Crystallography Open Database
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Searching journal of publication like 'Organic & biomolecular chemistry' volume of publication is 17
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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7157130 | CIF | C16 H12 F Fe I S | P -1 | 7.2; 10.0755; 11.5617 64.721; 78.205; 84.196 | 742.31 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157131 | CIF | C10 H7 Br Cl F Fe | P 1 21/n 1 | 6.5459; 10.4479; 15.037 90; 91.505; 90 | 1028 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157132 | CIF | C10 H7 F Fe I2 | P 1 21/c 1 | 12.21; 28.6668; 6.6319 90; 100.875; 90 | 2279.6 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157133 | CIF | C19 H20 F Fe I S Si | P 1 21/c 1 | 8.8626; 11.0153; 20.456 90; 98.537; 90 | 1974.9 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157134 | CIF | C14 H16 F Fe I O2 Si | P 1 21/n 1 | 6.7304; 13.738; 17.564 90; 100.433; 90 | 1597.2 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157135 | CIF | C26 H26 F Fe I O Si | P -1 | 8.1302; 10.5516; 14.7688 107.406; 93.634; 98.033 | 1189.6 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157136 | CIF | C10 H7 Cl F Fe I | P 1 21/c 1 | 6.6845; 15.913; 10.315 90; 99.375; 90 | 1082.6 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157137 | CIF | C13 H16 Br F Fe Si | P 1 21/c 1 | 17.276; 6.8553; 12.095 90; 100.988; 90 | 1406.2 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157138 | CIF | C21 H24 F Fe I O2 Si | P -1 | 8.514; 10.875; 11.472 86.069; 84.834; 82.271 | 1046.5 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157139 | CIF | C25 H25 F Fe I O P Si | P -1 | 8.1007; 10.7372; 14.989 108.19; 93.055; 97.786 | 1220.8 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157140 | CIF | C14 H16 F Fe I O Si | P 1 21/n 1 | 6.7234; 12.3647; 18.5635 90; 91.338; 90 | 1542.8 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157141 | CIF | C20 H20 F Fe I O S Si | P -1 | 7.148; 9.9469; 15.3417 108.069; 97.069; 91.763 | 1026.4 | Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J. From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space. Organic & biomolecular chemistry, 2019, 17, 9352-9359 |
7157142 | CIF | C19 H18 F N3 O3 | P 1 21/n 1 | 19.0038; 7.304; 25.2096 90; 108.964; 90 | 3309.26 | Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes. Organic & biomolecular chemistry, 2019, 17, 9390-9402 |
7157143 | CIF | C36 H32 Br2 N6 O6 | P 1 21/n 1 | 15.516; 9.876; 23.035 90; 104.61; 90 | 3416 | Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes. Organic & biomolecular chemistry, 2019, 17, 9390-9402 |
7157144 | CIF | C46 H45 Br2 N6 O6 | C 1 2/c 1 | 24.8162; 11.0757; 34.2851 90; 100.28; 90 | 9272.2 | Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes. Organic & biomolecular chemistry, 2019, 17, 9390-9402 |
7157145 | CIF | C27 H24 N2 O5 S | P 21 21 21 | 8.5917; 13.421; 21.279 90; 90; 90 | 2453.7 | Lu, Min; Li, Hong; Zou, Chuncheng; Li, Jianchang; Liu, Chengyu; Sun, Maolin; Ma, Yueyue; Cheng, Ruihua; Ye, Jinxing Primary amine catalyzed diastereo- and enantioselective Michael reaction of thiazolones and α,β-unsaturated ketones. Organic & biomolecular chemistry, 2019, 17, 9305-9312 |
7157147 | CIF | C25 H24 N2 O2 S | P 21 21 21 | 9.0518; 12.1315; 18.9731 90; 90; 90 | 2083.47 | Luo, Shao-Xiong; Liu, Yanzhou; Lambrecht, Michael J.; Ortwine, Daniel F.; DiPasquale, Antonio G.; Liang, Jun; Wang, Xiaojing; Zbieg, Jason R.; Li, Jun cis-Selective synthesis of 1,3-disubstituted tetrahydro-β-carbolines from N-sulfonyl N,S-acetals. Organic & biomolecular chemistry, 2019, 17, 9510 |
