Crystallography Open Database

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7116346 CIFC17 H15 Br OP 1 21/c 15.7276; 18.038; 13.687
90; 100.05; 90
1392.4Jing Chen; Chao Chen; Junjie Chen; Guohua Wang; Hongmei Qu
Cu-catalyzed intramolecular aryl-etherification reactions of alkoxyl alkynes with diaryliodonium salts via cleavage of a stable C-O bond
Chem.Commun., 2015, 51, 1356
7116347 CIFC22 H17 F N2 O4 S2P 1 21/c 19.0012; 11.6897; 19.0204
90; 92.744; 90
1999.06Bagineni Prasad; Raju Adepu; Atul Kumar Sharma; Manojit Pal
Creation of molecular complexities via a new Cu-catalyzed cascade reaction: a direct access to novel 2,2'-spirobiindole derivatives
Chem.Commun., 2015, 51, 1259
7116348 CIFC51 H51 Cl2 F6 Fe O P4P 1 21/n 112.7886; 17.372; 22.188
90; 92.649; 90
4924.1Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116349 CIFC50 H51 Fe O2 P3P 1 21/n 110.6741; 22.0513; 18.8153
90; 104.313; 90
4291.2Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116350 CIFC52 H53 Fe O P3P -110.9336; 13.3435; 16.5675
76.51; 77.792; 69.833
2183.44Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116351 CIFC52 H53 Fe O P3C 1 2/c 142.0668; 8.5013; 25.591
90; 111.301; 90
8526.7Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116352 CIFC29 H26 F6 N7 O3 P Ru SC 1 2/c 113.6846; 22.956; 20.732
90; 98.493; 90
6441.4Yue Zheng; Qianxiong Zhou; Wanhua Lei; Yuanjun Hou; Ke Li; Yongjie Chen; Baowen Zhang; Xuesong Wang
DNA photocleavage in anaerobic conditions by a Ru(II) complex: a new mechanism
Chem.Commun., 2015, 51, 428
7116353 CIFC33 H23.5 N O10.75 TbF d d 28.487; 34.829; 52.441
90; 90; 90
15501Zhiyong Guo; Xuezhi Song; Huaping Lei; Hailong Wang; Shengqun Su; Hui Xu; Guodong Qian; Hongjie Zhang; Banglin Chen
A ketone functionalized luminescent terbium metal-organic framework for sensing of small molecules
Chem.Commun., 2015, 51, 376
7116354 CIFC22 H20 N2 O2P b c n15.715; 12.1408; 9.9342
90; 90; 90
1895.4Digambar Balaji Shinde; Sharath Kandambeth; Pradip Pachfule; Raya Rahul Kumar; Rahul Banerjee
Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores
Chem.Commun., 2015, 51, 310
7116355 CIFC20 H16 N2 O2P 43 21 27.0094; 7.0094; 32.787
90; 90; 90
1610.88Digambar Balaji Shinde; Sharath Kandambeth; Pradip Pachfule; Raya Rahul Kumar; Rahul Banerjee
Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores
Chem.Commun., 2015, 51, 310
7116356 CIFC43 H60 Cl Cu4 N15 O28P 4/m n c13.3088; 13.3088; 20.4387
90; 90; 90
3620.2Di-ming Chen; Wei Shi; Peng Cheng
A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes
Chem.Commun., 2015, 51, 370
7116357 CIFC61 H84 Cl Cu4 N20 O29.5I 4/m m m13.959; 13.959; 20.0475
90; 90; 90
3906.3Di-ming Chen; Wei Shi; Peng Cheng
A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes
Chem.Commun., 2015, 51, 370
7116358 CIFC29 H74 Ge N2 Si8P 1 21/n 112.106; 23.293; 16.666
90; 103.081; 90
4577.6Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116359 CIFC32 H64 Ge Si8P 1 21/c 113.326; 18.718; 18.391
90; 102.16; 90
4484.5Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116360 CIFC29 H69 Ge P Si8P b c a25.174; 14.054; 25.198
90; 90; 90
8915Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116361 CIFC37 H75 Ge P Si8P -19.809; 14.698; 20.257
105.37; 97.24; 109.32
2583.1Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116362 CIFC34 H66 Ge Si8P 1 21/n 113.204; 19.641; 18.411
90; 109.7; 90
