Crystallography Open Database

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1554360 CIFC30 H42 B2 O5P -110.0513; 15.5408; 19.0622
88.904; 83.3; 87.795
2954.8Gao, Guoliang; Kuang, Zhijie; Song, Qiuling
Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2
Organic Chemistry Frontiers, 2018, 5, 2249
1554361 CIFC28 H31 Cl3 N2 PdP 1 21/n 110.3174; 12.4692; 20.4932
90; 96.89; 90
2617.4Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan
Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides
Organic Chemistry Frontiers, 2018, 5, 2484
1554362 CIFC28 H31 Cl N2 O PdP -110.0241; 11.2921; 11.727
92.4; 105.358; 106.802
1215.24Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan
Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides
Organic Chemistry Frontiers, 2018, 5, 2484
1554363 CIFC28 H28 Cl F3 N2 PdP b c a18.6245; 13.7023; 22.6048
90; 90; 90
5768.7Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan
Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides
Organic Chemistry Frontiers, 2018, 5, 2484
1554364 CIFC48 H39 Cl N2 PdP b c a18.9753; 19.6328; 20.1865
90; 90; 90
7520.2Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan
Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides
Organic Chemistry Frontiers, 2018, 5, 2484
1554365 CIFC35 H32 Br N3 O3P 1 21 112.6497; 9.0221; 14.1532
90; 113.568; 90
1480.53Mei, Hongjiang; Lin, Lili; Shen, Bin; Liu, Xiaohua; Feng, Xiaoming
Highly enantioselective desymmetrization of prochiral cyclic α,α-dicyanoalkenes via the direct vinylogous Michael/cyclization domino reaction
Organic Chemistry Frontiers, 2018, 5, 2505
1554366 CIFC18 H15 N O2 SP 1 21/c 118.6922; 5.447; 14.5323
90; 92.936; 90
1477.68Shen, Wen-Bo; Zhou, Bo; Zhang, Zhi-Xin; Yuan, Han; Fang, Wei; Ye, Long-Wu
Gold-catalyzed cascade cyclization of N-propargyl ynamides: rapid access to functionalized indeno[1,2-c]pyrroles
Organic Chemistry Frontiers, 2018, 5, 2468
1554367 CIFC10 H9 N OP 1 21 17.5235; 5.5446; 10.2976
90; 99.85; 90
423.23Wu, Qi; Li, Yabo; Wang, Chenyang; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
1,4-Refunctionalization of β-diketones to γ-keto nitriles via C–C single bond cleavage
Organic Chemistry Frontiers, 2018, 5, 2496
1554368 CIFC28 H17 F3 N2 O1.01P -17.933; 11.1848; 13.1762
72.919; 73.841; 84.499
1073.26Vivek Kumar, Sundaravel; Ellairaja, Sundaram; Satheesh, Vanaparthi; Sivasamy Vasantha, Vairathevar; Punniyamurthy, Tharmalingam
Rh-Catalyzed regioselective C‒H activation and C‒C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines
Organic Chemistry Frontiers, 2018, 5, 2630
1554369 CIFC43 H37 Cl3 N2 O2P 1 21 110.757; 12.558; 14.389
90; 99.306; 90
1918Lu, Yi-Nan; Ma, Chun; Lan, Jin-Ping; Zhu, Caiqiang; Mao, Yu-Jia; Mei, Guang-Jian; Zhang, Shu; Shi, Feng
Catalytic enantioselective and regioselective substitution of 2,3-indolyldimethanols with enaminones
Organic Chemistry Frontiers, 2018, 5, 2657
1554370 CIFC20 H18 O4C 1 2/c 122.7223; 5.7888; 25.159
90; 95.416; 90
3294.5Ma, Dengke; Song, Yulong; Fu, Chunling; Zhang, Fang; Guo, Yinlong; Huang, Xin; Ma, Shengming
E-Selective N-heterocyclic carbene-catalyzed reaction of aldehydes and butadienoates: effect of water and chloroform as the proton shuttle
Organic Chemistry Frontiers, 2018, 5, 2560
1554371 CIFC25 H22 Cl N O3 SP -110.2719; 10.4262; 11.7012
69.168; 73.012; 86.849
1118.45Wang, Hepan; Wang, Bingbing; Sun, Song; Cheng, Jiang
Copper-catalyzed radical Heck type cyclization: a three-component reaction of DABCO·(SO2)2, aryldiazonium tetrafluoroborates and dienes toward sulfonated benzo- seven-membered nitrogen heterocycles
Organic Chemistry Frontiers, 2018, 5, 2547
1554372 CIFC21 H19 Cl F N O6P -19.5372; 10.0615; 11.5029
74.116; 83.655; 71.87
1008.56Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L.
Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals
Organic Chemistry Frontiers, 2018, 5, 2588
1554373 CIFC16 H14 Cl F N2 O6P 1 21/c 116.4649; 6.9417; 15.0372
90; 93.483; 90
1715.5Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L.
Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals
Organic Chemistry Frontiers, 2018, 5, 2588
1554374 CIFC23 H31 N O2 SP -16.812; 11.371; 13.441
80.287; 84.84; 77.986
1002.1Han, Yulin; Ma, Shengming
Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes
Organic Chemistry Frontiers, 2018, 5, 2680
1554375 CIFC18 H23 N O2 SP 1 21/c 110.6868; 20.2; 8.0112
90; 101.747; 90
1693.2Han, Yulin; Ma, Shengming
Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes
Organic Chemistry Frontiers, 2018, 5, 2680
1554376 CIFC24 H30 O4P 1 21/c 18.9632; 26.894; 9.2793
90; 110.151; 90
2099.9Han, Yulin; Ma, Shengming
Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes
Organic Chemistry Frontiers, 2018, 5, 2680
1554377 CIFC36 H34 N O6P 1 21 111.0672; 24.0508; 11.3892
90; 91.3083; 90
3030.73Yue, Jing-Fei; Ran, Guang-Yao; Yang, Xing-Xing; Du, Wei; Chen, Ying-Chun
Asymmetric Diels–Alder cycloadditions of benzofulvene-based 2,4-dienals via trienamine activation
Organic Chemistry Frontiers, 2018, 5, 2676
1554378 CIFC24 H26 N2 O3P 1 21 110.2146; 11.7243; 10.2644
90; 119.315; 90
1071.84Zhang, Zi-Jing; Song, Jin
An isothiourea-catalyzed asymmetric formal [4 + 2] cycloaddition of in situ generated azoalkenes with C1 ammonium enolates
Organic Chemistry Frontiers, 2018, 5, 2578
1554379 CIFC32 H27 N O5 SP -110.276; 12.5669; 13.0463
66.455; 73.203; 66.317
1397.8Zhang, Changyuan; Chen, Lianfen; Chen, Kai; Wang, Chuntao; Xu, Zurong; Jiang, Huanfeng; Zhu, Shifa
Cu(i)-Catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition reaction
Organic Chemistry Frontiers, 2018, 5, 2510
1554380 CIFC29 H28 Cl N3 O7P 21 21 218.611; 11.3415; 28.819
90; 90; 90
2814.5Wei, Qinghua; Ma, Xiaochu; Chen, Jianghui; Niu, Li; Yang, Xi; Xia, Fei; Liu, Shunying
A triple-functionalised metal centre-catalyzed enantioselective multicomponent reaction
Organic Chemistry Frontiers, 2018, 5, 2799
1554381 CIFC29 H43 I Mg N2 OP -18.4477; 11.883; 15.889
97.79; 90.12; 96.968
1568.3Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554382 CIFC50 H66 Mg2 N4P 1 21/c 112.5799; 19.2069; 20.3357
90; 102.473; 90
4797.6Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554383 CIFC50 H66 Mg2 N4P n a 2121.9804; 19.3508; 11.283
90; 90; 90
4799.1Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554384 CIFC46 H58 Mg N4P -111.0139; 11.3202; 18.565
75.316; 83.401; 62.905
1993.3Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554385 CIFC54 H53 Mg N2P 1 21/c 111.4271; 17.954; 20.908
90; 93.495; 90
4281.6Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554386 CIFC48 H49 Cl2 N2P c c n21.607; 13.2782; 14.0261
90; 90; 90
4024.1Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554387 CIFC51 H55 I Mg N2 OC 1 2/c 125.689; 11.0511; 32.698
90; 105.996; 90
8923.3Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554388 CIFC58 H76 Cl2 Mg2 N4P 1 21/c 111.9804; 15.2444; 15.0882
90; 95.298; 90
