Crystallography Open Database
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Result: there are 90 entries in the selection
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Searching journal of publication like 'Green Chemistry' volume of publication is 20
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7230745 | CIF | C13 H12 O3 | P 1 21 1 | 11.11016; 9.04172; 15.58673 90; 95.3028; 90 | 1559.06 | Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J. Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen–Schmidt reactions of dihydrolevoglucosenone (Cyrene®) Green Chemistry, 2018, 20, 4423 |
| 7230820 | CIF | C22 H16 O5 S | P n a 21 | 7.7651; 16.4066; 14.1404 90; 90; 90 | 1801.5 | Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide Green Chemistry, 2018, 20, 3059 |
| 7230821 | CIF | C21 H13 Cl O4 S | P 1 c 1 | 12.8859; 5.6317; 25.025 90; 92.804; 90 | 1813.9 | Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide Green Chemistry, 2018, 20, 3059 |
| 7230882 | CIF | C18 H19 N O2 S | P -1 | 8.9159; 9.228; 10.159 105.035; 98.43; 102.959 | 767.8 | Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian Anodic benzylic C(sp3)–H amination: unified access to pyrrolidines and piperidines Green Chemistry, 2018, 20, 3191 |
| 7230883 | CIF | C14 H15 F6 N O3 S | C 1 2/c 1 | 39.756; 6.2412; 31.125 90; 123.261; 90 | 6457.7 | Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian Anodic benzylic C(sp3)–H amination: unified access to pyrrolidines and piperidines Green Chemistry, 2018, 20, 3191 |
| 7230887 | CIF | C18 H21 N O6 | P -1 | 8.9121; 10.6028; 10.607 107.362; 95.433; 110.176 | 875.81 | Wang, Yinling; Du, Yiman; He, Jianghua; Zhang, Yuetao Transformation of lignin model compounds to N-substituted aromatics via Beckmann rearrangement Green Chemistry, 2018, 20, 3318 |
| 7230903 | CIF | C20 H18 O | C 1 2/c 1 | 14.081; 14.4862; 16.112 90; 113.689; 90 | 3009.6 | Senadi, Gopal Chandru; Wang, Jeh-Jeng p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C–O scission strategy Green Chemistry, 2018, 20, 3420 |
| 7230904 | CIF | C19 H16 O2 | P -1 | 6.3828; 10.3101; 11.896 104.198; 100.779; 97.652 | 732.2 | Senadi, Gopal Chandru; Wang, Jeh-Jeng p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C–O scission strategy Green Chemistry, 2018, 20, 3420 |
| 7230905 | CIF | C12 H10 O3 | P 1 21/c 1 | 9.52; 13.2012; 8.3853 90; 112.716; 90 | 972.1 | Senadi, Gopal Chandru; Wang, Jeh-Jeng p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C–O scission strategy Green Chemistry, 2018, 20, 3420 |
| 7230906 | CIF | C53 H44 Cl F6 N4 P3 Ru | I -4 | 28.6436; 28.6436; 13.5364 90; 90; 90 | 11106 | Chakrabarti, Kaushik; Mishra, Anju; Panja, Dibyajyoti; Paul, Bhaskar; Kundu, Sabuj Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources Green Chemistry, 2018, 20, 3339 |
| 7230942 | CIF | C42 H36 Br Cl2 N2 O5.5 S2 | P -1 | 10.1352; 13.2429; 16.5954 110.962; 96.295; 91.276 | 2062.93 | Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles Green Chemistry, 2018, 20, 3271 |
| 7230943 | CIF | C25 H23 N O3 S | P 1 21/c 1 | 18.5095; 10.9007; 10.3745 90; 103.857; 90 | 2032.3 | Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles Green Chemistry, 2018, 20, 3271 |
| 7230944 | CIF | C31 H25 N O3 S | P 1 21/n 1 | 11.7246; 12.2563; 16.5665 90; 98.55; 90 | 2354.15 | Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles Green Chemistry, 2018, 20, 3271 |
| 7230945 | CIF | C21 H18 O4 | C 1 2/c 1 | 17.0463; 11.4307; 18.4621 90; 107.898; 90 | 3423.3 | Sha, Hong-Kai; Liu, Feng; Lu, Juan; Liu, Zhang-Qin; Hao, Wen-Juan; Tang, Jia-Le; Tu, Shu-Jiang; Jiang, Bo Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols Green Chemistry, 2018, 20, 3476 |
| 7230946 | CIF | C27 H23 N O3 | P 1 21/c 1 | 14.9117; 9.0532; 16.0374 90; 99.025; 90 | 2138.2 | Sha, Hong-Kai; Liu, Feng; Lu, Juan; Liu, Zhang-Qin; Hao, Wen-Juan; Tang, Jia-Le; Tu, Shu-Jiang; Jiang, Bo Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols Green Chemistry, 2018, 20, 3476 |
| 7231095 | CIF | C29 H29 N5 | P -1 | 9.7181; 11.6016; 12.0845 69.98; 78.308; 71.223 | 1205.45 | Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K. C–H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines Green Chemistry, 2018, 20, 3463 |
| 7231096 | CIF | C22 H25 N5 | P -1 | 8.154; 14.767; 16.628 90.056; 100.409; 90.188 | 1969.2 | Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K. C–H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines Green Chemistry, 2018, 20, 3463 |
| 7231097 | CIF | C26 H24 Cl N5 O | P 1 21 1 | 9.5211; 11.9295; 20.9205 90; 100.11; 90 | 2339.3 | Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K. C–H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines Green Chemistry, 2018, 20, 3463 |
| 7231098 | CIF | C26 H25 N5 | C 1 c 1 | 10.7702; 13.9788; 15.802 90; 109.391; 90 | 2244.11 | Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K. C–H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines Green Chemistry, 2018, 20, 3463 |
| 7231099 | CIF | C26 H25 N5 | P 1 21/c 1 | 13.8953; 9.4127; 16.851 90; 97.186; 90 | 2186.67 | Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K. C–H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines Green Chemistry, 2018, 20, 3463 |
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