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
7118279 CIFC16 H24 N2 O5P 1 21/n 16.9693; 12.1404; 19.3065
90; 90.623; 90		1633.43Eckshtain-Levi, Meital; Lavi, Ronit; Yufit, Dmitry S.; Daniel, Bareket; Green, Omer; Fleker, Ohad; Richman, Michal; Rahimipour, Shai; Gruzman, Arie; Benisvy, Laurent
A versatile water-soluble chelating and radical scavenging platform.
Chemical communications (Cambridge, England), 2016, 52, 2350-2353
7118280 CIFC32.5 H60 Cl N3 O5P 1 21/n 120.6006; 12.5488; 27.283
90; 92.36; 90		7047Eckshtain-Levi, Meital; Lavi, Ronit; Yufit, Dmitry S.; Daniel, Bareket; Green, Omer; Fleker, Ohad; Richman, Michal; Rahimipour, Shai; Gruzman, Arie; Benisvy, Laurent
A versatile water-soluble chelating and radical scavenging platform.
Chemical communications (Cambridge, England), 2016, 52, 2350-2353
7118281 CIFC32 H49 Cu N4 O11.5P -113.96; 14.092; 18.3587
89.637; 83.246; 85.326		3574.6Eckshtain-Levi, Meital; Lavi, Ronit; Yufit, Dmitry S.; Daniel, Bareket; Green, Omer; Fleker, Ohad; Richman, Michal; Rahimipour, Shai; Gruzman, Arie; Benisvy, Laurent
A versatile water-soluble chelating and radical scavenging platform.
Chemical communications (Cambridge, England), 2016, 52, 2350-2353
7118282 CIFC151 H146 Cl6 N8 O12P -114.438; 15.006; 16.156
104.214; 92.043; 94.227		3379Katoono, Ryo; Suzuki, Takanori
Planar chiral desymmetrization of a two-layered cyclophane and control of dynamic helicity through the arrangement of two nonstereogenic centers.
Chemical communications (Cambridge, England), 2016, 52, 1029-1031
7118283 CIFC27 H24 O3P 1 21/c 118.7438; 5.9398; 19.1345
90; 92.094; 90		2128.9Kumar, Atul; Maurya, Shivam; Pratap, Kemant; Srivastava, Suman
Betaine mediated synthesis of annulated dihydrofurans from oxobis(methylthio)ketene acetals and N-butyl-N'-methyl ethane-1,2-diamine as precursors via NHC elimination.
Chemical communications (Cambridge, England), 2016, 52, 2795-2798
7118284 CIFC2 H2 N4 O12P 1 21/c 17.5489; 7.2995; 8.3759
90; 97.935; 90		457.12Fischer, Dennis; Klapötke, Thomas M; Stierstorfer, Jörg
Tetranitratoethane.
Chemical communications (Cambridge, England), 2016, 52, 916-918
7118285 CIFC110 H108 Dy7 N24 O39 P3P 1 21/c 114.7481; 33.056; 25.607
90; 104.153; 90		12105Tian, Haiquan; Bao, Song-Song; Zheng, Li-Min
Cyclic single-molecule magnets: from the odd-numbered heptanuclear to a dimer of heptanuclear dysprosium clusters.
Chemical communications (Cambridge, England), 2016, 52, 2314-2317
7118286 CIFC212 H176 Dy14 N48 O70 P10C 1 2/c 122.068; 25.118; 44.977
90; 101.477; 90		24432Tian, Haiquan; Bao, Song-Song; Zheng, Li-Min
Cyclic single-molecule magnets: from the odd-numbered heptanuclear to a dimer of heptanuclear dysprosium clusters.
Chemical communications (Cambridge, England), 2016, 52, 2314-2317
7118287 CIFC40 H32 Br4 N2P b c a18.6729; 11.0827; 33.857
90; 90; 90		7006.58Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118288 CIFC52 H42 N2 O2 P2C 1 2/c 128.1262; 8.5442; 20.5029
90; 109.719; 90		4638.24Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118289 CIFC40 H34 Br2 N2P -111.0372; 12.6734; 13.6066
87.925; 67.674; 66.578		1600.69Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118290 CIFC46 H39 N2 O PP 1 21/c 110.7866; 32.189; 10.4301
90; 99.194; 90		3574.9Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118291 CIFC56 H66 N2 O2 P2C 1 2/c 129.5733; 8.868; 20.0015
90; 109.81; 90		4935.1Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118292 CIFC40 H47 Cl Hg O4P -114.6684; 16.1503; 16.8665
109.87; 99.8419; 95.2508		3653.9Slavík, Petr; Kohout, Michal; Böhm, Stanislav; Eigner, Václav; Lhoták, Pavel
Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation.
Chemical communications (Cambridge, England), 2016, 52, 2366-2369
7118293 CIFC40 H47 Cl Hg O4C 1 2/c 136.8232; 9.7905; 26.7317
90; 131.016; 90		7271.6Slavík, Petr; Kohout, Michal; Böhm, Stanislav; Eigner, Václav; Lhoták, Pavel
Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation.
Chemical communications (Cambridge, England), 2016, 52, 2366-2369
7118294 CIFC40 H46 O4P -110.5111; 17.7963; 19.3271
110.342; 96.592; 101.212		3259.1Slavík, Petr; Kohout, Michal; Böhm, Stanislav; Eigner, Václav; Lhoták, Pavel
Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation.
Chemical communications (Cambridge, England), 2016, 52, 2366-2369
7118295 CIFC106 H135 Fe6 N6 O50 Tb3C 1 2/c 129.189; 26.117; 20.479
90; 124.572; 90		12855Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118296 CIFC109 H143 Dy3 Fe6 N6 O51C 1 2/c 129.2726; 26.0163; 20.8386
90; 125.139; 90		12977.8Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118297 CIFC109 H143 Fe6 Ho3 N6 O51C 1 2/c 129.211; 25.894; 20.7929
90; 124.97; 90		12888Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118298 CIFC108 H139 Fe6 N6 O50 Tm3C 1 2/c 129.069; 25.935; 20.683
90; 124.822; 90		12801Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118299 CIFC112 H151 Fe6 N6 O52 Yb3P -119.6191; 22.3573; 31.163
77.52; 80.86; 71.74		12612.6Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118300 CIFC109 H143 Fe6 Lu3 N6 O51C 1 2/c 129.1226; 25.811; 20.8572
90; 125.126; 90		12822.9Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118301 CIFC108 H139 Fe6 N6 O50 Y3C 1 2/c 129.172; 25.835; 20.884
90; 125.552; 90		12805Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118302 CIFC107 H125 Cl6 Fe6 Gd3 N6 O47P 1 21/n 123.721; 20.6579; 26.078
90; 100.61; 90		12560.4Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118303 CIFC24 H38 B N6 S3 ZnR -3 :H13.3984; 13.3984; 27.542
90; 90; 120		4281.9Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118304 CIFC41 H57 B N6 S3 ZnR -3 c :H13.473; 13.473; 67.359
90; 90; 120		10589Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118305 CIFC34 H47 B N6 O2 S3 ZnP 1 21 110.3568; 19.5721; 10.5278
90; 119.424; 90		1858.8Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118306 CIFC41 H51 B Mo N6 O3 S3 ZnP -110.2866; 12.0489; 19.226
92.635; 93.904; 114.888		2149.3Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118307 CIFC27 H38 B F N6 S4 ZnP 1 21/n 113.199; 17.979; 13.504
90; 92.785; 90		3201Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118308 CIFCo6 H224 Li14 Na9 O250 P5 W36P -114.5199; 25.6135; 27.6975
94.512; 99.078; 93.145		10116.6Martin-Sabi, Mercè; Winter, Ross Stuart; Lydon, Claire; Cameron, Jamie M.; Long, De-Liang; Cronin, Leroy
Rearrangement of {α-P2W15} to {PW6} moieties during the assembly of transition-metal-linked polyoxometalate clusters.
