Crystallography Open Database

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7115294 CIFC15 H19 N OP 21 21 217.9717; 11.1704; 14.2796
90; 90; 90
1271.56Xusheng Zhang; Min Wang; Pinhua Li; Lei Wang
n-Bu4NI/TBHP-catalyzed direct amination of allylic and benzylic C(sp3)-H with anilines under metal-free conditions
Chem.Commun., 2014, 50, 8006
7115295 CIFC17 H15 Fe N OC 1 2/c 115.794; 10.62; 17.36
90; 102.863; 90
2838.8Masahiro Kamitani; Masaki Ito; Masumi Itazaki; Hiroshi Nakazawa
Effective dehydrogenation of 2-pyridylmethanol derivatives catalyzed by an iron complex
Chem.Commun., 2014, 50, 7941
7115296 CIFC35 H31 N7P 1 21/n 111.9764; 19.8384; 12.5324
90; 112.803; 90
2744.88Rampal Pandey; Gabor Mehes; Amit Kumar; Rakesh Kumar Gupta; Chihaya Adachic; Daya Shankar Pandey
Structural and mechanistic insights into an Fe3±triggered quinazoline based molecular rotor
Chem.Commun., 2014, 50, 8032
7115297 CIFC35 H27 Cl2 N7 O2C 1 2/c 115.7933; 11.5458; 17.1322
90; 99.286; 90
3083.1Rampal Pandey; Gabor Mehes; Amit Kumar; Rakesh Kumar Gupta; Chihaya Adachic; Daya Shankar Pandey
Structural and mechanistic insights into an Fe3±triggered quinazoline based molecular rotor
Chem.Commun., 2014, 50, 8032
7115298 CIFC20 H16 N4P 1 21/n 16.8611; 12.8045; 18.2363
90; 91.863; 90
1601.27Rampal Pandey; Gabor Mehes; Amit Kumar; Rakesh Kumar Gupta; Chihaya Adachic; Daya Shankar Pandey
Structural and mechanistic insights into an Fe3±triggered quinazoline based molecular rotor
Chem.Commun., 2014, 50, 8032
7115299 CIFC62 H60 N6P -19.1332; 11.8576; 13.566
84.777; 83.98; 72.609
1391.5D. S. Andrianov; V. B. Rybakov; A. V. Cheprakov
Between porphyrins and phthalocyanines: 10,20-diaryl-5,15-tetrabenzodiazaporphyrins
Chem.Commun., 2014, 50, 7953
7115300 CIFC71 H88 N6 O15P -115.0617; 15.8532; 20.3366
86.099; 78.81; 67.459
4399.6Jinchuan Hu; Long Chen; Jie Shen; Jian Luo; Pengchi Deng; Yi Ren; Huaqiang Zeng; Wen Feng; Lihua Yuan
Convergent heteroditopic cyclo[6]aramides as macrocyclic ion-pair receptors for constructing [2]pseudorotaxanes
Chem.Commun., 2014, 50, 8024
7115301 CIFC81 H114 Cl5 N7 O16P 1 21/n 115.3283; 24.6571; 23.0091
90; 107.044; 90
8314.4Jinchuan Hu; Long Chen; Jie Shen; Jian Luo; Pengchi Deng; Yi Ren; Huaqiang Zeng; Wen Feng; Lihua Yuan
Convergent heteroditopic cyclo[6]aramides as macrocyclic ion-pair receptors for constructing [2]pseudorotaxanes
Chem.Commun., 2014, 50, 8024
7115302 CIFC17 H24 O6P 1 21/c 112.9911; 10.5635; 12.5742
90; 105.22; 90
1665.05Lu-Feng Wang; Zi-Fa Shi; Xiao-Ping Cao; Bao-Sheng Li; Peng An
Construction of fused- and spiro-oxa-[n.2.1] skeletons by a tandem epoxide rearrangement/intramolecular [3+2] cycloaddition of cyclopropanes with carbonyls
Chem.Commun., 2014, 50, 8061
7115303 CIFC17 H24 O7P 1 21/n 110.9441; 13.9862; 11.3875
90; 99.729; 90
1717.97Lu-Feng Wang; Zi-Fa Shi; Xiao-Ping Cao; Bao-Sheng Li; Peng An
Construction of fused- and spiro-oxa-[n.2.1] skeletons by a tandem epoxide rearrangement/intramolecular [3+2] cycloaddition of cyclopropanes with carbonyls
Chem.Commun., 2014, 50, 8061
7115304 CIFC26 H34 Cl N2 O3P 1 21/c 115.6872; 19.328; 8.3731
90; 95.034; 90
2528.9Feng Lin; Tian-Guang Zhan; Tian-You Zhou; Kang-Da Zhang; Guang-Yu Li; Jian Wu; Xin Zhao
The construction of rigid supramolecular polymers in water through the self-assembly of rod-like monomers and cucurbit[8]uril
Chem.Commun., 2014, 50, 7982
7115305 CIFC35.5 H56.5 Cl1.5 N6 O9P 110.1668; 11.5055; 20.4107
87; 75.864; 65.519
2103.85Bryden A. F.; Le Bailly; Jonathan Clayden
Controlling the sign and magnitude of screw-sense preference from the C-terminus of an achiral helical foldamer
Chem.Commun., 2014, 50, 7949
7115306 CIFC17 H27 B F K O3.5P -111.369; 13.198; 13.395
102.149; 103.237; 90.795
1908.6Yusuke Makida; Enrico Marelli; Alexandra M. Z. Slawin; Steven P. Nolan
Nickel-catalysed carboxylation of organoboronates
Chem.Commun., 2014, 50, 8010
7115307 CIFC26 H28P 1 21/n 19.9322; 8.985; 43.0557
90; 91.32; 90
3841.3Hang Zhang; Bo Wang; Kang Wang; Guojun Xie; Changkun Li; Yan Zhang; Jianbo Wang
