Crystallography Open Database
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Searching year of publication is 2015
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1531044 | CIF | C30 H22 O4 | P 1 21 1 | 7.0717; 8.8439; 19.5443 90; 96.556; 90 | 1214.33 | Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones Chem. Sci., 2015, 6, 7319 |
1531045 | CIF | C38.5 H29 Cl O4 | C 1 2 1 | 16.8074; 10.9989; 16.649 90; 92.018; 90 | 3075.9 | Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones Chem. Sci., 2015, 6, 7319 |
1531046 | CIF | C27 H23 N O4 | P 1 21 1 | 8.1626; 12.2302; 11.0742 90; 101.402; 90 | 1083.72 | Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones Chem. Sci., 2015, 6, 7319 |
1531047 | CIF | C30 H21 F3 N2 | C 1 2/c 1 | 28.3793; 8.2635; 21.2253 90; 112.455; 90 | 4600.2 | Mukundam, Vanga; Kumar, Atul; Dhanunjayarao, Kunchala; Ravi, Arthi; Peruncheralathan, S.; Venkatasubbaiah, Krishnan Tetraaryl pyrazole polymers: versatile synthesis, aggregation induced emission enhancement and detection of explosives Polym. Chem., 2015, 6, 7764 |
1531166 | CIF | C28 H26 N2 O4 S2 | P -1 | 9.2332; 11.8033; 13.4383 78.564; 74.091; 80.538 | 1371.04 | Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines. Organic letters, 2015, 17, 4870-4873 |
1531170 | CIF | C28 H26 N2 O4 S2 | P 21 21 21 | 7.8395; 12.02537; 26.9644 90; 90; 90 | 2542.01 | Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines. Organic letters, 2015, 17, 4870-4873 |
1531174 | CIF | C28 H26 N2 O4 S2 | P 21 21 21 | 5.35547; 17.35361; 27.184 90; 90; 90 | 2526.39 | Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines. Organic letters, 2015, 17, 4870-4873 |
1531311 | CIF | C60 H79 B N3 O2 Sc Si | P -1 | 12.489; 12.502; 20.618 84.375; 75.312; 65.747 | 2839.1 | Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin Isolation, structure and reactivity of a scandium boryl oxycarbene complex Chem. Sci., 2015 |
1531312 | CIF | C54 H81 B N3 O2 Sc Si | P 1 21/n 1 | 13.706; 12.501; 31.255 90; 97.34; 90 | 5311 | Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin Isolation, structure and reactivity of a scandium boryl oxycarbene complex Chem. Sci., 2015 |
1531313 | CIF | C53 H75 B N3 O4 Sc Si | P -1 | 12.0903; 12.7458; 18.106 93.545; 99.571; 114.287 | 2481.3 | Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin Isolation, structure and reactivity of a scandium boryl oxycarbene complex Chem. Sci., 2015 |
1531314 | CIF | C59 H79 B N4 O Sc Si | P -1 | 12.7148; 14.2837; 15.4973 102.293; 99.228; 91.066 | 2710.3 | Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin Isolation, structure and reactivity of a scandium boryl oxycarbene complex Chem. Sci., 2015 |
1531315 | CIF | C50 H71 B N3 O2 Sc Si | P 1 21/c 1 | 12.8438; 20.755; 18.74 90; 108.462; 90 | 4738.5 | Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin Isolation, structure and reactivity of a scandium boryl oxycarbene complex Chem. Sci., 2015 |
1531316 | CIF | C24 H17 N O | P 1 21/n 1 | 12.9997; 21.3361; 13.502 90; 106.398; 90 | 3592.6 | Poudel, Tej Narayan; Lee, Yong Rok Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group Chem. Sci., 2015, 6, 7028 |
1531795 | CIF | C22 H26 O9 | P 1 21 1 | 6.58475; 12.3394; 13.1873 90; 101.317; 90 | 1050.66 | Wang, Yuezhou; Qi, Shuang; Zhan, Ying; Zhang, Nanwen; Wu, An-An; Gui, Fu; Guo, Kai; Yang, Yanru; Cao, Shugeng; Hu, Zhiyu; Zheng, Zhonghui; Song, Siyang; Xu, Qingyan; Shen, Yuemao; Deng, Xianming Aspertetranones A-D, Putative Meroterpenoids from the Marine Algal-Associated Fungus Aspergillus sp. ZL0-1b14. Journal of natural products, 2015, 78, 2405-2410 |
1531937 | CIF | C98 H96 B F24 N2 O Pd Tl | P -1 | 12.7422; 26.6786; 28.5026 99.098; 90.144; 90.509 | 9566.9 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531938 | CIF | C108 H102 B F24 N2 Pd Tl | P -1 | 12.5519; 20.2591; 21.647 105.597; 102.325; 97.308 | 5079.1 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531939 | CIF | C152 H172 Ag4 F12 N4 O12 Pt2 S4 | P 1 21/n 1 | 11.7798; 29.62; 20.9358 90; 90.39; 90 | 7304.7 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531940 | CIF | C81 H92 Ag F3 N2 O3 Pt S | P 1 21/n 1 | 18.6061; 19.7722; 20.9507 90; 106.515; 90 | 7389.5 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531941 | CIF | C71 H94 F3 N2 O5 Pt S Tl | P -1 | 13.95; 16.2777; 17.6213 66.887; 70.018; 71.465 | 3379.6 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531942 | CIF | C93 H134 Ag F3 N2 O10.5 Pd S | P 21 21 21 | 15.5936; 21.315; 24.141 90; 90; 90 | 8023.9 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531943 | CIF | C79 H106 Ag F3 N5 O4 Pt S | P 21 21 21 | 15.6478; 21.2503; 24.077 90; 90; 90 | 8006.1 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531944 | CIF | C84 H98 Ag F3 N2 O3 Pd S | P -1 | 14.5289; 15.663; 17.673 96.662; 109.412; 94.019 | 3742.1 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531945 | CIF | C98 H96 B F24 N2 O Pt Tl | P -1 | 12.7326; 26.642; 28.428 99.2; 90.224; 90.514 | 9518.8 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531946 | CIF | C94 H86 B F24 N2 Pt Tl | P -1 | 14.6265; 20.6542; 31.1986 76.597; 79.378; 89.566 | 9005.2 | Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S. Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding Chem. Sci., 2015, 6, 7169 |
1531947 | CIF | C3 H7 Cl3 I0 N O0 Pb | P 43 21 2 | 10.4482; 10.4482; 14.7573 90; 90; 90 | 1611 | Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission Chem. Sci., 2015, 6, 7222 |
1531948 | CIF | C80 H180 Cl59 N16 O2 Pb21 | P 1 21/c 1 | 21.2016; 15.9211; 26.4092 90; 91.811; 90 | 8910 | Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission Chem. Sci., 2015, 6, 7222 |
1532146 | CIF | C24 H12 N6 O6 | P b c n | 7.235; 41.244; 21.816 90; 90; 90 | 6510 | Zhan, Tian-Guang; Zhou, Tian-You; Qi, Qiao-Yan; Wu, Jian; Li, Guang-Yu; Zhao, Xin The construction of supramolecular polymers through anion bridging: from frustrated hydrogen-bonding networks to well-ordered linear arrays Polym. Chem., 2015, 6, 7586 |
