Crystallography Open Database
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Searching journal of publication like 'Organic Chemistry Frontiers' volume of publication is 5
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1553856 | CIF | C81 H82 O10 | P -1 | 12.0438; 14.5042; 22.049 72.623; 76.291; 77.888 | 3530.8 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553857 | CIF | C44 H48 O12 | P 1 21/n 1 | 12.791; 20.978; 14.779 90; 98.582; 90 | 3921 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553858 | CIF | C90 H125 N3 O10 | P -1 | 13.633; 15.357; 20.965 91.591; 94.087; 111.251 | 4073.6 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553859 | CIF | C42 H46 O11 | P 1 21 1 | 14.289; 23.102; 20.977 90; 108.428; 90 | 6570 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553860 | CIF | C119 H158 Cl9 O10 | P -1 | 14.89; 18.123; 21.671 81.371; 82.134; 87.707 | 5726 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553861 | CIF | C110 H140 O10 | C 1 2/c 1 | 43.045; 21.347; 23.043 90; 104.773; 90 | 20474 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553862 | CIF | C82 H85 O12 | P 1 21 1 | 16.77; 21.69; 18.89 90; 93.48; 90 | 6858 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553863 | CIF | C75 H110 O10 | P -1 | 16.619; 16.686; 16.858 95.191; 117.822; 114.325 | 3527.9 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553864 | CIF | C81 H84 O10 | P -1 | 12.31; 16.48; 18.98 83.427; 80.887; 69.254 | 3548 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553865 | CIF | C82 H86 Cl2 O10 | P -1 | 12.2178; 15.0675; 20.9593 78.186; 85.869; 67.284 | 3483.6 | Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H. A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state Organic Chemistry Frontiers, 2018, 5, 10 |
| 1553872 | CIF | C30 H30 I N3 O5 | P 21 21 21 | 12.1518; 12.3848; 19.412 90; 90; 90 | 2921.5 | Zhu, Jing-Yan; Yang, Wu-Lin; Liu, Yang-Zi; Shang, Shao-Jing; Deng, Wei-Ping A copper(i)-catalyzed asymmetric Mannich reaction of glycine Schiff bases with isatin-derived ketimines: enantioselective synthesis of 3-substituted 3-aminooxindoles Organic Chemistry Frontiers, 2018, 5, 70 |
| 1553873 | CIF | C13 H23 N O4 S | P 21 21 21 | 6.1598; 8.133; 31.1006 90; 90; 90 | 1558.07 | Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters Organic Chemistry Frontiers, 2018, 5, 36 |
| 1553874 | CIF | C21 H24 N2 O6 S | P 21 21 21 | 7.9925; 13.9906; 19.0487 90; 90; 90 | 2130.02 | Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters Organic Chemistry Frontiers, 2018, 5, 36 |
| 1553880 | CIF | C10 H8 Cl N O2 | P 1 21/c 1 | 3.8516; 11.2844; 21.4208 90; 89.074; 90 | 930.89 | Ledovskaya, Maria S.; Rodygin, Konstantin S.; Ananikov, Valentine P. Calcium-mediated one-pot preparation of isoxazoles with deuterium incorporation Organic Chemistry Frontiers, 2018, 5, 226 |
| 1553883 | CIF | C43 H60 N2 P Sc Si2 | P -1 | 10.8597; 13.0923; 18.0508 75.984; 74.865; 66.722 | 2247.6 | Gao, Hongjie; Su, Jianhong; Xu, Pengfei; Xu, Xin Scandium-catalyzed C(sp3)‒H alkylation of N,N-dimethyl anilines with alkenes Organic Chemistry Frontiers, 2018, 5, 59 |
