Crystallography Open Database
Search results
Result: there are 1096 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
Searching journal of publication like 'Green Chemistry'
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7230471 | CIF | C23 H18 N2 O5 S | P -1 | 9.1495; 11.0385; 11.775 68.418; 81.041; 68.191 | 1026.46 | Yao, Xinghui; Weng, Xin; Wang, Kaixuan; Xiang, Haifeng; Zhou, Xiangge Transition metal free oxygenation of 8-aminoquinoline amides in water Green Chemistry, 2018, 20, 2472 |
| 7230499 | CIF | C14 H10 N2 O | P 1 21/c 1 | 12.105; 7.6772; 11.507 90; 97.73; 90 | 1059.7 | Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage Green Chemistry, 2018, 20, 2449 |
| 7230500 | CIF | C19 H14 N2 O2 | P 1 21/c 1 | 10.351; 11.378; 12.992 90; 106.17; 90 | 1469.6 | Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage Green Chemistry, 2018, 20, 2449 |
| 7230578 | CIF | C12 H14 O4 | P 1 21/n 1 | 5.8802; 25.3608; 8.2156 90; 109.663; 90 | 1153.72 | Yang, Da; Liu, Huan; Wang, Dong-Liang; Luo, Zhoujie; Lu, Yong; Xia, Fei; Liu, Ye Co-catalysis over a bi-functional ligand-based Pd-catalyst for tandem bis-alkoxycarbonylation of terminal alkynes Green Chemistry, 2018, 20, 2588 |
| 7230581 | CIF | C15 H0 Br N O | C 1 c 1 | 29.72; 5.675; 7.425 90; 95.29; 90 | 1247 | Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones Green Chemistry, 2018, 20, 2722 |
| 7230582 | CIF | C20 H16 F3 N | P -1 | 8.585; 9.869; 10.0994 91.079; 103.819; 90.728 | 830.6 | Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones Green Chemistry, 2018, 20, 2722 |
| 7230705 | CIF | C13 H10 Cl N O S | P 1 21/n 1 | 10.4863; 9.6208; 12.383 90; 111.484; 90 | 1162.48 | Ma, Yan-Na; Guo, Chen-Yang; Zhao, Qianyi; Zhang, Jie; Chen, Xuenian Synthesis of dibenzothiazines from sulfides by one-pot N,O-transfer and intramolecular C‒H amination Green Chemistry, 2018, 20, 2953 |
| 7230721 | CIF | C80 H70 Cl2 N6 O11 | F d d 2 | 21.758; 50.304; 13.416 90; 90; 90 | 14684 | Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles Green Chemistry, 2018, 20, 2775 |
| 7230722 | CIF | C48 H49 Cl2 N3 O4 | P -1 | 12.043; 13.174; 13.616 98.819; 97.641; 98.079 | 2087 | Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles Green Chemistry, 2018, 20, 2775 |
| 7230738 | CIF | C11 H10 O4 | P 21 21 21 | 7.22158; 9.60997; 13.4791 90; 90; 90 | 935.44 | 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 |
| 7230739 | CIF | C13 H11 N O5 | P 1 21 1 | 8.36693; 7.08624; 19.5336 90; 93.2815; 90 | 1156.25 | 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 |
| 7230740 | CIF | C15 H14 O3 | P 65 | 13.5583; 13.5583; 45.7998 90; 90; 120 | 7291.3 | 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 |
| 7230741 | CIF | C11 H10 O3 S | P 21 21 21 | 6.32713; 10.32552; 15.23806 90; 90; 90 | 995.516 | 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 |
| 7230742 | CIF | C13 H12 O4 | P 21 21 21 | 9.50457; 9.59528; 11.4776 90; 90; 90 | 1046.75 | 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 |
| 7230743 | CIF | C14 H14 O3 | P 21 21 21 | 6.47958; 7.89044; 22.4589 90; 90; 90 | 1148.25 | 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 |
| 7230744 | CIF | C13 H11 Cl O3 | P 1 21 1 | 5.94601; 5.17983; 18.2456 90; 94.739; 90 | 560.03 | 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 |
| 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 |
