Crystallography Open Database
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Result: there are 123 entries in the selection
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Searching journal of publication like 'Green Chemistry' volume of publication is 24
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7244484 | CIF | C26 H29 N O3 | P 1 21 1 | 8.0026; 15.666; 8.8626 90; 93.268; 90 | 1109.3 | He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations Green Chemistry, 2022, 24, 2483-2491 |
| 7244523 | CIF | C26 H25 N3 O6 | P b c a | 12.6825; 14.325; 26.5675 90; 90; 90 | 4826.7 | Maiti, Debajit; Das, Ranajit; Prabakar, Tejas; Sen, Subhabrata Blue LED induced solvent-free multicomponent reactions among aryl diazoacetates, pyridine derivatives and maleimides: direct eco-friendly synthesis of densely functionalized itaconimides Green Chemistry, 2022, 24, 3001-3008 |
| 7244542 | CIF | C15 H20 O4 | P b c a | 16.3085; 7.9252; 21.384 90; 90; 90 | 2763.84 | Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J. Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2 Green Chemistry, 2022, 24, 2535-2541 |
| 7244543 | CIF | C16 H20 O5 S | P 1 21/n 1 | 13.9329; 6.1434; 19.2618 90; 96.736; 90 | 1637.34 | Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J. Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2 Green Chemistry, 2022, 24, 2535-2541 |
| 7244544 | CIF | C16 H20 O6 | P 1 21 1 | 10.8206; 6.2424; 12.0066 90; 109.921; 90 | 762.48 | Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J. Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2 Green Chemistry, 2022, 24, 2535-2541 |
| 7244545 | CIF | C15 H20 O3 S | P c a 21 | 21.6035; 7.9904; 16.8357 90; 90; 90 | 2906.19 | Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J. Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2 Green Chemistry, 2022, 24, 2535-2541 |
| 7244580 | CIF | C15 H12 N2 O | P 1 21/n 1 | 16.392; 7.1332; 20.1084 90; 95.662; 90 | 2339.75 | Ren, Jie; Pi, Chao; Cui, Xiuling; Wu, Yangjie Divergent C(sp2)–H arylation of heterocycles via organic photoredox catalysis Green Chemistry, 2022, 24, 3017-3022 |
| 7244581 | CIF | C15 H12 O3 | P 1 21/c 1 | 8.9535; 14.0575; 9.4542 90; 90.799; 90 | 1189.83 | Zhou, Bei; He, Yu-Juan; Tao, Yun-Feng; Liu, Lan-Xiang; Hu, Min; Chang, Zu-Hui; Lei, Hong; Lin, Jun; Lin, Tong; Du, Guan-Ben Electrocatalytic synthesis of α,α-gem-dihalide ketones from α-mono-halide ketones and unexpected dimer condensation Green Chemistry, 2022, 24, 2859-2870 |
| 7244591 | CIF | C19 H19 N O2 | P -1 | 7.9813; 11.4019; 17.8408 92.73; 90.852; 108.525 | 1536.9 | Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone Green Chemistry, 2022, 24, 2919-2926 |
| 7244592 | CIF | C18 H17 N O2 | P -1 | 8.21; 9.4039; 10.1909 111.938; 99.562; 97.455 | 703.68 | Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone Green Chemistry, 2022, 24, 2919-2926 |
| 7244593 | CIF | C18 H17 N O2 | P 1 21/n 1 | 11.7113; 9.8511; 25.285 90; 97.144; 90 | 2894.5 | Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone Green Chemistry, 2022, 24, 2919-2926 |
| 7244594 | CIF | C19 H19 N O2 | P 1 21/n 1 | 12.6474; 7.3679; 17.5437 90; 110.655; 90 | 1529.7 | Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone Green Chemistry, 2022, 24, 2919-2926 |
| 7244625 | CIF | C21 H18 N2 O S | P -1 | 11.9441; 12.2012; 13.45 76.259; 72.322; 79.906 | 1802.8 | Chen, Ziren; Xue, Fei; Liu, Tianxiang; Wang, Bin; Zhang, Yonghong; Jin, Weiwei; Xia, Yu; Liu, Chenjiang Synthesis of β-hydroxysulfides via visible-light-driven and EDA complex-promoted hydroxysulfenylation of styrenes with heterocyclic thiols in EtOH under photocatalyst-free conditions Green Chemistry, 2022, 24, 3250-3256 |
| 7244626 | CIF | C87 H71 Cl8 N8 O4 S4 | P 1 21/c 1 | 24.764; 12.538; 13.43 90; 91.148; 90 | 4169.1 | Chen, Ziren; Xue, Fei; Liu, Tianxiang; Wang, Bin; Zhang, Yonghong; Jin, Weiwei; Xia, Yu; Liu, Chenjiang Synthesis of β-hydroxysulfides via visible-light-driven and EDA complex-promoted hydroxysulfenylation of styrenes with heterocyclic thiols in EtOH under photocatalyst-free conditions Green Chemistry, 2022, 24, 3250-3256 |
| 7244644 | CIF | C24 H16 O5 | P 1 21/c 1 | 4.998; 19.0007; 18.7257 90; 96.275; 90 | 1767.6 | Karmakar, Indrajit; Brahmachari, Goutam Electrochemical and mechanochemical synthesis of dihydrofuro[3,2-c]chromenones via intramolecular Csp3–H cross-dehydrogenative oxygenation within warfarin frameworks: an efficient and straightforward dual approach Green Chemistry, 2022, 24, 2825-2838 |
| 7244664 | CIF | C29 H24 O5 | P -1 | 9.1359; 10.8744; 12.1839 83.076; 88.393; 84.055 | 1195 | Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides Green Chemistry, 2022, 24, 3623-3628 |
| 7244665 | CIF | C23 H20 O6 | P c c n | 12.0593; 16.1161; 20.7106 90; 90; 90 | 4025.1 | Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides Green Chemistry, 2022, 24, 3623-3628 |
| 7244666 | CIF | C28 H24 O5 | P b c a | 16.277; 14.959; 19.366 90; 90; 90 | 4715.4 | Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides Green Chemistry, 2022, 24, 3623-3628 |
| 7244667 | CIF | C28 H24 O5 | P n a 21 | 20.333; 6.4811; 35.365 90; 90; 90 | 4660.4 | Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides Green Chemistry, 2022, 24, 3623-3628 |
| 7244670 | CIF | C16 H14 Br N O | P 1 21/m 1 | 6.3843; 7.1053; 15.724 90; 100.963; 90 | 700.3 | Goh, Jeffrey; Ong, Seng Kheong; Tan, Yan Sheng; Loh, Teck-Peng Catalyst-free C–N bond formation under biocompatible reaction conditions Green Chemistry, 2022, 24, 3321-3325 |
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