Crystallography Open Database

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7212127 CIFC7 H15 N O3P 1 21/n 16.6199; 13.9451; 9.2587
90; 101.76; 90
836.78Smiglak, 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 CIFC18 H20 N2 O2P 1 21 18.4078; 8.3744; 11.4399
90; 98.698; 90
796.22Jida, 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 CIFC12 H17 N O4C 1 2 117.5352; 7.6758; 10.0025
90; 113.78; 90
1232Jida, 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 CIFC20 H15 N O2C 1 2/c 122.045; 9.268; 17.8038
90; 124.751; 90
2988.74Raihan, 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 CIFC15 H17 N O6P 1 21/n 17.1337; 26.8903; 7.6505
90; 90.614; 90
1467.49Raihan, 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 CIFC13 H13 N O2P c a b9.1168; 13.8294; 17.2443
90; 90; 90
2174.16Raihan, 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 CIFC11 H13 N O5P 21 21 218.449; 11.2583; 12.0738
90; 90; 90
1148.5Raihan, 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 CIFC13 H16 O2P 1 21/n 113.286; 5.6083; 15.808
90; 95.142; 90
1173.1Liu, 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 CIFC13 H17 N O2P -15.7313; 11.8701; 18.407
72.324; 85.809; 79.963
1174.6Feng, 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 CIFC48 H32 F8 N12 Ru2P 1 21/c 19.6596; 38.8963; 12.5248
90; 102.989; 90
4585.4Herrero, 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 CIFC48 H93 Cl5 Cu2 N6P -18.8041; 12.5714; 25.282
89.005; 89.757; 86.052
2791.1Stricker, 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 CIFC60 H112 Cu F6 N8 PP -111.7007; 13.6056; 21.043
91.893; 94.239; 100.766
3278.2Stricker, 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 CIFC90 H168 Cu6 I6 N12P -19.7553; 13.5795; 20.6572
106.873; 94.154; 95.814
2590.3Stricker, 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 CIFC64 H124 Br8 Cu4 N8P -110.3068; 16.172; 25.595
73.875; 87.515; 87.742
4092.9Stricker, 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 CIFC30 H56 Br2 Cu2 N4P -19.002; 9.454; 20.757
85.74; 87.75; 78.95
1728.4Stricker, 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 CIFC22 H19 N O2P -19.2376; 14.5788; 14.9383
66.775; 74.994; 74.785
1756.3Zhou, 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 CIFC14 H14 B Bi F4 O SP 1 21/c 113.8004; 11.5529; 9.8253
90; 93.005; 90
1564.34Qiu, 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 CIFC20 H26 O4 SP 21 21 219.3439; 13.2412; 15.8279
90; 90; 90
1958.3Rosini, 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 CIFC26 H26 F2 N2 O6 SP 1 21/c 114.6241; 20.681; 8.745
90; 90.538; 90
2644.7Ma, 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 CIFC20 H44 Cu F6 N8 O4 P5 S2P -110.4612; 11.6733; 15.4745
80.696; 70.225; 83.182
1750.69García-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 CIFC15 H12 I N3 SP 1 21/c 114.5177; 7.2359; 14.3593
90; 101.588; 90
1477.68García-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 CIFC20 H22 F3 N2 O4.5R -3 :H35.238; 35.238; 8.3319
90; 90; 120
8959.8Yan, 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 CIFK0.7 Na0.3 Nb O3A m m 23.970162; 5.67111; 5.69467
90; 90; 90
128.217Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212940 CIFK0.7 Na0.3 Nb O3A m m 23.96867; 5.67069; 5.69626
90; 90; 90
128.195Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212941 CIFK0.7 Na0.3 Nb O3A m m 23.97024; 5.662; 5.68624
90; 90; 90
127.82Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212942 CIFK0.7 Na0.3 Nb O3A m m 23.96136; 5.65428; 5.68474
90; 90; 90
127.33Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212943 CIFK0.93 Na0.07 Nb O3A m m 23.98381; 5.689; 5.70757
90; 90; 90
129.356Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212944 CIFK0.903 Na0.097 Nb O3A m m 23.981973; 5.68731; 5.70733
90; 90; 90
129.252Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212945 CIFK0.86 Na0.14 Nb O3A m m 23.977443; 5.68725; 5.70678
90; 90; 90
129.091Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212946 CIFK0.84 Na0.16 Nb O3A m m 23.973479; 5.68046; 5.70266
90; 90; 90
128.716Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212947 CIFK0.83 Na0.17 Nb O3A m m 23.973479; 5.68046; 5.70266
90; 90; 90
128.716Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212948 CIFK0.77 Na0.23 Nb O3A m m 23.972623; 5.68015; 5.7037
90; 90; 90
128.705Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212949 CIFK0.73 Na0.27 Nb O3A m m 23.97304; 5.67576; 5.69703
90; 90; 90
128.468Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212950 CIFK0.75 Na0.25 Nb O3A m m 23.970626; 5.67573; 5.69855
90; 90; 90
128.424Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212951 CIFK0.72 Na0.28 Nb O3A m m 23.96953; 5.6731; 5.69719
90; 90; 90
128.298Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7214116 CIFC25 H19 N O5P 1 21/c 120.6371; 11.0516; 20.5751
90; 119.356; 90
4090Muthusaravanan, 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 CIFC9 H21 N O3P c c n14.5983; 20.935; 8.5228
90; 90; 90
2604.7Vanderveen, Jesse R.; Durelle, Jeremy; Jessop, Philip G.