| 1553884 | CIF | C19 H20 O | P 1 21/c 1 | 8.859; 21.377; 8.0979 90; 106.44; 90 | 1470.9 | Zang, Wenqing; Wei, Yin; Shi, Min Gold(i) catalyzed cascade cyclization: intramolecular two-fold nucleophilic addition to vinylidenecyclopropanes (VDCPs) Organic Chemistry Frontiers, 2018, 5, 197 |
| 1553885 | CIF | C15 H12 Cl2 O2 | P -1 | 6.059; 8.893; 13.346 91.59; 93.75; 108.42 | 679.9 | Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes Organic Chemistry Frontiers, 2018, 5, 561 |
| 1553886 | CIF | C18 H20 O2 | P -1 | 8.26; 10.221; 10.602 102.5; 107.52; 109.03 | 756.2 | Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes Organic Chemistry Frontiers, 2018, 5, 561 |
| 1553887 | CIF | C18 H17 N O3 S | P 1 21/c 1 | 17.558; 9.331; 9.8891 90; 91.367; 90 | 1619.71 | Sun, Deli; Zhang, Ronghua Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides Organic Chemistry Frontiers, 2018, 5, 92 |
| 1553888 | CIF | C13 H15 N O3 S | P 1 21/c 1 | 15.8995; 8.3725; 9.9537 90; 100.406; 90 | 1303.2 | Sun, Deli; Zhang, Ronghua Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides Organic Chemistry Frontiers, 2018, 5, 92 |
| 1553889 | CIF | C18 H17 Cl N2 O3 S | P 1 21/n 1 | 13.2285; 9.3407; 14.9536 90; 95.087; 90 | 1840.4 | Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines Organic Chemistry Frontiers, 2018, 5, 189 |
| 1553890 | CIF | C17 H14 Cl2 N2 O2 S | P 1 21/n 1 | 11.6687; 8.7574; 17.8369 90; 96.512; 90 | 1810.9 | Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines Organic Chemistry Frontiers, 2018, 5, 189 |
| 1553891 | CIF | C27 H35 N O1.5 P | C 1 2/c 1 | 10.5217; 14.8118; 29.451 90; 94.42; 90 | 4576.1 | Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation Organic Chemistry Frontiers, 2018, 5, 88 |
| 1553892 | CIF | C28 H24 N O2 P | C 1 2/c 1 | 24.609; 9.508; 21.415 90; 115.972; 90 | 4504.7 | Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation Organic Chemistry Frontiers, 2018, 5, 88 |
| 1553893 | CIF | C30 H23 Au F3 N4 O3 P S | P 1 21/c 1 | 11.707; 16.717; 15.157 90; 96.39; 90 | 2948 | Huang, Ronghui; Yang, Yongchun; Wang, Duo-Sheng; Zhang, Liang; Wang, Dawei Where does Au coordinate to N-(2-pyridiyl)benzotriazole: gold-catalyzed chemoselective dehydrogenation and borrowing hydrogen reactions Organic Chemistry Frontiers, 2018, 5, 203 |
| 1553894 | CIF | C24 H20 N2 O5 | P 1 21 1 | 10.31419; 19.2062; 11.0205 90; 109.532; 90 | 2057.49 | Ruan, Sai; Lin, Xiaobin; Xie, Lihua; Lin, Lili; Feng, Xiaoming; Liu, Xiaohua Asymmetric synthesis of 3-aminodihydrocoumarins via the chiral guanidine catalyzed cascade reaction of azlactones Organic Chemistry Frontiers, 2018, 5, 32 |
| 1553895 | CIF | C21 H17 Br N2 O | P 1 21/n 1 | 8.7889; 8.9182; 22.444 90; 91.02; 90 | 1758.9 | Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones Organic Chemistry Frontiers, 2018, 5, 80 |
| 1553896 | CIF | C15 H14 N2 O | P 1 21/n 1 | 9.8465; 26.3558; 9.9725 90; 104.267; 90 | 2508.2 | Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones Organic Chemistry Frontiers, 2018, 5, 80 |
