Crystallography Open Database

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1550392 CIFCo Li0.5 O2R -3 m :H2.8127; 2.8127; 14.2754
90; 90; 120		97.806Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550393 CIFCo Li0.58 O2R -3 m :H2.8145; 2.8145; 14.2475
90; 90; 120		97.74Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550394 CIFCo Li0.79 O2R -3 m :H2.8165; 2.8165; 14.093
90; 90; 120		96.817Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550395 CIFCo Li0.89 O2R -3 m :H2.8175; 2.8175; 14.0598
90; 90; 120		96.658Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550396 CIFCo Li0.98 O2R -3 m :H2.8178; 2.8178; 14.0621
90; 90; 120		96.694Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550397 CIFCo Li O2R -3 m :H2.8185; 2.8185; 14.0664
90; 90; 120		96.772Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550398 CIFCo Li1.16 O2R -3 m :H2.8176; 2.8176; 14.061
90; 90; 120		96.673Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550399 CIFCo Li1.43 O2R -3 m :H2.8503; 2.8503; 14.139
90; 90; 120		99.48Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1552859 CIF
HKL
Paper		C36 H38 Cl4 Cu2 N6 O2P 1 21/n 112.004; 9.7942; 17.4116
90; 107.633; 90		1950.9Naugle, Mercedes S.; Keller, Brittany T.; Zeller, Matthias; Zaleski, Curtis M.
Di-μ-chlorido-bis[chlorido(dimethylformamide-κ<i>N</i>)(3,5-diphenyl-1<i>H</i>-pyrazole-κ<i>N</i>^2^)copper(II)]
IUCrData, 2018, 3, x181186
1552860 CIF
HKL
Paper		C34 H45 Li Mo N4 O4 P2P -111.7633; 12.5731; 13.7249
87.283; 75.537; 67.45		1812.66Höhne, Martha; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
Tetracarbonyl-2κ^4^<i>C</i>-[μ-5-methyl-1,1,3-triphenyl-2-(propan-2-yl)-2,4-diaza-1,3-diphosphahexan-4-ido-1κ<i>N</i>^4^:2κ<i>P</i>^1^,<i>P</i>^3^](<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-tetramethylethane-1,2-diamine-1κ^2^<i>N</i>,<i>N</i>')lithiummolybdenum
IUCrData, 2018, 3, x181149
1553182 CIFC20 H19 N O7P 1 21/c 111.3454; 13.013; 12.3899
90; 91.009; 90		1828.93Kulkarni, Anand M.; Srinivas, Kolluru; Deshpande, Mukund V.; Ramana, Chepuri V.
Cu-catalyzed sequential C–N bond formations: expeditious synthesis of tetracyclic indoloindol-3-ones
Organic Chemistry Frontiers, 2016, 3, 43
1553195 CIFC24 H22 N4 O4P 21 21 217.6889; 15.5382; 16.4272
90; 90; 90		1962.58Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang
Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach
Organic Chemistry Frontiers, 2016, 3, 24
1553196 CIFC24 H26 N4 O6P -19.32; 10.5489; 12.1772
95.818; 90.49; 111.805		1104.44Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang
Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach
Organic Chemistry Frontiers, 2016, 3, 24
1553197 CIFC15 H24 Br N O5P -18.8508; 10.0352; 10.7879
116.066; 107.114; 90.5266		811.83Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553198 CIFC14 H23 Cl2 N O5P 1 21/n 111.7775; 8.7429; 16.8595
90; 105.852; 90		1670Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553199 CIFC13 H19 N O4P 1 21/n 111.3134; 9.429; 12.7345
90; 110.991; 90		1268.29Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553200 CIFC15 H21 N O4P 1 21/c 117.0197; 16.271; 10.1414
90; 99.0774; 90		2773.26Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553201 CIFC13 H19 N O5P 1 21/n 110.9816; 9.2222; 13.0751
90; 107.689; 90		1261.57Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553202 CIFC25 H32 Cl Ir N2P 1 21/n 113.083; 9.848; 18.876
90; 93.26; 90		2428.1Tang, Guo-Dong; Pan, Cheng-Ling; Li, Xingwei
Iridium(iii)- and rhodium(iii)-catalyzed coupling of anilines with α-diazoesters via chelation-assisted C‒H activation
Organic Chemistry Frontiers, 2016, 3, 87
1553203 CIFC27 H29 N O2P 1 21/c 115.5737; 12.7774; 11.4615
90; 91.399; 90		2280.06Roy, Tony; Bhojgude, Sachin Suresh; Kaicharla, Trinadh; Thangaraj, Manikandan; Garai, Bikash; Biju, Akkattu T.
Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines
Organic Chemistry Frontiers, 2016, 3, 71
1553204 CIFC12 H14 O2P 1 21/c 19.8964; 7.7982; 13.421
90; 91.267; 90		1035.5Ling, Jesse; Lam, Sze Kui; Lo, Brian; Lam, Sarah; Wong, Wing-Tak; Sun, Jian; Chen, Guanhua; Chiu, Pauline
Epoxy and aziridinyl enolsilanes in diastereoselective inter- and intramolecular Friedel–Crafts alkylations
Organic Chemistry Frontiers, 2016, 3, 457
1553205 CIFC22 H20 Cl N O2 SI 1 a 111.4861; 14.0594; 13.486
90; 111.393; 90		2027.77Prabagar, B.; Nayak, Sanatan; Mallick, Rajendra K.; Prasad, Rangu; Sahoo, Akhila K.
Triphenylphosphine promoted regio and stereoselective α-halogenation of ynamides
Organic Chemistry Frontiers, 2016, 3, 110
1553206 CIFC27 H28 Br N3 O7 SP 1 21 111.0065; 8.788; 14.4392
90; 99.424; 90		1377.78Gerten, Anthony L.; Stanley, Levi M.
