Crystallography Open Database
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Searching journal of publication like 'Organic & biomolecular chemistry' volume of publication is 16
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7156189 | CIF | C20 H20 N2 O | P 1 21/n 1 | 9.5682; 18.4465; 9.7648 90; 104.808; 90 | 1666.25 | Mariappan, Arumugam; Das, Krishna Mohan; Jeganmohan, Masilamani Remote alkylation of N-(quinolin-8-yl)benzamides with alkyl bromides via ruthenium(ii)-catalyzed C-H bond activation. Organic & biomolecular chemistry, 2018, 16, 3419-3427 |
| 7156190 | CIF | C18 H22 O5 | P b c a | 13.248; 11.319; 21.558 90; 90; 90 | 3233 | Zhang, Wuxia; Xiao, Dehai; Wang, Bo A concise total synthesis of cochlearoid B. Organic & biomolecular chemistry, 2018, 16, 3358-3361 |
| 7156191 | CIF | C24 H24 Br N O7 | P -1 | 8.5808; 10.449; 27.944 83.51; 88.58; 66.94 | 2290 | Zhang, Wuxia; Xiao, Dehai; Wang, Bo A concise total synthesis of cochlearoid B. Organic & biomolecular chemistry, 2018, 16, 3358-3361 |
| 7156192 | CIF | C22 H29 F N2 O4 | P 1 21/c 1 | 10.7014; 14.4421; 14.1016 90; 106.984; 90 | 2084.36 | Aimon, Anthony; Karageorgis, George; Masters, Jacob; Dow, Mark; Craven, Philip G. E.; Ohsten, Martin; Willaume, Anthony; Morgentin, Rémy; Ruiz-Llamas, Nicolas; Lemoine, Hugues; Kalliokoski, Tuomo; Eatherton, Andrew J.; Foley, Daniel J.; Marsden, Stephen P.; Nelson, Adam Realisation of small molecule libraries based on frameworks distantly related to natural products. Organic & biomolecular chemistry, 2018, 16, 3160-3167 |
| 7156193 | CIF | C26 H24 N2 O3 | P -1 | 8.0151; 11.4152; 12.798 89.432; 71.763; 86.136 | 1109.52 | Waheed, Mohd; Ahmed, Naseem; Alsharif, Meshari A.; Alahmdi, Mohammed Issa; Mukhtar, Sayeed One-pot synthesis of 1,5-diketones from 3-acetyl-4-hydroxycoumarin and effective cyclization to unexpected 3,4-dihydropyridines. Organic & biomolecular chemistry, 2018, 16, 3428-3437 |
| 7156194 | CIF | C25 H24 O5 | P -1 | 7.746; 11.9902; 12.4618 70.558; 75.621; 79.609 | 1051.15 | Waheed, Mohd; Ahmed, Naseem; Alsharif, Meshari A.; Alahmdi, Mohammed Issa; Mukhtar, Sayeed One-pot synthesis of 1,5-diketones from 3-acetyl-4-hydroxycoumarin and effective cyclization to unexpected 3,4-dihydropyridines. Organic & biomolecular chemistry, 2018, 16, 3428-3437 |
| 7156195 | CIF | C30 H29 N3 O5 S2 | P 1 21 1 | 8.6001; 17.1655; 9.5808 90; 94.473; 90 | 1410.06 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156196 | CIF | C17 H17 N O5 S2 | P 21 21 21 | 5.8407; 14.9477; 19.3104 90; 90; 90 | 1685.9 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156197 | CIF | C24 H22 N2 O3 S2 | P 1 21 1 | 14.3941; 6.9252; 21.6163 90; 94.3263; 90 | 2148.62 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156198 | CIF | C19 H16 N2 O3 S2 | P b c a | 10.414; 15.8099; 