Crystallography Open Database
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Searching journal of publication like 'Green Chemistry'
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7212127 | CIF | C7 H15 N O3 | P 1 21/n 1 | 6.6199; 13.9451; 9.2587 90; 101.76; 90 | 836.78 | Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D. New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores Green Chemistry, 2010, 12, 491 |
| 7212281 | CIF | C18 H20 N2 O2 | P 1 21 1 | 8.4078; 8.3744; 11.4399 90; 98.698; 90 | 796.22 | Jida, Mouhamad; Deprez-Poulain, Rebecca; Malaquin, Sandra; Roussel, Pascal; Agbossou-Niedercorn, Francine; Deprez, Benoit; Laconde, Guillaume Solvent-free microwave-assisted Meyers’ lactamization Green Chemistry, 2010, 12, 961 |
| 7212282 | CIF | C12 H17 N O4 | C 1 2 1 | 17.5352; 7.6758; 10.0025 90; 113.78; 90 | 1232 | Jida, Mouhamad; Deprez-Poulain, Rebecca; Malaquin, Sandra; Roussel, Pascal; Agbossou-Niedercorn, Francine; Deprez, Benoit; Laconde, Guillaume Solvent-free microwave-assisted Meyers’ lactamization Green Chemistry, 2010, 12, 961 |
| 7212362 | CIF | C20 H15 N O2 | C 1 2/c 1 | 22.045; 9.268; 17.8038 90; 124.751; 90 | 2988.74 | Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa ‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB) Green Chemistry, 2010, 12, 1090 |
| 7212363 | CIF | C15 H17 N O6 | P 1 21/n 1 | 7.1337; 26.8903; 7.6505 90; 90.614; 90 | 1467.49 | Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa ‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB) Green Chemistry, 2010, 12, 1090 |
| 7212364 | CIF | C13 H13 N O2 | P c a b | 9.1168; 13.8294; 17.2443 90; 90; 90 | 2174.16 | Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa ‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB) Green Chemistry, 2010, 12, 1090 |
| 7212365 | CIF | C11 H13 N O5 | P 21 21 21 | 8.449; 11.2583; 12.0738 90; 90; 90 | 1148.5 | Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa ‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB) Green Chemistry, 2010, 12, 1090 |
| 7212382 | CIF | C13 H16 O2 | P 1 21/n 1 | 13.286; 5.6083; 15.808 90; 95.142; 90 | 1173.1 | Liu, Pei Nian; Xia, Fei; Wang, Qing Wei; Ren, Yu Jie; Chen, Jun Qin Triflic acid adsorbed on silica gel as an efficient and recyclable catalyst for the addition of β-dicarbonyl compounds to alcohols and alkenes Green Chemistry, 2010, 12, 1049 |
| 7212399 | CIF | C13 H17 N O2 | P -1 | 5.7313; 11.8701; 18.407 72.324; 85.809; 79.963 | 1174.6 | Feng, Li-Chun; Sun, Ya-Wei; Tang, Wei-Jun; Xu, Li-Jin; Lam, Kim-Lung; Zhou, Zhongyuan; Chan, Albert S. C. Highly efficient chemoselective construction of 2,2-dimethyl-6-substituted 4-piperidones via multi-component tandem Mannich reaction in ionic liquids Green Chemistry, 2010, 12, 949 |
| 7212674 | CIF | C48 H32 F8 N12 Ru2 | P 1 21/c 1 | 9.6596; 38.8963; 12.5248 90; 102.989; 90 | 4585.4 | Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Urbanos, Francisco A. First microwave synthesis of multiple metal-metal bond paddlewheel compounds Green Chemistry, 2010, 12, 965 |
| 7212698 | CIF | C48 H93 Cl5 Cu2 N6 | P -1 | 8.8041; 12.5714; 25.282 89.005; 89.757; 86.052 | 2791.1 | Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation Green Chemistry, 2010, 12, 1589 |