Chemical communications (Cambridge, England), 2016, 52, 919-921
7118309 CIFH120 Li12 Mn6 Na11 O198 P5 W36P -114.0471; 21.9582; 30.7558
87.466; 88.627; 86.131		9453.6Martin-Sabi, Mercè; Winter, Ross Stuart; Lydon, Claire; Cameron, Jamie M.; Long, De-Liang; Cronin, Leroy
Rearrangement of {α-P2W15} to {PW6} moieties during the assembly of transition-metal-linked polyoxometalate clusters.
Chemical communications (Cambridge, England), 2016, 52, 919-921
7118310 CIFH137 Li20 Mn9 Na5 O245 P8 W45P -114.0535; 29.6184; 31.8218
74.118; 81.242; 89.716		12582Martin-Sabi, Mercè; Winter, Ross Stuart; Lydon, Claire; Cameron, Jamie M.; Long, De-Liang; Cronin, Leroy
Rearrangement of {α-P2W15} to {PW6} moieties during the assembly of transition-metal-linked polyoxometalate clusters.
Chemical communications (Cambridge, England), 2016, 52, 919-921
7118311 CIFC68 H162 Br Cr Mo6 N5 O26P 1 21 116.314; 15.3614; 18.1903
90; 92.867; 90		4552.9Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118312 CIFC45 H109 Cr Mo6 N6 O29P -113.554; 13.7899; 21.0955
86.768; 88.944; 63.016		3508Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118313 CIFC46 H108 Cr Mo6 N5 O28P -113.6865; 13.7366; 21.5248
86.727; 83.692; 62.304		3561.4Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118314 CIFC68 H177 Br3 Cr Mo6 N6 O32.5P 1 21 123.7911; 15.3677; 28.4337
90; 96.193; 90		10335.1Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118315 CIFC68 H176 Br3 Cr Mo6 N6 O31P 1 21 124.0231; 15.1457; 28.6632
90; 95.967; 90		10372.5Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118316 CIFC67 H161 Br Cr Mo6 N4 O28P 1 21 116.5248; 15.1876; 18.3785
90; 93.071; 90		4605.9Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118317 CIFC11 H12 N6 O2P 17; 7.1645; 13.4574
94.095; 93.302; 105.223		647.52Pathigoolla, Atchutarao; Sureshan, Kana M.
The topochemical synthesis of triazole-linked homobasic DNA.
Chemical communications (Cambridge, England), 2016, 52, 886-888
7118318 CIFC37 H53 Br3 Co2 N3 O PP 1 21/c 114.965; 24.298; 15.796
90; 110.07; 90		5395Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118319 CIFC33 H45 Br Co N3 PP 1 21/c 112.8384; 17.0917; 16.7231
90; 116.587; 90		3281.5Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118320 CIFC66 H90 Co2 N8 P2P -114.852; 16.6741; 18.3766
66.34; 84.429; 66.37		3807.8Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118321 CIFC33 H45 Co N5 PC 1 2/c 125.681; 15.695; 18.634
90; 113.151; 90		6906Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118322 CIFC9 H9 I N2 O3P -18.154; 11.633; 12.467
67.55; 76.11; 76.47		1047.6Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118323 CIFC10 H12 I N2 O3.5P -19.7294; 11.427; 11.566
90.02; 110.88; 93.06		1199.5Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118324 CIFC15 H13 I N2 O3P 21 21 215.7923; 8.4216; 29.71
90; 90; 90		1449.3Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118325 CIFC12 H9 I N2 O4 SP 1 21/c 17.137; 22.707; 8.8248
90; 90.68; 90		1430Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118326 CIFC13 H11 I N2 O4 SP -17.2705; 8.7631; 12.765
109.12; 99.97; 90.54		754.9Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118327 CIFC18 H13 I N2 O4 SP 1 21/c 112.277; 10.283; 14.972
90; 106.71; 90		1810.3Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118328 CIFC12 H10 N2 O4 SP -16.8571; 8.4482; 11.3117
98.755; 106.766; 93.582		616.19Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118329 CIFC13 H12 N2 O4 SP 1 21/c 114.1204; 6.8482; 14.7897
90; 112.86; 90		1317.83Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118330 CIFC21 H20 Cl N O6P 21 21 215.79637; 13.3106; 25.2934
90; 90; 90		1951.47Shu, Tao; Ni, Qijian; Song, Xiaoxiao; Zhao, Kun; Wu, Tianyu; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter
Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction.
Chemical communications (Cambridge, England), 2016, 52, 2609-2611
7118331 CIFC21 H23 N O7P -18.6216; 9.7362; 13.104
91.924; 104.975; 108.523		999.5Gao, Qian; Hao, Wen-Juan; Liu, Feng; Tu, Shu-Jiang; Wang, Shu-Liang; Li, Guigen; Jiang, Bo
Unexpected isocyanide-based three-component bicyclization for the stereoselective synthesis of densely functionalized pyrano[3,4-c]pyrroles.
Chemical communications (Cambridge, England), 2016, 52, 900-903
7118332 CIFC16 H12 N6 SP c c n12.0045; 10.8025; 11.0878
90; 90; 90		1437.9Wang, Ying; Yi, Jin-Min; Zhang, Meng-Yuan; Xu, Ping; Zhao, Xiao-Jun
I2-induced SC-SC transformation within two-dimensional Zn(ii)-triazole framework: an ideal detector of cyano-containing molecules.
Chemical communications (Cambridge, England), 2016, 52, 3099-3102
7118333 CIFC28.5 H30 N7.5 O6.5 S ZnP -19.0152; 12.4589; 13.9479
105.422; 91.756; 94.9		1502.37Wang, Ying; Yi, Jin-Min; Zhang, Meng-Yuan; Xu, Ping; Zhao, Xiao-Jun
I2-induced SC-SC transformation within two-dimensional Zn(ii)-triazole framework: an ideal detector of cyano-containing molecules.
Chemical communications (Cambridge, England), 2016, 52, 3099-3102
7118334 CIFC44 H33 I N12 O7.5 S2 Zn2P -18.94; 15.624; 18.684
65.286; 84.924; 74.295		2281.3Wang, Ying; Yi, Jin-Min; Zhang, Meng-Yuan; Xu, Ping; Zhao, Xiao-Jun
I2-induced SC-SC transformation within two-dimensional Zn(ii)-triazole framework: an ideal detector of cyano-containing molecules.
Chemical communications (Cambridge, England), 2016, 52, 3099-3102
7118335 CIFC70 H68 N4 O7 Zn2P n n a17.8685; 23.0557; 18.5326
90; 90; 90		7634.89He, Shixiong; Wang, Fuli; Tong, Wah-Leung; Yiu, Shek-Man; Chan, Michael C. W.
Topologically diverse shape-persistent bis-(Zn-salphen) catalysts: efficient cyclic carbonate formation under mild conditions.
Chemical communications (Cambridge, England), 2016, 52, 1017-1020
7118336 CIFC39 H36 N2 O SP 1 21/c 113.163; 9.4788; 25.5497
90; 96.7832; 90		3165.5Ikezawa, Takahiro; Mutoh, Katsuya; Kobayashi, Yoichi; Abe, Jiro
Thiophene-substituted phenoxyl-imidazolyl radical complexes with high photosensitivity.
Chemical communications (Cambridge, England), 2016, 52, 2465-2468
7118337 CIFC33 H32 N2 O SP -111.58; 14.496; 18.428
67.834; 89.295; 70.014		2668Ikezawa, Takahiro; Mutoh, Katsuya; Kobayashi, Yoichi; Abe, Jiro
Thiophene-substituted phenoxyl-imidazolyl radical complexes with high photosensitivity.
Chemical communications (Cambridge, England), 2016, 52, 2465-2468
7118338 CIFC39 H36 N2 O SP 1 21/c 112.934; 9.3801; 26.147
90; 97.1867; 90		3147.3Ikezawa, Takahiro; Mutoh, Katsuya; Kobayashi, Yoichi; Abe, Jiro
Thiophene-substituted phenoxyl-imidazolyl radical complexes with high photosensitivity.