4495.2Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116363 CIFC26 H60 Ge Si8P 1 21/n 19.642; 18.886; 22.043
90; 98.58; 90
3969.1Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116364 CIFC30 H28 Cl6 Fe2 N2 OP 1 21/c 110.588; 11.729; 26.02
90; 91.42; 90
3230.3Martin Brzozowski; Jose A. Forni; G. Paul Savage; Anastasios Polyzos
The direct alpha-C(sp3)-H functionalisation of N-aryl tetrahydroisoquinolinesvia an iron-catalysed aerobic nitro-Mannich reaction and continuous flow processing
Chem.Commun., 2015, 51, 334
7116365 CIFC15 H12 O3P 1 21/c 19.0155; 14.112; 9.6804
90; 90.552; 90
1231.5Saikat Khamarui; Rituparna Maiti; Dilip K. Maiti
General base-tuned unorthodox synthesis of amides and ketoesters with water
Chem.Commun., 2015, 51, 384
7116366 CIFC39 H32 Au2 F10 N2P -112.3529; 12.613; 12.95
99.282; 107.229; 100.92
1840.7Zhao Chen; Jing Zhang; Min Song; Jun Yin; Guang-AoYu; Sheng Hua Liu
A novel fluorene-based aggregation-induced emission (AIE)-active gold(I) complex with crystallization-induced emission enhancement (CIEE) and reversible mechanochromism characteristics
Chem.Commun., 2015, 51, 326
7116367 CIFC20 H16 N2P 1 21/c 118.16; 5.8576; 14.864
90; 109.694; 90
1488.7Rajeshwer Vanjari; Tirumaleswararao Guntreddi; Saurabh Kumar; Krishna Nand Singh
Sulphur promoted C(sp3)-C(sp2) cross dehydrogenative cyclisation of acetophenonehydrazones with aldehydes: efficient synthesis of 3,4,5-trisubstituted 1H-pyrazoles
Chem.Commun., 2015, 51, 366
7116368 CIFC62 H60P -14.9784; 11.3963; 19.9225
95.603; 92.746; 93.2
1121.54Gaole Dai; Jingjing Chang; Wenhua Zhang; Shiqiang Bai; Kuo-Wei Huang; Jianwei Xu; Chunyan Chi
Dianthraceno[a,e]pentalenes: synthesis, crystallographic structures and applications in organic field-effect transistors
Chem.Commun., 2015, 51, 503
7116369 CIFC86 H78P -19.7359; 16.193; 22.166
99.203; 101.335; 101.921
3278.4Gaole Dai; Jingjing Chang; Wenhua Zhang; Shiqiang Bai; Kuo-Wei Huang; Jianwei Xu; Chunyan Chi
Dianthraceno[a,e]pentalenes: synthesis, crystallographic structures and applications in organic field-effect transistors
Chem.Commun., 2015, 51, 503
7116370 CIFC15 H14 Cl N3 O5P -16.0904; 7.695; 16.3916
83.899; 82.995; 87.213
757.65Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116371 CIFC15 H15 N3 O2C 1 c 119.9626; 4.6037; 15.3349
90; 112.829; 90
1298.91Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116372 CIFC33 H13 B F15 N3 OP -111.777; 12.266; 12.551
76.4; 64.72; 64.59
1477.8Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116373 CIFC18 H21 B N3 O1.5P -19.0122; 11.123; 17.8748
72.078; 87.907; 79.532
1676.14Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116374 CIFC44 H60 B N O2P 1 21/c 118.442; 11.9605; 19.592
90; 116.965; 90
3851.7Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116375 CIFC52 H79 B2 NP 1 21/c 120.9432; 12.5599; 17.1099
90; 91.099; 90
4499.8Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116376 CIFC50 H65 B N2P 1 21/c 112.3306; 13.0545; 25.512
90; 90.626; 90
4106.4Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116377 CIFC52 H69 B N OP 1 21/n 110.6296; 23.2451; 18.409
90; 104.193; 90
4409.8Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116378 CIFC40 H52 B N O2P 1 21/n 110.1073; 16.6024; 20.2451
90; 94.273; 90
3387.79Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116379 CIFC39 H54 B N OP 1 21/c 117.347; 10.634; 19.7137
90; 112.174; 90