1532452 | CIF | C15 H34 I2 N4 Ni O4 S2 | P -1 | 10.141; 11.619; 11.643 86.263; 69.71; 76.551 | 1251.3 | Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y. The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes Chem. Sci., 2015, 6, 7079 |
1532453 | CIF | C15 H29 Co N2 O6 S2 | P -1 | 7.5419; 8.0477; 16.687 78.174; 82.069; 86.421 | 981.2 | Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y. The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes Chem. Sci., 2015, 6, 7079 |
1532454 | CIF | C15 H28 Fe N2 O6 S2 | P -1 | 7.486; 8.04; 16.74 78.165; 82.235; 86.603 | 976.6 | Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y. The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes Chem. Sci., 2015, 6, 7079 |
1532455 | CIF | C30 H56 Cu2 N4 O12 S4 | C 1 2/c 1 | 19.683; 12.1661; 19.517 90; 106.346; 90 | 4484.7 | Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y. The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes Chem. Sci., 2015, 6, 7079 |
1532456 | CIF | C11 H24 N2 O2 S2 | P 1 21/c 1 | 9.6252; 12.3461; 12.2335 90; 103.606; 90 | 1413 | Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y. The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes Chem. Sci., 2015, 6, 7079 |
1532457 | CIF | C32 H40 S3 | P -1 | 9.799; 11.932; 13.735 84.22; 72.85; 66.98 | 1412.1 | Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji Synthesis and Properties of Ethene-Bridged Terthiophenes. Organic letters, 2015, 17, 4858-4861 |
1532458 | CIF | C32 H40 S3 | P -1 | 10.274; 10.828; 13.62 73.61; 83.52; 85.57 | 1443 | Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji Synthesis and Properties of Ethene-Bridged Terthiophenes. Organic letters, 2015, 17, 4858-4861 |
1532459 | CIF | C28 H32 S3 | P -1 | 7.769; 12.591; 12.753 93.524; 98.169; 101.228 | 1206.1 | Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji Synthesis and Properties of Ethene-Bridged Terthiophenes. Organic letters, 2015, 17, 4858-4861 |
1532460 | CIF | C24 H24 S3 | P 1 21/c 1 | 11.959; 22.114; 7.632 90; 97.436; 90 | 2001 | Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji Synthesis and Properties of Ethene-Bridged Terthiophenes. Organic letters, 2015, 17, 4858-4861 |
1532461 | CIF | C16 H8 S3 | P 1 21/c 1 | 13.033; 3.916; 24.464 90; 103.214; 90 | 1215.5 | Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji Synthesis and Properties of Ethene-Bridged Terthiophenes. Organic letters, 2015, 17, 4858-4861 |
1532465 | CIF | C47.5 H62.5 F6 N1.5 O6.5 P | P 1 2/c 1 | 15.9874; 18.0758; 18.1871 90; 107.85; 90 | 5002.8 | Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities Chem. Sci., 2015, 6, 6731 |
1532466 | CIF | C138 H129 F18 N3 O18 P3 | R -3 :H | 43.2165; 43.2165; 12.4664 90; 90; 120 | 20163.7 | Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities Chem. Sci., 2015, 6, 6731 |
1532468 | CIF | C82 H116 Cd2 N24 O25 | C 1 2/c 1 | 30.664; 17.225; 27.371 90; 105.9; 90 | 13904 | Sun, Chun-Yi; To, Wai-Pong; Wang, Xin-Long; Chan, Kaai-Tung; Su, Zhong-Min; Che, Chi-Ming Metal‒organic framework composites with luminescent gold(iii) complexes. Strongly emissive and long-lived excited states in open air and photo-catalysis Chem. Sci., 2015, 6, 7105 |
1532469 | CIF | C91.5 H111.5 Ge2 N2 Si2 | P -1 | 10.806; 18.897; 21.557 108.61; 90.43; 103.93 | 4032.1 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532470 | CIF | C104 H122 Ge2 N2 O2 Si2 | P 1 21/n 1 | 13.373; 21.643; 15.884 90; 102.62; 90 | 4486.3 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532471 | CIF | C46 H57 Ge N Si | P -1 | 10.783; 11.465; 16.298 97.01; 91.76; 92.77 | 1996.1 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532472 | CIF | C52 H61 Ge N Si | P 1 21/n 1 | 11.543; 23.7164; 16.3022 90; 97.979; 90 | 4419.7 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532473 | CIF | C49 H61 Ge N Si | P 1 21/c 1 | 10.319; 18.286; 22.437 90; 91.27; 90 | 4232.7 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532474 | CIF | C50 H63 Ge N Si | P 1 21 1 | 10.2741; 14.6818; 14.6417 90; 102.077; 90 | 2159.71 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532475 | CIF | C52 H67 Ge N Si | P 1 21/n 1 | 9.942; 15.413; 28.793 90; 97.18; 90 | 4377.5 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532476 | CIF | C46 H57 N Si Sn | P -1 | 10.673; 12.534; 15.493 82.27; 85.09; 73.63 | 1968 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532477 | CIF | C52 H68 N Si Sn | P -1 | 10.2591; 13.6505; 17.3164 99.111; 105.293; 95.189 | 2287.3 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532478 | CIF | C53 H61 Ge N Si | P 1 21/n 1 | 10.0813; 15.796; 28.096 90; 96.916; 90 | 4441.6 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532479 | CIF | C53 H61 N Si Sn | P 1 21/n 1 | 10.1088; 15.7379; 28.106 90; 96.853; 90 | 4439.5 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532480 | CIF | C52 H65 Ge N Si | P 1 21/n 1 | 10.003; 15.4017; 28.92 90; 97.698; 90 | 4415.4 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532481 | CIF | C49 H63 Ge N Si | P 1 21/n 1 | 11.374; 23.3065; 16.3439 90; 97.891; 90 | 4291.5 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532482 | CIF | C49 H62 Cl Ge N Si | P -1 | 10.731; 14.446; 15.647 77.83; 78.54; 69.06 | 2194.2 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532483 | CIF | C48 H63 Ge N O Si | P -1 | 10.399; 14.2109; 15.4524 90.483; 101.026; 105.118 | 2159.72 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532484 | CIF | C53 H70 N2 O Si Sn | P -1 | 14.604; 15.84; 20.773 88.61; 82.84; 84.99 | 4749.2 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532485 | CIF | C112 H154 Ge2 N2 O2 Si2 | P 1 21/n 1 | 15.0392; 12.4994; 26.2128 90; 93.127; 90 | 4920.17 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532486 | CIF | C112 H158 N2 O2 Si2 Sn2 | P -1 | 15.4827; 16.4448; 23.7823 72.311; 88.259; 62.908 | 5094.1 | Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes Chem. Sci., 2015, 6, 7249 |