| 7212699 | CIF | C60 H112 Cu F6 N8 P | P -1 | 11.7007; 13.6056; 21.043 91.893; 94.239; 100.766 | 3278.2 | Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation Green Chemistry, 2010, 12, 1589 |
| 7212700 | CIF | C90 H168 Cu6 I6 N12 | P -1 | 9.7553; 13.5795; 20.6572 106.873; 94.154; 95.814 | 2590.3 | Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation Green Chemistry, 2010, 12, 1589 |
| 7212701 | CIF | C64 H124 Br8 Cu4 N8 | P -1 | 10.3068; 16.172; 25.595 73.875; 87.515; 87.742 | 4092.9 | Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation Green Chemistry, 2010, 12, 1589 |
| 7212702 | CIF | C30 H56 Br2 Cu2 N4 | P -1 | 9.002; 9.454; 20.757 85.74; 87.75; 78.95 | 1728.4 | Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation Green Chemistry, 2010, 12, 1589 |
| 7212731 | CIF | C22 H19 N O2 | P -1 | 9.2376; 14.5788; 14.9383 66.775; 74.994; 74.785 | 1756.3 | Zhou, Yu; Zhai, Yun; Li, Jian; Ye, Deju; Jiang, Hualiang; Liu, Hong Metal-free tandem reaction in water: An efficient and regioselective synthesis of 3-hydroxyisoindolin-1-ones Green Chemistry, 2010, 12, 1397 |
| 7212732 | CIF | C14 H14 B Bi F4 O S | P 1 21/c 1 | 13.8004; 11.5529; 9.8253 90; 93.005; 90 | 1564.34 | Qiu, Renhua; Qiu, Yimiao; Yin, Shuangfeng; Song, Xingxing; Meng, Zhengong; Xu, Xinhua; Zhang, Xiaowen; Luo, Shenglian; Au, Chak-Tong; Wong, Wai-Yeung Facile separation catalyst system: direct diastereoselective synthesis of (E)-α,β-unsaturated ketones catalyzed by an air-stable Lewis acidic/basic bifunctional organobismuth complex in ionic liquids Green Chemistry, 2010, 12, 1767 |
| 7212907 | CIF | C20 H26 O4 S | P 21 21 21 | 9.3439; 13.2412; 15.8279 90; 90; 90 | 1958.3 | Rosini, Goffredo; Paolucci, Claudio; Boschi, Francesca; Marotta, Emanuela; Righi, Paolo; Tozzi, Francesco Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base Green Chemistry, 2010, 12, 1747 |
| 7212908 | CIF | C26 H26 F2 N2 O6 S | P 1 21/c 1 | 14.6241; 20.681; 8.745 90; 90.538; 90 | 2644.7 | Ma, Ning; Jiang, Bo; Zhang, Ge; Tu, Shu-Jiang; Wever, Walter; Li, Guigen New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines Green Chemistry, 2010, 12, 1357 |
| 7212909 | CIF | C20 H44 Cu F6 N8 O4 P5 S2 | P -1 | 10.4612; 11.6733; 15.4745 80.696; 70.225; 83.182 | 1750.69 | García-Álvarez, Joaquín; Díez, Josefina; Gimeno, José A highly efficient copper(i) catalyst for the 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes in water: regioselective synthesis of 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles Green Chemistry, 2010, 12, 2127 |
| 7212910 | CIF | C15 H12 I N3 S | P 1 21/c 1 | 14.5177; 7.2359; 14.3593 90; 101.588; 90 | 1477.68 | García-Álvarez, Joaquín; Díez, Josefina; Gimeno, José A highly efficient copper(i) catalyst for the 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes in water: regioselective synthesis of 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles Green Chemistry, 2010, 12, 2127 |
| 7212911 | CIF | C20 H22 F3 N2 O4.5 | R -3 :H | 35.238; 35.238; 8.3319 90; 90; 120 | 8959.8 | Yan, Shengjiao; Chen, Yulan; Liu, Lin; He, Nengqin; Lin, Jun Three-component solvent-free synthesis of highly substituted bicyclic pyridines containing a ring-junction nitrogen Green Chemistry, 2010, 12, 2043 |
