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 |
| 7156240 | CIF | C56 H47 N3 O5 S | P 1 21/c 1 | 14.816; 28.03; 12.06 90; 113.633; 90 | 4588 | Suzuki, Shin; Asako, Takashi; Itami, Kenichiro; Yamaguchi, Junichiro Modular synthesis of heptaarylindole. Organic & biomolecular chemistry, 2018, 16, 3771-3776 |
| 7156241 | CIF | C47 H44 Cl3 N O | P 1 21/c 1 | 11.365; 13.805; 25.674 90; 92.439; 90 | 4024.4 | Suzuki, Shin; Asako, Takashi; Itami, Kenichiro; Yamaguchi, Junichiro Modular synthesis of heptaarylindole. Organic & biomolecular chemistry, 2018, 16, 3771-3776 |
| 7156242 | CIF | C50 H41 Cl3 F3 N O3 S | P -1 | 9.7851; 10.7442; 22.106 103.099; 95.707; 98.173 | 2219.6 | Suzuki, Shin; Asako, Takashi; Itami, Kenichiro; Yamaguchi, Junichiro Modular synthesis of heptaarylindole. Organic & biomolecular chemistry, 2018, 16, 3771-3776 |
| 7156243 | CIF | C44 H40 N2 O3 S | P 1 21/n 1 | 14.744; 9.8309; 25.091 90; 94.077; 90 | 3627.7 | Suzuki, Shin; Asako, Takashi; Itami, Kenichiro; Yamaguchi, Junichiro Modular synthesis of heptaarylindole. Organic & biomolecular chemistry, 2018, 16, 3771-3776 |
| 7156244 | CIF | C31 H22 B4 Cl2 F8 N8 O2 S2 | P 1 21/c 1 | 9.0994; 17.118; 11.3594 90; 98.095; 90 | 1751.8 | Duan, Wenzeng; Liu, Qingsong; Huo, Yanmin; Cui, Jichun; Gong, Shuwen; Liu, Zhipeng AIE-active boron complexes based on benzothiazole-hydrazone chelates. Organic & biomolecular chemistry, 2018, 16, 4977-4984 |
| 7156245 | CIF | C39 H26 B4 Cl2 F8 N8 O2 S2 | P 1 21/n 1 | 10.6491; 22.7467; 17.0946 90; 104.248; 90 | 4013.5 | Duan, Wenzeng; Liu, Qingsong; Huo, Yanmin; Cui, Jichun; Gong, Shuwen; Liu, Zhipeng AIE-active boron complexes based on benzothiazole-hydrazone chelates. Organic & biomolecular chemistry, 2018, 16, 4977-4984 |
| 7156246 | CIF | C19 H11 B F2 N4 S | P 1 21/c 1 | 13.7279; 8.6809; 14.7591 90; 105.207; 90 | 1697.3 | Duan, Wenzeng; Liu, Qingsong; Huo, Yanmin; Cui, Jichun; Gong, Shuwen; Liu, Zhipeng AIE-active boron complexes based on benzothiazole-hydrazone chelates. Organic & biomolecular chemistry, 2018, 16, 4977-4984 |
| 7156247 | CIF | C15 H9 B F2 N4 O0 S | P 1 21/c 1 | 11.0689; 10.5398; 25.7733 90; 109.097; 90 | 2841.3 | Duan, Wenzeng; Liu, Qingsong; Huo, Yanmin; Cui, Jichun; Gong, Shuwen; Liu, Zhipeng AIE-active boron complexes based on benzothiazole-hydrazone chelates. Organic & biomolecular chemistry, 2018, 16, 4977-4984 |
| 7156248 | CIF | C15 H11 N O | P 21 21 21 | 6.4849; 7.9199; 21.9097 90; 90; 90 | 1125.28 | Wang, Zheng; Xu, Ming-Hua Highly enantioselective synthesis of α-tertiary chiral amino acid derivatives through rhodium-catalyzed asymmetric arylation of cyclic N-sulfonyl α-ketimino esters. Organic & biomolecular chemistry, 2018, 16, 4633-4640 |
| 7156249 | CIF | C24 H33 N3 O6 S | P 1 21/c 1 | 19.0398; 8.7917; 15.4377 90; 103.834; 90 | 2509.2 | Bakulina, Olga; Dar'in, Dmitry; Krasavin, Mikhail Mixed carboxylic-sulfonic anhydride in reaction with imines: a straightforward route to water-soluble β-lactams via a Staudinger-type reaction. Organic & biomolecular chemistry, 2018, 16, 3989-3998 |
| 7156250 | CIF | C38 H31 N O4 | P -1 | 9.843; 12.3941; 13.6713 75.947; 81.791; 66.836 | 1485.4 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156251 | CIF | C38 H31 N O5 | P -1 | 12.6224; 13.4198; 18.628 69.695; 86.767; 88.299 | 2954.4 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156252 | CIF | C37 H28 Cl N O4 | P 1 21/c 1 | 14.5654; 22.655; 8.9813 90; 103.56; 90 | 2881 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156253 | CIF | C36 H28 N2 O4 | P 1 21/c 1 | 9.215; 22.358; 17.565 90; 111.492; 90 | 3367.3 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156254 | CIF | C29 H27 N O3 | P 1 21/c 1 | 8.9074; 24.06; 11.549 90; 112.68; 90 | 2283.7 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156255 | CIF | C22 H20 Br N O3 | P b c a | 8.7048; 19.6596; 22.0693 90; 90; 90 | 3776.8 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156256 | CIF | C28 H24 N2 O5 | C 1 2/c 1 | 17.485; 23.214; 13.752 90; 90.437; 90 | 5582 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156257 | CIF | C28 H26 Cl2 N2 O3 | P 1 21/c 1 | 15.2237; 12.7126; 15.0411 90; 119.6; 90 | 2531.1 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156258 | CIF | C27 H24 N2 O3 | P -1 | 7.3088; 12.204; 12.7704 110.563; 96.8007; 96.6011 | 1043.87 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156259 | CIF | C21 H20 N2 O3 | P 1 21/c 1 | 12.2787; 8.6166; 16.4475 90; 103.03; 90 | 1695.4 | Cao, Jun; Sun, Jing; Yan, Chao-Guo Regioselective and diastereoselective synthesis of two functionalized 1,5-methanoindeno[1,2-d]azocines via a three-component reaction. Organic & biomolecular chemistry, 2018, 16, 4170-4175 |
| 7156260 | CIF | C23 H22 N2 O6 | P 21 21 21 | 9.6235; 13.3554; 16.7938 90; 90; 90 | 2158.4 | Chen, Jin-Quan; Mi, Yang; Shi, Zi-Fa; Cao, Xiao-Ping Construction of the tetracyclic core of (±)-cycloclavine and 4-amino Uhle's ketone. Organic & biomolecular chemistry, 2018, 16, 3801-3808 |
| 7156261 | CIF | C11 H21 Cl N2 O | P -1 | 10.1121; 10.442; 12.0205 95.695; 91.086; 97.671 | 1251.02 | Alzahrani, Abdullah; Mirallai, Styliana I.; Chalmers, Benjamin A.; McArdle, Patrick; Aldabbagh, Fawaz Synthesis of N-[(dialkylamino)methyl]acrylamides and N-[(dialkylamino)methyl]methacrylamides from Schiff base salts: useful building blocks for smart polymers. Organic & biomolecular chemistry, 2018, 16, 4108-4116 |
| 7156262 | CIF | C8 H18 Cl N O | P 1 21/c 1 | 11.319; 10.9194; 7.7658 90; 90.269; 90 | 959.8 | Alzahrani, Abdullah; Mirallai, Styliana I.; Chalmers, Benjamin A.; McArdle, Patrick; Aldabbagh, Fawaz Synthesis of N-[(dialkylamino)methyl]acrylamides and N-[(dialkylamino)methyl]methacrylamides from Schiff base salts: useful building blocks for smart polymers. Organic & biomolecular chemistry, 2018, 16, 4108-4116 |
| 7156263 | CIF | C16 H19 N3 O3 | P b c a | 10.2591; 9.6617; 30.5377 90; 90; 90 | 3026.9 | Maiden, T. M. M.; Mbelesi, N.; Procopiou, P. A.; Swanson, S.; Harrity, J. P. A. A convergent strategy towards febrifugine and related compounds. Organic & biomolecular chemistry, 2018, 16, 4159-4169 |