1532487 | CIF | C23 H32 O7 | P 21 21 21 | 9.772; 13.5369; 16.5519 90; 90; 90 | 2189.53 | Ma, Guoxu; Wu, Haifeng; Chen, Deli; Zhu, Nailiang; Zhu, Yindi; Sun, Zhonghao; Li, Pengfei; Yang, Junshan; Yuan, Jingquan; Xu, Xudong Antimalarial and Antiproliferative Cassane Diterpenes of Caesalpinia sappan. Journal of natural products, 2015, 78, 2364-2371 |
1532490 | CIF | C27 H30 B2 D3 N2 O2 | P -1 | 6.2435; 13.8921; 14.2338 100.533; 92.139; 100.164 | 1191.63 | Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene Chem. Sci., 2015, 6, 7150 |
1532491 | CIF | C30 H34 B2 N2 O2 | P -1 | 12.0335; 13.357; 17.045 73.663; 81.968; 79.686 | 2575 | Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene Chem. Sci., 2015, 6, 7150 |
1532492 | CIF | C31 H36 B2 N2 O2 | P 1 21/n 1 | 9.498; 9.09; 30.647 90; 94.119; 90 | 2639.1 | Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene Chem. Sci., 2015, 6, 7150 |
1532493 | CIF | C30 H33 B2 Br N2 O2 | P 1 21/n 1 | 9.5066; 9.248; 30.632 90; 94.399; 90 | 2685.1 | Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene Chem. Sci., 2015, 6, 7150 |
1532494 | CIF | C32 H39 B2 N2 O2 | P 1 21/n 1 | 8.8862; 21.985; 14.0495 90; 96.2349; 90 | 2728.5 | Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene Chem. Sci., 2015, 6, 7150 |
1532495 | CIF | C33 H52 I P2 Pd | P b c a | 14.978; 16.438; 29.361 90; 90; 90 | 7229 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532496 | CIF | C65 H64 B F24 I P2 Pd | P 1 21/n 1 | 14.0602; 28.6171; 16.9031 90; 92.0331; 90 | 6796.9 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532497 | CIF | C33 H53 I P2 Pd | P 1 21/c 1 | 12.8203; 14.834; 19.174 90; 106.641; 90 | 3493.7 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532498 | CIF | C40 H60 I N P2 Pd | P 1 21/n 1 | 17.0891; 14.014; 18.4206 90; 100.081; 90 | 4343.4 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532499 | CIF | C39 H57 I O P2 Pd | P -1 | 11.8764; 14.433; 25.1741 101.297; 93.5784; 111.2 | 3903 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532500 | CIF | C68 H72 B F24 I P3 Pd | P 1 21 1 | 10.0901; 23.7955; 31.205 90; 90.532; 90 | 7492 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532501 | CIF | C44 H67 F3 O4 P2 Pd S2 | P 21 21 21 | 14.0266; 15.2323; 21.3735 90; 90; 90 | 4566.6 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532502 | CIF | C50 H74 P2 Pd S2 | P 1 21/n 1 | 11.297; 11.59; 36.768 90; 92.926; 90 | 4808 | Cui, Peng; Iluc, Vlad M. Redox-induced umpolung of transition metal carbenes Chem. Sci., 2015, 6, 7343 |
1532507 | CIF | C8 H4 F S3 | P n m a | 7.784; 22.5821; 9.6099 90; 90; 90 | 1689.22 | Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S. Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization Polym. Chem., 2015, 6, 7658 |
1532508 | CIF | C16 H10 S6 | C 1 2/c 1 | 24.2039; 6.2548; 22.525 90; 103.733; 90 | 3312.6 | Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S. Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization Polym. Chem., 2015, 6, 7658 |
1532509 | CIF | C12 H6 S6 Se2 | P b c a | 16.5074; 8.21747; 23.5969 90; 90; 90 | 3200.9 | Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S. Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization Polym. Chem., 2015, 6, 7658 |
1532510 | CIF | C12 H6 S8 | P 1 21/c 1 | 8.3161; 20.227; 9.2199 90; 92.391; 90 | 1549.53 | Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S. Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization Polym. Chem., 2015, 6, 7658 |
1532833 | CIF | C21 H28 N2 O4 | P 21 21 21 | 8.7278; 9.6635; 46.6791 90; 90; 90 | 3937 | Chung, John Y. L.; Marcune, Benjamin; Strotman, Hallena R.; Petrova, Rositza I.; Moore, Jeffrey C.; Dormer, Peter G. Synthesis of ((3R,6R)-6-Methylpiperidin-3-yl)methanol via Biocatalytic Transamination and Crystallization-Induced Dynamic Resolution Organic Process Research & Development, 2015, 19, 1418 |
1533007 | CIF | C75 H88 Mo4 O8 P2 Sm2 | P -1 | 9.5023; 12.6103; 15.1418 97.784; 90.79; 100.069 | 1768.68 | Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W. The approach to 4d/4f-polyphosphides Chem. Sci., 2015, 6, 7179 |
1533008 | CIF | C68 H80 Mo4 O8 P2 Yb2 | P -1 | 9.4563; 12.5189; 14.9787 84.903; 71.669; 76.285 | 1635 | Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W. The approach to 4d/4f-polyphosphides Chem. Sci., 2015, 6, 7179 |
1533009 | CIF | C68 H86 Mo2 O4 P4 Sm2 | P -1 | 9.6185; 10.2667; 17.5096 83.519; 77.307; 78.461 | 1648.4 | Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W. The approach to 4d/4f-polyphosphides Chem. Sci., 2015, 6, 7179 |
1533010 | CIF | C81 H105 Mo3 O6 P5 Sm3 | P 1 21/m 1 | 10.13; 25.686; 15.724 90; 96.36; 90 | 4066.2 | Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W. The approach to 4d/4f-polyphosphides Chem. Sci., 2015, 6, 7179 |
1533011 | CIF | C78 H106 Mo2 O4 P6 Sm2 | P -1 | 11.1671; 12.7931; 14.7276 98.952; 110.227; 95.319 | 1925.7 | Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W. The approach to 4d/4f-polyphosphides Chem. Sci., 2015, 6, 7179 |
1533012 | CIF | C78 H106 Mo2 O4 P6 Yb2 | P -1 | 11.1924; 12.6285; 14.6371 99.581; 110.455; 94.847 | 1888.44 | Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W. The approach to 4d/4f-polyphosphides Chem. Sci., 2015, 6, 7179 |
1533373 | CIF | C28 H42 Au Cl3 N4 O | I 41/a | 37.1846; 37.1846; 9.743 90; 90; 90 | 13471.6 | Ramsay, William J.; Foster, Jonathan A.; Moore, Katharine L.; Ronson, Tanya K.; Mirgalet, Raphaël J.; Jefferson, David A.; Nitschke, Jonathan R. AuICl-bound N-heterocyclic carbene ligands form MII4(LAuCl)6integrally gilded cages Chem. Sci., 2015, 6, 7326 |