Enantioselective dearomative [3 + 2] cycloadditions of indoles with azomethine ylides derived from alanine imino esters
Organic Chemistry Frontiers, 2016, 3, 339
1553207 CIFC36 H29 Cl O6P 21 21 216.2154; 20.2473; 22.9882
90; 90; 90		2893Fu, Zhenqian; Wu, Xingxing; Chi, Yonggui Robin
Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters
Organic Chemistry Frontiers, 2016, 3, 145
1553208 CIFC24 H25 N3 O2P -17.1121; 8.5933; 18.426
94.339; 100.719; 105.418		1057.3Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing
Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes
Organic Chemistry Frontiers, 2016, 3, 184
1553209 CIFC28 H26 N2 O3P 1 21/c 115.8733; 11.8466; 12.3385
90; 99.402; 90		2289Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing
Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes
Organic Chemistry Frontiers, 2016, 3, 184
1553210 CIFC22 H24 Br2 N2P -19.1241; 10.2171; 11.3635
78.194; 82.379; 72.418		985.63Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan
Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)
Organic Chemistry Frontiers, 2016, 3, 324
1553211 CIFC20 H22 N2P -17.4987; 7.9073; 14.5997
77.721; 79.566; 69.529		787.06Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan
Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)
Organic Chemistry Frontiers, 2016, 3, 324
1553212 CIFC22 H32 N2 O4P 21 21 2110.016; 10.025; 21.596
90; 90; 90		2168.5Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng
Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine
Organic Chemistry Frontiers, 2016, 3, 62
1553213 CIFC17 H25 Cl N2 O2C 2 2 2110.351; 11.942; 26.963
90; 90; 90		3332.9Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng
Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine
Organic Chemistry Frontiers, 2016, 3, 62
1553214 CIFC23 H27 Cl6 I N2P 1 21/n 112.0005; 9.4272; 25.9285
90; 101.178; 90		2877.7Desens, Willi; Kohrt, Christina; Spannenberg, Anke; Werner, Thomas
A novel zinc based binary catalytic system for CO2utilization under mild conditions
Organic Chemistry Frontiers, 2016, 3, 156
1553215 CIFC16 H17 Cl2 N O4P 21 21 218.3061; 9.701; 20.7173
90; 90; 90		1669.35Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo
Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis
Organic Chemistry Frontiers, 2016, 3, 319
1553216 CIFC16 H17 Br2 N O4P 1 21 18.3327; 9.5492; 11.4501
90; 108.133; 90		865.84Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo
Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis
Organic Chemistry Frontiers, 2016, 3, 319
1553217 CIFC20 H16 O5P -17.1154; 11.1585; 11.1645
107.811; 95.51; 91.238		838.83Zhang, Wen-Zhen; Yang, Ming-Wang; Yang, Xu-Tong; Shi, Ling-Long; Wang, Hui-Bo; Lu, Xiao-Bing
Double carboxylation of o-alkynyl acetophenone with carbon dioxide
Organic Chemistry Frontiers, 2016, 3, 217
1553218 CIFC25 H27 N O2 SP 1 21/n 18.6446; 10.8046; 24.326
90; 99.922; 90		2238.1Li, Jiawen; Qin, Guiping; Liu, Yang; Huang, Hanmin
Palladium-catalysed coupling reaction of aminals with N-sulfonyl hydrazones to give allylic sulfones
Organic Chemistry Frontiers, 2016, 3, 259
1553219 CIFC20 H28 O2 SiP 1 21/n 17.5687; 30.831; 8.0907
90; 90.916; 90		1887.7Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553220 CIFC14 H11 F3 OP -17.3733; 11.2959; 14.9182
109.524; 92.663; 101.436		1139.24Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553221 CIFC14 H12 O3P 1 2/c 115.9874; 10.2887; 13.7969
90; 108.28; 90		2154.92Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553222 CIFC14 H13 F OP b c a34.01; 9.158; 7.196
90; 90; 90		2241Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553223 CIFC34 H24 N PP -19.9764; 11.8382; 12.5698
115.716; 100.125; 93.876		1299.22Fu, Wai Chung; Zhou, Zhongyuan; Kwong, Fuk Yee
A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses
Organic Chemistry Frontiers, 2016, 3, 273
1553224 CIFC19 H16 F N O5 SP 21 21 2110.342; 12.672; 13.549
90; 90; 90		1775.6Yu, Jin-Sheng; Zhou, Jian
Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines
Organic Chemistry Frontiers, 2016, 3, 298
1553225 CIFC17 H14 F2 N2 O4 SP 21 21 217.1956; 9.6833; 23.2873
90; 90; 90		1622.59Yu, Jin-Sheng; Zhou, Jian
Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines
Organic Chemistry Frontiers, 2016, 3, 298
1553226 CIFC23 H14 Cl2 N2 OP 1 21/c 18.9936; 20.9137; 10.6975
90; 112.585; 90		1857.78Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553227 CIFC24 H14 Cl2 N2 O2P -16.3775; 12.1686; 13.4121
80.819; 88.955; 75.537		994.7Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553228 CIFC24 H14 Cl2 N2 O2P -15.2005; 13.556; 15.6215
73.584; 85.49; 87.12		1052.7Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553229 CIFC24 H17 Cl N2 O2P 21 21 218.0462; 9.2337; 26.6656
90; 90; 90		1981.2Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553230 CIFC20 H15 N3 O3I 1 2/a 113.6461; 10.723; 22.268
90; 90.915; 90		3258Nack, W. A.; Wang, B.; Wu, X.; Jiao, R.; He, G.; Chen, G.
