# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2024-05-20T20:32:36+02:00
# Query:
# SELECT data.*
# FROM
#  data JOIN jaltnames
#  ON altname = journal
# WHERE
#  (status is null or status != 'retracted') and
#  (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'Organic & Biomolecular Chemistry') AND volume = 1 AND duplicateof IS NULL AND (status is NULL OR status != 'errors') AND (method is NULL OR method != 'theoretical'))
# ORDER BY file asc
file,a,siga,b,sigb,c,sigc,alpha,sigalpha,beta,sigbeta,gamma,siggamma,vol,sigvol,celltemp,sigcelltemp,diffrtemp,sigdiffrtemp,cellpressure,sigcellpressure,diffrpressure,sigdiffrpressure,thermalhist,pressurehist,compoundsource,nel,sg,sgHall,sgNumber,commonname,chemname,mineral,formula,calcformula,cellformula,Z,Zprime,acce_code,authors,title,journal,year,volume,issue,firstpage,lastpage,doi,method,radiation,wavelength,radType,radSymbol,Rall,Robs,Rref,wRall,wRobs,wRref,RFsqd,RI,gofall,gofobs,gofgt,gofref,duplicateof,optimal,status,flags,svnrevision,date,time,onhold
"7150447","17.511","0.005","14.597","0.003","22.804","0.005","90","","111.552","0.003","90","","5421","2","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C60 H72 O4 S2 -","- C60.004 H72 O4 S2 -","- C240.016 H288 O16 S8 -","4","1","","Zeng, Xianshun; Sun, Hao; Chen, Langxing; Leng, Xuebing; Xu, Fengbo; Li, Qinshan; He, Xiwen; Zhang, Wenqin; Zhang, Zheng-Zhi","Synthesis of a tweezer-like bis(arylthiaalkoxy)calix[4]arene as a cation sensor for ion-selective electrodes: an investigation of the influence of neighboring halogen atoms on cation selectivity","Organic & Biomolecular Chemistry","2003","1","6","1073","1079","10.1039/b211381c","","","0.71073","MoKα","","0.1864","0.0842","","","0.2423","0.3205","","","","","","1.013","","","","has coordinates,has disorder","180290","2020-10-21","18:00:00",""
"7150448","8.134","0.001","7.111","0.0008","12.699","0.002","90","","100.87","0.01","90","","721.34","0.17","100","2","100","2","","","","","","","","2","P 1 21/c 1","-P 2ybc","14","","octafluoro-1,2-dimethylenecyclobutane","","- C6 F8 -","- C6 F8 -","- C24 F32 -","4","1","","Lentz, Dieter; Patzschke, Mona; Bach, Ansgar; Scheins, Stephan; Luger, Peter","Experimental charge density of octafluoro-1,2-dimethylenecyclobutane: atomic volumes and charges in a perfluorinated hydrocarbon","Organic & Biomolecular Chemistry","2003","1","2","409","414","10.1039/b208704a","","","0.7107","MoKα","","","0.031","","","","0.041","","","","","","2.52","","","","has coordinates","274637","2022-04-22","16:02:08",""
"7150449","11.1034","0.0011","11.9818","0.0014","9.9624","0.0012","90","","109.214","0.008","90","","1251.6","0.3","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C27 H32 N2 O4 S -","- C27 H32 N2 O4 S -","- C54 H64 N4 O8 S2 -","2","1","","Miyabe, Hideto; Fujii, Kayoko; Naito, Takeaki","Radical addition to oxime ethers for asymmetric synthesis of β-amino acid derivatives","Organic & Biomolecular Chemistry","2003","1","2","381","","10.1039/b208823a","","","0.71069","MoKα","","0.0377","0.0297","","","0.0971","0.1054","","","","","","0.902","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150450","12.2395","0.0015","20.5642","0.0014","10.904","0.0016","90","","94.209","0.011","90","","2737.1","0.6","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C29 H38 N2 O4 S -","- C29 H38 N2 O4 S -","- C116 H152 N8 O16 S4 -","4","2","","Miyabe, Hideto; Fujii, Kayoko; Naito, Takeaki","Radical addition to oxime ethers for asymmetric synthesis of β-amino acid derivatives","Organic & Biomolecular Chemistry","2003","1","2","381","","10.1039/b208823a","","","1.54178","CuKα","","0.0507","0.0416","","","0.1229","0.1305","","","","","","0.97","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150451","7.688","0.0002","13.2934","0.0003","31.112","0.0009","90","","90","","90","","3179.64","0.14","180","2","180","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C32 H28 N8 O7 -","- C32 H28 N8 O7 -","- C128 H112 N32 O28 -","4","1","","Rosenbohm, Christoph; Christensen, Signe M.; Sørensen, Mads D.; Pedersen, Daniel Sejer; Larsen, Lotte-Emilie; Wengel, Jesper; Koch, Troels","Synthesis of 2'-amino-LNA: a new strategyElectronic supplementary information (ESI) available: further experimental details and the structure of compound S11 (.pdb file). See http://www.rsc.org/suppdata/ob/b2/b208864a/","Organic & Biomolecular Chemistry","2003","1","4","655","","10.1039/b208864a","","","0.71073","MoKα","","0.056","0.0427","","","0.0892","0.0964","","","","","","1.096","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150452","12.677","0.0002","12.7397","0.0002","13.0974","0.0002","102.147","0.001","95.218","0.001","91.166","0.001","2057.62","0.06","100","2","100","2","","","","","","","","4","P -1","-P 1","2","Compound X","","","- C18 H34 O5 Si -","- C18 H34 O5 Si -","- C72 H136 O20 Si4 -","4","2","","Johnston, Derek; Couché, Emmanuel; Edmonds, David J.; Muir, Kenneth W.; Procter, David J.","The first synthetic studies on pestalotiopsin A. A stereocontrolled approach to the functionalised bicyclic coreElectronic supplementary information (ESI) available: crystal structure analysis of 18a. See http://www.rsc.org/suppdata/ob/b2/b209066j/","Organic & Biomolecular Chemistry","2003","1","2","328","","10.1039/b209066j","","","0.71073","MoKα","","0.0492","0.0374","","","0.0871","0.0939","","","","","","1.04","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150453","12.368","0.003","17.711","0.004","21.575","0.004","90","","92.382","0.004","90","","4721.9","1.8","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","(2S)-2-((1R,8aR)-8a-methyl-1,2,3,4,6,7,8,8a-octahydro-1-naphthyl)propyl N-((1S)-1-(1-naphthyl)ethyl)carbamate","","- C27 H35 N O2 -","- C27 H35 N O2 -","- C216 H280 N8 O16 -","8","4","","Chen, Yong-Jun; Gao, Ling-Jie; Murad, Ibrahim; Verstuyf, Annemieke; Verlinden, Lieve; Verboven, Christel; Bouillon, Roger; Viterbo, Davide; Milanesio, Marco; Van Haver, Dirk; Vandewalle, Maurits; De Clercq, Pierre J.","Synthesis, biological activity, and conformational analysis of CD-ring modified trans-decalin 1α,25-dihydroxyvitamin D analogsElectronic supplementary information (ESI) available: Further experimental details. See http://www.rsc.org/suppdata/ob/b2/b209147j/","Organic & Biomolecular Chemistry","2003","1","2","257","","10.1039/b209147j","","","0.71073","MoKα","","0.0865","0.042","","","0.0867","0.112","","","","","","0.933","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150454","6.1182","0.0003","6.6921","0.0004","10.181","0.0005","90","","94.019","0.003","90","","415.82","0.04","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","Compound X","","","- C9 H14 O2 -","- C9 H14 O2 -","- C18 H28 O4 -","2","1","","Amelia García Fraile; David G. Morris; Antonio García Martínez; Santiago de la Moya Cerero; Kenneth W. Muir; Karl S. Ryder; Enrique Teso Vilar","Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols","Org. Biomol. Chem.","2003","1","4","700","704","10.1039/b209427d","","","0.71073","MoKα","","0.0541","0.0425","","","0.0878","0.0929","","","","","","1.042","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150455","5.9714","0.0001","20.5466","0.0005","22.5632","0.0006","90","","90","","90","","2768.32","0.11","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","Compound X","","","- C10 H16 O -","- C10 H16 O -","- C120 H192 O12 -","12","3","","Amelia García Fraile; David G. Morris; Antonio García Martínez; Santiago de la Moya Cerero; Kenneth W. Muir; Karl S. Ryder; Enrique Teso Vilar","Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols","Org. Biomol. Chem.","2003","1","4","700","704","10.1039/b209427d","","","0.71073","MoKα","","0.0671","0.0508","","","0.0996","0.1081","","","","","","1.087","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150456","10.7633","0.0001","10.7633","0.0001","31.3398","0.0005","90","","90","","90","","3630.67","0.08","100","2","100","2","","","","","","","","3","P 41 21 2","P 4abw 2nw","92","Compound X","","","- C10 H16 O -","- C10 H16 O -","- C160 H256 O16 -","16","2","","Amelia García Fraile; David G. Morris; Antonio García Martínez; Santiago de la Moya Cerero; Kenneth W. Muir; Karl S. Ryder; Enrique Teso Vilar","Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols","Org. Biomol. Chem.","2003","1","4","700","704","10.1039/b209427d","","","0.71073","MoKα","","0.0606","0.0482","","","0.1244","0.132","","","","","","1.046","","","","has coordinates,has disorder","176453","2020-10-21","18:00:00",""
"7150457","14.587","0.0002","7","0.0001","27.868","0.0004","90","","105.047","0.0011","90","","2748.01","0.07","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C48 H48 B20 N6 O4 -","- C48 H48 B20 N6 O4 -","- C96 H96 B40 N12 O8 -","2","0.5","","Frixa, Christophe; Mahon, Mary F.; Thompson, Andrew S.; Threadgill, Michael D.","Synthesis of meso-substituted porphyrins carrying carboranes and oligo(ethylene glycol) units for potential applications in boron neutron capture therapyElectronic supplementary information (ESI) available: experimental details for the synthesis of compounds 12‒15, 31 and 32. See http://www.rsc.org/suppdata/ob/b2/b209534c/","Organic & Biomolecular Chemistry","2003","1","2","306","","10.1039/b209534c","","","0.71073","MoKα","","0.1002","0.0757","","","0.2287","0.249","","","","","","1.019","","","","has coordinates,has disorder","180290","2020-10-21","18:00:00",""
"7150458","9.8532","0.0007","6.9944","0.0005","14.504","0.001","90","","105.737","0.003","90","","962.11","0.12","233","2","233","2","","","","","","","","5","P 1 21/m 1","-P 2yb","11","","","","- C22 H23 B F4 O -","- C22 H23 B F4 O -","- C44 H46 B2 F8 O2 -","2","0.5","","Laus, Gerhard; Schottenberger, Herwig; Wurst, Klaus; Schütz, Johannes; Ongania, Karl-Hans; Horvath, Ulrike Erika Ida; Schwärzler, Alexander","Solvatochromism, halochromism, and preferential solvation of new dipolar guaiazulenyl 1,4-benzoquinone methidesElectronic supplementary information (ESI) available: Absorption maxima of the dyes 6‒10 in seven binary solvent mixtures. See http://www.rsc.org/suppdata/ob/b2/b209555f/","Organic & Biomolecular Chemistry","2003","1","8","1409","","10.1039/b209555f","","","0.71073","MoKα","","0.0595","0.0423","","","0.0995","0.107","","","","","","1.048","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150459","14.324","0.0009","12.5501","0.0007","14.623","0.001","90","","100","0.003","90","","2588.8","0.3","228","2","228","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C30 H38 O -","- C30 H38 O -","- C120 H152 O4 -","4","1","","Laus, Gerhard; Schottenberger, Herwig; Wurst, Klaus; Schütz, Johannes; Ongania, Karl-Hans; Horvath, Ulrike Erika Ida; Schwärzler, Alexander","Solvatochromism, halochromism, and preferential solvation of new dipolar guaiazulenyl 1,4-benzoquinone methidesElectronic supplementary information (ESI) available: Absorption maxima of the dyes 6‒10 in seven binary solvent mixtures. See http://www.rsc.org/suppdata/ob/b2/b209555f/","Organic & Biomolecular Chemistry","2003","1","8","1409","","10.1039/b209555f","","","0.71073","MoKα","","0.0665","0.0505","","","0.1306","0.141","","","","","","1.028","","","","has coordinates,has disorder","213973","2020-10-21","18:00:00",""
"7150460","11.1081","0.0003","12.6796","0.0004","11.6659","0.0004","90","","101.259","0.0013","90","","1611.48","0.09","200","","","","","","","","","","Local laboratory","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H22 N2 O2 -","- C20 H22 N2 O2 -","- C80 H88 N8 O8 -","4","1","","Banwell, Martin G.; Edwards, Alison J.; Jolliffe, Katrina A.; Smith, Jason A.; Hamel, Ernest; Verdier-Pinard, Pascal","Total synthesis of (±)-rhazinal, an alkaloidal spindle toxin from Kopsia teoi","Organic & Biomolecular Chemistry","2003","1","2","296","","10.1039/b209992f","","","0.71073","MoKα","","","0.0973","","","","0.0854","","","","","","0.8346","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150461","9.3201","0.0004","12.5782","0.0004","17.9679","0.0004","90","","90","","90","","2106.38","0.12","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H23 N O7 -","- C22 H23 N O7 -","- C88 H92 N4 O28 -","4","1","","Anat Reizelman; Suzanne C. M. Wigchert; Cinzia del-Bianco; Binne Zwanenburg","Synthesis and bioactivity of labelled germination stimulants for the isolation and identification of the strigolactone receptor","Org. Biomol. Chem.","2003","1","6","950","959","10.1039/b210678g","","","1.54184","CuKα","","0.0484","0.0397","","0.1169","0.1094","0.1169","","","1.048","","","1.048","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150462","32.285","0.002","11.8982","0.0006","19.8475","0.0011","90","","90","","90","","7624.1","0.7","120","2","120","2","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C30 H21 N5 O6 -","- C30 H21 N5 O6 -","- C360 H252 N60 O72 -","12","1.5","","Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.","Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/","Organic & Biomolecular Chemistry","2003","1","4","741","","10.1039/b210848h","","","0.71073","MoKα","","0.3726","0.0941","","","0.1043","0.1634","","","","","","0.958","","","","has coordinates","180290","2020-10-21","18:00:00",""
"7150463","11.0659","0.0002","12.04","0.0002","15.9608","0.0004","84.462","0.001","81.333","0.001","64.306","0.001","1893.21","0.07","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C36 H36 N5 O9 S3 -","- C36 H36 N5 O9 S3 -","- C72 H72 N10 O18 S6 -","2","1","","Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.","Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/","Organic & Biomolecular Chemistry","2003","1","4","741","","10.1039/b210848h","","","0.71073","MoKα","","0.0675","0.0452","","","0.1118","0.1222","","","","","","1.022","","","","has coordinates,has disorder","180290","2020-10-21","18:00:00",""
"7150464","8.608","0.005","15.212","0.005","15.257","0.005","67.786","0.005","84.475","0.005","73.886","0.005","1776.8","1.3","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C34 H31 N7 O12 S2 -","- C34 H31 N7 O12 S2 -","- C68 H62 N14 O24 S4 -","2","1","","Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.","Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/","Organic & Biomolecular Chemistry","2003","1","4","741","","10.1039/b210848h","","","0.71069","MoKα","","0.1424","0.0559","","","0.0998","0.1242","","","","","","0.909","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150465","20.3034","0.0011","10.1636","0.0005","13.457","0.0006","90","","104.057","0.002","90","","2693.8","0.2","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C30 H19 N7 O10 -","- C30 H19 N7 O10 -","- C120 H76 N28 O40 -","4","1","","Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.","Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/","Organic & Biomolecular Chemistry","2003","1","4","741","","10.1039/b210848h","","","0.71073","MoKα","","0.1256","0.055","","","0.1074","0.1308","","","","","","0.928","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150466","13.408","0.005","15.847","0.005","17.023","0.005","73.042","0.005","74.733","0.005","68.046","0.005","3159.9","1.8","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C62 H90 Cl N9 O10 -","- C62 H90 Cl N9 O10 -","- C124 H180 Cl2 N18 O20 -","2","1","","Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.","Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/","Organic & Biomolecular Chemistry","2003","1","4","741","","10.1039/b210848h","","","0.71069","MoKα","","0.4834","0.133","","","0.1941","0.2967","","","","","","0.83","","","","has coordinates","180290","2020-10-21","18:00:00",""
"7150467","10.516","0.004","18.569","0.006","8.832","0.004","90","","100.21","0.04","90","","1697.3","1.2","122","0.5","122","0.5","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","1","4,6-bis(phenylseleno)-3-methoxyphenol","","- C19 H16 O2 Se2 -","- C19 H16 O2 Se2 -","- C76 H64 O8 Se8 -","4","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","Cu-Ka","","0.0325","0.0307","","","0.0787","0.0804","","","","","","1.076","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150468","7.2242","0.0015","7.9556","0.0011","11.007","0.002","83.594","0.014","73.236","0.016","86","0.014","601.47","0.19","122","0.5","122","0.5","","","","","","","","4","P -1","-P 1","2","2","2,3-dimethyl-4-(phenylseleno)phenol","","- C14 H14 O Se -","- C14 H14 O Se -","- C28 H28 O2 Se2 -","2","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.025","0.0247","","","0.0677","0.0678","","","","","","1.134","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150469","15.0339","0.0015","5.642","0.0007","18.9279","0.0013","90","","101.673","0.007","90","","1572.3","0.3","122","0.5","122","0.5","","","","","","","","4","P 1 21/n 1","-P 2yn","14","3","4,6-bis(phenylseleno)benzene-1,3-diol","","- C18 H14 O2 Se2 -","- C18 H14 O2 Se2 -","- C72 H56 O8 Se8 -","4","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.0302","0.0301","","","0.0837","0.0838","","","","","","1.224","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150470","8.5958","0.0017","11.37","0.003","12.388","0.003","116.25","0.02","100.28","0.017","104.48","0.02","991.4","0.5","122","0.5","122","0.5","","","","","","","","4","P -1","-P 1","2","4","1,2-diethoxy-4,5-bis(phenylseleno)benzene","","- C22 H22 O2 Se2 -","- C22 H22 O2 Se2 -","- C44 H44 O4 Se4 -","2","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.0355","0.0349","","","0.0863","0.0867","","","","","","1.094","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150471","7.1618","0.001","15.132","0.0019","8.2912","0.001","90","","103.609","0.011","90","","873.3","0.2","122","0.5","122","0.5","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","5","1,4-dimethoxy-2,5-bis(phenylseleno)benzene","","- C20 H18 O2 Se2 -","- C20 H18 O2 Se2 -","- C40 H36 O4 Se4 -","2","0.5","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.0352","0.0346","","","0.0958","0.0965","","","","","","1.104","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150472","7.2789","0.0007","9.4958","0.0008","19.043","0.003","90","","97.047","0.011","90","","1306.3","0.3","122","0.5","122","0.5","","","","","","","","4","P 1 21/n 1","-P 2yn","14","6","1-methoxy-3,5-dimethyl-4-(phenylseleno)benzene","","- C15 H16 O Se -","- C15 H16 O Se -","- C60 H64 O4 Se4 -","4","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.0262","0.0257","","","0.0692","0.0697","","","","","","1.065","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150473","8.7061","0.0011","10.3054","0.0008","11.8008","0.0013","92.369","0.008","90.07","0.01","94.027","0.009","1055.2","0.2","122","0.5","122","0.5","","","","","","","","4","P -1","-P 1","2","7","4-(phenylseleno)benzene-1,3-diol","","- C12 H10 O2 Se -","- C12 H10 O2 Se -","- C48 H40 O8 Se4 -","4","2","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.0292","0.0292","","","0.0782","0.0783","","","","","","1.115","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150474","14.991","0.002","9.9673","0.0018","15.93","0.002","90","","90","","90","","2380.3","0.6","122","0.5","122","0.5","","","","","","","","4","P b c a","-P 2ac 2ab","61","8","1-methoxy-4-methyl-2-(phenylseleno)benzene","","- C14 H14 O Se -","- C14 H14 O Se -","- C112 H112 O8 Se8 -","8","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","1.5418","CuKα","","0.0266","0.0262","","","0.0724","0.0727","","","","","","1.153","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150475","9.0416","0.0012","7.8911","0.001","17.6103","0.0018","90","","102.406","0.01","90","","1227.1","0.3","122","0.5","122","0.5","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","9","2,5-dimethyl-4-(phenylseleno)phenol","","- C14 H14 O Se -","- C14 H14 O Se -","- C56 H56 O4 Se4 -","4","1","","Oddershede, Jette; Henriksen, Lars; Larsen, Sine","Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures","Organic & Biomolecular Chemistry","2003","1","6","1053","","10.1039/b211130f","","","0.71073","MoKα","","0.0268","0.0265","","","0.0758","0.076","","","","","","1.1","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150476","7.917","0.002","19.736","0.005","21.32","0.005","90","","90","","90","","3331.2","1.4","295","2","295","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","Crystal 7 ((R)-1/4)","(R)-alpha-[[(1,1-dimethylethyl)amino]methyl]-3,5-dihydroxybenzenemethanol (2S,3S)-di-O-toluoyl tartrate hydrate","","- C32 H39 N O12 -","- C32 H39 N O12 -","- C128 H156 N4 O48 -","4","1","","Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen","Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/","Organic & Biomolecular Chemistry","2003","1","6","1080","","10.1039/b211327a","","","0.71073","MoKα","","0.152","0.0495","","","0.0759","0.0973","","","","","","0.796","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150477","7.512","0.001","18.733","0.004","11.599","0.002","90","","103.1","0.01","90","","1589.8","0.5","295","2","295","2","","","","","","","","4","P 1 21 1","P 2yb","4","Crystal 6((S)-1/4)","(S)-alpha-[[(1,1-dimethylethyl)amino]methyl]-3,5-dihydroxybenzenemethanol (2S,3S)-di-O-toluoyl tartrate","","- C32 H37 N O11 -","- C12.8 H14.8 N0.4 O4.4 -","- C64 H74 N2 O22 -","5","2.5","","Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen","Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/","Organic & Biomolecular Chemistry","2003","1","6","1080","","10.1039/b211327a","","","0.71073","MoKα","","0.0579","0.0418","","","0.1003","0.1066","","","","","","0.944","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150478","7.506","0.001","18.714","0.003","11.59","0.002","90","","103.03","0.01","90","","1586.1","0.4","295","2","295","2","","","","","","","","4","P 1 21 1","P 2yb","4","Crystal 5((S)-1/4)","(S)-alpha-[[(1,1-dimethylethyl)amino]methyl]-3,5-dihydroxybenzenemethanol (2S,3S)-di-O-toluoyl tartrate","","- C32 H37 N O11 -","- C32 H37 N O11 -","- C64 H74 N2 O22 -","2","1","","Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen","Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/","Organic & Biomolecular Chemistry","2003","1","6","1080","","10.1039/b211327a","","","0.71073","MoKα","","0.0676","0.045","","","0.1061","0.1151","","","","","","0.925","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150479","7.81","0.001","21.431","0.004","21.948","0.003","90","","90","","90","","3673.6","1","291","2","291","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","Crystal 8 ((R)-1/4)","Inclusion complex of (R)-alpha-[[(1,1-dimethylethyl)amino]methyl]- 3,5-dihydroxybenzenemethanol (2S,3S)-di-O-toluoyl tartrate hydrate and acetone","","- C35 H45 N O13 -","- C35 H45 N O13 -","- C140 H180 N4 O52 -","4","1","","Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen","Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/","Organic & Biomolecular Chemistry","2003","1","6","1080","","10.1039/b211327a","","","0.71073","MoKα","","0.0912","0.0464","","","0.099","0.1124","","","","","","0.862","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150480","6.4904","0.0004","16.785","0.0011","8.2216","0.0005","90","","102.454","0.001","90","","874.6","0.1","120","2","120","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","2-Ethoxyl-3,5-dinitropyridine","","- C7 H7 N3 O5 -","- C7 H7 N3 O5 -","- C28 H28 N12 O20 -","4","1","","Crampton, Michael R.; Emokpae, Thomas A.; Howard, Judith A. K.; Isanbor, Chukwuemeka; Mondal, Raju","Kinetic and equilibrium studies of σ-adduct formation and nucleophilic substitution in the reactions of 2-phenoxy-3,5-dinitropyridine and 2-ethoxy-3,5-dinitropyridine with aliphatic amines in dipolar aprotic solventsElectronic supplementary information (ESI) available: Tables 10‒15. See http://www.rsc.org/suppdata/ob/b2/b211639c/","Organic & Biomolecular Chemistry","2003","1","6","1004","","10.1039/b211639c","","","0.71073","MoKα","","0.0465","0.0378","","","0.0959","0.101","","","","","","1.044","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150481","5.9847","0.0012","7.3833","0.0015","12.375","0.003","94.29","0.03","95.28","0.03","91.8","0.03","542.6","0.2","120","2","120","2","","","","","","","","4","P -1","-P 1","2","NPIP","2-Piperidine-3,5-dinitropyridine","","- C10 H12 N4 O4 -","- C10 H12 N4 O4 -","- C20 H24 N8 O8 -","2","1","","Crampton, Michael R.; Emokpae, Thomas A.; Howard, Judith A. K.; Isanbor, Chukwuemeka; Mondal, Raju","Kinetic and equilibrium studies of σ-adduct formation and nucleophilic substitution in the reactions of 2-phenoxy-3,5-dinitropyridine and 2-ethoxy-3,5-dinitropyridine with aliphatic amines in dipolar aprotic solventsElectronic supplementary information (ESI) available: Tables 10‒15. See http://www.rsc.org/suppdata/ob/b2/b211639c/","Organic & Biomolecular Chemistry","2003","1","6","1004","","10.1039/b211639c","","","0.71073","MoKα","","0.0361","0.0332","","","0.0935","0.0963","","","","","","1.072","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150482","9.1922","0.0011","7.1341","0.0011","31.75","0.004","90","","90","","90","","2082.1","0.5","296","2","296","2","","","","","","","","4","P b c m","-P 2c 2b","57","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene 1,3-benzenedicarboxylic acid","","- C24 H20 N4 O4 -","- C24 H20 N4 O4 -","- C96 H80 N16 O16 -","4","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.0701","0.0666","","","0.1534","0.1577","","","","","","1.17","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150483","35.743","0.007","9.285","0.002","7.338","0.001","90","","90","","90","","2435.3","0.8","100","2","100","2","","","","","","","","4","A m a 2","A 2 -2a","40","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene 4,4'-oxybisbenzoic acid","","- C30 H24 N4 O5 -","- C30 H24 N4 O5 -","- C120 H96 N16 O20 -","4","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.055","0.0371","","","0.0788","0.0836","","","","","","0.985","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150484","7.281","0.003","24.097","0.006","8.919","0.003","90","","90","","90","","1564.8","0.9","296","2","296","2","","","","","","","","4","P n m a","-P 2ac 2n","62","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene oxalic acid","","- C18 H16 N4 O4 -","- C18 H16 N4 O4 -","- C72 H64 N16 O16 -","4","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","1.54178","CuKα","","0.0853","0.0352","","","0.0785","0.0853","","","","","","0.988","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150485","5.492","0.001","34.585","0.002","6.318","0.001","90","","102.81","0.01","90","","1170.2","0.3","130","2","130","2","","","","","","","","4","P 1 21/m 1","-P 2yb","11","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene sebacic acid","","- C26 H32 N4 O4 -","- C26 H32 N4 O4 -","- C52 H64 N8 O8 -","2","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.0811","0.0561","","","0.1135","0.1293","","","","","","1.122","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150486","7.251","0.004","24.325","0.005","9.185","0.003","90","","90","","90","","1620.1","1.1","100","2","100","2","","","","","","","","4","P n m a","-P 2ac 2n","62","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene squaric acid","","- C20 H16 N4 O4 -","- C20 H16 N4 O4 -","- C80 H64 N16 O16 -","4","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.1333","0.0838","","","0.1717","0.2047","","","","","","1.132","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150487","5.7015","0.0005","26.821","0.003","6.1015","0.0006","90","","104.708","0.008","90","","902.47","0.16","294","2","294","2","","","","","","","","4","P 1 21/m 1","-P 2yb","11","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene succinic acid","","- C20 H20 N4 O4 -","- C20 H20 N4 O4 -","- C40 H40 N8 O8 -","2","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","1.54178","CuKα","","0.0453","0.0372","","","0.1011","0.1064","","","","","","1.048","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150488","10.268","0.002","15.529","0.003","11.158","0.002","90","","105.47","0.03","90","","1714.7","0.6","294","2","294","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","N,N'-bis(2-pyridyl)-1,3-diaminobenzene 1,4-benzeneicarboxylic acid 2:1","","- C20 H17 N4 O2 -","- C20 H17 N4 O2 -","- C80 H68 N16 O8 -","4","1","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.05","0.0406","","","0.1168","0.1235","","","","","","1.097","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150489","9.117","0.002","14.433","0.004","19.312","0.006","90","","90","","90","","2541.2","1.2","296","2","296","2","","","","","","","","4","P b c n","-P 2n 2ab","60","","N,N'-bis(2-pyridyl)-1,4-diaminobenzene 2,2'-biphenyldicarboxylic acid co-crystal","","- C30 H24 N4 O4 -","- C30 H24 N4 O4 -","- C120 H96 N16 O16 -","4","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.1369","0.0398","","","0.0977","0.1129","","","","","","0.981","","","","has coordinates","180290","2020-10-21","18:00:00",""
