Crystallography Open Database

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Searching journal of publication like 'Organic & biomolecular chemistry' volume of publication is 2

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7153546 CIFC24 H18 O2P c a 217.7959; 20.639; 11.0953
90; 90; 90		1785.2Pathak, Rakhi; Vandayar, Kantharuby; van Otterlo, Willem A. L.; Michael, Joseph P.; Fernandes, Manuel A.; de Koning, Charles B.
The synthesis of angularly fused polyaromatic compounds by using a light-assisted, base-mediated cyclization reaction
Organic & Biomolecular Chemistry, 2004, 2, 3504-3509
7153545 CIFC74 H42 Cl3 N5 ZnP -112.6459; 15.6657; 16.2904
92.816; 111.014; 109.678		2783.2Shen, Zhen; Uno, Hidemitsu; Shimizu, Yusuke; Ono, Noboru
Controlling conformations and physical properties of meso-tetrakis(phenylethynyl)porphyrins by ring fusion: synthesis, properties and structural characterizations
Organic & Biomolecular Chemistry, 2004, 2, 3442-3447
7153544 CIFC78 H60 N4 O2 ZnC 1 2/c 130.864; 11.647; 18.709
90; 117.893; 90		5944Shen, Zhen; Uno, Hidemitsu; Shimizu, Yusuke; Ono, Noboru
Controlling conformations and physical properties of meso-tetrakis(phenylethynyl)porphyrins by ring fusion: synthesis, properties and structural characterizations
Organic & Biomolecular Chemistry, 2004, 2, 3442-3447
7153543 CIFC68 H62 N4P -110.785; 14.2; 17.438
94.857; 102.039; 90.567		2601.4Shen, Zhen; Uno, Hidemitsu; Shimizu, Yusuke; Ono, Noboru
Controlling conformations and physical properties of meso-tetrakis(phenylethynyl)porphyrins by ring fusion: synthesis, properties and structural characterizations
Organic & Biomolecular Chemistry, 2004, 2, 3442-3447
7153542 CIFC56 H78 F12 N8 O12 P2P 1 21/c 18.04; 28.57; 13.42
90; 93.41; 90		3077Cruz, Carla; Delgado, Rita; Drew, Michael G. B.; F�lix, V�tor
Supramolecular aggregates between carboxylate anions and an octaaza macrocyclic receptor
Organic & Biomolecular Chemistry, 2004, 2, 2911-2918
7153541 CIFC44 H70 F12 N8 O12 P2P -110.818; 11.701; 12.827
105.1; 101.25; 115.44		1325Cruz, Carla; Delgado, Rita; Drew, Michael G. B.; F�lix, V�tor
Supramolecular aggregates between carboxylate anions and an octaaza macrocyclic receptor
Organic & Biomolecular Chemistry, 2004, 2, 2911-2918
7153540 CIFC17 H19 N O4P 1 21/a 17.309; 15.546; 13.8909
90; 104.34; 90		1529.2Ando, Kumiko; Tsuji, Eriko; Ando, Yuko; Kunitomo, Jun-ichi; Yamashita, Masayuki; Ohta, Shunsaku; Nabe, Takeshi; Kohno, Shigekatsu; Yokomizo, Takehiko; Shimizu, Takao; Ohishi, Yoshitaka
Preparation of 2- and 4-(2-alkylcarbamoyl-1-methylvinyl)-7-alkyloxybenzo[b]furans having potent antagonistic activity against human leukotriene B4 BLT1 and/or BLT2 receptors
Organic & Biomolecular Chemistry, 2004, 2, 3427-3431
7153539 CIFC31 H31 N O4P -110.259; 16.12; 8.654
104.45; 105.78; 96.235		1309.5Ando, Kumiko; Tsuji, Eriko; Ando, Yuko; Kunitomo, Jun-ichi; Yamashita, Masayuki; Ohta, Shunsaku; Nabe, Takeshi; Kohno, Shigekatsu; Yokomizo, Takehiko; Shimizu, Takao; Ohishi, Yoshitaka
Preparation of 2- and 4-(2-alkylcarbamoyl-1-methylvinyl)-7-alkyloxybenzo[b]furans having potent antagonistic activity against human leukotriene B4 BLT1 and/or BLT2 receptors
Organic & Biomolecular Chemistry, 2004, 2, 3427-3431
7153538 CIFC19 H20 B F4 N O2P b c a14.1926; 14.1055; 18.319
90; 90; 90		3667.3Moncada, Margarida C.; Fern�ndez, Dami�n; Lima, Jo�o C.; Parola, A. Jorge; Lodeiro, Carlos; Folgosa, Filipe; Melo, M. Jo�o; Pina, Fernando
Multistate properties of 7-(N,N-diethylamino)-4?-hydroxyflavylium. An example of an unidirectional reaction cycle driven by pH
Organic & Biomolecular Chemistry, 2004, 2, 2802-2808
7153537 CIFC24 H37 N3 O4 S2P 21 21 2110.752; 11.183; 21.829
90; 90; 90		2624.7Scheuermann, J. Erik W.; Sibbons, Kevin F.; Benoit, David M.; Motevalli, Majid; Watkinson, Michael