Palladium-catalyzed arylation of β-methylene C(sp3)–H bonds at room temperature: desymmetrization of simple cycloalkyl carboxylic acids
Organic Chemistry Frontiers, 2016, 3, 561
1553231 CIFC23 H18 N2 O5P 1 21 17.6839; 11.0556; 12.4153
90; 106.486; 90		1011.32Jiao, Lihui; Zhao, Xiaowei; Liu, Huixin; Ye, Xinyi; Li, Yun; Jiang, Zhiyong
Organocatalytic asymmetric conjugate addition of diaryloxazolidin-2,4-diones to nitroolefins: an efficient approach to chiral α-aryl-α-hydroxy carboxylic acids
Organic Chemistry Frontiers, 2016, 3, 470
1553232 CIFC38 H34 N O4 P SP 1 21/c 113.83; 21.2702; 14.1309
90; 119.452; 90		3619.6Zhu, Yi-Long; Wang, De-Cai; Jiang, Bo; Hao, Wen-Juan; Wei, Ping; Wang, Ai-Fang; Qiu, Jiang-Kai; Tu, Shu-Jiang
Metal-free oxidative hydrophosphinylation of 1,7-enynes
Organic Chemistry Frontiers, 2016, 3, 385
1553233 CIFC13 H14 Br N O3 SP 1 21/c 120.218; 9.2121; 15.306
90; 95.315; 90		2838.5Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553234 CIFC13 H14 Br N O3 SP -17.8592; 9.0905; 9.748
79.19; 89.1; 77.31		667.1Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553235 CIFC16 H14 Br N O3 SP 1 21/c 111.83; 9.2659; 14.59
90; 97.6; 90		1585.2Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553236 CIFC16 H14 Br N O3 SP -18.3045; 9.415; 11.19
87.089; 73.797; 70.74		792.3Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553237 CIFC16 H14 Br N O3 SP 1 21/c 115.825; 8.982; 11.426
90; 109.905; 90		1527.1Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553238 CIFC22 H25 N O3P 1 21 18.1343; 27.626; 8.8172
90; 97.223; 90		1965.7Mu, Yucheng; Tan, Xiaodong; Zhang, Yemin; Jing, Xiaobi; Shi, Zhuangzhi
Pd(ii)-catalyzed β-C–H arylation of O-methyl ketoximes with iodoarenes
Organic Chemistry Frontiers, 2016, 3, 380
1553418 CIFC21 H15 Br F N OP -15.9396; 11.302; 13.413
96.05; 99.59; 101.21		862Sheng, Jinyu; Su, Xiang; Cao, Chengyao; Chen, Chao
Synthesis of benzo[1,3]oxazines via copper(i)-catalyzed cascade annulation of nitriles, aldehydes and diaryliodonium salts
Organic Chemistry Frontiers, 2016, 3, 501
1553419 CIFC28 H22 F3 N O5P 21 21 219.1158; 9.8126; 28.3116
90; 90; 90		2532.46Gao, Tai-Ping; Liu, Dan; Lin, Jun-Bing; Hu, Xiu-Qin; Wang, Zhu-Yin; Xu, Peng-Fei
Direct construction of chiral quaternary dihydropyranones through highly enantioselective organocatalytic hetero-Diels–Alder reactions of olefinic azlactones
Organic Chemistry Frontiers, 2016, 3, 598
1553420 CIFC25 H48 N2 O5 S SiP 1 21 112.5809; 8.9728; 13.319
90; 93.554; 90		1500.64Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553421 CIFC20 H28 Cl N2 O4.5 SP 21 21 2111.701; 14.628; 25.939
90; 90; 90		4439.8Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553422 CIFC250 H238 F24 N18 O12 P4 Ru2P n n n :222.824; 22.583; 47.813
90; 90; 90		24644.5Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553423 CIFC90 H102 F12 N10 O8 P2 RuP 1 21/n 120.3614; 15.5902; 30.5936
90; 94.4504; 90		9682.3Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553424 CIFC102 H130 F12 N10 O26 S4 Zn2P -111.0301; 12.3939; 21.8715
76.878; 78.788; 87.305		2856.3Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553425 CIFC155 H166 Cl22 F24 N12 O12 P4 Ru2P -115.004; 15.1525; 21.5611
98.4023; 98.0121; 108.321		4512.9Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553426 CIFC98 H98 Br2 F12 N16 O10 P2 RuP 1 21/n 114.556; 24.668; 26.949
90; 93.27; 90		9660.8Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.
Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 667
1553427 CIFC180 H194 F24 N22 O18 P4 Ru2P -113.6711; 16.967; 22.4266
71.073; 82.622; 68.288		4571.45Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.
Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 667
1553428 CIFC14 H16 O5P 1 21/c 119.5895; 7.0388; 9.2405
90; 91.626; 90		1273.63Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2016, 3, 714
1553429 CIFC14 H16 O5P 1 21/c 18.144; 14.5913; 11.013
90; 94.901; 90		1303.91Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2016, 3, 714
1553430 CIFC17 H16 Cl N O2P 21 21 218.1449; 10.8999; 16.4545
90; 90; 90		1460.81Vyas, Vijyesh K.; Bhanage, Bhalchandra M.
Asymmetric transfer hydrogenation of seven membered tricyclic ketones: N-substituted dibenzo[b,e]azepine-6,11-dione driven by nonclassical CH/O interactions
Organic Chemistry Frontiers, 2016, 3, 614
1553431 CIFC31 H28 N4 O3P 1 21 19.837; 10.113; 14.456
90; 106.063; 90		1382Zhu, Yi; Li, Yao; Meng, Qingbin; Li, Xin
An organocatalytic enantioselective vinylogous Mannich reaction of α,α-dicyanoolefins with isatin N-Boc ketimines
Organic Chemistry Frontiers, 2016, 3, 709
1553432 CIFC23 H15 Cl3 N2 O2P c a 217.7032; 16.441; 14.9629
90; 90; 90		1895Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen
Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling
Organic Chemistry Frontiers, 2016, 3, 799
1553433 CIFC21 H12 Cl N3 O2P -17.147; 7.9449; 16.405
101.767; 96.018; 106.731		859.9Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen
Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling
Organic Chemistry Frontiers, 2016, 3, 799
1553434 CIFC16 H11 Br O2P 1 21/c 19.986; 15.521; 8.74
90; 101.027; 90		1329.6Qiu, Guanyinsheng; Liu, Tong; Ding, Qiuping
Tandem oxidative radical brominative addition of activated alkynes and spirocyclization: switchable synthesis of 3-bromocoumarins and 3-bromo spiro-[4,5] trienone
Organic Chemistry Frontiers, 2016, 3, 510
1553435 CIFC37 H24 O3P -16.3266; 11.3868; 18.6894
94.305; 99.144; 100.166		1301Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553436 CIFC37 H26 O2P -16.514; 11.9444; 17.215
93.28; 94.949; 104.241		1289.2Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553437 CIFC38 H27 N O3.5P -112.8713; 12.9061; 18.4438
83.491; 70.221; 87.197		2864.3Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553438 CIFC41 H34 O6P 1 21/c 19.5936; 9.4163; 34.688
90; 93.15; 90		3128.8Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553439 CIFC38 H26 O2P -19.837; 10.766; 13.71
