu, Jhih-Yang; Cheng, Yen-Ju
Synthesis and Molecular Properties of Two Isomeric Dialkylated Tetrathienonaphthalenes.
Organic letters, 2016, 18, 368-371
1542675 CIFC34 H44 S4 Si2P -111.715; 12.209; 15.564
76.856; 75.796; 79.474		2082.4Chang, Shao-Ling; Lu, Chih-Wen; Lai, Yu-Ying; Hsu, Jhih-Yang; Cheng, Yen-Ju
Synthesis and Molecular Properties of Two Isomeric Dialkylated Tetrathienonaphthalenes.
Organic letters, 2016, 18, 368-371
1542676 CIFC24 H18 O3P 1 21/n 19.9595; 12.5319; 14.6208
90; 97.484; 90		1809.3More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542677 CIFC16 H12 O3P -17.6359; 8.6199; 10.087
80.935; 79.666; 69.242		607.6More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542678 CIFC19 H18 O4P 1 21/c 19.4895; 8.7747; 19.062
90; 101.174; 90		1557.2More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542679 CIFC17 H14 O3P 1 21/n 19.3485; 13.5764; 10.5947
90; 101.444; 90		1317.94More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542680 CIFC16 H12 O3P b c a10.0417; 18.527; 26.755
90; 90; 90		4977.6More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542681 CIFC22 H22 O5P -19.3342; 10.9832; 19.0771
103.527; 91.081; 99.292		1873.3More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542682 CIFC12 H11 Cl F3 N OP 1 21/n 110.761; 5.854; 19.673
90; 102.693; 90		1209Fu, Mingyang; Chen, Long; Jiang, Yongpeng; Jiang, Zhong-Xing; Yang, Zhigang
Copper-Catalyzed Intermolecular Chloro- and Bromotrifluoromethylation of Alkenes.
Organic letters, 2016, 18, 348-351
1542683 CIFC36 H36 Br N2 O4.5 SC 1 2 127.2716; 10.7113; 11.2422
90; 90.5644; 90		3283.85Wang, Shoulei; Rodriguez-Escrich, Carles; Pericàs, Miquel A
H-Bond-Directing Organocatalyst for Enantioselective [4 + 2] Cycloadditions via Dienamine Catalysis.
Organic letters, 2016, 18, 556-559
1542684 CIFC13 H10 N2 SP -13.9105; 10.8964; 12.403
97.328; 94.957; 92.265		521.54Sharma, Shivani; Pathare, Ramdas S.; Maurya, Antim K.; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M.; Pardasani, Ram T.
Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight.
Organic letters, 2016, 18, 356-359
1542685 CIFC14 H12 N2 O SP 1 21/c 113.1514; 12.8014; 7.2224
90; 105.094; 90		1173.99Sharma, Shivani; Pathare, Ramdas S.; Maurya, Antim K.; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M.; Pardasani, Ram T.
Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight.
Organic letters, 2016, 18, 356-359
1542686 CIFC26 H22 Cl2 N2 O4P 1 21/c 19.921; 17.9238; 12.9555
90; 90.022; 90		2303.8Zhou, Yunfei; Zhu, Jianming; Li, Bo; Zhang, Yong; Feng, Jia; Hall, Adrian; Shi, Jiye; Zhu, Weiliang
Access to Different Isomeric Dibenzoxazepinones through Copper-Catalyzed C-H Etherification and C-N Bond Construction with Controllable Smiles Rearrangement.
Organic letters, 2016, 18, 380-383
1542687 CIFC24 H17 Cl N2 O3P 1 21/c 114.8316; 16.4395; 7.8011
90; 93.277; 90		1898.99Zhou, Yunfei; Zhu, Jianming; Li, Bo; Zhang, Yong; Feng, Jia; Hall, Adrian; Shi, Jiye; Zhu, Weiliang
Access to Different Isomeric Dibenzoxazepinones through Copper-Catalyzed C-H Etherification and C-N Bond Construction with Controllable Smiles Rearrangement.