1533374 | CIF | C30 H33 Cl F3 Ir N2 O2 | P 1 21/n 1 | 11.3662; 17.1523; 15.528 90; 111.111; 90 | 2824.1 | Yellol, Jyoti; Pérez, Sergio A; Buceta, Alicia; Yellol, Gorakh; Donaire, Antonio; Szumlas, Piotr; Bednarski, Patrick J.; Makhloufi, Gamall; Janiak, Christoph; Espinosa, Arturo; Ruiz, José Novel C,N-Cyclometalated Benzimidazole Ruthenium(II) and Iridium(III) Complexes as Antitumor and Antiangiogenic Agents: A Structure-Activity Relationship Study. Journal of medicinal chemistry, 2015, 58, 7310-7327 |
1533375 | CIF | C30 H32 Cl F3 N2 O2 Ru | P 1 21/c 1 | 12.5656; 17.1429; 13.9971 90; 108.785; 90 | 2854.5 | Yellol, Jyoti; Pérez, Sergio A; Buceta, Alicia; Yellol, Gorakh; Donaire, Antonio; Szumlas, Piotr; Bednarski, Patrick J.; Makhloufi, Gamall; Janiak, Christoph; Espinosa, Arturo; Ruiz, José Novel C,N-Cyclometalated Benzimidazole Ruthenium(II) and Iridium(III) Complexes as Antitumor and Antiangiogenic Agents: A Structure-Activity Relationship Study. Journal of medicinal chemistry, 2015, 58, 7310-7327 |
1533376 | CIF | C25.5 H28 O12.5 | P 21 21 21 | 15.0788; 17.5135; 19.2065 90; 90; 90 | 5072.1 | Gan, Maoluo; Liu, Bin; Tan, Yi; Wang, Qiang; Zhou, Hongxia; He, Hongwei; Ping, Yuhui; Yang, Zhaoyong; Wang, Yiguang; Xiao, Chunling Saccharothrixones A-D, Tetracenomycin-Type Polyketides from the Marine-Derived Actinomycete Saccharothrix sp. 10-10. Journal of natural products, 2015, 78, 2260-2265 |
1534094 | CIF | C79 H60 Cl2 N10 O7 Ru | P -1 | 12.6643; 15.7605; 18.076 105.968; 97.219; 99.105 | 3370.1 | Fan, Congbin; Ye, Changqing; Wang, Xiaomei; Chen, Zhigang; Zhou, Yuyang; Liang, Zuoqin; Tao, Xutang Synthesis and Electrochromic Properties of New Terpyridine‒Triphenylamine Hybrid Polymers Macromolecules, 2015, 48, 6465 |
1534095 | CIF | C32 H40 N0 O8 | P 21 21 21 | 8.2474; 12.543; 29.019 90; 90; 90 | 3001.9 | Yang, Shanshan; Sun, Jiachen; Lu, Hong; Ma, Hong; Zhang, Yaozhou Bioactivity-guided isolation of anticancer compounds from Euphorbia lathyris Anal. Methods, 2015, 7, 9568 |
1534096 | CIF | C16 H16 Br N O2 | P 21 21 21 | 5.1904; 9.7263; 29.581 90; 90; 90 | 1493.3 | Pathipati, Stalin R.; Singh, Vipender; Eriksson, Lars; Selander, Nicklas Lewis Acid Catalyzed Annulation of Nitrones with Oxiranes, Aziridines, and Thiiranes. Organic letters, 2015, 17, 4506-4509 |
1534097 | CIF | C27 H21 N O4 | P 1 21/c 1 | 11.7836; 8.1908; 21.1196 90; 92.216; 90 | 2036.9 | Jung, Youngeun; Kim, Ikyon Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles. Organic letters, 2015, 17, 4600-4603 |
1534098 | CIF | C26 H21 N O3 | P 1 21/c 1 | 11.5406; 9.3427; 18.9135 90; 96.804; 90 | 2024.9 | Jung, Youngeun; Kim, Ikyon Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles. Organic letters, 2015, 17, 4600-4603 |
1534099 | CIF | C62 H60 Cl N4 O4 P | P 1 21 1 | 13.9954; 19.389; 14.02 90; 115.309; 90 | 3439.3 | Gao, Xing; Han, Jianwei; Wang, Limin Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles. Organic letters, 2015, 17, 4596-4599 |
1534100 | CIF | C65 H65 N4 O5 P | P 1 21 1 | 12.0658; 17.7295; 13.2309 90; 104.155; 90 | 2744.4 | Gao, Xing; Han, Jianwei; Wang, Limin Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles. Organic letters, 2015, 17, 4596-4599 |
1534101 | CIF | C24 H29 F N2 O5 | R 3 :H | 31.82; 31.82; 6.203 90; 90; 120 | 5439.2 | Bonetti, Andrea; Pellegrino, Sara; Das, Priyadip; Yuran, Sivan; Bucci, Raffaella; Ferri, Nicola; Meneghetti, Fiorella; Castellano, Carlo; Reches, Meital; Gelmi, Maria Luisa Dipeptide Nanotubes Containing Unnatural Fluorine-Substituted β(2,3)-Diarylamino Acid and l-Alanine as Candidates for Biomedical Applications. Organic letters, 2015, 17, 4468-4471 |
1534102 | CIF | C15 H17 N3 | P 1 21/c 1 | 9.507; 9.4923; 14.387 90; 90.344; 90 | 1298.3 | Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton. Organic letters, 2015, 17, 4518-4521 |
1534103 | CIF | C24 H21 N | P 1 21/c 1 | 7.4677; 18.793; 24.102 90; 94.988; 90 | 3369.7 | Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton. Organic letters, 2015, 17, 4518-4521 |
1534104 | CIF | C13 H14 B Cl F2 N2 | I 41/a :2 | 25.108; 25.108; 8.6289 90; 90; 90 | 5439.8 | Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride. Organic letters, 2015, 17, 4632-4635 |
1534105 | CIF | C16 H11 B Cl2 F2 N2 O | C 1 2/c 1 | 15.6318; 13.1816; 15.4701 90; 96.971; 90 | 3164.1 | Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride. Organic letters, 2015, 17, 4632-4635 |
1534106 | CIF | C12 H11 B Cl2 F2 N2 | P -1 | 10.1284; 11.8356; 12.656 91.216; 110.273; 107.739 | 1341.8 | Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride. Organic letters, 2015, 17, 4632-4635 |
1534107 | CIF | C20 H13 F3 O2 S | P -1 | 7.4471; 9.4405; 12.781 79.059; 79.842; 75.136 | 844.95 | Xu, Chunfa; Shen, Qilong Lewis Acid Mediated Trifluoromethylthio Lactonization/Lactamization. Organic letters, 2015, 17, 4561-4563 |
1534108 | CIF | C24 H21 N O4 S | P 1 21/n 1 | 8.2556; 14.406; 17.938 90; 93.63; 90 | 2129.1 | Liu, Hongxu; Yang, Yanyan; Wang, Shen; Wu, Jie; Wang, Xiao-Na; Chang, Junbiao Synthesis of 3-Substituted 2-Aminochromones via Sn(IV)-Promoted Annulation of Ynamides with 2-Methoxyaroyl Chlorides. Organic letters, 2015, 17, 4472-4475 |
1534109 | CIF | C14 H11 N O S | P -1 | 5.9946; 7.961; 12.7201 85.167; 84.614; 73.532 | 578.51 | Lemercier, Bérénice C; Pierce, Joshua G. Synthesis of 1,4,2-Oxathiazoles via Oxidative Cyclization of Thiohydroximic Acids. Organic letters, 2015, 17, 4542-4545 |
1534110 | CIF | C25 H22 Cl2 I N3 O4 S | P 1 21 1 | 10.469; 11.122; 11.473 90; 92.129; 90 | 1335 | Tripathi, Chandra Bhushan; Mukherjee, Santanu Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes. Organic letters, 2015, 17, 4424-4427 |
1534111 | CIF | C18 H16 I N O | P 1 21 1 | 9.9179; 5.7432; 14.186 90; 95.817; 90 | 803.88 | Tripathi, Chandra Bhushan; Mukherjee, Santanu Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes. Organic letters, 2015, 17, 4424-4427 |
1534112 | CIF | C21 H21 N O5 S | P 1 21 1 | 11.3632; 11.802; 15.831 90; 109.817; 90 | 1997.3 | Qiao, Baokun; Huang, Yin-Jun; Nie, Jing; Ma, Jun-An Highly Regio-, Diastereo-, and Enantioselective Mannich Reaction of Allylic Ketones and Cyclic Ketimines: Access to Chiral Benzosultam. Organic letters, 2015, 17, 4608-4611 |
