Crystallography Open Database

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Searching journal of publication like 'Chemical science' volume of publication is 9

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1549085 CIFC53 H75 B2 Li O3P 1 21 114.775; 19.9973; 17.9098
90; 109.105; 90
5000.2Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549086 CIFC61 H90 B2 Cl Li O8F d d 212.2698; 43.946; 21.961
90; 90; 90
11841.6Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549087 CIFC63 H87 B2 Li O4P 1 21/c 119.497; 24.7864; 23.972
90; 92.463; 90
11574Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549088 CIFC43 H54 B2P c a 2141.344; 14.272; 6.1349
90; 90; 90
3620Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549089 CIFC70 H84 B2 OP -110.4041; 11.5484; 25.736
79.323; 85.313; 81.22
2998.51Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549094 CIFC26 H32 O2 S2I 1 2/a 17.7604; 5.9132; 49.45
90; 95.879; 90
2257.3van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549095 CIFC26 H32 O2 S2I 1 2/a 17.856; 5.8413; 49.561
90; 95.46; 90
2264van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549096 CIFC26 H32 O2 S2I 1 2/a 18.0891; 5.7282; 49.849
90; 94.255; 90
2303.4van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549097 CIFC26 H32 O2 S2I 1 2/a 17.9306; 5.8288; 49.645
90; 95.171; 90
2285.5van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549098 CIFC26 H32 O2 S2I 1 2/a 17.9631; 5.8073; 49.723
90; 94.85; 90
2291.2van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549099 CIFC26 H32 O2 S2I 1 2/a 18.3546; 5.6236; 50.168
90; 93.146; 90
2353.5van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549100 CIFC26 H32 O2 S2I 1 2/a 18.0248; 5.7688; 49.827
90; 94.591; 90
2299.3van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549101 CIFC26 H32 O2 S2I 1 2/a 18.446; 5.58942; 50.2534
90; 92.829; 90
2369.48van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549102 CIFC26 H32 O2 S2I 1 2/a 17.8186; 5.8811; 49.458
90; 95.762; 90
2262.7van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549103 CIFC26 H32 O2 S2I 1 2/a 18.1615; 5.6918; 49.87
90; 93.819; 90
2311.5van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549104 CIFC26 H32 O2 S2I 1 2/a 18.2606; 5.6541; 49.944
90; 93.621; 90
2328van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549107 CIFC30 H60 Br2 F4 Ni2 P4P -111.059; 12.1681; 15.1847
75.96; 89.526; 89.997
1982.25Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549108 CIFC18 H30 F5 I Ni P2I 1 2 18.0074; 11.3665; 12.9665
90; 94.616; 90
1176.33Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549109 CIFC18 H30 F5 I Ni P2I 1 2 17.8675; 11.3291; 12.9347
90; 94.392; 90
1149.51Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549110 CIFC18 H30 F4 Ni P2P 43 21 28.13398; 8.13398; 31.6136
90; 90; 90
2091.61Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549111 CIFC18 H30 F4 I2 Ni P2C m c 2112.6196; 14.8011; 13.2994
90; 90; 90
2484.11Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549112 CIFC18 H30 F4 I2 Ni P2P b c a14.0519; 14.4485; 24.3473
90; 90; 90
4943.2Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549113 CIFC18 H30 F4 I2 Ni P2P 1 21/c 19.9032; 16.1922; 15.2884
90; 93.913; 90
2445.85Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549114 CIFC18 H30 F5 I Ni P2P 1 21 19.4116; 12.701; 9.727
90; 95.377; 90
1157.62Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549115 CIFC18 H30 F5 I Ni P2I 1 2 17.892; 11.3325; 12.9439
90; 94.434; 90
1154.19Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549116 CIFC18 H30 Cl F4 I Ni P2P 1 21/c 19.95341; 16.0611; 15.04577
90; 97.0034; 90
2387.31Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549117 CIFC18 H30 Br F4 I Ni P2P 1 21/c 19.95422; 16.0712; 15.0877
90; 95.7803; 90
2401.4Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549118 CIFC18 H30 F5 I Ni P2C 1 c 117.1652; 8.5185; 16.935
90; 96.803; 90
2458.8Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549119 CIFC18 H30 Cl F4 I Ni P2P 1 21 19.2736; 13.2118; 9.817
90; 95.22; 90
1197.8Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549120 CIFC26 H30 F4 I2 Ni P2P -17.8141; 12.9211; 14.7784
76.749; 79.7; 76.748