21.1096 90; 90; 90 | 3475.58 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156199 | CIF | C14 H12 N2 O S2 | P b c a | 10.3634; 12.0468; 21.0449 90; 90; 90 | 2627.37 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156200 | CIF | C14 H12 N2 O S2 | P -1 | 5.6439; 10.3733; 11.1733 88.811; 76.205; 88.281 | 634.93 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156201 | CIF | C19 H21 N O3 S2 | P b c a | 9.13571; 13.38135; 30.0335 90; 90; 90 | 3671.54 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156202 | CIF | C21 H16 N2 O3 S2 | P 1 21/c 1 | 11.8815; 6.2795; 23.859 90; 95.94; 90 | 1770.6 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156203 | CIF | C21 H16 N2 O3 S2 | P 1 21/c 1 | 11.0765; 18.7037; 17.8788 90; 91.808; 90 | 3702.1 | García de la Concepción, Juan; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor-acceptor interactions. Organic & biomolecular chemistry, 2018, 16, 3438-3452 |
| 7156204 | CIF | C93 H151 N25 O23 | P 21 21 21 | 9.2019; 33.434; 36.933 90; 90; 90 | 11362.7 | Ben Haj Salah, Khoubaib; Das, Sanjit; Ruiz, Nicolas; Andreu, Vanessa; Martinez, Jean; Wenger, Emmanuel; Amblard, Muriel; Didierjean, Claude; Legrand, Baptiste; Inguimbert, Nicolas How are 1,2,3-triazoles accommodated in helical secondary structures? Organic & biomolecular chemistry, 2018, 16, 3576-3583 |
| 7156205 | CIF | C142 H233 N33 O37 | P 1 | 9.0696; 21.623; 23.9383 111.419; 95.745; 98.514 | 4261.16 | Ben Haj Salah, Khoubaib; Das, Sanjit; Ruiz, Nicolas; Andreu, Vanessa; Martinez, Jean; Wenger, Emmanuel; Amblard, Muriel; Didierjean, Claude; Legrand, Baptiste; Inguimbert, Nicolas How are 1,2,3-triazoles accommodated in helical secondary structures? Organic & biomolecular chemistry, 2018, 16, 3576-3583 |
| 7156206 | CIF | C69 H113 N17 O18 | I 1 2 1 | 24.5384; 8.9796; 40.3241 90; 105.026; 90 | 8581.4 | Ben Haj Salah, Khoubaib; Das, Sanjit; Ruiz, Nicolas; Andreu, Vanessa; Martinez, Jean; Wenger, Emmanuel; Amblard, Muriel; Didierjean, Claude; Legrand, Baptiste; Inguimbert, Nicolas How are 1,2,3-triazoles accommodated in helical secondary structures? Organic & biomolecular chemistry, 2018, 16, 3576-3583 |
| 7156207 | CIF | C71 H114 N18 O17 | P 21 21 21 | 10.1857; 17.9944; 46.7774 90; 90; 90 | 8573.6 | Ben Haj Salah, Khoubaib; Das, Sanjit; Ruiz, Nicolas; Andreu, Vanessa; Martinez, Jean; Wenger, Emmanuel; Amblard, Muriel; Didierjean, Claude; Legrand, Baptiste; Inguimbert, Nicolas How are 1,2,3-triazoles accommodated in helical secondary structures? Organic & biomolecular chemistry, 2018, 16, 3576-3583 |
| 7156208 | CIF | C78 H133 N19 O19 | P 21 21 2 | 29.04; 33.47; 10.3 90; 90; 90 | 10011 | Ben Haj Salah, Khoubaib; Das, Sanjit; Ruiz, Nicolas; Andreu, Vanessa; Martinez, Jean; Wenger, Emmanuel; Amblard, Muriel; Didierjean, Claude; Legrand, Baptiste; Inguimbert, Nicolas How are 1,2,3-triazoles accommodated in helical secondary structures? Organic & biomolecular chemistry, 2018, 16, 3576-3583 |