87.68; 77.4; 71.54		1343.4Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553440 CIFC29 H20 OC 1 2/c 126.128; 8.1552; 21.487
90; 119.724; 90		3976Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553441 CIFC71 H64 O24P 1 21/c 119.7803; 8.925; 17.1219
90; 93.062; 90		3018.37Leowanawat, Pawaret; Nowak-Król, Agnieszka; Würthner, Frank
Tetramethoxy-bay-substituted perylene bisimides by copper-mediated cross-coupling
Organic Chemistry Frontiers, 2016, 3, 537
1553442 CIFC20 H24 N2P 1 21/n 113.1094; 8.943; 14.6031
90; 105.214; 90		1652.03Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke
Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles
Organic Chemistry Frontiers, 2016, 3, 609
1553443 CIFC23 H24 N2 SP 1 21/n 111.6939; 9.4598; 16.9069
90; 91.481; 90		1869.65Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke
Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles
Organic Chemistry Frontiers, 2016, 3, 609
1553444 CIFC16 H16 O3 SP 21 21 215.9262; 8.0475; 31.957
90; 90; 90		1524.06Phanindrudu, Mandalaparthi; Tiwari, Dipak Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar
Magnetically separable nano-copper catalyzed unprecedented stereoselective synthesis of E-vinyl sulfones from tosylmethyl isocyanide and alkynes: TosMIC as a source of the sulfonyl group
Organic Chemistry Frontiers, 2016, 3, 795
1553445 CIFC23 H20 Br2 N2 O2P 1 21/n 113.4028; 11.2931; 14.0439
90; 91.99; 90		2124.4Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone
Organic Chemistry Frontiers, 2016, 3, 759
1553446 CIFC36 H56 Au Cl N O P SP 1 21 112.5457; 22.382; 12.6621
90; 92.052; 90		3553.2Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone
Organic Chemistry Frontiers, 2016, 3, 759
1553447 CIFC26 H21 N O3 SC 1 2/c 121.51; 10.73; 19.7
90; 113.492; 90		4170Gong, Xinxing; Xia, Hongguang; Wu, Jie
A palladium-catalyzed tandem reaction of 2-alkynylbenzenesulfonamides with 2-(2-bromoarylidene)cyclobutanones
Organic Chemistry Frontiers, 2016, 3, 697
1553448 CIFC23 H21 F N4P -110.5273; 11.4221; 34.217
90.072; 98.137; 105.697		3917.7Jiang, Yu; Wang, Qiang; Sun, Run; Tang, Xiang-Ying; Shi, Min
Base-induced synthesis of N-dialkylaminomethyl-2H-1,2,3-triazoles from N-sulfonyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2016, 3, 744
1553449 CIFC32 H25 N O6P 21 21 219.02156; 9.44417; 30.948
90; 90; 90		2636.81Ran, Guang-Yao; Wang, Pan; Du, Wei; Chen, Ying-Chun
α-Regioselective [3 + 2] annulations with Morita‒Baylis‒Hillman carbonates of isatins and 2-nitro-1,3-enynes
Organic Chemistry Frontiers, 2016, 3, 861
1553450 CIFC21 H13 N SP -17.187; 10.356; 11.075
66.214; 86.273; 89.284		752.6Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming
Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2016, 3, 870
1553451 CIFC22 H17 N O2 SP -111.0789; 11.6353; 16.29
93.084; 106.29; 115.259		1786.1Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming
Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2016, 3, 870
1553452 CIFC19 H17 N O5P 1 21/n 113.5013; 18.6052; 13.6121
90; 106.649; 90		3275.9Görgen née Boersch, Christina; Lutsenko, Kiril; Merkul, Eugen; Frank, Walter; Müller, Thomas J. J.
Catalytic one-pot synthesis of 4-(hetero)aryl substituted 5-(2-oxoethyl) oxazol-2(3H)-ones by coupling–isomerization–elimination (CIE) sequence
Organic Chemistry Frontiers, 2016, 3, 887
1553453 CIFC48 H53 Cl2 N3 O6 Ru SP 1 21/c 18.4973; 40.566; 26.516
90; 97.469; 90		9063Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553454 CIFC44 H49 Cl2 N3 O3 Ru SP n a 2116.8326; 12.2762; 20.4575
90; 90; 90		4227.3Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553455 CIFC40 H47 Cl2 N3 O4 Ru SP 1 21/c 111.3136; 21.889; 16.102
90; 97.063; 90		3957.3Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553456 CIFC36 H46 Cl2 N2 O3 RuP 1 21/c 120.114; 8.8782; 20.665
90; 105.736; 90		3552Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553457 CIFC22 H26 Cl3 N2 O RuP 21 21 212.073; 18.008; 10.7084
90; 90; 90		2328.1Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553458 CIFC42 H43 Cl2 N3 O4 Ru SR -3 :H40.354; 40.354; 14.657
90; 90; 120		20670Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553459 CIFC14 H10 F12 N2P 1 21/n 110.0639; 8.163; 20.469
90; 101.995; 90		1644.8Xie, Jin; Li, Jian; Wurm, Thomas; Weingand, Vanessa; Sung, Hui-Ling; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K.
A general photoinduced electron transfer-directed chemoselective perfluoroalkylation of N,N-dialkylhydrazones
Organic Chemistry Frontiers, 2016, 3, 841
1553460 CIFC27 H26 Cl2 F3 N7 SP b c a16.558; 17.307; 19.571
90; 90; 90		5608Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553461 CIFC27 H23 F6 N7 S2P -19.817; 11.968; 13.149
102.73; 99.17; 104.43		1421.3Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553462 CIFC27 H23 F6 N7 S2P 1 21/c 114.717; 15.564; 12.282
90; 103.48; 90		2735.8Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553463 CIFC17 H25 Cl2 N3 O4 SP -110.82; 10.975; 11.163
74.634; 62.808; 65.132		1065.4Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of (2-oxoindolin-3-yl)methanesulfonohydrazides via a photo-induced reaction of N-(2-iodoaryl)acrylamide, DABSO, and hydrazine
Organic Chemistry Frontiers, 2016, 3, 865
1553464 CIFC22 H18 F3 N O6P -111.266; 12.1474; 16.278
73.095; 73.52; 84.96		2043.8Li, Zong-Rui; Bao, Xing-Xing; Sun, Jian; Shen, Jing; Wu, Dun-Qi; Liu, Yan-Kai; Deng, Qing-Hai; Liu, Feng
Iron-catalyzed trifluoromethylation of vinylcyclopropanes: facile synthesis of CF3–containing dihydronaphthalene derivatives
Organic Chemistry Frontiers, 2016, 3, 934
1553465 CIFC16 H16 B N3 O2I 1 2/a 125.856; 5.37038; 21.5154
90; 101.646; 90		2926.05Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.
“Click-fluors”: triazole-linked saccharide sensors
Organic Chemistry Frontiers, 2016, 3, 918
1553466 CIFC24 H24 B N3 O4P -17.1065; 9.0913; 17.685
81.994; 84.409; 68.79		1053.43Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.