Chemical communications (Cambridge, England), 2016, 52, 2465-2468
7118340 CIFC31 H29 Br N2 O5P 1 21 110.6073; 9.8229; 14.4413
90; 107.283; 90		1436.76Han, Jeng-Liang; Chang, Chia-Hao
An asymmetric assembly of spirooxindole dihydropyranones through a direct enantioselective organocatalytic vinylogous aldol-cyclization cascade reaction of 3-alkylidene oxindoles with isatins.
Chemical communications (Cambridge, England), 2016, 52, 2322-2325
7118341 CIFC16 H22 OP 1 c 15.6982; 18.9135; 13.0889
90; 95.097; 90		1405.05Pan, Jin-Long; Chen, Tao; Zhang, Zhi-Qiang; Li, Yi-Fan; Zhang, Xiao-Ming; Zhang, Fu-Min
A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 2382-2385
7118342 CIFC42 H58 N2 O4.5 P SiP -111.473; 13.299; 13.766
85.201; 86.909; 86.437		2086.5Lin, Chao-Yang; Ma, Peng-Ju; Sun, Zhao; Lu, Chong-Dao; Xu, Yan-Jun
Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides.
Chemical communications (Cambridge, England), 2016, 52, 912-915
7118343 CIFC24 H31 Br N2 O3 SP 21 21 219.891; 16.14; 16.21
90; 90; 90		2588Lin, Chao-Yang; Ma, Peng-Ju; Sun, Zhao; Lu, Chong-Dao; Xu, Yan-Jun
Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides.
Chemical communications (Cambridge, England), 2016, 52, 912-915
7118344 CIFC184 H162 Co6 Mn6 N24 O32 S8R -323.1209; 23.1209; 27.281
90; 90; 120		12629.9Jeon, Ie-Rang; David Harris, T.
An S = 12 semiquinoid radical-bridged Mn6 wheel complex assembled from an asymmetric redox-active bridging ligand.
Chemical communications (Cambridge, England), 2016, 52, 1006-1008
7118345 CIFC29 H33 N2 PP 1 21/c 111.3578; 9.9307; 22.539
90; 102.838; 90		2478.6Majhi, Paresh Kumar; Chow, Keith C. F.; Hsieh, Tom H. H.; Bowes, Eric G.; Schnakenburg, Gregor; Kennepohl, Pierre; Streubel, Rainer; Gates, Derek P.
Even the normal is abnormal: N-heterocyclic carbene C(2) binding to a phosphaalkene without breaking the P[double bond, length as m-dash]C π-bond.
Chemical communications (Cambridge, England), 2016, 52, 998-1001
7118346 CIFC58 H72 B2 N4 O P2C 1 2/c 125.984; 9.734; 21.55
90; 108.32; 90		5174.3Majhi, Paresh Kumar; Chow, Keith C. F.; Hsieh, Tom H. H.; Bowes, Eric G.; Schnakenburg, Gregor; Kennepohl, Pierre; Streubel, Rainer; Gates, Derek P.
Even the normal is abnormal: N-heterocyclic carbene C(2) binding to a phosphaalkene without breaking the P[double bond, length as m-dash]C π-bond.
Chemical communications (Cambridge, England), 2016, 52, 998-1001
7118347 CIFC17 H23 N O6P 1 21 19.223; 7.1694; 13.3259
90; 92.731; 90		880.153Riaño, Iker; Díaz, Estibaliz; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Vicario, Jose L.
Organocatalytic enantio- and diastereoselective synthesis of 3,5-disubstituted prolines.
Chemical communications (Cambridge, England), 2016, 52, 2330-2333
7118348 CIFC38 H70 Na3 O32 S3P -3 1 c27.0902; 27.0902; 30.1891
90; 90; 120		19186.9Garnett, Graham A. E.; Daze, Kevin D.; Peña Diaz, Jorge A; Fagen, Noah; Shaurya, Alok; Ma, Manuel C. F.; Collins, Mary S.; Johnson, Darren W.; Zakharov, Lev N.; Hof, Fraser
Attraction by repulsion: compounds with like charges undergo self-assembly in water that improves in high salt and persists in real biological fluids.
Chemical communications (Cambridge, England), 2016, 52, 2768-2771
7118349 CIFC29 H32 N2 O4 SP 1 21 112.959; 7.94026; 14.0403
90; 116.595; 90		1291.86Li, Guangxun; Liu, Hongxin; Wang, Yingwei; Zhang, Shiqi; Lai, Shujun; Tang, Ling; Zhao, Jinzhong; Tang, Zhuo
The catalytic enantioselective synthesis of tetrahydroquinolines containing all-carbon quaternary stereocenters via the formation of aza-ortho-xylylene with 1,2-dihydroquinoline as a precursor.
Chemical communications (Cambridge, England), 2016, 52, 2304-2306
7118350 CIFC23 H23 Br N2 O5P 1 21/n 114.4012; 10.1201; 15.5792
90; 97.623; 90		2250.47Zhang, Ya-Jun; Chen, Cheng; Tan, Bin; Cai, Li-Xuan; Yang, Xiao-Dong; Zhang, Jie
A dual-stimuli responsive small molecule organic material with tunable multi-state response showing turn-on luminescence and photocoloration.
Chemical communications (Cambridge, England), 2016, 52, 2835-2838
7118351 CIFC46 H58 Br2 N4 O16C 1 2/c 127.25; 13.662; 17.3
90; 110.04; 90		6051Zhang, Ya-Jun; Chen, Cheng; Tan, Bin; Cai, Li-Xuan; Yang, Xiao-Dong; Zhang, Jie
A dual-stimuli responsive small molecule organic material with tunable multi-state response showing turn-on luminescence and photocoloration.
Chemical communications (Cambridge, England), 2016, 52, 2835-2838
7118352 CIFC23 H21 F6 N2 O4 PP 1 21/c 16.821; 17.801; 19.7701
90; 98.215; 90		2375.9Zhang, Ya-Jun; Chen, Cheng; Tan, Bin; Cai, Li-Xuan; Yang, Xiao-Dong; Zhang, Jie
A dual-stimuli responsive small molecule organic material with tunable multi-state response showing turn-on luminescence and photocoloration.
Chemical communications (Cambridge, England), 2016, 52, 2835-2838
7118353 CIFC20 H18 Br N2 O2P 1 21/n 111.3148; 7.1192; 21.3182
90; 93.83; 90		1713.4Xu, Guo-Qiang; Li, Chen-Guang; Liu, Ming-Qian; Cao, Jian; Luo, Yong-Chun; Xu, Peng-Fei
Dual C-H functionalization of N-aryl tetrahydroisoquinolines: a highly diastereoselective synthesis of dibenzo[a,f]quinolizines via visible-light induced oxidation and inverse electron-demand aza-Diels-Alder reaction.
Chemical communications (Cambridge, England), 2016, 52, 1190-1193
7118354 CIFC20 H12 N O5.5 ZnP 65 2 215.9684; 15.9684; 33.649
90; 90; 120		7430.6Wen, Hui-Min; Li, Bin; Wang, Hailong; Krishna, Rajamani; Chen, Banglin
High acetylene/ethylene separation in a microporous zinc(ii) metal-organic framework with low binding energy.
Chemical communications (Cambridge, England), 2016, 52, 1166-1169
7118355 CIFC69 H87 Fe3 N6 S3P 63/m16.8444; 16.8444; 12.6713
90; 90; 120		3113.6Lee, Yousoon; Jeon, Ie-Rang; Abboud, Khalil A.; García-Serres, Ricardo; Shearer, Jason; Murray, Leslie J.
A [3Fe-3S](3+) cluster with exclusively μ-sulfide donors.