Pd-Catalyzed ring-opening cross-coupling of cyclopropenes with aryl iodides
Chem.Commun., 2014, 50, 8050
7115308 CIFC48 H39 N O4P 21 21 2111.0511; 14.426; 22.603
90; 90; 90
3603.4Jun Zheng; Shu-Li You
Rhodium-catalyzed direct coupling of biaryl pyridine derivatives with internal alkynes
Chem.Commun., 2014, 50, 8204
7115309 CIFC47 H32 Cl NP -18.7922; 9.5339; 21.234
96.76; 99.441; 90.583
1742.8Jun Zheng; Shu-Li You
Rhodium-catalyzed direct coupling of biaryl pyridine derivatives with internal alkynes
Chem.Commun., 2014, 50, 8204
7115310 CIFC57 H66 N3 O S2 UP 1 21/n 111.8172; 19.4061; 24.4379
90; 99.239; 90
5531.5John J. Kiernicki; Phillip E. Fanwick; Suzanne C. Bart
Utility of a redox-active pyridine(diimine) chelate in facilitating two electron oxidative addition chemistry at uranium
Chem.Commun., 2014, 50, 8189
7115311 CIFC45 H56 Cl2 N3 O UP 1 21/c 18.2201; 24.8482; 20.3997
90; 92.708; 90
4162.08John J. Kiernicki; Phillip E. Fanwick; Suzanne C. Bart
Utility of a redox-active pyridine(diimine) chelate in facilitating two electron oxidative addition chemistry at uranium
Chem.Commun., 2014, 50, 8189
7115312 CIFC47 H51 Cl N3 O0.12 Se UC 1 2/c 142.342; 8.3362; 24.4297
90; 101.179; 90
8459.4John J. Kiernicki; Phillip E. Fanwick; Suzanne C. Bart
Utility of a redox-active pyridine(diimine) chelate in facilitating two electron oxidative addition chemistry at uranium
Chem.Commun., 2014, 50, 8189
7115313 CIFC61 H72 N3 O2 Se2 UP 1 21/n 111.7186; 26.9121; 17.5708
90; 100.642; 90
5446.03John J. Kiernicki; Phillip E. Fanwick; Suzanne C. Bart
Utility of a redox-active pyridine(diimine) chelate in facilitating two electron oxidative addition chemistry at uranium
Chem.Commun., 2014, 50, 8189
7115314 CIFC4.5 H5 B0.5 N3 Pu0.17P 63/m11.7036; 11.7036; 13.5561
90; 90; 120
1608.07N. Magnani; E. Colineau; J.-C. Griveau; C. Apostolidis; O. Walter; R. Caciuffo
A plutonium-ased single-molecule magnet
Chem.Commun., 2014, 50, 8171
7115315 CIFC24 H40 Al2 Br2P 1 2/n 117.8044; 8.4388; 17.835
90; 100.799; 90
2632.21Tatsuya Wasano; Tomohiro Agou; Takahiro Sasamori; Norihiro Tokitoh
Synthesis, structure and reactivity of a 1-bromoalumole
Chem.Commun., 2014, 50, 8148
7115316 CIFC12 H38 B9 N4 TaP 1 21/n 111.08; 16.589; 12.2139
90; 97.377; 90
2226.4Li Xiang; Zuowei Xie
Conversion of (eta^5^-C2B9H10R)TaX3 (X = Me, NMe2) to (eta^6^-C2B9H10R)TaX' (X' = NMe2, azaallyl) in the absence of a reducing agent: synthesis and structure of tantallacarboranes incorporating an arachno-eta^6^-C2B9^4-^ ligand
Chem.Commun., 2014, 50, 8249
7115317 CIFC19 H37 B9 N3 TaP 1 21/n 110.076; 22.404; 11.47
90; 90.44; 90
2589.2Li Xiang; Zuowei Xie
Conversion of (eta^5^-C2B9H10R)TaX3 (X = Me, NMe2) to (eta^6^-C2B9H10R)TaX' (X' = NMe2, azaallyl) in the absence of a reducing agent: synthesis and structure of tantallacarboranes incorporating an arachno-eta^6^-C2B9^4-^ ligand
Chem.Commun., 2014, 50, 8249
7115318 CIFC19 H41 B9 N O2 TaP 1 21/n 19.5075; 14.0259; 21.3447
90; 96.654; 90
2827.2Li Xiang; Zuowei Xie
Conversion of (eta^5^-C2B9H10R)TaX3 (X = Me, NMe2) to (eta^6^-C2B9H10R)TaX' (X' = NMe2, azaallyl) in the absence of a reducing agent: synthesis and structure of tantallacarboranes incorporating an arachno-eta^6^-C2B9^4-^ ligand
Chem.Commun., 2014, 50, 8249
7115319 CIFC12 H17 B O2 SeP b c a12.6814; 13.1877; 16.1788
90; 90; 90
2705.7Xavier Sanz; Christopher M. Vogels; Andreas Decken; Carles Bo; Stephen A. Westcott; Elena Fernandez
Face to face activation of a phenylselenium borane with alpha,beta-unsaturated carbonyl substrates: facile synthesis of C-Se bonds
Chem.Commun., 2014, 50, 8420
7115320 CIFC76 H72 N4 O18 Zn3P 1 21 111.167; 22.145; 16.594
90; 108.31; 90
3895.8Takayoshi Arai; Noriyuki Sugiyama; Hyuma Masu; Sayaka Kado; Shinnosuke Yabe; Masahiro Yamanaka
A trinuclear Zn3(OAc)4-3,3'-bis(aminoimino)binaphthoxide complex for highly efficient catalytic asymmetric iodolactonization
Chem.Commun., 2014, 50, 8287
7115321 CIFC38 H80 Br N4 O15 Pd S2P 15.207; 8.066; 30.666
84.437; 89.103; 86.149
