Crystallography Open Database

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7117665 CIFC85 H76 Cl6 Mn14 O12 P8P -110.3548; 10.5563; 20.4728
79.072; 82.668; 83.529
2170.28Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117666 CIFC50 H44 Cl4 Mn8 O8 P4C 1 2/c 129.4777; 11.0635; 21.2608
90; 132.06; 90
5147.9Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117667 CIFC20 H16 Br N O6 SP 21 21 218.30101; 10.28989; 23.4389
90; 90; 90
2002.07Lewis S. Aitken; Lisa E. Hammond; Rajkumar Sundaram; Kenneth Shankland; Geoffrey D. Brown; Alexander J. A. Cobb
Asymmetric cyclopropanation of conjugated cyanosulfones using a novel cupreine organocatalyst: rapid access to delta^3^-amino acids
Chem.Commun., 2015, 51, 13558
7117668 CIFC18 H26 B F4 N RuP n a 2116.1385; 14.1014; 8.2801
90; 90; 90
1884.35Andrey I. Konovalov; Evgeniya O. Gorbacheva; Fedor M. Miloserdov; Vladimir V. Grushin
Ruthenium-catalyzed nucleophilic fluorination of halobenzenes
Chem.Commun., 2015, 51, 13527
7117669 CIFC12 H11 N O2P 1 21 17.7718; 5.5207; 11.7443
90; 91.969; 90
503.6Dipak Kumar Tiwari; Jaya Pogula; B. Sridhar; Dharmendra Kumar Tiwari; Pravin R. Likhar
Nano-copper catalysed highly regioselective synthesis of 2,4-disubstituted pyrroles from terminal alkynes and isocyanides
Chem.Commun., 2015, 51, 13646
7117670 CIFC20 H20 Br N O3P 1 21 15.3126; 9.6321; 18.149
90; 92.117; 90
928.1Francesco Berti; Federico Malossi; Fabio Marchetti; Mauro Pineschi
A highly enantioselective Mannich reaction of aldehydes with cyclic N-acyliminium ions by synergistic catalysis
Chem.Commun., 2015, 51, 13694
7117671 CIFC8 H8 F6 N4 Ni O2 SiP 4/m m m7.0148; 7.0148; 7.5655
90; 90; 90
372.28Osama Shekhah; Youssef Belmabkhout; Karim Adil; Prashant M. Bhatt; Amy J. Cairns; Mohamed Eddaoudi
A facile solvent-free synthesis route for the assembly of a highly CO2 selective and H2S tolerant NiSIFSIX metal-organic framework
Chem.Commun., 2015, 51, 13595
7117672 CIFC18 H16 Cl2 Hg N2 S2C 1 2/c 126.6229; 10.0005; 13.9461
90; 93.414; 90
3706.45Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117673 CIFC19 H19 Ag F3 N2 O3 S3C 1 2/c 123.7546; 9.6388; 18.5295
90; 93.688; 90
4233.84Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117674 CIFC20 H19 Cl2 N3 S2 ZnP 1 21/c 18.5494; 18.8079; 13.9638
90; 99.017; 90
2217.58Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117675 CIFC18 H12 Hg I2 N2 S2C 1 2/c 126.4973; 10.4756; 14.4782
90; 94.642; 90
4005.6Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117676 CIFC28 H22 Br F3 O4P 1 21 110.6758; 9.3185; 25.405
90; 99.557; 90
2492.3Bjarke S. Donslund; Alicia Monleon; Jesper Larsen; Lise Ibsen; Karl Anker Jorgensen
The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks
Chem.Commun., 2015, 51, 13666
7117677 CIFC24 H22 Br F3 O3P 21 21 219.671; 10.892; 21.822
90; 90; 90
2298.7Bjarke S. Donslund; Alicia Monleon; Jesper Larsen; Lise Ibsen; Karl Anker Jorgensen
The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks
Chem.Commun., 2015, 51, 13666
7117678 CIFC27 H27 N O5 SP -19.687; 10.731; 12.624
99.142; 109.67; 102.46
1168Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117679 CIFC28 H26 F3 N O7 S2P 1 21/n 110.689; 16.049; 16.697
