Crystallography Open Database

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1542543 CIFC9 H6.2 N6 O0.1R -3 m :H12.657; 12.657; 9.296
90; 90; 120
1289.7Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542544 CIFC12 H17 F9 N6 O7P b c n12.335; 21.047; 7.89
90; 90; 90
2048.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542545 CIFC14 H3.5 F10.5 N7P 41 3 215.8427; 15.8427; 15.8427
90; 90; 90
3976.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
7118161 CIFC9 H15 Dy N2 O14P 1 21/n 110.1045; 15.4994; 10.4754
90; 102.207; 90
1603.5Liang Qin; Li-Xian Lin; Zhi-Ping Fang; Shui-Ping Yang; Gui-Hua Qiu; Jin-Xiang Chen; Wen-Hua Chen
A water-stable metal-organic framework of a zwitterionic carboxylate with dysprosium: a sensing platform for Ebolavirus RNA sequences
Chem.Commun., 2016, 52, 132
7118162 CIFC12 H16 N2 O4P 1 21 15.1412; 26.4969; 9.2776
90; 105.207; 90
1219.59Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed
Gelation by supramolecular dimerization of mono(urea)s
Chem.Commun., 2016, 52, 198
7118163 CIFC11 H14 N2 O4P -14.6214; 8.2787; 14.248
92.962; 94.351; 95.33
540.25Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed
Gelation by supramolecular dimerization of mono(urea)s
Chem.Commun., 2016, 52, 198
7118164 CIFC12 H16 N2 O4P -14.529; 9.009; 15.234
101.869; 93.598; 101.742
592Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed
Gelation by supramolecular dimerization of mono(urea)s
Chem.Commun., 2016, 52, 198
7118165 CIFC93 H14 N O2 S2 Sc3P n a 2119.9441; 15.7417; 14.9924
90; 90; 90
4706.9Maira R. Ceron; Marta Izquierdo; Nuria Alegret; Juan A. Valdez; Antonio Rodriguez-Fortea; Marilyn M. Olmstead; Alan L. Balch; Josep M. Poblet; Luis Echegoyen
Reactivity differences of Sc3N at C2n (2n = 68 and 80). Synthesis of the first methanofullerene derivatives of Sc3N at D5h-C80
Chem.Commun., 2016, 52, 64
7118166 CIFC30 H49 B Fe N4 O2 Si2P 1 21/n 116.807; 12.849; 17.795
90; 114.07; 90
3509Holger Braunschweig; Rian D. Dewhurst; Katharina Ferkinghoff
Carbene-induced synthesis of the first borironium cations using the [(eta^5^-C5Me5)Fe(CO)2]^-^ anion as an unlikely leaving group
Chem.Commun., 2016, 52, 183
7118167 CIFC34 H57 B Fe N4 O2 Si2P 1 21/c 110.5605; 17.2867; 20.8645
90; 99.455; 90
3757.2Holger Braunschweig; Rian D. Dewhurst; Katharina Ferkinghoff
Carbene-induced synthesis of the first borironium cations using the [(eta^5^-C5Me5)Fe(CO)2]^-^ anion as an unlikely leaving group
Chem.Commun., 2016, 52, 183
7118168 CIFC71 H58 Cl4 N2 S2P 21 21 2113.4055; 15.0828; 29.1775
90; 90; 90
5899.5Ping Chen; Sheng-mei Lu; Wengang Guo; Yan Liu; Can Li
A highly enantioselective thiolation of sulfonyl indoles to access 3-sec-sulfur-substituted indoles in water
Chem.Commun., 2016, 52, 96
7118169 CIFC17 H19 Cl O5C 1 2 121.41; 9.115; 8.678
90; 90.827; 90
1693.4Qiang Sha; Hadi Arman; Michael P. Doyle
Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement
Chem.Commun., 2016, 52, 108
7118170 CIFC23 H22 Cl N O3P 21 21 219.258; 9.554; 22.789
90; 90; 90
2015.7Qiang Sha; Hadi Arman; Michael P. Doyle
Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement
Chem.Commun., 2016, 52, 108
7118171 CIFC96 H104 N7 O ReP -115.7923; 16.6247; 21.4456
70.8548; 70.4554; 71.4233
4872.6Jan Paulo T. Zaragoza; Maxime A. Siegler; David P. Goldberg
Rhenium(V)-oxo corrolazines: isolating redox-active ligand reactivity
Chem.Commun., 2016, 52, 167
7118172 CIFC18 H26 N3 Ni O2P 21 21 215.79; 10.095; 29.897
90; 90; 90
1747.5Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118173 CIFC24 H23 F2 N3 Ni O2P 21 21 2110.148; 11.913; 17.409
90; 90; 90
2104.6Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118174 CIFC21.5 H31 F N3 Ni O2.5P 21 21 2110.777; 10.97; 36.58
90; 90; 90
4325Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118175 CIFC15 H12 F2C 1 2/c 124.87; 5.944; 16.266
90; 107.995; 90
2287Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118176 CIFC15 H13 FC 1 c 17.74284; 17.2689; 8.39473
90; 91.1751; 90
1122.23Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118177 CIFC20 H26 N2 O6 SP 21 21 214.0216; 21.3117; 6.4976
90; 90; 90
1941.64Pedras, M. S. C.; To, Q. H.; Schatte, G.
Divergent reactivity of an indole glucosinolate yields Lossen or Neber rearrangement products: the phytoalexin rapalexin A or a unique β-d-glucopyranose fused heterocycle.
Chemical communications (Cambridge, England), 2016, 52, 2505-2508
7118178 CIFC60 H90 Li2 O12 ThR -3 :H14.8737; 14.8737; 24.3175
90; 90; 120
4658.9Pedrick, Elizabeth A.; Hrobárik, Peter; Seaman, Lani A.; Wu, Guang; Hayton, Trevor W.
Synthesis, structure and bonding of hexaphenyl thorium(iv): observation of a non-octahedral structure.
Chemical communications (Cambridge, England), 2015, 52, 689-692
7118179 CIFC60 H78 Li2 O10 ThP 1 21/n 116.5641; 16.7043; 21.3854
90; 108.682; 90
5605.4Pedrick, Elizabeth A.; Hrobárik, Peter; Seaman, Lani A.; Wu, Guang; Hayton, Trevor W.
Synthesis, structure and bonding of hexaphenyl thorium(iv): observation of a non-octahedral structure.
Chemical communications (Cambridge, England), 2015, 52, 689-692
7118185 CIFC29 H21 N OP 21 21 219.002; 13.225; 17.293
90; 90; 90
2058.8Barsu, Nagaraju; Sen, Malay; Premkumar, J. Richard; Sundararaju, Basker
Cobalt(iii) catalyzed C-8 selective C-H and C-O coupling of quinoline N-oxide with internal alkynes via C-H activation and oxygen atom transfer.
Chemical communications (Cambridge, England), 2016, 52, 1338-1341
7118186 CIFC12 H14 N6 O6P 1 21/n 19.22642; 9.71725; 18.0546
90; 101.605; 90
1585.6Erhardt, Hellmuth; Mohr, Fabian; Kirsch, Stefan F.
Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry.
Chemical communications (Cambridge, England), 2016, 52, 545-548
7118187 CIFC31 H25 N9 O6P 1 21/n 114.6712; 12.489; 17.0137
90; 106.677; 90
2986.3Erhardt, Hellmuth; Mohr, Fabian; Kirsch, Stefan F.
Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry.
Chemical communications (Cambridge, England), 2016, 52, 545-548
7118188 CIFC33 H35 Cl2 I N4 O PdP -110.7622; 12.8238; 13.4282
114.432; 100.558; 93.044
1641.4Vicente-Hernández, Inmaculada; Chicote, María-Teresa; Vicente, José; Bautista, Delia
A new type of oxidative addition of an iodoarene to a Pd(ii) complex.