1278.9Shohei Kumagai; Shinya Takaishi; Brian K. Breedlove; Hiroshi Okamoto; Hisaaki Tanaka; Shin-ichi Kuroda; Masahiro Yamashita
Bromide-bridged palladium(III) chain complexes showing charge bistability near room temperature
Chem.Commun., 2014, 50, 8382
7115322 CIFC18 H17 N O3 SP 1 21 19.9921; 8.095; 10.5243
90; 107.49; 90
811.91P.-F. Koh; P. Wang; J.-M. Huang; T.-P. Loh
Biomass derived furfural-based facile synthesis of protected (2S)-phenyl-3-piperidone, a common intermediate for many drugs
Chem.Commun., 2014, 50, 8324
7115323 CIFC23 H26 F3 N O4P -112.6844; 13.0079; 13.5817
83.347; 80.714; 83.78
2187.5P.-F. Koh; P. Wang; J.-M. Huang; T.-P. Loh
Biomass derived furfural-based facile synthesis of protected (2S)-phenyl-3-piperidone, a common intermediate for many drugs
Chem.Commun., 2014, 50, 8324
7115324 CIFC18 H17 N O4 SP 1 21/n 18.3044; 10.7213; 17.956
90; 91.819; 90
1597.9P.-F. Koh; P. Wang; J.-M. Huang; T.-P. Loh
Biomass derived furfural-based facile synthesis of protected (2S)-phenyl-3-piperidone, a common intermediate for many drugs
Chem.Commun., 2014, 50, 8324
7115325 CIFC20 H21 N O3 SP 1 21/n 110.5854; 16.1439; 11.1053
90; 113.485; 90
1740.58P.-F. Koh; P. Wang; J.-M. Huang; T.-P. Loh
Biomass derived furfural-based facile synthesis of protected (2S)-phenyl-3-piperidone, a common intermediate for many drugs
Chem.Commun., 2014, 50, 8324
7115326 CIFC21 H23 N O3 SP 1 21 19.789; 9.327; 11.044
90; 114.811; 90
915.3P.-F. Koh; P. Wang; J.-M. Huang; T.-P. Loh
Biomass derived furfural-based facile synthesis of protected (2S)-phenyl-3-piperidone, a common intermediate for many drugs
Chem.Commun., 2014, 50, 8324
7115327 CIFC163 H140 Dy F3 Ir6 N18 O29 P6 SP -115.736; 16.7879; 18.23
65.078; 83.173; 68.357
4055.7Dai Zeng; Min Ren; Song-Song Bao; Li Li; Li-Min Zheng
A luminescent heptanuclear DyIr6 complex showing field-induced slow magnetization relaxation
Chem.Commun., 2014, 50, 8356
7115328 CIFC17 H21 N OP -16.5188; 6.6901; 16.077
93.17; 91.18; 98.9
691.3Yang Gao; Yubing Huang; Wanqing Wu; Kefan Huang; Huanfeng Jiang
Pd-Catalyzed C-H activation/oxidative cyclization of acetanilide with norbornene: concise access to functionalized indolines
Chem.Commun., 2014, 50, 8370
7115329 CIFC36 H72 N4 O4 Zn2P 1 21/c 110.6599; 12.5644; 15.3343
90; 108.876; 90
1943.4Phillip Jochmann; Douglas W. Stephan
The synthesis and structure of [Zn(TEMPO)2]2 and [Zn(mu-H)(mu^2^-mu^1^:mu^1^-TEMPO)]6
Chem.Commun., 2014, 50, 8395
7115330 CIFC7.5 H15 N0.75 O0.75 Zn0.75R -3 :H19.8098; 19.8098; 14.692
90; 90; 120
4993.1Phillip Jochmann; Douglas W. Stephan
The synthesis and structure of [Zn(TEMPO)2]2 and [Zn(mu-H)(mu^2^-mu^1^:mu^1^-TEMPO)]6
Chem.Commun., 2014, 50, 8395
7115331 CIFC14 H22 N6 O8 ZnC 1 2/c 114.043; 12.4823; 12.349
90; 111.89; 90
2008.6Yuehong Wen; Tianlu Sheng; Zhihao Sun; Zhenzhen Xue; Yanlong Wang; Yong Wang; Shengmin Hu; Xiao Ma; Xintao Wu
A combination of the 'pillaring' strategy and chiral induction: an approach to prepare homochiral three-dimensional coordination polymers from achiral precursors
Chem.Commun., 2014, 50, 8320
7115332 CIFC14 H26 Mo N4 O8 ZnC 1 2 113.901; 12.713; 7.07
90; 91.139; 90
1249.2Yuehong Wen; Tianlu Sheng; Zhihao Sun; Zhenzhen Xue; Yanlong Wang; Yong Wang; Shengmin Hu; Xiao Ma; Xintao Wu
A combination of the 'pillaring' strategy and chiral induction: an approach to prepare homochiral three-dimensional coordination polymers from achiral precursors
Chem.Commun., 2014, 50, 8320
7115333 CIFC14 H30 Mo N4 O10 ZnC 1 2 113.971; 12.841; 7.137
90; 90.74; 90
1280Yuehong Wen; Tianlu Sheng; Zhihao Sun; Zhenzhen Xue; Yanlong Wang; Yong Wang; Shengmin Hu; Xiao Ma; Xintao Wu
A combination of the 'pillaring' strategy and chiral induction: an approach to prepare homochiral three-dimensional coordination polymers from achiral precursors
Chem.Commun., 2014, 50, 8320
7115334 CIFC14 H32 N4 O11 S ZnC 1 2 113.783; 12.697; 6.743
90; 90.759; 90
1179.9Yuehong Wen; Tianlu Sheng; Zhihao Sun; Zhenzhen Xue; Yanlong Wang; Yong Wang; Shengmin Hu; Xiao Ma; Xintao Wu