| 1553897 | CIF | C23 H20 Cl F3 N2 O3 | P b c a | 18.1727; 10.5743; 23.813 90; 90; 90 | 4576 | Sun, Yao-Liang; Wei, Yin; Shi, Min Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles Organic Chemistry Frontiers, 2018, 5, 210 |
| 1553898 | CIF | C20 H24 N2 O4 | P 1 21/c 1 | 18.416; 11.31; 9.759 90; 93.907; 90 | 2027.9 | Sun, Yao-Liang; Wei, Yin; Shi, Min Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles Organic Chemistry Frontiers, 2018, 5, 210 |
| 1553899 | CIF | C14 H19 N O3 S | P 21 21 21 | 5.36821; 11.71337; 21.6232 90; 90; 90 | 1359.66 | Reboredo, Silvia; García-Marijuan, Ainara; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Ugarriza, Iratxe; Vicario, Jose L. Highly diastereoselective C →N acyl rearrangement in polysubstituted pyrrolidine 2,2-dicarboxylates. Stereocontrolled synthesis of densely functionalized prolines Organic Chemistry Frontiers, 2018, 5, 933 |
| 1553900 | CIF | C13 H13 Br N2 O | P 1 21/c 1 | 9.673; 11.975; 10.6305 90; 96.144; 90 | 1224.3 | Zhao, He; Chen, Xiuwen; Jiang, Huanfeng; Zhang, Min Copper-catalysed dehydrogenative α-C(sp3)‒H amination of tetrahydroquinolines with O-benzoyl hydroxylamines Organic Chemistry Frontiers, 2018, 5, 539 |
| 1553901 | CIF | C17 H17 N O3 | P 21 21 21 | 6.5337; 8.4509; 26.0879 90; 90; 90 | 1440.46 | Xu, Youguo; Zhang, Sheng; Li, Lijun; Wang, Yukang; Zha, Zhenggen; Wang, Zhiyong l-Phenylalanine potassium catalyzed asymmetric formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone Organic Chemistry Frontiers, 2018, 5, 376 |
| 1553902 | CIF | C16 H36 Br Cl3 Fe N | P n n a | 18.4928; 11.5835; 11.4759 90; 90; 90 | 2458.3 | Li, Sanliang; Zhu, Bo; Lee, Richmond; Qiao, Baokun; Jiang, Zhiyong Visible light-induced selective aerobic oxidative transposition of vinyl halides using a tetrahalogenoferrate(iii) complex catalyst Organic Chemistry Frontiers, 2018, 5, 380 |
| 1553903 | CIF | C24 H13 F | P 1 21/n 1 | 10.4684; 7.428; 18.7773 90; 90.086; 90 | 1460.11 | Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation Organic Chemistry Frontiers, 2018, 5, 398 |
| 1553904 | CIF | C24 H14 Cl2 | C 1 2/c 1 | 16.8237; 11.333; 10.2994 90; 114.382; 90 | 1788.6 | Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation Organic Chemistry Frontiers, 2018, 5, 398 |
| 1553905 | CIF | C20 H22 N4 S | P 1 21/n 1 | 17.47; 5.702; 20.396 90; 114.211; 90 | 1853 | Amendola, Valeria; Boiocchi, Massimo; Fabbrizzi, Luigi; La Cognata, Sonia; Legnani, Laura; Lo Presti, Eliana; Mangano, Carlo; Miljkovic, Ana Anion-induced isomerization of fluorescent semi(thio)carbazones Organic Chemistry Frontiers, 2018, 5, 391 |
| 1553906 | CIF | C23 H25 N O2 | C 1 2 1 | 17.0278; 8.4534; 14.668 90; 110.034; 90 | 1983.59 | Shen, Hong-Qiang; Liu, Cong; Zhou, Ji; Zhou, Yong-Gui Enantioselective palladium-catalyzed C‒H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand Organic Chemistry Frontiers, 2018, 5, 611 |
| 1553907 | CIF | C25.5 H35 Cl2 Fe N3 O1.5 | P 1 21 1 | 16.1979; 9.8887; 17.2384 90; 100.854; 90 | 2711.8 | Chen, Jianhui; Xi, Tuo; Lu, Zhan 10 gram-scale synthesis of a chiral oxazoline iminopyridine ligand and its applications Organic Chemistry Frontiers, 2018, 5, 247 |