Design and evaluation of switchable-hydrophilicity solvents
Green Chemistry, 2014, 16, 1187
7214118 CIFC20 H14 N2 O3P 1 21/c 19.0629; 11.2174; 16.215
90; 104.835; 90
1593.5Das, 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 CIFC21 H16 N2 OP 1 21 110.0929; 6.337; 12.8314
90; 100.192; 90
807.73Das, 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 CIFC26 H17 N O5P -16.937; 11.638; 13.019
75.535; 89.874; 76.165
986.4Das, 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 CIFC22 H27 N3 O3P -18.6867; 11.0032; 12.0059
70.06; 84.209; 76.001
1046.5Das, 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 CIFC7 H5 Br2 O2 ReP 1 21/m 16.892; 8.967; 8.538
90; 112.7; 90
486.8Hernández, 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 CIFC7 H5 Br2 O2 ReP 1 21/m 16.34; 12.504; 6.4937
90; 109.161; 90
486.27Hernández, 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 CIFC7 H5 Cl2 O2 ReP 1 21/m 16.2456; 12.2155; 6.2656
90; 106.932; 90
457.3Hernández, 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 CIFC7 H5 I2 O2 ReC 1 2/m 113.389; 9.29; 9.128
90; 107.669; 90
1081.8Hernández, 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 CIFC23 H20 N2P 21 21 2110.2819; 10.7707; 15.6284
90; 90; 90
1730.7Solan, 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 CIFC28 H31 Cl N2 OP 1 21/n 15.7713; 16.573; 25.145
90; 92.354; 90
2403Solan, 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 CIFC8 H20 N2 O4P n a 2111.0906; 14.6981; 7.6029
90; 90; 90
1239.35Qi, 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 CIFC40 H86 Mo N2 O10P -19.7003; 10.0807; 26.1807
88.397; 82.073; 69.855
2379.99Chakravarthy, 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 CIFC10 H16 N2 O S2P 1 21/n 110.7382; 10.2853; 11.9959
90; 114.837; 90
1202.35Wang, 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 CIFC10 H16 N2 O S2P 1 21/n 17.0242; 15.4761; 11.2508
90; 92.082; 90
1222.24Wang, 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 CIFC10 H19 N2 O5P b c n12.1669; 12.065; 19.2806
90; 90; 90
2830.3Wang, 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 CIFC23 H15 N OP c a 2122.439; 5.3555; 13.393
90; 90; 90
1609.5Rao, 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 CIFC23 H21 Cl N2 O2C 1 2/c 111.9856; 18.2571; 9.0361
90; 94.463; 90
1971.3Silveira, 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 CIFC28 H30 N2 O2 S2C 1 2/c 120.704; 12.3263; 21.8634
90; 113.463; 90
5118.3Silveira, 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 CIFC27 H28 N3 O2 P SP 1 21/c 19.7499; 30.5632; 8.5329
90; 101.967; 90
2487.44Keller, 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 CIFC28 H30 N3 O2 P SP 1 21/c 116.0609; 18.7305; 8.9676
90; 98.481; 90
2668.2Keller, 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 CIFC21 H23 N2 O2 P SP -18.7642; 10.8437; 12.1558
94.396; 106.808; 109.396
1023.87Keller, 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 CIFC25 H56 Cl6 N8 O5 P4 Pd2 S2P 1 21/c 112.8415; 13.0797; 28.1381
90; 109.006; 90
4468.5García-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 CIFC17 H17 N3 O4P 1 21/n 111.6784; 5.6853; 23.4754
90; 96.479; 90
1548.7García-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 CIFC18 H24 N2 O3 SiP -19.893; 10.366; 10.379
102.062; 105.681; 103.638
952.6Bellachioma, 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 CIFC15 H16 N2 O2P 1 21/c 114.092; 8.462; 11.276
90; 96.819; 90
1335.1Bellachioma, 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 CIFC11 H10 Br N O3P b c a12.936; 12.022; 14.578
90; 90; 90
2267.1Zou, 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 CIFC23 H19 NP -19.2869; 9.636; 11.202
84.187; 72.065; 64.104
857.3Taheri, 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 CIFC20 H19 NP 1 21 17.859; 7.981; 23.406
90; 92.401; 90
1466.8Taheri, 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 CIFC20 H20 Br N O4P 1 21/n 110.7001; 11.3758; 17.0795
90; 103.62; 90
2020.5Chennapuram, 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 CIFC18 H18 N2 O3P 1 21/n 111.2762; 13.0441; 12.5041
90; 112.669; 90
1697.12Chennapuram, 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 CIFC17 H15 N3 OP 1 21/c 114.9957; 7.6225; 11.9828
90; 91.022; 90
1369.47Li, 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 CIFC27 H26 N2P 1 21/c 17.4217; 23.8402; 11.7942
90; 99.776; 90