3367.6Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116380 CIFC37 H50 B N O2P 1 21/n 113.4374; 14.3288; 18.5873
90; 105.742; 90
3444.6Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116381 CIFC49 H70 B NP -110.9523; 12.2836; 18.2004
77.103; 81.075; 65.736
2170.4Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116382 CIFC52.5 H81 B N2P -110.318; 12.8163; 17.8056
83.969; 86.164; 85.117
2329.1Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116383 CIFC34 H27 N O3 SP 1 21/c 16.1013; 15.039; 23.894
90; 90.877; 90
2192.2Seema Dhiman; S. S. V. Ramasastry
Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(I)/Bronsted acid catalysis
Chem.Commun., 2015, 51, 557
7116384 CIFC21 H20 Cl2 O3P 21 21 2110.9383; 11.4949; 15.5104
90; 90; 90
1950.2Yuxiao Liu; Yongming Deng; Peter Y. Zavalij; Renhua Liu; Michael P. Doyle
An efficient route to highly enantioenrichedtetrahydroazulenes and beta-tetralones by desymmetrization reactions of delta,delta-diaryldiazoaceto-acetates
Chem.Commun., 2015, 51, 565
7116385 CIFC126 H108 Eu2 N18 O12P 21 21 226.0606; 28.4219; 23.3299
90; 90; 90
17280.3Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116386 CIFC138 H90 Eu2 F18 N18 O18 S6P -116.679; 20.3099; 24.4218
87.025; 70.961; 89.269
7809.7Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116387 CIFC44 H40 N6 O4P 1 21 110.3285; 17.8133; 10.5822
90; 100.506; 90
1914.3Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116388 CIFC17 H17 N O3P 21 21 2110.2469; 10.4606; 13.5437
90; 90; 90
1451.7Zhao-Lin He; Chun-Jiang Wang
Ag(I)-catalyzed tandem [6+3] annulation/isomerization of isocyanoacetates with fulvenes: an expedient approach to synthesize fused dihydropyridines
Chem.Commun., 2015, 51, 534
7116389 CIFC98 H167 Ag12 N12 O0.5 P6 Si6P 1 21 115.889; 18.207; 23.994
90; 95.206; 90
6913Bahareh Khalili Najafabadi; John F. Corrigan
N-Heterocyclic carbene stabilized Ag-P nanoclusters
Chem.Commun., 2015, 51, 665
7116390 CIFC141 H250.8 Ag26 N16 P12 Si10P -117.285; 20.433; 29.512
95.465; 91.603; 90.317
10371Bahareh Khalili Najafabadi; John F. Corrigan
N-Heterocyclic carbene stabilized Ag-P nanoclusters
Chem.Commun., 2015, 51, 665
7116391 CIFC15.74 H19.56 N9.19 O Zn2P b c a15.504; 15.364; 18.127
90; 90; 90
4317.9Yichao Lin; Qiuju Zhang; Chongchong Zhao; Huailong Li; Chunlong Kong; Cai Shen; Liang Chen
An exceptionally stable functionalized metal-organic framework for lithium storage
Chem.Commun., 2015, 51, 697
7116392 CIFC30 H24 S2P 1 21/n 18.641; 10.6699; 25.373
90; 97.159; 90
2321.1Sengodagounder Muthusamy; Manickasamy Sivaguru; Eringathodi Suresh
Indium(III) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines
Chem.Commun., 2015, 51, 707
7116393 CIFC33 H29 Cl S2P -19.901; 11.029; 14.297
74.65; 76.568; 68.378
1383.7Sengodagounder Muthusamy; Manickasamy Sivaguru; Eringathodi Suresh
Indium(III) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines
Chem.Commun., 2015, 51, 707
7116394 CIFC39 H34 B N3P 21 21 218.621; 18.3501; 19.69
90; 90; 90
3114.9Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116395 CIFC25 H19 B F2 N2P 21 21 2110.9427; 12.7077; 14.9474
90; 90; 90
2078.5Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116396 CIFC27 H24 B F2 N3P -112.2723; 14.705; 14.7883
69.664; 67.961; 82.665
2319.6Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116397 CIFC37 H29 B N2P 1 21/n 110.9565; 19.2414; 13.7066