| 7212939 | CIF | K0.7 Na0.3 Nb O3 | A m m 2 | 3.970162; 5.67111; 5.69467 90; 90; 90 | 128.217 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212940 | CIF | K0.7 Na0.3 Nb O3 | A m m 2 | 3.96867; 5.67069; 5.69626 90; 90; 90 | 128.195 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212941 | CIF | K0.7 Na0.3 Nb O3 | A m m 2 | 3.97024; 5.662; 5.68624 90; 90; 90 | 127.82 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212942 | CIF | K0.7 Na0.3 Nb O3 | A m m 2 | 3.96136; 5.65428; 5.68474 90; 90; 90 | 127.33 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212943 | CIF | K0.93 Na0.07 Nb O3 | A m m 2 | 3.98381; 5.689; 5.70757 90; 90; 90 | 129.356 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212944 | CIF | K0.903 Na0.097 Nb O3 | A m m 2 | 3.981973; 5.68731; 5.70733 90; 90; 90 | 129.252 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212945 | CIF | K0.86 Na0.14 Nb O3 | A m m 2 | 3.977443; 5.68725; 5.70678 90; 90; 90 | 129.091 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212946 | CIF | K0.84 Na0.16 Nb O3 | A m m 2 | 3.973479; 5.68046; 5.70266 90; 90; 90 | 128.716 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212947 | CIF | K0.83 Na0.17 Nb O3 | A m m 2 | 3.973479; 5.68046; 5.70266 90; 90; 90 | 128.716 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212948 | CIF | K0.77 Na0.23 Nb O3 | A m m 2 | 3.972623; 5.68015; 5.7037 90; 90; 90 | 128.705 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212949 | CIF | K0.73 Na0.27 Nb O3 | A m m 2 | 3.97304; 5.67576; 5.69703 90; 90; 90 | 128.468 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212950 | CIF | K0.75 Na0.25 Nb O3 | A m m 2 | 3.970626; 5.67573; 5.69855 90; 90; 90 | 128.424 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7212951 | CIF | K0.72 Na0.28 Nb O3 | A m m 2 | 3.96953; 5.6731; 5.69719 90; 90; 90 | 128.298 | Handoko, Albertus D.; Goh, Gregory K. L. Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C Green Chemistry, 2010, 12, 680 |
| 7214116 | CIF | C25 H19 N O5 | P 1 21/c 1 | 20.6371; 11.0516; 20.5751 90; 119.356; 90 | 4090 | Muthusaravanan, Sivasubramanian; Sasikumar, Chinnathambi; Devi Bala, Balasubramanian; Perumal, Subbu An eco-friendly three-component regio- and stereoselective synthesis of highly functionalized dihydroindeno[1,2-b]pyrroles under grinding Green Chemistry, 2014, 16, 1297 |
| 7214117 | CIF | C9 H21 N O3 | P c c n | 14.5983; 20.935; 8.5228 90; 90; 90 | 2604.7 | Vanderveen, Jesse R.; Durelle, Jeremy; Jessop, Philip G. Design and evaluation of switchable-hydrophilicity solvents Green Chemistry, 2014, 16, 1187 |
| 7214118 | CIF | C20 H14 N2 O3 | P 1 21/c 1 | 9.0629; 11.2174; 16.215 90; 104.835; 90 | 1593.5 | Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester Green Chemistry, 2014, 16, 1426 |
| 7214119 | CIF | C21 H16 N2 O | P 1 21 1 | 10.0929; 6.337; 12.8314 90; 100.192; 90 | 807.73 | Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester Green Chemistry, 2014, 16, 1426 |
| 7214120 | CIF | C26 H17 N O5 | P -1 | 6.937; 11.638; 13.019 75.535; 89.874; 76.165 | 986.4 | Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester Green Chemistry, 2014, 16, 1426 |