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanesElectronic supplementary information (ESI) available: Molecular modelling methodology. Figs. S1?S4: Lowest energy conformation calculated for the protonated form of 6b, 6b�HOAc, the protonated form of 6a and 6a�HOAc. Figs. S5 and S6: Charge distribution calculated for the protonated forms of 6a and 6b. See http://www.rsc.org/suppdata/ob/b4/b409259g/
Organic & Biomolecular Chemistry, 2004, 2, 2664-2670
7153536 CIFC28 H41 N3 O5 S2P 21 21 217.476; 14.31; 26.388
90; 90; 90		2823.03Scheuermann, J. Erik W.; Sibbons, Kevin F.; Benoit, David M.; Motevalli, Majid; Watkinson, Michael
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanesElectronic supplementary information (ESI) available: Molecular modelling methodology. Figs. S1?S4: Lowest energy conformation calculated for the protonated form of 6b, 6b�HOAc, the protonated form of 6a and 6a�HOAc. Figs. S5 and S6: Charge distribution calculated for the protonated forms of 6a and 6b. See http://www.rsc.org/suppdata/ob/b4/b409259g/
Organic & Biomolecular Chemistry, 2004, 2, 2664-2670
7153535 CIFC25.17 H40.5 N4.17 O2.33P -113.0112; 17.31; 17.729
88.46; 81.647; 88.021		3947.3El Drubi Vega, Ismael; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Anion binding properties of 5,5?-dicarboxamido-dipyrrolylmethanes
Organic & Biomolecular Chemistry, 2004, 2, 2935-2941
7153534 CIFC23 H35 N3 O3P 1 21/c 113.788; 17.251; 9.9242
90; 107.786; 90		2247.7El Drubi Vega, Ismael; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Anion binding properties of 5,5?-dicarboxamido-dipyrrolylmethanes
Organic & Biomolecular Chemistry, 2004, 2, 2935-2941
7153533 CIFC30 H36 N4 O3P 21 21 2111.1668; 11.7777; 20.32
90; 90; 90		2672.47El Drubi Vega, Ismael; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Anion binding properties of 5,5?-dicarboxamido-dipyrrolylmethanes
Organic & Biomolecular Chemistry, 2004, 2, 2935-2941
7153532 CIFC23 H34 N2 OP 1 21 19.1902; 14.444; 15.8727
90; 94.398; 90		2100.8Whitby, Richard J.; Gustaf Saluste, C.; Furber, Mark
Synthesis of ?-iminoimidates by palladium catalysed double isonitrile insertion
Organic & Biomolecular Chemistry, 2004, 2, 1974-1976
7153531 CIFC17 H23 N O4 SP 21 21 218.23; 9.09; 22.57
90; 90; 90		1688Wang, Libo; Nakamura, Shuichi; Toru, Takeshi
Highly enantioselective reaction of lithiated N-Boc-thiazolidine: a new chiral formyl anion equivalent
Organic & Biomolecular Chemistry, 2004, 2, 2168-2169
7153530 CIFC23 H19 Cl3 N4 O SP 1 21/c 16.1798; 26.851; 13.65
90; 92.26; 90		2263.2Hughes, Gregory; Kreher, David; Wang, Changsheng; Batsanov, Andrei S.; Bryce, Martin R.
Ethynyl ?-extended 2,5-diphenyl-1,3,4-oxadiazoles and 2-phenyl 5-(2-thienyl)-1,3,4-oxadiazoles: synthesis, X-ray crystal structures and optical properties
Organic & Biomolecular Chemistry, 2004, 2, 3363-3367
7153529 CIFC26 H20 N2 O SP -16.345; 6.985; 23.672
94.24; 91.96; 91.93		1045Hughes, Gregory; Kreher, David; Wang, Changsheng; Batsanov, Andrei S.; Bryce, Martin R.
Ethynyl ?-extended 2,5-diphenyl-1,3,4-oxadiazoles and 2-phenyl 5-(2-thienyl)-1,3,4-oxadiazoles: synthesis, X-ray crystal structures and optical properties
Organic & Biomolecular Chemistry, 2004, 2, 3363-3367
7153528 CIFC24 H20 N2 O SP -16.1665; 6.9748; 22.943
83.55; 84.09; 83.67		970.45Hughes, Gregory; Kreher, David; Wang, Changsheng; Batsanov, Andrei S.; Bryce, Martin R.
Ethynyl ?-extended 2,5-diphenyl-1,3,4-oxadiazoles and 2-phenyl 5-(2-thienyl)-1,3,4-oxadiazoles: synthesis, X-ray crystal structures and optical properties
Organic & Biomolecular Chemistry, 2004, 2, 3363-3367
7153527 CIFC24 H20 N4 OP 1 21/a 122.881; 6.314; 28.86
90; 109.86; 90		3921.4Hughes, Gregory; Kreher, David; Wang, Changsheng; Batsanov, Andrei S.; Bryce, Martin R.
Ethynyl ?-extended 2,5-diphenyl-1,3,4-oxadiazoles and 2-phenyl 5-(2-thienyl)-1,3,4-oxadiazoles: synthesis, X-ray crystal structures and optical properties
Organic & Biomolecular Chemistry, 2004, 2, 3363-3367

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