Chemical communications (Cambridge, England), 2016, 52, 1174-1177
7118356 CIFC4.5 H1.5 Eu0.25 In0.25 O4P 42/m c m12.6261; 12.6261; 29.234
90; 90; 90		4660.4Qian, Jinjie; Li, Qipeng; Liang, Linfeng; Yang, Yan; Cao, Zhen; Yu, Panpan; Huang, Shaoming; Hong, Maochun
A photoluminescent indium-organic framework with discrete cages and one-dimensional channels for gas adsorption.
Chemical communications (Cambridge, England), 2016, 52, 9032-9035
7118357 CIFC14 H7 F5 N2P 21 21 217.6294; 12.6995; 25.8239
90; 90; 90		2502.1Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118358 CIFC14 H7 F5 N2P 1 21/c 17.6779; 23.7528; 13.8443
90; 90.3699; 90		2524.75Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118359 CIFC14 H7 F5 N2P n a 2125.3241; 6.535; 29.874
90; 90; 90		4943.9Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118360 CIFC14 H7 F5 N2P 1 21/c 113.9748; 7.4518; 11.8994
90; 104.487; 90		1199.77Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118361 CIFC26 H19 O3 PC 1 2/c 116.295; 14.157; 18.637
90; 104.42; 90		4164Fukazawa, Aiko; Suda, Shinji; Taki, Masayasu; Yamaguchi, Eriko; Grzybowski, Marek; Sato, Yoshikatsu; Higashiyama, Tetsuya; Yamaguchi, Shigehiro
Phospha-fluorescein: a red-emissive fluorescein analogue with high photobleaching resistance.
Chemical communications (Cambridge, England), 2016, 52, 1120-1123
7118362 CIFC8 H5 Cl3 F N OP 1 21/c 19.1964; 11.7747; 9.7412
90; 98.134; 90		1044.21Ghosh, Monisankar; Saha, Suchandrima; Dutta, Samir Kumar
'Dual hit' metabolic modulator LDCA selectively kills cancer cells by efficient competitive inhibition of LDH-A.
Chemical communications (Cambridge, England), 2016, 52, 2401-2404
7118363 CIFC26 H22C 2 2 219.937; 17.673; 10.223
90; 90; 90		1795.3Iwahara, Hideaki; Kushida, Tomokatsu; Yamaguchi, Shigehiro
A planarized 9-phenylanthracene: a simple electron-donating building block for fluorescent materials.
Chemical communications (Cambridge, England), 2016, 52, 1124-1127
7118364 CIFC20 H14P -16.247; 10.259; 10.779
84.94; 76.39; 77.39		654.7Iwahara, Hideaki; Kushida, Tomokatsu; Yamaguchi, Shigehiro
A planarized 9-phenylanthracene: a simple electron-donating building block for fluorescent materials.
Chemical communications (Cambridge, England), 2016, 52, 1124-1127
7118365 CIFC186 H102 N8 O71 S3 Zn20R -3 :H25.299; 25.299; 166.828
90; 90; 120		92471Xie, Wei; He, Wen-Wen; Du, Dong-Ying; Li, Shun-Li; Qin, Jun-Sheng; Su, Zhong-Min; Sun, Chun-Yi; Lan, Ya-Qian
A stable Alq3@MOF composite for white-light emission.
Chemical communications (Cambridge, England), 2016, 52, 3288-3291
7118366 CIFC12 H16 N3 O5 PP -17.6832; 9.6923; 10.0668
89.063; 82.389; 80.144		732.07Gao, Ming; Li, Yi; Xie, Lijuan; Chauvin, Remi; Cui, Xiuling
Direct phosphonation of quinoxalin-2(1H)-ones under transition-metal-free conditions.
Chemical communications (Cambridge, England), 2016, 52, 2846-2849
7118367 CIFC25 H38 O5 SiP 1 21/n 110.5246; 7.1824; 33.424
90; 94.7154; 90		2518Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118368 CIFC20 H23 Br O5P 1 21/c 17.1552; 17.356; 14.5825
90; 95.177; 90		1803.5Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118369 CIFC22 H20 O6P c a 2134.732; 13.1317; 8.2791
90; 90; 90		3776Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118370 CIFC23 H21 Br O6P 1 21/n 112.6704; 9.7676; 16.2166
90; 97.059; 90		1991.7Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118371 CIFC18 H20 O5P c a 2125.583; 6.8787; 17.4038
90; 90; 90		3062.7Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118372 CIFC18 H19 Br O5P 1 c 111.3068; 9.6829; 24.116
90; 103.091; 90		2571.7Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118373 CIFC19 H22 O5P 1 21/c 115.1059; 7.0831; 16.4912
90; 114.08; 90		1610.9Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118374 CIFC19 H21 Br O5P -18.854; 14.268; 14.396
94.289; 102.73; 95.207		1758.2Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118375 CIFC20 H23 Br O5P 1 21/n 112.0177; 6.6196; 23.898
90; 93.302; 90		1898Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118376 CIFC2 H10 N2 O12 S4 Zn3C 1 2/c 113.7379; 8.3487; 13.0277
90; 106.235; 90		1434.61Tiwari, Ranjay K.; Kumar, Jitendra; Behera, J. N.
The first organically templated open-framework metal-sulfites with layered and three-dimensional diamondoid structures.
Chemical communications (Cambridge, England), 2016, 52, 1282-1285
7118377 CIFC2 H12 N6 O6 S2 ZnF d d 214.4211; 12.1181; 14.0692
90; 90; 90		2458.7Tiwari, Ranjay K.; Kumar, Jitendra; Behera, J. N.
The first organically templated open-framework metal-sulfites with layered and three-dimensional diamondoid structures.
Chemical communications (Cambridge, England), 2016, 52, 1282-1285
7118378 CIFC28 H40 Cu I2 N8P 1 21/c 118.1909; 19.1754; 20.759
90; 112.85; 90		6672.9Roy, Subhasish; Sarma, Manas Jyoti; Kashyap, Bishwapran; Phukan, Prodeep
A quick Chan-Lam C-N and C-S cross coupling at room temperature in the presence of square pyramidal [Cu(DMAP)4I]I as a catalyst.
Chemical communications (Cambridge, England), 2016, 52, 1170-1173
7118379 CIFC20 H36 B6 Ir2P 1 21/n 19.1413; 19.4335; 28.6894
90; 98.911; 90		5035.1Borthakur, Rosmita; Mondal, Bijan; Nandi, Purbasha; Ghosh, Sundargopal
Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the "Rule-Breakers"(Cp* = η(5)-C5Me5).
Chemical communications (Cambridge, England), 2016, 52, 3199-3202
7118380 CIFC20 H37 B7 Ir2P -19.1768; 9.2116; 16.3496
99.379; 101.76; 102.741		1288.09Borthakur, Rosmita; Mondal, Bijan; Nandi, Purbasha; Ghosh, Sundargopal
Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the "Rule-Breakers"(Cp* = η(5)-C5Me5).
Chemical communications (Cambridge, England), 2016, 52, 3199-3202
7118381 CIFC20 H36 B6 Ir2P 1 21/c 116.4805; 19.9995; 16.6991
90; 117.242; 90		4893.5Borthakur, Rosmita; Mondal, Bijan; Nandi, Purbasha; Ghosh, Sundargopal
Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the "Rule-Breakers"(Cp* = η(5)-C5Me5).
Chemical communications (Cambridge, England), 2016, 52, 3199-3202
7118382 CIFC23 H26 N O3 PP -18.6783; 11.3201; 12.0032
111.032; 94.279; 105.86		1038.96Wang, Jieping; Siqueira, Gilberto; Müller, Georgina; Rentsch, Daniel; Huch, Anja; Tingaut, Philippe; Levalois-Grützmacher, Joëlle; Grützmacher, Hansjörg
Synthesis of new bis(acyl)phosphane oxide photoinitiators for the surface functionalization of cellulose nanocrystals.