A combination of the 'pillaring' strategy and chiral induction: an approach to prepare homochiral three-dimensional coordination polymers from achiral precursors
Chem.Commun., 2014, 50, 8320
7115335 CIFC14 H30 Cr N4 O10 ZnC 1 2 113.85; 12.77; 6.939
90; 91.45; 90
1227Yuehong Wen; Tianlu Sheng; Zhihao Sun; Zhenzhen Xue; Yanlong Wang; Yong Wang; Shengmin Hu; Xiao Ma; Xintao Wu
A combination of the 'pillaring' strategy and chiral induction: an approach to prepare homochiral three-dimensional coordination polymers from achiral precursors
Chem.Commun., 2014, 50, 8320
7115336 CIFC57 H40 Cl2 N2 SP -19.9886; 13.324; 16.9907
91.846; 100.777; 102.672
2160.93Young Mo Sung; Bartosz Szyszko; Radomir Mysliborski; Marcin Stepien; Juwon Oh; Minjung Son; Lechoslaw Latos-Grazynski; Dongho Kim
The effect of pi-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids
Chem.Commun., 2014, 50, 8367
7115337 CIFC49 H36 Cl2 N2 SP 1 21/n 115.054; 16.56; 15.22
90; 96.87; 90
3767Young Mo Sung; Bartosz Szyszko; Radomir Mysliborski; Marcin Stepien; Juwon Oh; Minjung Son; Lechoslaw Latos-Grazynski; Dongho Kim
The effect of pi-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids
Chem.Commun., 2014, 50, 8367
7115338 CIFC20 H21 I N2 O4 SP 1 21/n 18.0734; 17.0233; 15.3571
90; 96.854; 90
2095.5Manjusha V. Karkhelikar; Rajeev R. Jha; B. Sridhar; Pravin R. Likhar; Akhilesh K. Verma
An expedient approach to pyrrolo[3,2-c]quinolines via regioselective formation of the pyrrole nucleus over indoles
Chem.Commun., 2014, 50, 8526
7115339 CIFC25 H27 Cl3 N2 O6 SP 1 21/n 117.5098; 8.4729; 18.956
90; 94.435; 90
2803.9Manjusha V. Karkhelikar; Rajeev R. Jha; B. Sridhar; Pravin R. Likhar; Akhilesh K. Verma
An expedient approach to pyrrolo[3,2-c]quinolines via regioselective formation of the pyrrole nucleus over indoles
Chem.Commun., 2014, 50, 8526
7115340 CIFC23 H18 O3P 1 21/c 125.754; 6.0366; 23.164
90; 106.637; 90
3450.5Hai Xiao Siyang; Xu Rui Wu; Xiao Yue Ji; Xin Yan Wu; Pei Nian Liu
A copper(II) perchlorate-promoted tandem reaction of internal alkynol and salicyl N-tosylhydrazone: direct access to isochromeno[3,4-b]chromene
Chem.Commun., 2014, 50, 8514
7115341 CIFC50 H47.5 Co7 N2.5 O29R -3 :H14.997; 14.997; 52.244
90; 90; 120
10176Ya-Min Li; Hui-Jie Lun; Chang-Yu Xiao; Yan-Qing Xu; Ling Wu; Jing-He Yang; Jing-Yang Niu; Sheng-Chang Xiang
A bilayer triangular lattice with crown-like Co7 spin cluster SBUs exhibiting high spin frustration
Chem.Commun., 2014, 50, 8558
7115342 CIFC36 H24 N4P -19.0514; 12.8065; 12.889
98.181; 107.151; 103.624
1350.9Hiroaki Yamashita; Jiro Abe
Pentaarylbiimidazole, PABI: an easily synthesized fast photochromic molecule with superior durability
Chem.Commun., 2014, 50, 8468
7115343 CIFC36 H24 N4P n a 2115.8279; 14.7391; 11.544
90; 90; 90
2693.1Hiroaki Yamashita; Jiro Abe
Pentaarylbiimidazole, PABI: an easily synthesized fast photochromic molecule with superior durability
Chem.Commun., 2014, 50, 8468
7115344 CIFC23 H31 B Cl N3P b c a9.7748; 18.042; 24.277
90; 90; 90
4281.4Ying Kai Loh; Che Chang Chong; Rakesh Ganguly; Yongxin Li; Dragoslav Vidovic; Rei Kinjo
1,2,4,3-Triazaborole-based neutral oxoborane stabilized by a Lewis acid
Chem.Commun., 2014, 50, 8561
7115345 CIFC23 H32 B N3 OC 1 c 118.898; 13.4431; 17.569
90; 100.681; 90
4386Ying Kai Loh; Che Chang Chong; Rakesh Ganguly; Yongxin Li; Dragoslav Vidovic; Rei Kinjo
1,2,4,3-Triazaborole-based neutral oxoborane stabilized by a Lewis acid
Chem.Commun., 2014, 50, 8561
7115346 CIFC23 H32 Al B Cl3 N3 OP 1 21/n 19.7657; 17.593; 16.2032
90; 106.333; 90
2671.5Ying Kai Loh; Che Chang Chong; Rakesh Ganguly; Yongxin Li; Dragoslav Vidovic; Rei Kinjo
1,2,4,3-Triazaborole-based neutral oxoborane stabilized by a Lewis acid
Chem.Commun., 2014, 50, 8561
7115347 CIFC21 H18 N2 O5C 1 2/c 134.026; 8.1856; 13.2003
90; 94.279; 90
3666.3Shen Liu; Wenteng Chen; Jing Luo; Yongping Yu
[3+3] annulation of allylic phosphoryl-stabilized carbanions/phosphorus ylides and vinyl azides: a practice strategy for synthesis of polyfunctionalized anilines