| 7156209 | CIF | C184 H302 N50 O46 | P 1 21 1 | 12.0625; 35.0403; 31.1624 90; 100.906; 90 | 12933.6 | Ben Haj Salah, Khoubaib; Das, Sanjit; Ruiz, Nicolas; Andreu, Vanessa; Martinez, Jean; Wenger, Emmanuel; Amblard, Muriel; Didierjean, Claude; Legrand, Baptiste; Inguimbert, Nicolas How are 1,2,3-triazoles accommodated in helical secondary structures? Organic & biomolecular chemistry, 2018, 16, 3576-3583 |
| 7156210 | CIF | Ce H16 N7 O19 | C 1 2/c 1 | 11.0806; 8.8522; 17.7829 90; 102.82; 90 | 1700.8 | Wang, Tinghua; Nigudkar, Swati S.; Yasomanee, Jagodige P.; Rath, Nigam P.; Stine, Keith J.; Demchenko, Alexei V. Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2. Organic & biomolecular chemistry, 2018, 16, 3596-3604 |
| 7156211 | CIF | C14 H19 N O12 | P 21 21 21 | 5.5311; 13.8941; 23.168 90; 90; 90 | 1780.5 | Wang, Tinghua; Nigudkar, Swati S.; Yasomanee, Jagodige P.; Rath, Nigam P.; Stine, Keith J.; Demchenko, Alexei V. Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2. Organic & biomolecular chemistry, 2018, 16, 3596-3604 |
| 7156212 | CIF | C34 H27 N O12 | P 1 21 1 | 14.9257; 5.4551; 21.093 90; 95.99; 90 | 1708 | Wang, Tinghua; Nigudkar, Swati S.; Yasomanee, Jagodige P.; Rath, Nigam P.; Stine, Keith J.; Demchenko, Alexei V. Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2. Organic & biomolecular chemistry, 2018, 16, 3596-3604 |
| 7156213 | CIF | C28 H22 Cl F3 N4 O3 | P 21 21 21 | 10.3289; 13.752; 18.4669 90; 90; 90 | 2623.09 | Luo, Yuan; Xie, Ke-Xin; Yue, Deng-Feng; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng An organocatalytic asymmetric Mannich reaction of pyrazoleamides with cyclic trifluoromethyl ketimines: enantioselective access to dihydroquinazolinone skeletons. Organic & biomolecular chemistry, 2018, 16, 3372-3375 |
| 7156214 | CIF | C17 H12 O3 S | P -1 | 8.2863; 8.959; 10.6474 87.057; 70.068; 71.08 | 701.38 | Shen, Jinhui; Yang, Yang; Hou, Xiaoli; Zeng, Wenlei; Yu, Aimin; Zhao, Xiaowei; Meng, Xiangtai Darzens reaction of thioisatins and sulfonium salts: approach to the synthesis of thiochromenone derivatives with anticancer potency. Organic & biomolecular chemistry, 2018, 16, 3487-3494 |
| 7156215 | CIF | C25 H18 O4 S | P 1 21/c 1 | 7.2549; 20.063; 14.429 90; 101.37; 90 | 2059 | Shen, Jinhui; Yang, Yang; Hou, Xiaoli; Zeng, Wenlei; Yu, Aimin; Zhao, Xiaowei; Meng, Xiangtai Darzens reaction of thioisatins and sulfonium salts: approach to the synthesis of thiochromenone derivatives with anticancer potency. Organic & biomolecular chemistry, 2018, 16, 3487-3494 |