90; 95.002; 90
2878.6Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116398 CIFC81 H19 NC m c 2115.499; 27.568; 9.7851
90; 90; 90
4180.9T. W. Chamberlain; M. A. Lebedeva; W. Abuajwa; M. Suyetin; W. Lewis; E. Bichoutskaia; M. Schroder; A.; N.; Khlobystov'
Switching intermolecular interactions by confinement in carbon nanotubes
Chem.Commun., 2015, 51, 648
7116399 CIFC168 H192 Cl8 Fe4 N36 O32R 3 :H30.682; 30.682; 23.596
90; 90; 120
19237Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116400 CIFC168 H192 Cl8 Fe4 N36 O32R 3 :H30.825; 30.825; 22.939
90; 90; 120
18876Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116401 CIFC211.17 H272.75 Cl8 Fe4 N47.58 O47P 119.6065; 19.7357; 20.2252
116.621; 115.561; 94.4565
5944.6Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116402 CIFC192 H234 Cl8 Fe4 N42 O44P 119.7723; 19.7731; 20.282
115.476; 116.397; 94.961
6022.1Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116403 CIFC174 H189 Cl20 Fe4 N39 O32R 3 :H31.4702; 31.4702; 22.296
90; 90; 120
19123Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116404 CIFC H B N O ZnP 43 21 28.67; 8.67; 12.722
90; 90; 90
956.3Chun-Yang Pan; Li-Juan Zhong; Feng-Hua Zhao; Hong-Mei Yang; Jian Zhou
Zn(1,3-DAP)[B4O7]: a rare chiral zeolitic framework constructed of four-connected [B4O9] clusters with a single-stranded helical channel
Chem.Commun., 2015, 51, 753
7116405 CIFC21 H19 Br N3 O3C 1 2 119.7543; 6.8067; 15.8605
90; 98.736; 90
2107.89Bao-Dong Cui; Yong You; Jian-Qiang Zhao; Jian Zuo; Zhi-Jun Wu; Xiao-Ying Xu; Xiao-Mei Zhang; Wei-Cheng Yuan
3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3'-disubstituted oxindole derivatives
Chem.Commun., 2015, 51, 757
7116406 CIFC10 H9 N O3P 1 21/c 19.3511; 11.4869; 8.4156
90; 102.475; 90
882.62Jingjing Shi; Jie Zhou; Yunnan Yan; Jinlong Jia; Xuelei Liu; Huacan Song; H. Eric Xu; Wei Yi
One-pot cascade synthesis of N-methoxyisoquinolinediones via Rh(III)-catalyzed carbenoid insertion C-H activation/cyclization
Chem.Commun., 2015, 51, 668
7116407 CIFC52 H72 B2 Be N4P 1 21/n 112.855; 27.0697; 14.2004
90; 92.555; 90
4936.6T. Arnold; H. Braunschweig; W. C. Ewing; T. Kramer; J. Mies; J. K. Schuster
Beryllium bis(diazaborolyl): old neighbors finally shake hands
Chem.Commun., 2015, 51, 737
7116408 CIFC63 H86 B2 Be N6P 1 21 112.3713; 20.3783; 12.4856
90; 114.919; 90
2854.7T. Arnold; H. Braunschweig; W. C. Ewing; T. Kramer; J. Mies; J. K. Schuster
Beryllium bis(diazaborolyl): old neighbors finally shake hands
Chem.Commun., 2015, 51, 737
7116409 CIFC149 H248 B8 P8 Sn4P 1 21/c 114.0885; 26.577; 20.0509
90; 95.273; 90
7475.89Keith Izod; Casey M. Dixon; Ross W. Harrington; Michael R. Probert
Impact of a rigid backbone on the structure of an agostically-stabilised dialkylstannylene: isolation of an unusual bridged stannyl-stannylene
Chem.Commun., 2015, 51, 679
7116410 CIFC37 H38 N4 Ni O6P 1 21 18.2226; 39.325; 10.4346
90; 91.494; 90
3372.9Tingting Li; Shengbin Zhou; Jiang Wang; Jose Luis Acena; Vadim A. Soloshonok; Hong Liu
Asymmetric synthesis of alpha-(1-oxoisoindolin-3-yl)glycine: synthetic and mechanistic challenges
Chem.Commun., 2015, 51, 1624
7116411 CIFC36 H34 N4 Ni O5P 1 21/n 111.0249; 18.09; 15.8569
90; 91.288; 90
3161.7Tingting Li; Shengbin Zhou; Jiang Wang; Jose Luis Acena; Vadim A. Soloshonok; Hong Liu
Asymmetric synthesis of alpha-(1-oxoisoindolin-3-yl)glycine: synthetic and mechanistic challenges