“Click-fluors”: triazole-linked saccharide sensors
Organic Chemistry Frontiers, 2016, 3, 918
1553467 CIFC14 H10 Br N O2P 21 21 214.4197; 11.6677; 22.915
90; 90; 90		1181.7Zhang, Xu; Xu, Bin; Xu, Ming-Hua
Rhodium-catalyzed asymmetric arylation of N- and O-containing cyclic aldimines: facile and efficient access to highly optically active 3,4-dihydrobenzo[1,4]oxazin-2-ones and dihydroquinoxalinones
Organic Chemistry Frontiers, 2016, 3, 944
1553468 CIFC14 H15 Cl N2 PdP 1 c 19.4647; 12.7252; 11.5908
90; 108.624; 90		1322.9Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553469 CIFC16 H19 Cl N2 PdP 1 21/c 19.6575; 11.675; 26.2578
90; 92.079; 90		2958.7Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553470 CIFC16 H17 Cl N2 O PdP 1 21/n 16.9704; 17.1706; 12.2014
90; 97.943; 90		1446.33Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553471 CIFC24 H19 Cl N O P PdP 1 21/n 112.2558; 9.9099; 17.4367
90; 109.768; 90		1992.95Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553472 CIFC23 H17 Cl N O P PdP -19.0641; 9.6782; 12.7031
91.535; 108.207; 112.231		966.47Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553473 CIFC25 H17 N O SP 1 21/n 15.4373; 22.5643; 15.678
90; 91.295; 90		1923Singh, Radhey M.; Kumar, Ritush; Bharadwaj, Kishor Chandra; Gupta, Tanu
Pd catalyzed facile synthesis of cyclopenta[b]quinolin-1-one via sequential Sonogashira coupling and annulation. An unusual mode of ring closure, using sulphur as a soft nucleophile
Organic Chemistry Frontiers, 2016, 3, 1100
1553474 CIFC36 H26P -19.2253; 12.0172; 12.8207
65.023; 76.245; 83.655		1251.4He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553475 CIFC32 H24P 1 21/n 19.4248; 9.6366; 25.0543
90; 94.474; 90		2268.6He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553476 CIFC40 H28P 1 21/c 116.4844; 9.1722; 19.225
90; 107.472; 90		2772.7He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553477 CIFC40 H28P 1 21/n 111.3717; 15.9519; 15.1309
90; 93.429; 90		2739.83He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553478 CIFC42 H28P 1 21/c 19.5798; 10.2198; 29.4004
90; 96.324; 90		2860.89He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553479 CIFC28 H23 Cl N4 O7P 1 21 112.766; 16.24; 13.427
90; 107.96; 90		2648Li, Jun-Hua; Cui, Zhi-Hao; Du, Da-Ming
Diastereo- and enantioselective construction of cyclohexanone-fused spirospyrazolones containing four consecutive stereocenters through asymmetric sequential reactions
Organic Chemistry Frontiers, 2016, 3, 1087
1553480 CIFC17 H22 O2P 1 21/c 111.7876; 19.8876; 12.1607
90; 94.193; 90		2843.2Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles
Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers
Organic Chemistry Frontiers, 2016, 3, 999
1553481 CIFC17 H22 O2P 1 21/c 119.1606; 13.3348; 23.8068
90; 108.315; 90		5774.6Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles
Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers
Organic Chemistry Frontiers, 2016, 3, 999
1553482 CIFC23 H27 N O6 SP 1 21/n 18.2306; 9.8924; 26.999
90; 98.152; 90		2176.1Duan, Shuangshuang; Long, Dan; Zhao, Changgui; Zhao, Gaoyuan; Yuan, Ziyun; Xie, Xingang; Fang, Jianguo; She, Xuegong
Efficient construction of the A/C/D tricyclic skeleton of palhinine A
Organic Chemistry Frontiers, 2016, 3, 1137
1553483 CIFC23 H19 Br OP 1 21/n 110.005; 9.977; 18.125
90; 92.34; 90		1807.7Liu, Yu; Zhao, Peng; Zhang, Bo; Xi, Chanjuan
MeOTf-catalyzed annulation of aldehydes and arylalkynes leading to 2,3-disubstituted indanones
Organic Chemistry Frontiers, 2016, 3, 1116
1553484 CIFC23 H20 SP -19.756; 10.716; 10.881
65.921; 68.07; 63.361		902.7Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.
Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes
Organic Chemistry Frontiers, 2016, 3, 1126
1553485 CIFC20 H13 F SP 1 21/c 16.0606; 13.4845; 18.39
90; 91.36; 90		1502.5Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.
Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes
Organic Chemistry Frontiers, 2016, 3, 1126
1553486 CIFC20 H17 F3 I N OC 1 2/c 131.8; 8.994; 13.605
90; 110.595; 90		3642An, Yuanyuan; Kuang, Yunyan; Wu, Jie
Synthesis of trifluoromethylated 3,4-dihydroquinolin-2(1H)-ones via a photo-induced radical cyclization of benzene-tethered 1,7-enynes with Togni reagent
Organic Chemistry Frontiers, 2016, 3, 994
1553487 CIFC21 H19 Br N2 O4P 21 21 218.4058; 10.8659; 21.9188
90; 90; 90		2001.99Ma, Qiao; Gong, Lei; Meggers, Eric
Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter
Organic Chemistry Frontiers, 2016, 3, 1319
1553488 CIFC20 H18 N6 OP 1 21/c 120.5231; 9.5667; 20.3255
90; 115.091; 90		3614.1Liu, Hou-Lu; Jiang, Yu; Hao, Jian; Tang, Xiang-Ying; Shi, Min
A new method to access triazole-fused spiro-guanidines from the reaction of isothiocyanates tethered N-sulfonyl-1,2,3-triazoles and amines
Organic Chemistry Frontiers, 2016, 3, 1447
1553489 CIFC18 H11 I N2 OP -17.504; 8.467; 13.179
95.607; 102.6; 110.95		748.8Wu, Yan-Dong; Geng, Xiao; Gao, Qinghe; Zhang, Jingjing; Wu, Xia; Wu, An-Xin
Iodine-promoted sequential dual oxidative Csp3–H amination/Csp3–H iodination reactions: efficient synthesis of 1-iodoimidazo[1,5-a]pyridines
Organic Chemistry Frontiers, 2016, 3, 1430
1553490 CIFC60 H44 N4 O4 Pd2P c c n20.2007; 25.2676; 31.3498
90; 90; 90		16001.7Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi
Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules
Organic Chemistry Frontiers, 2016, 3, 1286
1553491 CIFC61 H45 Cl3 N4 O4 Pd2C 1 2/c 127.6181; 13.0551; 30.802
90; 113.65; 90		10173.2Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi
Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules
Organic Chemistry Frontiers, 2016, 3, 1286
1553492 CIFC29 H44 O6 SiP 21 21 2111.5223; 14.9948; 16.4141
90; 90; 90		2835.9Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553493 CIFC29 H40 O5 SiC 1 2 127.836; 7.8125; 14.1759
90; 92.711; 90		3079.4Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553494 CIFC17 H14 O2P 1 21/c 113.6594; 5.9624; 17.4715
90; 106.688; 90		1363Cui, Fei-Hu; Su, Shi-Xia; Xu, Yan-li; Liang, Ying; Wang, Heng-shan; Pan, Ying-Ming
Capture of CO2 in air for 4,5-disubstituted furan-2(5H)-ones
Organic Chemistry Frontiers, 2016, 3, 1304
1553495 CIFC38 H24 Cl2 N2 O6P 1 21/c 114.2296; 6.2823; 33.8457
90; 90.358; 90		3025.56Wirtanen, T.; Muuronen, M.; Hurmalainen, J.; Tuononen, H. M.; Nieger, M.; Helaja, J.