2056.5Yasmin, 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 CIFC28 H30 Cl2 N3 P RuP b c a11.8935; 13.1976; 33.9681
90; 90; 90
5331.8Li, 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 CIFC26 H18 Cu N2 O10C 1 2/c 110.118; 11.051; 21.051
90; 99.029; 90
2324.6Kathalikkattil, 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 CIFC19 H19 N OP 1 21/c 114.0947; 5.86763; 18.4634
90; 97.511; 90
1513.87Karu, Ramesh; Gedu, Satyanarayana
Microwave assisted domino heck cyclization and alkynylation: synthesis of alkyne substituted dihydrobenzofurans
Green Chemistry, 2018, 20, 369
7229581 CIFC15 H15 N O3 SP 1 21/c 115.2479; 5.5541; 16.8079
90; 95.501; 90
1416.88Wang, 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 CIFC82 H78 F12 N2 O P6 Pd2 S4P -19.3104; 10.7032; 21.2565
86.197; 78.5; 88.333
2070.87Jantan, 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 CIFC82 H78 F12 N2 O P6 Pd2 S4P 1 21/n 120.6104; 15.5218; 26.8129
90; 107.289; 90
8190.2Jantan, 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 CIFC94 H88 F12 N2 O P6 Pd2 S4I 1 a 133.0045; 10.85381; 26.7343
90; 106.511; 90
9182Jantan, 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 CIFC16 H15 N3 O5P -17.4889; 8.9633; 12.2743
98.953; 106.482; 98.679
763.71Qiao, 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 CIFC9 H8 Cl2 O2 SP 1 21 17.3712; 10.3338; 13.8683
90; 93.683; 90
1054.2Pye, 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 CIFC14 H18 O2 SP 1 21/n 17.8477; 7.955; 20.8582
90; 96.801; 90
1292.98Pye, 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 CIFC22 H16 F NP b c a19.293; 7.2555; 23.177
90; 90; 90
3244.3Ahmed, 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 CIFC39 H31 N O2 P2P 1 21/n 111.651; 11.814; 23.05
90; 101.391; 90
3110.2Wen, 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 CIFC20 H20 O2 SP n m a6.2278; 37.44; 7.3546
90; 90; 90
1714.9Nguyen, 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 CIFC42 H33 N3 OP -110.822; 12.45; 13.434
68.323; 84.539; 77.041
1639Albaladejo, 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 CIFC44 H37 N3 O3P -112.1335; 12.3113; 12.6442
87.101; 86.513; 69.271
1762.4Albaladejo, 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 CIFC11 H6 O2P -13.7722; 8.864; 25.643
86.384; 89.405; 81.479
846.27Chen, 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 CIFC11 H5 O2P 1 21/c 13.8398; 6.201; 35.222
90; 91.034; 90
838.5Chen, 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 CIFC32 H25 N O4 S2 Se3P 1 21/n 117.114; 11.241; 18.622
90; 116.978; 90
3192.6Wang, 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 CIFC32 H25 N O4 S2 Se2P -19.3039; 11.2838; 15.363
110.126; 99.341; 93.707
1481.6Wang, 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 CIFC18 H33 Mo12 N6 O40 PP -114.9687; 15.0798; 21.8498
86.944; 88.681; 85.622
4909.8Megías-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 CIFC24 H45 Mo12 N6 O40 PP -112.9158; 21.2163; 21.6946
95.876; 105.285; 101.08
5553.7Megías-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 CIFC30 H57 Mo12 N6 O40 PP b c a22.3846; 20.969; 26.0718
90; 90; 90
12237.7Megías-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 CIFC7 H22 O3 Si3P -4 21 c17.5199; 17.5199; 10.0567
90; 90; 90
3086.9Arzumanyan, 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 CIFC24 H19 N OP -19.4619; 9.7534; 10.5387
68.185; 78.205; 88.782
882.26Teng, 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 CIFC25 H19 Cl3 N2P 1 21/c 110.6279; 15.8991; 13.4801
90; 100.33; 90
2240.9Teng, 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 CIFC16 H24 O3P -16.0145; 8.0625; 16.0814
96.122; 94.613; 100.073
759.5Wang, 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 CIFC17 H26 O3P 1 21/c 115.6175; 8.4961; 12.67
90; 96.193; 90
1671.3Wang, 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 CIFC36 H56 O6P 1 21/c 112.9802; 8.6558; 32.2944
90; 94.115; 90
3619.1Wang, 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 CIFC18 H29 Cl2 Ir N4 O2P -19.1521; 9.681; 11.7658
88.195; 86.069; 89.089
1039.4Lu, 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 CIFC22 H25 N5 O4P -19.324; 9.76; 12.772
75.736; 70.173; 77.227
1047.6Zhang, 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 CIFC116 H88 Cl6 N8C 1 2/c 143.317; 23.984; 28.932
90; 117.762; 90
26598Ishizuka, 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

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