Chemical communications (Cambridge, England), 2016, 52, 594-596
7118189 CIFC40 H38 Cu2 N9 O12 S2P 4/n c c11.4766; 11.4766; 30.5554
90; 90; 90
4024.5Abrahams, C. T.; Abrahams, B. F.; Hudson, T. A.; Robson, R.
Templation of a square grid copper(ii) 4,4'-bipyridine network by a 3D PtS-related Cu(i)-Cu(ii) 4,4'-bipyridine crystal.
Chemical communications (Cambridge, England), 2016, 52, 609-612
7118190 CIFC20 H20 Cu N4 O8 S2P 4/n c c11.5095; 11.5095; 15.4286
90; 90; 90
2043.8Abrahams, C. T.; Abrahams, B. F.; Hudson, T. A.; Robson, R.
Templation of a square grid copper(ii) 4,4'-bipyridine network by a 3D PtS-related Cu(i)-Cu(ii) 4,4'-bipyridine crystal.
Chemical communications (Cambridge, England), 2016, 52, 609-612
7118196 CIFC77 H100 N4 O10 Pd SiP 1 21/c 124.3213; 10.002; 32.0407
90; 111.912; 90
7231.2Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André
Catenane-based mechanically-linked block copolymers.
Chemical communications (Cambridge, England), 2016, 52, 2149-2152
7118197 CIFC75 H96 N4 O10 Pd SiC 1 2/c 139.473; 12.053; 35.42
90; 114.26; 90
15364Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André
Catenane-based mechanically-linked block copolymers.
Chemical communications (Cambridge, England), 2016, 52, 2149-2152
7118198 CIFC75 H93 N4 O13 PdI 1 2/a 137.2375; 11.7434; 32.5955
90; 101.666; 90
13959.4Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André
Catenane-based mechanically-linked block copolymers.
Chemical communications (Cambridge, England), 2016, 52, 2149-2152
7118199 CIFC22 H29 O PP 1 21/c 115.6981; 7.4997; 16.6619
90; 93.155; 90
1958.65Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118200 CIFC22 H29 PP -18.3322; 8.5865; 13.0867
87.833; 85.945; 86.322
931.49Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118201 CIFC43 H37 B F15 O P SiP 1 21/c 110.8091; 25.3584; 16.9567
90; 96.133; 90
4621.25Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118202 CIFC25 H6 B F15 OP -19.4516; 12.1427; 12.2399
110.414; 100.07; 97.111
1269.99Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118203 CIFC96 H110 F12 N8 O18 P2P -112.01; 13.437; 16.32
106.161; 102.667; 98.007
2411Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118204 CIFC90 H96 F12 N2 O16 P2P -113.799; 15.7; 22.416
104.6; 96.36; 107.93
4377Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118205 CIFC80 H88 Cl6 F12 N2 O16 P2C 1 2/c 120.956; 17.451; 24.943
90; 109.498; 90
8599Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118206 CIFC92 H104 F12 N2 O20 P2P -112.778; 12.983; 14.022
108.815; 93.025; 100.752
2147Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118207 CIFC32 H29 N O2 SP 1 21/c 111.62; 11.0673; 21.125
90; 98.311; 90
2688.2Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118208 CIFC26 H25 N O2 SP 1 21/n 113.926; 10.6835; 14.955
90; 92.243; 90
2223.3Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118209 CIFC26 H27 N O3 SP 1 21/n 110.4657; 19.751; 12.477
90; 114.712; 90
2342.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118210 CIFC24 H21 N O2 SP 1 21/c 110.6663; 10.8826; 18.121
90; 103.78; 90
2042.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118211 CIFC24 H21 N O2 SP 1 21/c 114.001; 12.335; 11.587
90; 95.497; 90
1991.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118212 CIFC24 H21 N O2 SP 1 21/c 18.9249; 9.9995; 22.944
90; 107.13; 90
1956.8Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118213 CIFC54 H58 N3 P2 RhP 1 21/n 113.58; 21.768; 17.29
90; 111.548; 90
4754Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118214 CIFC48 H48 N3 P2 RhP 1 21/c 116.185; 18.144; 15.477
90; 118.406; 90
3998Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118215 CIFC72 H66 N3 P2 RhP 1 21/n 113.567; 28.198; 16.293
90; 109.213; 90
5886Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118216 CIFC98 H96 N6 P4 Rh2C 1 2/c 142.986; 17.237; 27.577
90; 119.527; 90
17779Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118217 CIFC60 H56 N3 P2 RhP 1 21/n 113.907; 27.103; 16.593
90; 112.133; 90
5793Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118218 CIFC36 H26 Br2 O4P 21 21 215.6288; 12.578; 41.669
90; 90; 90
2950.1Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118219 CIFC36 H28 O4P 21 21 219.263; 12.8186; 22.369
90; 90; 90
2656.1Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118220 CIFC36 H26 Br2 O4P 21 21 215.5911; 13.004; 40.623
90; 90; 90
2953.6Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118221 CIFC13 H11 F N2P -110.0641; 11.0425; 12.1824
114.924; 95.055; 111.476
1094.39Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak
'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks.