"7150490","17.29","0.002","4.0427","0.0005","24.72","0.003","90","","93.121","0.011","90","","1725.3","0.4","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","N,N'-bis(2-pyridyl)-1,4-diaminobenzene malonic acid co-crystal","","- C19 H18 N4 O4 -","- C19 H18 N4 O4 -","- C76 H72 N16 O16 -","4","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","1.54178","CuKα","","0.0657","0.0345","","","0.0871","0.0986","","","","","","1.021","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150491","8.4312","0.0009","10.1438","0.0012","15.0064","0.0015","85.842","0.009","73.025","0.009","78.006","0.009","1200.6","0.2","294","2","294","2","","","","","","","","4","P -1","-P 1","2","","N,N'-bis(2-pyridyl)-1,4-diaminobenzene sebacic acid","","- C26 H32 N4 O4 -","- C26 H32 N4 O4 -","- C52 H64 N8 O8 -","2","1","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.1829","0.0565","","","0.1004","0.1302","","","","","","0.864","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150492","3.842","0.001","9.062","0.002","12.098","0.002","87.23","0.03","81.25","0.03","78.18","0.03","407.41","0.16","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","N,N'-bis(2-pyridyl)-1,4-diaminobenzene squaric acid co-crystal","","- C20 H16 N4 O4 -","- C20 H16 N4 O4 -","- C20 H16 N4 O4 -","1","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.0693","0.051","","","0.096","0.1074","","","","","","1.127","","","","has coordinates","180290","2020-10-21","18:00:00",""
"7150493","7.767","0.0013","8.8044","0.0017","9.1959","0.0017","62.048","0.019","71.921","0.017","70.707","0.016","515.1","0.19","294","2","294","2","","","","","","","","4","P -1","-P 1","2","","N,N'-bis(2-pyridyl)-1,4-diaminobenzene 1,4-benzenedicarboxylic acid","","- C24 H20 N4 O4 -","- C24 H20 N4 O4 -","- C24 H20 N4 O4 -","1","0.5","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","1.54178","CuKα","","0.0546","0.0466","","","0.1237","0.1275","","","","","","1.069","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150494","8.783","0.0011","10.6035","0.0011","13.8087","0.0015","88.06","0.009","87.645","0.009","86.861","0.009","1282.4","0.3","294","2","294","2","","","","","","","","4","P -1","-P 1","2","","N,N'-bis(2-pyridyl)-4,4'-methylenebis(aminobenzene) 1,4-benzenedicarboxylic acid ethanol 2:1:2","","- C29 H29 N4 O3 -","- C29 H29 N4 O3 -","- C58 H58 N8 O6 -","2","1","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.1515","0.0713","","","0.1562","0.1934","","","","","","1.085","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150495","10.3442","0.0007","11.7028","0.0009","12.6687","0.0009","78.461","0.006","65.91","0.006","73.925","0.006","1338.68","0.18","294","2","294","2","","","","","","","","4","P -1","-P 1","2","","N,N'-bis(2-pyridyl)-4,4'-oxybis(aminobenzene) 1,4-benzenedicarboxylic acid hydrate 1:1:1","","- C30 H26 N4 O6 -","- C30 H26 N4 O6 -","- C60 H52 N8 O12 -","2","1","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.0571","0.0423","","","0.1193","0.1289","","","","","","1.058","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150496","28.8097","0.0018","7.8866","0.0006","18.5925","0.001","90","","98.004","0.005","90","","4183.3","0.5","294","2","294","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","N,N'-bis(2-pyridyl)-2,2'-oxybis(aminobenzene) fumaric acid co-crystal","","- C24 H20 N4 O3 -","- C24 H20 N4 O3 -","- C192 H160 N32 O24 -","8","1","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.0622","0.0489","","","0.1331","0.1452","","","","","","1.071","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150497","8.2875","0.0006","10.1511","0.0008","13.3739","0.001","78.828","0.007","87.705","0.006","84.019","0.006","1097.55","0.15","294","2","294","2","","","","","","","","4","P -1","-P 1","2","","N,N'-bis(2-pyridyl)-2,2'-oxybis(aminobenzene) 1,4-benzenedicarboxylic acid co-crystal","","- C26 H21 N4 O3 -","- C26 H21 N4 O3 -","- C52 H42 N8 O6 -","2","1","","Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz","Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5","Organic & Biomolecular Chemistry","2003","1","8","1425","","10.1039/b211675h","","","0.71073","MoKα","","0.0768","0.0478","","","0.1036","0.1204","","","","","","1.074","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150498","8.962","0.002","8.981","0.002","19.587","0.004","82.32","0.02","88.22","0.02","66.69","0.02","1434.4","0.6","298.2","","","","","","","","","","","3","P 1","P 1","1","","","","- C33 H32 O7 -","- C33 H32 O7 -","- C66 H64 O14 -","2","2","","Yamauchi, Satoshi; Uno, Hidemitsu","Syntheses of the stereoisomers of neolignans morinol C and D","Organic & Biomolecular Chemistry","2003","1","8","1323","","10.1039/b211801g","","","0.7107","MoKa","","","0.0581","","","","0.1486","","","","","","1.207","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150499","16.192","0.005","10.689","0.004","17.644","0.006","90","","91.95","0.02","90","","3052","1.8","298","","298","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C36 H36 Fe2 N2 O2 -","- C36 H36 Fe2 N2 O2 -","- C144 H144 Fe8 N8 O8 -","4","1","","Coutouli-Argyropoulou, Evdoxia; Tsitabani, Maria; Petrantonakis, Georgios; Terzis, Aris; Raptopoulou, Catherine","Labeling of organic biomolecules with ethynylferrocene","Organic & Biomolecular Chemistry","2003","1","8","1382","","10.1039/b300191a","","","1.5418","CuKα","","0.1223","0.059","","0.1955","0.1448","","","","1.05","1.126","1.126","","","","","has coordinates,has disorder","180290","2020-10-21","18:00:00",""
"7150500","9.589","0.006","13.179","0.007","13.454","0.007","110.43","0.03","100.31","0.03","101.43","0.03","1503.6","1.5","294","","","","","","","","","","","4","P -1","-P 1","2","","","","- C31 H19 Br6 N2 -","- C31 H19 Br6 N2 -","- C62 H38 Br12 N4 -","2","1","","Rahman, A. Noman M. M.; Bishop, Roger; Craig, Donald C.; Scudder, Marcia L.","Why a hexabromodiquinoline host preferentially includes small aromatic hydrocarbon guests","Organic & Biomolecular Chemistry","2003","1","8","1435","","10.1039/b300248a","","","0.71073","MoKα","","","0.043","","","","0.051","","","","","","1.6","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150501","10.107","0.005","11.121","0.005","14.41","0.007","74.44","0.04","72.35","0.04","79.62","0.03","1478.2","1.3","294","","","","","","","","","","","4","P -1","-P 1","2","","","","- C30 H20 Br6 N2 -","- C30 H20 Br6 N2 -","- C60 H40 Br12 N4 -","2","1","","Rahman, A. Noman M. M.; Bishop, Roger; Craig, Donald C.; Scudder, Marcia L.","Why a hexabromodiquinoline host preferentially includes small aromatic hydrocarbon guests","Organic & Biomolecular Chemistry","2003","1","8","1435","","10.1039/b300248a","","","0.71073","MoKα","","","0.079","","","","0.096","","","","","","1.72","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150502","9.596","0.005","12.682","0.006","13.545","0.007","107.47","0.03","96.61","0.03","106.84","0.02","1467.6","1.3","294","","","","","","","","","","","4","P -1","-P 1","2","","","","- C30 H20 Br6 N2 -","- C30 H20 Br6 N2 -","- C60 H40 Br12 N4 -","2","1","","Rahman, A. Noman M. M.; Bishop, Roger; Craig, Donald C.; Scudder, Marcia L.","Why a hexabromodiquinoline host preferentially includes small aromatic hydrocarbon guests","Organic & Biomolecular Chemistry","2003","1","8","1435","","10.1039/b300248a","","","0.71073","MoKα","","","0.06","","","","0.072","","","","","","1.66","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150503","9.212","0.005","15.384","0.006","17.735","0.007","90","","111.75","0.02","90","","2334.4","1.8","294","","","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H10 Br6 N2 -","- C22 H10 Br6 N2 -","- C88 H40 Br24 N8 -","4","1","","Rahman, A. Noman M. M.; Bishop, Roger; Craig, Donald C.; Scudder, Marcia L.","Why a hexabromodiquinoline host preferentially includes small aromatic hydrocarbon guests","Organic & Biomolecular Chemistry","2003","1","8","1435","","10.1039/b300248a","","","0.71073","MoKα","","","0.062","","","","0.068","","","","","","1.91","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150504","9.384","0.005","12.901","0.006","13.415","0.007","103.57","0.02","100.24","0.03","109.04","0.02","1434.1","1.3","294","","","","","","","","","","","4","P -1","-P 1","2","","","","- C29 H18 Br6 N2 -","- C29 H15 Br6 N2 -","- C58 H30 Br12 N4 -","2","1","","Rahman, A. Noman M. M.; Bishop, Roger; Craig, Donald C.; Scudder, Marcia L.","Why a hexabromodiquinoline host preferentially includes small aromatic hydrocarbon guests","Organic & Biomolecular Chemistry","2003","1","8","1435","","10.1039/b300248a","","","0.71073","MoKα","","","0.079","","","","0.095","","","","","","1.69","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150505","8.283","0.003","12.655","0.004","9.554","0.002","90","","90.09","0.02","90","","1001.5","0.5","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","(+/-)-2,4-dichloro-cis-3a,4,7,7a-tetrahydro-cis-4,7-epithio- 1-benzothiophene-trans-1-syn-8-dioxide","","- C8 H6 Cl2 O2 S2 -","- C8 H6 Cl2 O2 S2 -","- C32 H24 Cl8 O8 S8 -","4","1","","Boyd, Derek R.; Sharma, Narain D.; Gunaratne, Nimal; Haughey, Simon A.; Kennedy, Martina A.; Malone, John F.; Allen, Christopher C. R.; Dalton, Howard","Dioxygenase-catalysed oxidation of monosubstituted thiophenes: sulfoxidation versus dihydrodiol formation","Organic & Biomolecular Chemistry","2003","1","6","984","","10.1039/b300867n","","","1.54178","CuKα","","0.0744","0.0683","","","0.1779","0.1817","","","","","","1.056","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150506","11.1658","0.0009","6.6249","0.0005","13.2296","0.001","90","","111.526","0.0012","90","","910.37","0.12","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","(+/-)-6-acetyl-1-methyl-7lambda4-thiabicyclo[2.2.1]hepta-2-en-7-one","","- C9 H12 O2 S -","- C9 H12 O2 S -","- C36 H48 O8 S4 -","4","1","","Boyd, Derek R.; Sharma, Narain D.; Gunaratne, Nimal; Haughey, Simon A.; Kennedy, Martina A.; Malone, John F.; Allen, Christopher C. R.; Dalton, Howard","Dioxygenase-catalysed oxidation of monosubstituted thiophenes: sulfoxidation versus dihydrodiol formation","Organic & Biomolecular Chemistry","2003","1","6","984","","10.1039/b300867n","","","0.71073","MoKα","","0.1014","0.0912","","","0.2658","0.2759","","","","","","0.954","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150507","10.889","0.002","28.96","0.005","9.213","0.002","90","","106.59","0.02","90","","2784.3","1","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","9,10-Dicyano-9-(6-bromo-5-oxocyclohepta-1,3,6- trienyl)-10-(7-oxocyclohepta- 1,3,5-trienyl)-9,10- dihydroanthracene","","- C36 H23 Br N2 O2 -","- C36 H23 Br N2 O2 -","- C144 H92 Br4 N8 O8 -","4","1","","Mori, Akira; Kawakami, Hiroko; Kato, Nobuo; Wu, Shu-Ping; Takeshita, Hitoshi","Photochemical reactions of 2-bromotropone and 2,7-dibromotropone with 9,10-dicyanoanthracene","Organic & Biomolecular Chemistry","2003","1","10","1730","","10.1039/b300922j","","","1.54184","CuKα","","0.0718","0.048","","0.1446","0.1275","","","","1.039","1.068","1.068","","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150508","16.772","0.003","7.698","0.001","25.944","0.006","90","","94.46","0.02","90","","3339.5","1.1","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","2-Bromo-7-(10-cyano-9-anthryl)tropone","2-Bromo-7-(10-cyano-9-anthryl) cyclohepta-2,4,6-trien-1-one","","- C22 H12 Br N O -","- C22 H12 Br N O -","- C176 H96 Br8 N8 O8 -","8","1","","Mori, Akira; Kawakami, Hiroko; Kato, Nobuo; Wu, Shu-Ping; Takeshita, Hitoshi","Photochemical reactions of 2-bromotropone and 2,7-dibromotropone with 9,10-dicyanoanthracene","Organic & Biomolecular Chemistry","2003","1","10","1730","","10.1039/b300922j","","","1.54184","CuKα","","0.0557","0.0428","","0.1214","0.111","","","","1.059","1.083","1.083","","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150509","13.614","0.003","13.721","0.006","13.427","0.003","104.95","0.02","108.12","0.02","111.56","0.02","2010.8","1.3","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","9-(3-Bromo-2-oxocycloheptatrienyl)-9- cyanoanthran-5-one","","- C50 H30 Br2 N2 O4 -","- C50 H30 Br2 N2 O4 -","- C100 H60 Br4 N4 O8 -","2","1","","Mori, Akira; Kawakami, Hiroko; Kato, Nobuo; Wu, Shu-Ping; Takeshita, Hitoshi","Photochemical reactions of 2-bromotropone and 2,7-dibromotropone with 9,10-dicyanoanthracene","Organic & Biomolecular Chemistry","2003","1","10","1730","","10.1039/b300922j","","","1.54184","CuKα","","0.0504","0.0457","","0.1275","0.1236","","","","1.09","1.112","1.112","","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150510","11.026","0.002","23.928","0.004","9.7068","0.0011","90","","91.854","0.012","90","","2559.6","0.7","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","9-(6-Bromo-7-oxocycloheptatrienyl)- 9,10-dicyano-10-(4,5,6-tribromocyclohex-2-enyl)- 9,10-dihydroanthracene","","- C29 H18 Br4 N2 O -","- C29 H18 Br4 N2 O -","- C116 H72 Br16 N8 O4 -","4","1","","Mori, Akira; Kawakami, Hiroko; Kato, Nobuo; Wu, Shu-Ping; Takeshita, Hitoshi","Photochemical reactions of 2-bromotropone and 2,7-dibromotropone with 9,10-dicyanoanthracene","Organic & Biomolecular Chemistry","2003","1","10","1730","","10.1039/b300922j","","","1.54184","CuKα","","0.0592","0.053","","0.1441","0.1394","","","","1.063","1.091","1.091","","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150511","16.906","0.008","14.087","0.007","7.001","0.004","90","","90.368","0.01","90","","1667.3","1.5","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","4-Methyl-dihydro-1,3,4-benzotriazepin-5-ones","4-Methyl-dihydro-1,3,4-benzotriazepin-5-ones","","- C9 H9 N3 O -","- C9 H9 N3 O -","- C72 H72 N24 O8 -","8","2","","Zahra, Jalal A.; El-Abadelah, Mustafa M.; Nazer, Musa Z.; Ebraheem, Kais A. K.; Boese, Roland","Investigations on the structure of 4-methyldihydro-1,3,4-benzotriazepin-5-ones. Tautomer reassignment","Organic & Biomolecular Chemistry","2003","1","10","1798","","10.1039/b301047c","","","0.71073","MoKα","","0.1032","0.0714","","","0.1812","0.2077","","","","","","1.021","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7150512","8.0987","0.001","8.0844","0.0006","23.252","0.002","90","","99.511","0.011","90","","1501.5","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","Arene chromium complex","","","- C14 H16 Cr O6 -","- C14 H16 Cr O6 -","- C56 H64 Cr4 O24 -","4","1","","Kumar Tipparaju, Suresh; Puranik, Vedavati G.; Sarkar, Amitabha","Chelation-control in nucleophilic addition to Cr(CO)3-complexed aryl aldehydesElectronic supplementary information (ESI) available: 1) 200 and 300 MHz 1H NMR spectra of selected compounds; 2) Crystallographic tables of bond angles, bond lengths, torsional angles etc. for compounds 3a and 3a?. See http://www.rsc.org/suppdata/ob/b3/b301426f/","Organic & Biomolecular Chemistry","2003","1","10","1720","","10.1039/b301426f","","","0.7093","MoKα","","0.0527","0.035","","","0.0889","0.0949","","","","","","1.022","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150513","13.6389","0.0013","8.9939","0.0011","13.7401","0.0014","90","","113.594","0.007","90","","1544.6","0.3","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","Arene chromium complex","","","- C14 H16 Cr O6 -","- C14 H16 Cr O6 -","- C56 H64 Cr4 O24 -","4","1","","Kumar Tipparaju, Suresh; Puranik, Vedavati G.; Sarkar, Amitabha","Chelation-control in nucleophilic addition to Cr(CO)3-complexed aryl aldehydesElectronic supplementary information (ESI) available: 1) 200 and 300 MHz 1H NMR spectra of selected compounds; 2) Crystallographic tables of bond angles, bond lengths, torsional angles etc. for compounds 3a and 3a?. See http://www.rsc.org/suppdata/ob/b3/b301426f/","Organic & Biomolecular Chemistry","2003","1","10","1720","","10.1039/b301426f","","","0.7093","MoKα","","0.035","0.0289","","","0.0838","0.0861","","","","","","1.087","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150514","9.6207","0.0011","10.9214","0.0013","11.3237","0.0013","109.183","0.002","101.783","0.002","98.254","0.002","1071.1","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","5,5'-difluorophenylindigo‒3,3'-bis(4-fluorophenylimine)","","","- C28 H16 F4 N4 -","- C28 H16 F4 N4 -","- C56 H32 F8 N8 -","2","1","","Boeyens, Jan C. A.; Cook, Leanne M.; Ding, Yunxiang; Fernandes, Manuel A.; Reid, David H.","Thermal oligomerisation of aryl isocyanides: formation of pyrazino[1,2-a:4,5-a?]diindoles and indigo diarylimines","Organic & Biomolecular Chemistry","2003","1","12","2168","","10.1039/b302340k","","","0.71073","MoKα","","0.1138","0.0508","","","0.1222","0.1471","","","","","","0.996","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150515","7.977","0.0011","10.8182","0.0015","13.3466","0.0019","109.812","0.002","93.863","0.002","95.079","0.003","1073.5","0.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","7,14-di-(4-fluorophenylamino)-6,13-di-(4-fluorophenylimino)pyrazino [1,2-a:4,5-a']diindole","","","- C48 H38 F6 N8 O2 -","- C48 H38 F6 N8 O2 -","- C48 H38 F6 N8 O2 -","1","0.5","","Boeyens, Jan C. A.; Cook, Leanne M.; Ding, Yunxiang; Fernandes, Manuel A.; Reid, David H.","Thermal oligomerisation of aryl isocyanides: formation of pyrazino[1,2-a:4,5-a?]diindoles and indigo diarylimines","Organic & Biomolecular Chemistry","2003","1","12","2168","","10.1039/b302340k","","","0.71073","MoKα","","0.1095","0.0505","","","0.1259","0.1478","","","","","","0.991","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150516","26.112","0.003","9.913","0.001","16.461","0.002","90","","127.628","0.006","90","","3374.6","0.7","298","","298","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C17 H23 N O2 S -","- C17 H23 N O2 S -","- C136 H184 N8 O16 S8 -","8","1","","O'Mahony, Donogh J. R.; Belanger, David B.; Livinghouse, Tom","Substrate control of stereoselection in the rhodium(i) catalyzed intramolecular [4 + 2] cycloaddition reactionElectronic supplementary information (ESI) available: experimental procedures and spectroscopic data for compounds 4a?d and 6a?c. See http://www.rsc.org/suppdata/ob/b3/b302426c/","Organic & Biomolecular Chemistry","2003","1","12","2038","","10.1039/b302426c","","","0.7107","MoKα","","","0.0528","","0.0763","0.0481","","","","","","","1.371","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7150517","11.595","0.006","12.862","0.005","11.561","0.006","101.31","0.04","119.63","0.03","73.15","0.03","1431.5","1.3","296.2","","296.2","","","","","","","","","6","P -1","-P 1","2","","","","- C19 H36 Cl5 N3 O5 Os -","- C19 H36 Cl5 N3 O5 Os -","- C38 H72 Cl10 N6 O10 Os2 -","2","1","","Donohoe, Timothy J.; Mitchell, Lee; Waring, Michael J.; Helliwell, Madeleine; Bell, Andrew; Newcombe, Nicholas J.","Scope of the directed dihydroxylation: application to cyclic homoallylic alcohols and trihaloacetamides","Organic & Biomolecular Chemistry","2003","1","12","2173","","10.1039/b303081d","","","0.7107","MoKα","","0.066","0.0354","","0.0369","0.0316","","","","1.609","1.521","1.521","","","","","has coordinates","209482","2020-10-21","18:00:00",""
"7150518","11.19","0.02","11.405","0.01","15.857","0.01","90","","102.57","0.04","90","","1975","4","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C13 H24 Cl3 N3 O5 Os -","- C13 H24 Cl3 N3 O5 Os -","- C52 H96 Cl12 N12 O20 Os4 -","4","1","","Donohoe, Timothy J.; Mitchell, Lee; Waring, Michael J.; Helliwell, Madeleine; Bell, Andrew; Newcombe, Nicholas J.","Scope of the directed dihydroxylation: application to cyclic homoallylic alcohols and trihaloacetamides","Organic & Biomolecular Chemistry","2003","1","12","2173","","10.1039/b303081d","","","0.71069","MoKα","","0.0261","0.024","","","0.0619","0.0629","","","","","","1.023","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7150519","10.771","0.001","11.765","0.001","12.279","0.001","69.53","0.01","85.1","0.01","85.96","0.01","1451.1","0.2","120","0.2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H16 F18 N2 O6 -","- C24 H16 F18 N2 O6 -","- C48 H32 F36 N4 O12 -","2","1","","Chambers, Richard D.; Hoskin, Philip R.; Kenwright, Alan R.; Khalil, Ali; Richmond, Paul; Sandford, Graham; Yufit, Dmitrii S.; Howard, Judith A. K.","Polyhalogenated heterocyclic compounds. Macrocycles from perfluoro-4-isopropylpyridinePart 50. For part 49 see ref. 1.","Organic & Biomolecular Chemistry","2003","1","12","2137","","10.1039/b303443g","","","0.71073","MoKα","","0.2019","0.0762","","","0.1519","0.1921","","","","","","0.952","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150520","11.0542","0.0004","14.1784","0.0005","18.7552","0.0006","90","","102.96","0.001","90","","2864.64","0.17","120","2","120","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H16 F18 N2 O6 -","- C24 H16 F18 N2 O6 -","- C96 H64 F72 N8 O24 -","4","1","","Chambers, Richard D.; Hoskin, Philip R.; Kenwright, Alan R.; Khalil, Ali; Richmond, Paul; Sandford, Graham; Yufit, Dmitrii S.; Howard, Judith A. K.","Polyhalogenated heterocyclic compounds. Macrocycles from perfluoro-4-isopropylpyridinePart 50. For part 49 see ref. 1.","Organic & Biomolecular Chemistry","2003","1","12","2137","","10.1039/b303443g","","","0.71073","MoKα","","0.0532","0.0439","","","0.1101","0.1175","","","","","","1.053","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150521","13.473","0.003","23.261","0.005","11.079","0.002","90","","113.78","0.03","90","","3177.3","1.4","120","0.2","120","0.2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C30 H12 F18 N2 O4 -","- C30 H12 F18 N2 O4 -","- C120 H48 F72 N8 O16 -","4","1","","Chambers, Richard D.; Hoskin, Philip R.; Kenwright, Alan R.; Khalil, Ali; Richmond, Paul; Sandford, Graham; Yufit, Dmitrii S.; Howard, Judith A. K.","Polyhalogenated heterocyclic compounds. Macrocycles from perfluoro-4-isopropylpyridinePart 50. For part 49 see ref. 1.","Organic & Biomolecular Chemistry","2003","1","12","2137","","10.1039/b303443g","","","0.71073","MoKα","","0.1322","0.1168","","","0.2795","0.31","","","","","","1.095","","","","has coordinates,has disorder","180291","2020-10-21","18:00:00",""
"7150522","14.2011","0.0005","8.4725","0.0003","9.4479","0.0003","90","","102.114","0.001","90","","1111.45","0.07","120","0.2","120","0.2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","19,20-diaza-8,17-bis[1,2,2,2-tetrafluoromethyl)ethyl]-7,9,16,18-tetrafluoro-2,5,11,14-tetraoxatricyclo[13.3.1.1^6,10^]icosa-1(19),6,8,10(20),15,17-hexaene","","- C20 H8 F18 N2 O4 -","- C20 H8 F18 N2 O4 -","- C40 H16 F36 N4 O8 -","2","0.5","","Chambers, Richard D.; Hoskin, Philip R.; Kenwright, Alan R.; Khalil, Ali; Richmond, Paul; Sandford, Graham; Yufit, Dmitrii S.; Howard, Judith A. K.","Polyhalogenated heterocyclic compounds. Macrocycles from perfluoro-4-isopropylpyridinePart 50. For part 49 see ref. 1.","Organic & Biomolecular Chemistry","2003","1","12","2137","","10.1039/b303443g","","","0.71073","MoKα","","0.0643","0.0429","","","0.0997","0.1101","","","","","","1.022","","","","has coordinates","211399","2020-10-21","18:00:00",""