7157148 | CIF | C23 H26 N2 O3 S | P 21 21 21 | 9.2149; 11.3488; 19.7251 90; 90; 90 | 2062.81 | Luo, Shao-Xiong; Liu, Yanzhou; Lambrecht, Michael J.; Ortwine, Daniel F.; DiPasquale, Antonio G.; Liang, Jun; Wang, Xiaojing; Zbieg, Jason R.; Li, Jun cis-Selective synthesis of 1,3-disubstituted tetrahydro-β-carbolines from N-sulfonyl N,S-acetals. Organic & biomolecular chemistry, 2019, 17, 9510 |
7157149 | CIF | C22 H18 N2 S | P 1 21/c 1 | 9.6081; 15.136; 11.7745 90; 101.041; 90 | 1680.65 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157150 | CIF | C28 H20 N4 O4 S | P 1 21/c 1 | 13.0978; 8.4281; 21.7783 90; 103.164; 90 | 2340.92 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157151 | CIF | C22 H14 N2 O | P 1 n 1 | 8.7248; 8.5852; 11.534 90; 105.252; 90 | 833.5 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157152 | CIF | C40 H30 N8 O S2 | P -1 | 9.4466; 9.9176; 19.5777 79.604; 86.538; 70.029 | 1695.59 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157153 | CIF | C24 H16 N2 O4 S | P -1 | 8.8175; 10.9212; 10.9295 76.676; 67.685; 89.692 | 943.5 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157154 | CIF | C22 H16 N2 Se | P 1 21/c 1 | 9.6424; 15.1758; 11.7826 90; 101.61; 90 | 1688.9 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157155 | CIF | C22 H14 F2 N2 S | P 1 21/c 1 | 9.5114; 15.691; 11.5516 90; 98.966; 90 | 1702.9 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157156 | CIF | C72 H60 N6 Se3 | P -1 | 11.8825; 12.7306; 20.6914 90.924; 101.853; 111.378 | 2838.3 | Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L. Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling. Organic & biomolecular chemistry, 2019, 17, 9467 |
7157157 | CIF | C16 H13 N O2 S | P -1 | 6.4036; 7.8241; 14.538 85.37; 89.441; 70.995 | 686.3 | You, Guirong; Xi, Dan; Sun, Jian; Hao, Liqiang; Xia, Chengcai Transition-metal- and oxidant-free three-component reaction of quinoline N-oxides, sodium metabisulfite and aryldiazonium tetrafluoroborates via a dual radical coupling process. Organic & biomolecular chemistry, 2019, 17, 9479 |
7157158 | CIF | C25 H28 N2 O3 | P 1 21/n 1 | 13.4238; 10.0908; 16.9778 90; 96.486; 90 | 2285.04 | He, Yi; Narmon, Thomas; Wu, Danjun; Li, Zhenghua; Van Meervelt, Luc; Van der Eycken, Erik V. A gold-triggered dearomative spirocarbocyclization/Diels-Alder reaction cascade towards diverse bridged N-heterocycles. Organic & biomolecular chemistry, 2019, 17, 9529 |
7157159 | CIF | C24 H26 N2 O3 | P -1 | 11.7236; 11.754; 17.2404 73.252; 73.789; 71.074 | 2106.24 | He, Yi; Narmon, Thomas; Wu, Danjun; Li, Zhenghua; Van Meervelt, Luc; Van der Eycken, Erik V. A gold-triggered dearomative spirocarbocyclization/Diels-Alder reaction cascade towards diverse bridged N-heterocycles. Organic & biomolecular chemistry, 2019, 17, 9529 |
7157181 | CIF | C24 H36 Cl N3 O Pd Se | R -3 :H | 27.319; 27.319; 19.5324 90; 90; 120 | 12624.5 | Sharma, Kamal Nayan; Satrawala, Naveen; Srivastava, Avinash Kumar; Ali, Munsaf; Joshi, Raj Kumar Palladium(ii) ligated with a selenated (Se, C<sub>NHC</sub>, N<sup>-</sup>)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water. Organic & biomolecular chemistry, 2019, 17, 8969-8976 |
7157182 | CIF | C25 H21 N O3 | P 1 21/c 1 | 11.065; 11.521; 15.832 90; 97.78; 90 | 1999.68 | Zeng, Qian; Dong, Kuiyong; Huang, Jingjing; Qiu, Lihua; Xu, Xinfang Copper-catalyzed carbene/alkyne metathesis terminated with the Buchner reaction: synthesis of dihydrocyclohepta[b]indoles. Organic & biomolecular chemistry, 2019, 17, 2326-2330 |