| 7156264 | CIF | C15 H15 Cl N4 | P 1 21/n 1 | 10.585; 8.8309; 15.039 90; 96.741; 90 | 1396.1 | Jia, Feng-Cheng; Xu, Cheng; Wang, Yu-Wei; Chen, Zhi-Peng; Chen, Yun-Feng; Wu, An-Xin Copper-catalyzed ambient-temperature decarboxylative annulation of isatins with amidine hydrochlorides: a facile access to 2-(1,3,5-triazin-2-yl)aniline derivatives. Organic & biomolecular chemistry, 2018, 16, 4223-4226 |
| 7156265 | CIF | C30 H26 Br2 Cl0 N4 O2 Pd | P c a 21 | 40.319; 8.136; 8.974 90; 90; 90 | 2944 | Panyam, Pradeep Kumar Reddy; Sreedharan, Ramdas; Gandhi, Thirumanavelan Synthesis of topologically constrained naphthalimide appended palladium(ii)-N-heterocyclic carbene complexes - insights into additive controlled product selectivity. Organic & biomolecular chemistry, 2018, 16, 4357-4364 |
| 7156266 | CIF | C72 H112 N2 O8 P2 | P 1 21/c 1 | 21.0973; 11.579; 14.9601 90; 109.03; 90 | 3454.81 | Iadevaia, Giulia; Núñez-Villanueva, Diego; Stross, Alexander E.; Hunter, Christopher A. Backbone conformation affects duplex initiation and duplex propagation in hybridisation of synthetic H-bonding oligomers. Organic & biomolecular chemistry, 2018, 16, 4183-4190 |
| 7156267 | CIF | C18 H19 N O2 | P 1 21/n 1 | 5.4408; 10.1935; 27.458 90; 91.789; 90 | 1522.1 | Zhang, Yixin; Ma, Haojie; Liu, Xingxing; Cui, Xinfeng; Wang, Shaohua; Zhan, Zhenzhen; Pu, Jinghong; Huang, Guosheng The synthesis of multi-substituted pyrrolidinones via a direct [3 + 2] cycloaddition of azaoxyallyl cations with aromatic ethylenes. Organic & biomolecular chemistry, 2018, 16, 4439-4442 |
| 7156268 | CIF | C24 H32 Br O4 P | P -1 | 10.215; 11.4694; 12.0747 115.285; 93.898; 92.846 | 1271.3 | Gupta, Ashis Kumar; Ahamad, Shakir; Vaishanv, Narendra Kumar; Kant, Ruchir; Mohanan, Kishor Base-mediated 1,6-conjugate addition of the Seyferth-Gilbert reagent to para-quinone methides. Organic & biomolecular chemistry, 2018, 16, 4623-4627 |
| 7156269 | CIF | C27 H39 N2 O4 P | P 21 21 21 | 9.947; 15.743; 18.185 90; 90; 90 | 2847.7 | Gupta, Ashis Kumar; Ahamad, Shakir; Vaishanv, Narendra Kumar; Kant, Ruchir; Mohanan, Kishor Base-mediated 1,6-conjugate addition of the Seyferth-Gilbert reagent to para-quinone methides. Organic & biomolecular chemistry, 2018, 16, 4623-4627 |
| 7156270 | CIF | C H Br0 N O | P 1 21/n 1 | 7.8543; 20.6582; 8.3912 90; 116.689; 90 | 1216.46 | Wang, Rui-Xiang; Yuan, Si-Tian; Liu, Jin-Biao; Wu, Jie; Qiu, Guanyinsheng Regioselective 5-exo-dig oxy-cyclization of 2-alkynylbenzamide for the synthesis of isobenzofuran-1-imines and isobenzofuran. Organic & biomolecular chemistry, 2018, 16, 4501-4508 |
| 7156271 | CIF | C11 H7 F3 N2 O2 | P 1 21/c 1 | 4.568; 16.1861; 15.8035 90; 115.336; 90 | 1056.09 | You, Chang; Yuan, Tingting; Huang, Yanzhen; Pi, Chao; Wu, Yangjie; Cui, Xiuling Rhodium-catalyzed regioselective C8-H amination of quinoline N-oxides with trifluoroacetamide at room temperature. Organic & biomolecular chemistry, 2018, 16, 4728-4733 |
| 7156272 | CIF | C19 H21 N O5 | P -1 | 9.2521; 9.8028; 9.9294 75.679; 88.544; 79.757 | 858.51 | Chen, Rongxiang; Ogunlana, Abosede Adejoke; Fang, Shangwen; Long, Wenhao; Sun, Hongmei; Bao, Xiaoguang; Wan, Xiaobing In situ generation of nitrile oxides from copper carbene and tert-butyl nitrite: synthesis of fully substituted isoxazoles. Organic & biomolecular chemistry, 2018, 16, 4683-4687 |
| 7156273 | CIF | C15 H15 N O4 | P 1 21 1 | 6.2246; 26.4216; 8.1454 90; 93.774; 90 | 1336.72 | Malinowski, Maciej; Hensienne, Raphaël; Kern, Nicolas; Tardieu, Damien; Bodlenner, Anne; Hazelard, Damien; Compain, Philippe Stereocontrolled synthesis of polyhydroxylated bicyclic azetidines as a new class of iminosugars. Organic & biomolecular chemistry, 2018, 16, 4688-4700 |
| 7156274 | CIF | C26 H24 N2 O5 S | P -1 | 10.5259; 10.5345; 10.834 91.068; 104.536; 100.359 | 1141.4 | de la Concepción, Juan García; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. On the dual reactivity of a Janus-type mesoionic dipole: experiments and theoretical validation. Organic & biomolecular chemistry, 2018, 16, 4778-4783 |
| 7156275 | CIF | C31 H27 N3 O4 S | P n a 21 | 11.8735; 18.6709; 11.878 90; 90; 90 | 2633.22 | de la Concepción, Juan García; Ávalos, Martín; Cintas, Pedro; Jiménez, José L; Light, Mark E. On the dual reactivity of a Janus-type mesoionic dipole: experiments and theoretical validation. Organic & biomolecular chemistry, 2018, 16, 4778-4783 |
| 7156276 | CIF | C20 H19 Br O4 S | P -1 | 7.5123; 12.1628; 12.1719 63.522; 79.736; 89.681 | 976.11 | Hou, Yading; Zhang, Yuwen; Tong, Xiaofeng Phosphine-catalysed α-umpolung addition of nucleophiles to δ-acetoxy allenoates: stereoselective synthesis of 2,4-dienoates. Organic & biomolecular chemistry, 2018, 16, 5245-5249 |
| 7156277 | CIF | C32 H52 B N3 O2 | P b c a | 17.9063; 21.5998; 33.6902 90; 90; 90 | 13030.4 | Boghi, Michele; Hall, Dennis G. Valdecoxib vs. borazavaldecoxib: isoxazole BN/CC isosterism as a case study in designing and stabilizing boron heterocycles. Organic & biomolecular chemistry, 2018, 16, 4849-4856 |
| 7156278 | CIF | C16 H14 N2 O2 | P 1 21/c 1 | 8.9; 9.5626; 15.9864 90; 98.4476; 90 | 1345.8 | Boghi, Michele; Hall, Dennis G. Valdecoxib vs. borazavaldecoxib: isoxazole BN/CC isosterism as a case study in designing and stabilizing boron heterocycles. Organic & biomolecular chemistry, 2018, 16, 4849-4856 |
| 7156279 | CIF | C35 H50 B N3 O2 | P 1 21/c 1 | 9.7871; 17.5209; 19.0833 90; 94.1963; 90 | 3263.61 | Boghi, Michele; Hall, Dennis G. Valdecoxib vs. borazavaldecoxib: isoxazole BN/CC isosterism as a case study in designing and stabilizing boron heterocycles. Organic & biomolecular chemistry, 2018, 16, 4849-4856 |
| 7156280 | CIF | C17 H21 B N3 O3 S | P 1 21/c 1 | 12.7713; 7.9352; 17.9462 90; 94.7903; 90 | 1812.37 | Boghi, Michele; Hall, Dennis G. Valdecoxib vs. borazavaldecoxib: isoxazole BN/CC isosterism as a case study in designing and stabilizing boron heterocycles. Organic & biomolecular chemistry, 2018, 16, 4849-4856 |
| 7156281 | CIF | C28 H44 Br N O4 S | P 21 21 21 | 5.6897; 11.2486; 45.457 90; 90; 90 | 2909.3 | Guerola, Marta; Escolano, Marcos; Alzuet-Piña, Gloria; Gómez-Bengoa, Enrique; Ramírez de Arellano, Carmen; Sánchez-Roselló, María; Del Pozo, Carlos Synthesis of substituted piperidines by enantioselective desymmetrizing intramolecular aza-Michael reactions. Organic & biomolecular chemistry, 2018, 16, 4650-4658 |