| 7231100 | CIF | C1.61 H1.61 N0.3 | P 1 21/n 1 | 11.3769; 17.6453; 11.4216 90; 96.532; 90 | 2277.99 | 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 |
| 7231101 | CIF | C33 H31 N5 O2 | P 21 21 21 | 9.5012; 15.8064; 18.7456 90; 90; 90 | 2815.2 | 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 |
| 7231208 | CIF | C17 H14 N2 O2 S | P -1 | 8.4181; 9.1433; 10.4688 74.013; 72.64; 69.444 | 706.85 | Chen, En; Shao, Jiaan; Tang, Pai; Shu, Ke; Chen, Wenteng; Yu, Yongping Catalyst-free three-component sequencing for efficient assembly of [1,3] oxazine N-fused imidazole-2-thiones Green Chemistry, 2018, 20, 3696 |
| 7231242 | CIF | C12 H14 N2 O | P -1 | 5.8293; 9.3602; 10.5304 77.907; 80.183; 78.031 | 544.74 | Pelliccia, Sveva; Abbate, Vincenzo; Meneghetti, Fiorella; Frascione, Nunzianda; Hider, Robert Charles; Novellino, Ettore; Tron, Gian Cesare; Giustiniano, Mariateresa On-water pyrrolidine-mediated domino synthesis of 2-iminoisatins Green Chemistry, 2018, 20, 3912 |
| 7231243 | CIF | C90 H78 Cl N9 O5 P6 Ru2 | P 1 21/n 1 | 22.8345; 15.0703; 27.8444 90; 92.926; 90 | 9569.4 | Guan, Chao; Pan, Yupeng; Ang, Eleanor Pei Ling; Hu, Jinsong; Yao, Changguang; Huang, Mei-Hui; Li, Huaifeng; Lai, Zhiping; Huang, Kuo-Wei Conversion of CO2 from air into formate using amines and phosphorus-nitrogen PN3P-Ru(ii) pincer complexes Green Chemistry, 2018, 20, 4201 |
| 7231244 | CIF | C48 H40 N3 O P3 Ru | P -1 | 12.2479; 20.634; 25.309 106.192; 93.516; 106.236 | 5829.8 | Guan, Chao; Pan, Yupeng; Ang, Eleanor Pei Ling; Hu, Jinsong; Yao, Changguang; Huang, Mei-Hui; Li, Huaifeng; Lai, Zhiping; Huang, Kuo-Wei Conversion of CO2 from air into formate using amines and phosphorus-nitrogen PN3P-Ru(ii) pincer complexes Green Chemistry, 2018, 20, 4201 |
| 7231311 | CIF | C16 H14.5 F3 N3 O0.25 | P 1 21/c 1 | 5.6803; 22.15; 23.2022 90; 90.281; 90 | 2919.2 | Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents Green Chemistry, 2018, 20, 4023 |
| 7231312 | CIF | C18 H23 N3 O4 | P 1 21 1 | 5.35503; 10.169; 32.73 90; 92.72; 90 | 1780.31 | Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents Green Chemistry, 2018, 20, 4023 |
| 7231313 | CIF | C15 H12 F3 N | P n a 21 | 27.0703; 5.7522; 8.0156 90; 90; 90 | 1248.14 | Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents Green Chemistry, 2018, 20, 4023 |
| 7231314 | CIF | C18 H23 N3 O2 | P 1 21/c 1 | 12.8362; 11.1053; 11.7668 90; 92.584; 90 | 1675.65 | Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents Green Chemistry, 2018, 20, 4023 |
| 7231315 | CIF | C23 H21 N O2 | P 1 21 1 | 5.66625; 18.3197; 17.6253 90; 90.314; 90 | 1829.55 | Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents Green Chemistry, 2018, 20, 4023 |
| 7231316 | CIF | C21 H19 N3 O2 | P 1 21/c 1 | 12.8553; 5.5968; 24.4632 90; 92.11; 90 | 1758.9 | Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents Green Chemistry, 2018, 20, 4023 |
| 7231346 | CIF | C18 H26 Cl9 Ir N2 O4 S | P b c a | 11.2915; 16.6242; 32.7927 90; 90; 90 | 6155.6 | Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A. Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water Green Chemistry, 2018, 20, 4094 |
| 7231347 | CIF | C22 H27 Ir N2 O2 | P -1 | 8.592; 10.2464; 12.6648 78.655; 82.445; 67.017 | 1004.56 | Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A. Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water Green Chemistry, 2018, 20, 4094 |