90; 103.962; 90
2780Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117680 CIFC23 H27 N O5 SP 21 21 217.466; 13.997; 20.362
90; 90; 90
2128Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117681 CIFC17 H21 N O5 SP 1 21/n 113.648; 8.763; 14.28
90; 91.288; 90
1707.4Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117682 CIFC23 H27 N O6 SP 1 21/c 18.2174; 25.204; 10.5671
90; 95.161; 90
2179.7Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117683 CIFC27 H29 N O4 SP -18.05; 16.385; 18.274
94.603; 93.801; 94.487
2388.8Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117684 CIFC42 H46 N2 O2P 1 21/n 111.2948; 16.3779; 19.5856
90; 103.789; 90
3518.6Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117685 CIFC36 H34 N2 O2P b c a15.3406; 16.1078; 22.8598
90; 90; 90
5648.7Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117686 CIFC36 H36 N2 O2C 1 c 122.1106; 8.5517; 15.1278
90; 93.349; 90
2855.5Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117687 CIFC43 H51 B Cl2 F4 N2 OP 21 21 2112.1048; 16.0393; 21.3761
90; 90; 90
4150.22Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117688 CIFC43 H48 Cl0.5 N3.5 O2.5P -113.2188; 16.6509; 19.82
68.92; 86.793; 67.534
3744.8Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117689 CIFC32 H23 N3 O2C 1 2/c 133.04; 21.838; 7.2037
90; 95.946; 90
5169.7Rui Chen; Ru-Qiang Lu; Ke Shi; Fan Wu; Hong-Xun Fang; Zhe-Xuan Niu; Xiao-Yun Yan; Ming Luo; Xin-Chang Wang; Chi-Yuan Yang; Xiao-Ye Wang; Binbin Xu; Haiping Xia; Jian Pei; Xiao-Yu Cao
Corannulene derivatives with low LUMO levels and dense convex-concave packing for n-channel organic field-effect transistors
Chem.Commun., 2015, 51, 13768
7117690 CIFC30 H19 N3 O2I 1 2/a 17.2119; 21.7175; 31.966
90; 95.488; 90
4983.7Rui Chen; Ru-Qiang Lu; Ke Shi; Fan Wu; Hong-Xun Fang; Zhe-Xuan Niu; Xiao-Yun Yan; Ming Luo; Xin-Chang Wang; Chi-Yuan Yang; Xiao-Ye Wang; Binbin Xu; Haiping Xia; Jian Pei; Xiao-Yu Cao
Corannulene derivatives with low LUMO levels and dense convex-concave packing for n-channel organic field-effect transistors
Chem.Commun., 2015, 51, 13768
7117691 CIFC96 H86 F4 N2 Sn2P -110.1387; 14.5652; 15.407
109.721; 103.913; 101.78
1974.97C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117692 CIFC94 H86 N2 Sn2P -110.3114; 12.6833; 14.8438
101.757; 90.344; 99.28
1874.19C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117693 CIFC72 H66 Cl2 N2 Sb2P -110.5945; 12.3644; 12.5871
98.608; 105.285; 100.205
1531.5C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117694 CIFC48 H43 Cl4 F2 N Sb2P 1 21/n 116.2248; 10.8555; 26.4376
90; 106.24; 90
4470.6C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117695 CIFC74 H70 Bi Cl7 N2 SnP -110.519; 14.7566; 22.9059
75.62; 86.231; 80.569
3396.4C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117696 CIFC84 H76 Bi Cl3 F2 N2 SnP n a 2121.3654; 31.1166; 10.7124
90; 90; 90
7121.8C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117697 CIFC26 H36 N2 S4P -14.5302; 10.3934; 14.1186
81.405; 86.591; 82.721
651.44Te-Fang Yang; Sheng-Han Huang; Yi-Pang Chiu; Bo-Hsiang Chen; Yu-Wei Shih; Yu-Chang Chang; Jie-Yi Yao; Yao-Jen Lee; Ming-Yu Kuo