Organic letters, 2016, 18, 380-383
1542688 CIFC32 H16 Br8 O8C 1 2/c 121.0972; 15.0686; 14.2085
90; 128.249; 90		3547.3Kumar, Yogendra; Kumar, Sharvan; Kumar Keshri, Sudhir; Shukla, Jyoti; Singh, Shiv Shankar; Thakur, Tejender S.; Denti, Mitchell; Facchetti, Antonio; Mukhopadhyay, Pritam
Synthesis of Octabromoperylene Dianhydride and Diimides: Evidence of Halogen Bonding and Semiconducting Properties.
Organic letters, 2016, 18, 472-475
1542689 CIFC11 H10 N4 O3P b c a10.487; 13.0919; 16.145
90; 90; 90		2216.6Pawar, Govind Goroba; Brahmanandan, Abhilashamole; Kapur, Manmohan
Palladium(II)-Catalyzed, Heteroatom-Directed, Regioselective C-H Nitration of Anilines Using Pyrimidine as a Removable Directing Group.
Organic letters, 2016, 18, 448-451
1542690 CIFC34 H35 Br N2 OP 21 21 2110.839; 23.282; 24.36
90; 90; 90		6147Li, Xuanyi; Xu, Xiuyan; Wei, Weiwei; Lin, Aijun; Yao, Hequan
Organocatalyzed Asymmetric 1,6-Conjugate Addition of para-Quinone Methides with Dicyanoolefins.
Organic letters, 2016, 18, 428-431
1542691 CIFC14 H17 F N2 O2 SP 1 21 15.8834; 11.064; 11.101
90; 102.611; 90		705.2Hajra, Saumen; Aziz, Sk Mohammad; Jana, Bibekananda; Mahish, Prosenjit; Das, Dhiraj
Synthesis of Chiral Spiro-Aziridine Oxindoles via Aza-Corey-Chaykovsky Reaction of Isatin Derived N-tert-Butanesulfinyl Ketimines.
Organic letters, 2016, 18, 532-535
1542692 CIFC32 H31 N O5P 1 21/c 110.3073; 11.8581; 21.8138
90; 94.816; 90		2656.8Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong
Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines.
Organic letters, 2016, 18, 600-603
1542693 CIFC26 H20 F3 N OI 1 2/a 118.3718; 5.6809; 40.089
90; 100.975; 90		4107.5Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong
Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines.
Organic letters, 2016, 18, 600-603
1542694 CIFC29 H25 F2 N O3P -110.2357; 10.5168; 12.7893
71.454; 71.195; 73.002		1207.61Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong
Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines.
Organic letters, 2016, 18, 600-603
1542695 CIFC18 H24 O3P 21 21 217.8269; 8.7254; 23.407
90; 90; 90		1598.5Liu, Chenguang; Zeng, Zhixiong; Chen, Renzhi; Jiang, Xunjin; Wang, Yinglu; Zhang, Yandong
Total Synthesis of (+)-Fusarisetin A Driven by a One-Pot Four-Reaction Process.
Organic letters, 2016, 18, 624-627
1542696 CIFC18 H12 Br2 O2 SP -17.9582; 8.0654; 13.665
82.257; 84.908; 72.622		828.3Wang, Miao; Xiang, Jia-Chen; Cheng, Yan; Wu, Yan-Dong; Wu, An-Xin
Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit.
Organic letters, 2016, 18, 524-527
1542697 CIFC19 H16 O4 S2P -17.573; 8.012; 15.475
77.359; 78.217; 86.315		896.7Wang, Miao; Xiang, Jia-Chen; Cheng, Yan; Wu, Yan-Dong; Wu, An-Xin
Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit.
Organic letters, 2016, 18, 524-527
1542698 CIFC23.5 H14.5 Cl4.5 N3 O8P -19.645; 11.531; 23.18
92.059; 90.249; 95.534		2564.25Yoon, Ina; Suh, Sung-Eun; Barros, Stephanie A.; Chenoweth, David M.
Synthesis of 9-Substituted Triptycene Building Blocks for Solid-Phase Diversification and Nucleic Acid Junction Targeting.
Organic letters, 2016, 18, 1096
1542699 CIFC17 H16 F N OP -15.5492; 10.9097; 11.6094
102.644; 93.799; 96.078		679.03Wang, Yi-Feng; Hu, Ming; Hayashi, Hirohito; Xing, Bengang; Chiba, Shunsuke
Linking of Alcohols with Vinyl Azides.