| 7214121 | CIF | C22 H27 N3 O3 | P -1 | 8.6867; 11.0032; 12.0059 70.06; 84.209; 76.001 | 1046.5 | Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester Green Chemistry, 2014, 16, 1426 |
| 7214122 | CIF | C7 H5 Br2 O2 Re | P 1 21/m 1 | 6.892; 8.967; 8.538 90; 112.7; 90 | 486.8 | Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes Green Chemistry, 2014, 16, 1087 |
| 7214123 | CIF | C7 H5 Br2 O2 Re | P 1 21/m 1 | 6.34; 12.504; 6.4937 90; 109.161; 90 | 486.27 | Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes Green Chemistry, 2014, 16, 1087 |
| 7214124 | CIF | C7 H5 Cl2 O2 Re | P 1 21/m 1 | 6.2456; 12.2155; 6.2656 90; 106.932; 90 | 457.3 | Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes Green Chemistry, 2014, 16, 1087 |
| 7214125 | CIF | C7 H5 I2 O2 Re | C 1 2/m 1 | 13.389; 9.29; 9.128 90; 107.669; 90 | 1081.8 | Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes Green Chemistry, 2014, 16, 1087 |
| 7214126 | CIF | C23 H20 N2 | P 21 21 21 | 10.2819; 10.7707; 15.6284 90; 90; 90 | 1730.7 | Solan, Agnes; Nişanci, Bilal; Belcher, Miranda; Young, Jonathon; Schäfer, Christian; Wheeler, Kraig A.; Török, Béla; Dembinski, Roman Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones Green Chemistry, 2014, 16, 1120 |
| 7214127 | CIF | C28 H31 Cl N2 O | P 1 21/n 1 | 5.7713; 16.573; 25.145 90; 92.354; 90 | 2403 | Solan, Agnes; Nişanci, Bilal; Belcher, Miranda; Young, Jonathon; Schäfer, Christian; Wheeler, Kraig A.; Török, Béla; Dembinski, Roman Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones Green Chemistry, 2014, 16, 1120 |
| 7214128 | CIF | C8 H20 N2 O4 | P n a 21 | 11.0906; 14.6981; 7.6029 90; 90; 90 | 1239.35 | Qi, Feng; Stein, Robin S.; Friščić, Tomislav Mimicking mineral neogenesis for the clean synthesis of metal‒organic materials from mineral feedstocks: coordination polymers, MOFs and metal oxide separation Green Chemistry, 2014, 16, 121 |
| 7214305 | CIF | C40 H86 Mo N2 O10 | P -1 | 9.7003; 10.0807; 26.1807 88.397; 82.073; 69.855 | 2379.99 | Chakravarthy, Rajan Deepan; Ramkumar, Venkatachalam; Chand, Dillip Kumar A molybdenum based metallomicellar catalyst for controlled and selective sulfoxidation reactions in aqueous medium Green Chemistry, 2014, 16, 2190 |
| 7214306 | CIF | C10 H16 N2 O S2 | P 1 21/n 1 | 10.7382; 10.2853; 11.9959 90; 114.837; 90 | 1202.35 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation Green Chemistry, 2014, 16, 2266 |
| 7214307 | CIF | C10 H16 N2 O S2 | P 1 21/n 1 | 7.0242; 15.4761; 11.2508 90; 92.082; 90 | 1222.24 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation Green Chemistry, 2014, 16, 2266 |
| 7214308 | CIF | C10 H19 N2 O5 | P b c n | 12.1669; 12.065; 19.2806 90; 90; 90 | 2830.3 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation Green Chemistry, 2014, 16, 2266 |
| 7214309 | CIF | C23 H15 N O | P c a 21 | 22.439; 5.3555; 13.393 90; 90; 90 | 1609.5 | Rao, Yin; Li, Zhexian; Yin, Guodong Clean and efficient assembly of functionalized benzofuro[2,3-c]pyridines via metal-free one-pot domino reactions Green Chemistry, 2014, 16, 2213 |
| 7215076 | CIF | C23 H21 Cl N2 O2 | C 1 2/c 1 | 11.9856; 18.2571; 9.0361 90; 94.463; 90 | 1971.3 | Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S. CeIII-promoted oxidation. Efficient aerobic one-pot eco-friendly synthesis of oxidized bis(indol-3-yl)methanes and cyclic tetra(indolyl)dimethanes Green Chemistry, 2012, 14, 2912 |