| 1553908 | CIF | C21 H19 Br O2 | P 1 21/n 1 | 8.277; 19.206; 11.294 90; 93.738; 90 | 1791.6 | Qi, Jifeng; Zheng, Jing; Cui, Sunliang Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization Organic Chemistry Frontiers, 2018, 5, 222 |
| 1553909 | CIF | C26 H28 O2 | P -1 | 8.914; 9.542; 13.652 86.106; 80.322; 67.976 | 1061 | Qi, Jifeng; Zheng, Jing; Cui, Sunliang Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization Organic Chemistry Frontiers, 2018, 5, 222 |
| 1553910 | CIF | C38 H26 N4 O4 | P b c n | 21.1618; 11.9414; 23.2097 90; 90; 90 | 5865.1 | Zwoliński, K. M.; Sieroń, L.; Eilmes, J. One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges Organic Chemistry Frontiers, 2018, 5, 171 |
| 1553911 | CIF | C46 H50 N4 O8 S4 Zn | P 1 21 1 | 11.2639; 15.6341; 13.7495 90; 110.204; 90 | 2272.3 | Zwoliński, K. M.; Sieroń, L.; Eilmes, J. One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges Organic Chemistry Frontiers, 2018, 5, 171 |
| 1553912 | CIF | C3.8 H2.8 Br0.2 N0.2 O0.4 | P 1 21/c 1 | 17.1209; 6.8257; 14.2218 90; 100.2; 90 | 1635.72 | Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids Organic Chemistry Frontiers, 2018, 5, 415 |
| 1553913 | CIF | C24 H28 N O2 Rh | P -1 | 8.581; 10.888; 11.352 93.19; 106.92; 90.49 | 1012.8 | Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids Organic Chemistry Frontiers, 2018, 5, 415 |
| 1553914 | CIF | C2.44 H1.78 N0.22 O0.22 | P -1 | 7.1832; 10.3531; 12.7041 99.499; 102.356; 98.881 | 892.4 | Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids Organic Chemistry Frontiers, 2018, 5, 415 |
| 1553915 | CIF | C29 H32 O3 | C 1 2/c 1 | 30.962; 10.076; 20.18 90; 121.016; 90 | 5395.5 | Liu, Lina; Yuan, Zhenbo; Pan, Rui; Zeng, Yuye; Lin, Aijun; Yao, Hequan; Huang, Yue 1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans Organic Chemistry Frontiers, 2018, 5, 623 |
| 1553916 | CIF | C17 H13 Cl N2 O4 | P -1 | 10.1754; 13.7004; 13.8309 119.49; 102.929; 92.342 | 1609.7 | Daggupati, Ramana V.; Malapaka, Chandrasekharam Cu(i)-Catalyzed amidation/imidation of N-arylglycine ester derivatives via C‒N coupling under mild conditions Organic Chemistry Frontiers, 2018, 5, 788 |
| 1553917 | CIF | C16 H15 N3 O2 | P -1 | 6.0881; 7.8709; 14.5993 86.207; 88.891; 76.774 | 679.53 | Zhu, Chuanle; Zeng, Hao; Chen, Fulin; Liu, Chi; Zhu, Rui; Wu, Wanqing; Jiang, Huanfeng Copper-catalyzed coupling of oxime acetates and aryldiazonium salts: an azide-free strategy toward N-2-aryl-1,2,3-triazoles Organic Chemistry Frontiers, 2018, 5, 571 |
| 1553918 | CIF | C28 H26 N2 | P 1 21/c 1 | 6.4301; 13.8923; 12.2241 90; 103.031; 90 | 1063.85 | Grandl, Markus; Sun, Yu; Pammer, Frank Electronic and structural properties of N →B-ladder boranes with high electron affinity Organic Chemistry Frontiers, 2018, 5, 336 |
| 1553919 | CIF | C40 H54 B2 N2 | P -1 | 9.0141; 12.9277; 15.5179 111.75; 98.849; 99.031 | 1613.9 | Grandl, Markus; Sun, Yu; Pammer, Frank Electronic and structural properties of N →B-ladder boranes with high electron affinity Organic Chemistry Frontiers, 2018, 5, 336 |