Organic letters, 2016, 18, 992
1542700 CIFC22 H17 Cl2 F3 N2 O3P 21 21 217.6378; 15.9147; 18.2712
90; 90; 90		2220.9Li, Xiaoyuan; Su, Jinhuan; Liu, Zhourujun; Zhu, Yuanyuan; Dong, Zhenghao; Qiu, Shuai; Wang, Jiayi; Lin, Li; Shen, Zhiqiang; Yan, Wenjin; Wang, Kairong; Wang, Rui
Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block".
Organic letters, 2016, 18, 956
1542701 CIFC26 H20 Cl F3 N2 O3P 1 21 110.2811; 11.149; 11.3115
90; 115.56; 90		1169.7Li, Xiaoyuan; Su, Jinhuan; Liu, Zhourujun; Zhu, Yuanyuan; Dong, Zhenghao; Qiu, Shuai; Wang, Jiayi; Lin, Li; Shen, Zhiqiang; Yan, Wenjin; Wang, Kairong; Wang, Rui
Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block".
Organic letters, 2016, 18, 956
1542702 CIFC10 H6 F3 N3 OP -17.0244; 7.2782; 10.394
99.34; 92.323; 91.732		523.55Pieber, Bartholomäus; Kappe, C. Oliver
Generation and Synthetic Application of Trifluoromethyl Diazomethane Utilizing Continuous Flow Technologies.
Organic letters, 2016, 18, 1076
1542703 CIFC16 H15 F5 O3 SP -15.584; 11.7071; 12.0947
85.184; 83.294; 87.881		782.18Friese, Florian W.; Dreier, Anna-Lena; Matsnev, Andrej V.; Daniliuc, Constantin G.; Thrasher, Joseph S.; Haufe, Günter
Anti-Selective Aldol Reactions of Pentafluorosulfanylacetic Acid Esters with Aldehydes Mediated by Dicyclohexylchloroborane.
Organic letters, 2016, 18, 1012
1542704 CIFC17 H23 Cl2 F5 O3 SP -110.0879; 13.4704; 16.5159
66.318; 85.001; 89.698		2046.4Friese, Florian W.; Dreier, Anna-Lena; Matsnev, Andrej V.; Daniliuc, Constantin G.; Thrasher, Joseph S.; Haufe, Günter
Anti-Selective Aldol Reactions of Pentafluorosulfanylacetic Acid Esters with Aldehydes Mediated by Dicyclohexylchloroborane.
Organic letters, 2016, 18, 1012
1542705 CIFC19 H19 N O3P 1 21 19.2196; 6.1859; 14.23
90; 94.59; 90		809Wang, Jie; Wang, Mingyang; Chen, Kehao; Zha, Shanke; Song, Chao; Zhu, Jin
C-H Activation-Based Traceless Synthesis via Electrophilic Removal of a Directing Group. Rhodium(III)-Catalyzed Entry into Indoles from N-Nitroso and α-Diazo-β-keto Compounds.
Organic letters, 2016, 18, 1178
1542706 CIFC12 H14 N2 O5P 1 21/c 18.922; 19.474; 8.18
90; 111.49; 90		1322.4Wang, Jie; Wang, Mingyang; Chen, Kehao; Zha, Shanke; Song, Chao; Zhu, Jin
C-H Activation-Based Traceless Synthesis via Electrophilic Removal of a Directing Group. Rhodium(III)-Catalyzed Entry into Indoles from N-Nitroso and α-Diazo-β-keto Compounds.
Organic letters, 2016, 18, 1178
1542707 CIFC21 H29 N O6P 1 21/n 115.7725; 9.1679; 16.4313
90; 115.84; 90		2138.41Shen, Xin-Yue; Peng, Xiao-Shui; Wong, Henry N. C.
Total Synthesis of (±)-Gracilioether F.
Organic letters, 2016, 18, 1032
1542708 CIFC14 H18 F N O4 SP 21 21 217.0953; 12.6329; 16.757
90; 90; 90		1502Wu, Liang; Chen, Pinhong; Liu, Guosheng
Pd(II)-Catalyzed Aminofluorination of Alkenes in Total Synthesis 6-(R)-Fluoroswainsonine and 5-(R)-Fluorofebrifugine.