Chem.Commun., 2015, 51, 1624
7116412 CIFC24 H20 B Cl2 F2 N3 O SP 1 21/n 19.5908; 10.9141; 22.863
90; 99.059; 90
2363.3Hui Liu; Hua Lu; Zhikuan Zhou; Soji Shimizu; Zhifang Li; Nagao Kobayashi; Zhen Shen
Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties
Chem.Commun., 2015, 51, 1713
7116413 CIFC27 H26 B F2 N3 O2 SP 1 21/n 114.5722; 16.046; 22.1206
90; 107.66; 90
4928.61Hui Liu; Hua Lu; Zhikuan Zhou; Soji Shimizu; Zhifang Li; Nagao Kobayashi; Zhen Shen
Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties
Chem.Commun., 2015, 51, 1713
7116414 CIFC17 H14 F6 O2 S2P 1 21/c 19.9685; 10.863; 15.8102
90; 98.901; 90
1691.4Ryuhei Kodama; Kimio Sumaru; Kana Morishita; Toshiyuki Kanamori; Kengo Hyodo; Takashi Kamitanaka; Masakazu Morimoto; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
A diarylethene as the SO2 gas generator upon UV irradiation
Chem.Commun., 2015, 51, 1736
7116415 CIFC26 H27 O3 PP 1 21/c 118.332; 6.1364; 20.639
90; 107.621; 90
2212.8Yuzhen Gao; Xueqin Li; Jian Xu; Yile Wu; Weizhu Chen; Guo Tang; Yufen Zhao
Mn(OAc)3-mediated phosphonation-lactonization of alkenoic acids: synthesis of phosphono-gamma-butyrolactones
Chem.Commun., 2015, 51, 1605
7116416 CIFC H Cl SP -111.7098; 12.2432; 19.742
75.953; 72.973; 75.614
2576.9Ru-Qiang Lu; Yi-Nyu Zhou; Xiao-Yun Yan; Ke Shi; Yu-Qing Zheng; Ming Luo; Xin-Chang Wang; Jian Pei; Haiping Xia; Laura Zoppi; Kim K. Baldridge; Jay S. Siegel; Xiao-Yu Cao
Thiophene-fused bowl-shaped polycyclic aromatics with a dibenzo[a,g]corannulene core for organic field-effect transistors
Chem.Commun., 2015, 51, 1681
7116417 CIFC26 H17 NP 1 21/c 113.6965; 7.3314; 18.6691
90; 103.364; 90
1823.89Iyyanar Karthikeyan; Dhanarajan Arunprasath; Govindasamy Sekar
An efficient synthesis of pyrido[1,2-a]indoles through aza-Nazarov type cyclization
Chem.Commun., 2015, 51, 1701
7116418 CIFC27 H16 O4 ZnI b a m36.006; 6.013; 31.426
90; 90; 90
6803.9Xun-Gao Liu; Hui Wang; Bin Chen; Yang Zou; Zhi-Guo Gu; Zujin Zhao; Liang Shen
A luminescent metal-organic framework constructed using a tetraphenylethene-based ligand for sensing volatile organic compounds
Chem.Commun., 2015, 51, 1677
7116419 CIFC11 H13 B Cl2 N2P 1 21/n 17.839; 16.0342; 9.5567
90; 96.056; 90
1194.5Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deisshurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116420 CIFC13 H17 B Cl2 N2C 1 c 115.0371; 7.5273; 13.1615
90; 108.431; 90
1413.3Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116421 CIFC25 H25 B N2P 1 21/n 110.68; 14.1175; 13.6179
90; 93.975; 90
2048.3Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116422 CIFC27 H29 B N2P 1 21/n 111.205; 13.058; 16.087
90; 106.498; 90
2256.9Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116423 CIFC37 H55 B N2 P2 PtP -115.9324; 15.9875; 16.3672
63.872; 87.926; 79.834
3680.2Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116424 CIFC40.67 H53.33 N5 O4.17 RhR -3 :H34.6494; 34.6494; 16.6624
90; 90; 120
17324.5Eva Jurgens; Barbara Wucher; Frank Rominger; Karl W. Tornroos; Doris Kunz
Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex
Chem.Commun., 2015, 51, 1897
7116425 CIFC109 H134 N15 O7 Rh3P 1 21/n 121.7612; 21.6015; 23.3468
90; 90.011; 90
10974.7Eva Jurgens; Barbara Wucher; Frank Rominger; Karl W. Tornroos; Doris Kunz
Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex
Chem.Commun., 2015, 51, 1897