| 1553920 | CIF | C40 H54 B2 N2 | P 1 21/n 1 | 17.2519; 10.4002; 18.7527 90; 94.829; 90 | 3352.73 | Grandl, Markus; Sun, Yu; Pammer, Frank Electronic and structural properties of N →B-ladder boranes with high electron affinity Organic Chemistry Frontiers, 2018, 5, 336 |
| 1553921 | CIF | C44 H56 B2 N2 | P 1 21 1 | 10.7137; 14.9388; 11.2075 90; 101.824; 90 | 1755.7 | Grandl, Markus; Sun, Yu; Pammer, Frank Electronic and structural properties of N →B-ladder boranes with high electron affinity Organic Chemistry Frontiers, 2018, 5, 336 |
| 1553922 | CIF | C50 H29 B2 F20 N3 | P 1 2/n 1 | 13.3636; 12.765; 15.0491 90; 111.844; 90 | 2382.85 | Grandl, Markus; Sun, Yu; Pammer, Frank Electronic and structural properties of N →B-ladder boranes with high electron affinity Organic Chemistry Frontiers, 2018, 5, 336 |
| 1553923 | CIF | C60 H38 B2 F20 N2 | P -1 | 11.196; 13.488; 19.102 102.11; 104.06; 108.18 | 2528 | Grandl, Markus; Sun, Yu; Pammer, Frank Electronic and structural properties of N →B-ladder boranes with high electron affinity Organic Chemistry Frontiers, 2018, 5, 336 |
| 1553924 | CIF | C35 H37 Cl2 N3 O4 S2 | P 1 21/n 1 | 8.616; 21.777; 18.552 90; 100.259; 90 | 3425 | Cao, Bo; Wei, Yin; Shi, Min Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons Organic Chemistry Frontiers, 2018, 5, 423 |
| 1553925 | CIF | C8 H12 Cl Cu N4 O4 | P n a 21 | 24.106; 8.4201; 20.584 90; 90; 90 | 4178 | Cao, Bo; Wei, Yin; Shi, Min Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons Organic Chemistry Frontiers, 2018, 5, 423 |
| 1553926 | CIF | C33 H33 N3 O4 S2 | C 1 2/c 1 | 33.342; 14.1163; 13.8882 90; 113.533; 90 | 5993 | Cao, Bo; Wei, Yin; Shi, Min Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons Organic Chemistry Frontiers, 2018, 5, 423 |
| 1553927 | CIF | C33 H33 N3 O4 S2 | P 1 21/c 1 | 20.618; 12.7286; 11.5829 90; 96.577; 90 | 3019.8 | Cao, Bo; Wei, Yin; Shi, Min Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons Organic Chemistry Frontiers, 2018, 5, 423 |
| 1553928 | CIF | C36 H29 N3 | P 1 21/c 1 | 16.4746; 9.1306; 19.2167 90; 113.764; 90 | 2645.5 | Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones Organic Chemistry Frontiers, 2018, 5, 595 |
| 1553929 | CIF | C40.35 H35.05 N3 O1.67 | P -1 | 9.0006; 13.4106; 13.9272 73.859; 78.251; 71.617 | 1519.94 | Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones Organic Chemistry Frontiers, 2018, 5, 595 |
| 1553930 | CIF | C39 H29 N3 O2 | P 1 21/n 1 | 9.8591; 17.6789; 16.9614 90; 96.753; 90 | 2935.83 | Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones Organic Chemistry Frontiers, 2018, 5, 595 |
| 1553931 | CIF | C43 H29 N3 | P 1 21/n 1 | 9.7752; 18.4617; 18.0848 90; 102.389; 90 | 3187.7 | Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones Organic Chemistry Frontiers, 2018, 5, 595 |
| 1553932 | CIF | C44 H31 N3 O | P 1 21/c 1 | 9.9057; 18.2185; 17.9256 90; 94.694; 90 | 3224.13 | Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones Organic Chemistry Frontiers, 2018, 5, 595 |
| 1553933 | CIF | C10 H15 N O3 | P 1 c 1 | 9.9528; 5.6608; 10.1737 90; 119.444; 90 | 499.16 | Peter, Clovis; Geoffroy, Philippe; Miesch, Michel Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids Organic Chemistry Frontiers, 2018, 5, 566 |