| 7215077 | CIF | C28 H30 N2 O2 S2 | C 1 2/c 1 | 20.704; 12.3263; 21.8634 90; 113.463; 90 | 5118.3 | Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S. CeIII-promoted oxidation. Efficient aerobic one-pot eco-friendly synthesis of oxidized bis(indol-3-yl)methanes and cyclic tetra(indolyl)dimethanes Green Chemistry, 2012, 14, 2912 |
| 7215078 | CIF | C27 H28 N3 O2 P S | P 1 21/c 1 | 9.7499; 30.5632; 8.5329 90; 101.967; 90 | 2487.44 | Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings Green Chemistry, 2012, 14, 2807 |
| 7215079 | CIF | C28 H30 N3 O2 P S | P 1 21/c 1 | 16.0609; 18.7305; 8.9676 90; 98.481; 90 | 2668.2 | Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings Green Chemistry, 2012, 14, 2807 |
| 7215080 | CIF | C21 H23 N2 O2 P S | P -1 | 8.7642; 10.8437; 12.1558 94.396; 106.808; 109.396 | 1023.87 | Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings Green Chemistry, 2012, 14, 2807 |
| 7215081 | CIF | C25 H56 Cl6 N8 O5 P4 Pd2 S2 | P 1 21/c 1 | 12.8415; 13.0797; 28.1381 90; 109.006; 90 | 4468.5 | García-Álvarez, Joaquín; Díez, Josefina; Vidal, Cristian Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water Green Chemistry, 2012, 14, 3190 |
| 7215082 | CIF | C17 H17 N3 O4 | P 1 21/n 1 | 11.6784; 5.6853; 23.4754 90; 96.479; 90 | 1548.7 | García-Álvarez, Joaquín; Díez, Josefina; Vidal, Cristian Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water Green Chemistry, 2012, 14, 3190 |
| 7215777 | CIF | C18 H24 N2 O3 Si | P -1 | 9.893; 10.366; 10.379 102.062; 105.681; 103.638 | 952.6 | Bellachioma, Gianfranco; Castrica, Luca; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi Catalyst- and solvent-free conditions as an environmentally benign approach to 4-aryl-3-cyano-hexahydro-4H-1,2-benzoxazine-2-oxides Green Chemistry, 2008, 10, 327 |
| 7215778 | CIF | C15 H16 N2 O2 | P 1 21/c 1 | 14.092; 8.462; 11.276 90; 96.819; 90 | 1335.1 | Bellachioma, Gianfranco; Castrica, Luca; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi Catalyst- and solvent-free conditions as an environmentally benign approach to 4-aryl-3-cyano-hexahydro-4H-1,2-benzoxazine-2-oxides Green Chemistry, 2008, 10, 327 |
| 7215812 | CIF | C11 H10 Br N O3 | P b c a | 12.936; 12.022; 14.578 90; 90; 90 | 2267.1 | Zou, You-Quan; Guo, Wei; Liu, Feng-Lei; Lu, Liang-Qiu; Chen, Jia-Rong; Xiao, Wen-Jing Visible-light-induced photocatalytic formyloxylation reactions of 3-bromooxindoles with water and DMF: the scope and mechanism Green Chemistry, 2014, 16, 3787 |
| 7216184 | CIF | C23 H19 N | P -1 | 9.2869; 9.636; 11.202 84.187; 72.065; 64.104 | 857.3 | Taheri, Amir; Liu, Changhui; Lai, Bingbing; Cheng, Cheng; Pan, Xiaojuan; Gu, Yanlong Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones Green Chemistry, 2014, 16, 3715 |
| 7216185 | CIF | C20 H19 N | P 1 21 1 | 7.859; 7.981; 23.406 90; 92.401; 90 | 1466.8 | Taheri, Amir; Liu, Changhui; Lai, Bingbing; Cheng, Cheng; Pan, Xiaojuan; Gu, Yanlong Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones Green Chemistry, 2014, 16, 3715 |