1401.12Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549121 CIFC18 H30 F4 I2 Ni P2P 1 21/c 112.19004; 28.0191; 14.2344
90; 91.6129; 90
4859.89Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549122 CIFC69 H54 Fe N6 O4 P2P 1 21/c 117.9956; 14.2843; 23.6299
90; 111.37; 90
5656.57Lim, Jia Hui; Engelmann, Xenia; Corby, Sacha; Ganguly, Rakesh; Ray, Kallol; Soo, Han Sen
C-H activation and nucleophilic substitution in a photochemically generated high valent iron complex.
Chemical science, 2018, 9, 3992-4002
1549123 CIFC62 H34 F12 Fe N6 P2F d d 227.5449; 55.4159; 10.2412
90; 90; 90
15632Brandl, Thomas; Hoffmann, Viktor; Pannwitz, Andrea; Häussinger, Daniel; Neuburger, Markus; Fuhr, Olaf; Bernhard, Stefan; Wenger, Oliver S.; Mayor, Marcel
Chiral macrocyclic terpyridine complexes.
Chemical science, 2018, 9, 3837-3843
1549124 CIFC66 H44 F12 N6 O P2 RuP -4 21 c16.392; 16.392; 21.9038
90; 90; 90
5885.5Brandl, Thomas; Hoffmann, Viktor; Pannwitz, Andrea; Häussinger, Daniel; Neuburger, Markus; Fuhr, Olaf; Bernhard, Stefan; Wenger, Oliver S.; Mayor, Marcel
Chiral macrocyclic terpyridine complexes.
Chemical science, 2018, 9, 3837-3843
1549133 CIFC23 H23 Au F6 N O SbP 21 21 216.6287; 16.4246; 21.5858
90; 90; 90
2350.1Serra, Jordi; Font, Pau; Sosa Carrizo, E. Daiann; Mallet-Ladeira, Sonia; Massou, Stéphane; Parella, Teodor; Miqueu, Karinne; Amgoune, Abderrahmane; Ribas, Xavi; Bourissou, Didier
Cyclometalated gold(iii) complexes: noticeable differences between (N,C) and (P,C) ligands in migratory insertion.
Chemical science, 2018, 9, 3932-3940
1549134 CIFC24 H22 Au Cl4 NP -17.4651; 9.8244; 16.963
98.935; 91.454; 106.868
1172.83Serra, Jordi; Font, Pau; Sosa Carrizo, E. Daiann; Mallet-Ladeira, Sonia; Massou, Stéphane; Parella, Teodor; Miqueu, Karinne; Amgoune, Abderrahmane; Ribas, Xavi; Bourissou, Didier
Cyclometalated gold(iii) complexes: noticeable differences between (N,C) and (P,C) ligands in migratory insertion.
Chemical science, 2018, 9, 3932-3940
1549135 CIFC55 H62 N2 P2P 1 21/n 110.9502; 20.9614; 20.7528
90; 97.766; 90
4719.7Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549136 CIFC48 H52 P2P 1 21/c 18.3846; 21.347; 11.6195
90; 111.081; 90
1940.5Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549137 CIFC31 H37 N2 PP 1 21/c 18.304; 23.286; 13.9
90; 90.34; 90
2687.8Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549138 CIFC48 H52 O P2P b c a16.9466; 20.6986; 23.0289
90; 90; 90
8077.9Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549139 CIFC55 H64 N2 O P2P 1 21/n 116.228; 16.3739; 17.6769
90; 93.71; 90
4687.2Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549140 CIFC65 H42 F6 N4 O11P -110.6269; 14.921; 17.4851
108.065; 102.085; 91.766
2563.72Shaw, John S.; Vaiyapuri, Rajendran; Parker, Matthew P.; Murray, Claire A.; Lim, Kate J. C.; Pan, Cong; Knappert, Marcus; Cardin, Christine J.; Greenland, Barnaby W.; Grau-Crespo, Ricardo; Colquhoun, Howard M.
Elements of fractal geometry in the <sup>1</sup>H NMR spectrum of a copolymer intercalation-complex: identification of the underlying Cantor set.
Chemical science, 2018, 9, 4052-4061
1549141 CIFC34 H37 B N2P 1 21/c 122.653; 8.3251; 15.2916
90; 107.682; 90
2747.6Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549142 CIFC32 H36 B N SP 1 21/c 17.925; 21.8524; 16.0075
90; 98.766; 90
2739.8Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549143 CIFC34 H39 B N2P -110.294; 11.896; 13.128
66.239; 88.621; 75.243
1417.2Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549144 CIFC34 H39 B N2P 1 21/n 18.41; 34.22; 10.14
90; 97.87; 90
2891Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549145 CIFC32 H36 B N SP 1 21/c 17.9779; 21.8456; 15.7662
90; 98.411; 90
2718.2Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549146 CIFC35 H40 B N OP 1 21/c 17.2959; 22.3592; 17.984
90; 92.626; 90
2930.7Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549147 CIFC39 H43 B N2P -18.1029; 11.3778; 18.5298
87.821; 85.222; 71.032
1609.84Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549148 CIFC32 H34 B N SP n a 2132.54; 9.129; 9.286
90; 90; 90
2758Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855

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