Organic letters, 2016, 18, 960
1542709 CIFC22 H17 N3 O2P -13.8508; 12.3597; 18.3893
82.341; 88.727; 87.157		866.25Kumar, Gangam Srikanth; Kapur, Manmohan
Ruthenium-Catalyzed, Site-Selective C-H Allylation of Indoles with Allyl Alcohols as Coupling Partners.
Organic letters, 2016, 18, 1112
1542710 CIFC22 H18 Br N OP 21 21 219.7821; 10.3912; 35.968
90; 90; 90		3656.1Liu, Zhen-Ting; Wang, Ya-Hui; Zhu, Fu-Lin; Hu, Xiang-Ping
Enantioselective Copper-Catalyzed Formal [4 + 2] Cycloaddition of o-Aminophenol Derivatives with Propargylic Esters for Synthesis of Optically Active 3,4-Dihydro-2H-1,4-benzoxazines.
Organic letters, 2016, 18, 1190
1542711 CIFC15 H10 Br I OP 1 21/n 17.603; 10.723; 16.702
90; 91.919; 90		1360.9Sasaki, Teppei; Miyagi, Kotaro; Moriyama, Katsuhiko; Togo, Hideo
Direct Preparation of 3-Iodochromenes from 3-Aryl- and 3-Alkyl-2-propyn-1-ols with Diaryliodonium Salts and NIS.
Organic letters, 2016, 18, 944
1542712 CIFC18 H16 F N O4P 1 21/n 111.161; 9.295; 15.244
90; 94.06; 90		1577.5Yang, Chen; Liu, Yang; Yang, Jin-Dong; Li, Yi-He; Li, Xin; Cheng, Jin-Pei
Amination of 3-Substituted Benzofuran-2(3H)-ones Triggered by Single-Electron Transfer.
Organic letters, 2016, 18, 1036
1542713 CIFC79 H72 N6 O10C 1 2/c 138.088; 12.3446; 34.909
90; 107.222; 90		15678Bi, Jiahai; Zeng, Xiangfei; Tian, Demei; Li, Haibing
Temperature-Responsive Switch Constructed from an Anthracene-Functionalized Pillar[5]arene-Based Host-Guest System.
Organic letters, 2016, 18, 1092
1542714 CIFC30 H44 O4P 21 21 218.0564; 12.2225; 28.0933
90; 90; 90		2766.33Coffinier, Romain; Assal, Mourad El; Peixoto, Philippe A.; Bosset, Cyril; Miqueu, Karinne; Sotiropoulos, Jean-Marc; Pouységu, Laurent; Quideau, Stéphane
Total Synthesis of (-)-Bacchopetiolone via an Asymmetric Hydroxylative Phenol Dearomatization/[4+2]-Dimerization Cascade Promoted by a Novel Salen-Type Chiral Iodane.
Organic letters, 2016, 18, 1120
1542715 CIFC14 H10 N2 O2P 1 21/c 115.2095; 5.9093; 12.9247
90; 102.997; 90		1131.88Bhat, Shreesha V.; Robinson, David; Moses, John E.; Sharma, Pallavi
Synthesis of Oxadiazol-5-imines via the Cyclizative Capture of in Situ Generated Cyanamide Ions and Nitrile Oxides.
Organic letters, 2016, 18, 1100
1542716 CIFC114 H105 Br7 Cl9 N16 O19P 1 21/n 119.423; 23.548; 30.226
90; 98.09; 90		13687Li, Xuesong; Qi, Ting; Srinivas, Kolupula; Massip, Stéphane; Maurizot, Victor; Huc, Ivan
Synthesis and Multibromination of Nanosized Helical Aromatic Amide Foldamers via Segment-Doubling Condensation.
Organic letters, 2016, 18, 1044
1542717 CIFC699.6 H691.6 Br14 Cl64.8 N96 O101P 1 21/c 159.25; 37.63; 38.83
90; 104.6; 90		83779Li, Xuesong; Qi, Ting; Srinivas, Kolupula; Massip, Stéphane; Maurizot, Victor; Huc, Ivan
Synthesis and Multibromination of Nanosized Helical Aromatic Amide Foldamers via Segment-Doubling Condensation.