1534113 | CIF | C19 H18 N2 O2 | P 1 21/c 1 | 11.7071; 15.8544; 9.4636 90; 113.637; 90 | 1609.2 | Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles. Organic letters, 2015, 17, 4502-4505 |
1534114 | CIF | C14 H17 N3 O4 | P 1 21/c 1 | 6.9191; 16.135; 14.3518 90; 104.515; 90 | 1551.09 | Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles. Organic letters, 2015, 17, 4502-4505 |
1534115 | CIF | C33 H25 N3 O2 | P 1 21/n 1 | 16.9438; 7.2054; 21.3218 90; 95.864; 90 | 2589.49 | Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles. Organic letters, 2015, 17, 4490-4493 |
1534116 | CIF | C27 H20 N4 O4 | P 1 21/c 1 | 7.3218; 32.2827; 11.6678 90; 91.975; 90 | 2756.25 | Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles. Organic letters, 2015, 17, 4490-4493 |
1534117 | CIF | C21 H19 F3 N4 O2 | P 1 21/c 1 | 22.1268; 5.3611; 16.7753 90; 101.52; 90 | 1949.86 | Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines. Organic letters, 2015, 17, 4568-4571 |
1534118 | CIF | C20 H18 F3 N3 O2 | P c a 21 | 16.6564; 5.4719; 39.3699 90; 90; 90 | 3588.3 | Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines. Organic letters, 2015, 17, 4568-4571 |
1534119 | CIF | C53 H45 N2 O8 | P 21 21 21 | 11.4428; 15.4354; 24.3994 90; 90; 90 | 4309.5 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534120 | CIF | C48 H52 N4 O9 | P 21 21 2 | 14.958; 25.526; 11.093 90; 90; 90 | 4235.5 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534121 | CIF | C45 H42 I2 N4 O8 | C 1 2/c 1 | 35.02; 16.0741; 20.002 90; 111.769; 90 | 10456 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534122 | CIF | C59 H63 N6 O8 | C 1 2/c 1 | 20.0623; 15.4284; 19.2848 90; 120.843; 90 | 5125 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534123 | CIF | C47 H48 N4 O8 | P 1 21/c 1 | 13.787; 14.6; 24.867 90; 105.219; 90 | 4829.9 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534124 | CIF | C49 H50 Cl6 N4 O8 | P -1 | 13.203; 13.977; 14.658 90.494; 100.476; 113.249 | 2434.2 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534125 | CIF | C45 H44 N4 O8 | P -1 | 12.2439; 13.8398; 14.5323 91.544; 97.532; 110.103 | 2285.7 | Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection. Organic letters, 2015, 17, 4440-4443 |
1534135 | CIF | C40 H59 Cl2 N2 P Ru | P 1 21/n 1 | 12.2117; 18.0562; 18.2926 90; 103.741; 90 | 3918 | Lummiss, Justin A. M.; Higman, Carolyn S.; Fyson, Devon L.; McDonald, Robert; Fogg, Deryn E. The divergent effects of strong NHC donation in catalysis Chem. Sci., 2015, 6, 6739 |
1534136 | CIF | C39 H35 N O | P 1 21/c 1 | 19.39657; 15.07422; 10.4257 90; 98.9955; 90 | 3010.86 | Deng, Haiqin; He, Zikai; Lam, Jacky W. Y.; Tang, Ben Zhong Regio- and stereoselective construction of stimuli-responsive macromolecules by a sequential coupling-hydroamination polymerization route Polym. Chem., 2015, 6, 8297 |
1534348 | CIF | C20 H32 O3 | C 1 2 1 | 33.5582; 7.4109; 14.7554 90; 97.8284; 90 | 3635.4 | Du, Kun; De Mieri, Maria; Neuburger, Markus; Zietsman, Pieter C.; Marston, Andrew; van Vuuren, Sandy F.; Ferreira, Daneel; Hamburger, Matthias; van der Westhuizen, Jan H. Labdane and Clerodane Diterpenoids from Colophospermum mopane. Journal of natural products, 2015, 78, 2494-2504 |
1534351 | CIF | C16 H30 N2 O5 S | P 65 | 11.4458; 11.4458; 27.7551 90; 90; 120 | 3148.95 | Mazzier, Daniela; Carraro, Francesco; Crisma, Marco; Rancan, Marzio; Toniolo, Claudio; Moretto, Alessandro A terminally protected dipeptide: from crystal structure and self-assembly, through co-assembly with carbon-based materials, to a ternary catalyst for reduction chemistry in water. Soft matter, 2015, 12, 238-245 |
1534352 | CIF | C16 H30 N2 O5 S | P 21 21 21 | 5.08911; 12.09583; 32.4406 90; 90; 90 | 1996.95 | Mazzier, Daniela; Carraro, Francesco; Crisma, Marco; Rancan, Marzio; Toniolo, Claudio; Moretto, Alessandro A terminally protected dipeptide: from crystal structure and self-assembly, through co-assembly with carbon-based materials, to a ternary catalyst for reduction chemistry in water. Soft matter, 2015, 12, 238-245 |
1534401 | CIF | C38 H57 Cl F19 N7 O5 P3 Ru | P -1 | 10.036; 14.855; 18.895 73.62; 76.36; 87.09 | 2626 | Du, Jun; Zhang, Erlong; Zhao, Yao; Zheng, Wei; Zhang, Yang; Lin, Yu; Wang, Zhaoying; Luo, Qun; Wu, Kui; Wang, Fuyi Discovery of a dual-targeting organometallic ruthenium complex with high activity inducing early stage apoptosis of cancer cells. Metallomics : integrated biometal science, 2015, 7, 1573-1583 |
1538419 | CIF | C24.5 H27 Br2 Cl O6 | P 21 21 21 | 9.7566; 19.1985; 27.6028 90; 90; 90 | 5170.34 | Hans, Marcus; Charpentier, Maël; Huch, Volker; Jauch, Johann; Bruhn, Torsten; Bringmann, Gerhard; Quandt, Dietmar Stereoisomeric Composition of Natural Myrtucommulone A. Journal of natural products, 2015, 78, 2381-2389 |
1538420 | CIF | C48 H55 F3 O10 | P 1 21 1 | 6.4479; 40.961; 17.888 90; 91.687; 90 | 4722.4 | Hans, Marcus; Charpentier, Maël; Huch, Volker; Jauch, Johann; Bruhn, Torsten; Bringmann, Gerhard; Quandt, Dietmar Stereoisomeric Composition of Natural Myrtucommulone A. Journal of natural products, 2015, 78, 2381-2389 |
1539135 | CIF | C20 H15 Cl N2 O3 | P 1 21/n 1 | 16.571; 5.5448; 20.45 90; 111.604; 90 | 1747 | Li, Danyang; Yu, Ming; Zhang, Jitan; Liu, Zhanxiang; Zhang, Yuhong Synthesis of Benzyl Esters via Functionalization of Multiple C-H Bonds by Palladium Catalysis. Organic letters, 2015, 17, 5300-5303 |
1540018 | CIF | C24 H20 Dy2 N2 O17 | C 1 2/c 1 | 18.3085; 9.0788; 19.6464 90; 97.068; 90 | 3240.8 | Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet. Inorganic chemistry, 2015, 54, 10224-10231 |
1540019 | CIF | C26 H28 Dy2 N2 O19 | C 1 2/c 1 | 18.465; 9.2442; 19.699 90; 102.18; 90 | 3286.8 | Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet. Inorganic chemistry, 2015, 54, 10224-10231 |