Chem.Commun., 2014, 50, 8539
7115349 CIFC37 H36 N O3 P PdP 21 21 2110.0641; 11.7975; 26.192
90; 90; 90
3109.81Renta Jonathan Chew; Kai Yuan Teo; Yinhua Huang; Bin-Bin Li; Yongxin Li; Sumod A. Pullarkat; Pak-Hing Leung
Enantioselective phospha-Michael addition of diarylphosphines to beta,gamma-unsaturated alpha-ketoesters and amides
Chem.Commun., 2014, 50, 8768
7115350 CIFC18 H12 OC 1 c 134.4472; 7.3598; 9.8621
90; 98.492; 90
2472.87Shinaj K. Rajagopal; Abbey M. Philip; Kalaivanan Nagarajan; Mahesh Hariharan
Progressive acylation of pyrene engineers solid state packing and colour via C-H...H-C, C-H...O and pi-pi interactions
Chem.Commun., 2014, 50, 8644
7115351 CIFC20 H14 O2P n m a7.3519; 16.6654; 11.3344
90; 90; 90
1388.72Shinaj K. Rajagopal; Abbey M. Philip; Kalaivanan Nagarajan; Mahesh Hariharan
Progressive acylation of pyrene engineers solid state packing and colour via C-H...H-C, C-H...O and pi-pi interactions
Chem.Commun., 2014, 50, 8644
7115352 CIFC20 H14 O2P 1 21/n 19.243; 7.463; 10.095
90; 98.88; 90
688Shinaj K. Rajagopal; Abbey M. Philip; Kalaivanan Nagarajan; Mahesh Hariharan
Progressive acylation of pyrene engineers solid state packing and colour via C-H...H-C, C-H...O and pi-pi interactions
Chem.Commun., 2014, 50, 8644
7115353 CIFC20 H14 O2P 1 21/c 18.1941; 23.0417; 7.402
90; 93.824; 90
1394.43Shinaj K. Rajagopal; Abbey M. Philip; Kalaivanan Nagarajan; Mahesh Hariharan
Progressive acylation of pyrene engineers solid state packing and colour via C-H...H-C, C-H...O and pi-pi interactions
Chem.Commun., 2014, 50, 8644
7115354 CIFC22 H16 O3P 1 21/c 111.0402; 20.0564; 7.2682
90; 96.682; 90
1598.44Shinaj K. Rajagopal; Abbey M. Philip; Kalaivanan Nagarajan; Mahesh Hariharan
Progressive acylation of pyrene engineers solid state packing and colour via C-H...H-C, C-H...O and pi-pi interactions
Chem.Commun., 2014, 50, 8644
7115355 CIFC24 H18 O4C 1 2 120.1864; 39.606; 7.0261
90; 109.988; 90
5279Shinaj K. Rajagopal; Abbey M. Philip; Kalaivanan Nagarajan; Mahesh Hariharan
Progressive acylation of pyrene engineers solid state packing and colour via C-H...H-C, C-H...O and pi-pi interactions
Chem.Commun., 2014, 50, 8644
7115356 CIFC27 H28 B Cu N6I 1 2/a 120.7069; 9.4597; 28.7537
90; 104.04; 90
5464Tian Wen; De-Xiang Zhang; Hai-Xia Zhang; Hua-Bin Zhang; Jian Zhang; Dong-Sheng Li
Redox-active Cu(I) boron imidazolate framework for mechanochromic and catalytic applications
Chem.Commun., 2014, 50, 8754
7115357 CIFC24 H23 N3 OP 21 21 217.5448; 9.2205; 28.088
90; 90; 90
1954Lianke Wang; Yanfang Shen; Mingdi Yang; Xiuzhen Zhang; Weinan Xu; Qiuju Zhu; Jieying Wu; Yupeng Tian; Hongping Zhou
Novel highly emissive H-aggregates with aggregate fluorescence change in a phenylbenzoxazole-based system
Chem.Commun., 2014, 50, 8723
7115358 CIFC20 H14 N2 O2P 1 21/c 126.467; 4.692; 12.387
90; 101.332; 90
1508.3Lianke Wang; Yanfang Shen; Mingdi Yang; Xiuzhen Zhang; Weinan Xu; Qiuju Zhu; Jieying Wu; Yupeng Tian; Hongping Zhou
Novel highly emissive H-aggregates with aggregate fluorescence change in a phenylbenzoxazole-based system
Chem.Commun., 2014, 50, 8723
7115359 CIFC24 H23 N3 O2P 21 21 217.516; 9.49; 27.807
90; 90; 90
1983.4Lianke Wang; Yanfang Shen; Mingdi Yang; Xiuzhen Zhang; Weinan Xu; Qiuju Zhu; Jieying Wu; Yupeng Tian; Hongping Zhou
Novel highly emissive H-aggregates with aggregate fluorescence change in a phenylbenzoxazole-based system
Chem.Commun., 2014, 50, 8723
7115360 CIFC16 H32 N2 Na2 O20 S2 UP -18.422; 9.3646; 19.946
89.043; 88.581; 72.24
1497.6C. A. Hawkins; C. G. Bustillos; R. Copping; B. L. Scott; I. May; M. Nilsson
Challenging conventional f-element separation chemistry - reversing uranyl(VI)/lanthanide(III) solvent extraction selectivity
Chem.Commun., 2014, 50, 8670
7115361 CIFC50 H36 Eu3 N4 O23I m -337.9826; 37.9826; 37.9826
90; 90; 90
54797Bo Liu; Wei-Ping Wu; Lei Hou; Yao-Yu Wang
Four uncommon nanocage-based Ln-MOFs: highly selective luminescent sensing for Cu2+ ions and selective CO2 capture
Chem.Commun., 2014, 50, 8731