Pyromellitic dithioimides: thionation improves air-stability and electron mobility of N-type organic field-effect transistors
Chem.Commun., 2015, 51, 13772
7117698 CIFC19 H19 N O4 S2P -18.0274; 8.1297; 14.6961
76.433; 74.709; 85.528
899.17Sridhar Undeela; Srinivas Thadkapally; Jagadeesh Babu Nanubolu; Kiran Kumar Singarapu; Rajeev S. Menon
Catalyst-controlled divergence in cycloisomerisation reactions of N-propargyl-N-vinyl sulfonamides: gold-catalysed synthesis of 2-sulfonylmethyl pyrroles and dihydropyridines
Chem.Commun., 2015, 51, 13748
7117699 CIFC22 H14 N2P -15.8666; 11.4535; 12.2113
83.981; 81.526; 76.578
787.26Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117700 CIFC22 H15 N O2P 1 21/c 110.0557; 10.3647; 15.6302
90; 97.658; 90
1614.5Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117701 CIFC16 H10 N2P 1 21/n 111.476; 6.7685; 15.8831
90; 106.572; 90
1182.5Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117702 CIFC24 H16 N2 OP 1 21/c 113.1944; 9.7945; 14.6162
90; 100.206; 90
1859Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117703 CIFC94 H116 N8 O17P 1 21 118.7521; 23.0271; 25.3314
90; 89.8645; 90
10938.2Hanna Jedrzejewska; Marcin Kwit; Agnieszka Szumna
Switching of inherent chirality driven by self-assembly
Chem.Commun., 2015, 51, 13799
7117704 CIFFe11 H78 Na27 O258 Sb6 W60P -117.5189; 24.8676; 25.0737
60.828; 74.889; 72.982
9028.7Xiaoqiang Du; Yong Ding; Fangyuan Song; Baochun Ma; Junwei Zhao; Jie Song
Efficient photocatalytic water oxidation catalyzed by polyoxometalate [Fe11(H2O)14(OH)2(W3O10)2(alpha-SbW9O33)6]^27-^ based on abundant metals
Chem.Commun., 2015, 51, 13925
7117705 CIFC50 H70 F12 N4 O2.93 P2P 1 21/c 115.137; 14.675; 13.735
90; 114.58; 90
2774.6Saioa Cobo; Frederic Lafolet; Eric Saint-Aman; Christian Philouze; Christophe Bucher; Serena Silvi; Alberto Credi; Guy Royal
Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen
Chem.Commun., 2015, 51, 13886
7117706 CIFC39 H32 Br2 Fe N2P 1 21/n 113.1652; 12.2178; 20.8109
90; 107.514; 90
3192.3C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117707 CIFC47 H55 Fe N2 Na O3P 1 21/n 121.2714; 16.1257; 24.0679
90; 99.18; 90
8149.9C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117708 CIFC67.63 H55.63 Fe3 N4 O0.63P 21 21 225.8932; 14.78371; 13.25563
90; 90; 90
5074.22C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117709 CIFC274 H230 Fe4 N16 O3P n a 2126.9704; 17.93806; 21.5915
90; 90; 90
10445.9C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117710 CIFC44 H44P -110.4488; 12.4887; 13.5525
71.996; 79.884; 82.754
1650.87C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117711 CIFC58 H47 Fe N2P -110.1232; 14.1732; 15.1866
103.795; 93.762; 92.887
2106.63C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117712 CIFC36 H34 N2 O2P 1 21/c 18.9045; 8.871; 17.5783
90; 96.259; 90
1380.3C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117713 CIFC17 H17 N O3P -16.0589; 8.071; 15.6647
100.41; 96.485; 93.141
746.38Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117714 CIFC12 H12 Cl3 N O3P -18.6581; 11.8588; 14.7395
101.56; 104.761; 90.004
1431.65Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976

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