Chemical communications (Cambridge, England), 2016, 52, 2141-2144
7118222 CIFC13 H10 F2 N2P 1 21/c 112.7028; 8.3775; 11.5509
90; 117.017; 90
1095.1Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak
'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks.
Chemical communications (Cambridge, England), 2016, 52, 2141-2144
7118223 CIFC41 H33 N3 O6P 1 21/c 111.1829; 11.5006; 26.2259
90; 92.219; 90
3370.4Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118224 CIFC41 H33 Cd Cl0 I2 N3 O6R -3 :H54.6374; 54.6374; 8.9458
90; 90; 120
23127.6Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118225 CIFC42.17 H36 Br Cd I2 N3 O6.33R -3 :H54.5811; 54.5811; 8.9081
90; 90; 120
22982.7Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118226 CIFC42 H35 Cd I4 N3 O6R -3 :H54.772; 54.772; 8.8733
90; 90; 120
23053.3Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118227 CIFC41 H33 Cd I2 N3 O6R -3 :H54.8819; 54.8819; 8.8759
90; 90; 120
23152.7Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118230 CIFC26 H18 Br Cl4 N2 O4P 1 21 113.0622; 8.2259; 13.1485
90; 106.33; 90
1355.79Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian
Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles.
Chemical communications (Cambridge, England), 2016, 52, 2537-2540
7118231 CIFC27 H21 Br Cl2 N2 O5P 21 21 2112.315; 13.9146; 15.2049
90; 90; 90
2605.49Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian
Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles.
Chemical communications (Cambridge, England), 2016, 52, 2537-2540
7118232 CIFC31 H30 Br N3 O5I 1 2 114.6406; 9.57209; 19.5953
90; 97.003; 90
2725.62Zhao, Kun; Zhi, Ying; Li, Xinyi; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter
Asymmetric synthesis of 3,3'-pyrrolidinyl-dispirooxindoles via a one-pot organocatalytic Mannich/deprotection/aza-Michael sequence.
Chemical communications (Cambridge, England), 2016, 52, 2249-2252
7118241 CIFC40 H24 In N2 O8C 1 2/c 128.286; 20.9422; 27.5862
90; 120.798; 90
14037Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun
The dynamic response of a flexible indium based metal-organic framework to gas sorption.
Chemical communications (Cambridge, England), 2016, 52, 2277-2280
7118242 CIFC40 H24 In N2 O8I 1 2/c 126.9793; 21.3293; 26.4721
90; 97.001; 90
15119.8Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun
The dynamic response of a flexible indium based metal-organic framework to gas sorption.
Chemical communications (Cambridge, England), 2016, 52, 2277-2280
7118243 CIFC25 H32 B F6 I2 N8 O P WP 1 21/n 18.352; 22.5729; 18.2914
90; 100.772; 90
3387.69Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W.
Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex.