7115362 CIFC50 H36 Gd3 N4 O23I m -337.9569; 37.9569; 37.9569
90; 90; 90
54686Bo Liu; Wei-Ping Wu; Lei Hou; Yao-Yu Wang
Four uncommon nanocage-based Ln-MOFs: highly selective luminescent sensing for Cu2+ ions and selective CO2 capture
Chem.Commun., 2014, 50, 8731
7115363 CIFC29.5 H29 N O5.5 S2C 1 2/c 124.428; 12.34; 22.946
90; 113.081; 90
6363.2Xiao Liu; Lingjuan Zhang; Xianxiu Xu; Shan Wang; Ling Pan; Qian Zhang; Qun Liu
Aerobic copper-catalyzed oxidative [6C+1C] annulation: an efficient route to seven-membered carbocycles
Chem.Commun., 2014, 50, 8764
7115364 CIFC26.5 H26 Br Cl N2 O5P 21 2 2148.787; 11.8679; 9.6762
90; 90; 90
5602.5Haifeng Zheng; Peng He; Yangbin Liu; Yulong Zhang; Xiaohua Liu; Lili Lin; Xiaoming Feng
Efficient synthesis of carbazolespirooxindole skeletons via asymmetric Diels-Alder reaction of 3-vinylindoles and methyleneindolinones
Chem.Commun., 2014, 50, 8794
7115365 CIFC97 H97 Fe2 N8 O12 Zn2C 1 2 114.4; 37.7; 27.2
90; 100; 90
14542Zhiwei Yang; Chengfeng Zhu; Zijian Li; Yan Liu; Guohua Liu; Yong Cui
Engineering chiral Fe(salen)-based metal-organic frameworks for asymmetric sulfide oxidation
Chem.Commun., 2014, 50, 8775
7115366 CIFC104 H100 Cd2 Fe2 N8 O13F 2 2 219.2468; 54.9054; 64.1439
90; 90; 90
67784Zhiwei Yang; Chengfeng Zhu; Zijian Li; Yan Liu; Guohua Liu; Yong Cui
Engineering chiral Fe(salen)-based metal-organic frameworks for asymmetric sulfide oxidation
Chem.Commun., 2014, 50, 8775
7115367 CIFC57.5 H91 Cu4 N4 Zn4I -4 3 m16.8803; 16.8803; 16.8803
90; 90; 90
4809.9Kerstin Freitag; Hung Banh; Christian Gemel; Rudiger W. Seidel; Samia Kahlal; Jean-Yves Saillard; Roland A. Fischer
Molecular brass: Cu4Zn4, a ligand protected superatom cluster
Chem.Commun., 2014, 50, 8681
7115368 CIFC16 H31 N3 O4P 18.5557; 14.0932; 16.307
77.134; 81.935; 80.958
1881.71Nicola H. Powell; Guy J. Clarkson; Rebecca Notman; Piotr Raubo; Nathaniel G. Martin; Michael Shipman
Synthesis and structure of oxetane containing tripeptide motifs
Chem.Commun., 2014, 50, 8797
7115369 CIFC19.1 H29.4 N3 O4.1P 18.4127; 9.5002; 13.3202
96.096; 104.312; 90.121
1025.26Nicola H. Powell; Guy J. Clarkson; Rebecca Notman; Piotr Raubo; Nathaniel G. Martin; Michael Shipman
Synthesis and structure of oxetane containing tripeptide motifs
Chem.Commun., 2014, 50, 8797
7115370 CIFC89 H105 B Ir2 N7 OP 1 21 111.8882; 23.2366; 15.133
90; 95.97; 90
4157.69Friedrich Angersbach-Bludau; Christopher Schulz; Julia Schoffel; Peter Burger
Syntheses and electronic structures of mu-nitrido bridged pyridine, diimine iridium complexes
Chem.Commun., 2014, 50, 8735
7115371 CIFC54 H60.5 F3 Ir2 N7 O3.75 SC 1 2/c 123.7205; 15.3311; 16.5083
90; 122.479; 90
5064.4Friedrich Angersbach-Bludau; Christopher Schulz; Julia Schoffel; Peter Burger
Syntheses and electronic structures of mu-nitrido bridged pyridine, diimine iridium complexes
Chem.Commun., 2014, 50, 8735
7115372 CIFC54 H62 Ir2 N7 Na OP 1 21/n 110.6929; 26.4273; 16.8108
90; 94.351; 90
4736.78Friedrich Angersbach-Bludau; Christopher Schulz; Julia Schoffel; Peter Burger
Syntheses and electronic structures of mu-nitrido bridged pyridine, diimine iridium complexes
Chem.Commun., 2014, 50, 8735
7115373 CIFC58 H62 F3 Ir2 N9 O3 SP 1 21/c 118.049; 15.45; 20.89
90; 97.103; 90
5780.6Friedrich Angersbach-Bludau; Christopher Schulz; Julia Schoffel; Peter Burger
Syntheses and electronic structures of mu-nitrido bridged pyridine, diimine iridium complexes
Chem.Commun., 2014, 50, 8735
7115374 CIFC26 H22 N2.5 O2F d d 241.923; 11.1; 19.335
90; 90; 90
8997K. C. Gowri Sreedevi; Ajesh P. Thomas; K. H. Aparna; Renuka Pradhan; M. L. P. Reddy; U. Lourderaj; A. Srinivasan
Photoenolization via excited state double proton transfer induces 'turn on' fluorescence in diformyl diaryl dipyrromethane
Chem.Commun., 2014, 50, 8667
7115375 CIFC63 H69 In3 N9 O30.5F d d 233.493; 53.707; 22.036
90; 90; 90
39639Dongmei Wang; Tingting Zhao; Yu Cao; Shuo Yao; Guanghua Li; Qisheng Huo; Yunling Liu
High performance gas adsorption and separation of natural gas in two microporous metal-organic frameworks with ternary building units