Organic letters, 2016, 18, 1044
1542718 CIFC19 H23 N O3 SP 21 21 216.101; 15.371; 19.086
90; 90; 90		1789.9Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542719 CIFC16 H19 N O3 SP 1 21 15.804; 22.592; 6.639
90; 115.905; 90		783.1Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542720 CIFC18 H18 Br N O5 SP 21 21 218.115; 11.495; 19.441
90; 90; 90		1813.5Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542721 CIFC16 H19 N O4 SP 21 21 217.758; 10.373; 19.137
90; 90; 90		1540Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542722 CIFC17 H13 Br F3 N O4 SP 21 21 2114.6; 14.941; 16.318
90; 90; 90		3559.6Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542723 CIFC16 H18 Br N O3 SP 1 21 15.9781; 19.198; 7.657
90; 108.46; 90		833.6Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542724 CIFC16 H18 N4 O3 SP 21 21 215.4849; 12.639; 24.563
90; 90; 90		1702.8Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542725 CIFC17 H16 Br N O4 SP 1 21 17.819; 11.246; 9.64
90; 94.539; 90		845Pan, Hongjie; Huang, Hu; Liu, Weigang; Tian, Hua; Shi, Yian
Phosphine Oxide-Sc(OTf)3 Catalyzed Highly Regio- and Enantioselective Bromoaminocyclization of (E)-Cinnamyl Tosylcarbamates. An Approach to a Class of Synthetically Versatile Functionalized Molecules.
Organic letters, 2016, 18, 896
1542726 CIF
HKL
Paper		C14 H16 O3C 1 2/c 116.401; 6.9386; 20.666
90; 97.089; 90		2333.8Lough, Alan J.; Carlson, Emily; Tam, William
(1a<i>R</i>*,2<i>R</i>*,7<i>S</i>*,7a<i>S</i>*)-<i>rel</i>-3,6-Dimethoxy-2-methyl-1a,2,7,7a-tetrahydro-2,7-epoxy-1<i>H</i>-cyclopropa[<i>b</i>]naphthalene
IUCrData, 2016, 1, x160341
1542727 CIF
HKL
Paper		C76 H72 Ag2 Cl N O5 P4 S2P -112.44; 13.07; 13.579
93.489; 117.157; 115.354		1682.6Li, Yun-Hua; Shao, Yong-Liang
μ-Chlorido-bis[(dimethyl sulfoxide-κ<i>O</i>)bis(triphenylphosphane-κ<i>P</i>)silver(I)] nitrate
IUCrData, 2016, 1, x160332
1542728 CIF
HKL
Paper		C13 H19 N O3P -15.2542; 10.374; 11.341
94.937; 102.429; 102.811		582.8Moriguchi, Tetsuji; Kamoto, Ryota; Jalli, Venkataprasad; Tsuge, Akihiko
<i>N</i>-Hexyl-3,4-dihydroxybenzamide
IUCrData, 2016, 1, x160346
1542729 CIF
HKL
Paper		C32 H48 Cl4 Cu2 N6 O20P 1 21/n 115.262; 9.355; 15.832
90; 92.858; 90		2257.6Zhu, Xian-Hong; Li, Peng; Chen, Xiao-Wei; Ke, Wen-Shan; Chen, Fei; Zhang, Hua-Xin
[μ-<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-Tetrakis(pyridin-2-ylmethyl)butane-1,4-diamine]bis[(dimethanol-κ<i>O</i>)(perchlorato-κ<i>O</i>)copper(II)] bis(perchlorate)
IUCrData, 2016, 1, x160344
1542730 CIFC22 H18P n a 2122.283; 10.1485; 6.7864
90; 90; 90		1534.7Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Divergent reaction pathways in gold-catalyzed cycloisomerization of 1,5-enynes containing a cyclopropane ring: dramatic ortho substituent and temperature effects
Chem. Sci., 2016, 7, 4318
1542731 CIFC24 H18P 1 21/n 17.4014; 11.2513; 19.726
90; 91.021; 90		1642.4Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Divergent reaction pathways in gold-catalyzed cycloisomerization of 1,5-enynes containing a cyclopropane ring: dramatic ortho substituent and temperature effects
Chem. Sci., 2016, 7, 4318
1542732 CIFC19 H18 OP 1 21/n 19.9373; 5.8477; 23.768