1540020 | CIF | C24 H20 Dy2 N2 O17 | P n m a | 8.6326; 28.1206; 15.3462 90; 90; 90 | 3725.3 | Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet. Inorganic chemistry, 2015, 54, 10224-10231 |
1540021 | CIF | C10 H12 B F4 N O2 Ru | P 1 21/n 1 | 8.7303; 9.7841; 15.4342 90; 91.525; 90 | 1317.89 | Nyawade, Eunice A.; Friedrich, Holger B.; Omondi, Bernard; Mpungose, Philani Synthesis and Characterization of New (η5-Cyclopentadienyl)dicarbonylruthenium(II) Amine Complexes: Their Application as Homogeneous Catalysts in Styrene Oxidation Organometallics, 2015, 34, 4922 |
1540022 | CIF | C14 H14 B F4 N O2 Ru | P 1 21/n 1 | 10.4488; 9.7788; 31.7901 90; 99.236; 90 | 3206.1 | Nyawade, Eunice A.; Friedrich, Holger B.; Omondi, Bernard; Mpungose, Philani Synthesis and Characterization of New (η5-Cyclopentadienyl)dicarbonylruthenium(II) Amine Complexes: Their Application as Homogeneous Catalysts in Styrene Oxidation Organometallics, 2015, 34, 4922 |
1540024 | CIF | C42 H49 Cl2 Eu N12 O16 Zn | P -1 | 13.8641; 14.5627; 15.19 96.519; 113.081; 109.85 | 2543.6 | Anastasiadis, Nikolaos C.; Polyzou, Christina D.; Kostakis, George E.; Bekiari, Vlasoula; Lan, Yanhua; Perlepes, Spyros P.; Konidaris, Konstantis F.; Powell, Annie K. Dinuclear lanthanide(iii)/zinc(ii) complexes with methyl 2-pyridyl ketone oxime. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19791-19795 |
1540025 | CIF | C28 H29 Dy N10 O10 Zn | C 1 c 1 | 15.9387; 9.3158; 22.5168 90; 94.59; 90 | 3332.6 | Anastasiadis, Nikolaos C.; Polyzou, Christina D.; Kostakis, George E.; Bekiari, Vlasoula; Lan, Yanhua; Perlepes, Spyros P.; Konidaris, Konstantis F.; Powell, Annie K. Dinuclear lanthanide(iii)/zinc(ii) complexes with methyl 2-pyridyl ketone oxime. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19791-19795 |
1540029 | CIF | C28 H20 Cu O7 | P 1 21/n 1 | 12.3691; 13.9416; 13.8663 90; 100.45; 90 | 2351.5 | Jochyms, Quentin; Guillot, Pierre; Mignard, Emmanuel; Vincent, Jean-Marc A fluorosurfactant and photoreducible Cu(II)-tren click catalyst: surfactant and catalytic properties at liquid/liquid interfaces. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19700-19707 |
1540030 | CIF | C46 H58 Dy2 N14 O24 | P -1 | 9.931; 10.841; 14.4817 82.775; 71.167; 74.627 | 1421.48 | Kuo, Che-Jung; Holmberg, Rebecca J.; Lin, Po-Heng Slight synthetic changes eliciting different topologies: synthesis, structure and magnetic properties of novel dinuclear and nonanuclear dysprosium complexes. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19758-19762 |
1540031 | CIF | C80 H92 Dy9 N24 O46 | C 1 2/c 1 | 34.8579; 24.5497; 24.2872 90; 120.453; 90 | 17916.6 | Kuo, Che-Jung; Holmberg, Rebecca J.; Lin, Po-Heng Slight synthetic changes eliciting different topologies: synthesis, structure and magnetic properties of novel dinuclear and nonanuclear dysprosium complexes. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19758-19762 |
1540032 | CIF | C28.5 H63 Cl2 Cu2 N4 O19 Zn2 | P -1 | 10.9593; 13.8454; 17.4039 109.186; 90.177; 108.009 | 2355.8 | Heras Ojea, María José; Wilson, Claire; Coles, Simon J.; Tuna, Floriana; Murrie, Mark Directed synthesis of {CuZn} and {CuZn} heterometallic complexes. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19275-19281 |
1540033 | CIF | C88 H232 Cl8 Cu8 N16 O96 Zn8 | P 4/n | 26.5574; 26.5574; 13.1186 90; 90; 90 | 9252.5 | Heras Ojea, María José; Wilson, Claire; Coles, Simon J.; Tuna, Floriana; Murrie, Mark Directed synthesis of {CuZn} and {CuZn} heterometallic complexes. Dalton transactions (Cambridge, England : 2003), 2015, 44, 19275-19281 |
1540373 | CIF | C135 H42 Cl3 O2 | C 1 2/c 1 | 20.4242; 25.5132; 32.3262 90; 105.672; 90 | 16218.5 | Abeyratne Kuragama, Peumie L.; Fronczek, Frank R.; Sygula, Andrzej Bis-corannulene Receptors for Fullerenes Based on Klärner's Tethers: Reaching the Affinity Limits. Organic letters, 2015, 17, 5292-5295 |
1540374 | CIF | C16 H26 N2 O6 S | P 21 21 21 | 6.2372; 11.1508; 28.596 90; 90; 90 | 1988.8 | Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones. Organic letters, 2015, 17, 5408-5411 |
1540375 | CIF | C13 H21 N O6 | P 21 21 21 | 6.282; 9.924; 24.859 90; 90; 90 | 1549.8 | Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones. Organic letters, 2015, 17, 5408-5411 |
1540376 | CIF | C16 H27 N O8 | P 1 21 1 | 10.248; 9.553; 11.932 90; 99.477; 90 | 1152.2 | Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones. Organic letters, 2015, 17, 5408-5411 |
1540377 | CIF | C17 H28 N2 O6 | P 1 21 1 | 10.375; 17.5559; 10.8576 90; 95.023; 90 | 1970 | Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones. Organic letters, 2015, 17, 5408-5411 |
1540378 | CIF | C19 H24 N2 O6 S | P 1 21 1 | 11.0948; 6.112; 15.1863 90; 92.704; 90 | 1028.7 | Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones. Organic letters, 2015, 17, 5408-5411 |
1540379 | CIF | C20 H26 N2 O6 | P 1 21 1 | 9.6081; 10.7346; 20.0544 90; 91.493; 90 | 2067.7 | Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones. Organic letters, 2015, 17, 5408-5411 |
1540380 | CIF | C84 H153 Ag3 Au15 O2 S14 | C 1 2/c 1 | 24.9951; 18.5586; 51.826 90; 90.478; 90 | 24040 | Xiang, Ji; Li, Peng; Song, Yongbo; Liu, Xia; Chong, Hanbao; Jin, Shan; Pei, Yong; Yuan, Xiaoyou; Zhu, Manzhou X-Ray crystal structure, and optical and electrochemical properties of the Au15Ag3(SC6H11)14 nanocluster with a core-shell structure. Nanoscale, 2015, 7, 18278-18283 |
1540381 | CIF | C21 H24 Cl Co N7 Ni | P 1 21/n 1 | 14.4536; 9.9877; 14.7366 90; 101.065; 90 | 2087.8 | Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C. Configuring Bonds between First-Row Transition Metals. Accounts of chemical research, 2015, 48, 2885-2894 |
1540382 | CIF | C41 H64 Fe N4 O0.5 P3 Ti | P -1 | 12.35; 19.4587; 19.7453 113.034; 95.547; 101.183 | 4204.9 | Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C. Configuring Bonds between First-Row Transition Metals. Accounts of chemical research, 2015, 48, 2885-2894 |