| 1553934 | CIF | C16 H14 O7 | P -1 | 6.934; 9.4461; 12.5549 77.759; 76.1; 88.981 | 779.63 | Xu, Li-Chen; Zhou, Peng; Li, Jia-Zhuo; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo Thiazolium salt-catalyzed [3 + 2 + 1] cyclization for the synthesis of trisubstituted 2-pyrones using arylglyoxals as a carbonyl source Organic Chemistry Frontiers, 2018, 5, 753 |
| 1553935 | CIF | C65 H63 F6 N8 O12 P S6 | P -1 | 14.18; 16.43; 16.973 65.7; 71.841; 79.491 | 3417.8 | Zhao, Meng-Yao; Guo, Qing-Hui; Wang, Mei-Xiang Understanding the driving force for the molecular recognition of S6-corona[3]arene[3]pyridazine toward organic ammonium cations Organic Chemistry Frontiers, 2018, 5, 760 |
| 1553936 | CIF | C26 H28 Cl2 N3 O5 P Ru | P 21 21 21 | 8.4287; 10.7538; 30.9419 90; 90; 90 | 2804.59 | de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A. Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst Organic Chemistry Frontiers, 2018, 5, 841 |
| 1553937 | CIF | C33 H30 Cl2 N3 O4 P Ru | P 4 | 28.3195; 28.3195; 8.539 90; 90; 90 | 6848.2 | de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A. Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst Organic Chemistry Frontiers, 2018, 5, 841 |
| 1553938 | CIF | C27 H23 N3 O | I 41 c d | 31.825; 31.825; 8.303 90; 90; 90 | 8410 | Zhang, Chen; Pi, Junxia; Chen, Shu; Liu, Ping; Sun, Peipei Construction of a 4H-pyrido[4,3,2-gh]phenanthridin-5(6H)-one skeleton via a catalyst-free radical cascade addition/cyclization using azo compounds as radical sources Organic Chemistry Frontiers, 2018, 5, 793 |
| 1553939 | CIF | C22 H22 Si | P b c a | 8.8464; 13.6195; 30.1026 90; 90; 90 | 3626.9 | Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)‒Si bond cleavage Organic Chemistry Frontiers, 2018, 5, 860 |
| 1553940 | CIF | C21 H20 Si | P 1 21/n 1 | 12.2864; 9.5206; 14.4288 90; 96.731; 90 | 1676.16 | Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)‒Si bond cleavage Organic Chemistry Frontiers, 2018, 5, 860 |
| 1553941 | CIF | C23 H22 N2 O7 | P 1 | 9.297; 11.515; 11.957 61.974; 80.333; 67.602 | 1044.6 | Han, Jianxin; Niu, Sheng-Tong; Liu, Yushuang; Gan, Lishe; Wang, Tianfu; Lu, Chong-Dao; Yuan, Tao Robustanoids A and B, two novel pyrrolo[2,3-b]indole alkaloids from Coffea canephora: isolation and total synthesis Organic Chemistry Frontiers, 2018, 5, 586 |
| 1553942 | CIF | C28 H21 N5 O | P -1 | 7.483; 12.28; 13.156 73.055; 75.131; 76.779 | 1102.1 | Gao, Qinghe; He, Shuang; Wu, Xia; Zhang, Jingjing; Bai, Suping; Wu, Yandong; Wu, Anxin Selective access to dipyrazolo-fused pyridines via formal [3 + 2 + 1] heteroannulation of methyl ketones with pyrazol-5-amines Organic Chemistry Frontiers, 2018, 5, 765 |
| 1553943 | CIF | C83 H54 Cl2 N2 O2 | P -1 | 9.6948; 10.6078; 14.8224 105.266; 103.77; 93.623 | 1415.35 | Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D. A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence Organic Chemistry Frontiers, 2018, 5, 640 |