"7150523","7.014","0.001","7.085","0.001","14.149","0.002","77.79","0.02","89.21","0.01","77.4","0.02","670.28","0.18","243","2","243","2","","","","","","","","3","P -1","-P 1","2","","","","- C15 H10 N4 -","- C15 H10 N4 -","- C30 H20 N8 -","2","1","","Nicolle N. P. Moonen; Robin Gist; Corinne Boudon; Jean-Paul Gisselbrecht; Paul Seiler; Tsuyoshi Kawai; Atsushi Kishioka; Maurice Gross; Masahiro Irie; François Diederich","Donor-substituted cyanoethynylethenes: powerful chromophores for opto-electronic applications","Org. Biomol. Chem.","2003","1","12","2032","2034","10.1039/b303879c","","","1.5418","CuKα","","0.064","0.0583","","","0.1721","0.1787","","","","","","1.09","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7150524","3.9477","0.0002","11.1064","0.0004","22.3725","0.0009","90","","93.769","0.002","90","","978.79","0.07","120","2","120","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 N4 -","- C24 H20 N4 -","- C48 H40 N8 -","2","0.5","","Nicolle N. P. Moonen; Robin Gist; Corinne Boudon; Jean-Paul Gisselbrecht; Paul Seiler; Tsuyoshi Kawai; Atsushi Kishioka; Maurice Gross; Masahiro Irie; François Diederich","Donor-substituted cyanoethynylethenes: powerful chromophores for opto-electronic applications","Org. Biomol. Chem.","2003","1","12","2032","2034","10.1039/b303879c","","","0.7107","MoKα","","0.1077","0.0531","","","0.1081","0.1582","","","","","","1.267","","","","has coordinates","180291","2020-10-21","18:00:00",""
"7151357","5.5947","0.0009","9.6504","0.0017","31.93","0.006","90","","90","","90","","1723.9","0.5","193","2","193","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C19 H30 O3 -","- C19 H30 O3 -","- C76 H120 O12 -","4","1","","Sorensen, John L.; Auclair, Karine; Kennedy, Jonathan; Richard Hutchinson, C.; Vederas, John C.","Transformations of cyclic nonaketides by Aspergillus terreus mutants blocked for lovastatin biosynthesis at the lovA and lovC genes","Organic & Biomolecular Chemistry","2003","1","1","50","","10.1039/b207721c","","","0.71073","MoKα","","0.2881","0.062","","","0.1103","0.2159","","","","","","0.779","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151358","5.5318","0.0011","9.7123","0.0019","32.163","0.007","90","","90","","90","","1728","0.6","193","2","193","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C19 H30 O4 -","- C19 H30 O4 -","- C76 H120 O16 -","4","1","","Sorensen, John L.; Auclair, Karine; Kennedy, Jonathan; Richard Hutchinson, C.; Vederas, John C.","Transformations of cyclic nonaketides by Aspergillus terreus mutants blocked for lovastatin biosynthesis at the lovA and lovC genes","Organic & Biomolecular Chemistry","2003","1","1","50","","10.1039/b207721c","","","0.71073","MoKα","","0.0885","0.0538","","","0.0944","0.1044","","","","","","1.016","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151359","17.092","0.002","30.493","0.003","16.382","0.002","90","","90","","90","","8538.1","1.7","299.2","","299.2","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C48 H48 O12 -","- C48 H48 O12 -","- C384 H384 O96 -","8","1","","Ashram, Muhammad; Mizyed, Shehadeh; Georghiou, Paris E.","Ester derivatives of hexahomotrioxacalix[3]naphthalenes: conformational and binding properties with alkali metal cations","Organic & Biomolecular Chemistry","2003","1","3","599","","10.1039/b209046p","","","1.5418","CuKα","","0.1917","0.087","","0.091","","0.08","","","1.571","","","2.01","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151360","7.295","0.003","18.22","0.008","20.779","0.007","90","","95.67","0.03","90","","2748.3","1.9","188","2","188","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C18 H16 Fe -","- C18 H16 Fe -","- C144 H128 Fe8 -","8","2","","Baldridge, Kim K.; Donovan-Merkert, Bernadette T.; O'Connor, Joseph M.; Lee, Linda I.; Closson, Adam; Fandrick, Daniel; Tran, Tuan; Bunker, Kevin D.; Fouzi, Mouffouk; Gantzel, Peter","Ring-strain effects on the oxidation potential of enediynes and enediyne complexes","Organic & Biomolecular Chemistry","2003","1","5","763","","10.1039/b209285a","","","0.71073","MoKα","","0.0931","0.0544","","0.1308","0.1082","","","","1.026","1.057","1.057","","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151361","7.316","0.005","11.656","0.008","17.244","0.017","75.28","0.07","80.66","0.07","76.67","0.05","1375","2","190","2","190","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H16 Fe -","- C18 H16 Fe -","- C72 H64 Fe4 -","4","2","","Baldridge, Kim K.; Donovan-Merkert, Bernadette T.; O'Connor, Joseph M.; Lee, Linda I.; Closson, Adam; Fandrick, Daniel; Tran, Tuan; Bunker, Kevin D.; Fouzi, Mouffouk; Gantzel, Peter","Ring-strain effects on the oxidation potential of enediynes and enediyne complexes","Organic & Biomolecular Chemistry","2003","1","5","763","","10.1039/b209285a","","","0.71073","MoKα","","0.0806","0.0611","","0.1733","0.1522","","","","1.043","1.069","1.069","","","","","has coordinates,has disorder","180299","2020-10-21","18:00:00",""
"7151362","10.055","0.007","11.047","0.006","14.409","0.008","107.38","0.04","91.75","0.05","103.08","0.05","1479.5","1.6","186","2","186","2","","","","","","","","3","P -1","-P 1","2","","","","- C19 H18 Fe -","- C19 H18 Fe -","- C76 H72 Fe4 -","4","2","","Baldridge, Kim K.; Donovan-Merkert, Bernadette T.; O'Connor, Joseph M.; Lee, Linda I.; Closson, Adam; Fandrick, Daniel; Tran, Tuan; Bunker, Kevin D.; Fouzi, Mouffouk; Gantzel, Peter","Ring-strain effects on the oxidation potential of enediynes and enediyne complexes","Organic & Biomolecular Chemistry","2003","1","5","763","","10.1039/b209285a","","","0.71073","MoKα","","0.0795","0.0572","","","0.1365","0.1521","","","","","","1.056","","","","has coordinates,has disorder","180299","2020-10-21","18:00:00",""
"7151363","7.7426","0.0003","12.4048","0.0005","24.867","0.001","90","","90","","90","","2388.36","0.16","100","","100","2","","","","","","","see text","5","P 21 21 21","P 2ac 2ab","19","","","","- C29 H24 N2 O2 S2 -","- C29 H24 N2 O2 S2 -","- C116 H96 N8 O8 S8 -","4","1","","van Delden, Richard A.; Koumura, Nagatoshi; Schoevaars, Annemarie; Meetsma, Auke; Feringa, Ben L.","A donor–acceptor substituted molecular motor: unidirectional rotation driven by visible light","Organic & Biomolecular Chemistry","2003","1","1","33","35","10.1039/b209378b","","","0.71073","MoKα","","0.0291","0.0285","","","0.0763","0.0769","","","","","","1.037","","","","has coordinates","288193","2023-12-08","17:12:24",""
"7151364","9.413","0.003","9.609","0.006","12.855","0.004","100.19","0.04","95.29","0.03","109.46","0.05","1064.6","0.9","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C23 H33 N3 -","- C23 H33 N3 -","- C46 H66 N6 -","2","1","","Malassene, Richard; Vanquelef, Enguerran; Toupet, Loic; Hurvois, Jean-Pierre; Moinet, Claude","Diastereoselective preparation of 2,4,6-trisubstituted-2'-cyanopiperidines: application to the construction of the carbon framework of perhydrohistrionicotoxin","Organic & Biomolecular Chemistry","2003","1","3","547","","10.1039/b209387a","","","0.71069","MoKα","","0.1071","0.0615","","","0.1911","0.2077","","","","","","1.095","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151365","12.3997","0.0002","20.171","0.0004","30.6428","0.0006","90","","90","","90","","7664.2","0.2","100","2","100","2","","","","","","","Sandoz-Novartis","4","P 21 21 21","P 2ac 2ab","19","cyclosporin G","cyclosporin G crystal form I ex MeOH LT","","- C63.5 H119.8 N11 O14.9 -","- C63.5 H119.8 N11 O14.9 -","- C254 H479.2 N44 O59.6 -","4","1","","Potter, Brian; Palmer, Rex A.; Withnall, Robert; Jenkins, Terence C.; Chowdhry, Babur Z.","Two new cyclosporin folds observed in the structures of the immunosuppressant cyclosporin G and the formyl peptide receptor antagonist cyclosporin H at ultra-high resolution","Organic & Biomolecular Chemistry","2003","1","9","1466","","10.1039/b210086j","","","0.71073","MoKα","","0.1427","0.0661","","","0.1489","0.1813","","","","","","1.008","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151366","12.43","0.0017","20.256","0.003","30.617","0.004","90","","90","","90","","7708.8","1.9","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","cyclosporin G","cyclosporin G crystal form II ex MeOH and Mg (ClO4)2 LT","","- C64 H121.8 N11 O15.4 -","- C64 H121.8 N11 O15.4 -","- C256 H487.2 N44 O61.6 -","4","1","","Potter, Brian; Palmer, Rex A.; Withnall, Robert; Jenkins, Terence C.; Chowdhry, Babur Z.","Two new cyclosporin folds observed in the structures of the immunosuppressant cyclosporin G and the formyl peptide receptor antagonist cyclosporin H at ultra-high resolution","Organic & Biomolecular Chemistry","2003","1","9","1466","","10.1039/b210086j","","","0.71073","MoKα","","0.0726","0.0558","","","0.1386","0.1485","","","","","","1.042","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151367","17.2986","0.0008","19.69","0.001","24.137","0.004","90","0","90","0","90","0","8221.3","1.5","293","2","293","2","","","","","","","Sandoz-Novartis","4","P 21 21 21","P 2ac 2ab","19","cyclosporin H","cyclosporin H crystal form I ex MeOH RT","","- C62 H123 N11 O18 -","- C62 H123 N11 O18 -","- C248 H492 N44 O72 -","4","1","","Potter, Brian; Palmer, Rex A.; Withnall, Robert; Jenkins, Terence C.; Chowdhry, Babur Z.","Two new cyclosporin folds observed in the structures of the immunosuppressant cyclosporin G and the formyl peptide receptor antagonist cyclosporin H at ultra-high resolution","Organic & Biomolecular Chemistry","2003","1","9","1466","","10.1039/b210086j","","","1.5418","CuKα","","0.1343","0.0892","","","0.2212","0.2418","","","","","","1.06","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151368","17.358","0.002","19.515","0.001","23.225","0.003","90","0","90","0","90","0","7867.3","1.4","293","2","293","2","","","","","","","Sandoz-Novartis","4","P 21 21 21","P 2ac 2ab","19","cyclosporin H","cyclosporin H crystal form II ex MeOH+Mg(ClO4)2 RT","","- C62 H123.8 N11 O18.4 -","- C62 H123.8 N11 O18.4 -","- C248 H495.2 N44 O73.6 -","4","1","","Potter, Brian; Palmer, Rex A.; Withnall, Robert; Jenkins, Terence C.; Chowdhry, Babur Z.","Two new cyclosporin folds observed in the structures of the immunosuppressant cyclosporin G and the formyl peptide receptor antagonist cyclosporin H at ultra-high resolution","Organic & Biomolecular Chemistry","2003","1","9","1466","","10.1039/b210086j","","","1.5418","CuKα","","0.0937","0.0582","","","0.1429","0.1555","","","","","","0.964","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151369","9.1016","0.0009","9.3289","0.0007","11.1653","0.0012","90","","96.651","0.013","90","","941.64","0.16","153","2","153","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C24 H24 N2 O -","- C24 H24 N2 O -","- C48 H48 N4 O2 -","2","1","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.0351","0.0278","","","0.0639","0.0664","","","","","","0.949","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151370","10.8641","0.0016","6.36","0.0008","13.0544","0.0017","90","","90.312","0.01","90","","902","0.2","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C23 H22 N2 -","- C23 H22 N2 -","- C46 H44 N4 -","2","1","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.085","0.0494","","","0.0967","0.1118","","","","","","1.119","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151371","6.6825","0.0005","7.4085","0.0004","23.4403","0.0018","90","","94.08","0.01","90","","1157.53","0.14","153","2","153","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C25 H25 Cl3 N2 O -","- C25 H25 Cl3 N2 O -","- C50 H50 Cl6 N4 O2 -","2","1","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.0403","0.0299","","","0.0657","0.0684","","","","","","0.923","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151372","11.4989","0.0005","14.7712","0.0008","25.141","0.0016","90","","90","","90","","4270.3","0.4","153","2","153","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C54 H50 N4 -","- C54 H50 N4 -","- C216 H200 N16 -","4","1","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.076","0.0326","","","0.0487","0.0558","","","","","","0.73","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151373","20.7692","0.0018","6.0863","0.0004","14.9639","0.0013","90","","99.673","0.01","90","","1864.7","0.3","153","2","153","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C48 H46 N4 O2 -","- C48 H46 N4 O2 -","- C96 H92 N8 O4 -","2","0.5","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.0425","0.0334","","","0.0819","0.0847","","","","","","1.026","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151374","6.1546","0.0005","13.5496","0.0013","17.5877","0.0016","90","","90","","90","","1466.7","0.2","153","2","153","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H17 Br N2 -","- C17 H17 Br N2 -","- C68 H68 Br4 N8 -","4","1","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.0705","0.0315","","","0.051","0.0574","","","","","","0.783","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151375","11.4893","0.0008","20.8542","0.0016","6.4198","0.0004","90","","90","","90","","1538.19","0.19","153","2","153","2","","","","","","","","3","P 21 21 2","P 2 2ab","18","","","","- C34 H50 N4 -","- C34 H50 N4 -","- C68 H100 N8 -","2","0.5","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","0.71073","MoKα","","0.0774","0.0417","","","0.0841","0.0926","","","","","","0.834","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151376","6.5403","0.0008","11.3397","0.001","20.395","0.002","90","","90","","90","","1512.6","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H17 Br N2 -","- C17 H17 Br N2 -","- C68 H68 Br4 N8 -","4","1","","Mathias Düggeli; Catherine Goujon-Ginglinger; Sarah Richard Ducotterd; David Mauron; Christophe Bonte; Alexander von Zelewsky; Helen Stoeckli-Evans; Antonia Neels","Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings","Org. Biomol. Chem.","2003","1","11","1894","1899","10.1039/b210625f","","","1.5418","CuKα","","0.032","0.0314","","","0.0801","0.0808","","","","","","1.075","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151377","12.915","0.002","5.694","0.001","27.08","0.003","90","","98.69","","90","","1968.5","0.5","291","2","291","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","2-hydroxy-6-(4-methoxybencyliden)-2-(1-(4- methoxyphenyl)ethyl)cyclohexanone","2-hydroxy-6-(4-methoxybencyliden)-2-[1-(4-methoxyphenyl)ethyl]cyclohexanone","","- C23 H26 O4 -","- C23 H26 O4 -","- C92 H104 O16 -","4","1","","Klimova, Elena I.; García, Marcos Martínez; Klimova, Tatiana; Ortega, S. Hernandez; Bakinovsky, Leon V.","1,3-Bis(diarylmethylidene)-2-methylidenecyclohexanes in cycloaddition and cyclodimerization reactions. The role of stereoelectronic factors","Organic & Biomolecular Chemistry","2003","1","7","1210","","10.1039/b210890a","","","1.54178","CuKα","","0.0533","0.0423","","","0.1037","0.1124","","","","","","1.041","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151378","15.243","0.006","8.697","0.004","15.245","0.01","90","","108.21","0.04","90","","1919.8","1.8","298","2","298","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H23 N O5 -","- C22 H23 N O5 -","- C88 H92 N4 O20 -","4","1","","Heaney, Frances; Fenlon, Julie; McArdle, Patrick; Cunningham, Desmond","α-Keto amides as precursors to heterocycles—generation and cycloaddition reactions of piperazin-5-one nitrones","Organic & Biomolecular Chemistry","2003","1","7","1122","","10.1039/b210943n","","","0.71069","MoKα","","0.0918","0.0648","","","0.1562","0.1726","","","","","","1.063","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151379","8.4604","0.0016","19.74","0.002","16.8","0.002","90","","90","","90","","2805.7","0.7","298","2","298","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C15 H16 N2 O4 -","- C15 H16 N2 O4 -","- C120 H128 N16 O32 -","8","1","","Heaney, Frances; Fenlon, Julie; McArdle, Patrick; Cunningham, Desmond","α-Keto amides as precursors to heterocycles—generation and cycloaddition reactions of piperazin-5-one nitrones","Organic & Biomolecular Chemistry","2003","1","7","1122","","10.1039/b210943n","","","0.71069","MoKα","","0.0488","0.0435","","","0.1055","0.1105","","","","","","1.026","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151380","14.013","0.001","14.151","0.001","17.216","0.001","88.99","0.01","70.38","0.01","68.04","0.01","2959.5","0.5","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","9-{N-tosylpyrrolo[3,4-d]-1,3-dithiol-2-ylidene}-10-{4,5- bis(methylsulfanyl)-1,3-dithiol-2-ylidene}-9,10-dihydroanthracene","","- C31 H23 N O2 S7 -","- C31 H23 N O2 S7 -","- C124 H92 N4 O8 S28 -","4","2","","Christensen, Christian A.; Bryce, Martin R.; Batsanov, Andrei S.; Becher, Jan","New strategies and building blocks for functionalised 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives, including pyrrolo-annelated derivatives and π-extended systems with intramolecular charge-transferThis paper is Molecular Saddles Part 10. For Part 9 see reference 5c.Electronic supplementary information (ESI) available: NOE spectra for compound 23. See http://www.rsc.org/suppdata/ob/b2/b211153p/","Organic & Biomolecular Chemistry","2003","1","3","511","","10.1039/b211153p","","","0.71073","MoKα","","0.0455","0.0347","","","0.086","0.0921","","","","","","1.021","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151381","9.226","0.001","12.541","0.001","12.76","0.002","99.64","0.01","95.44","0.01","108.73","0.01","1360.9","0.3","120","2","120","2","","","","","","","","4","P -1","-P 1","2","","9-{pyrrolo[3,4-d]-1,3-dithiol-2-ylidene}-10-{4,5-bis(butylsulfanyl)- 1,3-dithiol-2-ylidene}-9,10-dihydroanthracene","","- C30 H29 N S6 -","- C30 H29 N S6 -","- C60 H58 N2 S12 -","2","1","","Christensen, Christian A.; Bryce, Martin R.; Batsanov, Andrei S.; Becher, Jan","New strategies and building blocks for functionalised 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives, including pyrrolo-annelated derivatives and π-extended systems with intramolecular charge-transferThis paper is Molecular Saddles Part 10. For Part 9 see reference 5c.Electronic supplementary information (ESI) available: NOE spectra for compound 23. See http://www.rsc.org/suppdata/ob/b2/b211153p/","Organic & Biomolecular Chemistry","2003","1","3","511","","10.1039/b211153p","","","0.71073","MoKα","","0.0355","0.0305","","","0.0812","0.0846","","","","","","1.031","","","","has coordinates,has disorder","180299","2020-10-21","18:00:00",""
"7151382","12.276","0.003","9.688","0.002","25.605","0.005","90","","100.73","0.01","90","","2992","1.1","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","9-{N-methylpyrrolo[3,4-d]-1,3-dithiol-2-ylidene}-10-{4,5- bis(butylsulfanyl)-1,3-dithiol-2-ylidene}-9,10-dihydroanthracene","","- C31 H31 N S6 -","- C31 H31 N S6 -","- C124 H124 N4 S24 -","4","1","","Christensen, Christian A.; Bryce, Martin R.; Batsanov, Andrei S.; Becher, Jan","New strategies and building blocks for functionalised 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives, including pyrrolo-annelated derivatives and π-extended systems with intramolecular charge-transferThis paper is Molecular Saddles Part 10. For Part 9 see reference 5c.Electronic supplementary information (ESI) available: NOE spectra for compound 23. See http://www.rsc.org/suppdata/ob/b2/b211153p/","Organic & Biomolecular Chemistry","2003","1","3","511","","10.1039/b211153p","","","0.71073","MoKα","","0.0717","0.0488","","","0.1169","0.1331","","","","","","1.019","","","","has coordinates,has disorder","180299","2020-10-21","18:00:00",""
"7151383","11.413","0.017","13.296","0.017","32.14","0.04","81.631","0.01","81.645","0.01","67.077","0.01","4423","10","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C81.5 H93 Cl4 I4 N0 O11.5 -","- C81.5 H77 Cl4 I4 O11.49 -","- C163 H154 Cl8 I8 O22.98 -","2","1","","Matthews, Susan E.; Felix, Vitor; Drew, Michael G. B.; Beer, Paul D.","Halo-Derivatised Calix[4]tubes","Organic & Biomolecular Chemistry","2003","1","7","1232","","10.1039/b211303a","","","0.71073","MoKα","","0.1154","0.0905","","","0.2436","0.2674","","","","","","1.034","","","","has coordinates,has disorder","176453","2020-10-21","18:00:00",""
"7151384","32.85","0.04","13.692","0.019","47.55","0.06","90","","98.546","0.01","90","","21150","5","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C109 H114 Br4 O7 -","- C96 H101 Br4 O14 -","- C768 H808 Br32 O112 -","8","1","","Matthews, Susan E.; Felix, Vitor; Drew, Michael G. B.; Beer, Paul D.","Halo-Derivatised Calix[4]tubes","Organic & Biomolecular Chemistry","2003","1","7","1232","","10.1039/b211303a","","","0.71073","MoKα","","0.2825","0.1262","","","0.31","0.3511","","","","","","0.918","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151385","13.949","0.005","8.165","0.003","12.755","0.005","90","","117.15","0.007","90","","1292.6","0.8","203","2","203","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","3-Oxo-2H-2-[N-(methylphenylhydrazono)]benzothiophene","","- C15 H12 N2 O S -","- C15 H12 N2 O S -","- C60 H48 N8 O4 S4 -","4","1","","Zahra, Jalal A.; Abu Thaher, Bassam A.; El-Abadelah, Mustafa M.; Boese, Roland","An alternative synthesis of 2-(N-arylhydrazono)-1-benzothiophen-3-ones","Organic & Biomolecular Chemistry","2003","1","5","822","","10.1039/b211458p","","","0.71073","MoKα","","0.1283","0.0669","","","0.1423","0.1716","","","","","","0.935","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151386","15.1929","0.0006","7.2142","0.0003","7.2588","0.0003","90","","90","","90","","795.6","0.06","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","1-(2-hydroxy-5-nitrophenyl)ethanone","1-(2-hydroxy-5-nitrophenyl)ethanone","","- C8 H7 N O4 -","- C8 H7 N O4 -","- C32 H28 N4 O16 -","4","1","","Hibbs, David E.; Overgaard, Jacob; Piltz, Ross O.","X‒N Charge density analysis of the hydrogen bonding motif in 1-(2-hydroxy-5-nitrophenyl)ethanoneElectronic supplementary information (ESI) available: multipole population coefficients and pseudoatom parameterization. See http://www.rsc.org/suppdata/ob/b2/b211683a/","Organic & Biomolecular Chemistry","2003","1","7","1191","","10.1039/b211683a","","neutron","1.235","Neutron","","0.0235","0.0226","","","0.0548","0.0554","","","","","","1.18","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151387","15.2399","","7.2338","","7.2773","","90","","90","","90","","802.267","","100","1","100","","","","","","","","","4","P c a 21","P 2c -2ac","29","1-(2-hydroxy-5-nitrophenyl)ethanone","1-(2-hydroxy-5-nitrophenyl)ethanone","","- C8 H7 N O4 -","- C8 H7 N O4 -","- C32 H28 N4 O16 -","4","1","","Hibbs, David E.; Overgaard, Jacob; Piltz, Ross O.","X‒N Charge density analysis of the hydrogen bonding motif in 1-(2-hydroxy-5-nitrophenyl)ethanoneElectronic supplementary information (ESI) available: multipole population coefficients and pseudoatom parameterization. See http://www.rsc.org/suppdata/ob/b2/b211683a/","Organic & Biomolecular Chemistry","2003","1","7","1191","","10.1039/b211683a","","","0.71073","MoKα","","0.027","0.026","","","0.022","0.022","","","","","","2","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151388","12.031","0.005","14.718","0.007","9.702","0.003","107.6","0.03","102.69","0.03","68.07","0.03","1507.9","1.1","293.2","","","","","","","","","","","3","P -1","-P 1","2","","","","- C38 H34 O5 -","- C38 H34 O5 -","- C76 H68 O10 -","2","1","","Yoshitake, Yasuyuki; Misaka, Junichi; Abe, Masaki; Yamasaki, Masatoshi; Eto, Masashi; Harano, Kazunobu","Carboxylic acid clathrate hosts of Diels‒Alder adducts of phencyclone and 2-alkenoic acids. Role of bidentate C‒H⋯O hydrogen bonds between the phenanthrene and carbonyl groups in host‒host networksElectronic supplementary information (ESI) available: structures and packing diagrams. See http://www.rsc.org/suppdata/ob/b2/b212129h/","Organic & Biomolecular Chemistry","2003","1","7","1240","","10.1039/b212129h","","","0.7107","MoKα","","","0","","","","0.0732","","","","","","1.608","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151389","11.899","0.001","13.792","0.001","11.684","0.001","98.192","0.008","111.951","0.007","67.864","0.007","1647.4","0.3","293.2","","","","","","","","","","","3","P -1","-P 1","2","","","","- C43 H36 O4 -","- C43 H36 O4 -","- C86 H72 O8 -","2","1","","Yoshitake, Yasuyuki; Misaka, Junichi; Abe, Masaki; Yamasaki, Masatoshi; Eto, Masashi; Harano, Kazunobu","Carboxylic acid clathrate hosts of Diels‒Alder adducts of phencyclone and 2-alkenoic acids. Role of bidentate C‒H⋯O hydrogen bonds between the phenanthrene and carbonyl groups in host‒host networksElectronic supplementary information (ESI) available: structures and packing diagrams. See http://www.rsc.org/suppdata/ob/b2/b212129h/","Organic & Biomolecular Chemistry","2003","1","7","1240","","10.1039/b212129h","","","0.7107","MoKα","","","0.04","","","","0.0705","","","","","","1.039","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151390","11.882","0.005","12.857","0.003","10.411","0.005","98.94","0.03","104.64","0.04","63.49","0.02","1375.4","1","293.2","","","","","","","","","","","4","P -1","-P 1","2","","","","- C34 H31 N O3 -","- C34 H31 N O3 -","- C68 H62 N2 O6 -","2","1","","Yoshitake, Yasuyuki; Misaka, Junichi; Abe, Masaki; Yamasaki, Masatoshi; Eto, Masashi; Harano, Kazunobu","Carboxylic acid clathrate hosts of Diels‒Alder adducts of phencyclone and 2-alkenoic acids. Role of bidentate C‒H⋯O hydrogen bonds between the phenanthrene and carbonyl groups in host‒host networksElectronic supplementary information (ESI) available: structures and packing diagrams. See http://www.rsc.org/suppdata/ob/b2/b212129h/","Organic & Biomolecular Chemistry","2003","1","7","1240","","10.1039/b212129h","","","0.7107","MoKα","","","0.0532","","","","0.0914","","","","","","1.152","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151391","3.9188","0.0008","30.25","0.006","11.013","0.002","90","","100.187","0.004","90","","1284.9","0.4","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H13 F O2 -","- C17 H13 F O2 -","- C68 H52 F4 O8 -","4","1","","Xu, Wei; Chen, Qing-Yun","A novel approach of cycloaddition of difluorocarbene to α,β-unsaturated aldehydes and ketones: synthesis of gem-difluorocyclopropyl ketones and 2-fluorofurans","Organic & Biomolecular Chemistry","2003","1","7","1151","","10.1039/b212232d","","","0.71073","MoKα","","0.0818","0.0425","","","0.0803","0.0905","","","","","","0.823","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151392","4.5249","0.0002","19.144","0.0009","13.5302","0.0004","90","","94.715","0.001","90","","1168.08","0.08","293","2","293","2","","","","","","","synthesis as described","5","P 1 21/n 1","-P 2yn","14","","N-3,5-dichlorosalicylideneaniline","","- C13 H9 Cl2 N O -","- C13 H9 Cl2 N O -","- C52 H36 Cl8 N4 O4 -","4","1","","Fukuda, Hisatane; Amimoto, Kiichi; Koyama, Hiroyuki; Kawato, Toshio","Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals","Organic & Biomolecular Chemistry","2003","1","9","1578","","10.1039/b212295b","","x-ray","0.71069","MoKα","","0.1217","0.1115","","","0.3221","0.3322","","","","","","1.17","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151393","12.717","0.001","9.179","0.003","13.527","0.002","90","","116.965","0.009","90","","1407.3","0.5","293","2","293","2","","","","","","","synthesis as described","5","P 1 21/c 1","-P 2ybc","14","","N-(3,5-dichlorosalicylidene)-2,6-dimethylaniline","","- C15 H13 Cl2 N O -","- C15 H13 Cl2 N O -","- C60 H52 Cl8 N4 O4 -","4","1","","Fukuda, Hisatane; Amimoto, Kiichi; Koyama, Hiroyuki; Kawato, Toshio","Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals","Organic & Biomolecular Chemistry","2003","1","9","1578","","10.1039/b212295b","","x-ray","0.71073","MoKα","","0.0493","0.0344","","","0.0965","0.1056","","","","","","1.027","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151394","11.228","0.0007","14.8658","0.0008","22.7359","0.0013","90","","91.153","0.003","90","","3794.2","0.4","293","2","293","2","","","","","","","synthesis as described","5","P 1 21/n 1","-P 2yn","14","","N-(3,5-dichlorosalicylidene)-2,6-diisopropylaniline","","- C19 H21 Cl2 N O -","- C19 H21 Cl2 N O -","- C152 H168 Cl16 N8 O8 -","8","2","","Fukuda, Hisatane; Amimoto, Kiichi; Koyama, Hiroyuki; Kawato, Toshio","Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals","Organic & Biomolecular Chemistry","2003","1","9","1578","","10.1039/b212295b","","x-ray","0.71069","MoKα","","0.0997","0.0614","","","0.1601","0.19","","","","","","1.06","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151395","13.805","0.0004","11.639","0.0003","15.6289","0.0004","90","","97.051","0.001","90","","2492.2","0.12","293","2","293","2","","","","","","","synthesis as described","5","P 1 21/n 1","-P 2yn","14","","N-(3,5-dichlorosalicylidene)-2,4,6-tri-tert-butylaniline","","- C25 H33 Cl2 N O -","- C25 H33 Cl2 N O -","- C100 H132 Cl8 N4 O4 -","4","1","","Fukuda, Hisatane; Amimoto, Kiichi; Koyama, Hiroyuki; Kawato, Toshio","Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals","Organic & Biomolecular Chemistry","2003","1","9","1578","","10.1039/b212295b","","x-ray","0.71069","MoKα","","0.1867","0.0883","","","0.1711","0.2128","","","","","","1.104","","","","has coordinates,has disorder","213973","2020-10-21","18:00:00",""