2743.8Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554389 CIFC68 H96 B2 Mg2 N4 O6P -413.2295; 13.2295; 19.2267
90; 90; 90
3365.1Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554390 CIFC18 H36 B2 O6P 1 21/c 110.58; 10.4047; 10.785
90; 118.687; 90
1041.5Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554391 CIFC52 H70 Mg2 N4P c c n17.7085; 33.2898; 17.0054
90; 90; 90
10024.9Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao
Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds
Organic Chemistry Frontiers, 2018, 5, 3538
1554392 CIFC30 H21 Cl N2 O2P -18.5511; 10.4286; 14.3935
88.875; 87.601; 68.209
1190.78Xu, Hui; Chen, Kuan; Liu, Hong-Wei; Wang, Guan-Wu
Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions
Organic Chemistry Frontiers, 2018, 5, 2864
1554393 CIFC22 H24 Cl3 F6 N4 P RuP 1 21/n 18.1716; 30.1115; 10.9853
90; 95.159; 90
2692.1Wu, Qiang; Pan, Le; Du, Guangming; Zhang, Chi; Wang, Dawei
Preparation of pyridyltriazole ruthenium complexes as effective catalysts for the selective alkylation and one-pot C‒H hydroxylation of 2-oxindole with alcohols and mechanism exploration
Organic Chemistry Frontiers, 2018, 5, 2668
1554394 CIFC17 H13 F2 N O2P b c a8.3324; 18.0049; 18.9382
90; 90; 90
2841.2Ma, Xingxing; Deng, Shuilin; Song, Qiuling
Halodifluoroacetates as formylation reagents for various amines via unprecedented quadruple cleavage
Organic Chemistry Frontiers, 2018, 5, 3505
1554395 CIFC14 H17 N OP -16.32; 11.047; 16.999
90.548; 95.825; 90.542
1180.6Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco
Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study
Organic Chemistry Frontiers, 2018, 5, 3231
1554396 CIFC12 H26 Cl2 N2 Ni O7P -16.9966; 12.0579; 12.9998
63.724; 88.61; 86.344
981.4Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco
Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study
Organic Chemistry Frontiers, 2018, 5, 3231
1554397 CIFC22 H25 N O6P 1 21/c 110.9821; 9.771; 21.137
90; 119.629; 90
1971.56Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.
Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2829
1554398 CIFC23 H29 N O7P 1 c 17.0556; 15.3824; 10.7866
90; 108.471; 90
1110.38Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.
Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2829
1554399 CIFC22 H25 N O6P 1 21/c 115.7969; 8.7827; 14.6012
90; 103.801; 90
1967.28Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.
Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2829
1554400 CIFC43 H26 N2 O2P -19.516; 11.551; 13.616
91.24; 106.05; 99.94
1412.9Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław
Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin
Organic Chemistry Frontiers, 2018, 5, 3068
1554401 CIFC61 H45 B F4 N2 O2P 1 21/n 114.154; 17.553; 19.832
90; 106.78; 90
4717.4Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław
Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin
Organic Chemistry Frontiers, 2018, 5, 3068
1554402 CIFC86 H54 B8 F22 N4 O7P -18.09; 12.074; 24.254
82.58; 89.11; 70.85
2218.3Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław
Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin
Organic Chemistry Frontiers, 2018, 5, 3068
1554404 CIFC29 H37 N O7P 1 21 112.2892; 11.6999; 19.3795
90; 103.521; 90
2709.2Fan, Yaqin; Wang, Yi; Fu, Peng; Chairoungdua, Arthit; Piyachaturawat, Pawinee; Zhu, Weiming
Secopaxilline A, an indole-diterpenoid derivative from an aciduric Penicillium fungus, its identification and semisynthesis
Organic Chemistry Frontiers, 2018, 5, 2835
1554405 CIFC28 H24 O5P 1 21/n 19.5523; 9.8572; 23.9209
90; 99.141; 90
2223.76Zhao, Yinsong; Zheng, Qinze; Yu, Chuangui; Liu, Zheng; Wang, Deping; You, Jingsong; Gao, Ge
Rh(iii)-Catalyzed regioselective C–H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes
Organic Chemistry Frontiers, 2018, 5, 2875
1554406 CIFC30 H31 Br N2 O3P 1 21 113.248; 7.6262; 27.213
90; 97.298; 90
2727.1Yuan, Yang; Zheng, Zhan-Jiang; Ye, Fei; Ma, Jun-Han; Xu, Zheng; Bai, Xing-Feng; Li, Li; Xu, Li-Wen
Highly efficient desymmetrization of cyclopropenes to azabicyclo[3.1.0]hexanes with five continuous stereogenic centers by copper-catalyzed [3 + 2] cycloadditions
Organic Chemistry Frontiers, 2018, 5, 2759
1554407 CIFC23 H28 O6P 1 21 17.3005; 12.1224; 11.9121
90; 105.259; 90
1017.05Zhang, Xun; Li, Zhongle; Yong, Huaya; Xie, Zhixiang
Biomimetic syntheses of C23 terpenoids: structural revision of salyunnanin A and confirmation of hassanane
Organic Chemistry Frontiers, 2018, 5, 3469
1554408 CIFC14 H10 Br N O4P b c a7.5983; 16.424; 20.8458
90; 90; 90
2601.44Maezono, Shizuka Mei Bautista; Kim, Sung Hong; Lee, Yong Rok
Copper-catalyzed [3 + 2 + 1] annulation for functionalized pyridines as potent and dynamic UV absorbers
Organic Chemistry Frontiers, 2018, 5, 3368
1554409 CIFC18 H18 O2P 1 21/n 19.0575; 12.288; 12.993
90; 94.793; 90
1441Yang, Binmiao; Zhai, Xuejie; Feng, Shubo; Shao, Zhihui
Dearomatization of naphthols using oxy-allyl cations: efficient construction of α-all-carbon quaternary center-containing 2-(2-oxocycloalkyl)cycloalkyl diketones
Organic Chemistry Frontiers, 2018, 5, 2794
1554410 CIFC44 H42 Cl N5 O8P -117.135; 17.343; 20.802
106.696; 98.131; 118.106
4934.7Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo
Domino aza/oxa-hetero-Diels–Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine]
Organic Chemistry Frontiers, 2018, 5, 2754
1554411 CIFC42 H38 Cl N5 O6P -112.086; 12.455; 17.13
96.558; 109.996; 107.812
2236.9Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo
Domino aza/oxa-hetero-Diels–Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine]
Organic Chemistry Frontiers, 2018, 5, 2754
1554412 CIFC28 H22P -19.7638; 10.0633; 10.6246
100.341; 103.17; 95.285
990.28Chuskit, Deachen; Chaudhary, Renu; Venugopalan, Paloth; König, Burkhard; Natarajan, Palani
Oxidative homodimerization of substituted olefins by DDQ visible light photocatalysis
Organic Chemistry Frontiers, 2018, 5, 3553
1554413 CIFC18 H25 N O7 SP 1 21/c 110; 14.827; 13.344
90; 101.939; 90
1935.7Lei, Meng; Li, Yanjun; Cao, Shi; Hou, Xinyi; Gong, Lei
Alkylation–peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3–H functionalization
Organic Chemistry Frontiers, 2018, 5, 3083
1554414 CIFC19 H24 F3 N O2P -112.1127; 13.1333; 13.1505
76.939; 79.228; 63.194
1810.2Long, Hao; Song, Jinshuai; Xu, Hai-Chao
Electrochemical synthesis of 7-membered carbocycles through cascade 5-exo-trig/7-endo-trig radical cyclization
Organic Chemistry Frontiers, 2018, 5, 3129
1554415 CIFC30 H29 N3 O4 SP 1 21 18.6306; 10.9636; 14.5139
90; 90.644; 90
1373.25Huang, Qiuhong; Cheng, Yuyu; Yuan, Huijun; Chang, Xiaoyong; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective Mannich-type addition of 5H-thiazol-4-ones to isatin-derived imines: access to 3-substituted 3-amino-2-oxindoles featured by vicinal sulfur-containing tetrasubstituted stereocenters
Organic Chemistry Frontiers, 2018, 5, 3226
1554416 CIFC24 H22 N4 O4P 1 21/c 118.2546; 9.1982; 13.3199
90; 108.231; 90