| 7156282 | CIF | C20 H19 N3 O | P b c a | 19.497; 8.597; 19.553 90; 90; 90 | 3277.4 | Kumar, Avnish; Tiwari, Dharmendra Kumar; Sridhar, Balasubramanian; Likhar, Pravin R. Unprecedented synthesis of 1,2,3-triazolo-cinnolinone via Sonogashira coupling and intramolecular cyclization. Organic & biomolecular chemistry, 2018, 16, 4840-4848 |
| 7156283 | CIF | C10 H10 F2 N4 O8 | P b c n | 12.1505; 10.471; 10.2881 90; 90; 90 | 1308.9 | Zhang, Jian; Ling, Yi-Fei; Wang, Gui-Xiang; Zhang, Lin; Luo, Jun Synthesis of two new gem-fluoronitro containing tetranitroadamantanes and property comparison with their nitro and gem-dinitro analogues. Organic & biomolecular chemistry, 2018, 16, 4784-4788 |
| 7156284 | CIF | C25 H38 N2 O3 S | C 1 2 1 | 25.58; 7.18; 16.94 90; 125.27; 90 | 2540 | Kennington, Stuart C. D.; Gómez-Palomino, Alejandro; Salomó, Ernest; Romea, Pedro; Urpí, Fèlix; Font-Bardia, Mercè General and stereoselective aminoxylation of biradical titanium(iv) enolates with TEMPO: a detailed study on the effect of the chiral auxiliary. Organic & biomolecular chemistry, 2018, 16, 4807-4815 |
| 7156285 | CIF | C19 H16 Br N3 O5 S | P -1 | 7.3579; 8.8158; 15.8511 85.431; 88.543; 72.739 | 978.77 | Zhao, Mei-Xin; Dong, Zhi-Wen; Zhu, Guang-Yu; Zhao, Xiao-Li; Shi, Min Diastereo- and enantioselective Mannich/cyclization cascade reaction of isocyanoacetates with cyclic sulfamide ketimines by cinchona alkaloid squaramide/AgOAc cooperative catalysis. Organic & biomolecular chemistry, 2018, 16, 4641-4649 |
| 7156286 | CIF | C29 H26 N2 O3 | P b c a | 10.1449; 11.6133; 40.0056 90; 90; 90 | 4713.29 | Xu, Yulong; Chen, Hao; Li, Wei; Xie, Qiong; Yu, Linqian; Shao, Liming Synthetic access to isoxazoline-functionalized isoquinolines via microwave-assisted iminoxyl radical-participated cascade cyclization of vinyl isocyanides. Organic & biomolecular chemistry, 2018, 16, 4996-5005 |
| 7156287 | CIF | C14 H11 N3 O3 S | P 1 21/n 1 | 10.471; 10.038; 13.551 90; 101.028; 90 | 1398 | Wang, Qijun; Wang, Chang; Shi, Wangyu; Xiao, Yumei; Guo, Hongchao Pd-Catalyzed diastereoselective [3 + 2] cycloaddition of vinylcyclopropanes with sulfamate-derived cyclic imines. Organic & biomolecular chemistry, 2018, 16, 4881-4887 |
| 7156288 | CIF | C36 H40 Cl N3 Ni O4 | P 21 21 21 | 6.2383; 15.367; 32.9494 90; 90; 90 | 3158.66 | Takeda, Ryosuke; Kawamura, Akie; Kawashima, Aki; Sato, Tatsunori; Moriwaki, Hiroki; Izawa, Kunisuke; Abe, Hidenori; Soloshonok, Vadim A. Second-order asymmetric transformation and its application for the practical synthesis of α-amino acids. Organic & biomolecular chemistry, 2018, 16, 4968-4972 |
| 7156289 | CIF | C14 H14 O4 | P b c a | 10.287; 11.291; 20.866 90; 90; 90 | 2423.6 | Hsu, Day-Shin; Liou, Chang-Yan Total synthesis and structural revision of (±)-nidemone. Organic & biomolecular chemistry, 2018, 16, 4990-4995 |
| 7156290 | CIF | C56 H40 F24 N4 P4 | P 1 21/c 1 | 14.1176; 22.1778; 11.231 90; 100.087; 90 | 3462.05 | Chen, Long; Lim, Kate J. C.; Babra, Tahkur S.; Taylor, James O.; PiŽl, Martin; Evans, Robert; Chippindale, Ann M.; Hartl, František; Colquhoun, Howard M.; Greenland, Barnaby W. A macrocyclic receptor containing two viologen species connected by conjugated terphenyl groups. Organic & biomolecular chemistry, 2018, 16, 5006-5015 |
| 7156291 | CIF | C21 H28 N2 O2 | C 1 2/c 1 | 23.0931; 6.0038; 29.114 90; 99.674; 90 | 3979.15 | Wei, Yuanyuan; Wang, Jie; Wang, Yajun; Yao, Xiaoqiang; Yang, Caixia; Huo, Congde Auto-oxidation promoted sp<sup>3</sup> C-H arylation of glycine derivatives. Organic & biomolecular chemistry, 2018, 16, 4985-4989 |
| 7156292 | CIF | C31 H25 B Cl2 F4 N2 | P -1 | 8.8458; 12.0478; 13.9043 89.408; 83.302; 72.134 | 1400.22 | Wang, Zhuo; Li, Tongyu; Xing, Siyang; Zhu, Bolin Facile and practical synthesis of β-carbolinium salts and γ-carbolinium salts via rhodium-catalyzed three-component reactions. Organic & biomolecular chemistry, 2018, 16, 5021-5026 |
| 7156293 | CIF | C25 H26 Cl Ir N2 | P 1 21 1 | 7.5213; 16.0289; 17.7564 90; 91.742; 90 | 2139.69 | Wang, Zhuo; Li, Tongyu; Xing, Siyang; Zhu, Bolin Facile and practical synthesis of β-carbolinium salts and γ-carbolinium salts via rhodium-catalyzed three-component reactions. Organic & biomolecular chemistry, 2018, 16, 5021-5026 |
| 7156294 | CIF | C30 H23 Cl2 F6 N2 P | P 1 21/n 1 | 13.7632; 12.7539; 16.2519 90; 99.002; 90 | 2817.6 | Wang, Zhuo; Li, Tongyu; Xing, Siyang; Zhu, Bolin Facile and practical synthesis of β-carbolinium salts and γ-carbolinium salts via rhodium-catalyzed three-component reactions. Organic & biomolecular chemistry, 2018, 16, 5021-5026 |
| 7156295 | CIF | C26 H32 O4 Si | P 1 21/c 1 | 11.66; 12.07; 18.027 90; 100.58; 90 | 2494 | Acharyya, Ranjan Kumar; Nanda, Samik Asymmetric total synthesis of naturally occurring spirocyclic tetranorsesquiterpenoid lanceolactone A. Organic & biomolecular chemistry, 2018, 16, 5027-5035 |
| 7156296 | CIF | C20 H17 B F5 N3 O S | P 1 21/c 1 | 17.347; 8.8962; 14.148 90; 112.523; 90 | 2016.8 | Lugovik, Kseniya I.; Eltyshev, Alexander K.; Suntsova, Polina O.; Smoluk, Leonid T.; Belousova, Anna V.; Ulitko, Maria V.; Minin, Artem S.; Slepukhin, Pavel A.; Benassi, Enrico; Belskaya, Nataliya P. Fluorescent boron complexes based on new N,O-chelates as promising candidates for flow cytometry. Organic & biomolecular chemistry, 2018, 16, 5150-5162 |
| 7156297 | CIF | C19 H18 Cl N O3 S | P b c a | 15.5285; 12.2909; 18.3647 90; 90; 90 | 3505.1 | Maheshwar Rao, B.; Yadav, J. S.; Sridhar, B.; Subba Reddy, B. V. Silver(i)-catalyzed sequential hydroamination and Prins type cyclization for the synthesis of fused benzo-δ-sultams. Organic & biomolecular chemistry, 2018, 16, 5163-5166 |
| 7156301 | CIF | C22 H27 N3 O2 | P -1 | 8.0402; 9.8828; 13.696 99.883; 90.997; 109.551 | 1007 | Bąk, Krzysztof M; Chabuda, Krzysztof; Montes, Helena; Quesada, Roberto; Chmielewski, Michał J 1,8-Diamidocarbazoles: an easily tuneable family of fluorescent anion sensors and transporters. Organic & biomolecular chemistry, 2018, 16, 5188-5196 |