Chem.Commun., 2014, 50, 8648
7115376 CIFC54 H43 N3 O24 Zn5C 1 2/c 129.372; 15.784; 19.14
90; 107.16; 90
8478Dongmei Wang; Tingting Zhao; Yu Cao; Shuo Yao; Guanghua Li; Qisheng Huo; Yunling Liu
High performance gas adsorption and separation of natural gas in two microporous metal-organic frameworks with ternary building units
Chem.Commun., 2014, 50, 8648
7115377 CIFC10 H11 Ag2 N5 O4P 1 21/n 110.4687; 12.697; 11.0554
90; 115.122; 90
1330.49Ji Zheng; Ya-Dong Yu; Fang-Fang Liu; Bao-Yu Liu; Gang Wei; Xiao-Chun Huang
Modulation of argentophilic interactions by bridging amine ligands: photoluminescence tuneable by excitation energy or temperature
Chem.Commun., 2014, 50, 9000
7115378 CIFC10 H11 Ag2 N5 O4P 1 21/n 110.4635; 12.5188; 11.0115
90; 115.202; 90
1305.1Ji Zheng; Ya-Dong Yu; Fang-Fang Liu; Bao-Yu Liu; Gang Wei; Xiao-Chun Huang
Modulation of argentophilic interactions by bridging amine ligands: photoluminescence tuneable by excitation energy or temperature
Chem.Commun., 2014, 50, 9000
7115379 CIFC20 H26 Ag4 N10 O10P 1 21/n 16.879; 11.7678; 17.321
90; 92.741; 90
1400.5Ji Zheng; Ya-Dong Yu; Fang-Fang Liu; Bao-Yu Liu; Gang Wei; Xiao-Chun Huang
Modulation of argentophilic interactions by bridging amine ligands: photoluminescence tuneable by excitation energy or temperature
Chem.Commun., 2014, 50, 9000
7115380 CIFC20 H26 Ag4 N10 O10P 1 21/n 16.7585; 11.7522; 17.2702
90; 92.669; 90
1370.24Ji Zheng; Ya-Dong Yu; Fang-Fang Liu; Bao-Yu Liu; Gang Wei; Xiao-Chun Huang
Modulation of argentophilic interactions by bridging amine ligands: photoluminescence tuneable by excitation energy or temperature
Chem.Commun., 2014, 50, 9000
7115381 CIFC24 H26 Ag4 N10 O8P 1 21/c 18.9949; 14.1156; 11.5353
90; 104.168; 90
1420.07Ji Zheng; Ya-Dong Yu; Fang-Fang Liu; Bao-Yu Liu; Gang Wei; Xiao-Chun Huang
Modulation of argentophilic interactions by bridging amine ligands: photoluminescence tuneable by excitation energy or temperature
Chem.Commun., 2014, 50, 9000
7115382 CIFC26 H30 Ag4 N10 O8P 1 21/c 114.2975; 11.9979; 19.3757
90; 109.377; 90
3135.4Ji Zheng; Ya-Dong Yu; Fang-Fang Liu; Bao-Yu Liu; Gang Wei; Xiao-Chun Huang
Modulation of argentophilic interactions by bridging amine ligands: photoluminescence tuneable by excitation energy or temperature
Chem.Commun., 2014, 50, 9000
7115383 CIFC32 H35 Dy N4 O14 ZnP -111.132; 12.522; 13.219
105.888; 91.753; 94.464
1764.3Apoorva Upadhyay; Saurabh Kumar Singh; Chinmoy Das; Ranajit Mondol; Stuart K. Langley; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
Enhancing the effective energy barrier of a Dy(III) SMM using a bridged diamagnetic Zn(II) ion
Chem.Commun., 2014, 50, 8838
7115384 CIFC28 H26 Dy N5 O13A b a 217.654; 54.092; 9.5502
90; 90; 90
9120Apoorva Upadhyay; Saurabh Kumar Singh; Chinmoy Das; Ranajit Mondol; Stuart K. Langley; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
Enhancing the effective energy barrier of a Dy(III) SMM using a bridged diamagnetic Zn(II) ion
Chem.Commun., 2014, 50, 8838
7115385 CIFC12 H30 Na2 O Zn3P 65 2 28.7801; 8.7801; 43.327
90; 90; 120
2892.6L. Zane Miller; Michael Shatruka; D. Tyler McQuade
Alkali metal oxides trapped by diethylzinc
Chem.Commun., 2014, 50, 8937
7115386 CIFC16 H40 K2 O Zn4P 4/n n c9.0272; 9.0272; 14.145
90; 90; 90
1152.7L. Zane Miller; Michael Shatruka; D. Tyler McQuade
Alkali metal oxides trapped by diethylzinc
Chem.Commun., 2014, 50, 8937
7115387 CIFC16 H40 O Rb2 Zn4P 4/n n c9.446; 9.446; 14.199
90; 90; 90
1266.9L. Zane Miller; Michael Shatruka; D. Tyler McQuade
Alkali metal oxides trapped by diethylzinc
Chem.Commun., 2014, 50, 8937
7115388 CIFC19 H19 N O3P -17.949; 9.913; 11.241
96.837; 105.663; 109.836
780.3Kazunari Nakajima; Mai Kitagawa; Yuya Ashida; Yoshihiro Miyake; Yoshiaki Nishibayashi
Synthesis of nitrogen heterocycles via alpha-aminoalkyl radicals generated from alpha-silyl secondary amines under visible light irradiation
Chem.Commun., 2014, 50, 8900
7115389 CIFC26 H15 F N O4 P WP n a 2115.8144; 19.0204; 7.3213
90; 90; 90