Intermolecular oxidative dehydrogenative 3,3′-coupling of benzo[b]furans and benzo[b]thiophenes promoted by DDQ/H+: total synthesis of shandougenine B
Organic Chemistry Frontiers, 2016, 3, 1738
1553496 CIFC62 H61 N7 O20 S4P 1 21/n 113.909; 20.264; 22.762
90; 91.41; 90		6414Gaeta, Carmine; Della Sala, Paolo; Talotta, Carmen; De Rosa, Margherita; Soriente, Annunziata; Brancatelli, Giovanna; Geremia, Silvano; Neri, Placido
A tetrasulfate-resorcin[6]arene cavitand as the host for organic ammonium guests
Organic Chemistry Frontiers, 2016, 3, 1276
1553498 CIFC14 H17 N5 O4P 21 21 217.51038; 17.3551; 23.2172
90; 90; 90		3026.21Naik, Siddhi D.; Chandra, Girish; Sahu, Pramod K.; Kim, Hong-Rae; Qu, Shuhao; Yoon, Ji-seong; Jeong, Lak Shin
Stereo- and regio-selective synthesis of 3′-C-substituted-(N)-methanocarba adenosines as potential anticancer agents
Organic Chemistry Frontiers, 2016, 3, 1472
1553499 CIFC16 H12 F3 N O2P 1 21/c 112.057; 8.771; 14.736
90; 113.287; 90		1431.4Mizuta, Satoshi; Otaki, Hiroki; Kitamura, Kanami; Nishi, Kodai; Watanabe, Ken; Makau, Juliann Nzembi; Hashimoto, Ryo; Usui, Toshiya; Chiba, Kenya
3,3-Dibromo-2-trifluoromethyl acrylic acid ethyl ester: a versatile platform for the stereoselective preparation of functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones
Organic Chemistry Frontiers, 2016, 3, 1661
1553500 CIFC17 H10 Cl F3 N2 OP -18.165; 9.432; 10.126
85.485; 83.241; 73.145		740.3Jin, Li-Kun; Lu, Guo-Ping; Cai, Chun
Copper-catalyzed 8-amido chelation-induced regioselective C–H fluoroalkylation of quinolines
Organic Chemistry Frontiers, 2016, 3, 1309
1553501 CIFC24 H15 NP 21 21 214.8217; 10.1093; 31.14
90; 90; 90		1517.89Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553502 CIFC22 H13 N SP c a 2116.3471; 11.2916; 8.0242
90; 90; 90		1481.15Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553503 CIFC23 H24 N2P -16.202; 10.169; 14.7158
75.057; 85.343; 84.132		890.56Liu, Cheng-Guo; Gu, Zheng-Yang; Bai, Hui-Wen; Wang, Shun-Yi; Ji, Shun-Jun
An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions
Organic Chemistry Frontiers, 2016, 3, 1299
1553504 CIFC22 H25 N2 O4 PP -18.9115; 11.1099; 11.8272
83.858; 86.228; 67.922		1078.45Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates
Organic Chemistry Frontiers, 2016, 3, 1646
1553505 CIFC22 H25 N2 O4 PP c c n15.3031; 18.1046; 15.6855
90; 90; 90		4345.8Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates
Organic Chemistry Frontiers, 2016, 3, 1646
1553506 CIFC31 H27 N2 O2P 21 21 218.681; 17.323; 32.77
90; 90; 90		4928Chen, Zhen; Huo, Yuwen; An, Ping; Wang, Xichao; Song, Chun; Ma, Yudao
[2.2]Paracyclophane-based N-heterocyclic carbene as efficient catalyst or as ligand for copper catalyst for asymmetric α-silylation of N-tosylaldimines
Organic Chemistry Frontiers, 2016, 3, 1725
1553507 CIFC17 H31 N O4P 21 21 217.643; 16.144; 6.601
90; 90; 90		1880.2Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553508 CIFC17 H31 N O4P 21 21 216.03; 16.334; 18.224
90; 90; 90		1795Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553509 CIFC13 H21 N O3P 1 21 110.178; 21.78; 11.615
90; 90.547; 90		2574.7Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553510 CIFC13 H21 N O3P 21 21 216.078; 10.204; 19.957
90; 90; 90		1237.73Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553511 CIFC26 H42 N2 O6P 1 21 17.252; 25.57; 14.465
90; 100.17; 90		2640.2Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553512 CIFC41 H31 Cl2 N O2P -19.1392; 13.2716; 13.7699
77.608; 76.026; 84.909		1581.79Seifert, Sabine; Schmidt, David; Würthner, Frank
A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides
Organic Chemistry Frontiers, 2016, 3, 1435
1553513 CIFC79 H66 Cl2 N2 O4P 1 21/c 113.3641; 15.796; 14.8901
90; 112.839; 90		2896.9Seifert, Sabine; Schmidt, David; Würthner, Frank
A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides
Organic Chemistry Frontiers, 2016, 3, 1435
1553514 CIFC24 H20 O2 SP 1 21/n 19.2961; 10.1519; 20.823
90; 102.267; 90		1920.26Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo
Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones
Organic Chemistry Frontiers, 2016, 3, 1452
1553515 CIFC27 H20 O2 SP 1 21/c 17.0521; 28.03; 10.4649
90; 100.069; 90		2036.7Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo
Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones
Organic Chemistry Frontiers, 2016, 3, 1452
1553516 CIFC33 H35 N O4 SP 1 21/c 115.4186; 11.3388; 16.9081