7157183 | CIF | C29 H22 N2 O3 S | P -1 | 12.875; 13.03; 15.195 76.583; 78.566; 72.177 | 2338.2 | Kundal, Sandip; Chakraborty, Baitan; Paul, Kartick; Jana, Umasish Efficient two-step synthesis of structurally diverse indolo[2,3-b]quinoline derivatives. Organic & biomolecular chemistry, 2019, 17, 2321-2325 |
7157184 | CIF | C19 H16 N2 S | P 1 21/n 1 | 8.5086; 17.1346; 22.5907 90; 99.192; 90 | 3251.2 | Zhang, Xi; Wang, Tong-Lin; Liu, Xiao-Jun; Wang, Xi-Cun; Quan, Zheng-Jun The solvent-controlled chemoselective construction of C-S/S-S bonds via the Michael reaction/thiol coupling of quinoline-2-thiones. Organic & biomolecular chemistry, 2019, 17, 2379-2383 |
7157185 | CIF | C14 H15 F6 N3 O | P 1 21/n 1 | 11.79; 7.792; 16.696 90; 103.74; 90 | 1489.9 | Moraes, Paulo A.; Lobo, Marcio M.; Marangoni, Mário A; Meyer, Alexandre R.; Frizzo, Clarissa P.; Bonacorso, Helio G.; Martins, Marcos A. P.; Zanatta, Nilo Chemo- and regioselective reactions of 5-bromo enones/enaminones with pyrazoles. Organic & biomolecular chemistry, 2019, 17, 2384-2392 |
7157186 | CIF | C14 H17 F6 N3 O | P b c a | 11.65; 18.43; 15.238 90; 90; 90 | 3272 | Moraes, Paulo A.; Lobo, Marcio M.; Marangoni, Mário A; Meyer, Alexandre R.; Frizzo, Clarissa P.; Bonacorso, Helio G.; Martins, Marcos A. P.; Zanatta, Nilo Chemo- and regioselective reactions of 5-bromo enones/enaminones with pyrazoles. Organic & biomolecular chemistry, 2019, 17, 2384-2392 |
7157187 | CIF | C24 H24 Br2 O5 | P 21 21 21 | 17.353; 24.435; 5.4165 90; 90; 90 | 2296.7 | Shit, Sudip; Devi, Namita; Devi, Ngangbam Renubala; Saikia, Anil K. Stereoselective synthesis of hexahydrofuro[3,4-b]furan-4-ol and its dimer via tandem Prins and pinacol rearrangement. Organic & biomolecular chemistry, 2019, 17, 7398-7407 |
7157188 | CIF | C12 H13 Br O3 | P 1 21 1 | 5.845; 7.6852; 12.8843 90; 100.457; 90 | 569.15 | Shit, Sudip; Devi, Namita; Devi, Ngangbam Renubala; Saikia, Anil K. Stereoselective synthesis of hexahydrofuro[3,4-b]furan-4-ol and its dimer via tandem Prins and pinacol rearrangement. Organic & biomolecular chemistry, 2019, 17, 7398-7407 |
7157189 | CIF | C32 H32 N2 O7 | P 21 21 21 | 13; 13.405; 17.492 90; 90; 90 | 3048 | Sharma, Arun; Sharma, Vivek; Chimni, Swapandeep Singh Organocatalytic enantioselective conjugate addition of pyrazolin-5-ones to arylomethylidene malonates. Organic & biomolecular chemistry, 2019, 17, 9514 |
7157225 | CIF | C24 H24 N4 O2 | P -1 | 9.145; 11.501; 11.649 117.55; 94.48; 91.05 | 1080.9 | Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Organic & biomolecular chemistry, 2019, 17, 9585-9604 |
7157226 | CIF | C17 H12 O5 S2 | P 1 21/c 1 | 8.7498; 18.5113; 9.4511 90; 99.3488; 90 | 1510.46 | Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Organic & biomolecular chemistry, 2019, 17, 9585-9604 |
7157227 | CIF | C23 H23 N3 O2 | I 41/a :2 | 38.315; 38.315; 5.547 90; 90; 90 | 8143.2 | Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Organic & biomolecular chemistry, 2019, 17, 9585-9604 |
7157228 | CIF | C23 H25 N O4 S | P 1 21/n 1 | 11.6856; 14.0485; 13.2869 90; 96.0216; 90 | 2169.2 | Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Organic & biomolecular chemistry, 2019, 17, 9585-9604 |
7157229 | CIF | C22 H16 O3 S | P 1 21/n 1 | 8.8058; 20.394; 9.6437 90; 99.794; 90 | 1706.6 | Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Organic & biomolecular chemistry, 2019, 17, 9585-9604 |
7157230 | CIF | C24 H23 N O3 S | P 1 21/n 1 | 9.6018; 12.4113; 16.8115 90; 96.978; 90 | 1988.6 | Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Organic & biomolecular chemistry, 2019, 17, 9585-9604 |
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