Chemical communications (Cambridge, England), 2016, 52, 2616-2619
7118244 CIFC33 H38 B F6 N8 O2 P WP 1 21/n 125.7178; 11.6201; 25.7435
90; 97.686; 90
7624.2Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W.
Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex.
Chemical communications (Cambridge, England), 2016, 52, 2616-2619
7118245 CIFC20 H21 Br O5P 1 21/c 112.3928; 8.3243; 18.5364
90; 95.888; 90
1902.15Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang
Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation.
Chemical communications (Cambridge, England), 2016, 52, 2257-2260
7118246 CIFC21 H23 Br O5P 1 21/c 19.2166; 9.0685; 23.2491
90; 99.08; 90
1918.83Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang
Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation.
Chemical communications (Cambridge, England), 2016, 52, 2257-2260
7118247 CIFC27 H24 N2 O3P -110.9476; 11.03; 11.0714
86.1003; 64.8281; 60.6087
1037.28Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118249 CIFC31 H24 N2 O2P -19.365; 11.4265; 11.9971
74.104; 80.112; 71.016
1162.72Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118250 CIFC25 H20 N3 OP 1 21/c 118.817; 10.53; 9.5207
90; 96.996; 90
1872.4Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118251 CIFC28 H28 Cl N O3P -19.469; 10.0316; 13.1967
83.975; 70.468; 85.668
1173.8Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118252 CIFC19 H15 N O4P 1 21/c 18.3566; 17.7311; 10.5304
90; 101.637; 90
1528.24Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118253 CIFC27 H26 N2 O3P -18.2128; 12.0722; 12.1473
80.826; 73.356; 74.316
1106.54Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118254 CIFC18 H19 N O3P n m a15.9415; 14.8517; 6.2573
90; 90; 90
1481.5Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118255 CIFC14 H15 N O5P 1 21/c 19.5866; 19.5978; 7.6285
90; 111.316; 90
1335.17Baumann, A. N.; Music, A.; Karaghiosoff, K.; Didier, D.
Highly diastereoselective approach to methylenecyclopropanes via boron-homologation/allylboration sequences.
Chemical communications (Cambridge, England), 2016, 52, 2529-2532
7118256 CIFC45 H37 Cl N5 O P RuP 1 21/n 113.9666; 12.6444; 21.018
90; 95.457; 90
3694.9Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K.
Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst.
Chemical communications (Cambridge, England), 2016, 52, 2901-2904
7118257 CIFC39 H31 Cl N5 O3 P RuP 1 21/c 116.1333; 12.495; 16.9891
90; 98.709; 90
3385.27Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K.
Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst.
Chemical communications (Cambridge, England), 2016, 52, 2901-2904
7118258 CIFC38 H42 Cl6 Cu2 N6P -18.2153; 11.1662; 11.5343
85.272; 84.43; 77.543
1026.24Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118259 CIFC38 H42 Cl6 Cu2 N6P -18.1887; 10.9691; 11.3579
85.0163; 85.1738; 77.5551
990.21Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118260 CIFC40 H46 Cl6 Cu2 N6P -18.3056; 11.1055; 11.873
86.315; 89.284; 77.72
1067.9Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118261 CIFC40 H46 Cl6 Cu2 N6P -18.3293; 10.9929; 11.7343
86.079; 89.732; 77.869
1047.9Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118262 CIFC38 H40 Cl8 Cu2 N6P -18.253; 10.948; 11.802
85.792; 89.721; 78.477
1042Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118263 CIFC40 H46 Cl6 Cu2 N6 O2P -18.292; 10.995; 12.277
84.743; 86.68; 78.394
1090.9Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118264 CIFC18 H18 Cl Cu N4 O2P 21 21 219.0636; 9.6375; 20.925
90; 90; 90
1827.8Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118265 CIFC21 H25 Cl Cu N3P 1 21/c 19.5545; 8.8034; 23.9329
90; 96.6239; 90
1999.61Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118266 CIFC36 H38 Cl2 Cu2 N6P 1 21/n 110.0169; 15.969; 10.7209
90; 95.056; 90
1708.24Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118267 CIFC43.5 H37 Al Au Cl F36 N2 O4 P4P 1 21/n 110.7137; 38.3822; 14.7478
90; 90.909; 90
6063.8Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop
Functionalization of P4 in the coordination sphere of coinage metal cations.