Chemical communications (Cambridge, England), 2016, 52, 2823-2826
7118383 CIFC20 H15 N3 OP 1 21/n 19.7059; 15.7541; 10.525
90; 95.513; 90		1601.91Sadhu, Pradeep; Punniyamurthy, Tharmalingam
Copper(ii)-mediated regioselective N-arylation of pyrroles, indoles, pyrazoles and carbazole via dehydrogenative coupling.
Chemical communications (Cambridge, England), 2016, 52, 2803-2806
7118384 CIFC25 H17 F N2 O2P 1 21/c 110.9284; 18.6077; 10.9054
90; 118.516; 90		1948.6Rajkumar, Subramani; Antony Savarimuthu, S.; Senthil Kumaran, Rajendran; Nagaraja, C. M.; Gandhi, Thirumanavelan
Expedient synthesis of new cinnoline diones by Ru-catalyzed regioselective unexpected deoxygenation-oxidative annulation of propargyl alcohols with phthalazinones and pyridazinones.
Chemical communications (Cambridge, England), 2016, 52, 2509-2512
7118385 CIFC23 H15 N3 O4P 1 21/c 122.748; 10.773; 15.613
90; 102.346; 90		3737.7Rajkumar, Subramani; Antony Savarimuthu, S.; Senthil Kumaran, Rajendran; Nagaraja, C. M.; Gandhi, Thirumanavelan
Expedient synthesis of new cinnoline diones by Ru-catalyzed regioselective unexpected deoxygenation-oxidative annulation of propargyl alcohols with phthalazinones and pyridazinones.
Chemical communications (Cambridge, England), 2016, 52, 2509-2512
7118386 CIFC11 H14 O2 SP 1 21/c 123.952; 5.752; 14.804
90; 100.445; 90		2005.8Albarghouti, Ghassan; Kotikalapudi, Ramesh; Lankri, David; Valerio, Viviana; Tsvelikhovsky, Dmitry
Cascade Pd(ii)-catalyzed Wacker lactonization-Heck reaction: rapid assembly of spiranoid lactones.
Chemical communications (Cambridge, England), 2016, 52, 3095-3098
7118387 CIFC53 H100 N12 Ni2 O24P 1 2/c 118.257; 8.475; 28.615
90; 129.59; 90		3412Jiang, Xiang; Kou, Hui-Zhong
Solid state reconstructive phase transition from porous supramolecular network to porous coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 2952-2955
7118388 CIFC57 H92 N12 Ni2 O16I 41/a27.286; 27.286; 8.343
90; 90; 90		6212Jiang, Xiang; Kou, Hui-Zhong
Solid state reconstructive phase transition from porous supramolecular network to porous coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 2952-2955
7118389 CIFC20 H28 Cu N2 O4P -17.5787; 8.0875; 9.6138
72.4479; 68.0319; 85.0439		520.8Paquet, C.; Lacelle, T.; Deore, B.; Kell, A. J.; Liu, X.; Korobkov, I.; Malenfant, P. R. L.
Pyridine-copper(ii) formates for the generation of high conductivity copper films at low temperatures.
Chemical communications (Cambridge, England), 2016, 52, 2605-2608
7118392 CIFCs1.5 H130 Na14.5 Ni7 O180 P4 W30P -112.7488; 12.7765; 25.7791
92.399; 101.831; 104.172		3966Bassil, Bassem S.; Xiang, Yixian; Haider, Ali; Hurtado, Jaime; Novitchi, Ghenadie; Powell, Annie K.; Bossoh, A. Martin; Mbomekallé, Israël M; de Oliveira, Pedro; Kortz, Ulrich
Heptanickel(ii) double-cubane core in wells-dawson heteropolytungstate, [Ni7(OH)6(H2O)6(P2W15O56)2](16.).
Chemical communications (Cambridge, England), 2016, 52, 2601-2604
7118393 CIFC25 H17 N O2 S2P 1 21/c 111.3452; 17.9768; 10.1595
90; 110.197; 90		1944.63Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118394 CIFC41 H32 Cl2 N2 O2 S3C 1 2/c 120.7971; 11.4101; 15.4184
90; 98.56; 90		3618Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118395 CIFC42 H34 N2 O2 S3I 1 2/a 112.7719; 13.6832; 19.915
90; 98.962; 90		3437.9Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118396 CIFC42 H34 N2 O3 S3P 1 21/c 111.6805; 15.8659; 19.4344
90; 98.323; 90		3563.68Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118397 CIFC26 H26 N2 Ni O6P b c a11.4913; 18.0722; 22.1742
90; 90; 90		4605Shao, Haiyan; Muduli, Subas K.; Tran, Phong D.; Soo, Han Sen
Enhancing electrocatalytic hydrogen evolution by nickel salicylaldimine complexes with alkali metal cations in aqueous media.
Chemical communications (Cambridge, England), 2016, 52, 2948-2951
7118398 CIFC26 H26 F6 K N2 Ni O6 PP 1 21/n 19.4723; 18.6903; 15.7123
90; 96.0152; 90		2766.4Shao, Haiyan; Muduli, Subas K.; Tran, Phong D.; Soo, Han Sen
Enhancing electrocatalytic hydrogen evolution by nickel salicylaldimine complexes with alkali metal cations in aqueous media.
Chemical communications (Cambridge, England), 2016, 52, 2948-2951
7118399 CIFC160 H112 O34P -112.8218; 15.8756; 38.6736
93.295; 93.991; 102.38		7649.3Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118400 CIFC80 H72 N4 O18P -114.5203; 16.0332; 18.9168
103.209; 94.7721; 106.869		4049.79Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118401 CIFC166 H126 N2 O36P -115.3014; 20.3447; 28.1624
101.571; 99.3676; 103.554		8144.6Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118402 CIFC68 H44 O14P -114.5303; 14.9461; 20.2579
102.355; 101.544; 99.0611		4117.4Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118403 CIFC60 H36 O12P -115.4431; 20.9868; 28.0527
103.362; 98.9655; 105.805		8275.7Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118404 CIFC68 H44 O14P -119.1278; 22.403; 22.3984
60.046; 87.4093; 81.0545		8209.05Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118405 CIFC33 H39 Cl3 N2 O3 Ru SP 1 21 17.7787; 22.469; 9.7911
90; 104.593; 90		1656.08B. Vilhanova; J. Vaclavik; P. Sot; J. Pechacek; J. Zapal; R. Pazout; J. Maixner; M. Kuzmac; P. Kacer
Enantioselective hydrogenation of cyclic imines catalysed by Noyori-Ikariya half-sandwich complexes and their analogues
Chem.Commun., 2016, 52, 362
7118406 CIFC200 H274 Dy18 N18 O135 Zn12C 1 2/c 135.409; 30.501; 31.789
90; 115.52; 90		30983Nikoleta Stavgianoudaki; Milosz Siczek; Tadeusz Lis; Ross Inglis; Constantinos J. Milios
A triacontanuclear [Zn12Dy18] cluster: a ring of [Dy4] cubes
Chem.Commun., 2016, 52, 343
7118407 CIFC16 H13 NP b c a16.7246; 7.1468; 20.102
90; 90; 90		2402.7Kai Chen; Zi-Zhong Zhu; Jia-Xin Liu; Xiang-Ying Tang; Yin Wei; Min Shi
Substrate-controlled Rh(II)-catalyzed single-electron-transfer (SET): divergent synthesis of fused indoles
Chem.Commun., 2016, 52, 350
7118408 CIFC19 H17 N OP 1 21/n 19.2535; 14.994; 10.714
90; 101.697; 90		1455.7Kai Chen; Zi-Zhong Zhu; Jia-Xin Liu; Xiang-Ying Tang; Yin Wei; Min Shi