| 7156216 | CIF | C29 H26 N2 O5 | P -1 | 9.05; 10.2; 27.541 89.877; 93.866; 111.112 | 2365.6 | Tang, Xue; Gao, Ying-Juan; Deng, Hui-Qing; Lei, Jin-Ju; Liu, Si-Wei; Zhou, Lin; Shi, Yin; Liang, Hao; Qiao, Jie; Guo, Li; Han, Bo; Cui, Hai-Lei Catalyst-free [3 + 2] cyclization of dihydroisoquinoline imines and isatin-derived Morita-Baylis-Hillman carbonates via 1,5-electrocyclization: synthesis of tetrahydroisoquinoline-fused spirooxindoles. Organic & biomolecular chemistry, 2018, 16, 3362-3366 |
| 7156217 | CIF | C60 H50 N2 O14 S3 | P 1 21/c 1 | 20.451; 29.075; 9.8797 90; 103.894; 90 | 5702.7 | Mishra, Richa; Jana, Asim; Panday, Anoop Kumar; Choudhury, Lokman H. Synthesis of fused pyrroles containing 4-hydroxycoumarins by regioselective metal-free multicomponent reactions. Organic & biomolecular chemistry, 2018, 16, 3289-3302 |
| 7156218 | CIF | C13 H16 O3 S | P 1 21/c 1 | 13.4091; 7.5272; 13.3823 90; 114.262; 90 | 1231.41 | Dang, Hang T.; Nguyen, Vu T.; Nguyen, Viet D.; Arman, Hadi D.; Larionov, Oleg V. Efficient synthesis of 3-sulfolenes from allylic alcohols and 1,3-dienes enabled by sodium metabisulfite as a sulfur dioxide equivalent. Organic & biomolecular chemistry, 2018, 16, 3605-3609 |
| 7156219 | CIF | C56 H60 Cl2 N6 Ni O S2 | C 1 2/c 1 | 39.247; 12.6465; 21.5421 90; 93.847; 90 | 10668.1 | Smith, Martin J.; Blake, Iain M.; Clegg, William; Anderson, Harry L. Push-pull quinoidal porphyrins. Organic & biomolecular chemistry, 2018, 16, 3648-3654 |
| 7156220 | CIF | C58 H68 Cl2 N4 Ni S2 Si | P 1 21 1 | 26.289; 15.6605; 28.462 90; 109.794; 90 | 11025.4 | Smith, Martin J.; Blake, Iain M.; Clegg, William; Anderson, Harry L. Push-pull quinoidal porphyrins. Organic & biomolecular chemistry, 2018, 16, 3648-3654 |
| 7156221 | CIF | C103 H109 N9 Ni O S2 Zn | P -1 | 14.218; 20.122; 21.975 69.445; 72.044; 82.393 | 5598 | Smith, Martin J.; Blake, Iain M.; Clegg, William; Anderson, Harry L. Push-pull quinoidal porphyrins. Organic & biomolecular chemistry, 2018, 16, 3648-3654 |
| 7156222 | CIF | C58 H56 N6 S2 | P 1 21/n 1 | 36.962; 14.668; 40.822 90; 91.783; 90 | 22121 | Smith, Martin J.; Blake, Iain M.; Clegg, William; Anderson, Harry L. Push-pull quinoidal porphyrins. Organic & biomolecular chemistry, 2018, 16, 3648-3654 |
| 7156223 | CIF | C54 H52 N8 | I 1 2/a 1 | 34.85; 13.785; 40.21 90; 92.378; 90 | 19301 | Smith, Martin J.; Blake, Iain M.; Clegg, William; Anderson, Harry L. Push-pull quinoidal porphyrins. Organic & biomolecular chemistry, 2018, 16, 3648-3654 |
| 7156224 | CIF | C26 H22 Cl2 F3 N O2 | P -1 | 9.3021; 11.1033; 11.8279 81.577; 80.92; 72.384 | 1143.41 | Cheng, Bin; Zu, Bing; Li, Yuntong; Tao, Cheng; Zhang, Chen; Wang, Renqi; Li, Yun; Zhai, Hongbin Synthesis of CF<sub>3</sub>-containing spiro-epoxyoxindoles via the Corey-Chaykovsky reaction of N-alkyl isatins with Ph<sub>2</sub>S<sup>+</sup>CH<sub>2</sub>CF<sub>3</sub>OTf<sup/>. Organic & biomolecular chemistry, 2018, 16, 3564-3567 |