1540383 | CIF | C43 H68 N4 Ni O P3 Ti | P -1 | 12.5471; 14.0969; 24.6228 91.787; 98.742; 94.687 | 4286 | Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C. Configuring Bonds between First-Row Transition Metals. Accounts of chemical research, 2015, 48, 2885-2894 |
1540384 | CIF | C69 H91 B Co Cr N5 O P3 | P 1 21/c 1 | 17.8979; 14.3708; 26.8674 90; 99.446; 90 | 6816.8 | Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C. Configuring Bonds between First-Row Transition Metals. Accounts of chemical research, 2015, 48, 2885-2894 |
1540385 | CIF | C39 H60 B Cr F4 N4 Ni P3 | R -3 :H | 12.4121; 12.4121; 57.067 90; 90; 120 | 7613.9 | Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C. Configuring Bonds between First-Row Transition Metals. Accounts of chemical research, 2015, 48, 2885-2894 |
1540386 | CIF | C21 H24 Cl Co N7 Ni | P 1 21/n 1 | 14.4978; 10.0084; 14.7758 90; 100.944; 90 | 2105 | Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C. Configuring Bonds between First-Row Transition Metals. Accounts of chemical research, 2015, 48, 2885-2894 |
1540387 | CIF | C78 H196 Cu6 Li4 Mn4 N12 O104 | P 4/m m m | 36.71; 36.71; 15.414 90; 90; 90 | 20772 | Grancha, Thais; Acosta, Alvaro; Cano, Joan; Ferrando-Soria, Jesús; Seoane, Beatriz; Gascon, Jorge; Pasán, Jorge; Armentano, Donatella; Pardo, Emilio Cation Exchange in Dynamic 3D Porous Magnets: Improvement of the Physical Properties. Inorganic chemistry, 2015, 54, 10834-10840 |
1540388 | CIF | C78 H198 Cu6 K4 Mn4 N12 O105 | P 4/m m m | 37.492; 37.492; 15.557 90; 90; 90 | 21868 | Grancha, Thais; Acosta, Alvaro; Cano, Joan; Ferrando-Soria, Jesús; Seoane, Beatriz; Gascon, Jorge; Pasán, Jorge; Armentano, Donatella; Pardo, Emilio Cation Exchange in Dynamic 3D Porous Magnets: Improvement of the Physical Properties. Inorganic chemistry, 2015, 54, 10834-10840 |
1540389 | CIF | C19 H24 F2 N3 Na O7 S | P 1 21/c 1 | 15.929; 10.828; 13.718 90; 91.62; 90 | 2365.1 | Jiang, Chen; Wang, Yongli; Yan, Jiaqi; Yang, Jingxiang; Xiao, Liping; Hao, Hongxun Formation Mechanism and Phase Transformation Behaviors of Pantoprazole Sodium Heterosolvate Organic Process Research & Development, 2015, 19, 1752 |
1540392 | CIF | Ba0.1 O4 Si Sr1.9 | P m n b | 5.674; 7.086; 9.745 90; 90; 90 | 391.81 | Li, Xiaojun; Hua, Youjie; Ma, Hongping; Deng, Degang; Xu, Shiqing Modification of the crystal structure of Sr2−xBaxSi(O,N)4: Eu2+phosphors to improve their luminescence properties CrystEngComm, 2015, 17, 9123 |
1540393 | CIF | Ba0.15 N O4 Si Sr2.85 | P m n b | 5.6796; 7.1386; 9.7639 90; 90; 90 | 395.87 | Li, Xiaojun; Hua, Youjie; Ma, Hongping; Deng, Degang; Xu, Shiqing Modification of the crystal structure of Sr2−xBaxSi(O,N)4: Eu2+phosphors to improve their luminescence properties CrystEngComm, 2015, 17, 9123 |
1540394 | CIF | C17 H16 B Mo N6 O2 P3 | P -1 | 8.7379; 9.957; 13.2391 104.609; 96.252; 107.11 | 1044.19 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540395 | CIF | C38 H38 B2 Fe N12 P6 | P -1 | 10.981; 13.5289; 15.9001 91.94; 99.962; 111.752 | 2148.4 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540396 | CIF | C34.5 H34 B2 Cd N12 P6 | P -1 | 14.048; 14.097; 14.1551 66.977; 61.712; 61.256 | 2115.4 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540397 | CIF | C38 H38 B2 Co N12 P6 | P -1 | 11.132; 13.749; 15.6951 90.726; 99.272; 112.266 | 2186.9 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540398 | CIF | C38 H38 B2 N12 Ni P6 | P -1 | 11.091; 13.6971; 15.735 90.977; 99.368; 112.091 | 2177.3 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540399 | CIF | C32 H30 B3 Cl6 Co F4 N12 P6 | C 1 2/c 1 | 11.2374; 17.1902; 24.3814 90; 97.463; 90 | 4669.9 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540400 | CIF | C12 H11 B N6 P3 Tl | P n m a | 9.144; 10.3091; 17.5949 90; 90; 90 | 1658.61 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540401 | CIF | C12 H11 B Cl3 N6 P3 Ti | P 1 21/m 1 | 8.281; 10.292; 11.4621 90; 102.607; 90 | 953.34 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540402 | CIF | C15 H11 B Mn N6 O3 P3 | P 1 21/c 1 | 16.962; 10.482; 24.6311 90; 112.579; 90 | 4043.6 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540403 | CIF | C21 H23 B N7 P3 Pd | P 1 21/c 1 | 9.404; 15.931; 16.528 90; 100.27; 90 | 2436.5 | Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan The first scorpionate ligand based on diazaphosphole. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253 |
1540404 | CIF | C22 H16 Cu N14 O | P -1 | 12.3344; 14.2954; 15.4511 95.631; 107.583; 108.242 | 2410.1 | Saha, Manideepa; Das, Mriganka; Nasani, Rajendar; Choudhuri, Indrani; Yousufuddin, Muhammed; Nayek, Hari Pada; Shaikh, Mobin M.; Pathak, Biswarup; Mukhopadhyay, Suman Targeted water soluble copper-tetrazolate complexes: interactions with biomolecules and catecholase like activities. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20154-20167 |
1540405 | CIF | C29 H23 Cu N12 O3.5 | P -1 | 11.9248; 11.9276; 13.4576 71.6; 68.381; 70.668 | 1637.7 | Saha, Manideepa; Das, Mriganka; Nasani, Rajendar; Choudhuri, Indrani; Yousufuddin, Muhammed; Nayek, Hari Pada; Shaikh, Mobin M.; Pathak, Biswarup; Mukhopadhyay, Suman Targeted water soluble copper-tetrazolate complexes: interactions with biomolecules and catecholase like activities. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20154-20167 |
1540406 | CIF | C24.65 H18 Cr Gd N8 Ni O10.65 | P 1 21/c 1 | 13.071; 12.139; 21.735 90; 106.84; 90 | 3300.8 | Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199 |
1540407 | CIF | C24.63 H20.52 Cr N8 Ni O10.63 Tb | P 1 21/c 1 | 13.051; 12.15; 21.711 90; 106.89; 90 | 3294.2 | Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199 |
1540408 | CIF | C25 H18 Fe N8 Ni O11 Tb | P 1 21/c 1 | 12.861; 12.014; 21.577 90; 106.73; 90 | 3192.8 | Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199 |