Substrate-controlled Rh(II)-catalyzed single-electron-transfer (SET): divergent synthesis of fused indoles
Chem.Commun., 2016, 52, 350
7118409 CIFC66 H49 N6 O8 TlP 1 21/n 114.4652; 17.501; 23.3205
90; 91.874; 90		5900.6Victoria Ndoyom; Luca Fusaro; Thierry Roisnel; Stephane Le Gac; Bernard Boitrel
Spontaneous Tl(I)-to-Tl(III) oxidation in dynamic heterobimetallic Hg(II)/Tl(I) porphyrin complexes
Chem.Commun., 2016, 52, 517
7118410 CIFC95.5 H129.25 F12 N3.75 O24 P2C 1 c 131.6051; 13.3823; 24.6753
90; 90.155; 90		10436.4Danyu Xia; Peifa Wei; Bingbing Shi; Feihe Huang
A pillar[6]arene-based [2]pseudorotaxane in solution and in the solid state and its photo-responsive self-assembly behavior in solution
Chem.Commun., 2016, 52, 513
7118411 CIFC19 H18 Eu N3 O10P 1 21 19.7675; 7.1607; 15.8901
90; 107.9; 90		1057.59Hai-Yang Li; Hong Xu; Shuang-Quan Zang; Thomas C. W. Mak
A viologen-functionalized chiral Eu-MOF as a platform for multifunctional switchable material
Chem.Commun., 2016, 52, 525
7118412 CIFC35 H48 F3 Ge N3 O3 SP 1 21/n 111.7454; 24.4796; 13.3037
90; 115.166; 90		3462Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118413 CIFC36 H47 Cr Ge N3 O6P 1 21/c 110.2157; 22.5884; 15.2996
90; 97.648; 90		3499.07Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118414 CIFC36 H47 Ge Mo N3 O6P 1 21/c 110.3172; 22.6231; 15.3939
90; 97.423; 90		3562.9Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118415 CIFC36 H47 Ge N3 O6 WP 1 21/c 110.3691; 22.617; 15.3476
90; 97.055; 90		3572Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118416 CIFC33 H33 N3P -18.299; 12.11; 13.39
76.13; 87.13; 87.08		1304Qitao Tan; Huanhuan Chen; Huaida Xia; Bingxin Liu; Bin Xu
Parent and trisubstituted triazacoronenes: synthesis, crystal structure and physicochemical properties
Chem.Commun., 2016, 52, 537
7118417 CIFC16 H23 F12 N3 Ru Sb2P 1 21/c 18.3829; 18.5671; 17.8534
90; 98.919; 90		2745.21Zhao, Yinsong; He, Zhen; Li, Shiqing; Tang, Junbin; Gao, Ge; Lan, Jingbo; You, Jingsong
An air-stable half-sandwich Ru(II) complex as an efficient catalyst for [3+2] annulation of 2-arylcyclo-2-enones with alkynes.
Chemical communications (Cambridge, England), 2016, 52, 4613-4616
7118418 CIFC20 H18 OP 1 21/c 19.7368; 8.7212; 17.6929
90; 97.34; 90		1490.11Zhao, Yinsong; He, Zhen; Li, Shiqing; Tang, Junbin; Gao, Ge; Lan, Jingbo; You, Jingsong
An air-stable half-sandwich Ru(II) complex as an efficient catalyst for [3+2] annulation of 2-arylcyclo-2-enones with alkynes.
Chemical communications (Cambridge, England), 2016, 52, 4613-4616
7118419 CIFC18 H14 Cl3 N SP -17.7687; 9.4304; 12.8027
101.342; 104.75; 102.507		853.44Yu, Liu-Zhu; Hu, Xu-Bo; Xu, Qin; Shi, Min
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: facile synthesis of furoquinoline and thienoquinoline derivatives.
Chemical communications (Cambridge, England), 2016, 52, 2701-2704
7118420 CIFC17 H12 Cl N OP -18.277; 8.861; 20.949
78.278; 83.751; 64.58		1358.4Yu, Liu-Zhu; Hu, Xu-Bo; Xu, Qin; Shi, Min
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: facile synthesis of furoquinoline and thienoquinoline derivatives.
Chemical communications (Cambridge, England), 2016, 52, 2701-2704
7118421 CIFC17 H13 Cl2 N OP -17.7899; 9.516; 11.134
99.138; 97.433; 109.903		751.1Yu, Liu-Zhu; Hu, Xu-Bo; Xu, Qin; Shi, Min
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: facile synthesis of furoquinoline and thienoquinoline derivatives.
Chemical communications (Cambridge, England), 2016, 52, 2701-2704
7118422 CIFC18 H22 N2 O8 TiP 1 21/n 110.9669; 14.7049; 13.0353
90; 113.016; 90		1934.82Brennan, Bradley J.; Chen, Jeffrey; Rudshteyn, Benjamin; Chaudhuri, Subhajyoti; Mercado, Brandon Q.; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Molecular titanium-hydroxamate complexes as models for TiO2 surface binding.
Chemical communications (Cambridge, England), 2016, 52, 2972-2975
7118423 CIFC54 H72 N6 O21 S6 Ti3R -3 c :H15.7049; 15.7049; 53.457
90; 90; 120		11418.4Brennan, Bradley J.; Chen, Jeffrey; Rudshteyn, Benjamin; Chaudhuri, Subhajyoti; Mercado, Brandon Q.; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Molecular titanium-hydroxamate complexes as models for TiO2 surface binding.
Chemical communications (Cambridge, England), 2016, 52, 2972-2975
7118424 CIFC36 H40 Cl8 N4 O10 Ti2P 1 21/n 112.1927; 10.0654; 19.3484
90; 102.042; 90		2322.3Brennan, Bradley J.; Chen, Jeffrey; Rudshteyn, Benjamin; Chaudhuri, Subhajyoti; Mercado, Brandon Q.; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Molecular titanium-hydroxamate complexes as models for TiO2 surface binding.
Chemical communications (Cambridge, England), 2016, 52, 2972-2975
7118425 CIFC24 O25 Zn4R -3 m :H18.2657; 18.2657; 22.3708
90; 90; 120		6463.8Bai, Linyi; Tu, Binbin; Qi, Yi; Gao, Qiang; Liu, Dong; Liu, Zhizhou; Zhao, Lingzhi; Li, Qiaowei; Zhao, Yanli
Enhanced performance in gas adsorption and Li ion batteries by docking Li(+) in a crown ether-based metal-organic framework.
Chemical communications (Cambridge, England), 2016, 52, 3003-3006
7118426 CIFC99 H152 Ge2 Si4P -116.3223; 17.6076; 18.3797
71.478; 77.643; 67.458		4600.3Nieder, David; Yildiz, Cem B.; Jana, Anukul; Zimmer, Michael; Huch, Volker; Scheschkewitz, David
Dimerization of a marginally stable disilenyl germylene to tricyclic systems: evidence for reversible NHC-coordination.
Chemical communications (Cambridge, England), 2016, 52, 2799-2802
7118427 CIFC95.5 H152 Ge2 Si4C 1 2/c 133.8499; 26.2285; 20.2919
90; 97.911; 90		17844.3Nieder, David; Yildiz, Cem B.; Jana, Anukul; Zimmer, Michael; Huch, Volker; Scheschkewitz, David
Dimerization of a marginally stable disilenyl germylene to tricyclic systems: evidence for reversible NHC-coordination.
Chemical communications (Cambridge, England), 2016, 52, 2799-2802
7118428 CIFC22 H18 F3 N O2P 1 21/c 113.9588; 8.5515; 16.218
90; 104.782; 90		1871.8Jiang, Quanbin; Guo, Tenglong; Wu, Kaikai; Yu, Zhengkun
Rhodium(iii)-catalyzed sp(2) C-H bond addition to CF3-substituted unsaturated ketones.