90; 98.064; 90		1367.5Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Divergent reaction pathways in gold-catalyzed cycloisomerization of 1,5-enynes containing a cyclopropane ring: dramatic ortho substituent and temperature effects
Chem. Sci., 2016, 7, 4318
1542733 CIFC19 H19 Cl O5P -17.9475; 10.528; 11.586
93.439; 108.109; 96.394		911.1Che, Chao; Huang, Qianwen; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed cascade annulation of unsaturated α-bromocarbonyls with enynals: a facile access to ketones from aldehydes
Chem. Sci., 2016, 7, 4134
1542734 CIFC20 H22 O5P -18.172; 9.085; 13.302
85.887; 79.292; 63.379		867.4Che, Chao; Huang, Qianwen; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed cascade annulation of unsaturated α-bromocarbonyls with enynals: a facile access to ketones from aldehydes
Chem. Sci., 2016, 7, 4134
1542735 CIFC19 H19 Cl O6P -19.9793; 11.954; 15.515
90.309; 90.735; 101.28		1814.9Che, Chao; Huang, Qianwen; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed cascade annulation of unsaturated α-bromocarbonyls with enynals: a facile access to ketones from aldehydes
Chem. Sci., 2016, 7, 4134
1542736 CIFC22 H19 F6 N4 O8 Os S2P 1 21/n 114.8667; 23.2445; 16.5946
90; 91.203; 90		5733.31Sugimoto, Hideki; Kanetake, Takayuki; Maeda, Kazuki; Itoh, Shinobu
Oxidative Cyclization of 1,5-Dienes with Hydrogen Peroxide Catalyzed by an Osmium(III) Complex: Synthesis of cis-Tetrahydrofurans.
Organic letters, 2016, 18, 1246-1249
1542737 CIFC15 H15 N O5C 1 2/c 128.1106; 5.872; 21.0927
90; 130.543; 90		2645.79Wendler, Felix; Rudolph, Tobias; Görls, Helmar; Jasinski, Nils; Trouillet, Vanessa; Barner-Kowollik, Christopher; Schacher, Felix H.
Maleimide-functionalized poly(2-ethyl-2-oxazoline): synthesis and reactivity
Polym. Chem., 2016, 7, 2419
1542738 CIFC14 H6 N2 O2P 16.061; 3.384; 11.575
90; 90; 90		237.4Fratini, Albert V.; Cross, Elisa M.; O'brien, Joseph F.; Adams, W. Wade
The structure of poly-2,5-benzoxazole (ABPBO) and poly-2,6-benzothiazole (ABPBT) fibers by X-ray diffraction
Journal of Macromolecular Science, Part B, 1985, 24, 159-179
1542739 CIFC14 H6 N2 S2P 16.044; 3.417; 12.194
90; 90; 90		251.8Fratini, Albert V.; Cross, Elisa M.; O'brien, Joseph F.; Adams, W. Wade
The structure of poly-2,5-benzoxazole (ABPBO) and poly-2,6-benzothiazole (ABPBT) fibers by X-ray diffraction
Journal of Macromolecular Science, Part B, 1985, 24, 159-179
1542740 CIFCe0.12 O2 Zr0.88P 42/n m c :13.627; 3.627; 5.2336
90; 90; 90		68.849Wang, X.-L.; Hubbard, C.R.; Alexander, K.B.; Becher, P.F.
Neutron diffraction measurements of the residual stresses in Al2O3 - ZrO2 (CeO2) ceramic composites
Journal of the American Ceramic Society, 1994, 77, 1569-1575
1542741 CIFC27 H19 N3 OP 1 21/c 14.832; 30.042; 13.79
90; 90.81; 90		2001.6Wang, Fen; Wang, He; Wang, Qiang; Yu, Songjie; Li, Xingwei
Co(III)-Catalyzed Synthesis of Quinazolines via C-H Activation of N-Sulfinylimines and Benzimidates.
Organic letters, 2016, 18, 1306-1309
1542742 CIFC33 H40 O7 SP 1 21 111.0077; 9.7685; 14.9709
90; 103.216; 90		1567.17Vibhute, Amol M.; Dhaka, Arun; Athiyarath, Vignesh; Sureshan, Kana M.