| 7216460 | CIF | C20 H20 Br N O4 | P 1 21/n 1 | 10.7001; 11.3758; 17.0795 90; 103.62; 90 | 2020.5 | Chennapuram, Madhu; Emmadi, Narender Reddy; Bingi, Chiranjeevi; Nanubolu, Jagadeesh Babu; Atmakur, Krishnaiah Group-assisted purification (GAP) chemistry for dihydrofurans: water as a medium for catalyst free synthesis in a one pot four component reaction Green Chemistry, 2014, 16, 3237 |
| 7216461 | CIF | C18 H18 N2 O3 | P 1 21/n 1 | 11.2762; 13.0441; 12.5041 90; 112.669; 90 | 1697.12 | Chennapuram, Madhu; Emmadi, Narender Reddy; Bingi, Chiranjeevi; Nanubolu, Jagadeesh Babu; Atmakur, Krishnaiah Group-assisted purification (GAP) chemistry for dihydrofurans: water as a medium for catalyst free synthesis in a one pot four component reaction Green Chemistry, 2014, 16, 3237 |
| 7216462 | CIF | C17 H15 N3 O | P 1 21/c 1 | 14.9957; 7.6225; 11.9828 90; 91.022; 90 | 1369.47 | Li, Wenjun; Du, Zhiyun; Huang, Jiayao; Jia, Qianfa; Zhang, Kun; Wang, Jian Direct access to 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of allyl ketones with azides Green Chemistry, 2014, 16, 3003 |
| 7216643 | CIF | C27 H26 N2 | P 1 21/c 1 | 7.4217; 23.8402; 11.7942 90; 99.776; 90 | 2056.5 | Yasmin, Lyzu; Eggers, Paul K.; Skelton, Brian W.; Stubbs, Keith A.; Raston, Colin L. Thin film microfluidic synthesis of fluorescent highly substituted pyridines Green Chemistry, 2014, 16, 3450 |
| 7216644 | CIF | C28 H30 Cl2 N3 P Ru | P b c a | 11.8935; 13.1976; 33.9681 90; 90; 90 | 5331.8 | Li, Wei; Xie, Jian-Hua; Yuan, Ming-Lei; Zhou, Qi-Lin Ruthenium complexes of tetradentate bipyridine ligands: highly efficient catalysts for the hydrogenation of carboxylic esters and lactones Green Chemistry, 2014, 16, 4081 |
| 7218341 | CIF | C26 H18 Cu N2 O10 | C 1 2/c 1 | 10.118; 11.051; 21.051 90; 99.029; 90 | 2324.6 | Kathalikkattil, Amal Cherian; Kim, Dong-Woo; Tharun, Jose; Soek, Han-Geul; Roshan, Roshith; Park, Dae-Won Aqueous-microwave synthesized carboxyl functional molecular ribbon coordination framework catalyst for the synthesis of cyclic carbonates from epoxides and CO2 Green Chemistry, 2014, 16, 1607 |
| 7229415 | CIF | C19 H19 N O | P 1 21/c 1 | 14.0947; 5.86763; 18.4634 90; 97.511; 90 | 1513.87 | Karu, Ramesh; Gedu, Satyanarayana Microwave assisted domino heck cyclization and alkynylation: synthesis of alkyne substituted dihydrobenzofurans Green Chemistry, 2018, 20, 369 |
| 7229581 | CIF | C15 H15 N O3 S | P 1 21/c 1 | 15.2479; 5.5541; 16.8079 90; 95.501; 90 | 1416.88 | Wang, Bin; Tang, Lin; Liu, Liyan; Li, Yanan; Yu, Yang; Wang, Zhiyong Base-mediated tandem sulfonylation and oximation of alkenes in water Green Chemistry, 2017 |
| 7229599 | CIF | C82 H78 F12 N2 O P6 Pd2 S4 | P -1 | 9.3104; 10.7032; 21.2565 86.197; 78.5; 88.333 | 2070.87 | Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James From recovered metal waste to high-performance palladium catalysts Green Chemistry, 2017 |
| 7229600 | CIF | C82 H78 F12 N2 O P6 Pd2 S4 | P 1 21/n 1 | 20.6104; 15.5218; 26.8129 90; 107.289; 90 | 8190.2 | Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James From recovered metal waste to high-performance palladium catalysts Green Chemistry, 2017 |