Chemical communications (Cambridge, England), 2016, 52, 2913-2915
7118429 CIFC18 H32 N O6 SiP 21 21 216.826; 9.791; 30.82
90; 90; 90		2059.8Jian-Liang Ye; Yang Liu; Zhi-Ping Yang; Pei-Qiang Huang
The asymmetric total synthesis of (+)-N-acetyl norloline
Chem.Commun., 2016, 52, 561
7118430 CIFC24 H21 B F2 N4P -18.4892; 8.7454; 14.2585
83.179; 79.851; 84.564		1031.68Dan Wu; Li Shao; Yang Li; Qinglian Hu; Feihe Huang; Guocan Yu; Guping Tang
A boron difluoride dye showing the aggregation-induced emission feature and high sensitivity to intra- and extra-cellular pH changes
Chem.Commun., 2016, 52, 541
7118431 CIFC43 H52 Ni P2 SiP 1 21/c 120.474; 22.468; 17.673
90; 110.92; 90		7594LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118432 CIFC46 H58 Ni P2 SiP 1 21/c 115.1784; 13.3439; 21.4058
90; 110.73; 90		4054.82LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118433 CIFC46 H58 Ni O3 P2 SiP 1 21/c 115.514; 13.3974; 21.723
90; 112.905; 90		4159.06LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118434 CIFC33 H48 Ni P2 SiP 1 21/c 118.2625; 8.1482; 21.5259
90; 93.717; 90		3196.5LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118435 CIFC31 H42 Ni O P2C 1 2/c 130.7146; 10.0835; 20.284
90; 114.295; 90		5725.82LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118436 CIFC43 H52 Ni P2 SiP 21 21 2112.91; 15.492; 19.254
90; 90; 90		3850.8LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118437 CIFC20 H24 Fe N5 O3 SP -18.394; 9.35; 13.675
82.26; 73.44; 82.14		1013.9Phonsri, Wasinee; Martinez, Victor; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Murray, Keith S.
Ligand effects in a heteroleptic bis-tridentate iron(iii) spin crossover complex showing a very high T1/2 value.
Chemical communications (Cambridge, England), 2016, 52, 1443-1446
7118438 CIFC30 H17 B F13 O3 P SP 1 21/c 110.0309; 16.5754; 17.784
90; 96.069; 90		2940.3Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118439 CIFC29 H18 B F10 PP -111.8789; 12.5298; 12.6592
61.284; 72.907; 67.981		1516.86Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118440 CIFC41 H19 B2 F20 PP 1 21/c 112.7173; 24.4025; 16.3076
90; 111.724; 90		4701.4Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118441 CIFC41 H19 B2 F20 PC 1 2/c 124.6726; 20.3084; 19.6095
90; 124.093; 90		8136.8Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118442 CIFC48 H25 B2 F20 O PP 1 21/n 113.2593; 22.2116; 19.2412
90; 101.101; 90		5560.7Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118443 CIFC42 H19 B2 F20 O PP -111.3678; 11.6324; 16.8035
70.245; 82.445; 79.967		2052.93Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118444 CIFC15 H21 N O SP 1 21/n 18.24752; 12.7555; 13.60131
90; 100.427; 90		1407.24Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118445 CIFC15 H21 N O SP 21 21 217.0524; 17.7693; 22.6194
90; 90; 90		2834.6Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118446 CIFC10 H17 N O2 SP 21 21 216.51691; 11.9691; 29.6051
90; 90; 90		2309.24Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118447 CIFC9 H15 N O2 SP 1 21 19.6985; 6.50545; 17.186
90; 94.266; 90		1081.31Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118448 CIFC14 H10 Cl F3 N2 O3 SP 21 21 2110.2939; 10.7278; 14.0751
90; 90; 90		1554.33Hou, Xuhe; Ma, Hongli; Zhang, Zhenhua; Xie, Lei; Qin, Zhaohai; Fu, Bin
An efficient approach for the construction of trifluoromethylated all-carbon quaternary stereocenters: enantioselective Ni(ii)-catalyzed Michael addition of 2-acetyl azaarene to β,β-disubstituted nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 1470-1473
7118449 CIFC44 H63 Cl3 N2 O0.5 P2C 1 2/c 127.4838; 17.6558; 21.9216
90; 118.269; 90		9368.7Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118450 CIFC45 H56 Cl6 F Ga N2 P2P 1 21/c 110.7484; 13.6179; 33.6481
90; 94.25; 90		4911.6Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118451 CIFC53 H61 Cl3 F7 N2 O3 P2 SP 1 21/c 112.2639; 12.5384; 36.3192
90; 99.262; 90		5511.98Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118452 CIFC42 H60 Cl6 Ga N2 P3P -113.8028; 17.4286; 21.7529
107.609; 98.701; 97.42		4844.6Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118457 CIFC34 H33 Br N2 O7P 19.5019; 10.4381; 18.819
93.77; 102.375; 116.062		1610.3Zhang, Zhenhua; Sun, Wangsheng; Zhu, Gongming; Yang, Junxian; Zhang, Ming; Hong, Liang; Wang, Rui
Chiral phosphoric acid catalyzed enantioselective 1,3-dipolar cycloaddition reaction of azlactones.
Chemical communications (Cambridge, England), 2016, 52, 1377-1380
7118458 CIFC150 H116 Cl2 Cu3 La6 N12 O56P 63 2 213.008; 13.008; 50.2913
90; 90; 120		7369.6Fang, Wei-Hui; Zhang, Lei; Zhang, Jian; Yang, Guo-Yu
Halogen dependent symmetry change in two series of wheel cluster organic frameworks built from La18 tertiary building units.
Chemical communications (Cambridge, England), 2016, 52, 1455-1457
7118459 CIFC150 H101 Br3 Cu4 La6 N12 O39P -3 c 113.0109; 13.0109; 51.3152
90; 90; 120		7523Fang, Wei-Hui; Zhang, Lei; Zhang, Jian; Yang, Guo-Yu
Halogen dependent symmetry change in two series of wheel cluster organic frameworks built from La18 tertiary building units.
Chemical communications (Cambridge, England), 2016, 52, 1455-1457
7118460 CIFC150 H101 Cu4 I3 La6 N12 O39P -3 c 113.0142; 13.0142; 51.3233
90; 90; 120		7528Fang, Wei-Hui; Zhang, Lei; Zhang, Jian; Yang, Guo-Yu
Halogen dependent symmetry change in two series of wheel cluster organic frameworks built from La18 tertiary building units.
Chemical communications (Cambridge, England), 2016, 52, 1455-1457
7118461 CIFC77.5 H46 O10.5P 1 21/c 117.323; 22.428; 15.591
90; 95.051; 90		6033.9Suzuki, Akira; Kondo, Kei; Sei, Yoshihisa; Akita, Munetaka; Yoshizawa, Michito
A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water.
Chemical communications (Cambridge, England), 2016, 52, 3151-3154
7118462 CIFC25 H31 N3 O4P b c a9.302; 15.8206; 32.7189
90; 90; 90		4815Diedrich, D.; Hamacher, A.; Gertzen, C. G. W.; Alves Avelar, L. A.; Reiss, G. J.; Kurz, T.; Gohlke, H.; Kassack, M. U.; Hansen, F. K.
Rational design and diversity-oriented synthesis of peptoid-based selective HDAC6 inhibitors.
Chemical communications (Cambridge, England), 2016, 52, 3219-3222
7118463 CIFC14 H20 F3 N O3P b c a7.7764; 15.755; 25.521
90; 90; 90		3126.8Yagafarov, Niyaz Z.; Kolesnikov, Pavel N.; Usanov, Dmitry L.; Novikov, Valentin V.; Nelyubina, Yulia V.; Chusov, Denis
The synthesis of sterically hindered amines by a direct reductive amination of ketones.
Chemical communications (Cambridge, England), 2016, 52, 1397-1400
7118464 CIFC90 H72 B2 N8 O6P -114.124; 15.235; 17.465
87.755; 69.97; 89.95		3527.8Copley, Graeme; Oh, Juwon; Yoshida, Kota; Shimizu, Daiki; Kim, Dongho; Osuka, Atsuhiro
Intramolecular electron transfer reactions in meso-(4-nitrophenyl)-substituted subporphyrins.