| 7156225 | CIF | C25 H20 F3 N O2 | P 1 21/c 1 | 9.33; 11.138; 19.656 90; 95.194; 90 | 2034.2 | Cheng, Bin; Zu, Bing; Li, Yuntong; Tao, Cheng; Zhang, Chen; Wang, Renqi; Li, Yun; Zhai, Hongbin Synthesis of CF<sub>3</sub>-containing spiro-epoxyoxindoles via the Corey-Chaykovsky reaction of N-alkyl isatins with Ph<sub>2</sub>S<sup>+</sup>CH<sub>2</sub>CF<sub>3</sub>OTf<sup/>. Organic & biomolecular chemistry, 2018, 16, 3564-3567 |
| 7156226 | CIF | C14 H14 F3 N O2 | P b c a | 8.7429; 13.5554; 21.9361 90; 90; 90 | 2599.7 | Cheng, Bin; Zu, Bing; Li, Yuntong; Tao, Cheng; Zhang, Chen; Wang, Renqi; Li, Yun; Zhai, Hongbin Synthesis of CF<sub>3</sub>-containing spiro-epoxyoxindoles via the Corey-Chaykovsky reaction of N-alkyl isatins with Ph<sub>2</sub>S<sup>+</sup>CH<sub>2</sub>CF<sub>3</sub>OTf<sup/>. Organic & biomolecular chemistry, 2018, 16, 3564-3567 |
| 7156227 | CIF | C21 H12 Br N3 | P 1 21/c 1 | 18.8659; 10.1158; 8.8637 90; 99.138; 90 | 1670.11 | Kopchuk, Dmitry S.; Nikonov, Igor L.; Khasanov, Albert F.; Giri, Kousik; Santra, Sougata; Kovalev, Igor S.; Nosova, Emiliya V.; Gundala, Sravya; Venkatapuram, Padmavathi; Zyryanov, Grigory V.; Majee, Adinath; Chupakhin, Oleg N. Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels-Alder reaction versus aryne-mediated domino process. Organic & biomolecular chemistry, 2018, 16, 5119-5135 |
| 7156228 | CIF | C28 H22 N4 O2 | P b c a | 9.2421; 17.3468; 28.1793 90; 90; 90 | 4517.7 | Kopchuk, Dmitry S.; Nikonov, Igor L.; Khasanov, Albert F.; Giri, Kousik; Santra, Sougata; Kovalev, Igor S.; Nosova, Emiliya V.; Gundala, Sravya; Venkatapuram, Padmavathi; Zyryanov, Grigory V.; Majee, Adinath; Chupakhin, Oleg N. Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels-Alder reaction versus aryne-mediated domino process. Organic & biomolecular chemistry, 2018, 16, 5119-5135 |
| 7156229 | CIF | C21 H13 N5 | P 1 21/c 1 | 13.2575; 15.3061; 7.8541 90; 98.654; 90 | 1575.61 | Kopchuk, Dmitry S.; Nikonov, Igor L.; Khasanov, Albert F.; Giri, Kousik; Santra, Sougata; Kovalev, Igor S.; Nosova, Emiliya V.; Gundala, Sravya; Venkatapuram, Padmavathi; Zyryanov, Grigory V.; Majee, Adinath; Chupakhin, Oleg N. Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels-Alder reaction versus aryne-mediated domino process. Organic & biomolecular chemistry, 2018, 16, 5119-5135 |
| 7156230 | CIF | C15 H12 Cl N | P -1 | 9.463; 9.9221; 13.5665 102.387; 94.259; 98.976 | 1221.2 | Gattu, Radhakrishna; Bhattacharjee, Suchandra; Mahato, Karuna; Khan, Abu T. Electronic effect of substituents on anilines favors 1,4-addition to trans-β-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles. Organic & biomolecular chemistry, 2018, 16, 3760-3770 |