7116426 CIFC39 H39 Ir N2 O2 S2P b c a13.4876; 18.3802; 27.8072
90; 90; 90
6893.5Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116427 CIFC60 H65 Cl2 Ir N2 O2 S2P -112.8835; 14.7285; 16.0114
103.949; 93.493; 103.298
2847.71Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116428 CIFC31.25 H24 Ir N2 O2.25 S2P -118.4383; 18.6855; 19.9281
107.775; 99.052; 117.763
5407.5Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116429 CIFC58 H58 N10 O18 S4P -17.8554; 13.428; 14.296
74.64; 83.39; 82.18
1435.6Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116430 CIFC58 H74 N10 O26 S4P -110.5682; 12.4098; 13.8043
70.117; 82.636; 85.85
1687.7Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116431 CIFC58 H61 N10 O19.5 S4P -112.2027; 13.5862; 19.851
72.658; 78.079; 72.902
2977Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116432 CIFC65 H68 N11 O18.5 S4P -114.085; 16.457; 16.585
80.08; 66.96; 72.44
3366.4Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116433 CIFC65 H69 N11 O19 S4P -113.9; 16.237; 16.444
79.98; 66.84; 73.12
3257.7Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116434 CIFC62 H69 N10 O21.5 S4P -114.166; 16.38; 18.029
103.04; 109.53; 98.05
3733.8Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116435 CIFC96 H144 Br4 N8 O22P 1 21/c 110.8583; 18.3496; 22.4335
90; 91.834; 90
4467.5Wei Zhang; Yi Li; Jing-Hua Sun; Cai-Ping Tan; Liang-Nian Ji; Zong-Wan Mao
Supramolecular self-assembled nanoparticles for chemo-photodynamic dual therapy against cisplatin resistant cancer cells
Chem.Commun., 2015, 51, 1807
7116436 CIFC56 H42C 1 2/c 123.491; 10.5581; 16.883
90; 99.21; 90
4133.3Guoying Zhang; Yinjun Xie; Zhengkun Wang; Yang Liu; Hanmin Huang
Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies
Chem.Commun., 2015, 51, 1850
7116437 CIFC74 H80 O SP -114.3679; 14.8455; 16.0061
75.95; 83.391; 83.523
3277.2Guoying Zhang; Yinjun Xie; Zhengkun Wang; Yang Liu; Hanmin Huang
Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies
Chem.Commun., 2015, 51, 1850
7116438 CIFC132 H120 N24P 21 21 2123.855; 26.655; 27.082
90; 90; 90
17220Huimin Ding; Yihui Yang; Bijian Li; Feng Pan; Guozhu Zhu; Matthias Zeller; Daqiang Yuan; Cheng Wang
Targeted synthesis of a large triazine-based [4+6] organic molecular cage: structure, porosity and gas separation
Chem.Commun., 2015, 51, 1976
7116439 CIFC65 H90 F6 N8 Na O10 P Rh4P 1 21/c 116.7562; 16.3493; 27.6506
90; 91.707; 90
7571.6Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116440 CIFC65 H92 B F4 N8 Na O11 Rh4P 1 21/c 116.662; 16.4372; 27.4724
90; 94.94; 90
7496.1Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116441 CIFC66 H87 N12 Na O12 Rh4P b c a22.6289; 21.7265; 29.7275
90; 90; 90
14615.4Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116442 CIFC62 H97.5 Ca N10.5 O22 Rh4P -111.3211; 18.6735; 18.7302
89.602; 75.171; 87.676
3824.6Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116443 CIFC62 H83 La N12 O19 Rh4P 21 21 218.7826; 19.9113; 10.6111
90; 90; 90
3968.4Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116444 CIFC62 H83 Eu N12 O19 Rh4P 21 21 218.4641; 19.8783; 10.5405
90; 90; 90
3868.7Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116445 CIFC66 H86 Dy N13 O20 Rh4P 1 21/c 113.9749; 18.7743; 28.0431
90; 93.975; 90
7339.9Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889

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