| 7156302 | CIF | C26 H19 N3 O2 | P 1 21/c 1 | 9.955; 15.804; 13.546 90; 108.143; 90 | 2025.2 | Bąk, Krzysztof M; Chabuda, Krzysztof; Montes, Helena; Quesada, Roberto; Chmielewski, Michał J 1,8-Diamidocarbazoles: an easily tuneable family of fluorescent anion sensors and transporters. Organic & biomolecular chemistry, 2018, 16, 5188-5196 |
| 7156303 | CIF | C49 H60 N4 O4 | P -1 | 8.6576; 15.744; 16.1197 89.599; 78.285; 84.114 | 2139.9 | Bąk, Krzysztof M; Chabuda, Krzysztof; Montes, Helena; Quesada, Roberto; Chmielewski, Michał J 1,8-Diamidocarbazoles: an easily tuneable family of fluorescent anion sensors and transporters. Organic & biomolecular chemistry, 2018, 16, 5188-5196 |
| 7156304 | CIF | C45 H68 N4 O4 | P 1 21/n 1 | 13.6871; 18.5215; 18.0498 90; 108.711; 90 | 4333.9 | Bąk, Krzysztof M; Chabuda, Krzysztof; Montes, Helena; Quesada, Roberto; Chmielewski, Michał J 1,8-Diamidocarbazoles: an easily tuneable family of fluorescent anion sensors and transporters. Organic & biomolecular chemistry, 2018, 16, 5188-5196 |
| 7156305 | CIF | C33 H39 N2 O3 | P 1 21/n 1 | 9.683; 21.363; 14.386 90; 109.097; 90 | 2812.1 | Liu, Qi; Liu, Jie-Jie; Cheng, Liang; Wang, Dong; Liu, Li TEMPO promoted direct multi-functionalization of terminal alkynes with 2-oxindoles/benzofuran-2(3H)-one. Organic & biomolecular chemistry, 2018, 16, 5228-5231 |
| 7156306 | CIF | C34 H46 N4 O3 S2 | P 21 21 21 | 13.5505; 14.85; 16.762 90; 90; 90 | 3372.9 | Huang, Yin-Hui; Jin, Xian-Yi; Zhao, Yong-Yi; Cong, Hang; Tao, Zhu A fluorescence-enhanced chemosensor based on multifarene[2,2] and its recognition of metal cations. Organic & biomolecular chemistry, 2018, 16, 5343-5349 |
| 7156307 | CIF | C15 H11 N3 O3 | P -1 | 7.8053; 8.2606; 11.869 91.064; 108.89; 113.92 | 651.9 | Murugan, Arumugavel; Gorantla, Koteswar Rao; Mallik, Bhabani S.; Sharada, Duddu S. Iron promoted C3-H nitration of 2H-indazole: direct access to 3-nitro-2H-indazoles. Organic & biomolecular chemistry, 2018, 16, 5113-5118 |
| 7156308 | CIF | C43 H38 N2 O | P 21 21 21 | 8.7773; 16.6542; 21.9525 90; 90; 90 | 3209 | Wu, Jia-Le; Wang, Cong-Shuai; Wang, Jin-Rong; Mei, Guang-Jian; Shi, Feng A catalytic asymmetric interrupted Nazarov-type cyclization of 2-indolylmethanols with cyclic enaminones. Organic & biomolecular chemistry, 2018, 16, 5457-5464 |
| 7156309 | CIF | C18 H17 Br N2 | P 1 21/n 1 | 9.541; 14.222; 12.432 90; 110.54; 90 | 1579.7 | Yadav, Pratik; Shaw, Ranjay; Elagamy, Amr; Kumar, Abhinav; Pratap, Ramendra Base controlled diverse reactivity of allyl cyanide for synthesis of multi-substituted benzenes. Organic & biomolecular chemistry, 2018, 16, 5465-5473 |
| 7156310 | CIF | C23 H25 F N3 O4 | P 1 21/c 1 | 11.8968; 18.4254; 10.7033 90; 103.556; 90 | 2280.8 | Mukhopadhyay, Soumendranath; Pan, Subhas Chandra An organocatalytic asymmetric Mannich reaction for the synthesis of 3,3-disubstituted-3,4-dihydro-2-quinolones. Organic & biomolecular chemistry, 2018, 16, 5407-5411 |
| 7156311 | CIF | C23.5 H28 Cl3 N3 O6 S2 | P -1 | 8.139; 13.44; 13.65 102.732; 104.959; 107.249 | 1304.4 | Liu, Guotao; Chen, Weijie; Xu, Zhiqiang; Ye, Fengying; Pan, Yingle; Chen, Xiaoqiang; Liu, Sheng Hua; Zeng, Lintao; Yin, Jun Regulating glutathione-responsiveness of naphthalimide-based fluorescent probes by an oxidation strategy. Organic & biomolecular chemistry, 2018, 16, 5517-5523 |
| 7156312 | CIF | C23 H27 Cl2 N3 O5 S2 | P -1 | 9.0264; 9.0426; 17.336 76.843; 80.437; 65.448 | 1249.2 | Liu, Guotao; Chen, Weijie; Xu, Zhiqiang; Ye, Fengying; Pan, Yingle; Chen, Xiaoqiang; Liu, Sheng Hua; Zeng, Lintao; Yin, Jun Regulating glutathione-responsiveness of naphthalimide-based fluorescent probes by an oxidation strategy. Organic & biomolecular chemistry, 2018, 16, 5517-5523 |
| 7156313 | CIF | C18 H25 N O3 S | P 1 21/c 1 | 11.6879; 18.2014; 8.4879 90; 102.767; 90 | 1761.04 | Wen, Ke; Wu, Zhengxing; Chen, Buyun; Chen, Jianzhong; Zhang, Wanbin Pd(ii)-Catalyzed aerobic 1,2-difunctionalization of conjugated dienes: efficient synthesis of morpholines and 2-morpholones. Organic & biomolecular chemistry, 2018, 16, 5618-5625 |
| 7156314 | CIF | C18 H25 N O4 S | P -1 | 8.2097; 11.3718; 11.432 63.44; 84.691; 84.975 | 949.27 | Wen, Ke; Wu, Zhengxing; Chen, Buyun; Chen, Jianzhong; Zhang, Wanbin Pd(ii)-Catalyzed aerobic 1,2-difunctionalization of conjugated dienes: efficient synthesis of morpholines and 2-morpholones. Organic & biomolecular chemistry, 2018, 16, 5618-5625 |
| 7156315 | CIF | C13 H15 N O4 S | P 1 21 1 | 10.8106; 5.454; 11.7245 90; 104.012; 90 | 670.72 | Wen, Ke; Wu, Zhengxing; Chen, Buyun; Chen, Jianzhong; Zhang, Wanbin Pd(ii)-Catalyzed aerobic 1,2-difunctionalization of conjugated dienes: efficient synthesis of morpholines and 2-morpholones. Organic & biomolecular chemistry, 2018, 16, 5618-5625 |
| 7156316 | CIF | C20 H21 N O4 S | P 1 21/c 1 | 17.4085; 6.2355; 17.4828 90; 99.565; 90 | 1871.39 | Wen, Ke; Wu, Zhengxing; Chen, Buyun; Chen, Jianzhong; Zhang, Wanbin Pd(ii)-Catalyzed aerobic 1,2-difunctionalization of conjugated dienes: efficient synthesis of morpholines and 2-morpholones. Organic & biomolecular chemistry, 2018, 16, 5618-5625 |
| 7156317 | CIF | C15 H21 N O3 S | P 1 21/c 1 | 9.1241; 13.2825; 25.2487 90; 94.118; 90 | 3052.01 | Wen, Ke; Wu, Zhengxing; Chen, Buyun; Chen, Jianzhong; Zhang, Wanbin Pd(ii)-Catalyzed aerobic 1,2-difunctionalization of conjugated dienes: efficient synthesis of morpholines and 2-morpholones. Organic & biomolecular chemistry, 2018, 16, 5618-5625 |
| 7156318 | CIF | C20 H23 N O3 S | C 1 2/c 1 | 27.193; 8.6013; 16.525 90; 101.302; 90 | 3790.2 | Wen, Ke; Wu, Zhengxing; Chen, Buyun; Chen, Jianzhong; Zhang, Wanbin Pd(ii)-Catalyzed aerobic 1,2-difunctionalization of conjugated dienes: efficient synthesis of morpholines and 2-morpholones. Organic & biomolecular chemistry, 2018, 16, 5618-5625 |
| 7156319 | CIF | C24 H14 F4 O2 | P 1 21/n 1 | 15.92; 5.8083; 20.4496 90; 100.147; 90 | 1861.4 | Yamada, Shigeyuki; Morita, Masato; Agou, Tomohiro; Kubota, Toshio; Ichikawa, Takahiro; Konno, Tsutomu Thermoresponsive luminescence properties of polyfluorinated bistolane-type light-emitting liquid crystals. Organic & biomolecular chemistry, 2018, 16, 5609-5617 |