"7151396","23.502","0.009","15.453","0.003","13.68","0.004","90","","118.66","0.02","90","","4360","2","296.2","","296.2","","","","","","","","","7","C 1 c 1","C -2yc","9","","","","- C22 H54.123 Cl9.877 N6 O3.123 Pt Zn3 -","- C22 H48 Cl9.877 N6 O3.123 Pt Zn3 -","- C88 H192 Cl39.508 N24 O12.492 Pt4 Zn12 -","4","1","","Kylie N. Brown; Rodney J. Geue; Trevor W. Hambley; David C. R. Hockless; A. David Rae; Alan M. Sargeson","Specificity in template syntheses of hexaaza-macrobicyclic cages: [Pt(Me5-tricosatrieneN6)]4+ and [Pt(Me5-tricosaneN6)]4+","Org. Biomol. Chem.","2003","1","9","1598","1608","10.1039/b212326f","","","0.7107","MoKα","","0.038","0.0277","","0.0379","","0.0364","","","1.619","","","1.704","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151397","14.724","0.005","14.724","0.005","55.8","0.01","90","","90","","120","","10477","5","294.2","","294.2","","","","","","","","","7","R -3 c :H","-R 3 2""c","167","","","","- C22 H46 Cl7 N6 O2 Pt Zn1.5 -","- C22 H46.0002 Cl6.9999 N6 O2.0001 Pt Zn1.5 -","- C264 H552.002 Cl83.9988 N72 O24.0012 Pt12 Zn18 -","12","0.333333","","Kylie N. Brown; Rodney J. Geue; Trevor W. Hambley; David C. R. Hockless; A. David Rae; Alan M. Sargeson","Specificity in template syntheses of hexaaza-macrobicyclic cages: [Pt(Me5-tricosatrieneN6)]4+ and [Pt(Me5-tricosaneN6)]4+","Org. Biomol. Chem.","2003","1","9","1598","1608","10.1039/b212326f","","","0.7107","MoKα","","0.0622","0.0459","","0.102","","0.088","","","1.932","","","1.964","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151398","12.3217","0.0002","15.4829","0.0002","22.9369","0.0002","90","","90","","90","","4375.8","0.1","203","2","203","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C49 H48 N4 O6 Si Zn -","- C49 H48 N4 O6 Si Zn -","- C196 H192 N16 O24 Si4 Zn4 -","4","1","","Felber, Beatrice; Calle, Carlos; Seiler, Paul; Schweiger, Arthur; Diederich, François","Dendritic metalloporphyrins with a distal H-bond donor as mimics of haemoglobinElectronic supplementary information (ESI) available: procedures for the synthesis of 1 and 5 and iron(ii) insertion into the dendritic porphyrins including full spectral characterisation and complete EPR characterisation of the complex 22·Co(dmim) and the corresponding oxygenated complex. See http://www.rsc.org/suppdata/ob/b2/b212468h/","Organic & Biomolecular Chemistry","2003","1","7","1090","","10.1039/b212468h","","","0.7107","MoKα","","0.0472","0.037","","","0.0765","0.0813","","","","","","1.036","","","","has coordinates","180299","2020-10-21","18:00:00",""
"7151399","18.827","0.004","5.097","0.001","16.083","0.003","90","","96.99","0.02","90","","1531.9","0.5","160","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C15 H26 O5 -","- C15 H26 O5 -","- C60 H104 O20 -","4","1","","McCullough, Kevin J.; Tokuhara, Hidekazu; Masuyama, Araki; Nojima, Masatomo","New approaches to the synthesis of spiro-peroxylactones","Organic & Biomolecular Chemistry","2003","1","9","1522","","10.1039/b300342f","","","0.71073","MoKα","","0.0564","0.0417","","","0.1016","0.1125","","","","","","1.024","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151400","9.726","0.003","18.482","0.005","11.049","0.003","90","","102.86","0.03","90","","1936.3","1","293","2","293","2","","","","","","","chemical synthesis","4","P 1 21/c 1","-P 2ybc","14","PNOX","","","- C24 H19 N O5 -","- C24 H19 N O5 -","- C96 H76 N4 O20 -","4","1","","Christophe Roussel; Rachid Fihi; Kabula Ciamala; Joël Vebrel; Touria Zair; Claude Riche","Spiroheterocycles from reaction of nitrones with methylene-γ-butyrolactones and some of their rearrangements","Org. Biomol. Chem.","2003","1","15","2689","2698","10.1039/b300628j","","","1.5418","CuKα","","0.0573","0.04","","0.1188","","0.1022","","","1.039","","","1.071","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151401","7.474","0.004","12.744","0.004","15.237","0.003","90","","91.49","0.03","90","","1450.8","0.9","296.2","","296.2","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 Cl2 O2 -","- C16 H12 Cl2 O2 -","- C64 H48 Cl8 O8 -","4","1","","Lee T. Boulton; Ian C. Lennon; Raymond McCague","Asymmetric hydrogenation of a 4,4-diaryl-3-butenoate; a novel approach to sertraline","Org. Biomol. Chem.","2003","1","7","1094","1096","10.1039/b301175p","","","0.7107","MoKα","","0.157","0.0575","","","0.0906","0.1135","","","","","","1.022","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151402","8.266","0.0005","8.644","0.0006","12.532","0.001","80.053","0.003","81.737","0.003","75.392","0.003","848.73","0.1","293","2","293","2","","","","","","","","5","P -1","-P 1","2","1,4,7,10,13-pentaoxacyclopentadecane ethanedithioamide clathrate","1,4,7,10,13-pentaoxacyclopentadecane ethanedithioamide clathrate","","- C12 H24 N2 O5 S2 -","- C12 H24 N2 O5 S2 -","- C24 H48 N4 O10 S4 -","2","1","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.71073","MoKα","","0.1092","0.0938","","","0.2308","0.2389","","","","","","1.122","","","","has coordinates,has disorder","213973","2020-10-21","18:00:00",""
"7151403","23.72","0.0001","7.655","0.0002","18.364","0.0003","90","","106.981","0.0006","90","","3189.1","0.1","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","cis-syn-cis (A) isomer (2,3,11,12-dicyclohexano- 1,4,7,10,13,16-hexaoxacyclooctadecane bis(ethanedithioamide) clathrate","cis-syn-cis (A) isomer (2,3,11,12-dicyclohexano-1,4,7,10,13,16- hexaoxacyclooctadecane bis(ethanedithioamide) clathrate","","- C24 H44 N4 O6 S4 -","- C24 H44 N4 O6 S4 -","- C96 H176 N16 O24 S16 -","4","0.5","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.7107","MoKα","","0.0582","0.0424","","","0.0966","0.1033","","","","","","1.067","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151404","12.654","0.003","7.57","0.0015","17.129","0.003","90","","106.14","0.03","90","","1576.1","0.6","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","cis-anti-cis (B) isomer (2,3,11,12-dicyclohexano- 1,4,7,10,13,16-hexaoxacyclooctadecane bis(ethanedithioamide) clathrate","cis-anti-cis (B) isomer (2,3,11,12-dicyclohexano-1,4,7,10,13,16- hexaoxacyclooctadecane bis(ethanedithioamide) clathrate","","- C24 H44 N4 O6 S4 -","- C24 H44 N4 O6 S4 -","- C48 H88 N8 O12 S8 -","2","0.5","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.71073","MoKα","","0.0494","0.0421","","","0.1103","0.1144","","","","","","1.097","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151405","14.196","0.003","7.187","0.002","19.552","0.003","90","","92.18","0.02","90","","1993.4","0.8","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","1,4,7,10,13,16-hexaoxacyclooctadecane N,N'- (thiocarbamoyl)hydrazine clathrate","1,4,7,10,13,16-hexaoxacyclooctadecane N,N'-(thiocarbamoyl)hydrazine clathrate","","- C14 H30 N4 O6 S2 -","- C14 H30 N4 O6 S2 -","- C56 H120 N16 O24 S8 -","4","1","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.7107","MoKα","","0.0452","0.0334","","","0.0746","0.0782","","","","","","1.023","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151406","12.489","0.002","7.509","0.002","14.639","0.003","90","","93.61","0.03","90","","1370.1","0.5","293","2","293","2","","","","","","","","5","P 1 n 1","P -2yac","7","cis-anti-cis isomer (B) (2,3,11,12-dicyclohexano- 1,4,7,10,13,16-hexaoxacyclooctadecane N,N'-(thiocarbamoyl)hydrazine clathrate","cis-anti-cis isomer (B) (2,3,11,12-dicyclohexano- 1,4,7,10,13,16-hexaoxacyclooctadecane N,N'-(thiocarbamoyl)hydrazine clathrate","","- C22 H42 N4 O6 S2 -","- C22 H42 N4 O6 S2 -","- C44 H84 N8 O12 S4 -","2","1","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.71073","MoKα","","0.0315","0.0303","","","0.0789","0.0796","","","","","","1.067","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151407","13.632","0.003","9.475","0.002","19.185","0.004","90","","90","","90","","2478","0.9","293","2","293","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","1,4,7,10,13-pentaoxacyclopentadecane bis(N,N'- (thiocarbamoyl)hydrazine) clathrate","1,4,7,10,13-pentaoxacyclopentadecane bis[N,N'-(thiocarbamoyl)hydrazine] clathrate","","- C14 H32 N8 O5 S4 -","- C14 H32 N8 O5 S4 -","- C56 H128 N32 O20 S16 -","4","0.5","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.71073","MoKα","","0.0519","0.0411","","","0.0917","0.0971","","","","","","1.079","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151408","18.475","0.004","18.445","0.004","9.443","0.002","90","","90","0.03","90","","3217.9","1.2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","1,4,7,10-tetraoxacyclododecane N,N'-(thiocarbamoyl)hydrazine clathrate","1,4,7,10-tetraoxacyclododecane N,N'-(thiocarbamoyl)hydrazine clathrate","","- C10 H22 N4 O4 S2 -","- C10 H22 N4 O4 S2 -","- C80 H176 N32 O32 S16 -","8","2","","Simonov, Yurii A.; Fonari, Marina S.; Zaworotko, Michael J.; Abourahma, Heba; Lipkowski, Janusz; Ganin, Edward V.; Yavolovskii, Arkadii A.","From 1D strands to extended molecular assemblies in the binary compounds of dithiooxamide and dithiobiurea with crown ethers","Organic & Biomolecular Chemistry","2003","1","16","2922","","10.1039/b301379k","","","0.71073","MoKα","","0.0448","0.0343","","","0.079","0.0828","","","","","","0.926","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151409","12.419","0.001","10.721","0.001","9.853","0.001","90","","90","","90","","1311.9","0.2","295","2","295","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C12 H13 N O3 S -","- C12 H13 N O3 S -","- C48 H52 N4 O12 S4 -","4","1","","Jackson, Richard F. W.; Dunn, Sara F. C.; McCamley, Andrew; Clegg, William","Synthesis and crystal structures of 2-substituted-2-phenylsulfonyloxiranes: evidence for a generalised anomeric effect in 2-phenylsulfonyloxiranesElectronic supplementary information (ESI) available: PDB files of the crystal structures of compounds 5, 6b and 7. See http://www.rsc.org/suppdata/ob/b3/b301409f/","Organic & Biomolecular Chemistry","2003","1","14","2527","","10.1039/b301409f","","","1.54184","CuKα","","0.061","0.0605","","","0.16","0.1609","","","","","","1.09","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151410","9.117","0.001","14.592","0.002","25.69","0.004","90","","90","","90","","3417.7","0.8","200","2","200","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C17 H18 O4 S2 -","- C17 H18 O4 S2 -","- C136 H144 O32 S16 -","8","1","","Jackson, Richard F. W.; Dunn, Sara F. C.; McCamley, Andrew; Clegg, William","Synthesis and crystal structures of 2-substituted-2-phenylsulfonyloxiranes: evidence for a generalised anomeric effect in 2-phenylsulfonyloxiranesElectronic supplementary information (ESI) available: PDB files of the crystal structures of compounds 5, 6b and 7. See http://www.rsc.org/suppdata/ob/b3/b301409f/","Organic & Biomolecular Chemistry","2003","1","14","2527","","10.1039/b301409f","","","0.71073","MoKα","","0.0614","0.0353","","","0.0878","0.1018","","","","","","1.064","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151411","9.399","0.001","14.683","0.001","25.747","0.003","90","","90","","90","","3553.2","0.6","295","2","295","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C17 H18 O5 S2 -","- C17 H18 O5 S2 -","- C136 H144 O40 S16 -","8","1","","Jackson, Richard F. W.; Dunn, Sara F. C.; McCamley, Andrew; Clegg, William","Synthesis and crystal structures of 2-substituted-2-phenylsulfonyloxiranes: evidence for a generalised anomeric effect in 2-phenylsulfonyloxiranesElectronic supplementary information (ESI) available: PDB files of the crystal structures of compounds 5, 6b and 7. See http://www.rsc.org/suppdata/ob/b3/b301409f/","Organic & Biomolecular Chemistry","2003","1","14","2527","","10.1039/b301409f","","","0.71073","MoKα","","0.1736","0.062","","","0.1461","0.1974","","","","","","1.045","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151412","8.519","0.001","9.782","0.001","18.631","0.002","90","","90","","90","","1552.6","0.3","294","1","294","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","1-OXO-4B,6B-DIYL-S(S)-CYCLIC SULPHITE","1-OXO-4B,6B-DIYL-S(S)-CYCLIC SULPHITE","","- C15 H24 O4 S -","- C15 H24 O4 S -","- C60 H96 O16 S4 -","4","1","","Andrés García-Granados; María C. Gutiérrez; Francisco Rivas","Improved microbiological hydroxylation of sesquiterpenoids: semisynthesis, structural determination and biotransformation studies of cyclic sulfite eudesmane derivatives","Org. Biomol. Chem.","2003","1","13","2314","2320","10.1039/b301577g","","","0.71073","MoKα","","0.0535","0.0409","","","0.1006","0.1086","","","","","","1.028","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151413","9.321","0.002","7.996","0.002","11.132","0.002","90","","106.32","0.03","90","","796.2","0.3","294","1","294","1","","","","","","","","4","P 1 21 1","P 2yb","4","1-OXO-4B,6B-DIYL-S(R)-CYCLIC SULPHITE","1-OXO-4B,6B-DIYL-S(R)-CYCLIC SULPHITE","","- C15 H24 O4 S -","- C15 H24 O4 S -","- C30 H48 O8 S2 -","2","1","","Andrés García-Granados; María C. Gutiérrez; Francisco Rivas","Improved microbiological hydroxylation of sesquiterpenoids: semisynthesis, structural determination and biotransformation studies of cyclic sulfite eudesmane derivatives","Org. Biomol. Chem.","2003","1","13","2314","2320","10.1039/b301577g","","","0.71073","MoKα","","0.105","0.0672","","","0.1455","0.173","","","","","","1.167","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151414","6.751","0.002","24.363","0.009","8.091","0.001","90","","101.75","0.02","90","","1302.9","0.6","293","2","293","2","","","","","","","","5","P 1 21/a 1","-P 2yab","14","","","","- C8 H17 F2 O5 P -","- C8 H17 F2 O5 P -","- C32 H68 F8 O20 P4 -","4","1","","Arnaud Henry-dit-Quesnel; Loic Toupet; Jean-Claude Pommelet; Thierry Lequeux","A difluorosulfide as a Freon-free source of phosphonodifluoromethyl carbanion","Org. Biomol. Chem.","2003","1","14","2486","2491","10.1039/b301729j","","","0.71069","MoKα","","0.0664","0.0446","","","0.124","0.1349","","","","","","1.054","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151415","10.5516","0.0006","26.343","0.002","11.8322","0.0009","90","","101.243","0.005","90","","3225.8","0.4","213.1","","","","","","","","","","","2","P 1 21/n 1","-P 2yn","14","","","","- C42 H34 -","- C42 H34 -","- C168 H136 -","4","1","","Toyota, Shinji; Iida, Taku; Kunizane, Chinatsu; Tanifuji, Naoki; Yoshida, Yukihiro","Rotational isomerism involving an acetylenic carbon IV: synthesis and structure of bis(1,1';3',1''-terphenyl-2'-yl)ethynes: molecular design of sterically congested alkynes toward restricted rotation about acetylenic axis","Organic & Biomolecular Chemistry","2003","1","13","2298","2302","10.1039/b302016a","","","0.7107","MoKα","","","0.053","","","","0.152","","","","","","1.028","","","","has coordinates","275253","2022-05-09","02:22:47",""
"7151416","12.818","0.007","10.012","0.005","29.263","0.014","90","","90","","90","","3755","3","115","2","115","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C16 H24 O2 Si2 -","- C16 H24 O2 Si2 -","- C128 H192 O16 Si16 -","8","2","","Sankararaman, Sethuraman; Srinivasan, Manivannan","Synthesis of differentially protected/functionalised acetylenic building blocks from p-benzoquinone and their use in the synthesis of new enediynesElectronic supplementary information (ESI) available: 400 MHz 1H NMR and 13C NMR spectra. See http://www.rsc.org/suppdata/ob/b3/b302323k/","Organic & Biomolecular Chemistry","2003","1","13","2388","","10.1039/b302323k","","","0.71073","MoKα","","0.159","0.0757","","","0.1745","0.2075","","","","","","0.846","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151417","12.9389","0.0002","11.7515","0.0003","16.957","0.0004","90","","111.055","0.0008","90","","2406.2","0.09","200","","","","","","","","","","Local laboratory","4","P 1 21/a 1","-P 2yab","14","","","","- C27 H34 O3 Si -","- C27 H34 O3 Si -","- C108 H136 O12 Si4 -","4","1","","Chaplin, Jason H.; Edwards, Alison J.; Flynn, Bernard L.","An enantioselective double Diels?Alder approach to the tetracyclic framework of colombiasin AElectronic supplementary information (ESI) available: Detailed procedures for the preparation of all compounds and their spectral data. See http://www.rsc.org/suppdata/ob/b3/b302522e/","Organic & Biomolecular Chemistry","2003","1","11","1842","","10.1039/b302522e","","","0.71073","MoKα","","","0.0349","","","","0.0409","","","","","","1.0528","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151418","37.608","0.006","8.6937","0.0014","15.053","0.003","90","","99.163","0.003","90","","4858.8","1.5","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","1,2-Di(methoxycarbonyl)-1,10b-dihydropyrolo(2,1-a)isoquinolin- 3-yl-(10H-phenothiazin-10-yl)-1-methanone","1,2-Di(methoxycarbonyl)-1,10b-dihydropyrolo[2,1-a]isoquinolin-3-yl- (10H-phenothiazin-10-yl)-1-methanone","","- C29 H22 N2 O5 S -","- C29 H22 N2 O5 S -","- C232 H176 N16 O40 S8 -","8","1","","Elena Bâcu; Dalila Samson-Belei; Guy Nowogrocki; Axel Couture; Pierre Grandclaudon","Benzoindolizine derivatives of N-acylphenothiazine. Synthesis and characterization","Org. Biomol. Chem.","2003","1","13","2377","2382","10.1039/b302662k","","","0.71073","MoKα","","0.0611","0.0459","","","0.1219","0.1295","","","","","","1.121","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151419","20.18","0.004","18.259","0.004","14.878","0.003","90","","125.498","0.003","90","","4463.1","1.6","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","1-ethoxycarbonyl-2,3-dihydropyrolo(2,1-a)isoquinolin-3-yl- (10H-phenothiazin-10-yl)-1-methanone","1-ethoxycarbonyl-2,3-dihydropyrolo[2,1-a]isoquinolin-3-yl- (10H-phenothiazin-10-yl)-1-methanone","","- C28 H22 N2 O3 S -","- C28 H22 N2 O3 S -","- C224 H176 N16 O24 S8 -","8","1","","Elena Bâcu; Dalila Samson-Belei; Guy Nowogrocki; Axel Couture; Pierre Grandclaudon","Benzoindolizine derivatives of N-acylphenothiazine. Synthesis and characterization","Org. Biomol. Chem.","2003","1","13","2377","2382","10.1039/b302662k","","","0.71073","MoKα","","0.0705","0.0501","","","0.1291","0.1394","","","","","","1.089","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151420","11.16","0.004","28.552","0.009","9.773","0.004","90","","108.615","0.005","90","","2951.2","1.9","173.2","","","","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","","","","- C38 H23 Cl2 F6 N2 O2 P S -","- C32 H23 Cl F6 N O P S -","- C128 H92 Cl4 F24 N4 O4 P4 S4 -","4","1","","Ito, Shunji; Kubo, Takahiro; Kondo, Mao; Kabuto, Chizuko; Morita, Noboru; Asao, Toyonobu; Fujimori, Kunihide; Watanabe, Masataka; Harada, Nobuyuki; Yasunami, Masafumi","Synthesis, stability and bonding situation of tris-, bis- and mono[9-(azuleno[1,2-b]thienyl)]methyl cationsElectronic supplementary information (ESI) available: CV waves of compounds 7a, 8a and 9a, redox details of compounds 7a,b, 8a,b, and 9a,b along with those of 4a, 5a and 6a, ORTEP drawings and details of the X-ray analyses of compounds 2b and 9b and NMR details of the compounds reported. See http://www.rsc.org/suppdata/ob/b3/b302688d/","Organic & Biomolecular Chemistry","2003","1","14","2572","","10.1039/b302688d","","","0.7107","MoKα","","0.0692","0.0411","","","0.0816","0.0916","","","","","","1.069","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151421","9.228","0.004","6.064","0.002","22.113","0.009","90","","106.348","0.005","90","","1187.4","0.8","173.2","","","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C15 H14 S -","- C15 H14 S -","- C60 H56 S4 -","4","1","","Ito, Shunji; Kubo, Takahiro; Kondo, Mao; Kabuto, Chizuko; Morita, Noboru; Asao, Toyonobu; Fujimori, Kunihide; Watanabe, Masataka; Harada, Nobuyuki; Yasunami, Masafumi","Synthesis, stability and bonding situation of tris-, bis- and mono[9-(azuleno[1,2-b]thienyl)]methyl cationsElectronic supplementary information (ESI) available: CV waves of compounds 7a, 8a and 9a, redox details of compounds 7a,b, 8a,b, and 9a,b along with those of 4a, 5a and 6a, ORTEP drawings and details of the X-ray analyses of compounds 2b and 9b and NMR details of the compounds reported. See http://www.rsc.org/suppdata/ob/b3/b302688d/","Organic & Biomolecular Chemistry","2003","1","14","2572","","10.1039/b302688d","","","0.7107","MoKα","","0.0458","0.0356","","","0.0873","0.0928","","","","","","1.041","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151422","10.031","0.003","27.595","0.006","11.908","0.005","90","","124.13","0.05","90","","2728","2","298","","","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","1-Phenyl-2,5-bis(5-(tricyanoethenyl)-2- thienyl)pyrrole/toluene complex","","","- C63 H30 N14 S4 -","- C63 H22 N14 S4 -","- C126 H44 N28 S8 -","2","0.5","","Ogura, Katsuyuki; Zhao, Rui; Mizuoka, Takashi; Akazome, Motohiro; Matsumoto, Shoji","Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest","Organic & Biomolecular Chemistry","2003","1","21","3845","","10.1039/b302689b","","","1.5418","CuKα","","0.077","0.051","","0.116","0.11","0.111","","","1.457","1.012","1.012","1.022","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151423","9.935","0.003","27.547","0.01","12.211","0.006","90","","124.93","0.05","90","","2740","3","298","","","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","1-Phenyl-2,5-bis(5-(tricyanoethenyl)-2-thienyl)pyrrole/p- xylene complex","","","- C64 H32 N14 S4 -","- C64 H32 N14 S4 -","- C128 H64 N28 S8 -","2","0.5","","Ogura, Katsuyuki; Zhao, Rui; Mizuoka, Takashi; Akazome, Motohiro; Matsumoto, Shoji","Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest","Organic & Biomolecular Chemistry","2003","1","21","3845","","10.1039/b302689b","","","1.54178","CuKα","","0.112","0.061","","0.153","0.132","0.134","","","2.516","0.978","0.978","1.018","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151424","9.979","0.003","27.55","0.006","12.035","0.005","90","","124.31","0.05","90","","2733","2","298","","","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","1-Phenyl-2,5-bis(5-(tricyanoethenyl)-2- thienyl)pyrrole/anisole complex","","","- C63 H30 N14 O S4 -","- C63.6 H22 N14 O1.3 S4 -","- C127.2 H44 N28 O2.6 S8 -","2","0.5","","Ogura, Katsuyuki; Zhao, Rui; Mizuoka, Takashi; Akazome, Motohiro; Matsumoto, Shoji","Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest","Organic & Biomolecular Chemistry","2003","1","21","3845","","10.1039/b302689b","","","1.54178","CuKα","","0.059","0.042","","0.089","0.087","0.087","","","1.44","1.008","1.008","1.007","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151425","12.38","0.007","27.61","0.02","16.338","0.01","90","","93.22","0.05","90","","5576","6","298","","","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","1-Phenyl-2,5-bis(5-(tricyanoethenyl)-2-thienyl)pyrrole/m- dimethoxybenzene complex","","","- C64 H32 N14 O2 S4 -","- C64 H32 N14 O2 S4 -","- C256 H128 N56 O8 S16 -","4","1","","Ogura, Katsuyuki; Zhao, Rui; Mizuoka, Takashi; Akazome, Motohiro; Matsumoto, Shoji","Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest","Organic & Biomolecular Chemistry","2003","1","21","3845","","10.1039/b302689b","","","1.54178","CuKα","","0.089","0.053","","0.117","0.11","0.111","","","1.615","1.001","1.001","1.04","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151426","9.829","0.005","27.691","0.01","12.488","0.007","90","","125.32","0.06","90","","2773","3","298","","","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","1-Phenyl-2,5-bis(5-(tricyanoethenyl)-2-thienyl)pyrrole/p- dimethoxybenzene complex","","","- C64 H32 N14 O2 S4 -","- C64 H32 N14 O2 S4 -","- C128 H64 N28 O4 S8 -","2","0.5","","Ogura, Katsuyuki; Zhao, Rui; Mizuoka, Takashi; Akazome, Motohiro; Matsumoto, Shoji","Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest","Organic & Biomolecular Chemistry","2003","1","21","3845","","10.1039/b302689b","","","1.54178","CuKα","","0.064","0.045","","0.091","0.088","0.089","","","1.568","1.004","1.004","1.003","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151427","10.168","0.006","27.708","0.012","11.785","0.011","90","","124.03","0.09","90","","2752","4","298","","","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","1-Phenyl-2,5-bis(5-(tricyanoethenyl)-2-thienyl)pyrrole/indene complex","","","- C65 H30 N14 S4 -","- C65 H22 N14 S4 -","- C130 H44 N28 S8 -","2","0.5","","Ogura, Katsuyuki; Zhao, Rui; Mizuoka, Takashi; Akazome, Motohiro; Matsumoto, Shoji","Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest","Organic & Biomolecular Chemistry","2003","1","21","3845","","10.1039/b302689b","","","1.54178","CuKα","","0.079","0.064","","0.213","0.212","0.212","","","1.428","1.011","1.011","1.006","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151428","15.087","0.002","6.443","0.002","16.736","0.002","90","","106.84","0.01","90","","1557.1","0.6","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H17 N O3 S2 -","- C16 H17 N O3 S2 -","- C64 H68 N4 O12 S8 -","4","1","","Aggarwal, Varinder K.; Grainger, Richard S.; Newton, Gary K.; Spargo, Peter L.; Hobson, Adrian D.; Adams, Harry","Highly diastereoselective 1,3-dipolar cycloaddition reactions of trans-2-methylene-1,3-dithiolane 1,3-dioxide with 3-oxidopyridinium and 3-oxidopyrylium betaines: a route to the tropane skeleton","Organic & Biomolecular Chemistry","2003","1","11","1884","","10.1039/b302834h","","","0.71073","MoKα","","0.0538","0.0418","","0.1117","0.103","","","","1.075","1.109","1.109","","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151429","21.864","0.009","6.091","0.003","20.852","0.009","90","","109.83","0.03","90","","2612","2","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C14 H22 O4 -","- C14 H22 O4 -","- C112 H176 O32 -","8","1","","Jean-François Berrien; Olivier Provot; Joëlle Mayrargue; Michel Coquillay; Liliane Cicéron; Frédérick Gay; Martin Danis; Anne Robert; Bernard Meunier","Alkylation of manganese(II) tetraphenylporphyrin by a synthetic antimalarial trioxane","Org. Biomol. Chem.","2003","1","16","2859","2864","10.1039/b302835f","","","0.71073","MoKα","","0.1045","0.0502","","","0.13","0.1542","","","","","","1.013","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151430","19.555","0.003","19.555","0.003","15.475","0.004","90","","90","","120","","5124.8","1.7","150","2","150","2","","","","","","","","5","P 65","P 65","170","","","","- C30 H39 N3 O6 S3 -","- C30 H39 N3 O6 S3 -","- C180 H234 N18 O36 S18 -","6","1","","Stones, Graham; Argouarch, Gilles; Kennedy, Alan R.; Sherrington, David C.; Gibson, Colin L.","The synthesis of an isopropyl substituted 1,4,7-triazacyclononane via an in situ sequential macrocyclisation method","Organic & Biomolecular Chemistry","2003","1","13","2357","","10.1039/b302887a","","","0.71069","MoKα","","0.1141","0.046","","","0.1105","0.1292","","","","","","1.024","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151431","8.375","0.001","7.653","0.001","9.691","0.001","90","","100.634","0.001","90","","610.47","0.13","173","2","173","2","","","","","","","","4","P 1 21 1","P 2yb","4","(3aS,11bS,11cR)-3a,4,5,11c-Tetrahydro-10b-hydroxy-furo-(3',2':3,4) pyrido(2,1-a)isoindol-2(1H),7(11bH)-dione","(3aS,11bS,11cR)-3a,4,5,11c-Tetrahydro-10b-hydroxy-furo-[3',2' :3,4] pyrido[2,1-a]isoindol-2(1H),7(11bH)-dione","","- C14 H13 N O4 -","- C14 H13 N O4 -","- C28 H26 N2 O8 -","2","1","","Hunter, Roger; Richards, Philip","Stereoselective tetrapyrido[2,1-a]isoindolone synthesis via carbanionic and radical intermediates: a model study for the Tacaman alkaloid D/E ring fusionElectronic supplementary information (ESI) available: Experimental details for compounds 21?23. See http://www.rsc.org/suppdata/ob/b3/b303031h/","Organic & Biomolecular Chemistry","2003","1","13","2348","","10.1039/b303031h","","","0.71073","MoKα","","0.0338","0.0291","","","0.0675","0.0701","","","","","","1.032","","","","has coordinates","205752","2020-10-21","18:00:00",""
"7151432","12.579","0.002","11.92","0.002","12.202","0.002","90","","92.68","0.01","90","","1827.6","0.5","293.2","","293.2","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","?","- C24 H14 N2 Te -","- C96 H56 N8 Te4 -","4","1","","Levy, Amalia; Cohen, Shmuel; Agranat, Israel","Overcrowded 1,8-diazafluorenylidene-chalcoxanthenes. Introducing nitrogens at the fjord regions of bistricyclic aromatic enes","Organic & Biomolecular Chemistry","2003","1","15","2755","","10.1039/b303041e","","","0.7107","MoKalpha","","","0.047","","","0.065","","","","","2.08","2.08","","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151433","18.713","0.003","9.553","0.002","4.831","0.001","90","","90","","90","","863.6","0.3","293.2","","293.2","","","","","","","","","4","P m n 21","P 2ac -2","31","","","","?","- C24 H14 N2 Se -","- C48 H28 N4 Se2 -","2","0.5","","Levy, Amalia; Cohen, Shmuel; Agranat, Israel","Overcrowded 1,8-diazafluorenylidene-chalcoxanthenes. Introducing nitrogens at the fjord regions of bistricyclic aromatic enes","Organic & Biomolecular Chemistry","2003","1","15","2755","","10.1039/b303041e","","","0.7107","MoKalpha","","","0.036","","","0.042","","","","","1.4","1.4","","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151434","18.811","0.004","9.702","0.003","4.639","0.001","90","","90","","90","","846.6","0.4","293.2","","293.2","","","","","","","","","4","P m n 21","P 2ac -2","31","","","","?","- C24 H14 N2 S -","- C48 H28 N4 S2 -","2","0.5","","Levy, Amalia; Cohen, Shmuel; Agranat, Israel","Overcrowded 1,8-diazafluorenylidene-chalcoxanthenes. Introducing nitrogens at the fjord regions of bistricyclic aromatic enes","Organic & Biomolecular Chemistry","2003","1","15","2755","","10.1039/b303041e","","","1.5418","CuKalpha","","","0.038","","","0.05","","","","","2.7","2.7","","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151435","7.448","0.001","15.243","0.001","31.849","0.001","90","","90","","90","","3615.8","0.6","293","2","293","2","","","","","","","","3","P c n b","-P 2b 2ac","60","","bisnaphthalene-2,3-diol 2,3-di(p-methylbenzoyloxy)naphthalene complex","","- C46 H36 O8 -","- C46 H36 O8 -","- C184 H144 O32 -","4","0.5","","Nakamatsu, Seiken; Yoshizawa, Kazuhiro; Toyota, Sinji; Toda, Fumio; Matijasic, Ivanka","Isolation of an inclusion complex of naphthol and its benzoate as an intermediate in the solvent-free benzoylation reaction of naphthol","Organic & Biomolecular Chemistry","2003","1","13","2231","","10.1039/b303060c","","","1.5418","CuKα","","0.058","0.0434","","","0.116","0.1272","","","","","","1.027","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7151436","17.7588","0.001","7.8904","0.0004","13.1044","0.0007","90","","91.161","0.003","90","","1835.86","0.17","150","2","150","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C18 H30 O8 -","- C18 H30 O8 -","- C72 H120 O32 -","4","0.5","","Bartlett, Stephen; Hodgson, Robert; Holland, Joanne M.; Jones, Matthew; Kilner, Colin; Nelson, Adam; Warriner, Stuart","Exploiting predisposition in the stereoselective synthesis of mono-, bi- and tetracyclic oxygen heterocycles: Equilibration between, and trapping of, alternative di- and tetraacetals","Organic & Biomolecular Chemistry","2003","1","13","2393","","10.1039/b303089j","","","0.71073","MoKα","","0.068","0.0481","","","0.1274","0.1395","","","","","","1.05","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151437","10.5524","0.0002","10.8377","0.0002","16.4357","0.0004","90","","101.829","0.0008","90","","1839.73","0.07","295","","295","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","(3E,4E)-4-(dimethylamino)-5-[(E)-phenyldiazenyl]pent-4-ene-2,3-dione 3-(phenylhydrazone)","","- C19 H21 N5 O -","- C19 H21 N5 O -","- C76 H84 N20 O4 -","4","1","","Petr Šimůnek; Valerio Bertolasi; Antonín Lyčka; Vladimír Macháček","An NMR and X-ray study of the structure of the azo coupling product of 4-dimethylaminopent-3-en-2-one and benzenediazonium-tetrafluoroborate","Org. Biomol. Chem.","2003","1","18","3250","3256","10.1039/b303206j","","","0.7107","MoKα","","0.0873","0.054","","","0.1307","0.1634","","","","","","1.078","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151438","9.2515","0.0001","28.6084","0.0004","9.4481","0.0001","90","","99.928","0.0006","90","","2463.19","0.05","150","","150","","","","","","","","?","4","P 1 21 1","P 2yb","4","","","","- C27 H20 N2 O4 -","- C27 H32 N2 O4 -","- C108 H128 N8 O16 -","4","2","","Elena Buñuel; Steven D. Bull; Stephen G. Davies; A. Christopher Garner; Edward D. Savory; Andrew D. Smith; Richard J. Vickers; David J. Watkin","Asymmetric synthesis of substituted 1-aminocyclopropane-1-carboxylic acids via diketopiperazine methodology","Org. Biomol. Chem.","2003","1","14","2531","2542","10.1039/b303348a","","","0.71073","MoKα","","0.0657","0.0657","","0.1407","0.1407","0.1407","","","","","","0.9234","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151439","10.4793","0.0002","10.531","0.0003","12.038","0.0004","90","","96.237","0.001","90","","1320.62","0.06","190","","190","","","","","","","","?","4","P 1 21 1","P 2yb","4","","(1S,3R,6S)-4,7-bis(4-methoxybenzyl)-6-isopropyl-1-phenyl-4,7-diaza- spiro[2.5]octane-5,8-dione","","- C31 H34 N2 O4 -","- C31 H34 N2 O4 -","- C62 H68 N4 O8 -","2","1","","Elena Buñuel; Steven D. Bull; Stephen G. Davies; A. Christopher Garner; Edward D. Savory; Andrew D. Smith; Richard J. Vickers; David J. Watkin","Asymmetric synthesis of substituted 1-aminocyclopropane-1-carboxylic acids via diketopiperazine methodology","Org. Biomol. Chem.","2003","1","14","2531","2542","10.1039/b303348a","","","0.71073","MoKα","","","0.0507","","","","0.0496","","","","","","1.0366","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151440","10.066","0.001","12.92","0.002","19.424","0.002","90","","90","","90","","2526.1","0.5","120","","120","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","CuCl2(1-Np-box)","2,2'-Isopropylidenebis(4-(1-naphthyl)-2-oxazoline) -copper-dichloride","","- C29 H26 Cl2 Cu N2 O2 -","- C29 H26 Cl2 Cu N2 O2 -","- C116 H104 Cl8 Cu4 N8 O8 -","4","1","","Hester L. van Lingen; Wei Zhuang; Tore Hansen; Floris P. J. T. Rutjes; Karl Anker Jørgensen","Formation of optically active chromanes by catalytic asymmetric tandem oxa-Michael addition‒Friedel‒Crafts alkylation reactions","Org. Biomol. Chem.","2003","1","11","1953","1958","10.1039/b303353h","","","0.71073","MoKα","","","0.028","","","","0.035","","","","","","1.21","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151441","10.2389","0.0009","13.089","0.001","19.466","0.002","90","","90","","90","","2608.8","0.4","120","","120","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","CuBr2(1-Np-box)","2,2'-Isopropylidenebis(4-(1-naphthyl)-2-oxazoline) -copper-dibromide","","- C29 H26 Br2 Cu N2 O2 -","- C29 H26 Br2 Cu N2 O2 -","- C116 H104 Br8 Cu4 N8 O8 -","4","1","","Hester L. van Lingen; Wei Zhuang; Tore Hansen; Floris P. J. T. Rutjes; Karl Anker Jørgensen","Formation of optically active chromanes by catalytic asymmetric tandem oxa-Michael addition‒Friedel‒Crafts alkylation reactions","Org. Biomol. Chem.","2003","1","11","1953","1958","10.1039/b303353h","","","0.71073","MoKα","","","0.033","","","","0.035","","","","","","0.9","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151442","15.388","0.005","7.129","0.001","16.839","0.006","90","","112.56","0.03","90","","1705.9","0.9","130","0.2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H22 N2 O6 -","- C17 H22 N2 O6 -","- C68 H88 N8 O24 -","4","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.061","0.0421","","","0.1032","0.1147","","","","","","1.046","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151443","16.441","0.002","5.981","0.002","18.722","0.002","90","","109.47","0.02","90","","1735.7","0.7","130","0.2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H22 N2 O6 -","- C17 H22 N2 O6 -","- C68 H88 N8 O24 -","4","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","1.5418","CuKα","","0.0405","0.036","","","0.1014","0.1048","","","","","","1.012","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151444","9.654","0.001","6.026","0.002","13.044","0.002","90","","107.09","0.01","90","","725.3","0.3","130","0.2","130","0.2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C12 H19 Cl3 O2 -","- C12 H19 Cl3 O2 -","- C24 H38 Cl6 O4 -","2","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","1.5418","CuKα","","0.0382","0.0371","","","0.0966","0.0988","","","","","","0.846","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151445","6.9757","0.0003","36.6182","0.0008","7.0342","0.0002","90","","107.555","0.001","90","","1713.12","0.1","130","0.2","130","0.2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H22 Cl N O4 -","- C17 H22 Cl N O4 -","- C68 H88 Cl4 N4 O16 -","4","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.077","0.0417","","","0.0865","0.0947","","","","","","1.042","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151446","6.179","0.002","11.071","0.003","11.13","0.002","100.57","0.02","90.17","0.02","95.16","0.02","745.3","0.3","130","0.2","130","0.2","","","","","","","","4","P -1","-P 1","2","","","","- C16 H23 N O3 -","- C16 H23 N O3 -","- C32 H46 N2 O6 -","2","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.0531","0.0439","","","0.1252","0.1332","","","","","","1.022","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151447","6.237","0.0001","12.7728","0.0002","20.4391","0.0004","90","","97.722","0.001","90","","1613.49","0.05","130","0.2","130","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H23 N O4 -","- C17 H23 N O4 -","- C68 H92 N4 O16 -","4","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.0697","0.0463","","","0.0943","0.1033","","","","","","1.025","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151448","24.7358","0.0003","6.2022","0.0001","20.9387","0.0004","90","","100.487","0.001","90","","3158.68","0.09","130","2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H24 O3 S -","- C16 H24 O3 S -","- C128 H192 O24 S8 -","8","2","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.0816","0.0443","","","0.0989","0.1112","","","","","","1.036","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151449","6.268","0.0014","10.409","0.0015","13.19","0.0019","94.3","0.011","95.04","0.015","98.83","0.015","843.6","0.3","130","0.2","130","0.2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H26 O3 S -","- C17 H26 O3 S -","- C34 H52 O6 S2 -","2","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","1.5418","CuKα","","0.0442","0.0375","","","0.0954","0.1009","","","","","","1.055","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151450","6.767","0.002","9.556","0.003","10.887","0.003","99.43","0.03","90.68","0.02","105.38","0.02","668.5","0.4","130","0.2","130","0.2","","","","","","","","4","P -1","-P 1","2","","","","- C16 H19 N O3 -","- C16 H19 N O3 -","- C32 H38 N2 O6 -","2","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","1.5418","CuKα","","0.0359","0.0355","","","0.0896","0.0898","","","","","","1.045","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151451","29.1896","0.0006","7.0518","0.0001","15.415","0.0003","90","","93.717","0.001","90","","3166.34","0.1","130","0.2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H18 N2 O6 -","- C17 H18 N2 O6 -","- C136 H144 N16 O48 -","8","2","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.0797","0.0481","","","0.1377","0.168","","","","","","1.137","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151452","7.539","0.003","8.479","0.002","12.043","0.003","75.3","0.02","76.86","0.02","88.83","0.03","724.6","0.4","130","0.2","130","0.2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H19 N O4 -","- C17 H19 N O4 -","- C34 H38 N2 O8 -","2","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","1.5418","CuKα","","0.042","0.0402","","","0.1096","0.1113","","","","","","1.07","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151453","11.7354","0.0009","11.125","0.001","11.132","0.001","90","","104.382","0.007","90","","1407.8","0.2","130","0.2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H20 O3 S -","- C16 H20 O3 S -","- C64 H80 O12 S4 -","4","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","1.5418","CuKα","","0.0355","0.0308","","","0.0781","0.0813","","","","","","1.057","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151454","9","0.002","9.594","0.004","26.225","0.007","90","","90","","90","","2264.4","1.2","130","0.2","130","0.2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C11 H18 O3 S -","- C11 H18 O3 S -","- C88 H144 O24 S8 -","8","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.0545","0.0375","","","0.0918","0.1012","","","","","","1.051","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151455","10.1245","0.0001","12.5511","0.0002","12.4094","0.0001","90","","106.86","0.001","90","","1509.13","0.03","130","0.2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H22 O3 S -","- C17 H22 O3 S -","- C68 H88 O12 S4 -","4","1","","Spiniello, Marisa; White, Jonathan M.","Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative ?-donor ability of C?H and C?C bonds","Organic & Biomolecular Chemistry","2003","1","17","3094","","10.1039/b303453d","","","0.71069","MoKα","","0.0436","0.0377","","","0.1143","0.1199","","","","","","0.997","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151456","13.5954","0.0002","9.5961","0.0001","9.123","0.0002","90","","108.318","0.001","90","","1129.9","0.03","200","2","200","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C11 H14 S2 -","- C11 H14 S2 -","- C44 H56 S8 -","4","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0573","0.0432","","","0.1086","0.1183","","","","","","1.026","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151457","20.021","0.0017","20.021","0.0017","5.685","0.0006","90","","90","","90","","2278.8","0.4","200","2","200","2","","","","","","","","3","I -4","I -4","82","","","","- C11 H14 S2 -","- C11 H14 S2 -","- C88 H112 S16 -","8","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0674","0.0404","","","0.0758","0.0846","","","","","","1.02","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151458","4.5402","0.0001","13.4819","0.0002","9.713","0.0002","90","","96.274","0.001","90","","590.98","0.02","200","2","200","2","","","","","","","","3","P 1 c 1","P -2yc","7","","","","- C12 H16 S2 -","- C12 H16 S2 -","- C24 H32 S4 -","2","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0254","0.0238","","","0.062","0.063","","","","","","1.058","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151459","18.2162","0.0002","9.0748","0.0001","16.3181","0.0002","90","","103.177","0.001","90","","2626.49","0.05","200","2","200","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C13 H18 S2 -","- C13 H18 S2 -","- C104 H144 S16 -","8","2","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0575","0.0379","","","0.0925","0.1098","","","","","","1.056","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151460","9.1023","0.0002","16.8216","0.0003","9.1905","0.0002","90","","90","","90","","1407.21","0.05","200","2","200","2","","","","","","","","3","P n m a","-P 2ac 2n","62","","","","- C14 H20 S2 -","- C14 H20 S2 -","- C56 H80 S8 -","4","0.5","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0425","0.0337","","","0.0878","0.0943","","","","","","1.028","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151461","14.4829","0.0002","10.9233","0.0002","9.0174","0.0001","90","","94.972","0.001","90","","1421.19","0.04","200","2","200","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C14 H20 S2 -","- C14 H20 S2 -","- C56 H80 S8 -","4","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0368","0.0307","","","0.0802","0.0844","","","","","","1.043","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151462","4.5938","0.0002","17.1826","0.0009","9.9664","0.0005","90","","93.166","0.001","90","","785.48","0.07","200","2","200","2","","","","","","","","3","P 1 c 1","P -2yc","7","","","","- C16 H24 S2 -","- C16 H24 S2 -","- C32 H48 S4 -","2","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0416","0.0334","","","0.0786","0.0889","","","","","","1.041","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151463","15.4224","0.0013","15.4224","0.0013","4.8824","0.0006","90","","90","","90","","1161.3","0.2","200","2","200","2","","","","","","","","3","P -4","P -4","81","","","","- C11 H14 Se2 -","- C11 H14 Se2 -","- C44 H56 Se8 -","4","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0563","0.0426","","","0.1026","0.1111","","","","","","1.074","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151464","9.8259","0.0003","4.7316","0.0001","14.5466","0.0004","90","","103.726","0.001","90","","656.99","0.03","200","2","200","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C12 H16 Te2 -","- C12 H16 Te2 -","- C24 H32 Te4 -","2","1","","Schulte, J. Hilko; Werz, Daniel B.; Rominger, Frank; Gleiter, Rolf","Syntheses and solid state structures of cyclic diynes with two chalcogen centres ? a competition between weak interactions","Organic & Biomolecular Chemistry","2003","1","15","2788","","10.1039/b303653g","","","0.71073","MoKα","","0.0444","0.0335","","","0.079","0.0853","","","","","","1.002","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151465","7.005","0.0002","12.8848","0.0004","13.7023","0.0005","91.151","0.001","94.66","0.001","90.007","0.002","1232.4","0.07","200","","200","","","","","","","","?","4","P -1","-P 1","2","","","","- C14 H11 N O4 -","- C14 H11 N O4 -","- C56 H44 N4 O16 -","4","2","","Easton, Christopher J.; Edwards, Alison J.; McNabb, Stephen B.; Merrett, Martin C.; O'Connell, Jenny L.; Simpson, Gregory W.; Simpson, Jamie S.; Willis, Anthony C.","Allylic halogenation of unsaturated amino acidsElectronic supplementary information (ESI) available: synthesis and characterisation of compounds 14?20 and 24?26. See http://www.rsc.org/suppdata/ob/b3/b303719c/","Organic & Biomolecular Chemistry","2003","1","14","2492","","10.1039/b303719c","","","0.71069","MoKα","","","0.0456","","","","0.0507","","","","","","1.0651","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151466","7.4491","0.0005","13.6937","0.001","13.8646","0.001","90","","91.317","0.003","90","","1413.9","0.17","200","","","","","","","","","","Local laboratory","5","P 1 21/a 1","-P 2yab","14","","","","- C14 H11 Cl2 N O4 -","- C14 H11 Cl2 N O4 -","- C56 H44 Cl8 N4 O16 -","4","1","","Easton, Christopher J.; Edwards, Alison J.; McNabb, Stephen B.; Merrett, Martin C.; O'Connell, Jenny L.; Simpson, Gregory W.; Simpson, Jamie S.; Willis, Anthony C.","Allylic halogenation of unsaturated amino acidsElectronic supplementary information (ESI) available: synthesis and characterisation of compounds 14?20 and 24?26. See http://www.rsc.org/suppdata/ob/b3/b303719c/","Organic & Biomolecular Chemistry","2003","1","14","2492","","10.1039/b303719c","","","0.71073","MoKα","","","0.0864","","","","0.0944","","","","","","1.0057","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151467","11.559","0.0003","11.8196","0.0003","15.3885","0.0004","90","","90","","90","","2102.42","0.09","150","","150","","","","","","","","synthesis as described","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H27 N O7 -","- C21 H27 N O7 -","- C84 H108 N4 O28 -","4","1","","Hussaini, Syed Raziullah; Moloney, Mark G.","2,5-Disubstituted pyrrolidines: versatile regioselective and diastereoselective synthesis by enamine reduction and subsequent alkylation","Organic & Biomolecular Chemistry","2003","1","11","1838","","10.1039/b303789d","","","0.71073","MoKα","","","0.0305","","","","0.0346","","","","","","1.0751","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151468","5.8063","0.0002","16.1078","0.0002","22.717","0.0004","90","","90","","90","","2124.65","0.09","150","","150","","","","","","","","synthesis as described","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H29 N O7 -","- C22 H29 N O7 -","- C88 H116 N4 O28 -","4","1","","Hussaini, Syed Raziullah; Moloney, Mark G.","2,5-Disubstituted pyrrolidines: versatile regioselective and diastereoselective synthesis by enamine reduction and