| 7231348 | CIF | C18 H29 Cl2 F6 Ir N2 O8 S2 | P 1 21/c 1 | 11.2529; 21.6653; 12.9575 90; 111.582; 90 | 2937.5 | Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A. Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water Green Chemistry, 2018, 20, 4094 |
| 7231363 | CIF | C8 H19 N3 Si2 | P 1 21/c 1 | 6.7038; 9.1027; 21.146 90; 91.335; 90 | 1290 | Roshandel, Sahar; Suri, Suresh C.; Marcischak, Jacob C.; Rasul, Golam; Surya Prakash, G. K. Catalyst and solvent free microwave-assisted synthesis of substituted 1,2,3-triazoles Green Chemistry, 2018, 20, 3700 |
| 7231382 | CIF | C14 H7 F4 N | P 1 21/c 1 | 13.274; 14.344; 6.1256 90; 101.518; 90 | 1142.8 | Charpe, Vaibhav Pramod; Hande, Aniket A.; Sagadevan, Arunachalam; Hwang, Kuo Chu Visible-light induced copper(i)-catalysed denitrogenative oxidative coupling of hydrazinylpyridines with terminal alkynes Green Chemistry, 2018, 20, 4859 |
| 7231389 | CIF | C15 H45 Cl9 N3 O4.5 Sn3 | C 1 c 1 | 15.459; 9.19; 23.79 90; 95.25; 90 | 3365.62 | Bayu, Asep; Yoshida, Akihiro; Karnjanakom, Surachai; Kusakabe, Katsuki; Hao, Xiaogang; Prakoso, Tirto; Abudula, Abuliti; Guan, Guoqing Catalytic conversion of biomass derivatives to lactic acid with increased selectivity in an aqueous tin(ii) chloride/choline chloride system Green Chemistry, 2018, 20, 4112 |
| 7231395 | CIF | C90 H101 N6 O12 | P -1 | 19.911; 20.945; 23.811 106.471; 107.031; 108.096 | 8223 | Zhu, Xin-Qi; Yuan, Han; Sun, Qing; Zhou, Bo; Han, Xiao-Qin; Zhang, Zhi-Xin; Lu, Xin; Ye, Long-Wu Benign catalysis with zinc: atom-economical and divergent synthesis of nitrogen heterocycles by formal [3 + 2] annulation of isoxazoles with ynol ethers Green Chemistry, 2018, 20, 4287 |
| 7231603 | CIF | C40 H45 B Cl2 F4 Ir N3 P2 | P -1 | 11.0544; 13.3742; 14.3388 84.204; 84.669; 72.812 | 2010.4 | Iturmendi, Amaia; Iglesias, Manuel; Munarriz, Julen; Polo, Victor; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.; Oro, Luis A. A highly efficient Ir-catalyst for the solventless dehydrogenation of formic acid: the key role of an N-heterocyclic olefin Green Chemistry, 2018, 20, 4875 |
| 7231604 | CIF | C38 H41 B Cl2 F4 Ir N3 P2 | P 1 21/n 1 | 15.5008; 11.5673; 21.116 90; 97.583; 90 | 3753 | Iturmendi, Amaia; Iglesias, Manuel; Munarriz, Julen; Polo, Victor; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.; Oro, Luis A. A highly efficient Ir-catalyst for the solventless dehydrogenation of formic acid: the key role of an N-heterocyclic olefin Green Chemistry, 2018, 20, 4875 |
| 7231651 | CIF | C20 H22 F3 N O3 | P -1 | 8.318; 11.515; 11.539 61.6; 78.05; 75.08 | 934.8 | He, Yu-Tao; Kang, Dahye; Kim, Inwon; Hong, Sungwoo Metal-free photocatalytic trifluoromethylative pyridylation of unactivated alkenes Green Chemistry, 2018, 20, 5209 |
| 7231666 | CIF | C13.75 H12.5 N1.25 O1.25 S0.25 | P 1 21/c 1 | 8.6319; 18.0068; 7.8624 90; 99.001; 90 | 1207.03 | Xing, Zhimin; Yang, Mingyang; Sun, Haiyu; Wang, Zemin; Chen, Peng; Liu, Lin; Wang, Xiaolei; Xie, Xingang; She, Xuegong Visible-light promoted dithioacetalization of aldehydes with thiols under aerobic and photocatalyst-free conditions Green Chemistry, 2018, 20, 5117 |
| 7231667 | CIF | C51 H37 F12 N5 O9 Zn2 | C 1 2/c 1 | 27.538; 7.887; 23.328 90; 99.24; 90 | 5000.9 | Joharian, Monika; Morsali, Ali; Azhdari Tehrani, Alireza; Carlucci, Lucia; Proserpio, Davide M. Water-stable fluorinated metal‒organic frameworks (F-MOFs) with hydrophobic properties as efficient and highly active heterogeneous catalysts in aqueous solution Green Chemistry, 2018, 20, 5336 |