2124.27Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun
Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors
Organic Chemistry Frontiers, 2018, 5, 3206
1554417 CIFC12 H12 N2 O3P 1 21/c 111.2278; 13.7389; 7.4364
90; 107.173; 90
1095.98Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun
Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors
Organic Chemistry Frontiers, 2018, 5, 3206
1554418 CIFC24 H20 N4 O5P 1 21/c 113.145; 14.0218; 12.9264
90; 114.416; 90
2169.47Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun
Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors
Organic Chemistry Frontiers, 2018, 5, 3206
1554421 CIFC24 H19 Cl N2 OP 1 21/c 15.628; 19.385; 17.569
90; 91.36; 90
1916.2Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei
Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines
Organic Chemistry Frontiers, 2018, 5, 2945
1554422 CIFC24 H19 Cl N2 OP -15.7976; 9.4263; 17.097
87.715; 87.737; 86.465
931.2Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei
Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines
Organic Chemistry Frontiers, 2018, 5, 2945
1554423 CIFC17 H0.25 N OP 21 21 216.229; 13.6065; 14.6177
90; 90; 90
1238.92Xu, Xin-Ming; Lei, Chuan-Hu; Tong, Shuo; Zhu, Jieping; Wang, Mei-Xiang
Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides
Organic Chemistry Frontiers, 2018, 5, 3138
1554424 CIFC27 H25 F N2 O5 SP 1 21 113.42; 5.3749; 17.821
90; 105.381; 90
1239.4Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing
Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F⋯H–N interactions on reactivity
Organic Chemistry Frontiers, 2018, 5, 2960
1554425 CIFC18 H16 Br F O2P 16.6841; 8.7074; 14.4482
87.391; 81.591; 78.532
815.14Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing
Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F⋯H–N interactions on reactivity
Organic Chemistry Frontiers, 2018, 5, 2960
1554426 CIFC14 H13 N O3P 1 21 110.0137; 10.3706; 11.987
90; 109.801; 90
1171.23Kim, Simon J.; Batey, Robert A.
Enantioselective isoquinuclidine synthesis via sequential Diels–Alder/visible-light photoredox C–C bond cleavage: a formal synthesis of the indole alkaloid catharanthine
Organic Chemistry Frontiers, 2018, 5, 2934
1554427 CIFC42 H50 O2 Si2P -17.6019; 7.7795; 17.7908
94.036; 92.577; 114.867
948.98Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan
Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs
Organic Chemistry Frontiers, 2018, 5, 2912
1554428 CIFC48 H50 N4 Si2C 1 2/c 139.755; 10.0294; 11.4351
90; 102.874; 90
4444.8Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan
Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs
Organic Chemistry Frontiers, 2018, 5, 2912
1554429 CIFC33 H35 N O6P 1 21/n 117.45405; 8.11896; 19.929
90; 91.5647; 90
2823.06Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin
Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction
Organic Chemistry Frontiers, 2018, 5, 3003
1554430 CIFC30 H26 Cl3 N O3P 1 21/c 111.083; 21.629; 12.241
90; 116.92; 90
2616Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin
Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction
Organic Chemistry Frontiers, 2018, 5, 3003
1554431 CIFC36 H37 O4 P SP 1 21/c 18.7333; 32.515; 11.3552
90; 92.555; 90
3221.3Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei
Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation
Organic Chemistry Frontiers, 2018, 5, 3567
1554432 CIFC45 H41 O4 P SP -110.244; 13.1272; 15.4443
85.216; 77.319; 69.981
1903.71Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei
Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation
Organic Chemistry Frontiers, 2018, 5, 3567
1554433 CIFC40 H39 O3 P SP 1 21/c 110.9576; 24.0001; 13.0509
90; 94.036; 90
3423.7Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei
Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation
Organic Chemistry Frontiers, 2018, 5, 3567
1554434 CIFC37 H35 O3 P SP 1 21/c 112.3705; 13.8788; 19.1238
90; 106.702; 90
3144.8Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei
Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation
Organic Chemistry Frontiers, 2018, 5, 3567
1554435 CIFC22 H24 N2P 1 21/c 122.09; 8.574; 9.447
90; 101.6; 90
1752.7Liu, Siyuan; Zhang, Wenzhu; Qu, Jingping; Wang, Baomin
Engaging 2-methyl indolenines in a tandem condensation/1,5-hydride transfer/cyclization process: construction of a novel indolenine–tetrahydroquinoline assembly
Organic Chemistry Frontiers, 2018, 5, 3008
1554436 CIFC21 H21 Br N O7 P SP 21 21 218.8385; 14.3341; 17.8495
90; 90; 90
2261.4Sun, Jun; Mou, Chengli; Liu, Changyi; Huang, Ruoyan; Zhang, Shupeng; Zheng, Pengcheng; Chi, Yonggui Robin
Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines
Organic Chemistry Frontiers, 2018, 5, 2992
1554441 CIFC28 H29 Co P SP 1 21/n 19.0319; 18.9034; 14.4632
90; 96.64; 90
2452.8Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang
Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives
Organic Chemistry Frontiers, 2018, 5, 2997
1554442 CIFC22 H18 N O2P 1 21/n 112.766; 7.3952; 18.2702
90; 103.067; 90
1680.17Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang
Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives
Organic Chemistry Frontiers, 2018, 5, 2997
1554443 CIFC30 H23 N O2P -17.3192; 11.4476; 14.2878
109.541; 103.435; 90.85
1091.7Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang
Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives
Organic Chemistry Frontiers, 2018, 5, 2997
1554444 CIFC26 H21 N O2P -17.4718; 10.17; 13.6849
80.313; 76.092; 74.405
966.3Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang
Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives
Organic Chemistry Frontiers, 2018, 5, 2997
1554445 CIFC28 H29 Br Co P SP n a 2116.6717; 10.051; 14.516
90; 90; 90
2432.4Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang
Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives
Organic Chemistry Frontiers, 2018, 5, 2997
1554448 CIFC28 H33 Br O3I 1 2 126.357; 7.5712; 24.9141
90; 92.458; 90
4967.1Liu, Lin; Song, Huayue; Chen, Peng; Yuan, Ziyun; Feng, Shangbiao; Zhang, Weiwei; Fang, Bowen; Xie, Xingang; She, Xuegong
Total synthesis of (−)-8-epi-chromazonarol enabled by a unique N2H4·H2O promoted intramolecular oxa-Michael cyclization reaction
Organic Chemistry Frontiers, 2018, 5, 3013
1554451 CIFC26 H23 N O2 SC 1 c 112.1152; 14.1577; 24.768
90; 93.519; 90
4240.3Zhang, Jia-hao; Wei, Yin; Shi, Min
Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2980
1554452 CIFC26 H23 N O2 SP 1 21/n 110.875; 11.83; 16.54
90; 98.8; 90
2103Zhang, Jia-hao; Wei, Yin; Shi, Min
Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2980
1554453 CIFC26 H23 N O4 SC 1 2/c 120.5631; 27.2351; 9.3277
90; 92.088; 90
5220.4Zhang, Jia-hao; Wei, Yin; Shi, Min
Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2980
1554454 CIFC20 H11 F12 O5 PP 1 21/c 115.787; 10.811; 13.977
90; 112.816; 90
2199Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.
Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Organic Chemistry Frontiers, 2018, 5, 3113
1554455 CIFC12 H20 N O4 PP 1 21 17.266; 11.409; 8.573
90; 96.695; 90
705.8Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.
Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Organic Chemistry Frontiers, 2018, 5, 3113
1554456 CIFC6 H7 O5 PP 21 21 214.6005; 10.122; 16.4334
90; 90; 90
765.24Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.
Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Organic Chemistry Frontiers, 2018, 5, 3113
1554457 CIFC24 H21 F6 O9 PP -110.7892; 11.1562; 11.7122
101.788; 99.647; 106.558
1283.93Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.
Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Organic Chemistry Frontiers, 2018, 5, 3113
1554458 CIFC18 H13 Cl6 O5 PI 41/a :227.972; 27.972; 11.844
90; 90; 90
9267Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.
Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Organic Chemistry Frontiers, 2018, 5, 3113
1554459 CIFC40 H40 N O2 SP -18.8009; 12.3786; 16.3465
102.889; 95.068; 108.26
1624.3Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang
Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells
Organic Chemistry Frontiers, 2018, 5, 3324
1554460 CIFC44 H42 N O2 SP -17.1299; 14.678; 17.037
74.911; 81.895; 89.178
1703.8Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang
Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells
Organic Chemistry Frontiers, 2018, 5, 3324
1554461 CIFC84 H80 N2 O4 S4P 1 21/c 113.5245; 24.687; 20.6534
90; 102.064; 90
6743.4Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang
Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells
Organic Chemistry Frontiers, 2018, 5, 3324
1554462 CIFC92 H81 N2 O4 S4P -114.3142; 16.7266; 18.5616
105.723; 109.469; 90.336
4010.6Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang
Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells
Organic Chemistry Frontiers, 2018, 5, 3324
1554467 CIFC19 H16 N2 O6 SP 1 21/c 19.7218; 7.7915; 24.097
90; 99.734; 90
1799Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang
Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines
Organic Chemistry Frontiers, 2018, 5, 3574
1554468 CIFC20 H19 N O4 SP -16.4452; 11.7323; 12.5163
105.865; 90.612; 93.872
907.9Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang
Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines
Organic Chemistry Frontiers, 2018, 5, 3574
1554469 CIFC33 H26 Cl N O2 SP 1 21/n 110.2302; 24.9417; 10.532
90; 94.66; 90
2678.4Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang
Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines
Organic Chemistry Frontiers, 2018, 5, 3574
1554470 CIFC26 H30 N4 O9I 1 2 19.9349; 5.4755; 25.351
90; 101.162; 90
1353Chen, Jinhong; Li, Junfang; Zhu, Longqing; Peng, Xue; Feng, Yiyue; Lu, Yingmei; Hu, Xiaoling; Liang, Jianpin; Zhao, Quanyi; Wang, Zhen
Total synthesis and structure revision of chrysamide B
Organic Chemistry Frontiers, 2018, 5, 3402
1554471 CIFC26 H30 O6P 1 21/n 111.6963; 8.9597; 23.096
90; 90.67; 90
2420.2Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans
Organic Chemistry Frontiers, 2018, 5, 3483
1554472 CIFC27 H28 Cl I N2 O5P -110.805; 11.7571; 12.8689
106.048; 95.01; 114.103
1396.3Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans
Organic Chemistry Frontiers, 2018, 5, 3483
1554473 CIFC14 H12 F6 N2 O4 S2P 1 21/n 18.4088; 17.398; 12.1982
90; 101.318; 90
1749.85Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554474 CIFC20 H15 F6 N O5 S2P 1 21/n 112.6441; 11.3643; 16.2034
90; 111.751; 90
2162.5Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554475 CIFC21 H19 F6 N O6 S3P 1 21/n 113.0371; 14.5605; 14.0643
90; 113.617; 90
2446.2Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554476 CIFC14 H11 Cl F6 N2 O5 S2C 1 2/c 131.442; 7.7594; 16.3435
90; 91.74; 90
3985.5Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554477 CIFC13 H8 F6 O7 S2P 1 21/n 15.7308; 13.6484; 21.184
90; 95.748; 90
1648.6Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554478 CIFC13 H10 F6 N2 O4 S2P 1 21/c 114.266; 6.0883; 18.922
90; 94.123; 90
1639.2Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554479 CIFC9 H10 F6 N2 O5 S2P b c a17.2641; 14.8304; 23.9088
90; 90; 90
6121.5Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554480 CIFC15 H14 F6 N2 O5 S2P n a 2127.2048; 18.3507; 12.2694
90; 90; 90
6125.2Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito
Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
Organic Chemistry Frontiers, 2018, 5, 3163
1554481 CIFC29 H28 N2 O S2P 1 21/n 117.607; 5.4871; 25.7682
90; 106.169; 90
2391Weldeab, Asmerom O.; Li, Lei; Cekli, Seda; Abboud, Khalil A.; Schanze, Kirk S.; Castellano, Ronald K.
Pyridine-terminated low gap π-conjugated oligomers: design, synthesis, and photophysical response to protonation and metalation
Organic Chemistry Frontiers, 2018, 5, 3170
1554482 CIFC26 H22 Br N O9P 1 21/c 111.2685; 18.6581; 12.8795
90; 111.426; 90
2520.8Agafonova, Anastasiya V.; Smetanin, Ilia A.; Rostovskii, Nikolai V.; Khlebnikov, Alexander F.; Novikov, Mikhail S.