| 7229601 | CIF | C94 H88 F12 N2 O P6 Pd2 S4 | I 1 a 1 | 33.0045; 10.85381; 26.7343 90; 106.511; 90 | 9182 | Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James From recovered metal waste to high-performance palladium catalysts Green Chemistry, 2017 |
| 7229614 | CIF | C16 H15 N3 O5 | P -1 | 7.4889; 8.9633; 12.2743 98.953; 106.482; 98.679 | 763.71 | Qiao, Kai; Yuan, Xin; Wan, Li; Zheng, Mingwei; Zhang, Dong; Fan, Bingbing; Di, Zhechen; Fang, Zheng; Guo, Kai Highly efficient synthesis of β-nitrate ester carboxamides through the ring-opening of 2-oxazolines Green Chemistry, 2017 |
| 7229619 | CIF | C9 H8 Cl2 O2 S | P 1 21 1 | 7.3712; 10.3338; 13.8683 90; 93.683; 90 | 1054.2 | Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L. Organic oxidations promoted in vortex driven thin films under continuous flow Green Chemistry, 2018, 20, 118 |
| 7229620 | CIF | C14 H18 O2 S | P 1 21/n 1 | 7.8477; 7.955; 20.8582 90; 96.801; 90 | 1292.98 | Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L. Organic oxidations promoted in vortex driven thin films under continuous flow Green Chemistry, 2018, 20, 118 |
| 7229621 | CIF | C22 H16 F N | P b c a | 19.293; 7.2555; 23.177 90; 90; 90 | 3244.3 | Ahmed, Waqar; Zhang, Sheng; Yu, Xiaoqiang; Yamamoto, Yoshinori; Bao, Ming Brønsted acid-catalyzed metal- and solvent-free quinoline synthesis fromN-alkyl anilines and alkynes or alkenes Green Chemistry, 2018, 20, 261 |
| 7229669 | CIF | C39 H31 N O2 P2 | P 1 21/n 1 | 11.651; 11.814; 23.05 90; 101.391; 90 | 3110.2 | Wen, Li-Rong; Sun, Yong-Xu; Zhang, Jin-Wei; Guo, Wei-Si; Li, Ming Catalyst- and solvent-free bisphosphinylation of isothiocyanates: a practical method for the synthesis of bisphosphinoylaminomethanes Green Chemistry, 2018, 20, 125 |
| 7229731 | CIF | C20 H20 O2 S | P n m a | 6.2278; 37.44; 7.3546 90; 90; 90 | 1714.9 | Nguyen, Thanh Binh; Retailleau, Pascal Sulfurative self-condensation of ketones and elemental sulfur: a three-component access to thiophenes catalyzed by aniline acid‒base conjugate pairs Green Chemistry, 2018, 20, 387 |
| 7229831 | CIF | C42 H33 N3 O | P -1 | 10.822; 12.45; 13.434 68.323; 84.539; 77.041 | 1639 | Albaladejo, María José; González-Soria, María José; Alonso, Francisco Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes Green Chemistry, 2018, 20, 701 |
| 7229832 | CIF | C44 H37 N3 O3 | P -1 | 12.1335; 12.3113; 12.6442 87.101; 86.513; 69.271 | 1762.4 | Albaladejo, María José; González-Soria, María José; Alonso, Francisco Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes Green Chemistry, 2018, 20, 701 |
| 7229843 | CIF | C11 H6 O2 | P -1 | 3.7722; 8.864; 25.643 86.384; 89.405; 81.479 | 846.27 | Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide Green Chemistry, 2018, 20, 989 |
| 7229844 | CIF | C11 H5 O2 | P 1 21/c 1 | 3.8398; 6.201; 35.222 90; 91.034; 90 | 838.5 | Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide Green Chemistry, 2018, 20, 989 |
| 7229845 | CIF | C32 H25 N O4 S2 Se3 | P 1 21/n 1 | 17.114; 11.241; 18.622 90; 116.978; 90 | 3192.6 | Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides Green Chemistry, 2018, 20, 604 |
| 7229846 | CIF | C32 H25 N O4 S2 Se2 | P -1 | 9.3039; 11.2838; 15.363 110.126; 99.341; 93.707 | 1481.6 | Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides Green Chemistry, 2018, 20, 604 |