| 7231688 | CIF | C114 H126 N24 Nd4 O42 Zn3 | R -3 c | 17.8928; 17.8928; 69.099 90; 90; 120 | 19158.4 | Wang, Li; Zhang, Ruilian; Han, Qing-Xin; Xu, Cong; Chen, Wan-Min; Yang, Huan; Gao, Guoshu; Qin, Wenwu; Liu, Wei-Sheng Amide-functionalized heterometallic helicate cages as highly efficient catalysts for CO2 conversion under mild condition Green Chemistry, 2018 |
| 7231689 | CIF | C114 H126 Eu4 N24 O42 Zn3 | R -3 c | 17.8497; 17.8497; 68.762 90; 90; 120 | 18973.2 | Wang, Li; Zhang, Ruilian; Han, Qing-Xin; Xu, Cong; Chen, Wan-Min; Yang, Huan; Gao, Guoshu; Qin, Wenwu; Liu, Wei-Sheng Amide-functionalized heterometallic helicate cages as highly efficient catalysts for CO2 conversion under mild condition Green Chemistry, 2018 |
| 7231775 | CIF | C12 H11 N O2 S | P 1 21/c 1 | 11.1231; 11.9525; 8.5577 90; 99.993; 90 | 1120.48 | Wang, Ming; Fan, Qiaoling; Jiang, Xuefeng Metal-free construction of primary sulfonamides through three diverse salts Green Chemistry, 2018, 20, 5469 |
| 7231898 | CIF | C16 H12 N2 O | P 1 21 1 | 3.9878; 12.0606; 24.7189 90; 93.93; 90 | 1186.07 | Mishra, Manisha; Twardy, Dylan; Ellstrom, Clifford; Wheeler, Kraig A.; Dembinski, Roman; Török, Béla Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination Green Chemistry, 2019, 21, 99 |
| 7231899 | CIF | C17 H14 N2 | P 1 21/c 1 | 13.2669; 11.5841; 16.4623 90; 100.794; 90 | 2485.2 | Mishra, Manisha; Twardy, Dylan; Ellstrom, Clifford; Wheeler, Kraig A.; Dembinski, Roman; Török, Béla Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination Green Chemistry, 2019, 21, 99 |
| 7231952 | CIF | C40 H36 N8 O4 S2 | P -1 | 10.651; 12.816; 14.137 100.211; 107.686; 101.151 | 1745.4 | Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K. A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer Green Chemistry, 2019, 21, 69 |
| 7231953 | CIF | C26 H26 N4 O2 | C 1 2/c 1 | 20.3152; 14.7532; 16.39 90; 110.119; 90 | 4612.6 | Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K. A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer Green Chemistry, 2019, 21, 69 |
| 7231954 | CIF | C22 H20 N4 O2 | P 1 21/c 1 | 10.9372; 9.1286; 35.781 90; 95.129; 90 | 3558.1 | Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K. A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer Green Chemistry, 2019, 21, 69 |
| 7231992 | CIF | C20 H26 Cl F6 Ir N3 O P | P n m a | 13.5409; 12.9814; 13.6168 90; 90; 90 | 2393.6 | Huang, Ming; Li, Yinwu; Liu, Jiahao; Lan, Xiao-Bing; Liu, Yan; Zhao, Cunyuan; Ke, Zhuofeng A bifunctional strategy for N-heterocyclic carbene-stabilized iridium complex-catalyzed N-alkylation of amines with alcohols in aqueous media Green Chemistry, 2019, 21, 219 |
| 7231993 | CIF | C37 H54 Cl N2 P2 Rh | R -3 c :H | 26.6194; 26.6194; 27.22 90; 90; 120 | 16703.8 | Lam, Raphael H.; McQueen, Caitlin M. A.; Pernik, Indrek; McBurney, Roy T.; Hill, Anthony F.; Messerle, Barbara A. Selective formylation or methylation of amines using carbon dioxide catalysed by a rhodium perimidine-based NHC complex Green Chemistry, 2019, 21, 538 |