Expedient synthesis of 3-hydroxypyrroles via Bu3SnH-triggered ionic 5-exo-trig-cyclization of 5-chloro-3-azamuconoate derivatives
Organic Chemistry Frontiers, 2018, 5, 3396
1554483 CIFC16 H9 Cl F3 N O3 SI b a 215.569; 29.973; 7.0564
90; 90; 90
3292.9Yi, Ruxia; Li, Xincheng; Wan, Boshun
Ring-opening and cyclization of aziridines with aryl azides: metal-free synthesis of 6-(triflyloxy)quinolines
Organic Chemistry Frontiers, 2018, 5, 3488
1554484 CIFC11 H9 F O2P 21 21 214.9693; 5.8579; 31.3863
90; 90; 90
913.64Han, Sang Hoon; Pandey, Ashok Kumar; Lee, Heeyoung; Kim, Saegun; Kang, Dahye; Jung, Young Hoon; Kim, Hyung Sik; Hong, Sungwoo; Kim, In Su
One-pot synthesis of 2-naphthols from nitrones and MBH adducts via decarboxylative N–O bond cleavage
Organic Chemistry Frontiers, 2018, 5, 3210
1554486 CIFC14 H8 N3 OP 1 21/n 15.7918; 13.738; 13.4519
90; 101.436; 90
1049.09Li, Ping-Gui; Yan, Cheng; Zhu, Shuai; Liu, Shu-Hui; Zou, Liang-Hua
Direct construction of benzimidazo[l,2-c]quinazolin-6-ones via metal-free oxidative C‒C bond cleavage
Organic Chemistry Frontiers, 2018, 5, 3464
1554487 CIFC37 H31 N3 O4 SP 1 21 113.6363; 8.5322; 15.2209
90; 116.205; 90
1588.9Gu, Bo-Qi; Yang, Wu-Lin; Wu, Shu-Xiao; Wang, Yan-Bing; Deng, Wei-Ping
Organocatalytic asymmetric synthesis of tetrahydrocarbazoles via an inverse-electron-demand Diels–Alder reaction of 2,3-indole-dienes with enals
Organic Chemistry Frontiers, 2018, 5, 3430
1554488 CIFC17 H18 N O5 PP -19.5039; 10.0075; 10.6869
64.045; 69.351; 83.294
854.35Wang, Jie; Li, Jun; Wei, Yuanyuan; Yang, Jingya; Huo, Congde
Copper-catalyzed oxidative phosphonation of 3,4-dihydro-1,4-benzoxazin-2-ones
Organic Chemistry Frontiers, 2018, 5, 3534
1556101 CIFC52 H48 N4 O3P -19.935; 15.483; 15.666
66.557; 76.89; 77.978
2134.4McCarthy, Jason R.; Jenkins, Hilary A.; Brückner, Christian
Free base meso-tetraaryl-morpholinochlorins and porpholactone from meso-tetraaryl-2,3-dihydroxy-chlorin.
Organic letters, 2003, 5, 19-22
1556102 CIFC19 H18 I N O4P 21 21 219.2879; 9.8237; 19.8438
90; 90; 90
1810.6Li, Guigen; Xu, Xin; Chen, Dianjun; Timmons, Cody; Carducci, Michael D.; Headley, Allan D.
Asymmetric halo aldol reaction (AHA).
Organic letters, 2003, 5, 329-331
1556103 CIFC68 H92 Se10P -110.459; 12.983; 13.711
101.621; 96.648; 94.94
1799.9Pietschnig, Rudolf; Schäfer, Sven; Merz, Klaus
Self-addition of a sterically hindered alkynylselenolate.
Organic letters, 2003, 5, 1867-1869
1556104 CIFC19 H19 N O3 SP 1 21/c 111.0472; 7.6308; 19.6869
90; 92.423; 90
1658.1Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince
New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
Organic letters, 2003, 5, 2181-2184
1556105 CIFC13 H14 N2 O3P 21 21 217.572; 10.031; 15.754
90; 90; 90
1196.59Magnus, Philip; Matthews, Kenneth S.; Lynch, Vince
New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
Organic letters, 2003, 5, 2181-2184
1556106 CIFC28 H16 F6 O2C c c 219.3494; 20.3274; 22.3761
90; 90; 90
8801Brizius, Glen; Billingsley, Kelvin; Smith, Mark D.; Bunz, Uwe H. F.
Conformational and electronic engineering of twisted diphenylacetylenes.
Organic letters, 2003, 5, 3951-3954
1556107 CIFC27 H40 O Si2 SnP 1 c 111.8381; 11.6026; 22.301
90; 104.522; 90
2965.2Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R.
Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne.
Organic letters, 2003, 5, 3971-3974
1556108 CIFC24.6 H32.8 Cl O1.3 Si2I 41/a :233.3269; 33.3269; 9.8038
90; 90; 90
10888.9Simpkins, Simon M. E.; Kariuki, Benson M.; Aricó, Caterina S; Cox, Liam R.
Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne.
Organic letters, 2003, 5, 3971-3974
1556486 CIFC104 H112 F48 K8 N8 O8P 1 21/n 114.2195; 11.8504; 39.8155
90; 97.526; 90
6651.4Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y.
K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides
Inorganics, 2017, 5, 13
1556487 CIFC48 H64 F24 K4 N4 O4P -113.9764; 14.1787; 16.1077
84.831; 81.56; 80.187
3104.31Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y.
K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides
Inorganics, 2017, 5, 13
1556488 CIFC12 H16 F6 K N OP -4 21 c13.5114; 13.5114; 17.556
90; 90; 90
3205Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y.
K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides
Inorganics, 2017, 5, 13
1556489 CIFC32 H48 F24 K4 N4 O4P 1 21/n 118.9136; 10.774; 24.7556
90; 108.265; 90
4790.4Rosca, S.-C.; Roueindeji, H.; Dorcet, V.; Roisnel, T.; Carpentier, J.-F.; Sarazin, Y.
K+...Cpi and K+...F Non-Covalent Interactions in pi-Functionalized Potassium Fluoroalkoxides
Inorganics, 2017, 5, 13
1556490 CIFC26 H70 Be2 Cl2 O2 Si8P 1 21/n 110.3667; 18.8628; 11.387
90; 98.15; 90
2204.2Naglav, D.; Tobey, B.; Dzialkowski, K.; Jansen, G.; Wolper, C.; Schulz, S.
Insights into Molecular Beryllium-Silicon Bonds
Inorganics, 2017, 5, 22
1556491 CIFC26 H45 Na O3 SiP 1 21/c 18.1123; 14.1264; 24.7662
90; 99.36; 90
2800.4Seifert, T.; Roesky, P.W.
Alkali and Alkaline Earth Metal Complexes Ligated by an Ethynyl Substituted Cyclopentadienyl Ligand
Inorganics, 2017, 5, 28
1556492 CIFC22 H37 K O2 SiP 21 21 2110.287; 11.429; 20.495
90; 90; 90
2409.6Seifert, T.; Roesky, P.W.
Alkali and Alkaline Earth Metal Complexes Ligated by an Ethynyl Substituted Cyclopentadienyl Ligand
Inorganics, 2017, 5, 28
1556493 CIFC44 H74 Ca2 I2 O4 Si2P 1 21/n 19.4746; 14.9924; 21.7467
90; 101.49; 90
3027.1Seifert, T.; Roesky, P.W.