A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors
Chem. Sci., 2016, 7, 4259
1542743 CIFC22 H16 Cl N O2 SP 1 21/c 110.375; 16.767; 10.757
90; 97.534; 90		1855.1Zhang, Liangliang; Chen, Su; Gao, Yuzhen; Zhang, Pengbo; Wu, Yile; Tang, Guo; Zhao, Yufen
tert-Butyl Hydroperoxide Mediated Cascade Synthesis of 3-Arylsulfonylquinolines.
Organic letters, 2016, 18, 1286-1289
1542744 CIFC14 H17 N O3P b c a9.1055; 9.4967; 30.8939
90; 90; 90		2671.46Zhu, Chuanle; Li, Jiawei; Chen, Pengquan; Wu, Wanqing; Ren, Yanwei; Jiang, Huanfeng
Transition-Metal-Free Cyclopropanation of 2-Aminoacrylates with N-Tosylhydrazones: A General Route to Cyclopropane α-Amino Acid with Contiguous Quaternary Carbon Centers.
Organic letters, 2016, 18, 1470-1473
1542745 CIFC16 H19 N O5P 1 21/c 18.8082; 19.624; 9.7487
90; 95.42; 90		1677.5Zhu, Chuanle; Li, Jiawei; Chen, Pengquan; Wu, Wanqing; Ren, Yanwei; Jiang, Huanfeng
Transition-Metal-Free Cyclopropanation of 2-Aminoacrylates with N-Tosylhydrazones: A General Route to Cyclopropane α-Amino Acid with Contiguous Quaternary Carbon Centers.
Organic letters, 2016, 18, 1470-1473
1542746 CIFC48 H191 Co5 N40 O126 Sb9 W24P 21 327.1499; 27.1499; 27.1499
90; 90; 90		20012.7Zhang, Zhi-Ming; Duan, Xiaopin; Yao, Shuang; Wang, Zhishu; Lin, Zekai; Li, Yang-Guang; Long, La-Sheng; Wang, En-Bo; Lin, Wenbin
Cation-mediated optical resolution and anticancer activity of chiral polyoxometalates built from entirely achiral building blocks
Chem. Sci., 2016, 7, 4220
1542747 CIFC60 H235 Cl Co4 N49 O133 Sb9 W24P 1 21/c 121.9241; 26.104; 42.1665
90; 119.618; 90		20979Zhang, Zhi-Ming; Duan, Xiaopin; Yao, Shuang; Wang, Zhishu; Lin, Zekai; Li, Yang-Guang; Long, La-Sheng; Wang, En-Bo; Lin, Wenbin
Cation-mediated optical resolution and anticancer activity of chiral polyoxometalates built from entirely achiral building blocks
Chem. Sci., 2016, 7, 4220
1542748 CIFC48 H47 N10 O10.5 S2P -116.853; 17.211; 18.087
99.16; 91.7; 96.78		5136.9Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L.
Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening
Chem. Sci., 2016, 7, 4148
1542749 CIFC48 H52 N10 O13 S2P 1 21/n 113.49; 18.126; 20.197
90; 101.26; 90		4843.5Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L.
Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening
Chem. Sci., 2016, 7, 4148
1542750 CIFC54 H68 F12 N10 O10 P2P -110.032; 10.288; 15.459
80.45; 80.06; 80.81		1535.6Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L.
Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening
Chem. Sci., 2016, 7, 4148
1542751 CIFC40 H39 F12 N11 O2 P2P 1 21/n 111.353; 20.065; 19.117
90; 98.58; 90		4306.1Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L.
Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening
Chem. Sci., 2016, 7, 4148
1542752 CIFC40 H41 F12 N11 O3 P2C 1 2/c 128.552; 13.685; 22.641
90; 103.63; 90		8597Shang, Jia; Rambo, Brett M.; Hao, Xiang; Xiang, Jun-Feng; Gong, Han-Yuan; Sessler, Jonathan L.
Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening
Chem. Sci., 2016, 7, 4148
1542753 CIFC20 H18 O6P 1 21/c 111.2187; 15.6963; 9.3981
90; 90.354; 90		1654.9Do, Lien T. M.; Aree, Thammarat; Siripong, Pongpun; Pham, Tuyen N. K.; Nguyen, Phung K. P.; Tip-pyang, Santi
Bougainvinones A–H, Peltogynoids from the Stem Bark of PurpleBougainvillea spectabilisand Their Cytotoxic Activity
Journal of Natural Products, 2016

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