1540409 | CIF | C24 H18 Fe Gd N8 Ni O11 | P 1 21/c 1 | 12.862; 12.012; 21.58 90; 106.72; 90 | 3193.1 | Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations. Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199 |
1540410 | CIF | C142 H120 Gd7 N11 O24 | P -1 | 15.5132; 20.762; 24.831 106.288; 103.085; 105.827 | 6977.1 | Mazarakioti, Eleni C.; Cunha-Silva, Luís; Bekiari, Vlasoula; Escuer, Albert; Stamatatos, Theocharis C. New structural topologies in 4f-metal cluster chemistry from vertex-sharing butterfly units: {LnIII7} complexes exhibiting slow magnetization relaxation and ligand-centred emissions RSC Advances, 2015, 5, 92534-92538 |
1540411 | CIF | C23 H20 N2 O | P -1 | 9.7936; 10.0349; 10.3079 110.403; 101.163; 102.888 | 883.8 | Dandia, Anshu; Sharma, Amit; Parewa, Vijay; Kumawat, Begraj; Rathore, Kuldeep S.; Sharma, Amit Amidic C–N bond cleavage of isatin: chemoselective synthesis of pyrrolo[2,3,4- <i>kl</i> ]acridin-1-ones using Ag NPs decorated rGO composite as an efficient and recoverable catalyst under microwave irradiation RSC Advances, 2015, 5, 91888-91902 |
1540412 | CIF | C29 H24 N2 O2 Se | P 21 21 21 | 8.7794; 14.6701; 37.5122 90; 90; 90 | 4831.4 | Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication RSC Advances, 2015, 5, 97113-97120 |
1540413 | CIF | C31 H28 N2 O3 Se | P 1 21 1 | 8.6504; 9.7776; 16.3783 90; 98.688; 90 | 1369.38 | Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication RSC Advances, 2015, 5, 97113-97120 |
1540414 | CIF | C22 H23 Br N2 O2 S Se | P 1 21 1 | 11.244; 7.6728; 12.837 90; 98.983; 90 | 1093.9 | Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication RSC Advances, 2015, 5, 97113-97120 |
1540415 | CIF | C16 H15 N Se | P 1 21/n 1 | 14.8679; 10.004; 18.5854 90; 98.871; 90 | 2731.3 | Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication RSC Advances, 2015, 5, 97113-97120 |
1540425 | CIF | C18 H14 N O4 | C 2 2 21 | 6.8797; 17.32; 26.023 90; 90; 90 | 3100.8 | Artuso, Emma; Ghibaudi, Elena; Lace, Beatrice; Marabello, Domenica; Vinciguerra, Daniele; Lombardi, Chiara; Koltai, Hinanit; Kapulnik, Yoram; Novero, Mara; Occhiato, Ernesto G.; Scarpi, Dina; Parisotto, Stefano; Deagostino, Annamaria; Venturello, Paolo; Mayzlish-Gati, Einav; Bier, Ariel; Prandi, Cristina Stereochemical Assignment of Strigolactone Analogues Confirms Their Selective Biological Activity. Journal of natural products, 2015, 78, 2624-2633 |
1540426 | CIF | C32 H32 O15 | P 21 21 21 | 7.0833; 13.9608; 31.0735 90; 90; 90 | 3072.81 | Wu, Guangwei; Yu, Guihong; Kurtán, Tibor; Mándi, Attila; Peng, Jixing; Mo, Xiaomei; Liu, Ming; Li, Hui; Sun, Xinhua; Li, Jing; Zhu, Tianjiao; Gu, Qianqun; Li, Dehai Versixanthones A-F, Cytotoxic Xanthone-Chromanone Dimers from the Marine-Derived Fungus Aspergillus versicolor HDN1009. Journal of natural products, 2015, 78, 2691-2698 |
1540465 | CIF | C28 H40 O8 | P 43 21 2 | 10.5228; 10.5228; 52.456 90; 90; 90 | 5808.4 | Nguyen, Ha T. T.; Truong, Ngan B.; Doan, Huong T. M.; Litaudon, Marc; Retailleau, Pascal; Do, Thao T.; Nguyen, Hung V.; Chau, Minh V.; Pham, Cuong V. Cytotoxic Clerodane Diterpenoids from the Leaves of Casearia grewiifolia. Journal of natural products, 2015, 78, 2726-2730 |
1540466 | CIF | C38.5 H52 O10.5 | P 31 | 18.4501; 18.4501; 9.9236 90; 90; 120 | 2925.5 | Nguyen, Ha T. T.; Truong, Ngan B.; Doan, Huong T. M.; Litaudon, Marc; Retailleau, Pascal; Do, Thao T.; Nguyen, Hung V.; Chau, Minh V.; Pham, Cuong V. Cytotoxic Clerodane Diterpenoids from the Leaves of Casearia grewiifolia. Journal of natural products, 2015, 78, 2726-2730 |
1540468 | CIF | C20 H16 Br N O | P 21 21 21 | 5.616; 13.1439; 22.937 90; 90; 90 | 1693.1 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540469 | CIF | C16 H15 Br N | P b c a | 16.0499; 7.6796; 22.6554 90; 90; 90 | 2792.4 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540470 | CIF | C22 H20 Br N O | P 1 21/n 1 | 9.5118; 19.672; 9.821 90; 91.45; 90 | 1837.1 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540471 | CIF | C17 H18 Br N | P b c a | 17.503; 8.0333; 21.133 90; 90; 90 | 2971.4 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540472 | CIF | C23 H22 Br N O | C 1 2/c 1 | 18.368; 9.0221; 23.995 90; 102.82; 90 | 3877.3 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540473 | CIF | C18 H20 Br N | P b c a | 16.319; 8.0724; 24.455 90; 90; 90 | 3221.5 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540474 | CIF | C24 H24 Br N O | P 1 21/n 1 | 5.7109; 12.738; 28.186 90; 90.021; 90 | 2050.4 | Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect Chem. Sci., 2015 |
1540475 | CIF | C18 H19 N O3 | P 21 21 21 | 6.1323; 7.4365; 33.4178 90; 90; 90 | 1523.95 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540476 | CIF | C19 H21 N O3 | P 1 21 1 | 8.719; 5.6224; 17.2361 90; 96.032; 90 | 840.26 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540477 | CIF | C18 H21 N O4 | C 1 2 1 | 14.0792; 6.7979; 17.748 90; 95.958; 90 | 1689.47 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540478 | CIF | C19 H21 N O3 | P 21 21 21 | 7.3552; 13.6032; 17.2196 90; 90; 90 | 1722.89 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540479 | CIF | C18 H19 N O3 | P 21 21 21 | 5.9065; 7.9113; 32.9027 90; 90; 90 | 1537.48 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540480 | CIF | C18 H17 N O2 | P 21 21 21 | 6.0722; 8.115; 29.7039 90; 90; 90 | 1463.69 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540481 | CIF | C21 H19 N O4 | P b c a | 9.4116; 15.8331; 24.7415 90; 90; 90 | 3686.8 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
1540482 | CIF | C19 H21 N O3 | P 1 21 1 | 8.5617; 5.5085; 17.2021 90; 103.015; 90 | 790.45 | Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung γ- and δ-Lactams from the Leaves of Clausena lansium. Journal of natural products, 2015, 78, 2521-2530 |
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