subsequent alkylation","Organic & Biomolecular Chemistry","2003","1","11","1838","","10.1039/b303789d","","","0.71073","MoKα","","","0.0414","","","","0.0492","","","","","","1.0012","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151469","6.9448","0.0005","20.84","0.0015","30.325","0.002","90","","90","","90","","4388.9","0.5","298","2","298","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C10 H15 Br Cl N O4 -","- C10 H15 Br Cl N O4 -","- C120 H180 Br12 Cl12 N12 O48 -","12","3","","Paul J. Dransfield; Paul M. Gore; Ivan Prokeš; Michael Shipman; Alexandra M. Z. Slawin","Preparation and reactivity of imino glycals: stereocontrolled, divergent approach to imino sugars","Org. Biomol. Chem.","2003","1","15","2723","2733","10.1039/b303817c","","","0.71073","MoKα","","0.081","0.0349","","","0.053","0.0606","","","","","","0.733","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151470","14.089","0.003","6.305","0.002","25.875","0.005","90","","90","","90","","2298.5","1","150","","150","","","","","","","","?","5","P 21 21 21","P 2ac 2ab","19","","","","- C26 H26 N2 O4 S -","- C26 H26 N2 O4 S -","- C104 H104 N8 O16 S4 -","4","1","","Anwar, Muhammed; Bailey, Jonathan H.; Dickinson, Laura C.; Edwards, Hermia J.; Goswami, Rajesh; Moloney, Mark G.","Pyrrolidinones derived from (S)-pyroglutamic acid: penmacric acid and analoguesPart V. For parts I?IV see refs. 20?22, 24","Organic & Biomolecular Chemistry","2003","1","13","2364","","10.1039/b303924b","","","1.5418","CuKα","","","0.1136","","","","0.1407","","","","","","0.9854","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151471","7.348","0.002","8.642","0.002","9.832","0.003","103.7","0.02","109.61","0.02","97.53","0.02","556.1","0.3","296","2","293","2","","","","","","","synthesis as described","5","P -1","-P 1","2","","","","- C11 H13 Cl N2 O -","- C11 H13 Cl N2 O -","- C22 H26 Cl2 N4 O2 -","2","1","","Ebner, Sieglinde; Wallfisch, Bianca; Andraos, John; Aitbaev, Ilyas; Kiselewsky, Michael; Bernhardt, Paul V.; Kollenz, Gert; Wentrup, Curt","N-Aminopyrroledione?hydrazonoketene?pyrazolium oxide?pyrazolone rearrangements and pyrazolone tautomerismElectronic supplementary information (ESI) available: calculated and observed IR spectra of 8a and X-ray structure, packing diagram, bond lengths and angles for compound 14. See http://www.rsc.org/suppdata/ob/b3/b304070d","Organic & Biomolecular Chemistry","2003","1","14","2550","","10.1039/b304070d","","x-ray","0.71073","MoKα","","0.1272","0.0692","","","0.1896","0.2244","","","","","","1.063","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151472","7.2668","0.0007","8.1141","0.0009","12.9245","0.0015","87.864","0.009","80.786","0.009","84.422","0.009","748.5","0.14","200","2","200","2","","","","","","","","6","P -1","-P 1","2","","","","- C13 H12 Br2 N2 O Zn -","- C13 H12 Br2 N2 O Zn -","- C26 H24 Br4 N4 O2 Zn2 -","2","1","","Merino, Pedro; Tejero, Tomas; Laguna, Mariano; Cerrada, Elena; Moreno, Ana; Lopez, Jose A.","An investigation of the Lewis acid mediated 1,3-dipolar cycloaddition between N-benzyl-C-(2-pyridyl)nitrone and allylic alcohol. Direct entry to isoxazolidinyl C-nucleosidesElectronic supplementary information (ESI) available: optimized geometries (PDB format). See http://www.rsc.org/suppdata/ob/b3/b304112c/","Organic & Biomolecular Chemistry","2003","1","13","2336","","10.1039/b304112c","","","0.71073","MoKα","","0.0513","0.0375","","","0.0942","0.1024","","","","","","1.028","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151473","10.978","0.002","11.643","0.002","12.334","0.002","100.93","0.01","100.53","0.02","111.47","0.01","1384.6","0.5","","","253","2","","","","","","","","7","P -1","-P 1","2","","","","- C52 H50 Ag2 Cl2 N4 O10 P2 -","- C52 H30 Ag2 Cl2 N4 O10 P2 -","- C52 H30 Ag2 Cl2 N4 O10 P2 -","1","0.5","","Merino, Pedro; Tejero, Tomas; Laguna, Mariano; Cerrada, Elena; Moreno, Ana; Lopez, Jose A.","An investigation of the Lewis acid mediated 1,3-dipolar cycloaddition between N-benzyl-C-(2-pyridyl)nitrone and allylic alcohol. Direct entry to isoxazolidinyl C-nucleosidesElectronic supplementary information (ESI) available: optimized geometries (PDB format). See http://www.rsc.org/suppdata/ob/b3/b304112c/","Organic & Biomolecular Chemistry","2003","1","13","2336","","10.1039/b304112c","","","0.71073","MoKα","","0.1401","0.0657","","","0.1415","0.1749","","","","","","1.023","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151474","10.2189","0.0003","15.3206","0.0005","27.7208","0.0006","90","","90","","90","","4340","0.2","173","2","173","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C15 H25 N3 O5 -","- C15 H25 N3 O5 -","- C120 H200 N24 O40 -","8","2","","Hitchcock, Peter B.; Papadopoulos, Konstantinos; Young, Douglas W.","?-Lactams as versatile synthons for homochiral ibotenate analogues with potential for activity at glutamate receptors1","Organic & Biomolecular Chemistry","2003","1","15","2670","","10.1039/b304607a","","","0.71073","MoKα","","0.0793","0.0657","","","0.1961","0.2092","","","","","","1.065","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151475","8.994","0.002","8.994","0.002","43.134","0.006","90","","90","","120","","3021.7","1","293","2","293","2","","","","","","","synthesis as described","4","P 61","P 61","169","","","","- C18 H25 N O7 -","- C18 H25 N O7 -","- C108 H150 N6 O42 -","6","1","","Peter B. Hitchcock; Shazia Rahman (née Masood); Douglas W. Young","An alternative to the use of δ-lactam urethanes in the “ring switch” approach to higher homologues of AMPA-type glutamate antagonists","Org. Biomol. Chem.","2003","1","15","2682","2688","10.1039/b304609p","","x-ray","0.71073","MoKα","","0.0616","0.0451","","","0.1081","0.1198","","","","","","0.968","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151476","7.3952","0.0004","22.4561","0.0011","13.7894","0.0009","90","","106.786","0.004","90","","2192.4","0.2","120","2","120","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","Wood","","","- C2 K N O2 S2 -","- C2 K N O2 S2 -","- C32 K16 N16 O32 S32 -","16","4","","Wood, Mark E.; Cane-Honeysett, Daniel J.; Dowle, Michael D.; Coles, Simon J.; Hursthouse, Michael B.","Synthetic and structural studies on 1,2,4-dithiazolidine-3,5-dione derivatives","Organic & Biomolecular Chemistry","2003","1","17","3015","","10.1039/b305096c","","","0.71073","MoKα","","0.0952","0.0593","","","0.1596","0.1847","","","","","","1.131","","","","has coordinates","187017","2020-10-21","18:00:00",""
"7151477","6.8589","0.0011","10.727","0.002","20.398","0.003","90","","90","","90","","1500.8","0.4","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C16 H26 O2 -","- C16 H26 O2 -","- C64 H104 O8 -","4","1","","Anderson, James C.; Blake, Alexander J.; Graham, Jonathan P.; Wilson, Claire","Investigation of the asymmetric ionic Diels?Alder reaction for the synthesis of cis-decalins","Organic & Biomolecular Chemistry","2003","1","16","2877","","10.1039/b305116a","","","0.71073","MoKα","","0.0485","0.0423","","","0.115","0.12","","","","","","1.06","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7151478","5.9429","0.001","12.548","0.002","20.128","0.004","90","","90","","90","","1501","0.5","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C16 H26 O3 -","- C16 H26 O3 -","- C64 H104 O12 -","4","1","","Anderson, James C.; Blake, Alexander J.; Graham, Jonathan P.; Wilson, Claire","Investigation of the asymmetric ionic Diels?Alder reaction for the synthesis of cis-decalins","Organic & Biomolecular Chemistry","2003","1","16","2877","","10.1039/b305116a","","","0.71073","MoKα","","0.0479","0.0365","","","0.0834","0.0876","","","","","","0.98","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7151479","6.1489","0.0009","14.787","0.002","23.008","0.003","90","","90","","90","","2092","0.5","120","2","120","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C23 H34 O4 -","- C23 H34 O4 -","- C92 H136 O16 -","4","1","","Anderson, James C.; Blake, Alexander J.; Graham, Jonathan P.; Wilson, Claire","Investigation of the asymmetric ionic Diels?Alder reaction for the synthesis of cis-decalins","Organic & Biomolecular Chemistry","2003","1","16","2877","","10.1039/b305116a","","","0.71073","MoKα","","0.1432","0.0934","","","0.1562","0.1767","","","","","","1.129","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151480","14.28","0.0004","25.481","0.002","10.83","0.0003","92.549","0.008","111.862","0.003","85.841","0.009","3647","0.3","296.2","","","","","","","","","","","6","P -1","-P 1","2","","","","- C31 H57 Cl N2 P2 S -","- C31 H57 Cl N2 P2 S -","- C124 H228 Cl4 N8 P8 S4 -","4","2","","Liang, Hongze; Ito, Shigekazu; Yoshifuji, Masaaki","Preparation, structure and coordination properties of 3,3-bis(diisopropylamino)-3-thioxo-1-(2,4,6-tri-tert-butylphenyl)-1,3-diphosphapropene","Organic & Biomolecular Chemistry","2003","1","17","3054","","10.1039/b305216h","","","0.7107","MoKα","","","0.1372","","","","0.1851","","","","","","1.758","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151481","11.0215","0.0006","21.108","0.001","16.2925","0.0005","90","","92.524","0.002","90","","3786.6","0.3","296.2","","","","","","","","","","","7","P 1 21/a 1","-P 2yab","14","","","","- C31 H57 Cl3 N2 P2 Pt S -","- C31 H57 Cl3 N2 P2 Pt S -","- C124 H228 Cl12 N8 P8 Pt4 S4 -","4","1","","Liang, Hongze; Ito, Shigekazu; Yoshifuji, Masaaki","Preparation, structure and coordination properties of 3,3-bis(diisopropylamino)-3-thioxo-1-(2,4,6-tri-tert-butylphenyl)-1,3-diphosphapropene","Organic & Biomolecular Chemistry","2003","1","17","3054","","10.1039/b305216h","","","0.7107","MoKα","","","0.0406","","","","0.0542","","","","","","1.571","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151482","20.7395","0.0007","16.555","0.0005","11.8561","0.0006","90","","90.06","0.002","90","","4070.7","0.3","296.2","","","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C34.5 H61 Cl3 N2 P2 Pt S -","- C34.5 H57 Cl3 N2 P2 Pt S -","- C138 H228 Cl12 N8 P8 Pt4 S4 -","4","1","","Liang, Hongze; Ito, Shigekazu; Yoshifuji, Masaaki","Preparation, structure and coordination properties of 3,3-bis(diisopropylamino)-3-thioxo-1-(2,4,6-tri-tert-butylphenyl)-1,3-diphosphapropene","Organic & Biomolecular Chemistry","2003","1","17","3054","","10.1039/b305216h","","","0.7107","MoKα","","","0.0555","","","","0.0651","","","","","","1.466","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151483","7.4271","0.0007","9.2771","0.0009","9.6627","0.0009","113.68","0.001","106.518","0.002","96.026","0.002","566.05","0.09","173","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C13 H13 Cl N2 O -","- C13 H13 Cl N2 O -","- C26 H26 Cl2 N4 O2 -","2","1","","Ihmels, Heiko; Faulhaber, Katja; Wissel, Kathrin; Viola, Giampietro; Vedaldi, Daniela","6-Aminoacridizinium bromide: a fluorescence probe which lights up in AT-rich regions of DNA","Organic & Biomolecular Chemistry","2003","1","17","2999","3001","10.1039/b305439j","","","0.71073","MoKα","","0.0466","0.046","","","0.1302","0.1309","","","","","","1.19","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151484","14.396","0.003","8.9008","0.0018","15.043","0.003","90","","105.83","0.03","90","","1854.4","0.7","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H20 N2 O5 S -","- C20 H20 N2 O5 S -","- C80 H80 N8 O20 S4 -","4","1","","Moody, Christopher J.; Slawin, Alexandra M. Z.; Willows, David","Dirhodium(ii) tetraacetate catalysed reactions of diazo thioamides: isolation and cycloaddition of anhydro-4-hydroxy-1,3-thiazolium hydroxides (thioisom�nchnones), an approach to analogues of dehydrogliotoxin","Organic & Biomolecular Chemistry","2003","1","15","2716","","10.1039/b305698h","","","1.54178","CuKα","","0.0627","0.0454","","","0.123","0.1358","","","","","","1.033","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151485","7.8459","0.0007","9.6884","0.0009","24.179","0.002","90","","96.467","0.002","90","","1826.3","0.3","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C19 H17 N O6 S -","- C19 H17 N O6 S -","- C76 H68 N4 O24 S4 -","4","1","","Moody, Christopher J.; Slawin, Alexandra M. Z.; Willows, David","Dirhodium(ii) tetraacetate catalysed reactions of diazo thioamides: isolation and cycloaddition of anhydro-4-hydroxy-1,3-thiazolium hydroxides (thioisom�nchnones), an approach to analogues of dehydrogliotoxin","Organic & Biomolecular Chemistry","2003","1","15","2716","","10.1039/b305698h","","","0.71073","MoKα","","0.0926","0.0456","","","0.1062","0.1253","","","","","","0.925","","","","has coordinates","180300","2020-10-21","18:00:00",""
"7151486","8.48","0.04","18.39","0.09","10.41","0.05","90","","99.58","0.05","90","","1601","13","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H17 N O3 S -","- C17 H17 N O3 S -","- C68 H68 N4 O12 S4 -","4","1","","Moody, Christopher J.; Slawin, Alexandra M. Z.; Willows, David","Dirhodium(ii) tetraacetate catalysed reactions of diazo thioamides: isolation and cycloaddition of anhydro-4-hydroxy-1,3-thiazolium hydroxides (thioisom�nchnones), an approach to analogues of dehydrogliotoxin","Organic & Biomolecular Chemistry","2003","1","15","2716","","10.1039/b305698h","","","0.71073","MoKα","","0.163","0.0654","","","0.1506","0.1889","","","","","","0.976","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151487","5.2341","0.0002","12.3751","0.0005","14.2381","0.0007","90","","97.688","0.001","90","","913.95","0.07","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H24 O7 S -","- C16 H24 O7 S -","- C32 H48 O14 S2 -","2","1","","Karisalmi, Kaisa; Rissanen, Kari; Koskinen, Ari M. P.","An enantioselective synthesis of the C(33)?C(37) fragment of Amphotericin BElectronic supplementary information (ESI) available: Tables S1?S5: crystal data and structure refinement, atomic coordinates and equivalent isotropic displacement parameters, bond lengths and angles, anisotropic displacement parameters and torsion angles for compound 7b. See http://www.rsc.org/suppdata/ob/b3/b305845j/","Organic & Biomolecular Chemistry","2003","1","18","3193","","10.1039/b305845j","","","0.71073","MoKα","","0.0583","0.0435","","","0.103","0.1099","","","","","","1.021","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151488","17.6824","0.0003","17.9641","0.0004","11.6546","0.0003","90","","90","","90","","3702.07","0.14","253","2","253","2","","","","","","","","8","P 21 21 21","P 2ac 2ab","19","(h3-Allyl)[(aS)-2-[4,4-dimethyl-oxazol-2-yl]-2^[$B!G^[(B-diphenylphosphino- 1,1^[$B!G^[(B-binaphthyl]palladium(II) hexafluoroantimonate","","","- C37 H30 F6 N O P Pd Sb -","- C40 H35 F6 N O P Pd Sb -","- C160 H140 F24 N4 O4 P4 Pd4 Sb4 -","4","1","","Hatano, Manabu; Mikami, Koichi","Highly enantioselective alkaloid synthesis via ene-type cyclizations catalyzed by cationic chiral palladium(ii) complexes of PN-ligands with an achiral oxazoline unitElectronic supplementary information (ESI) available: spectral data of substrates, cyclized products and PN-ligands and crystallographic data of Pd complexes. See http://www.rsc.org/suppdata/ob/b3/b305865b/","Organic & Biomolecular Chemistry","2003","1","22","3871","","10.1039/b305865b","","","0.71069","MoKα","","0.038","0.0343","","","0.0793","0.0807","","","","","","1.098","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151489","6.271","0.001","21.359","0.003","6.932","0.001","90","","108.27","0.01","90","","881.7","0.2","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","2-phenyl-5-bromopyrimidine","2-phenyl-5-bromopyrimidine","","- C10 H7 Br N2 -","- C10 H7 Br N2 -","- C40 H28 Br4 N8 -","4","1","","Hughes, Gregory; Wang, Changsheng; Batsanov, Andrei S.; Fern, Michael; Frank, Stephen; Bryce, Martin R.; Perepichka, Igor F.; Monkman, Andrew P.; Lyons, Benjamin P.","New pyrimidine- and fluorene-containing oligo(arylene)s: synthesis, crystal structures, optoelectronic properties and a theoretical study Electronic supplementary information (ESI) available: experimental synthetic procedures for compounds 4, 9 and 10; HF/6?31G(d,p) and B3LYP/6?31G(d,p) calculated geometries and frontier orbitals for compounds 13E, 14E and 16E?21E. See http://www.rsc.org/suppdata/ob/b3/b305870k/","Organic & Biomolecular Chemistry","2003","1","17","3069","","10.1039/b305870k","","","0.71073","MoKα","","0.0375","0.0287","","","0.0746","0.0786","","","","","","1.058","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151490","7.444","0.002","5.731","0.002","26.932","0.008","90","","92.82","0.01","90","","1147.6","0.6","103","2","103","2","","","","","","","","3","I 1 2/a 1","-I 2ya","15","2,5-diphenylpyrimidine","2,5-diphenylpyrimidine","","- C16 H12 N2 -","- C16 H12 N2 -","- C64 H48 N8 -","4","0.5","","Hughes, Gregory; Wang, Changsheng; Batsanov, Andrei S.; Fern, Michael; Frank, Stephen; Bryce, Martin R.; Perepichka, Igor F.; Monkman, Andrew P.; Lyons, Benjamin P.","New pyrimidine- and fluorene-containing oligo(arylene)s: synthesis, crystal structures, optoelectronic properties and a theoretical study Electronic supplementary information (ESI) available: experimental synthetic procedures for compounds 4, 9 and 10; HF/6?31G(d,p) and B3LYP/6?31G(d,p) calculated geometries and frontier orbitals for compounds 13E, 14E and 16E?21E. See http://www.rsc.org/suppdata/ob/b3/b305870k/","Organic & Biomolecular Chemistry","2003","1","17","3069","","10.1039/b305870k","","","0.71073","MoKα","","0.0517","0.042","","","0.1141","0.1234","","","","","","1.057","","","","has coordinates,has disorder","180300","2020-10-21","18:00:00",""
"7151491","10.244","0.003","10.979","0.003","13.52","0.003","93.37","0.01","93.99","0.01","95.14","0.01","1507.6","0.7","100","2","100","2","","","","","","","","4","P -1","-P 1","2","2,7-bis(5-bromo-2-pyrimidyl)-9,9-dihexylfluorene","2,7-bis(5-bromo-2-pyrimidyl)-9,9-dihexylfluorene","","- C33 H36 Br2 N4 -","- C33 H36 Br2 N4 -","- C66 H72 Br4 N8 -","2","1","","Hughes, Gregory; Wang, Changsheng; Batsanov, Andrei S.; Fern, Michael; Frank, Stephen; Bryce, Martin R.; Perepichka, Igor F.; Monkman, Andrew P.; Lyons, Benjamin P.","New pyrimidine- and fluorene-containing oligo(arylene)s: synthesis, crystal structures, optoelectronic properties and a theoretical study Electronic supplementary information (ESI) available: experimental synthetic procedures for compounds 4, 9 and 10; HF/6?31G(d,p) and B3LYP/6?31G(d,p) calculated geometries and frontier orbitals for compounds 13E, 14E and 16E?21E. See http://www.rsc.org/suppdata/ob/b3/b305870k/","Organic & Biomolecular Chemistry","2003","1","17","3069","","10.1039/b305870k","","","0.71073","MoKα","","0.1197","0.0941","","","0.2573","0.278","","","","","","1.107","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151492","7.5858","0.0001","8.444","0.0001","43.4801","0.0007","90","","90","","90","","2785.1","0.07","180","2","180","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H34 N2 O7 Si -","- C28 H34 N2 O7 Si -","- C112 H136 N8 O28 Si4 -","4","1","","Fleming, Ian; Maiti, Pranab; Ramarao, Chandrashekar","Stereocontrol of 1,5-related stereocentres using an intermediate silyl group?the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group","Organic & Biomolecular Chemistry","2003","1","22","3989","","10.1039/b305880h","","","0.71073","MoKα","","0.0654","0.0423","","","0.0776","0.0853","","","","","","1.078","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151493","7.1067","0.0001","14.8638","0.0004","26.2267","0.0007","90","","90","","90","","2770.39","0.11","180","2","180","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C27 H32 N2 O7 Si -","- C27 H32 N2 O7 Si -","- C108 H128 N8 O28 Si4 -","4","1","","Fleming, Ian; Maiti, Pranab; Ramarao, Chandrashekar","Stereocontrol of 1,5-related stereocentres using an intermediate silyl group?the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group","Organic & Biomolecular Chemistry","2003","1","22","3989","","10.1039/b305880h","","","0.71073","MoKα","","0.057","0.0405","","","0.0825","0.0889","","","","","","1.048","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151494","12.1915","0.0003","15.2706","0.0006","8.8616","0.0003","90","","90","","90","","1649.78","0.09","180","2","180","2","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C17 H24 O Si -","- C17 H24 O Si -","- C68 H96 O4 Si4 -","4","1","","Fleming, Ian; Maiti, Pranab; Ramarao, Chandrashekar","Stereocontrol of 1,5-related stereocentres using an intermediate silyl group?the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group","Organic & Biomolecular Chemistry","2003","1","22","3989","","10.1039/b305880h","","","0.71069","MoKα","","0.0487","0.0333","","0.1175","0.0763","","","","1.044","1.056","1.056","","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151495","6.822","0.001","23.501","0.005","23.73","0.005","90","","90","","90","","3804.5","1.3","293","2","150","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C19 H24.5 N2 O7.5 -","- C19 H24.5 N2 O7.5 -","- C152 H196 N16 O60 -","8","1","","Lech Kozerski; Bogdan Kamieński; Robert Kawęcki; Zofia Urbanczyk-Lipkowska; Wojciech Bocian; Elżbieta Bednarek; Jerzy Sitkowski; Katarzyna Zakrzewska; Kim T. Nielsen; Poul Erik Hansen","Solution and solid state 13C NMR and X-ray studies of genistein complexes with amines. Potential biological function of the C-7, C-5, and C-4'-OH groups","Org. Biomol. Chem.","2003","1","20","3578","3585","10.1039/b305991j","","","1.54178","CuKα","","0.0718","0.0643","","","0.1467","0.152","","","","","","1.257","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151496","10.323","0.001","8.328","0.001","15.665","0.001","90","1","108.3","0.01","90","1","1278.6","0.2","298","","","","","","","","","","Per Wiklund: Organic Chemistry CNT Biosciences, Karolinska Institute, Novum 141 57 Huddinge, Sweden","5","P 1 21/c 1","-P 2ybc","14","(()3a-Pentafluoroethyl-3,4-dioxa-9b-aza- cyclopenta(a)naphthalene-2,5-dione","(()3a-Pentafluoroethyl-3,4-dioxa-9b-aza-cyclopenta[a]naphthalene-2,5-dione","","- C12 H6 F5 N O4 -","- C12 H6 F5 N O4 -","- C48 H24 F20 N4 O16 -","4","1","","Wiklund, Per; Romero, Ivan; Bergman, Jan","Products from dehydration of dicarboxylic acids derived from anthranilic acid","Organic & Biomolecular Chemistry","2003","1","19","3396","","10.1039/b306032b","","","0.71073","MoKα","","0.138","0.05","","0.172","0.06","0.06","","","2.455","1.554","1.554","1.554","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151497","10.483","0.005","9.356","0.004","12.297","0.003","90","","101.14","0.03","90","","1183.4","0.8","298","2","298","2","","","","","","","","4","P 1 21/a 1","-P 2yab","14","","","","- C11 H16 N4 O -","- C11 H16 N4 O -","- C44 H64 N16 O4 -","4","1","","Blake, Alexander J.; Clarke, David; Mares, Richard W.; McNab, Hamish","Synthesis and chemistry of 3-tert-butyl-1,5-diaminopyrazole.","Organic & biomolecular chemistry","2003","1","23","4268","4274","10.1039/b306058f","","","0.71073","MoKα","","0.139","0.057","","","0.136","0.171","","","","","","1.009","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7151498","9.974","0.003","14.182","0.005","16.104","0.005","90","","107.088","0.005","90","","2177.4","1.2","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H25 N O4 -","- C25 H25 N O4 -","- C100 H100 N4 O16 -","4","1","","Gillson, Ashley-Mae E.; Glover, Stephen A.; Tucker, David J.; Turner, Peter","Crystal structures and properties of mutagenic N-acyloxy-N-alkoxyamides ? ?most pyramidal? acyclic amides","Organic & Biomolecular Chemistry","2003","1","19","3430","","10.1039/b306098p","","","0.71073","MoKα","","0.046","0.0349","","","0.0908","0.0951","","","","","","1.465","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151499","9.291","0.0019","17.063","0.004","18.64","0.004","90","","98.007","0.004","90","","2926.2","1.1","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H41 N O4 -","- C33 H41 N O4 -","- C132 H164 N4 O16 -","4","1","","Gillson, Ashley-Mae E.; Glover, Stephen A.; Tucker, David J.; Turner, Peter","Crystal structures and properties of mutagenic N-acyloxy-N-alkoxyamides ? ?most pyramidal? acyclic amides","Organic & Biomolecular Chemistry","2003","1","19","3430","","10.1039/b306098p","","","0.71073","MoKα","","0.0607","0.0425","","","0.0863","0.0909","","","","","","1.318","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151500","7.9079","0.0008","12.48","0.002","7.7913","0.0007","90","","92.89","0.01","90","","767.95","0.16","293","","293","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C6 H10 N4 S -","- C6 H10 N4 S -","- C24 H40 N16 S4 -","4","1","","Thanyasirikul, Yupa; Pakawatchai, Chaveng; Cole, Marcus L.; Junk, Peter C.; Skelton, Brian W.; White, Allan H.","Reappraising the formation of Jaff�'s base: studies of the treatment of imidazolidine-2-thione with mild oxidising agents","Organic & Biomolecular Chemistry","2003","1","18","3217","","10.1039/b306647a","","","0.71073","MoKα","","0.099","0.049","","0.062","","0.052","","","1.181","","","1.327","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151501","15.295","0.003","6.895","0.007","9.063","0.002","90","","90","","90","","955.8","1","293","","293","","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C6 H11 Br N4 S -","- C6 H11 Br N4 S -","- C24 H44 Br4 N16 S4 -","4","0.5","","Thanyasirikul, Yupa; Pakawatchai, Chaveng; Cole, Marcus L.; Junk, Peter C.; Skelton, Brian W.; White, Allan H.","Reappraising the formation of Jaff�'s base: studies of the treatment of imidazolidine-2-thione with mild oxidising agents","Organic & Biomolecular Chemistry","2003","1","18","3217","","10.1039/b306647a","","","0.71073","MoKα","","0.051","0.033","","0.059","","0.049","","","1.115","","","1.148","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7151502","13.42","0.001","12.95","0.001","14.439","0.001","90","","90","","90","","2509.3","0.3","150","","150","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C6 