| 7156320 | CIF | C28 H21 F5 O | P n a 21 | 11.4515; 4.9051; 39.555 90; 90; 90 | 2221.8 | Yamada, Shigeyuki; Morita, Masato; Agou, Tomohiro; Kubota, Toshio; Ichikawa, Takahiro; Konno, Tsutomu Thermoresponsive luminescence properties of polyfluorinated bistolane-type light-emitting liquid crystals. Organic & biomolecular chemistry, 2018, 16, 5609-5617 |
| 7156321 | CIF | C19 H14 N2 | C m c 21 | 23.851; 7.4217; 7.8859 90; 90; 90 | 1395.92 | Hu, Zhiyuan; Hou, Jiao; Liu, Jie; Yu, Wenquan; Chang, Junbiao Synthesis of imidazo[1,5-a]pyridines via I<sub>2</sub>-mediated sp<sup>3</sup> C-H amination. Organic & biomolecular chemistry, 2018, 16, 5653-5660 |
| 7156322 | CIF | C26 H18 N2 O7 | P -1 | 7.4307; 10.8091; 14.322 88.506; 89.846; 83.022 | 1141.42 | Wang, Zhi-Peng; He, Yun; Shao, Pan-Lin Transition-metal-free synthesis of polysubstituted pyrrole derivatives via cyclization of methyl isocyanoacetate with aurone analogues. Organic & biomolecular chemistry, 2018, 16, 5422-5426 |
| 7156323 | CIF | C30 H28 N2 | P 1 21/c 1 | 15.8276; 16.5142; 15.0083 90; 114.514; 90 | 3569.3 | Huang, Li; Cao, Ying-Juan; Sun, Xiang-Ying; Liu, Bin; Shen, Jiang-Shan Diverse applications of TMB-based sensing probes. Organic & biomolecular chemistry, 2018, 16, 5667-5676 |
| 7156324 | CIF | C17 H11 N O2 | P -1 | 9.812; 15.26; 18.464 108.25; 98.59; 92.69 | 2583.2 | Zhang, Wei; Yang, Chen; Pan, Yu-Liang; Li, Xin; Cheng, Jin-Pei Synthesis of 3-cyanomethylated coumarins by a visible-light-mediated direct cyanomethylation of aryl alkynoates. Organic & biomolecular chemistry, 2018, 16, 5788-5792 |
| 7156325 | CIF | C17 H10 Br N O2 | P 1 21/n 1 | 10.067; 9.1332; 15.755 90; 103.76; 90 | 1407 | Zhang, Wei; Yang, Chen; Pan, Yu-Liang; Li, Xin; Cheng, Jin-Pei Synthesis of 3-cyanomethylated coumarins by a visible-light-mediated direct cyanomethylation of aryl alkynoates. Organic & biomolecular chemistry, 2018, 16, 5788-5792 |
| 7156326 | CIF | C24 H24 Br N3 O4 S2 | P 21 21 21 | 8.7914; 16.8836; 17.728 90; 90; 90 | 2631.4 | Xu, Han; Kang, Tian-Chen; Sha, Feng; Wu, Xin-Yan Enantioselective Mannich reaction between rhodanines and isatin-derived ketimines to construct vicinal tetrasubstituted stereocenters. Organic & biomolecular chemistry, 2018, 16, 5780-5787 |
| 7156327 | CIF | C21 H32 N2 O6 | P 42 | 27.1192; 27.1192; 6.0742 90; 90; 90 | 4467.3 | Niwetmarin, Worawat; Rego Campello, Hugo; Sparkes, Hazel A.; Aggarwal, Varinder K.; Gallagher, Timothy (-)-Cytisine: Access to a stereochemically defined and functionally flexible piperidine scaffold. Organic & biomolecular chemistry, 2018, 16, 5823-5832 |
| 7156328 | CIF | C26 H25 N3 O5 | P 1 21 1 | 7.1313; 8.764; 17.546 90; 91.71; 90 | 1096.1 | Niwetmarin, Worawat; Rego Campello, Hugo; Sparkes, Hazel A.; Aggarwal, Varinder K.; Gallagher, Timothy (-)-Cytisine: Access to a stereochemically defined and functionally flexible piperidine scaffold. Organic & biomolecular chemistry, 2018, 16, 5823-5832 |
| 7156329 | CIF | C21 H30 N2 O7 | P 21 21 21 | 8.5893; 11.638; 22.452 90; 90; 90 | 2244.4 | Niwetmarin, Worawat; Rego Campello, Hugo; Sparkes, Hazel A.; Aggarwal, Varinder K.; Gallagher, Timothy (-)-Cytisine: Access to a stereochemically defined and functionally flexible piperidine scaffold. Organic & biomolecular chemistry, 2018, 16, 5823-5832 |
| 7156330 | CIF | C50 H44 Cl12 O12 | P -1 | 9.0593; 12.1761; 12.5506 74.493; 89.579; 84.484 | 1327.6 | Wang, Denan; Ivanov, Maxim V.; Mirzaei, Saber; Lindeman, Sergey V.; Rathore, Rajendra An electron-transfer induced conformational transformation: from non-cofacial "sofa" to cofacial "boat" in cyclotetraveratrylene (CTTV) and formation of charge transfer complexes. Organic & biomolecular chemistry, 2018, 16, 5712-5717 |
| 7156331 | CIF | C49.55 H48.64 Cl11.68 N2 O10 | P -1 | 10.0667; 16.1954; 19.0021 111.109; 94.141; 100.255 | 2812.4 | Wang, Denan; Ivanov, Maxim V.; Mirzaei, Saber; Lindeman, Sergey V.; Rathore, Rajendra An electron-transfer induced conformational transformation: from non-cofacial "sofa" to cofacial "boat" in cyclotetraveratrylene (CTTV) and formation of charge transfer complexes. Organic & biomolecular chemistry, 2018, 16, 5712-5717 |
| 7156332 | CIF | C28 H23 Cl2 N3 O2 | P -1 | 9.1731; 12.2931; 12.4614 64.335; 84.712; 79.181 | 1244 | Liao, Huiwu; Peng, Xiangjun; Hu, Dan; Xu, Xianyun; Huang, Panpan; Liu, Qian; Liu, Liangxian CoCl<sub>2</sub>-promoted TEMPO oxidative homocoupling of indoles: access to tryptanthrin derivatives. Organic & biomolecular chemistry, 2018, 16, 5699-5706 |
| 7156333 | CIF | C23 H17 N3 O3 | P 1 21/c 1 | 10.7906; 10.2626; 17.5715 90; 102.945; 90 | 1896.41 | Liao, Huiwu; Peng, Xiangjun; Hu, Dan; Xu, Xianyun; Huang, Panpan; Liu, Qian; Liu, Liangxian CoCl<sub>2</sub>-promoted TEMPO oxidative homocoupling of indoles: access to tryptanthrin derivatives. Organic & biomolecular chemistry, 2018, 16, 5699-5706 |
| 7156334 | CIF | C15 H9 Cl N2 O4 | P 1 21/c 1 | 12.899; 7.78; 13.924 90; 94.602; 90 | 1392.8 | Ieronimo, Gabriella; Palmisano, Giovanni; Maspero, Angelo; Marzorati, Alessandro; Scapinello, Luca; Masciocchi, Norberto; Cravotto, Giancarlo; Barge, Alessandro; Simonetti, Marco; Ameta, Keshav Lalit; Nicholas, Kenneth M.; Penoni, Andrea A novel synthesis of N-hydroxy-3-aroylindoles and 3-aroylindoles. Organic & biomolecular chemistry, 2018, 16, 6853-6859 |
| 7156335 | CIF | C18 H21 N O4 S | P n a 21 | 19.409; 22.804; 7.899 90; 90; 90 | 3496 | Devi, Runjun; Das, Jonali; Sarma, Bipul; Das, Sajal Kumar Phenolate-induced intramolecular ring-opening cyclization of N-tosylaziridines: access to functionalized benzoxacycles. Organic & biomolecular chemistry, 2018, 16, 5846-5858 |
| 7156336 | CIF | C20 H21 Cl N2 O3 | P 1 21 1 | 9.114; 8.76; 11.937 90; 98.233; 90 | 943.2 | Xu, Gang; Tong, Chaodi; Cui, Sunliang; Dai, Liyan A silver catalyzed domino reaction of N-cyanamide alkenes and 1,3-dicarbonyls for the synthesis of quinazolinones. Organic & biomolecular chemistry, 2018, 16, 5899-5906 |