Chemical communications (Cambridge, England), 2016, 52, 1424-1427
7118465 CIFC104 H100 Cd2 N8 O13.63 V2P 2 2 2117.046; 24.0462; 28.8442
90; 90; 90		11823Bhunia, Asamanjoy; Dey, Subarna; Moreno, José María; Diaz, Urbano; Concepcion, Patricia; Van Hecke, Kristof; Janiak, Christoph; Van Der Voort, Pascal
A homochiral vanadium-salen based cadmium bpdc MOF with permanent porosity as an asymmetric catalyst in solvent-free cyanosilylation.
Chemical communications (Cambridge, England), 2016, 52, 1401-1404
7118466 CIFC27 H27 N3 O4 S2P -19.8347; 10.7763; 13.371
77.323; 76.332; 67.333		1257.5Chen, Yu-Ling; Sharma, Pankaj; Liu, Rai-Shung
Sulfonamide-directed gold-catalyzed [2+2+2]-cycloadditions of nitriles with two discrete ynamides to construct 2,4-diaminopyridine cores.
Chemical communications (Cambridge, England), 2016, 52, 3187-3190
7118478 CIFC60 H90 Li2 O12 ThR -3 :H14.8737; 14.8737; 24.3175
90; 90; 120		4658.9Elizabeth A. Pedrick; Peter Hrobarik; Lani A. Seaman; Guang Wu; Trevor W. Hayton
Synthesis, structure and bonding of hexaphenyl thorium(IV): observation of a non-octahedral structure
Chem.Commun., 2016, 52, 689
7118479 CIFC60 H78 Li2 O10 ThP 1 21/n 116.5641; 16.7043; 21.3854
90; 108.682; 90		5605.4Elizabeth A. Pedrick; Peter Hrobarik; Lani A. Seaman; Guang Wu; Trevor W. Hayton
Synthesis, structure and bonding of hexaphenyl thorium(IV): observation of a non-octahedral structure
Chem.Commun., 2016, 52, 689
7118480 CIFC36 H26 Br2 O4P 21 21 215.6288; 12.578; 41.669
90; 90; 90		2950.1Zhan-Yong Wang; Ya-Li Ding; Gang Wang; Ying Cheng
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation
Chem.Commun., 2016, 52, 788
7118481 CIFC36 H28 O4P 21 21 219.263; 12.8186; 22.369
90; 90; 90		2656.1Zhan-Yong Wang; Ya-Li Ding; Gang Wang; Ying Cheng
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation
Chem.Commun., 2016, 52, 788
7118482 CIFC36 H26 Br2 O4P 21 21 215.5911; 13.004; 40.623
90; 90; 90		2953.6Zhan-Yong Wang; Ya-Li Ding; Gang Wang; Ying Cheng
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation
Chem.Commun., 2016, 52, 788
7118484 CIFC19 H21 N3C 1 2/c 121.0859; 8.8941; 8.6908
90; 110.448; 90		1527.18Hong, Seung Youn; Kwak, Jaesung; Chang, Sukbok
Rhodium-catalyzed selective CH functionalization of NNN tridentate chelating compounds via a rollover pathway.
Chemical communications (Cambridge, England), 2016, 52, 3159-3162
7118485 CIFC31 H39 N3C 1 2/c 130.5673; 9.9939; 8.7408
90; 106.271; 90		2563.2Hong, Seung Youn; Kwak, Jaesung; Chang, Sukbok
Rhodium-catalyzed selective CH functionalization of NNN tridentate chelating compounds via a rollover pathway.
Chemical communications (Cambridge, England), 2016, 52, 3159-3162
7118486 CIFC15 H15 Cl N2 OP 21 21 216.0936; 8.4244; 26.374
90; 90; 90		1353.9Feng, Qi; Li, Yuanyuan; Wang, Lili; Li, Chen; Wang, Jinmin; Liu, Yuanyuan; Li, Kai; Hou, Hongwei
Multiple-color aggregation-induced emission (AIE) molecules as chemodosimeters for pH sensing.
Chemical communications (Cambridge, England), 2016, 52, 3123-3126
7118487 CIFC16 H18 N2 O2P 1 21/c 114.9189; 5.968; 20.9971
90; 130.968; 90		1411.6Feng, Qi; Li, Yuanyuan; Wang, Lili; Li, Chen; Wang, Jinmin; Liu, Yuanyuan; Li, Kai; Hou, Hongwei
Multiple-color aggregation-induced emission (AIE) molecules as chemodosimeters for pH sensing.
Chemical communications (Cambridge, England), 2016, 52, 3123-3126
7118488 CIFC15 H16 N2 OP b c a11.278; 8.2043; 27.475
90; 90; 90		2542.2Feng, Qi; Li, Yuanyuan; Wang, Lili; Li, Chen; Wang, Jinmin; Liu, Yuanyuan; Li, Kai; Hou, Hongwei
Multiple-color aggregation-induced emission (AIE) molecules as chemodosimeters for pH sensing.
Chemical communications (Cambridge, England), 2016, 52, 3123-3126
7118489 CIFC78 H121 Cu6 N17 O54P 4/m n c26.956; 26.956; 39.145
90; 90; 90		28444Liu, Bing; Yao, Shuo; Shi, Chao; Li, Guanghua; Huo, Qisheng; Liu, Yunling
Significant enhancement of gas uptake capacity and selectivity via the judicious increase of open metal sites and Lewis basic sites within two polyhedron-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2016, 52, 3223-3226
7118490 CIFC87 H126 Cu6 N20 O48P 4/m n c27.405; 27.405; 39.362
90; 90; 90		29562Liu, Bing; Yao, Shuo; Shi, Chao; Li, Guanghua; Huo, Qisheng; Liu, Yunling
Significant enhancement of gas uptake capacity and selectivity via the judicious increase of open metal sites and Lewis basic sites within two polyhedron-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2016, 52, 3223-3226
7118491 CIFC3 H18 Bi2 I9 N3P 63/m m c8.5843; 8.5843; 21.69
90; 90; 120		1384.2Eckhardt, Kai; Bon, Volodymyr; Getzschmann, Jürgen; Grothe, Julia; Wisser, Florian M.; Kaskel, Stefan
Crystallographic insights into (CH3NH3)3(Bi2I9): a new lead-free hybrid organic-inorganic material as a potential absorber for photovoltaics.
Chemical communications (Cambridge, England), 2016, 52, 3058-3060
7118492 CIFC18 H12 O4C 1 2/c 121.876; 22.174; 15.3753
90; 130.23; 90		5694Reddy, Baddigam Kiran; Gadekar, Santosh C.; Anand, Venkataramanarao G.
The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.
Chemical communications (Cambridge, England), 2016, 52, 3007-3009
7118493 CIFC98 H14 F10 O4F d d 235.203; 55.389; 12.2274
90; 90; 90		23842Reddy, Baddigam Kiran; Gadekar, Santosh C.; Anand, Venkataramanarao G.
The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.
Chemical communications (Cambridge, England), 2016, 52, 3007-3009
7118494 CIFC84.86 H11.14 F8.57 O3.43F d -357.756; 57.756; 57.756
90; 90; 90		192660Reddy, Baddigam Kiran; Gadekar, Santosh C.; Anand, Venkataramanarao G.
The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.
Chemical communications (Cambridge, England), 2016, 52, 3007-3009
7118495 CIFC18 H19 N O3P 1 21/n 19.6614; 9.005; 18.1004
90; 91.9684; 90		1573.82Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218
7118496 CIFC17 H16 N2 SP 1 21/c 19.0979; 9.836; 17.0069
90; 102.321; 90		1486.84Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218
7118497 CIFC16 H16 Br N OP 1 21/n 112.4037; 9.4552; 13.0281
90; 100.594; 90		1501.88Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218

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