Alkali and Alkaline Earth Metal Complexes Ligated by an Ethynyl Substituted Cyclopentadienyl Ligand
Inorganics, 2017, 5, 28
1556494 CIFC53 H64 Mg N2 P2P 1 21/c 118.7343; 11.6636; 23.279
90; 106.937; 90
4866Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A.
Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide
Inorganics, 2017, 5, 29
1556495 CIFC122 H132 Mg2 N4 P4C 1 2/c 120.547; 22.5; 22
90; 90.34; 90
10171Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A.
Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide
Inorganics, 2017, 5, 29
1556496 CIFC49 H57 Al N2 P2P 1 21/c 113.149; 18.972; 17.427
90; 99.58; 90
4286.8Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A.
Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide
Inorganics, 2017, 5, 29
1556497 CIFC134 H144 Mg2 N4 P4C 1 2/c 119.08; 34.382; 16.79
90; 90.56; 90
11014Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A.
Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide
Inorganics, 2017, 5, 29
1556498 CIFC114 H140 Mg2 N4 O4 P4P -113.51; 14.4; 29.43
100.84; 100.81; 100.62
5379Sindlinger, C.P.; Lawrence, S.R.; Cordes, D.B.; Slawin, A.M.Z.; Stasch, A.
Methanediide Formation via Hydrogen Elimination in Magnesium versus Aluminium Hydride Complexes of a Sterically Demanding Bis(iminophosphoranyl)methanediide
Inorganics, 2017, 5, 29
1556499 CIFC17 H25 N OP c c n12.3641; 16.3858; 15.4945
90; 90; 90
3139.1Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556500 CIFC14 H19 N OP 1 21/n 110.0068; 9.8961; 12.7933
90; 99.138; 90
1250.82Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556501 CIFC18 H27 N OP 21 21 216.7423; 13.9706; 18.0631
90; 90; 90
1701.44Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556502 CIFC15 H21 N OC 1 2/c 118.8762; 8.0097; 19.0037
90; 107.543; 90
2739.6Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556503 CIFC42 H64 Li2 N2 O4P -19.406; 10.7931; 11.9959
69.04; 73.616; 67.016
1032.5Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556504 CIFC36 H52 Li2 N2 O4P 1 21/c 18.0148; 15.0628; 14.5918
90; 103.855; 90
1710.35Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556505 CIFC44 H68 Li2 N2 O4P 1 21/n 120.843; 10.495; 21.365
90; 112.886; 90
4305.6Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556506 CIFC63 H80 Li4 N4 O4P 21 21 2113.753; 18.3062; 24.0904
90; 90; 90
6065.1Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556507 CIFC72 H104 Li4 N4 O4P 1 21/n 114.3398; 27.504; 19.8735
90; 107.487; 90
7475.9Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556508 CIFC60 H80 Li4 N4 O4P 1 21/n 113.0543; 26.647; 16.4965
90; 91.218; 90
5737.1Gietz, T.; Boere, R.T.
Backbone-Substituted beta-Ketoimines and Ketoiminate Clusters: Transoid Li2O2 Squares and D2-Symmetric Li4O4 Cubanes. Synthesis, Crystallography and DFT Calculations
Inorganics, 2017, 5, 30
1556509 CIFC49 H62 I Mg N3 OP 1 21/n 18.9827; 23.6098; 22.1855
90; 90.818; 90
4704.62Vindus, D.; Niemeyer, M.
Hetero- and Homoleptic Magnesium Triazenides
Inorganics, 2017, 5, 33
1556510 CIFC48 H52 I Mg N3 OP 1 21/c 119.848; 9.373; 23.033
90; 90.386; 90
4284.9Vindus, D.; Niemeyer, M.
Hetero- and Homoleptic Magnesium Triazenides
Inorganics, 2017, 5, 33
1556511 CIFC90 H104 I4 Mg3 N6P b c a20.4142; 22.2202; 39.3523
90; 90; 90
17850.5Vindus, D.; Niemeyer, M.
Hetero- and Homoleptic Magnesium Triazenides
Inorganics, 2017, 5, 33
1556512 CIFC88 H84 I4 Mg3 N6P -116.9933; 17.5771; 17.8005
93.427; 99.534; 109.991
4888.5Vindus, D.; Niemeyer, M.
Hetero- and Homoleptic Magnesium Triazenides
Inorganics, 2017, 5, 33
1556513 CIFC47.5 H50 Mg0.5 N3P 1 2/n 115.0589; 13.0937; 20.3232
90; 99.013; 90
3957.8Vindus, D.; Niemeyer, M.
Hetero- and Homoleptic Magnesium Triazenides
Inorganics, 2017, 5, 33
1556514 CIFC81.5 H84 Mg N6P 1 21/n 113.302; 21.531; 24.332
90; 101.877; 90
6819.6Vindus, D.; Niemeyer, M.
Hetero- and Homoleptic Magnesium Triazenides
Inorganics, 2017, 5, 33
1556515 CIFC11 H27 Li O Si2P 1 21/n 19.493; 9.9165; 16.7191
90; 92.527; 90
1572.4Von Pilgrim, M.; Mondeshki, M.; Klett, J.
[Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands
Inorganics, 2017, 5, 39
1556516 CIFC13 H35 Li N2 Si2P 1 21/c 118.7636; 13.2303; 17.7299
90; 112.04; 90
4079.8Von Pilgrim, M.; Mondeshki, M.; Klett, J.
[Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands
Inorganics, 2017, 5, 39
1556517 CIFC11 H27 Na O Si2P 1 21/n 111.347; 9.7379; 14.622
90; 90.876; 90
1615.5Von Pilgrim, M.; Mondeshki, M.; Klett, J.
[Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands
Inorganics, 2017, 5, 39
1556518 CIFC32 H86 N6 Na2 Si4P 1 21/n 110.45; 17.414; 14.258
90; 100.824; 90
2548.5Von Pilgrim, M.; Mondeshki, M.; Klett, J.
[Bis(Trimethylsilyl)Methyl]Lithium and -Sodium: Solubility in Alkanes and Complexes with O- and N- Donor Ligands
Inorganics, 2017, 5, 39
1556519 CIFC40 H22 Fe N8 Ni O2 S4P -111.5777; 13.6154; 13.9687
66.134; 84.758; 65.272
1821Takahashi, K.; Sakurai, T.; Zhang, W.-M.; Okubo, S.; Ohta, H.; Yamamoto, T.; Einaga, Y.; Mori, H.
Spin-Singlet Transition in the Magnetic Hybrid Compound from a Spin-Crossover Fe(III) Cation and pi-Radical Anion
Inorganics, 2017, 5, 54
1556520 CIFC40 H22 Fe N8 Ni O2 S4P -111.4218; 13.7207; 13.8041
67.123; 84.938; 65.324
1804Takahashi, K.; Sakurai, T.; Zhang, W.-M.; Okubo, S.; Ohta, H.; Yamamoto, T.; Einaga, Y.; Mori, H.
Spin-Singlet Transition in the Magnetic Hybrid Compound from a Spin-Crossover Fe(III) Cation and pi-Radical Anion
Inorganics, 2017, 5, 54
1556521 CIFC40 H22 Fe N8 Ni O2 S4P -111.7638; 13.5893; 14.1
65.962; 85.184; 65.815
1868.6Takahashi, K.; Sakurai, T.; Zhang, W.-M.; Okubo, S.; Ohta, H.; Yamamoto, T.; Einaga, Y.; Mori, H.