| 7156337 | CIF | C30 H30 Br N3 O3 | P -1 | 10.5691; 12.489; 13.082 113.373; 95.324; 113.736 | 1384 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156338 | CIF | C25 H22 Br N3 O4 | P 1 21/c 1 | 6.8547; 15.209; 23.124 90; 98.52; 90 | 2384.1 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156339 | CIF | C25 H16 Br N O2 | P 1 21/c 1 | 5.3424; 19.837; 19.534 90; 103.226; 90 | 2015.2 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156340 | CIF | C24 H20 Br Cl N2 O2 | P -1 | 9.2635; 11.3364; 11.3467 86.529; 72.466; 78.713 | 1114.23 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156341 | CIF | C30 H30 Cl N3 O4 | P -1 | 10.1744; 12.6935; 13.136 113.581; 93.921; 112.484 | 1386.7 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156342 | CIF | C25 H22 Br2 N2 O2 | P 1 21/c 1 | 6.8119; 15.187; 22.922 90; 98.315; 90 | 2346.4 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156343 | CIF | C24 H20 Br N3 O4 | P -1 | 9.0719; 11.2308; 11.5065 80.422; 76.363; 70.848 | 1071.15 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156344 | CIF | C29 H28 Cl N3 O3 | P -1 | 9.933; 12.4636; 23.3748 93.564; 97.108; 113.474 | 2614.1 | Jiang, Wang; Sun, Jing; Liu, Ru-Zhang; Yan, Chao-Guo Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles. Organic & biomolecular chemistry, 2018, 16, 5816-5822 |
| 7156345 | CIF | C17 H20 F N O4 | P 1 21/c 1 | 6.44998; 20.5679; 23.9334 90; 94.4481; 90 | 3165.5 | Griggs, Samuel D.; Thompson, Nathan; Tape, Daniel T.; Fabre, Marie; Clarke, Paul A. Synthesis of highly substituted 2-spiropiperidines. Organic & biomolecular chemistry, 2018, 16, 6663-6674 |
| 7156346 | CIF | C24 H19 I N2 O S | P -1 | 8.6049; 11.226; 12.391 113.15; 98.39; 96.47 | 1069.6 | Wu, Jing; Kong, Yuanfang; Liu, Lingyan; Chang, Weixing; Li, Jing Metal-free multicomponent cascade reactions of homopropargylic amines and acyl chlorides as well as potassium thiocyanate and diiodine: an access to thiazine imides. Organic & biomolecular chemistry, 2018, 16, 5955-5959 |
| 7156347 | CIF | C19 H14 N2 O3 | P c c n | 10.8798; 18.4104; 14.5081 90; 90; 90 | 2905.99 | Butler, Nicholas M.; Hendra, Rudi; Bremner, John B.; Willis, Anthony C.; Lucantoni, Leonardo; Avery, Vicky M.; Keller, Paul A. Cascade reactions of indigo with oxiranes and aziridines: efficient access to dihydropyrazinodiindoles and spiro-oxazocinodiindoles. Organic & biomolecular chemistry, 2018, 16, 6006-6016 |
| 7156348 | CIF | C31 H25 N3 O4 S | P 1 21/c 1 | 23.5193; 11.6263; 9.3856 90; 90.966; 90 | 2566.1 | Butler, Nicholas M.; Hendra, Rudi; Bremner, John B.; Willis, Anthony C.; Lucantoni, Leonardo; Avery, Vicky M.; Keller, Paul A. Cascade reactions of indigo with oxiranes and aziridines: efficient access to dihydropyrazinodiindoles and spiro-oxazocinodiindoles. Organic & biomolecular chemistry, 2018, 16, 6006-6016 |
| 7156349 | CIF | C23 H18 N2 O6 | C 1 2/c 1 | 23.9584; 9.6484; 16.009 90; 90.165; 90 | 3700.6 | Butler, Nicholas M.; Hendra, Rudi; Bremner, John B.; Willis, Anthony C.; Lucantoni, Leonardo; Avery, Vicky M.; Keller, Paul A. Cascade reactions of indigo with oxiranes and aziridines: efficient access to dihydropyrazinodiindoles and spiro-oxazocinodiindoles. Organic & biomolecular chemistry, 2018, 16, 6006-6016 |
| 7156350 | CIF | C42 H35.85 Cl4.15 N4 O8 | P 21 21 21 | 10.5565; 14.9406; 25.9563 90; 90; 90 | 4093.84 | Butler, Nicholas M.; Hendra, Rudi; Bremner, John B.; Willis, Anthony C.; Lucantoni, Leonardo; Avery, Vicky M.; Keller, Paul A. Cascade reactions of indigo with oxiranes and aziridines: efficient access to dihydropyrazinodiindoles and spiro-oxazocinodiindoles. Organic & biomolecular chemistry, 2018, 16, 6006-6016 |
| 7156351 | CIF | C22 H18 N2 O4 | P 21 21 21 | 8.6464; 11.41283; 17.69376 90; 90; 90 | 1746.02 | Butler, Nicholas M.; Hendra, Rudi; Bremner, John B.; Willis, Anthony C.; Lucantoni, Leonardo; Avery, Vicky M.; Keller, Paul A. Cascade reactions of indigo with oxiranes and aziridines: efficient access to dihydropyrazinodiindoles and spiro-oxazocinodiindoles. Organic & biomolecular chemistry, 2018, 16, 6006-6016 |
| 7156352 | CIF | C28 H28 O12 | P -1 | 9.4743; 10.9625; 15.3255 69.302; 81.446; 65.245 | 1352.17 | Duong, Thuc-Huy; Beniddir, Mehdi A.; Genta-Jouve, Grégory; Aree, Thammarat; Chollet-Krugler, Marylène; Boustie, Joël; Ferron, Solenn; Sauvager, Aurélie; Nguyen, Huu-Hung; Nguyen, Kim-Phi-Phung; Chavasiri, Warinthorn; Le Pogam, Pierre Tsavoenones A-C: unprecedented polyketides with a 1,7-dioxadispiro[4.0.4.4]tetradecane core from the lichen Parmotrema tsavoense. Organic & biomolecular chemistry, 2018, 16, 5913-5919 |
| 7156353 | CIF | C25 H22 N4 O6 | P 1 21/c 1 | 7.6583; 11.7333; 25.007 90; 95.687; 90 | 2236 | Gao, Xing; Shan, Chunhui; Chen, Zhihao; Liu, Yan; Zhao, Xia; Zhang, Ao; Yu, Peng; Galons, Hervé; Lan, Yu; Lu, Kui One-pot synthesis of β-lactams by the Ugi and Michael addition cascade reaction. Organic & biomolecular chemistry, 2018, 16, 6096-6105 |
| 7156354 | CIF | C55 H58 N2 O9 S | P 21 21 21 | 11.1611; 18.4375; 23.2735 90; 90; 90 | 4789.3 | Łęczycka-Wilk, Katarzyna; Ulatowski, Filip; Cmoch, Piotr; Jarosz, Sławomir "Choose-a-size" control in the synthesis of sucrose based urea and thiourea macrocycles. Organic & biomolecular chemistry, 2018, 16, 6063-6069 |
| 7156355 | CIF | C34 H33 N3 O6 | P -1 | 11.2505; 11.5713; 13.0127 86.119; 84.314; 65.589 | 1534.3 | Guo, Jiaomei; Zhao, Yang; Fang, Dongmei; Wang, Qilin; Bu, Zhanwei Diastereoselective construction of pyrrolo[2,1-a]isoquinoline-based bispirooxindoles through a three-component [3 + 2] cycloaddition. Organic & biomolecular chemistry, 2018, 16, 6025-6034 |
| 7156356 | CIF | C11 H6 F7 N2 | P b c a | 9.1202; 8.3186; 33.169 90; 90; 90 | 2516.4 | Wang, Hui; Tu, Yuan-Hong; Liu, De-Yong; Hu, Xiang-Guo Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines. Organic & biomolecular chemistry, 2018, 16, 6634-6637 |
| 7156357 | CIF | C9 H8 F2 N2 | P 1 21/n 1 | 4.3659; 22.675; 8.74 90; 92.88; 90 | 864.1 | Wang, Hui; Tu, Yuan-Hong; Liu, De-Yong; Hu, Xiang-Guo Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines. Organic & biomolecular chemistry, 2018, 16, 6634-6637 |