H9 I3 N2 S -","- C6 H9 I3 N2 S -","- C48 H72 I24 N16 S8 -","8","1","","Thanyasirikul, Yupa; Pakawatchai, Chaveng; Cole, Marcus L.; Junk, Peter C.; Skelton, Brian W.; White, Allan H.","Reappraising the formation of Jaff�'s base: studies of the treatment of imidazolidine-2-thione with mild oxidising agents","Organic & Biomolecular Chemistry","2003","1","18","3217","","10.1039/b306647a","","","0.71073","MoKα","","0.059","0.037","","0.049","","0.044","","","1.066","","","1.116","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7151503","8.4698","0.0002","6.4952","0.0002","20.0695","0.0004","90","","94.0089","0.0006","90","","1101.38","0.05","150","","150","","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","","","","- C22 H32 O4 Si -","- C22 H32 O4 Si -","- C44 H64 O8 Si2 -","2","1","","Godage, H. Yasmin; Chambers, David J.; Evans, Graham R.; Fairbanks, Antony J.","Stereoselective synthesis of C-glycosides from carboxylic acids: the tandem Tebbe?Claisen approachThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3772","","10.1039/b306675b","","","0.71073","MoKα","","","0.0319","","","","0.0373","","","","","","1.0489","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151504","5.8009","0.0002","13.1214","0.0004","18.5666","0.0005","90","","90","","90","","1413.21","0.08","150","","150","","","","","","","","synthesis as derscribed","3","P 21 21 21","P 2ac 2ab","19","","","","- C16 H18 O4 -","- C16 H18 O4 -","- C64 H72 O16 -","4","1","","Godage, H. Yasmin; Chambers, David J.; Evans, Graham R.; Fairbanks, Antony J.","Stereoselective synthesis of C-glycosides from carboxylic acids: the tandem Tebbe?Claisen approachThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3772","","10.1039/b306675b","","","0.71073","MoKα","","","0.0289","","","","0.0319","","","","","","1.0546","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151505","5.1126","0.0005","14.2991","0.0002","19.1347","0.0008","90","","90","","90","","1398.85","0.15","150","","150","","","","","","","","synthesis as described","3","P 21 21 21","P 2ac 2ab","19","","","","- C16 H18 O4 -","- C16 H18 O4 -","- C64 H72 O16 -","4","1","","Godage, H. Yasmin; Chambers, David J.; Evans, Graham R.; Fairbanks, Antony J.","Stereoselective synthesis of C-glycosides from carboxylic acids: the tandem Tebbe?Claisen approachThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3772","","10.1039/b306675b","","","0.71073","MoKα","","","0.0315","","","","0.0355","","","","","","1.041","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151506","13.7851","0.0003","17.4951","0.0004","17.3777","0.0004","90","","102.901","0.0015","90","","4085.22","0.16","150","","150","","","","","","","","?","5","P 1 21/c 1","-P 2ybc","14","","","","- C96 H94 Cl2 N4 Si2 -","- C96 H94 Cl2 N4 Si2 -","- C192 H188 Cl4 N8 Si4 -","2","0.5","","Krivokapic, Alexander; Anderson, Harry L.","Synthesis and crystal structure of a meso-trialkynyl-[28]hexaphyrinThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3639","","10.1039/b306725b","","","0.71073","MoKα","","0.0907","0.0634","","0.0981","0.075","0.0749","","","","","","1.1072","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151507","32.9322","0.0014","8.629","0.0004","36.665","0.002","90","","99.019","0.002","90","","10290.3","0.9","150","","150","","","","","","","","?","5","P 1 21/a 1","-P 2yab","14","","","","- C112 H111 Cl3 N6 Si3 -","- C112 H111 Cl3 N6 Si3 -","- C448 H444 Cl12 N24 Si12 -","4","1","","Krivokapic, Alexander; Anderson, Harry L.","Synthesis and crystal structure of a meso-trialkynyl-[28]hexaphyrinThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3639","","10.1039/b306725b","","","0.71073","MoKα","","0.2122","0.1833","","0.2016","0.1626","0.1611","","","","","","0.9523","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151508","8.6168","0.0008","9.3641","0.0009","56.595","0.003","90","","90","","90","","4566.6","0.7","180","2","180","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C44 H70 N2 O12 -","- C44 H70 N2 O12 -","- C176 H280 N8 O48 -","4","1","","Critchley, P.; Clarkson, G. J.","Carbohydrate-protein interactions at interfaces: comparison of the binding of Ricinus communis lectin to two series of synthetic glycolipids using surface plasmon resonance studies.","Organic & biomolecular chemistry","2003","1","23","4148","4159","10.1039/b306784j","","","0.71073","MoKα","","0.1301","0.0652","","","0.1065","0.1276","","","","","","1.02","","","","has coordinates,has disorder","180301","2020-10-21","18:00:00",""
"7151509","10.747","0.0003","8.3113","0.0002","13.5613","0.0004","90","","100.432","0.0012","90","","1191.29","0.06","200","","200","","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","","","","- C20 H24 O11 S2 -","- C20 H24 O11 S2 -","- C40 H48 O22 S4 -","2","1","","Hollowood, Christopher J.; Ley, Steven V.","Reductive decomplexation of ?-allyltricarbonyliron lactone complexes using sodium naphthalenide as a route to stereodefined 1,7-diols and 2,3-diene-1,7-diols","Organic & Biomolecular Chemistry","2003","1","18","3197","","10.1039/b306861g","","","0.71073","MoKα","","","0.0417","","","","0.0465","","","","","","1.0631","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151510","15.0086","0.0005","8.0675","0.0003","15.1036","0.0005","90","","98.916","0.002","90","","1806.67","0.11","150","","150","","","","","","","","synthesis as described","4","P 1 21/a 1","-P 2yab","14","","","","- C20 H23 N O4 -","- C20 H23 N O4 -","- C80 H92 N4 O16 -","4","1","","John E. Moses; Jack E. Baldwin; Sébastien Brückner; Serena J. Eade; Robert M. Adlington","Biomimetic studies on polyenes","Org. Biomol. Chem.","2003","1","21","3670","3684","10.1039/b306933h","","","0.71073","MoKα","","","0.043","","","","0.0527","","","","","","1.0561","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151511","8.0506","0.0004","12.3846","0.0005","13.2746","0.0007","64.465","0.002","86.93","0.002","73.06","0.002","1138.44","0.1","150","","150","","","","","","","","synthesis as described","4","P -1","-P 1","2","","","","- C25 H23 N3 O8 -","- C25 H23 N3 O8 -","- C50 H46 N6 O16 -","2","1","","John E. Moses; Jack E. Baldwin; Sébastien Brückner; Serena J. Eade; Robert M. Adlington","Biomimetic studies on polyenes","Org. Biomol. Chem.","2003","1","21","3670","3684","10.1039/b306933h","","","0.71073","MoKα","","","0.0495","","","","0.0578","","","","","","1.0525","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151512","9.5061","0.0002","11.9924","0.0003","12.1678","0.0003","73.7785","0.0011","84.7859","0.0009","80.7467","0.0013","1313.04","0.05","150","","150","","","","","","","","synthesis as described","4","P -1","-P 1","2","","","","- C28 H27 N3 O8 -","- C28 H27 N3 O8 -","- C56 H54 N6 O16 -","2","1","","John E. Moses; Jack E. Baldwin; Sébastien Brückner; Serena J. Eade; Robert M. Adlington","Biomimetic studies on polyenes","Org. Biomol. Chem.","2003","1","21","3670","3684","10.1039/b306933h","","","0.71073","MoKα","","","0.0383","","","","0.0427","","","","","","1.0616","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151513","13.1953","0.0002","8.0054","0.0002","19.1169","0.0004","90","","107.708","0.0008","90","","1923.7","0.07","150","","150","","","","","","","","synthesis as described","4","P 1 21/n 1","-P 2yn","14","4,6,8-trimethyldec-2,4,6,8-tetraenyl 3,5-dinitrobenzoate","4,6,8-trimethyldec-2,4,6,8-tetraenyl 3,5-dinitrobenzoate","","- C20 H22 N2 O6 -","- C20 H22 N2 O6 -","- C80 H88 N8 O24 -","4","1","","John E. Moses; Jack E. Baldwin; Sébastien Brückner; Serena J. Eade; Robert M. Adlington","Biomimetic studies on polyenes","Org. Biomol. Chem.","2003","1","21","3670","3684","10.1039/b306933h","","","0.71073","MoKα","","","0.0384","","","","0.0513","","","","","","1.0033","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151514","11.289","0.001","11.4013","0.0008","19.344","0.004","96.03","0.01","95.87","0.01","112.82","0.007","2254.2","0.6","293","","293","","","","","","","","?","4","P -1","-P 1","2","","tert-butyl(1RS,2SR,3RS)-3-methyl-2-(N,N-dibenzylamino)- cyclopentane-1-carboxylate","","- C25 H33 N O2 -","- C25 H33 N O2 -","- C100 H132 N4 O8 -","4","2","","Bunnage, Mark E.; Chippindale, Ann M.; Davies, Stephen G.; Parkin, Richard M.; Smith, Andrew D.; Withey, Jonathan M.","Asymmetric synthesis of (1R,2S,3R)-3-methylcispentacin and (1S,2S,3R)-3-methyltranspentacin by kinetic resolution of tert-butyl (�)-3-methylcyclopentene-1-carboxylateThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3698","","10.1039/b306935b","","","1.5418","CuKα","","","0.0596","","","","0.0669","","","","","","1.0356","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7151515","9.9698","0.0008","10.8697","0.0009","21.974","0.004","90","","90","","90","","2381.3","0.5","293","","293","","","","","","","","see paper","4","P 21 2 21","P 2ac 2ac","18","","tert-butyl(1R,2S,3R,aS)-3-methyl-2-(N-benzylamino)- cyclopentane-1-carboxylate","","- C26 H35 N O2 -","- C26 H35 N O2 -","- C104 H140 N4 O8 -","4","1","","Bunnage, Mark E.; Chippindale, Ann M.; Davies, Stephen G.; Parkin, Richard M.; Smith, Andrew D.; Withey, Jonathan M.","Asymmetric synthesis of (1R,2S,3R)-3-methylcispentacin and (1S,2S,3R)-3-methyltranspentacin by kinetic resolution of tert-butyl (�)-3-methylcyclopentene-1-carboxylateThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3698","","10.1039/b306935b","","","1.5418","CuKα","","","0.0408","","","","0.0508","","","","","","1.0059","","","","has coordinates","211332","2020-10-21","18:00:00",""
"7151516","14.905","0.008","17.292","0.003","9.515","0.002","90","","93.09","0.02","90","","2448.8","1.5","160","2","160","2","","","","","","","synthesis as described","5","P 1 21 1","P 2yb","4","","","","- C24 H33 N2 O5.5 S2 -","- C24 H33 N2 O5.5 S2 -","- C96 H132 N8 O22 S8 -","4","2","","Pulacchini, Sonia; Nasser, Rima; Sibbons, Kevin F.; Motevalli, Majid; Hawkes, Geoffrey E.; Kroemer, Romano T.; Bento, Edson S.; Watkinson, Michael","Structure, modelling and dynamic behaviour of aza- and azaoxamacrocyclic ligands derived from (R,R)-1,2-diaminocyclohexaneElectronic supplementary information (ESI) available: different views of compounds 6, 6a and 6b. See http://www.rsc.org/suppdata/ob/b3/b306963j/","Organic & Biomolecular Chemistry","2003","1","22","4058","","10.1039/b306963j","","x-ray","0.71073","MoKα","","0.0948","0.0461","","","0.0987","0.1129","","","","","","1.038","","","","has coordinates","209363","2020-10-21","18:00:00",""
"7151517","22.981","0.003","13.623","0.003","10.142","0.002","90","","90","","90","","3175.2","1","293","2","293","2","","","","","","","synthesis as described","5","P 21 21 21","P 2ac 2ab","19","","","","- C31 H39 N3 O6 S3 -","- C31 H39 N3 O6 S3 -","- C124 H156 N12 O24 S12 -","4","1","","Pulacchini, Sonia; Nasser, Rima; Sibbons, Kevin F.; Motevalli, Majid; Hawkes, Geoffrey E.; Kroemer, Romano T.; Bento, Edson S.; Watkinson, Michael","Structure, modelling and dynamic behaviour of aza- and azaoxamacrocyclic ligands derived from (R,R)-1,2-diaminocyclohexaneElectronic supplementary information (ESI) available: different views of compounds 6, 6a and 6b. See http://www.rsc.org/suppdata/ob/b3/b306963j/","Organic & Biomolecular Chemistry","2003","1","22","4058","","10.1039/b306963j","","x-ray","0.71073","MoKα","","0.0778","0.0402","","","0.1085","0.1408","","","","","","1.078","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151518","13.5011","0.0004","15.4181","0.0004","16.111","0.0005","102.337","0.002","98.236","0.001","95.617","0.001","3213.69","0.16","153","2","153","2","","","","","","","","5","P -1","-P 1","2","","","","- C66 H91 Br2 N5 O2 -","- C58 H71 Br2 N5 -","- C116 H142 Br4 N10 -","2","1","","Jonathan L. Sessler; Julian M. Davis; Vladimir Král; Thomas Kimbrough; Vincent Lynch","Water soluble sapphyrins: potential fluorescent phosphate anion sensors","Org. Biomol. Chem.","2003","1","22","4113","4123","10.1039/b306964h","","","0.71073","MoKα","","0.1128","0.065","","","0.1461","0.1579","","","","","","1.148","","","","has coordinates,has disorder","180301","2020-10-21","18:00:00",""
"7151519","10.747","0.0003","8.3113","0.0002","13.5613","0.0004","90","","100.432","0.0012","90","","1191.29","0.06","200","","200","","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","","","","- C20 H24 O11 S2 -","- C20 H24 O11 S2 -","- C40 H48 O22 S4 -","2","1","","Gamblin, David P.; Garnier, Philippe; Ward, Sarah J.; Oldham, Neil J.; Fairbanks, Antony J.; Davis, Benjamin G.","Glycosyl phenylthiosulfonates (Glyco-PTS): novel reagents for glycoprotein synthesisThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.Electronic supplementary information (ESI) available: experimental procedures, characterization, protein ESI-MS spectra and crystal data. See http://www.rsc.org/suppdata/ob/b3/b306990g/","Organic & Biomolecular Chemistry","2003","1","21","3642","","10.1039/b306990g","","","0.71073","MoKα","","","0.0417","","","","0.0465","","","","","","1.0631","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151520","10.517","0.004","10.678","0.004","12.532","0.005","104.199","0.004","100.115","0.004","112.747","0.003","1199.3","0.8","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C28 H36 Fe2 N2 -","- C28 H36 Fe2 N2 -","- C56 H72 Fe4 N4 -","2","1","","Anderson, James C.; Blake, Alexander J.; Arnall-Culliford, Jennifer C.","Synthesis of planar chiral ferrocenyl 1,3-diamines and 1,3-amino ethers","Organic & Biomolecular Chemistry","2003","1","20","3586","","10.1039/b307014j","","x-ray","0.71073","MoKα","","0.0353","0.0261","","","0.0637","0.0694","","","","","","1.037","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151521","9.286","0.002","18.246","0.002","10.204","0.002","90","","90.77","0.02","90","","1728.7","0.5","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H20 N O5 S -","- C17 H20 N O5 S -","- C68 H80 N4 O20 S4 -","4","1","","Heaney, Frances; Fenlon, Julie; O'Mahony, Colm; McArdle, Patrick; Cunningham, Desmond","Alpha-oximono-esters as precursors to heterocycles‒generation of oxazinone N-oxides and cycloaddition to alkene dipolarophiles.","Organic & biomolecular chemistry","2003","1","23","4302","4316","10.1039/b307077h","","","0.71069","MoKα","","0.0856","0.0696","","","0.183","0.1956","","","","","","1.035","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151522","8.385","0.001","11.271","0.001","16.603","0.002","90","","90","","90","","1569.1","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H19 N O5 S -","- C15 H19 N O5 S -","- C60 H76 N4 O20 S4 -","4","1","","Heaney, Frances; Fenlon, Julie; O'Mahony, Colm; McArdle, Patrick; Cunningham, Desmond","Alpha-oximono-esters as precursors to heterocycles‒generation of oxazinone N-oxides and cycloaddition to alkene dipolarophiles.","Organic & biomolecular chemistry","2003","1","23","4302","4316","10.1039/b307077h","","","0.71069","MoKα","","0.0283","0.0256","","","0.0667","0.068","","","","","","0.859","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151523","8.728","0.001","11.841","0.001","14.929","0.002","71.632","0.009","80.69","0.01","81.7","0.01","1437.8","0.3","123.2","","","","","","","","","","","5","P -1","-P 1","2","","","","- C60 H44 F20 N4 O10 -","- C60 H44 F20 N4 O10 -","- C60 H44 F20 N4 O10 -","1","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0551","","","","0.1264","","","","","","1.403","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151524","9.599","0.001","11.653","0.002","15.605","0.002","110.08","0.01","95.75","0.01","106.7","0.01","1531.4","0.4","298.2","","","","","","","","","","","5","P -1","-P 1","2","","","","- C62 H46 F20 N6 O10 -","- C62 H46 F20 N6 O10 -","- C62 H46 F20 N6 O10 -","1","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0605","","","","0.1588","","","","","","1.104","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151525","15.963","0.001","15.963","0.001","20.165","0.002","90","","90","","90","","5138.4","0.7","296.2","","","","","","","","","","","5","I 41/a :2","-I 4ad","88","","","","- C48 H24 Cl8 F12 N4 -","- C48 H24 Cl8 F12 N4 -","- C192 H96 Cl32 F48 N16 -","4","0.25","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0692","","","","0.2018","","","","","","1.647","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151526","13.102","0.002","13.102","0.002","27.375","0.003","90","","90","","90","","4699.3","1.1","298.2","","","","","","","","","","","6","I 41/a :2","-I 4ad","88","","","","- C48 H28 Cl8 F12 N4 O2 -","- C48 H28 Cl8 F12 N4 O2 -","- C192 H112 Cl32 F48 N16 O8 -","4","0.25","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0528","","","","0.1404","","","","","","1.109","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151527","18.886","0.002","18.183","0.002","9.886","0.002","90","","90.428","0.003","90","","3394.8","0.9","173.2","","","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C74 H28 F40 N4 O2 -","- C74 H28 F40 N4 O2 -","- C148 H56 F80 N8 O4 -","2","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.069","","","","0.1418","","","","","","1.209","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151528","15.679","0.003","10.995","0.004","23.426","0.003","90","","100.47","0.01","90","","3971.2","1.7","298.2","","","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C76 H28 Cl6 F40 N6 O2 -","- C76 H28 Cl6 F40 N6 O2 -","- C152 H56 Cl12 F80 N12 O4 -","2","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0769","","","","0.2003","","","","","","1.327","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151529","25.555","0.009","15.884","0.002","25.659","0.008","90","","90","","90","","10415","5","288.1","","","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C88 H70 Cl24 N6 O12 -","- C84 H66 Cl12 N6 O12 -","- C336 H264 Cl48 N24 O48 -","4","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","0.0928","0.0872","","","0.2452","0.2491","","","","","","1.15","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151530","18.487","0.002","15.093","0.002","19.312","0.001","90","","94.823","0.007","90","","5369.4","1","296.2","","","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C108 H86 Cl16 N6 O12 -","- C108 H86 Cl16 N6 O12 -","- C216 H172 Cl32 N12 O24 -","2","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.088","","","","0.2471","","","","","","1.668","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151531","18.487","0.002","15.093","0.002","19.312","0.001","90","","94.823","0.007","90","","5369.4","1","296.1","","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C108 H86 Cl16 N6 O12 -","- C84 H66 Cl12 N6 O12 -","- C168 H132 Cl24 N12 O24 -","2","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.71069","MoKa","","0.148","0.0622","","","0.1819","0.2006","","","","","","0.82","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7151532","14.02","0.003","18.711","0.003","14.289","0.003","90","","117.76","0.01","90","","3317","1.2","298.2","","","","","","","","","","","5","P 1 21/a 1","-P 2yab","14","","","","- C68 H48 Cl10 N4 O8 -","- C68 H48 Cl10 N4 O8 -","- C136 H96 Cl20 N8 O16 -","2","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.07","","","","0.1792","","","","","","1.104","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151533","21.856","0.003","25.827","0.003","19.842","0.003","90","","115.244","0.003","90","","10131","2","173.2","","","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C56 H26 F20 N4 O8 -","- C56 H26 F20 N4 O8 -","- C448 H208 F160 N32 O64 -","8","1","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0513","","","","0.1266","","","","","","1.239","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151534","21.093","0.003","25.7","0.003","19.961","0.002","90","","107.1","0.003","90","","10342","2","123.2","","","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C59 H28.5 Cl0.5 F20 N4 O8 -","- C59 H30.5 Cl0.5 F20 N4 O8 -","- C472 H244 Cl4 F160 N32 O64 -","8","1","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0479","","","","0.1103","","","","","","1.015","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151535","14.995","0.003","12.084","0.002","15.045","0.003","90","","116.761","0.004","90","","2434.2","0.8","173.2","","","","","","","","","","","5","P 1 21/a 1","-P 2yab","14","","","","- C48 H18 Cl8 F12 N4 -","- C48 H18 Cl8 F12 N4 -","- C96 H36 Cl16 F24 N8 -","2","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0742","","","","0.1869","","","","","","1.665","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151536","25.555","0.009","15.884","0.002","25.659","0.008","90","","90","","90","","10415","5","288.2","","","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C88 H70 Cl24 N6 O12 -","- C88 H70 Cl24 N6 O12 -","- C352 H280 Cl96 N24 O48 -","4","0.5","","Uno, Hidemitsu; Inoue, Kentarou; Inoue, Takashi; Ono, Noboru","Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at ?-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogensElectronic Supporting Information Available: Ortep drawings of 3d�2EtOH, 3d�2DMF, 3e, 3e�2H2O, 3g�2(i-PrOH), 3g�2DMF�2CHCl3, 4a�4CHCl3, 4a�4PhCl, 5a�2PhCl, 5d, 5d��PhCl, and 5e; packing diagrams of 5d and 5d��PhCl; and their X-ray analyses data in CIF format. See http://www.rsc.org/suppdata/ob/b3/b307132d/","Organic & Biomolecular Chemistry","2003","1","21","3857","","10.1039/b307132d","","","0.7107","MoKa","","","0.0727","","","","0.176","","","","","","1.976","","","","has coordinates","193981","2020-10-21","18:00:00",""
"7151537","21.2","0.003","26.956","0.006","9.205","0.0011","90","","90","","90","","5260.4","1.5","298","","","","","","","","","","Local laboratory","4","P c c n","-P 2ab 2ac","56","","","","- C23 H41 N5 O2 -","- C23 H41 N5 O2 -","- C184 H328 N40 O16 -","8","1","","Yabuuchi, Kazuhiro; Marfo-Owusu, Emmanuel; Kato, Takashi","A new urea gelator: incorporation of intra- and intermolecular hydrogen bonding for stable 1D self-assembly","Organic & Biomolecular Chemistry","2003","1","19","3464","","10.1039/b307149a","","","0.71073","MoKα","","0.179","0.094","","0.237","0.233","0.162","","","0.778","1.216","1.216","0.814","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151538","39.501","0.009","13.177","0.003","24.959","0.006","90","","98.709","0.005","90","","12841","5","153","2","153","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C67 H83 F3 N Na O9 S -","- C67 H83 F3 N Na O9 S -","- C536 H664 F24 N8 Na8 O72 S8 -","8","1","","Abidi, Rym; Baklouti, Lassaad; Harrowfield, Jack M.; Sobolev, Alexandre N.; Vicens, Jacques; White, Allan H.","Alkali metal ion complexes of functionalised calixarenes ? competition between pendent arm and anion bonding to sodium","Organic & Biomolecular Chemistry","2003","1","18","3144","","10.1039/b307193f","","","0.71073","MoKα","","0.1896","0.0965","","","0.241","0.3137","","","","","","0.999","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151539","40.086","0.008","13.339","0.003","25.135","0.005","90","","98.58","0.03","90","","13289","5","295","2","295","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C67 H83 F3 N Na O9 S -","- C67 H83 F3 N Na O9 S -","- C536 H664 F24 N8 Na8 O72 S8 -","8","1","","Abidi, Rym; Baklouti, Lassaad; Harrowfield, Jack M.; Sobolev, Alexandre N.; Vicens, Jacques; White, Allan H.","Alkali metal ion complexes of functionalised calixarenes ? competition between pendent arm and anion bonding to sodium","Organic & Biomolecular Chemistry","2003","1","18","3144","","10.1039/b307193f","","","0.71073","MoKα","","0.3098","0.142","","","0.362","0.47","","","","","","1.019","","","","has coordinates,has disorder","180301","2020-10-21","18:00:00",""