Spin-Singlet Transition in the Magnetic Hybrid Compound from a Spin-Crossover Fe(III) Cation and pi-Radical Anion
Inorganics, 2017, 5, 54
1556522 CIFC20 H19 Au Cl N3 O2P -19.3874; 9.8339; 12.0913
69.669; 70.888; 76.465
979.82Lanoe, P.-H.; Najjari, B.; Hallez, F.; Gontard, G.; Amouri, H.
N-Heterocyclic Carbene Coinage Metal Complexes Containing Naphthalimide Chromophore: Design, Structure, and Photophysical Properties
Inorganics, 2017, 5, 58
1556523 CIFC76 H78 F12 Mn4 N8 O12 P2P -111.388; 11.8845; 15.3829
75.0794; 75.9749; 84.3937
1950.38Sukhikh, T.S.; Vostrikova, K.E.
Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV)
Inorganics, 2017, 5, 59
1556524 CIFC67 H64 Mn2 N11 O18 P ReP -114.2002; 15.7993; 18.047
84.638; 82.694; 65.057
3637.9Sukhikh, T.S.; Vostrikova, K.E.
Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV)
Inorganics, 2017, 5, 59
1556525 CIFC237 H224 Cl2 F6 Mn12 N45 O30 P Re3P -113.813; 15.0609; 30.1361
94.447; 93.223; 94.144
6222.1Sukhikh, T.S.; Vostrikova, K.E.
Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV)
Inorganics, 2017, 5, 59
1556526 CIFC133 H160 F12 Mn6 N19 O20 P2 ReP 1 21/n 123.738; 20.5122; 29.8804
90; 93.37; 90
14524.2Sukhikh, T.S.; Vostrikova, K.E.
Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV)
Inorganics, 2017, 5, 59
1556527 CIFC96 H100 B2 Mn2 N10 O11P 1 21/c 115.9891; 27.544; 21.779
90; 108.762; 90
9081.9Sukhikh, T.S.; Vostrikova, K.E.
Assembly of Mn(III) Schiff Base Complexes with Heptacyanorhenate (IV)
Inorganics, 2017, 5, 59
1556528 CIFC24 H28.5 B2 F8 Fe N10.5 P SP 21 21 2111.3421; 15.3291; 36.7355
90; 90; 90
6387Stock, P.; Wiedemann, D.; Petzold, H.; Horner, G.
Structural Dynamics of Spin Crossover in Iron(II) Complexes with Extended-Tripod Ligands
Inorganics, 2017, 5, 60
1556529 CIFC24 H28.5 Cl2 N10.5 O8 P S ZnP 1 21/c 19.0934; 31.653; 16.281
90; 136.39; 90
3232.3Stock, P.; Wiedemann, D.; Petzold, H.; Horner, G.
Structural Dynamics of Spin Crossover in Iron(II) Complexes with Extended-Tripod Ligands
Inorganics, 2017, 5, 60
1556530 CIFC50 H32 Fe N6 S2I b a m9.602; 18.9796; 23.8123
90; 90; 90
4339.6Iwai, S.; Yoshinami, K.; Nakashima, S.
Structure and Spin State of Iron(II) Assembled Complexes Using 9,10-Bis(4-pyridyl)anthracene as Bridging Ligand
Inorganics, 2017, 5, 61
1556531 CIFC64 H54 B4 F16 Fe2 N20 O3P -113.837; 13.855; 20.684
77.43; 77.58; 86.73
3779.5Craze, A.R.; Sciortino, N.F.; Badbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F.
Investigation of the Spin Crossover Properties of Three Dinulear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type
Inorganics, 2017, 5, 62
1556532 CIFC65 H57 B4 F16 Fe2 N19.5C 1 2/c 121.131; 17.391; 21.069
90; 107; 90
7404Craze, A.R.; Sciortino, N.F.; Badbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F.
Investigation of the Spin Crossover Properties of Three Dinulear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type
Inorganics, 2017, 5, 62
1556533 CIFC64 H54 B4 F15.5 Fe2 N20 S3P -19.521; 16.723; 23.621
95.29; 100.29; 92.93
3675.9Craze, A.R.; Sciortino, N.F.; Badbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F.
Investigation of the Spin Crossover Properties of Three Dinulear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type
Inorganics, 2017, 5, 62
1556545 CIFC10 H22 O5 Si2P 1 21/c 111.5359; 6.7079; 10.1493
90; 115.83; 90
706.9Kahr, J.; Belaj, F.; Pietschnig, R.
Preparation and Molecular Structure of a Cyclopentyl-Substituted Cage Hexasilsesquioxane T6 (T = cyclopentyl-SiO1.5) Starting from the Corresponding Silanetriol
Inorganics, 2017, 5, 66
1556546 CIFC10 H22 O5 Si2C m c e10.1476; 20.7484; 6.7022
90; 90; 90
1411.12Kahr, J.; Belaj, F.; Pietschnig, R.
Preparation and Molecular Structure of a Cyclopentyl-Substituted Cage Hexasilsesquioxane T6 (T = cyclopentyl-SiO1.5) Starting from the Corresponding Silanetriol
Inorganics, 2017, 5, 66
1556547 CIFC30 H54 O9 Si6C c c a :216.2855; 22.346; 19.6563
90; 90; 90
7153.2Kahr, J.; Belaj, F.; Pietschnig, R.
Preparation and Molecular Structure of a Cyclopentyl-Substituted Cage Hexasilsesquioxane T6 (T = cyclopentyl-SiO1.5) Starting from the Corresponding Silanetriol
Inorganics, 2017, 5, 66
1556548 CIFC69 H45 Cl2 F18 N3 P4 RuC 1 2/c 121.594; 27.753; 23.938
90; 93.631; 90
14317Van de Watering, F.F.; Heijtbrink, N.; Van der Vlugt, J.I.; Dzik, W.I.; De Bruin, B.; Reek, J.N.H.
3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation
Inorganics, 2017, 5, 73
1556549 CIFC69 H45 F18 N5 P4 RuP 1 21/c 114.2851; 18.909; 29.8721
90; 97.011; 90
8008.6Van de Watering, F.F.; Heijtbrink, N.; Van der Vlugt, J.I.; Dzik, W.I.; De Bruin, B.; Reek, J.N.H.
3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation
Inorganics, 2017, 5, 73
1556550 CIFC65 H55 Cl6 N3 P4 RuP 1 21/n 119.1879; 18.1604; 19.7879
90; 91.012; 90
6894.2Van de Watering, F.F.; Heijtbrink, N.; Van der Vlugt, J.I.; Dzik, W.I.; De Bruin, B.; Reek, J.N.H.
3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation
Inorganics, 2017, 5, 73
1556551 CIFC41 H39 I Ni P3P n a 2120.526; 10.367; 17.0858
90; 90; 90
3635.7Iffland, L.; Petuker, A.; Van Gastel, M.; Apfel, U.-P.
Mechanistic Implications for the Ni(I)-Catalyzed Kumada Cross-Coupling Reaction
Inorganics, 2017, 5, 78
1556552 CIFC31.5 H27 O2.5P -110.337; 10.816; 12.119
72.216; 84.13; 69.554
1208.9Nguyen, H.N.; Tashima, N.; Ikariya, T.; Kuwata, S.