| 7156358 | CIF | C26 H29 N3 O4 | P 1 21 1 | 8.9053; 29.8896; 10.0393 90; 113.921; 90 | 2442.69 | Cai, Yue; Gu, Qing; You, Shu-Li Chemoselective N-H functionalization of indole derivatives via the Reissert-type reaction catalyzed by a chiral phosphoric acid. Organic & biomolecular chemistry, 2018, 16, 6146-6154 |
| 7156359 | CIF | C23 H14 O2 | P b c n | 9.1068; 13.5461; 26.1677 90; 90; 90 | 3228.1 | Addepalli, Yesu; Yu, Zhimei; Ji, Jie; Zou, Cheng; Wang, Zhen; He, Yun Tandem Diels-Alder/oxidation-aromatization reactions involving 2-styrylchromones and arynes. Organic & biomolecular chemistry, 2018, 16, 6077-6085 |
| 7156360 | CIF | C16 H14 Cl N O2 | P 41 | 10.1392; 10.1392; 28.1205 90; 90; 90 | 2890.9 | Shao, Ling-Yan; Xu, Zhi; Wang, Cun-Ying; Fu, Xiao-Pan; Chen, Miao-Miao; Liu, Hong-Wei; Ji, Ya-Fei Palladium-catalyzed direct mono-aroylation of O-arylmethyl and aryl-substituted acetoxime ethers. Organic & biomolecular chemistry, 2018, 16, 6284-6294 |
| 7156361 | CIF | C21 H17 N3 O | P 1 21 1 | 8.863; 6.941; 14.038 90; 104.114; 90 | 837.52 | Shinde, Vikki N.; Dhiman, Shiv; Krishnan, Rangan; Kumar, Dalip; Kumar, Anil Synthesis of imidazopyridine-fused indoles via one-pot sequential Knoevenagel condensation and cross dehydrogenative coupling. Organic & biomolecular chemistry, 2018, 16, 6123-6132 |
| 7156362 | CIF | C24 H19 N3 O3 | P 1 21/n 1 | 9.4056; 7.0317; 28.179 90; 94.395; 90 | 1858.2 | Shinde, Vikki N.; Dhiman, Shiv; Krishnan, Rangan; Kumar, Dalip; Kumar, Anil Synthesis of imidazopyridine-fused indoles via one-pot sequential Knoevenagel condensation and cross dehydrogenative coupling. Organic & biomolecular chemistry, 2018, 16, 6123-6132 |
| 7156363 | CIF | C18 H19 N O6 | C 1 2/c 1 | 9.2351; 14.6347; 25.4336 90; 96.9605; 90 | 3412.09 | Tateishi, Keiichiro; Noguchi, Keiichi; Saito, Akio 2-Picoline catalyst-triggered [2 + 2 + 2] cycloaddition-type reaction of acetylenedicarboxylates, aldehydes and alkenes. Organic & biomolecular chemistry, 2018, 16, 5965-5968 |
| 7156364 | CIF | C17 H19 Br O6 | P 1 21/n 1 | 5.15537; 43.3613; 8.36326 90; 111.741; 90 | 1736.56 | Tateishi, Keiichiro; Noguchi, Keiichi; Saito, Akio 2-Picoline catalyst-triggered [2 + 2 + 2] cycloaddition-type reaction of acetylenedicarboxylates, aldehydes and alkenes. Organic & biomolecular chemistry, 2018, 16, 5965-5968 |
| 7156365 | CIF | C18 H19 N O6 | P 1 21/n 1 | 9.59148; 8.88839; 20.6593 90; 95.3754; 90 | 1753.52 | Tateishi, Keiichiro; Noguchi, Keiichi; Saito, Akio 2-Picoline catalyst-triggered [2 + 2 + 2] cycloaddition-type reaction of acetylenedicarboxylates, aldehydes and alkenes. Organic & biomolecular chemistry, 2018, 16, 5965-5968 |
| 7156366 | CIF | C44 H43 N3 O8 | P 1 21 1 | 13.6734; 10.41568; 27.6271 90; 103.065; 90 | 3832.73 | Knudsen, Ida M. B.; Hedberg, Christinne; Ladefoged, Lucy Kate; Ide, Daisuke; Brinkø, Anne; Eikeland, Espen Z.; Kato, Atsushi; Jensen, Henrik H. Divergent synthesis of new α-glucosidase inhibitors obtained through a vinyl Grignard-mediated carbocyclisation. Organic & biomolecular chemistry, 2018, 16, 6250-6261 |
| 7156367 | CIF | C17 H10 Cl F2 N O2 | P 41 | 8.1375; 8.1375; 22.67 90; 90; 90 | 1501.18 | Sun, Zhou; Xiang, Kuirong; Tao, Hua; Guo, Liqun; Li, Ying Synthesis of 2-substituted 3-chlorobenzofurans via TMSCl-mediated nucleophilic annulation of isatin-derived propargylic alcohols. Organic & biomolecular chemistry, 2018, 16, 6133-6139 |
| 7156368 | CIF | C30 H22 N2 O | P -1 | 9.6135; 10.5171; 12.3679 72.018; 70.4; 89.928 | 1113.15 | Yang, Kai; Bao, Xiaoze; Yao, Ye; Qu, Jingping; Wang, Baomin Iodine-mediated cross-dehydrogenative coupling of pyrazolones and alkenes. Organic & biomolecular chemistry, 2018, 16, 6275-6283 |
| 7156369 | CIF | C30 H31 N3 O4 | P -1 | 8.6452; 11.1356; 15.0205 108.623; 91.819; 111.122 | 1260.49 | Murphy, Rhys B.; Pham, Duc-Truc; White, Jonathan M.; Lincoln, Stephen F.; Johnston, Martin R. Molecular tweezers with a rotationally restricted linker and freely rotating porphyrin moieties. Organic & biomolecular chemistry, 2018, 16, 6206-6223 |
| 7156370 | CIF | C28 H28 N2 O4.06 | P -1 | 10.5365; 10.715; 11.866 64.644; 70.132; 77.884 | 1135.3 | Murphy, Rhys B.; Pham, Duc-Truc; White, Jonathan M.; Lincoln, Stephen F.; Johnston, Martin R. Molecular tweezers with a rotationally restricted linker and freely rotating porphyrin moieties. Organic & biomolecular chemistry, 2018, 16, 6206-6223 |
| 7156371 | CIF | C18 H21 B Br N O4 | P 1 21/n 1 | 6.9737; 23.8115; 11.0278 90; 98.529; 90 | 1810.96 | Pang, Yadong; Kojima, Ryoto; Ito, Hajime Copper(i)-catalysed stereoselective debromoborylation of aliphatic 1,1-dibromo-1-alkenes with bis(pinacolato)diboron. Organic & biomolecular chemistry, 2018, 16, 6187-6190 |
| 7156372 | CIF | C29 H42 O3 | P 1 21 1 | 10.811; 11.3987; 11.7982 90; 104.616; 90 | 1406.86 | Shan, Huanyu; Pan, Rihuang; Lin, Xufeng Synthesis and application of a new chiral monodentate spiro phosphoramidite ligand based on hexamethyl-1,1'-spirobiindane backbone in asymmetric hydroamination/arylation of alkenes. Organic & biomolecular chemistry, 2018, 16, 6183-6186 |
| 7156373 | CIF | C16 H20 B Br O4 | P 1 21/c 1 | 7.2446; 10.9482; 21.3662 90; 98.091; 90 | 1677.8 | Zi, You; Schömberg, Fritz; Seifert, Fabian; Görls, Helmar; Vilotijevic, Ivan trans-Hydroboration vs. 1,2-reduction: divergent reactivity of ynones and ynoates in Lewis-base-catalyzed reactions with pinacolborane. Organic & biomolecular chemistry, 2018, 16, 6341-6349 |
| 7156374 | CIF | C15 H11 N O2 S | P 1 21/c 1 | 14.1337; 10.2364; 8.868 90; 97.306; 90 | 1272.6 | Li, Xiao-Fang; Shi, Lin-Feng; Zhang, Xing-Guo; Zhang, Xiao-Hong Pd-Catalyzed C(sp<sup>2</sup>)-H aminocarbonylation using the Langlois reagent as a carbonyl source. Organic & biomolecular chemistry, 2018, 16, 6438-6442 |
| 7156375 | CIF | C23 H28 Cl N3 O2 | C 1 c 1 | 27.492; 10.71; 20.869 90; 131.125; 90 | 4628.6 | Ren, Zhi-Lin; He, Ping; Lu, Wen-Ting; Sun, Mei; Ding, Ming-Wu Synthesis of iminoisoindolinones via a cascade of the three-component Ugi reaction, palladium catalyzed isocyanide insertion, hydroxylation and an unexpected rearrangement reaction. Organic & biomolecular chemistry, 2018, 16, 6322-6331 |