| 7232134 | CIF | C8 H12 N2 O2 | P c a 21 | 13.4813; 8.2397; 6.9346 90; 90; 90 | 770.31 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232135 | CIF | C13 H23 N3 O2 | P 1 21/n 1 | 10.9982; 9.2785; 14.3717 90; 105.714; 90 | 1411.77 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232136 | CIF | C12 H21 N3 O2 | P 1 21/c 1 | 9.3632; 18.2488; 8.129 90; 114.812; 90 | 1260.76 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232137 | CIF | C13 H19 N3 | P 21 21 21 | 9.9385; 10.0425; 24.7502 90; 90; 90 | 2470.25 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232138 | CIF | C8 H14 N2 O3 | P 1 21/n 1 | 7.7428; 11.1556; 10.4925 90; 98.844; 90 | 895.52 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232139 | CIF | C9 H17 N3 O3 | P 1 21/n 1 | 8.1469; 10.0659; 12.9174 90; 104.799; 90 | 1024.16 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232140 | CIF | C23 H29 N3 | P 1 21/n 1 | 12.5296; 8.0939; 19.7181 90; 98.5378; 90 | 1977.52 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232141 | CIF | C16 H29 N3 O2 | P 1 21/c 1 | 14.3302; 9.2194; 12.9756 90; 104.588; 90 | 1659.02 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232142 | CIF | C13 H23 N3 O2 | C 1 c 1 | 10.3765; 13.1188; 11.2806 90; 114.605; 90 | 1396.17 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232143 | CIF | C15 H30 B F4 N3 | P 1 21/c 1 | 15.2506; 10.8267; 10.8569 90; 90.09; 90 | 1792.62 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232144 | CIF | C8 H13 N3 O2 | P 1 21/c 1 | 6.6679; 14.6889; 9.6025 90; 104.13; 90 | 912.05 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232145 | CIF | C19.5 H31.5 N3 O2 | P 1 21/c 1 | 14.6071; 41.9109; 14.5422 90; 117.159; 90 | 7921.1 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232146 | CIF | C16 H29 N3 O2 | P 41 | 11.8565; 11.8565; 24.0309 90; 90; 90 | 3378.2 | Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts Green Chemistry, 2019, 21, 640 |
| 7232175 | CIF | C27 H31 N O3 | P 1 21/c 1 | 10.8693; 19.0667; 11.8343 90; 102.11; 90 | 2398 | Chen, Ke; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo Metal-free synthesis of triarylated (Z)-nitrones via H2O-mediated 1,3-dipolar transfer under aerobic conditions Green Chemistry, 2019, 21, 675 |
| 7232200 | CIF | C27 H20 Cl2 N O P | P 1 21/n 1 | 9.594; 11.0586; 21.6374 90; 93.293; 90 | 2291.86 | Pan, Jiaoting; Zhao, Runmin; Guo, Jiami; Ma, Dumei; Xia, Ying; Gao, Yuxing; Xu, Pengxiang; Zhao, Yufen Three-component 3-(phosphoryl)methylindole synthesis from indoles, H-phosphine oxides and carbonyl compounds under metal-free conditions Green Chemistry, 2019, 21, 792 |
| 7232201 | CIF | C30 H27 Cl N O P | P 1 21/c 1 | 8.6081; 16.0745; 18.0657 90; 99.465; 90 | 2465.74 | Pan, Jiaoting; Zhao, Runmin; Guo, Jiami; Ma, Dumei; Xia, Ying; Gao, Yuxing; Xu, Pengxiang; Zhao, Yufen Three-component 3-(phosphoryl)methylindole synthesis from indoles, H-phosphine oxides and carbonyl compounds under metal-free conditions Green Chemistry, 2019, 21, 792 |
| 7232299 | CIF | C14 H10 N2 O | P 1 21/c 1 | 12.1056; 7.802; 11.6256 90; 97.574; 90 | 1088.43 | Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng Sustainable methine sources for the synthesis of heterocycles under metal- and peroxide-free conditions Green Chemistry, 2019, 21, 979 |
| 7232300 | CIF | C14 H9 F N2 O | P 1 21/c 1 | 12.4895; 7.7667; 11.5802 90; 96.718; 90 | 1115.59 | Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng Sustainable methine sources for the synthesis of heterocycles under metal- and peroxide-free conditions Green Chemistry, 2019, 21, 979 |
| 7232306 | CIF | C13 H9 N O3 | P -1 | 6.561; 7.0809; 12.0629 89.067; 87.281; 78.757 | 549.03 | Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones Green Chemistry, 2019, 21, 991 |