| 1553944 | CIF | C34 H29 Cl2 N O3 | P 1 21/c 1 | 14.1223; 10.4359; 19.4476 90; 97.282; 90 | 2843.05 | Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D. A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence Organic Chemistry Frontiers, 2018, 5, 640 |
| 1553945 | CIF | C13 H9 Br Cl F4 N S | P 1 21/c 1 | 6.18585; 19.014; 13.0299 90; 104.086; 90 | 1486.46 | Das, Prajwalita; Takada, Masahiro; Tokunaga, Etsuko; Saito, Norimichi; Shibata, Norio Synthesis of pyridine trans-tetrafluoro-λ6-sulfane derivatives via radical addition Organic Chemistry Frontiers, 2018, 5, 719 |
| 1553946 | CIF | C16 H12 Cl N O2 S | C 1 2/c 1 | 24.908; 13.4385; 8.7528 90; 93.042; 90 | 2925.7 | Zhao, Lang; Liao, Wei-Wei Pd-Catalyzed intramolecular C‒H addition to the cyano-group: construction of functionalized 2,3-fused thiophene scaffolds Organic Chemistry Frontiers, 2018, 5, 801 |
| 1553947 | CIF | C16 H18 N2 O2 | P 1 21/n 1 | 9.5527; 12.362; 12.0679 90; 92.577; 90 | 1423.66 | Yue, Qiang; Xiao, Zhen; Ran, Ziyao; Yuan, Songdong; Zhang, Qian; Li, Dong Copper-catalyzed α-C‒H amidation of simple ethers through C(sp3)‒H/N‒H cross dehydrogenative coupling Organic Chemistry Frontiers, 2018, 5, 967 |
| 1553948 | CIF | C17 H15.5 N2 O3.5 S | P 1 21 1 | 13.1217; 8.2301; 15.9865 90; 109.525; 90 | 1627.15 | Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters Organic Chemistry Frontiers, 2018, 5, 929 |
| 1553949 | CIF | C19 H17 F3 N O3.5 | P 21 21 21 | 8.0275; 13.876; 31.686 90; 90; 90 | 3529.5 | Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters Organic Chemistry Frontiers, 2018, 5, 929 |
| 1553950 | CIF | C28 H20 N4 | P 1 21/c 1 | 10.4482; 7.41078; 13.6312 90; 105.538; 90 | 1016.88 | Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes Organic Chemistry Frontiers, 2018, 5, 1096 |
| 1553951 | CIF | C25 H30 N2 O3.5 Rh | P -1 | 8.5997; 11.3141; 23.5957 89.88; 86.923; 89.086 | 2292.21 | Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes Organic Chemistry Frontiers, 2018, 5, 1096 |
| 1553952 | CIF | C24 H22 S6 Si2 | C 1 2/c 1 | 31.277; 16.691; 10.668 90; 93.503; 90 | 5559 | Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene Organic Chemistry Frontiers, 2018, 5, 1257 |
| 1553953 | CIF | C22 H20 S7 Si2 | P 1 21/c 1 | 19.71; 13.215; 10.489 90; 103.753; 90 | 2653.7 | Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene Organic Chemistry Frontiers, 2018, 5, 1257 |
| 1553954 | CIF | C11 H11 Br S3 Si | P n m a | 12.594; 7.353; 15.175 90; 90; 90 | 1405.3 | Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene Organic Chemistry Frontiers, 2018, 5, 1257 |
| 1553955 | CIF | C11 H11 Br S3 Si | P 1 21/c 1 | 11.5286; 15.8164; 8.4588 90; 110.19; 90 | 1447.6 | Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene Organic Chemistry Frontiers, 2018, 5, 1257 |
| 1553956 | CIF | C53 H49 Cl2 N3 O3 | P 1 21/n 1 | 11.566; 31.513; 12.0437 90; 92.279; 90 | 4386.2 | Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones Organic Chemistry Frontiers, 2018, 5, 1202 |
| 1553957 | CIF | C50.5 H49 Cl I N3 O5 | C 1 2/c 1 | 29.069; 16.647; 23.834 90; 124.203; 90 | 9538.8 | Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones Organic Chemistry Frontiers, 2018, 5, 1202 |