Chemical communications (Cambridge, England), 2016, 52, 3284-3287
7118268 CIFC94 H97 Al Au2 F36 N4 O4 P4C 1 2/c 139.9091; 25.1072; 22.5843
90; 100.38; 90
22259.3Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop
Functionalization of P4 in the coordination sphere of coinage metal cations.
Chemical communications (Cambridge, England), 2016, 52, 3284-3287
7118269 CIFC27 H24 Br N O3P 21 21 218.8669; 14.7074; 17.9059
90; 90; 90
2335.1Li, Mingfeng; Guo, Xin; Jin, Weifeng; Zheng, Qing; Liu, Shunying; Hu, Wenhao
An enantioselective three-component reaction of diazoacetates with indoles and enals by iridium/iminium co-catalysis.
Chemical communications (Cambridge, England), 2016, 52, 2736-2739
7118270 CIFC18 H32 O3 SiC 1 2/c 129.017; 11.4978; 12.6967
90; 111.472; 90
3942Stepherson, Jacob R.; Fronczek, Frank R.; Kartika, Rendy
An expedient synthesis of functionalized 1,4-diketone-derived compounds via silyloxyallyl cation intermediates.
Chemical communications (Cambridge, England), 2016, 52, 2300-2303
7118271 CIFC52 H44 N2 O20 Zn3P -19.4533; 18.614; 19.976
68.27; 82.61; 82.18
3223.2Chakraborty, Anindita; Bhattacharyya, Sohini; Hazra, Arpan; Ghosh, Ashta Chandra; Maji, Tapas Kumar
Post-synthetic metalation in an anionic MOF for efficient catalytic activity and removal of heavy metal ions from aqueous solution.
Chemical communications (Cambridge, England), 2016, 52, 2831-2834
7118272 CIFC15 H26 Cl N WP n a 2113.1669; 12.7572; 20.0394
90; 90; 90
3366.07Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot
Tungsten imido catalysts for selective ethylene dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 2850-2853
7118273 CIFC16 H25 Cl4 N O WP -18.5941; 14.1186; 17.4478
95.806; 98.562; 97.484
2059.88Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot
Tungsten imido catalysts for selective ethylene dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 2850-2853
7118274 CIFC22 H21 N O4P -111.0068; 18.8343; 19.829
72.08; 89.811; 77.711
3813.1Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua
Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine.
Chemical communications (Cambridge, England), 2016, 52, 2177-2180
7118275 CIFC22 H21 N O4P -19.035; 13.258; 16.686
90.402; 103.495; 105.139
1871.2Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua
Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine.
Chemical communications (Cambridge, England), 2016, 52, 2177-2180
7118276 CIFC24 H27 N O3C 1 2/c 144.225; 11.0988; 15.9916
90; 99.538; 90
7740.9Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua
Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine.
Chemical communications (Cambridge, England), 2016, 52, 2177-2180
7118277 CIFC90 H187 O100P 1 21 115.517; 9.825; 21.953
90; 90.05; 90
3346.8Rutenberg, R.; Leitus, G.; Fallik, E.; Poverenov, E.
Discovery of a non classic host guest complexation mode in a β-cyclodextrin/propionic acid model.
Chemical communications (Cambridge, England), 2016, 52, 2565-2568
7118278 CIFC30 H25 F N2 O3 SP 1 21 15.552; 17.133; 13.413
90; 93.446; 90
1273.6Sun, Xiao-Xue; Zhang, Hong-Hao; Li, Guo-Hao; Meng, Li; Shi, Feng
Diastereo- and enantioselective construction of an indole-based 2,3-dihydrobenzofuran scaffold via catalytic asymmetric [3+2] cyclizations of quinone monoimides with 3-vinylindoles.
Chemical communications (Cambridge, England), 2016, 52, 2968-2971

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