| 7156231 | CIF | C24 H20 F2 N2 O4 S | P 1 21/c 1 | 10.457; 18.104; 11.424 90; 98.239; 90 | 2140 | Yang, Xing; Zhang, Feng; Zhou, Yang; Huang, Yi-Yong Neighboring phenolic group-activated gem-difluoroallylboration of imines for the catalyst-free synthesis of gem-difluorohomoallylamines. Organic & biomolecular chemistry, 2018, 16, 3367-3371 |
| 7156233 | CIF | C18 H11 N3 O | P 1 c 1 | 11.8242; 5.6357; 20.6262 90; 99.544; 90 | 1355.46 | Liu, Xiaozu; Zhou, Yuxiang; Chen, Guojun; Yang, Zhongqin; Li, Qin; Liu, Peijun Iodine-catalyzed oxidative annulation of 3-cyanoacetylindoles with benzylamines: facile access to 5-(3-indolyl)oxazoles. Organic & biomolecular chemistry, 2018, 16, 3572-3575 |
| 7156234 | CIF | C15 H12 Br N3 O | P 1 21/n 1 | 10.7721; 9.4199; 14.3014 90; 107.313; 90 | 1385.44 | Liao, Zhen-Yuan; Yeh, Wen-Hsiung; Liao, Pen-Yuan; Liu, Yu-Ting; Chen, Ying-Cheng; Chen, Yi-Hung; Hsieh, Tsung-Han; Lin, Chia-Chi; Lu, Ming-Hsuan; Chen, Yi-Song; Hsu, Ming-Chih; Li, Tsai-Kun; Chien, Tun-Cheng Regioselective synthesis and biological evaluation of N-substituted 2-aminoquinazolin-4-ones. Organic & biomolecular chemistry, 2018, 16, 4482-4494 |
| 7156235 | CIF | C15 H12 Br N3 O | P 1 21/n 1 | 6.4056; 22.7204; 9.3434 90; 100.885; 90 | 1335.35 | Liao, Zhen-Yuan; Yeh, Wen-Hsiung; Liao, Pen-Yuan; Liu, Yu-Ting; Chen, Ying-Cheng; Chen, Yi-Hung; Hsieh, Tsung-Han; Lin, Chia-Chi; Lu, Ming-Hsuan; Chen, Yi-Song; Hsu, Ming-Chih; Li, Tsai-Kun; Chien, Tun-Cheng Regioselective synthesis and biological evaluation of N-substituted 2-aminoquinazolin-4-ones. Organic & biomolecular chemistry, 2018, 16, 4482-4494 |
| 7156236 | CIF | C26 H16 N2 O | P -1 | 8.9209; 9.161; 12.7949 101.938; 106.434; 107.197 | 908.67 | Sun, Hongwei; Tang, Shi; Li, Dengke; Zhou, Yali; Huang, Jinbo; Zhu, Qiang Cascade double isocyanide insertion and C-N coupling of 2-iodo-2'-isocyano-1,1'-biphenyls. Organic & biomolecular chemistry, 2018, 16, 3893-3896 |
| 7156237 | CIF | C21 H17 N3 O2 | P 1 21/n 1 | 5.834; 36.798; 8.5249 90; 103.941; 90 | 1776.2 | Zhang, Wenzheng; Xu, Guangyang; Qiu, Lin; Sun, Jiangtao Gold-catalyzed C5-alkylation of indolines and sequential oxidative aromatization: access to C5-functionalized indoles. Organic & biomolecular chemistry, 2018, 16, 3889-3892 |
| 7156238 | CIF | C30 H41 O4 P S | C 1 2 1 | 21.157; 6.917; 20.174 90; 98; 90 | 2923.6 | Prechelmacher, Susanne; Mereiter, Kurt; Hammerschmidt, Friedrich The α-hydroxyphosphonate-phosphate rearrangement of a noncyclic substrate - some new observations. Organic & biomolecular chemistry, 2018, 16, 3672-3680 |
| 7156239 | CIF | C99 H100 N2 O3 | P -1 | 13.339; 18.203; 18.304 106.445; 110.829; 95.262 | 3891 | Suzuki, Shin; Asako, Takashi; Itami, Kenichiro; Yamaguchi, Junichiro Modular synthesis of heptaarylindole. Organic & biomolecular chemistry, 2018, 16, 3771-3776 |
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