"7151540","19.214","0.006","16.341","0.004","7.1838","0.0009","90","","90","","90","","2255.5","0.9","145","","145","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(1S,2S,3S,6R,8S)-4-Benzyl-2-O-(tert-butyldimethylsilyl)-3-methyl-11-oxa-4-aza- tricyclo-[6.2.1.01.6] undec-9-en-5-one","","- C23 H33 N O3 Si -","- C23 H33 N O3 Si -","- C92 H132 N4 O12 Si4 -","4","1","","Tromp, Reynier A.; Brussee, Johannes; van der Gen, Arne","Stereochemistry of intramolecular Diels?Alder furan (IMDAF) reactions of furyl-substituted chiral ethanolamides","Organic & Biomolecular Chemistry","2003","1","20","3592","","10.1039/b307275d","","","0.71073","MoKalpha","","0.084","0.042","","0.05","0.045","","","","1.684","2.039","2.039","","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7151541","15.752","0.006","11.767","0.004","8.688","0.003","90","","103.607","0.007","90","","1565.2","1","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","7-Fluoro-4-(4-fluorophenyl)-1-methylbenzo[f][1,4]diazepine-2,3-dicarboxylic anhydride","","- C18 H12 F2 N2 O3 -","- C18 H12 F2 N2 O3 -","- C72 H48 F8 N8 O12 -","4","1","","Cheng, Ying; Yang, Hua; Meth-Cohn, Otto","The surprising nucleophilic addition of aminochlorocarbenes to diethyl acetylenedicarboxylate and to oxalyl chloride: quinolines and benzo[1,4]diazepines from N-alkylformanilides and oxalyl chloride in the presence of H�nig's base","Organic & Biomolecular Chemistry","2003","1","20","3605","","10.1039/b307278a","","","0.71073","MoKα","","0.2534","0.0569","","","0.1063","0.1883","","","","","","0.932","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151542","8.312","0.012","8.487","0.013","19.91","0.03","78.19","0.03","81.52","0.03","88.99","0.03","1360","4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","Diethyl 2-(2-chloro-1,2-bis(ethoxy-carbonyl)vinyl)- 6-methoxy1-1-methyl-1,2-dihydroquinoline-3,4-dicarboxylate","","- C25 H30 Cl N O9 -","- C25 H30 Cl N O9 -","- C50 H60 Cl2 N2 O18 -","2","1","","Cheng, Ying; Yang, Hua; Meth-Cohn, Otto","The surprising nucleophilic addition of aminochlorocarbenes to diethyl acetylenedicarboxylate and to oxalyl chloride: quinolines and benzo[1,4]diazepines from N-alkylformanilides and oxalyl chloride in the presence of H�nig's base","Organic & Biomolecular Chemistry","2003","1","20","3605","","10.1039/b307278a","","","0.71073","MoKα","","0.1848","0.0803","","","0.1756","0.2216","","","","","","0.998","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151543","12.0481","0.0011","14.5004","0.0017","16.407","0.002","81.45","0.03","83.18","0.05","67.32","0.017","2609.4","0.6","293","2","293","2","","","","","","","","4","P -1","-P 1","2","1-Benzyl-7-methoxy-4-(4-methoxyphenyl)-5- phenylbenzo(f)(1,4)diazepine-2,3-dicarbox-ylic anhydride","1-Benzyl-7-methoxy-4-(4-methoxyphenyl)-5-phenylbenzo[f][1,4]diazepine- 2,3-dicarbox-ylic anhydride","","- C32 H26 N2 O5 -","- C32 H26 N2 O5 -","- C128 H104 N8 O20 -","4","2","","Cheng, Ying; Yang, Hua; Meth-Cohn, Otto","The surprising nucleophilic addition of aminochlorocarbenes to diethyl acetylenedicarboxylate and to oxalyl chloride: quinolines and benzo[1,4]diazepines from N-alkylformanilides and oxalyl chloride in the presence of H�nig's base","Organic & Biomolecular Chemistry","2003","1","20","3605","","10.1039/b307278a","","","0.71073","MoKα","","0.2119","0.0481","","","0.0726","0.0918","","","","","","0.641","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151544","9.939","0.007","12.907","0.005","20.16","0.003","90","","90","","90","","2586","2","293","2","","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C19 H24 N2 O9 S -","- C19 H24 N2 O9 S -","- C76 H96 N8 O36 S4 -","4","1","","Marietta Tóth; Katalin E. Kövér; Attila Bényei; László Somsák","C-Glycosylmethylene carbenes: synthesis of anhydro-aldose tosylhydrazones as precursors; generation and a new synthetic route to exo-glycals","Org. Biomol. Chem.","2003","1","22","4039","4046","10.1039/b307378e","","x-ray","0.71073","MoKα","","","0.0533","","","","0.1828","","","","","","1.029","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151545","7.632","0.002","15.352","0.004","18.943","0.008","90","","94.83","0.03","90","","2211.6","1.2","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","3,3-diethyl-1,2-diferrocenylcyclopropene","","- C27 H28 Fe2 -","- C27 H28 Fe2 -","- C108 H112 Fe8 -","4","1","","Elena I. Klimova; Tatiana Klimova Berestneva; Arnaldo Cinquantini; Maddalena Corsini; Piero Zanello; Ruben A. Toscano; Simón Hernández-Ortega; Marcos Martínez García","3,3-Diethyl- and 3,3-dibenzyl-1,2-diferrocenylcyclopropenes","Org. Biomol. Chem.","2003","1","24","4458","4464","10.1039/b307408k","","","0.71073","MoKα","","0.1389","0.0711","","","0.1517","0.1872","","","","","","1.007","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151546","11.0169","0.0008","7.8226","0.0005","13.1321","0.0009","90","","102.329","0.001","90","","1105.63","0.13","291","2","291","2","","","","","","","","4","P 1 21 1","P 2yb","4","","4,5-DIFERROCEN-1-YL-HEPTAN-3-ONE","","- C27 H30 Fe2 O -","- C27 H30 Fe2 O -","- C54 H60 Fe4 O2 -","2","1","","Elena I. Klimova; Tatiana Klimova Berestneva; Arnaldo Cinquantini; Maddalena Corsini; Piero Zanello; Ruben A. Toscano; Simón Hernández-Ortega; Marcos Martínez García","3,3-Diethyl- and 3,3-dibenzyl-1,2-diferrocenylcyclopropenes","Org. Biomol. Chem.","2003","1","24","4458","4464","10.1039/b307408k","","","0.71073","MoKα","","0.0511","0.039","","","0.0749","0.0784","","","","","","0.968","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151547","17.709","0.003","7.553","0.002","19.656","0.002","90","","100.926","0.008","90","","2581.5","0.9","296.2","","","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C29 H26 N4 O5 -","- C29 H26 N4 O5 -","- C116 H104 N16 O20 -","4","1","","Tsuji, Eriko; Ando, Kumiko; Kunitomo, Jun-ichi; Yamashita, Masayuki; Ohta, Shunsaku; Kohno, Shigekatsu; Ohishi, Yoshitaka","Preparation of 3-acetoacetylaminobenzo[b]furan derivatives with cysteinyl leukotriene receptor 2 antagonistic activity","Organic & Biomolecular Chemistry","2003","1","18","3139","","10.1039/b307468d","","","1.5418","CuKα","","","0.0585","","","","0.1703","","","","","","1.491","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151548","13.4019","0.0002","8.1355","0.0001","7.8447","0.0001","90","","101.744","0.001","90","","837.41","0.02","299","2","299","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C6 H6 N6 S -","- C6 H6 N6 S -","- C24 H24 N24 S4 -","4","1","","Volkova, Natalya N.; Tarasov, Evgeniy V.; Kodess, Mikhail I.; Meervelt, Luc Van; Dehaen, Wim; Bakulev, Vasiliy A.","Reaction of 5-halo-1,2,3-thiadiazoles with aliphatic diamines. Synthesis and intramolecular cyclization of bis(1,2,3-triazolyl-1,2,3-thiadiazolyl)sulfides","Organic & Biomolecular Chemistry","2003","1","22","4030","","10.1039/b307693h","","","1.54178","CuKα","","0.0448","0.0437","","","0.1384","0.1405","","","","","","1.001","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151549","27.462","0.017","20.459","0.012","18.66","0.006","90","","103.03","0.04","90","","10214","9","203","2","203","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C112 H120 N6 O12 P4 -","- C112 H120 N6 O12 P4 -","- C448 H480 N24 O48 P16 -","4","1","","Christian Schmidt; Mohamed Saadioui; Volker Böhmer; Valéry Host; Marie-Rose Spirlet; Jean F. Desreux; Fréderic Brisach; Françoise Arnaud-Neu; Jean-François Dozol","Modification of calix[4]arenes with CMPO-functions at the wide rim. Synthesis, solution behavior, and separation of actinides from lanthanides","Org. Biomol. Chem.","2003","1","22","4089","4096","10.1039/b307929e","","","0.71073","MoKα","","0.1613","0.068","","","0.1445","0.1794","","","","","","0.922","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151550","5.7655","0.0003","9.7432","0.0004","19.338","0.001","83.041","0.005","85.348","0.006","85.954","0.004","1072.72","0.09","293","2","293","2","","","","","","","","4","P 1","P 1","1","","","","- C19 H36 Ho0 O6 -","- C19 H36 O6 -","- C38 H72 O12 -","2","2","","Cuzzupe, Anthony N.; Florio, Romina Di; White, Jonathan M.; Rizzacasa, Mark A.","Enantiospecific synthesis of the phospholipase A2 inhibitors (?)-cinatrin C1 and (+)-cinatrin C3","Organic & Biomolecular Chemistry","2003","1","20","3572","","10.1039/b308028e","","","1.5418","CuKα","","0.0633","0.0398","","","0.0909","0.1033","","","","","","1.018","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151551","25.207","0.004","7.631","0.002","17","0.003","90","0","95.5","0.1","90","0","3255","1.3","296","","296","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C16 H19 Cl N4 O -","- C16 H19 Cl N4 O -","- C128 H152 Cl8 N32 O8 -","8","2","","Greci, Lucedio; Castagna, Riccardo; Carloni, Patricia; Stipa, Pierluigi; Rizzoli, Corrado; Righi, Lara; Sgarabotto, Paolo","Nitrenium ions.Part 5. For Part 4 see ref. 1 Reactions of N,N-dimethyl-p-benzoyloxyaniline-iminium chloride with indoles and indolizines. X-ray structure of unexpected [2-chloro-4-(4-dimethylaminophenyl-ONN-azoxy)phenyl]dimethylamine (azoxy derivative)","Organic & Biomolecular Chemistry","2003","1","21","3768","","10.1039/b308088a","","","1.54178","CuKα","","0.1326","0.0501","","0.0943","","0.0677","","","0.87","","","1.235","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7151559","12.2184","0.0006","6.3844","0.0003","14.8429","0.0009","90","","108.081","0.002","90","","1100.68","0.1","180","2","180","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C18 H23 Cl3 N2 O5 -","- C18 H23 Cl3 N2 O5 -","- C36 H46 Cl6 N4 O10 -","2","1","","Ley, Steven V.; Cleator, Ed; Hewitt, Peter R.","A rapid stereocontrolled synthesis of the 3a-hydroxy-pyrrolo[2,3-b]indole skeleton, a building block for 10b-hydroxy-pyrazino[1?,2?:1,5]pyrrolo[2,3-b]indole-1,4-diones","Organic & Biomolecular Chemistry","2003","1","20","3492","","10.1039/b308288a","","","0.71073","MoKα","","0.0705","0.0577","","","0.156","0.1757","","","","","","1.09","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151560","25.6379","0.0012","9.2441","0.0004","12.2274","0.0006","90","","90","","90","","2897.9","0.2","110","2","110","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C16 H40 Cl4 N8 O8 Zn2 -","- C16 H40 Cl4 N8 O8 Zn2 -","- C64 H160 Cl16 N32 O32 Zn8 -","4","1","","Gao, Jian; Reibenspies, Joseph H.; Martell, Arthur E.","Selective recognition of thymidylylthymidine (TpT) and antitumor effects of a macrocyclic dizinc(II) complex.","Organic & biomolecular chemistry","2003","1","23","4242","4247","10.1039/b308358f","","","0.71073","MoKα","","0.06","0.0498","","","0.1255","0.1382","","","","","","1.14","","","","has coordinates,has disorder","180301","2020-10-21","18:00:00",""
"7151561","7.9103","0.0004","9.9556","0.0005","15.8702","0.0009","90","","90","","90","","1249.81","0.11","115","2","115","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H20 N2 O3 -","- C13 H20 N2 O3 -","- C52 H80 N8 O12 -","4","1","","Jean-Paul R. Hermet; David W. Porter; Michael J. Dearden; Justin R. Harrison; Tobias Koplin; Peter O'Brien; Jérôme Parmene; Vladimir Tyurin; Adrian C. Whitwood; John Gilday; Neil M. Smith","Synthesis of sparteine-like chiral diamines and evaluation in the enantioselective lithiation‒substitution of N-(tert-butoxycarbonyl)pyrrolidine","Org. Biomol. Chem.","2003","1","22","3977","3988","10.1039/b308410h","","","0.71073","MoKα","","0.0362","0.0333","","","0.0877","0.0898","","","","","","1.061","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151562","8.8117","0.0002","11.0726","0.0002","11.2477","0.0003","79.339","0.001","73.059","0.001","86.946","0.001","1031.68","0.04","123","2","123","2","","","","","","","","4","P -1","-P 1","2","","7-Carboxy-2,4-dimethyl-5H-benzo[b][1,4]diazepin-ium picrate","","- C19 H19 N5 O10 -","- C19 H19 N5 O10 -","- C38 H38 N10 O20 -","2","1","","Schmidt, Andreas; Shilabin, Abbas Gholipour; Nieger, Martin","On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines.","Organic & biomolecular chemistry","2003","1","23","4342","4350","10.1039/b308412d","","","0.71073","MoKα","","0.0519","0.0431","","","0.1165","0.1218","","","","","","1.074","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151563","12.334","0.003","12.813","0.003","14.026","0.003","90","","91.62","0.03","90","","2215.7","0.9","180","2","180","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C23 H30 O7 -","- C23 H30 O7 -","- C92 H120 O28 -","4","2","","Lee, Ai-Lan; Ley, Steven V.","The synthesis of the anti-malarial natural product polysphorin and analogues using polymer-supported reagents and scavengers","Organic & Biomolecular Chemistry","2003","1","22","3957","","10.1039/b308761a","","","0.71073","MoKα","","0.0931","0.0704","","","0.1715","0.1906","","","","","","1.064","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151564","22.4427","0.0004","11.0768","0.0003","12.8817","0.0002","90","","114.475","0.002","90","","2914.55","0.11","180","2","180","2","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C28 H34 N2 O9 S -","- C28 H34 N2 O9 S -","- C112 H136 N8 O36 S4 -","4","1","","Lee, Ai-Lan; Ley, Steven V.","The synthesis of the anti-malarial natural product polysphorin and analogues using polymer-supported reagents and scavengers","Organic & Biomolecular Chemistry","2003","1","22","3957","","10.1039/b308761a","","","0.71073","MoKα","","0.0572","0.0449","","","0.0951","0.1023","","","","","","1.085","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151565","8.5195","0.0011","10.0386","0.0013","19.37","0.002","90","","90","","90","","1656.6","0.3","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C19 H28 O2 -","- C19 H28 O2 -","- C76 H112 O8 -","4","1","","Dang, Hai-Shan; Roberts, Brian P.; Tocher, Derek A.","Thiol-catalysed radical-chain redox rearrangement reactions of benzylidene acetals derived from terpenoid diols","Organic & Biomolecular Chemistry","2003","1","22","4073","","10.1039/b309060b","","","0.71073","MoKα","","0.0682","0.0535","","","0.1178","0.1251","","","","","","1.07","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151566","10.6743","0.0007","16.4346","0.001","16.6813","0.001","90","","90","","90","","2926.4","0.3","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C34 H42 O4 -","- C34 H42 O4 -","- C136 H168 O16 -","4","1","","Dang, Hai-Shan; Roberts, Brian P.; Tocher, Derek A.","Thiol-catalysed radical-chain redox rearrangement reactions of benzylidene acetals derived from terpenoid diols","Organic & Biomolecular Chemistry","2003","1","22","4073","","10.1039/b309060b","","","0.71073","MoKα","","0.0507","0.0426","","","0.1077","0.1136","","","","","","1.015","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151567","8.804","0.003","10.274","0.003","18.428","0.005","90","","90","","90","","1666.9","0.9","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C19 H28 O2 -","- C19 H28 O2 -","- C76 H112 O8 -","4","1","","Dang, Hai-Shan; Roberts, Brian P.; Tocher, Derek A.","Thiol-catalysed radical-chain redox rearrangement reactions of benzylidene acetals derived from terpenoid diols","Organic & Biomolecular Chemistry","2003","1","22","4073","","10.1039/b309060b","","","0.71073","MoKα","","0.0817","0.0579","","","0.122","0.1329","","","","","","0.987","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151568","9.9643","0.0004","11.133","0.0004","17.3159","0.0007","90","","90","","90","","1920.9","0.13","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C17 H25 N O6 S -","- C17 H25 N O6 S -","- C68 H100 N4 O24 S4 -","4","1","","Foresti, Elisabetta; Palmieri, Gianni; Petrini, Marino; Profeta, Roberto","Highly diastereoselective addition of nitromethane anion to chiral alpha-amidoalkylphenyl sulfones. Synthesis of optically active alpha-amino acid derivatives.","Organic & biomolecular chemistry","2003","1","23","4275","4281","10.1039/b309211a","","","0.71073","MoKα","","0.0376","0.0358","","","0.0931","0.0951","","","","","","1.086","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151569","7.0666","0.0004","7.0975","0.0004","18.3293","0.0013","88.437","0.003","86.586","0.003","62.907","0.003","816.98","0.09","180","2","180","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H21 N O4 -","- C18 H21 N O4 -","- C36 H42 N2 O8 -","2","1","","Davies, John E.; Fleming, Ian; Goodman, Jonathan M.","A tricycloheptane product in cationic rearrangements","Organic & Biomolecular Chemistry","2003","1","20","3570","","10.1039/b309329h","","","0.71073","MoKα","","0.1793","0.1113","","","0.266","0.3102","","","","","","1.037","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151570","28.047","0.006","11.272","0.002","13.562","0.003","90","","103.05","0.03","90","","4176.8","1.6","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C17 H26 N5 O3 P -","- C17 H26 N5 O3 P -","- C136 H208 N40 O24 P8 -","8","1","","Brel, Valery K.; Belsky, Vitaly K.; Stash, Adam I.; Zavodnik, Valery E.; Stang, Peter J.","Synthesis and molecular structure of new acyclic analogues of nucleotides with a 1,2-alkadienic skeleton.","Organic & biomolecular chemistry","2003","1","23","4220","4226","10.1039/b309684j","","","0.71073","MoKα","","0.0597","0.0597","","","0.1621","0.1621","","","","","","1.065","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151571","14.135","0.003","8.272","0.002","14.408","0.003","90","","106.97","0.03","90","","1611.3","0.7","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C14 H20 N2 O5 P -","- C14 H19 N2 O5 P -","- C56 H76 N8 O20 P4 -","4","1","","Brel, Valery K.; Belsky, Vitaly K.; Stash, Adam I.; Zavodnik, Valery E.; Stang, Peter J.","Synthesis and molecular structure of new acyclic analogues of nucleotides with a 1,2-alkadienic skeleton.","Organic & biomolecular chemistry","2003","1","23","4220","4226","10.1039/b309684j","","","0.71073","MoKα","","0.0376","0.0376","","","0.1059","0.1059","","","","","","1.068","","","","has coordinates","213973","2020-10-21","18:00:00",""
"7151572","6.444","0.001","11.612","0.002","12.764","0.002","90","","98","0.01","90","","945.8","0.3","120","2","120","2","","","","","","","","4","P 1 21 1","P 2yb","4","","methyl 2-N-benzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside","","- C21 H25 N O5 -","- C21 H25 N O5 -","- C42 H50 N2 O10 -","2","1","","Emmerson, Daniel P. G.; Villard, Renaud; Mugnaini, Claudia; Batsanov, Andrei; Howard, Judith A. K.; Hems, William P.; Tooze, Robert P.; Davis, Benjamin G.","Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc?aldehyde additionsThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3826","","10.1039/b309715n","","","0.71073","MoKα","","0.0358","0.0344","","","0.0932","0.0948","","","","","","1.064","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151573","6.282","0.001","19.484","0.004","10.205","0.002","90","","90.22","0.01","90","","1249.1","0.4","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside","","- C28 H31 N O5 -","- C28 H31 N O5 -","- C56 H62 N2 O10 -","2","1","","Emmerson, Daniel P. G.; Villard, Renaud; Mugnaini, Claudia; Batsanov, Andrei; Howard, Judith A. K.; Hems, William P.; Tooze, Robert P.; Davis, Benjamin G.","Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc?aldehyde additionsThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3826","","10.1039/b309715n","","","0.71073","MoKα","","0.0329","0.0311","","","0.0773","0.0785","","","","","","1.051","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151574","10.073","0.001","19.17","0.001","13.434","0.001","90","","105.6","0.01","90","","2498.5","0.4","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside","","- C28 H31 N O5 -","- C28 H31 N O5 -","- C112 H124 N4 O20 -","4","2","","Emmerson, Daniel P. G.; Villard, Renaud; Mugnaini, Claudia; Batsanov, Andrei; Howard, Judith A. K.; Hems, William P.; Tooze, Robert P.; Davis, Benjamin G.","Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc?aldehyde additionsThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.","Organic & Biomolecular Chemistry","2003","1","21","3826","","10.1039/b309715n","","","0.71073","MoKα","","0.0566","0.0422","","","0.0839","0.0918","","","","","","1.069","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151578","7.511","0.0002","12.0412","0.0005","19.598","0.0007","90","","90","","90","","1772.47","0.11","150","2","150","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H31 Br2 N3 -","- C13 H31 Br2 N3 -","- C52 H124 Br8 N12 -","4","1","","Argouarch, Gilles; Stones, Graham; Gibson, Colin L.; Kennedy, Alan R.; Sherrington, David C.","Bifurcated, modular syntheses of chiral annulet triazacyclononanes","Organic & Biomolecular Chemistry","2003","1","24","4408","","10.1039/b310492c","","","0.71073","MoKα","","0.0526","0.0349","","","0.0639","0.0685","","","","","","1.039","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151579","8.0587","0.0008","11.2534","0.0011","22.104","0.003","90","","98.529","0.013","90","","1982.4","0.4","293","","293","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C21 H16 Cl N9 -","- C21 H16 Cl N9 -","- C84 H64 Cl4 N36 -","4","1","","Angel Díaz-Ortiz; José Elguero; Concepción Foces-Foces; Antonio de la Hoz; Andrés Moreno; Sergio Moreno; Ana Sánchez-Migallón; Gema Valiente","Synthesis, structural determination and dynamic behavior of 2-chloro-4,6-bis(pyrazolylamino)-1,3,5-triazines","Org. Biomol. Chem.","2003","1","24","4451","4457","10.1039/b310693d","","","1.54178","CuK\α","","0.054","0.043","","0.062","","0.055","","","0.984","","","0.972","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151580","4.0483","0.001","10.844","0.003","13.748","0.003","90","","97.19","0.005","90","","598.8","0.3","295","2","295","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","4-Chloro[1,3]dithiole-2-thione","","- C3 H Cl S3 -","- C3 H Cl S3 -","- C12 H4 Cl4 S12 -","4","1","","Suizu, Rie; Imakubo, Tatsuro","Synthesis and properties of hetero-halogenated TTFsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/ob/b3/b310822h/","Organic & Biomolecular Chemistry","2003","1","21","3629","","10.1039/b310822h","","","0.71073","MoKα","","0.0403","0.0378","","","0.1098","0.1112","","","","","","1.17","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151581","6.7584","0.0015","4.0939","0.0009","22.946","0.005","90","","97.097","0.004","90","","630","0.2","293","2","293","2","","","","","","","","7","P 1 n 1","P -2yac","7","","","","- C8 H2 Cl I N2 S2 Se2 -","- C8 H2 Cl I N2 S2 Se2 -","- C16 H4 Cl2 I2 N4 S4 Se4 -","2","1","","Suizu, Rie; Imakubo, Tatsuro","Synthesis and properties of hetero-halogenated TTFsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/ob/b3/b310822h/","Organic & Biomolecular Chemistry","2003","1","21","3629","","10.1039/b310822h","","","0.71073","MoKα","","0.0628","0.0602","","","0.1572","0.1595","","","","","","1.119","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151582","10.1391","0.0005","8.2152","0.0004","14.6853","0.0005","90","","96.703","0.003","90","","1214.85","0.09","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H17 F3 O2 -","- C13 H17 F3 O2 -","- C52 H68 F12 O8 -","4","1","","DiMartino, Gianluca; Hursthouse, Michael B.; Light, Mark E.; Percy, Jonathan M.; Spencer, Neil S.; Tolley, Malcolm","Syntheses of selectively fluorinated cyclodecenones: the first deployment of the neutral oxy-Cope rearrangement in organofluorine chemistry","Organic & Biomolecular Chemistry","2003","1","24","4423","","10.1039/b311261f","","","0.71073","MoKα","","0.0503","0.0352","","","0.0858","0.0933","","","","","","1.063","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151583","8.7576","0.0004","13.7337","0.001","9.8743","0.0004","90","","106.53","0.002","90","","1138.54","0.11","150","2","150","2","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C10 H10 Cl F5 O -","- C10 H10 Cl F5 O -","- C40 H40 Cl4 F20 O4 -","4","2","","DiMartino, Gianluca; Hursthouse, Michael B.; Light, Mark E.; Percy, Jonathan M.; Spencer, Neil S.; Tolley, Malcolm","Syntheses of selectively fluorinated cyclodecenones: the first deployment of the neutral oxy-Cope rearrangement in organofluorine chemistry","Organic & Biomolecular Chemistry","2003","1","24","4423","","10.1039/b311261f","","","0.71073","MoKα","","0.0272","0.0254","","","0.0594","0.0604","","","","","","1.068","","","","has coordinates,has disorder","180301","2020-10-21","18:00:00",""
"7151584","7.979","0.001","9.742","0.001","14.053","0.002","90","","90","","90","","1092.4","0.2","150","2","150","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C10 H10 Cl F5 O -","- C10 H10 Cl F5 O -","- C40 H40 Cl4 F20 O4 -","4","1","","DiMartino, Gianluca; Hursthouse, Michael B.; Light, Mark E.; Percy, Jonathan M.; Spencer, Neil S.; Tolley, Malcolm","Syntheses of selectively fluorinated cyclodecenones: the first deployment of the neutral oxy-Cope rearrangement in organofluorine chemistry","Organic & Biomolecular Chemistry","2003","1","24","4423","","10.1039/b311261f","","","0.71073","MoKα","","0.0334","0.0283","","","0.0598","0.0621","","","","","","1.054","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7151585","5.996","0.001","8.007","0.002","11.386","0.002","80.9","0.03","87.03","0.03","78.66","0.03","529.1","0.2","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C10 H10 F6 O -","- C10 H10 F6 O -","- C20 H20 F12 O2 -","2","1","","DiMartino, Gianluca; Hursthouse, Michael B.; Light, Mark E.; Percy, Jonathan M.; Spencer, Neil S.; Tolley, Malcolm","Syntheses of selectively fluorinated cyclodecenones: the first deployment of the neutral oxy-Cope rearrangement in organofluorine chemistry","Organic & Biomolecular Chemistry","2003","1","24","4423","","10.1039/b311261f","","","0.71073","MoKα","","0.0493","0.0425","","","0.1189","0.1248","","","","","","1.059","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151586","11.1132","0.0002","11.0996","0.0002","13.8507","0.0003","90","","102.89","0.0012","90","","1665.46","0.06","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H20 F5 N O3 -","- C15 H20 F5 N O3 -","- C60 H80 F20 N4 O12 -","4","1","","DiMartino, Gianluca; Hursthouse, Michael B.; Light, Mark E.; Percy, Jonathan M.; Spencer, Neil S.; Tolley, Malcolm","Syntheses of selectively fluorinated cyclodecenones: the first deployment of the neutral oxy-Cope rearrangement in organofluorine chemistry","Organic & Biomolecular Chemistry","2003","1","24","4423","","10.1039/b311261f","","","0.71073","MoKα","","0.0454","0.0344","","","0.08","0.0854","","","","","","1.04","","","","has coordinates","180301","2020-10-21","18:00:00",""
"7151587","6.6969","0.0004","7.0489","0.0006","10.9328","0.0007","77.964","0.006","75.679","0.009","80.977","0.008","486.04","0.06","293","","293","","","","","","","","","3","P -1","-P 1","2","","","","- C12 H14 O2 -","- C12 H14 O2 -","- C24 H28 O4 -","2","1","","Hue, Bui T. B.; Dijkink, Jan; Kuiper, Sanne; Larson, Kimberly K.; Guziec, Jr, Frank S; Goubitz, Kees; Fraanje, Jan; Schenk, Henk; van Maarseveen, Jan H.; Hiemstra, Henk","Synthesis of the cyclobutanone core of solanoeclepin A intramolecular allene butenolide photocycloaddition.","Organic & biomolecular chemistry","2003","1","24","4364","4366","10.1039/b311415e","","","1.5418","CuKα","","0.085","0.079","","0.104","","0.099","","","0.989","","","0.996","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7151588","7.0166","0.0003","10.5703","0.0006","13.7222","0.0013","90","","102.88","0.005","90","","992.13","0.12","293","","293","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C11 H16 O2 -","- C11 H16 O2 -","- C44 H64 O8 -","4","1","","Hue, Bui T. B.; Dijkink, Jan; Kuiper, Sanne; Larson, Kimberly K.; Guziec, Jr, Frank S; Goubitz, Kees; Fraanje, Jan; Schenk, Henk; van Maarseveen, Jan H.; Hiemstra, Henk","Synthesis of the cyclobutanone core of solanoeclepin A intramolecular allene butenolide photocycloaddition.","Organic & biomolecular chemistry","2003","1","24","4364","4366","10.1039/b311415e","","","1.5418","CuKα","","0.078","0.071","","0.066","","0.064","","","1.031","","","1.09","","","","has coordinates","191942","2020-10-21","18:00:00",""