90; 107.55; 90		2818.4Lv, Leiyang; Bai, Xiaohui; Yan, Xiaoyu; Li, Zhiping
Iron-catalyzed decarbonylation initiated [2 + 2 + m] annulation of benzene-linked 1,n-enynes with aliphatic aldehydes
Organic Chemistry Frontiers, 2016, 3, 1509
1553517 CIFC29 H26 N2 O5 SP -18.3151; 8.625; 18.7838
99.74; 96.686; 104.017		1270.61Sharma, Pankaj; Kumar, Niggula Praveen; Krishna, Namballa Hari; Prasanna, Daasi; Sridhar, Balasubramanian; Shankaraiah, Nagula
Silver(i)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds
Organic Chemistry Frontiers, 2016, 3, 1503
1553518 CIFC14 H17 F3 N2 O3 SP 1 21/n 18.849; 10.773; 17.758
90; 91.599; 90		1692.2Li, Yuewen; Xiang, Yuanchao; Li, Zhiming; Wu, Jie
Direct vicinal difunctionalization of alkynes through trifluoromethylation and aminosulfonylation via insertion of sulfur dioxide under catalyst-free conditions
Organic Chemistry Frontiers, 2016, 3, 1493
1553528 CIFC22 H32 O2 SiP b c a12.7034; 11.6077; 28.683
90; 90; 90		4229.5Liu, Zhen; Xia, Ying; Feng, Sheng; Zhang, Yan; Wang, Jianbo
Rh(i)-Catalyzed coupling of 2-bromoethyl aryldiazoacetates with tertiary propargyl alcohols through carbene migratory insertion
Organic Chemistry Frontiers, 2016, 3, 1691
1553529 CIFC24 H19 N O3P -19.3034; 9.6541; 11.6687
101.875; 106.962; 96.397		964.39Duan, Jindian; Cheng, Yuyu; Li, Rou; Li, Pengfei
Synthesis of spiro[indane-1,3-dione-1-pyrrolines] via copper-catalyzed heteroannulation of ketoxime acetates with 2-arylideneindane-1,3-diones
Organic Chemistry Frontiers, 2016, 3, 1614
1553532 CIFC18 H16 O SP b c a11.1348; 10.8734; 24.741
90; 90; 90		2995.5An, Zhenyu; She, Yue; Yang, Xiaodong; Pang, Xiaobo; Yan, Rulong
Metal-free synthesis of 3-methylthiofurans from homopropargylic alcohols and DMSO via a tandem sulfenylation/cyclization reaction in a one-pot manner
Organic Chemistry Frontiers, 2016, 3, 1746
1553533 CIFC24 H21 N OP 1 21/c 19.2943; 18.714; 20.557
90; 95.79; 90		3557.3Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553534 CIFC24 H19 NP b c a11.335; 7.4991; 37.869
90; 90; 90		3219Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553535 CIFC42 H34 Cl7 N3 PdP -110.641; 10.978; 17.744
100.04; 106.43; 93.41		1944.7Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553536 CIFC44 H40 Cl N3 PdR -3 :H36.49; 36.49; 21.305
90; 90; 120		24567Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553537 CIFC33 H25 Cl3 N2 O PdP 1 21/c 111.611; 19.188; 13.466
90; 113.15; 90		2758.5Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553538 CIFC34 H27 Cl N2 O PdP 1 21/n 114.187; 12.38; 14.674
90; 92.59; 90		2574.6Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553539 CIFC40 H33 N3 O0P 1 21/c 111.91; 32.793; 9.4655
90; 113.37; 90		3393.6Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553540 CIFC50 H50 N2 O6 S2P 1 21/c 112.0255; 18.091; 10.1121
90; 105.935; 90		2115.4Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent
Catalytic applications of [IPr·GaX2][SbF6] and related species
Organic Chemistry Frontiers, 2016, 3, 1603
1553541 CIFC18 H22 O4P b c a7.6825; 17.5861; 22.9639
90; 90; 90		3102.5Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent
Catalytic applications of [IPr·GaX2][SbF6] and related species
Organic Chemistry Frontiers, 2016, 3, 1603
1553542 CIFC20 H13 F SP 1 21/c 16.0149; 13.4117; 18.2153
90; 91.601; 90		1468.86Wang, Xiaoming; Gensch, Tobias; Glorius, Frank
Highly selective synthesis of 6-substituted benzothiophenes by Sc(OTf)3-catalyzed intermolecular cyclization and sulfur migration
Organic Chemistry Frontiers, 2016, 3, 1619
1553546 CIFC24 H28 O8P 1 21/c 116.1503; 8.3426; 18.1574
90; 108.184; 90		2324.3Cao, Tao; Ma, Shengming
Nickel-catalyzed alkyl-zincation and carboxylation of diynes
Organic Chemistry Frontiers, 2016, 3, 1711
1553553 CIFC19 H17 Cl OP 1 21 15.828; 8.2327; 16.8844
90; 98.492; 90		801.23Luo, Hongwen; Yu, Yihua; Ma, Shengming
Suzuki coupling for preparation of allenes – ligand effects and chirality transfer
Organic Chemistry Frontiers, 2016, 3, 1705
1553655 CIFC72 H84 N12R -3 :H24.741; 24.741; 19.826
90; 90; 120		10510Slater, A. G.; Little, M. A.; Briggs, M. E.; Jelfs, K. E.; Cooper, A. I.
A solution-processable dissymmetric porous organic cage
Molecular Systems Design & Engineering, 2018, 3, 223
1553656 CIFC73.1 H89.96 Cl1.55 N12 O1.89R -3 :H24.483; 24.483; 19.6123
90; 90; 120		10181Slater, A. G.; Little, M. A.; Briggs, M. E.; Jelfs, K. E.; Cooper, A. I.