| 7156376 | CIF | C31 H26 N4 O6 S | P 1 21 1 | 7.5644; 19.5682; 9.8133 90; 105.002; 90 | 1403.07 | Sharma, Vivek; Kaur, Anmolpreet; Sahoo, Subash Chandra; Chimni, Swapandeep Singh Enantioselective 1,4-Michael addition reaction of pyrazolin-5-one derivatives with 2-enoylpyridines catalyzed by Cinchona derived squaramides. Organic & biomolecular chemistry, 2018, 16, 6470-6478 |
| 7156377 | CIF | C66 H76 Cl12 N10 | P 1 21/c 1 | 11.7078; 23.2759; 12.9884 90; 90.62; 90 | 3539.3 | Liebold, Martin; Sharikow, Eugen; Seikel, Elisabeth; Trombach, Lukas; Harms, Klaus; Zimcik, Petr; Novakova, Veronika; Tonner, Ralf; Sundermeyer, Jörg An experimental and computational study on isomerically pure, soluble azaphthalocyanines and their complexes and boron azasubphthalocyanines of a varying number of aza units. Organic & biomolecular chemistry, 2018, 16, 6586-6599 |
| 7156378 | CIF | C49 H56 B Cl3 N6 | C m c 21 | 24.8236; 16.309; 10.9728 90; 90; 90 | 4442.3 | Liebold, Martin; Sharikow, Eugen; Seikel, Elisabeth; Trombach, Lukas; Harms, Klaus; Zimcik, Petr; Novakova, Veronika; Tonner, Ralf; Sundermeyer, Jörg An experimental and computational study on isomerically pure, soluble azaphthalocyanines and their complexes and boron azasubphthalocyanines of a varying number of aza units. Organic & biomolecular chemistry, 2018, 16, 6586-6599 |
| 7156379 | CIF | C60 H70 N12 O Zn | P 1 21/c 1 | 6.0419; 16.2175; 31.008 90; 95.305; 90 | 3025.3 | Liebold, Martin; Sharikow, Eugen; Seikel, Elisabeth; Trombach, Lukas; Harms, Klaus; Zimcik, Petr; Novakova, Veronika; Tonner, Ralf; Sundermeyer, Jörg An experimental and computational study on isomerically pure, soluble azaphthalocyanines and their complexes and boron azasubphthalocyanines of a varying number of aza units. Organic & biomolecular chemistry, 2018, 16, 6586-6599 |
| 7156380 | CIF | C22 H24 F N O5 | P 1 21 1 | 7.53; 5.649; 23.594 90; 96.387; 90 | 997.4 | Wu, Xiao-Na; You, Zhi-Hao; Liu, Yan-Kai Different hybridized oxygen atoms controlled chemoselective formation of oxocarbenium ions: synthesis of chiral heterocyclic compounds. Organic & biomolecular chemistry, 2018, 16, 6507-6520 |
| 7156381 | CIF | C140 H160 N8 O24 | P 21 21 21 | 7.9683; 16.3532; 23.8547 90; 90; 90 | 3108.4 | Wu, Xiao-Na; You, Zhi-Hao; Liu, Yan-Kai Different hybridized oxygen atoms controlled chemoselective formation of oxocarbenium ions: synthesis of chiral heterocyclic compounds. Organic & biomolecular chemistry, 2018, 16, 6507-6520 |
| 7156382 | CIF | C40 H40 Br2 N2 O10 | P 1 21 1 | 6.6706; 25.351; 11.3316 90; 89.9; 90 | 1916.2 | Wu, Xiao-Na; You, Zhi-Hao; Liu, Yan-Kai Different hybridized oxygen atoms controlled chemoselective formation of oxocarbenium ions: synthesis of chiral heterocyclic compounds. Organic & biomolecular chemistry, 2018, 16, 6507-6520 |
| 7156383 | CIF | C19 H15 F2 N O2 | P -1 | 9.5617; 9.7384; 10.228 75.27; 68.659; 61.422 | 775.3 | Mai, Wen-Peng; Wang, Fei; Zhang, Xiao-Feng; Wang, Shi-Min; Duan, Qun-Peng; Lu, Kui Nickel-catalysed radical tandem cyclisation/arylation: practical synthesis of 4-benzyl-3,3-difluoro-γ-lactams. Organic & biomolecular chemistry, 2018, 16, 6491-6498 |
| 7156384 | CIF | C21 H21 N O | P b c a | 14.3887; 9.1859; 24.515 90; 90; 90 | 3240.2 | Zhang, Xiao-Yu; Yang, Song; Wei, Yin; Shi, Min Thermally-induced intramolecular [2 + 2] cycloaddition of acrylamide-tethered alkylidenecyclopropanes. Organic & biomolecular chemistry, 2018, 16, 6399-6404 |
| 7156385 | CIF | C21 H21 N O | P -1 | 9.4746; 9.4905; 9.7931 78.081; 70.166; 77.527 | 800.24 | Zhang, Xiao-Yu; Yang, Song; Wei, Yin; Shi, Min Thermally-induced intramolecular [2 + 2] cycloaddition of acrylamide-tethered alkylidenecyclopropanes. Organic & biomolecular chemistry, 2018, 16, 6399-6404 |
| 7156386 | CIF | C45 H45 Cl N O7 P Pd | P 21 21 21 | 9.1935; 14.7832; 30.8543 90; 90; 90 | 4193.39 | Russell, David A.; Freudenreich, Julien J.; Stewart, Hannah L.; Bond, Andrew D.; Sore, Hannah F.; Spring, David R. Semi-syntheses of the 11-hydroxyrotenoids sumatrol and villosinol. Organic & biomolecular chemistry, 2018, 16, 6395-6398 |
| 7156387 | CIF | C17 H14 N2 O2 S | P b c a | 14.4456; 9.07642; 22.7259 90; 90; 90 | 2979.69 | Bandyopadhyay, Debashruti; Thirupathi, Annaram; Dhage, Nagsen Munjaji; Mohanta, Nirmala; Peruncheralathan, S. Nickel catalyzed site selective C-H functionalization of α-aryl-thioamides. Organic & biomolecular chemistry, 2018, 16, 6405-6409 |
| 7156388 | CIF | C17 H14 N2 O2 S | P 1 21/c 1 | 11.7047; 10.3186; 13.6857 90; 113.046; 90 | 1520.99 | Bandyopadhyay, Debashruti; Thirupathi, Annaram; Dhage, Nagsen Munjaji; Mohanta, Nirmala; Peruncheralathan, S. Nickel catalyzed site selective C-H functionalization of α-aryl-thioamides. Organic & biomolecular chemistry, 2018, 16, 6405-6409 |
| 7156389 | CIF | C26 H20 Cl N3 O8 S | P -1 | 5.6165; 13.983; 16.7686 65.52; 88.6; 86.77 | 1196.6 | Jiang, Yan; Yu, Shuo-Wen; Yang, Yi; Liu, Ying-Le; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng Synthesis of polycyclic spirooxindoles via an asymmetric catalytic one-pot stepwise Aldol/chloroetherification/aromatization procedure. Organic & biomolecular chemistry, 2018, 16, 6647-6651 |
| 7156390 | CIF | C23 H23 Cl N2 O4 | P 1 21 1 | 8.8442; 10.8918; 11.5077 90; 90.266; 90 | 1108.52 | Jiang, Yan; Yu, Shuo-Wen; Yang, Yi; Liu, Ying-Le; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng Synthesis of polycyclic spirooxindoles via an asymmetric catalytic one-pot stepwise Aldol/chloroetherification/aromatization procedure. Organic & biomolecular chemistry, 2018, 16, 6647-6651 |
| 7156391 | CIF | C26 H29 O3 P | P 1 21/n 1 | 9.6804; 24.788; 10.418 90; 109.906; 90 | 2350.5 | Chen, Yao-Zhong; Zhu, Jie; Wu, Jin-Jin; Wu, Lei Organobase catalyzed straightforward synthesis of phosphinyl functionalized 2H-pyran cores from allenylphosphine oxides and 1,3-diones. Organic & biomolecular chemistry, 2018, 16, 6675-6679 |
| 7156393 | CIF | C18 H19 Cl O2 | P 1 21/n 1 | 10.9261; 10.6284; 12.9254 90; 90.813; 90 | 1500.84 | Wu, Wanqing; Li, Can; Li, Jianxiao; Jiang, Huanfeng Palladium-catalyzed cascade carboesterification of norbornene with alkynes. Organic & biomolecular chemistry, 2018, 16, 8495-8504 |
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