| 7232307 | CIF | C18 H12 F3 N O3 | P -1 | 6.7109; 9.819; 12.7318 75.919; 82.43; 80.639 | 799.18 | Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones Green Chemistry, 2019, 21, 991 |
| 7232308 | CIF | C18 H15 N O4 | P b c a | 6.04; 19.12; 26.355 90; 90; 90 | 3043.6 | Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones Green Chemistry, 2019, 21, 991 |
| 7232363 | CIF | C21 H14 F5 N3 O4 | P -1 | 8.2387; 9.1226; 15.647 78.884; 77.335; 63.875 | 1023.9 | Du, Xuan-Xuan; Zi, Quan-Xing; Wu, Yu-Meng; Jin, Yi; Lin, Jun; Yan, Sheng-Jiao An environmentally benign multi-component reaction: regioselective synthesis of fluorinated 2-aminopyridines using diverse properties of the nitro group Green Chemistry, 2019, 21, 1505 |
| 7232364 | CIF | C23 H19 F5 N2 O2 | P -1 | 8.6308; 9.4049; 13.955 78.895; 81.887; 74.726 | 1067.4 | Du, Xuan-Xuan; Zi, Quan-Xing; Wu, Yu-Meng; Jin, Yi; Lin, Jun; Yan, Sheng-Jiao An environmentally benign multi-component reaction: regioselective synthesis of fluorinated 2-aminopyridines using diverse properties of the nitro group Green Chemistry, 2019, 21, 1505 |
| 7232431 | CIF | C52 H28 Br16 N4 O9 V | P c a b | 20.733; 26.304; 28.112 90; 90; 90 | 15331 | Dar, Tawseef Ahmad; Uprety, Bhawna; Sankar, Muniappan; Maurya, Mannar R. Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media Green Chemistry, 2019, 21, 1757 |
| 7232432 | CIF | C27.5 H22 N3 O5 V0.5 | P c c n | 13.829; 14.439; 26.153 90; 90; 90 | 5222 | Dar, Tawseef Ahmad; Uprety, Bhawna; Sankar, Muniappan; Maurya, Mannar R. Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media Green Chemistry, 2019, 21, 1757 |
| 7232441 | CIF | C17 H14 N2 O2 | P 1 21/c 1 | 11.954; 7.454; 15.468 90; 95.33; 90 | 1372.3 | Botla, Vinayak; Pilli, NavyaSree; Malapaka, Chandrasekharam Uncatalyzed, on water oxygenative cleavage of inert C‒N bond with concomitant 8,7-amino shift in 8-aminoquinoline derivatives Green Chemistry, 2019, 21, 1735 |
| 7232442 | CIF | C2 H4 N8 O4 Zn | P 1 21/c 1 | 6.294; 10.6563; 5.5677 90; 95.069; 90 | 371.97 | Zhang, Qi; Chen, Dong; Jing, Dong; Fan, Guijuan; He, Liu; Li, Hongzhen; Wang, Wentao; Nie, Fude Access to green primary explosives via constructing coordination polymers based on bis-tetrazole oxide and non-lead metals Green Chemistry, 2019, 21, 1947 |
| 7232466 | CIF | C15 H12 O2 | P 1 21/n 1 | 9.6376; 8.3094; 14.8885 90; 92.042; 90 | 1191.6 | Tang, Zhi; Tong, Zhou; Xu, Zhihui; Au, Chak-Tong; Qiu, Renhua; Yin, Shuang-Feng Recyclable nickel-catalyzed C‒H/O‒H dual functionalization of phenols with mandelic acids for the synthesis of 3-aryl benzofuran-2(3H)-ones under solvent-free conditions Green Chemistry, 2019, 21, 2015 |
| 7232467 | CIF | C19 H26 Cl4 Ir N3 O | P 1 21/n 1 | 12.768; 14.165; 13.588 90; 111.994; 90 | 2278.7 | Chakrabarti, Kaushik; Maji, Milan; Kundu, Sabuj Cooperative iridium complex-catalyzed synthesis of quinoxalines, benzimidazoles and quinazolines in water Green Chemistry, 2019, 21, 1999 |
| 7232468 | CIF | C13 H17 N2 O3 | P 1 21/c 1 | 9.9995; 10.3691; 12.6092 90; 101.192; 90 | 1282.53 | Sun, Zhen; Li, Zheng; Liao, Wei-Wei An organocatalytic hydroalkoxylation/Claisen rearrangement/Michael addition tandem sequence: divergent synthesis of multi-substituted 2,3-dihydrofurans and 2,3-dihydropyrroles from cyanohydrins Green Chemistry, 2019, 21, 1614 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!