Ruthenium-Catalyzed Dimerization of 1,1-Diphenylpropargyl Alcohol to a Hydroxybenzocyclobutene and Related Reactions
Inorganics, 2017, 5, 80
1556553 CIFC55 H50 O3 RuP 1 21/c 117.089; 12.512; 20.001
90; 107.378; 90
4081.4Nguyen, H.N.; Tashima, N.; Ikariya, T.; Kuwata, S.
Ruthenium-Catalyzed Dimerization of 1,1-Diphenylpropargyl Alcohol to a Hydroxybenzocyclobutene and Related Reactions
Inorganics, 2017, 5, 80
1556554 CIFC38 H78 N4 Pd4 Si3P 1 21/n 110.8179; 22.0783; 22.8654
90; 92.1391; 90
5457.4Sunada, Y.; Taniyama, N.; Shimamoto, K.; Kyushin, S.; Nagashima, H.
Construction of a Planar Tetrapalladium Cluster by the Reaction of Palladium(0) Bis(isocyanide) with Cyclic Tetrasilane
Inorganics, 2017, 5, 84
1556555 CIFC51 H100 N6 Pd4 Si3P -114.505; 15.339; 15.655
89.593; 63.724; 81.301
3080.2Sunada, Y.; Taniyama, N.; Shimamoto, K.; Kyushin, S.; Nagashima, H.
Construction of a Planar Tetrapalladium Cluster by the Reaction of Palladium(0) Bis(isocyanide) with Cyclic Tetrasilane
Inorganics, 2017, 5, 84
1556556 CIFC36 H75 O9 P3 Pd3 Si3P -111.2891; 12.711; 19.549
81.516; 85.854; 64.096
2495.6Sunada, Y.; Taniyama, N.; Shimamoto, K.; Kyushin, S.; Nagashima, H.
Construction of a Planar Tetrapalladium Cluster by the Reaction of Palladium(0) Bis(isocyanide) with Cyclic Tetrasilane
Inorganics, 2017, 5, 84
1556557 CIFC13 H28 Cl2 N4 ZnP 21 21 2113.4778; 15.173; 17.57
90; 90; 90
3593Metz, A.; Heck, J.; Gohlke, C.M.; Krockert, K.; Louven, Y.; McKeown, P.; Hoffmann, A.; Jones, M.D.; Herres-Pawlis, S.
Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide
Inorganics, 2017, 5, 85
1556558 CIFC13 H26 Cl2 N4 ZnP 1 21 19.4718; 18.095; 10.1331
90; 103.908; 90
1685.8Metz, A.; Heck, J.; Gohlke, C.M.; Krockert, K.; Louven, Y.; McKeown, P.; Hoffmann, A.; Jones, M.D.; Herres-Pawlis, S.
Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide
Inorganics, 2017, 5, 85
1556559 CIFC13 H26 Br2 N4 ZnP 1 21 19.2972; 14.257; 13.2
90; 101.844; 90
1712.4Metz, A.; Heck, J.; Gohlke, C.M.; Krockert, K.; Louven, Y.; McKeown, P.; Hoffmann, A.; Jones, M.D.; Herres-Pawlis, S.
Reactivity of Zinc Halide Complexes Containing Camphor-Derived Guanidine Ligands with Technical rac-Lactide
Inorganics, 2017, 5, 85
1556756 CIFNi Se5 Ta2C m c m3.5029; 12.8699; 15.6768
90; 90; 90
706.74Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi
Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>.
IUCrJ, 2018, 5, 158-165
1556757 CIFNi Se5 Ta2C m c m3.4375; 12.375; 15.4437
90; 90; 90
656.96Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi
Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>.
IUCrJ, 2018, 5, 158-165
1556758 CIFNi Se5 Ta2P m n m :23.437; 5.861; 15.512
90; 90; 90
312.48Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi
Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>.
IUCrJ, 2018, 5, 158-165
1556759 CIFNi Se5 Ta2P 1 2/n 13.437; 5.849; 15.512
90; 90.53; 90
311.8Nakano, Akitoshi; Sugawara, Kento; Tamura, Shinya; Katayama, Naoyuki; Matsubayashi, Kazuyuki; Okada, Taku; Uwatoko, Yoshiya; Munakata, Kouji; Nakao, Akiko; Sagayama, Hajime; Kumai, Reiji; Sugimoto, Kunihisa; Maejima, Naoyuki; Machida, Akihiko; Watanuki, Tetsu; Sawa, Hiroshi
Pressure-induced coherent sliding-layer transition in the excitonic insulator Ta<sub>2</sub>NiSe<sub>5</sub>.
IUCrJ, 2018, 5, 158-165
1556829 CIFC30 H29 Cl2 Cu2 I2 N O2 S2P -111.7925; 11.9665; 13.4375
93.29; 95.681; 118.683
1643.38Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung
Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes.
IUCrJ, 2018, 5, 45-53
1556830 CIFC29 H27 Cd2 I4 N O2 S2C 1 2/c 123.3017; 13.4569; 26.9935
90; 102.963; 90
8248.6Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung
Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes.
IUCrJ, 2018, 5, 45-53
1556831 CIFC58 H54 Cd4 I8 N2 O4 S4P -111.66; 12.147; 12.585
75.142; 87.056; 86.996
1719.2Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung
Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes.
IUCrJ, 2018, 5, 45-53
1556832 CIFC116 H106 Cd8 I16 N4 O8 S8P -111.3166; 13.4404; 24.586
86.655; 89.396; 78.371
3656.5Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung
Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes.
IUCrJ, 2018, 5, 45-53
1556833 CIFC29 H27 Cd Cu I3 N O2 S2P -18.9645; 14.4098; 14.8826
65.853; 73.386; 81.546
1680.04Park, In-Hyeok; Kang, Yunji; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Seo, Sujin; Jung, Jong Hwa; Lee, Shim Sung
Snapshot and crystallographic observations of kinetic and thermodynamic products for NO<sub>2</sub>S<sub>2</sub> macrocyclic complexes.
IUCrJ, 2018, 5, 45-53
1556834 CIFC0.26 Na0.01 O2 SiF d -3 m :219.442; 19.442; 19.442
90; 90; 90
7348.9Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607
1556835 CIFC0.26 Na0.01 O2 SiF d -3 m :219.4214; 19.4214; 19.4214
90; 90; 90
7325.6Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607
1556836 CIFC0.58 Na0.02 O4.53 Si2.27A 1 2/n 123.7844; 13.732; 23.784
90; 109.47; 90
7324Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607
1556837 CIFC0.26 Na0.01 O2 SiF d -3 m :219.4199; 19.4199; 19.4199
90; 90; 90
7323.9Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607
1556838 CIFC0.58 Na0.02 O4.53 Si2.27A 1 2/n 123.834; 13.76; 23.833
90; 109.47; 90
7369Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607
1556839 CIFC0.26 Na0.01 O2 SiF d -3 m :219.3944; 19.3944; 19.3944
90; 90; 90
7295.1Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607
1556840 CIFC0.58 Na0.02 O4.53 Si2.27A 1 2/n 123.834; 13.76; 23.833
90; 109.47; 90
7369Scheidl, K. S.; Effenberger, H. S.; Yagi, T.; Momma, K.; Miletich, Ronald
The hydrocarbon-bearing clathrasil chibaite and its host-guest structure at low temperature.
IUCrJ, 2018, 5, 595-607

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