| 7230013 | CIF | C18 H33 Mo12 N6 O40 P | P -1 | 14.9687; 15.0798; 21.8498 86.944; 88.681; 85.622 | 4909.8 | Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship Green Chemistry, 2018, 20, 1042 |
| 7230014 | CIF | C24 H45 Mo12 N6 O40 P | P -1 | 12.9158; 21.2163; 21.6946 95.876; 105.285; 101.08 | 5553.7 | Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship Green Chemistry, 2018, 20, 1042 |
| 7230015 | CIF | C30 H57 Mo12 N6 O40 P | P b c a | 22.3846; 20.969; 26.0718 90; 90; 90 | 12237.7 | Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship Green Chemistry, 2018, 20, 1042 |
| 7230209 | CIF | C7 H22 O3 Si3 | P -4 21 c | 17.5199; 17.5199; 10.0567 90; 90; 90 | 3086.9 | Arzumanyan, Ashot V.; Goncharova, Irina K.; Novikov, Roman A.; Milenin, Sergey A.; Boldyrev, Konstantin L.; Solyev, Pavel N.; Tkachev, Yaroslav V.; Volodin, Alexander D.; Smol'yakov, Alexander F.; Korlyukov, Alexander A.; Muzafarov, Aziz M. Aerobic Co or Cu/NHPI-catalyzed oxidation of hydride siloxanes: synthesis of siloxanols Green Chemistry, 2018, 20, 1467 |
| 7230285 | CIF | C24 H19 N O | P -1 | 9.4619; 9.7534; 10.5387 68.185; 78.205; 88.782 | 882.26 | Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones Green Chemistry, 2018, 20, 2007 |
| 7230286 | CIF | C25 H19 Cl3 N2 | P 1 21/c 1 | 10.6279; 15.8991; 13.4801 90; 100.33; 90 | 2240.9 | Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones Green Chemistry, 2018, 20, 2007 |
| 7230301 | CIF | C16 H24 O3 | P -1 | 6.0145; 8.0625; 16.0814 96.122; 94.613; 100.073 | 759.5 | Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process Green Chemistry, 2018, 20, 1998 |
| 7230302 | CIF | C17 H26 O3 | P 1 21/c 1 | 15.6175; 8.4961; 12.67 90; 96.193; 90 | 1671.3 | Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process Green Chemistry, 2018, 20, 1998 |
| 7230303 | CIF | C36 H56 O6 | P 1 21/c 1 | 12.9802; 8.6558; 32.2944 90; 94.115; 90 | 3619.1 | Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process Green Chemistry, 2018, 20, 1998 |
| 7230313 | CIF | C18 H29 Cl2 Ir N4 O2 | P -1 | 9.1521; 9.681; 11.7658 88.195; 86.069; 89.089 | 1039.4 | Lu, Sheng-Mei; Wang, Zhijun; Wang, Jijie; Li, Jun; Li, Can Hydrogen generation from formic acid decomposition on a highly efficient iridium catalyst bearing a diaminoglyoxime ligand Green Chemistry, 2018, 20, 1835 |
| 7230342 | CIF | C22 H25 N5 O4 | P -1 | 9.324; 9.76; 12.772 75.736; 70.173; 77.227 | 1047.6 | Zhang, Furen; Li, Chunmei; Liang, Xuezheng Solid acid-catalyzed domino cyclization reaction: regio- and diastereoselective synthesis of pyrido[2,3-d]pyrimidine derivatives bearing three contiguous stereocenters Green Chemistry, 2018, 20, 2057 |
| 7230380 | CIF | C116 H88 Cl6 N8 | C 1 2/c 1 | 43.317; 23.984; 28.932 90; 117.762; 90 | 26598 | Ishizuka, Tomoya; Ohkawa, Shumpei; Ochiai, Hidemi; Hashimoto, Muneaki; Ohkubo, Kei; Kotani, Hiroaki; Sadakane, Masahiro; Fukuzumi, Shunichi; Kojima, Takahiko A supramolecular photocatalyst composed of a polyoxometalate and a photosensitizing water-soluble porphyrin diacid for the oxidation of organic substrates in water Green Chemistry, 2018, 20, 1975 |
| 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 |
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