A solution-processable dissymmetric porous organic cage
Molecular Systems Design & Engineering, 2018, 3, 223
1553657 CIFC4 H18 N2 O22 Se6 V3P -110.0027; 10.4765; 12.2924
74.478; 72.643; 79.707		1177.8Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553658 CIFC4 H12 N2 O10 Se2 V2P 1 21/c 110.0879; 6.2047; 10.6765
90; 116.566; 90		597.71Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553659 CIFC8 H44 N4 O48 Se12 V6C 1 2/c 118.816; 7.934; 34.439
90; 95.85; 90		5114Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553660 CIFC8 H58.67 N6 O65.33 Se16 V8P 1 21/c 117.999; 15.658; 26.0344
90; 113.803; 90		6713.1Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553661 CIFC8 H43 N4 O47 Se12 V6P 1 21/c 124.713; 7.9212; 34.399
90; 130.376; 90		5129.9Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1554236 CIFC25 H20 SP 18.886; 10.971; 11.261
64.477; 78.704; 77.452		960.5Wang, Can; Yu, Yun; Chai, Zhaofei; He, Fangdi; Wu, Chaozheng; Gong, Yanbin; Han, Mengmeng; Li, Qianqian; Li, Zhen
Recyclable mechanoluminescent luminogen: different polymorphs, different self-assembly effects of the thiophene moiety and recovered molecular packing via simple thermal-treatment
Materials Chemistry Frontiers, 2019, 3, 32
1554237 CIFC25 H20 SP 21 21 215.988; 7.36; 45.02
90; 90; 90		1984.1Wang, Can; Yu, Yun; Chai, Zhaofei; He, Fangdi; Wu, Chaozheng; Gong, Yanbin; Han, Mengmeng; Li, Qianqian; Li, Zhen
Recyclable mechanoluminescent luminogen: different polymorphs, different self-assembly effects of the thiophene moiety and recovered molecular packing via simple thermal-treatment
Materials Chemistry Frontiers, 2019, 3, 32
1554238 CIFC61 H55 N5 O2 SP -113.5619; 13.7951; 15.3779
110.309; 101.188; 97.849		2581.1Yu, Hai-Xia; Zhi, Junge; Chang, Zheng-Feng; Shen, Tianjiao; Ding, Wei-Lu; Zhang, Xiaoling; Wang, Jin-Liang
Rational design of aggregation-induced emission sensor based on Rhodamine B for turn-on sensing of trivalent metal cations, reversible data protection, and bioimaging
Materials Chemistry Frontiers, 2019, 3, 151
1554239 CIFC40 H37 F6 N O2 PP 1 21/c 111.951; 15.59; 18.828
90; 97.29; 90		3479.6Ren, Fei; Liu, Pai; Gao, Yu; Shi, Jianbing; Tong, Bin; Cai, Zhengxu; Dong, Yuping
Real time bioimaging for mitochondria by taking the aggregation process of aggregation-induced emission near-infrared dyes with wash-free staining
Materials Chemistry Frontiers, 2019, 3, 57
1554240 CIFC25 H14 N4 O SP 1 21/c 117.804; 9.217; 12.5258
90; 107.795; 90		1957.1Wang, Ya-Kun; Huang, Chen-Chao; Kumar, Sarvendra; Wu, Sheng-Fan; Yuan, Yi; Aziz Khan, Aziz Khan; Jiang, Zuo-Quan; Fung, Man-Keung; Liao, Liang-Sheng
The roles of thermally activated delayed fluorescence sensitizers for efficient red fluorescent organic light-emitting diodes with D–A–A type emitters
Materials Chemistry Frontiers, 2019, 3, 161
1554241 CIFC109 H80 N16 O10 S4P -111.8289; 20.0485; 21.3871
105.379; 102.037; 99.001		4660.7Wang, Ya-Kun; Huang, Chen-Chao; Kumar, Sarvendra; Wu, Sheng-Fan; Yuan, Yi; Aziz Khan, Aziz Khan; Jiang, Zuo-Quan; Fung, Man-Keung; Liao, Liang-Sheng
The roles of thermally activated delayed fluorescence sensitizers for efficient red fluorescent organic light-emitting diodes with D‒A‒A type emitters
Materials Chemistry Frontiers, 2019, 3, 161
1554242 CIFC23 H17 N3 O3P 1 21 110.83; 7.65; 12.063
90; 103.07; 90		973.5He, Yanling; Li, Yuanyuan; Su, Huifang; Si, Yue; Liu, Yuanyuan; Peng, Qiuchen; He, Juan; Hou, Hongwei; Li, Kai
An o-phthalimide-based multistimuli-responsive aggregation-induced emission (AIE) system
Materials Chemistry Frontiers, 2019, 3, 50
1554243 CIFC47 H38 Cl2 N2 OP 1 21/c 120.728; 11.337; 17.818
90; 107.633; 90		3990Lin, Tingting; Su, Xing; Wang, Kai; Li, Minjie; Guo, Hongwei; Liu, Lulu; Zou, Bo; Zhang, Yu-Mo; Liu, Yifei; Zhang, Sean Xiao-An
An AIE fluorescent switch with multi-stimuli responsive properties and applications for quantitatively detecting pH value, sulfite anion and hydrostatic pressure
Materials Chemistry Frontiers, 2019, 3, 1052
1554244 CIFC41 H33 N3 O2P 1 21/c 115.538; 13.276; 16.39
90; 101.907; 90		3308.2Shimizu, Masaki; Tamagawa, Tomokazu; Nishimura, Kenta
4,5-Diaminophthalimides: highly efficient solid-state fluorophores and turn-on type fluorescent probes for hydrazine
Materials Chemistry Frontiers, 2019, 3, 563
1554245 CIFC29 H20 N2P c a 218.7745; 11.508; 20.298
90; 90; 90		2049.6Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554246 CIFC29 H23 N OP c a 2145.21; 6.1483; 7.449
90; 90; 90		2070.6Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554247 CIFC31 H27 NC 1 c 142.454; 11.064; 9.786
90; 94.49; 90		4582.5Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554248 CIFC29 H23 N OC 1 2/c 131.66; 5.901; 22.932
90; 100.11; 90		4217.8Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554249 CIFC32 H27 N3 OP 1 21/c 123.528; 6.0582; 17.914
90; 93.56; 90		2548.5Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554250 CIFC29 H20 N2P -18.4662; 15.145; 17.692
106.62; 95.32; 91.57		2160.9Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554251 CIFC37 H36 N4 O4 SP 1 21/n 111.695; 19.14; 15.289
90; 111.7; 90		3179.8Liu, Xuedan; Li, Aisen; Xu, Weiqing; Ma, Zhiyong; Jia, Xinru
An ESIPT-based fluorescent switch with AIEE, solvatochromism, mechanochromism and photochromism
Materials Chemistry Frontiers, 2019, 3, 620
1554252 CIFC45 H29 N5P -18.9145; 13.2762; 14.5859
110.467; 98.648; 96.716		1571.88Cao, Chen; Chen, Wen-Cheng; Tian, Shuang; Chen, Jia-Xiong; Wang, Zhong-Yi; Zheng, Xu-Hui; Ding, Chong-Wei; Li, Jing-Hong; Zhu, Jie-Ji; Zhu, Ze-Lin; Tong, Qing-Xiao; Lee, Chun-Sing
A novel D–π–A blue fluorophore based on [1,2,4]triazolo[1,5-a]pyridine as an electron acceptor and its application in organic light-emitting diodes
Materials Chemistry Frontiers, 2019, 3, 1071
1554611 CIFC63 H46 Cu F6 N4 O P3P -111.2628; 12.4158; 21.9828
83.055; 78.448; 87.667		2989.2Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael
Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety
Sustainable Energy & Fuels, 2019, 3, 692
1554612 CIFC48 H28 Cu F6 N8 PP -18.1362; 10.6863; 22.4625
86.186; 81.28; 87.085		1924.5Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael
Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety
Sustainable Energy & Fuels, 2019, 3, 692
1554613 CIFC22.5 H28 K0.5 N6 Ni0.5 O3P -112.9939; 13.5751; 14.0727
78.667; 85.315; 77.907		2377.8Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554614 CIFC36 H44 K2 N10 O3P 1 21/c 123.3268; 7.362; 22.2054
90; 94.794; 90		3800Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554615 CIFC24 H20 N10 NiP 1 21/n 17.7492; 16.392; 8.8505
90; 101.096; 90		1103.2Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554632 CIFC39 H32 F6 Ir N3 O0 S2C 1 2/c 126.026; 12.94; 22.386
90; 97.214; 90		7479.4Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860

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