| 1553958 | CIF | C52 H47 N3 O3 | P 1 21/n 1 | 13.605; 13.333; 23.507 90; 101.393; 90 | 4180 | Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones Organic Chemistry Frontiers, 2018, 5, 1202 |
| 1553959 | CIF | C20 H19 N O2 | P 1 21/c 1 | 7.6879; 13.3936; 15.696 90; 103.359; 90 | 1572.46 | Chen, Wei; Zhang, Yicheng; Li, Pinhua; Wang, Lei tert-Butyl peroxybenzoate mediated formation of 3-alkylated quinolines from N-propargylamines via a cascade radical addition/cyclization reaction Organic Chemistry Frontiers, 2018, 5, 855 |
| 1553960 | CIF | C51 H51 Cl5 N4 O2 P2 Ru | P 1 21/c 1 | 12.074; 22.964; 17.711 90; 93.931; 90 | 4899 | Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols Organic Chemistry Frontiers, 2018, 5, 1008 |
| 1553961 | CIF | C22 H28 Cl F6 N4 P Ru | P n a 21 | 24.447; 12.95; 7.9 90; 90; 90 | 2501.1 | Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols Organic Chemistry Frontiers, 2018, 5, 1008 |
| 1553962 | CIF | C48 H44 Cl2 N4 P2 Ru | P 1 21/c 1 | 9.679; 19.168; 21.719 90; 91.489; 90 | 4028 | Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols Organic Chemistry Frontiers, 2018, 5, 1008 |
| 1553963 | CIF | C23 H21 N O2 S | P 21 21 21 | 8.0484; 10.6055; 21.9053 90; 90; 90 | 1869.8 | Li, Yun; Chen, Jingchao; He, Zhenxiu; Qin, Hongyu; Zhou, Yongyun; Khan, Ruhima; Fan, Baomin Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides Organic Chemistry Frontiers, 2018, 5, 1108 |
| 1553964 | CIF | C26 H27 Br O3 | P 21 21 2 | 14.839; 17.596; 8.652 90; 90; 90 | 2259.1 | Li, Shoulei; Liu, Bin; Chen, Li; Li, Xin; Cheng, Jin-Pei N-Heterocyclic carbene promoted enantioselective desymmetrization reaction of diarylalkane-bisphenols Organic Chemistry Frontiers, 2018, 5, 1101 |
| 1553965 | CIF | C10 H8 N4 | P 1 21/c 1 | 4.3504; 24.437; 8.5476 90; 102.442; 90 | 887.36 | Qiao, Kai; Zhang, Dong; Zhang, Kai; Yuan, Xin; Zheng, Ming-Wei; Guo, Tian-Fo; Fang, Zheng; Wan, Li; Guo, Kai Iron(ii)-catalyzed C-2 cyanomethylation of indoles and pyrroles via direct oxidative cross-dehydrogenative coupling with acetonitrile derivatives Organic Chemistry Frontiers, 2018, 5, 1129 |
| 1553966 | CIF | C18 H21 N O2 S | P 21 21 21 | 9.4077; 9.9254; 17.562 90; 90; 90 | 1639.9 | Song, Bo; Chen, Mu-Wang; Zhou, Yong-Gui Synthesis of chiral sultams with two adjacent stereocenters via palladium-catalyzed dynamic kinetic resolution Organic Chemistry Frontiers, 2018, 5, 1113 |
| 1553967 | CIF | C15 H7 Cl F N O | P 1 21/n 1 | 8.9388; 9.7832; 13.5584 90; 107.86; 90 | 1128.54 | Liu, Jianming; Yan, Xuyang; Liu, Na; Zhang, Yanyan; Zhao, Shufang; Wang, Xiaopei; Zhuo, Kelei; Yue, Yuanyuan Elemental sulfur accelerated the reactivity of the 3-position of indole for the construction of chromeno[2,3-b]indoles Organic Chemistry Frontiers, 2018, 5, 1034 |
| 1553968 | CIF | C26 H27 N O3 | P -1 | 9.2089; 10.5763; 10.9769 100.503; 95.221; 91.16 | 1046.09 | Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines Organic Chemistry Frontiers, 2018, 5, 1160 |
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