2202.2Antonia Loibl; Iris de Krom; Evgeny A. Pidko; Manuela Weber; Jelena Wiecko; Christian Muller
Tuning the electronic effects of aromatic phosphorus heterocycles: an unprecedented phosphinine with significant P(pi)-donor properties
Chem.Commun., 2014, 50, 8842
7115390 CIFC19 H14 N2 O3I b a 216.678; 25.506; 7.5764
90; 90; 90
3222.9Fang-Le Hu; Yin Wei; Min Shi
Phosphine-catalyzed asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters
Chem.Commun., 2014, 50, 8912
7115391 CIFC30 H22 Br Cl2 N3 O6P 21 21 2113.339; 15.3601; 30.918
90; 90; 90
6334.7Fang-Le Hu; Yin Wei; Min Shi
Phosphine-catalyzed asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters
Chem.Commun., 2014, 50, 8912
7115392 CIFC13 H14 N4 O2P 1 21 18.1976; 12.7958; 11.9888
90; 104.227; 90
1218.99Estela Haldon; Eleuterio Alvarez; M. Carmen Nicasio; Pedro J. Perez
1,2,3-Triazoles from carbonyl azides and alkynes: filling the gap
Chem.Commun., 2014, 50, 8978
7115393 CIFC13 H13 Br N4 O2C 1 2/c 128.3878; 5.0616; 18.7871
90; 95.781; 90
2685.7Estela Haldon; Eleuterio Alvarez; M. Carmen Nicasio; Pedro J. Perez
1,2,3-Triazoles from carbonyl azides and alkynes: filling the gap
Chem.Commun., 2014, 50, 8978
7115394 CIFC11 H12 N4 O2 SP 1 21/n 15.2958; 11.8997; 18.8466
90; 93.808; 90
1185.06Estela Haldon; Eleuterio Alvarez; M. Carmen Nicasio; Pedro J. Perez
1,2,3-Triazoles from carbonyl azides and alkynes: filling the gap
Chem.Commun., 2014, 50, 8978
7115395 CIFC9 H14 N4 O3P 1 n 14.7202; 13.9971; 8.1756
90; 92.621; 90
539.59Estela Haldon; Eleuterio Alvarez; M. Carmen Nicasio; Pedro J. Perez
1,2,3-Triazoles from carbonyl azides and alkynes: filling the gap
Chem.Commun., 2014, 50, 8978
7115396 CIFC27 H21 Br N2 O4P 21 21 2110.3254; 10.3246; 26.4259
90; 90; 90
2817.1Tai-Ping Gao; Jun-Bing Lin; Xiu-Qin Hu; Peng-Fei Xu
A catalytic asymmetric hetero-Diels-Alder reaction of olefinic azlactones and isatins: facile access to chiral spirooxindole dihydropyranones
Chem.Commun., 2014, 50, 8934
7115397 CIFC12.33333 H14.33333 Cl N2 O SR -3 :H22.059; 22.059; 14.679
90; 90; 120
6186Hideo Ikota; Takayuki Ishida; Chihiro Tsukano; Yoshiji Takemoto
Synthesis of 3,3-disubstituted indoline-2-thiones catalysed by an N-heterocyclic carbene
Chem.Commun., 2014, 50, 8871
7115398 CIFC4 Ag N3I m a 27.9645; 10.138; 6.1945
90; 90; 90
500.2Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115399 CIFC4 Ag N3I m a 28.0121; 9.646; 6.2169
90; 90; 90
480.5Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115400 CIFC4 Ag N3I m a 28.0667; 9.7791; 6.2784
90; 90; 90
495.27Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115401 CIFC4 Ag N3I m a 28.0636; 9.7766; 6.2791
90; 90; 90
495.01Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115402 CIFC4 Ag N3I m a 28.047; 9.871; 6.261
90; 90; 90
497.3Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115403 CIFC4 Ag N3I m a 28.0584; 9.8752; 6.2692
90; 90; 90
498.89Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115404 CIFC4 Ag N3I m a 28.026; 9.968; 6.2459
90; 90; 90
499.69Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115405 CIFC4 Ag N3I m a 28.028; 9.9637; 6.2461
90; 90; 90
499.62Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115406 CIFC4 Ag N3I m a 28.0174; 10.0853; 6.2353
90; 90; 90
504.17Hodgson, Sarah A.; Adamson, Jasper; Hunt, Sarah J.; Cliffe, Matthew J.; Cairns, Andrew B.; Thompson, Amber L.; Tucker, Matthew G.; Funnell, Nicholas P.; Goodwin, Andrew L.
Negative area compressibility in silver(I) tricyanomethanide.
Chemical communications (Cambridge, England), 2014, 50, 5264-5266
7115407 CIFC15 H18 B F2 N3P 1 21/n 18.3942; 12.6829; 14.0136
90; 95.074; 90
1486.08Bhausaheb Dhokale; Thaksen Jadhav; Shaikh M. Mobin; Rajneesh Misra
Meso enamine substituted BODIPYs
Chem.Commun., 2014, 50, 9119
7115408 CIFC17 H22 B F2 N3P 1 21/c 19.2376; 14.714; 15.929
90; 127.73; 90
1712.4Bhausaheb Dhokale; Thaksen Jadhav; Shaikh M. Mobin; Rajneesh Misra
Meso enamine substituted BODIPYs
Chem.Commun., 2014, 50, 9119
7115409 CIFC17 H22 B F2 N3P 1 21/n 111.1777; 11.3773; 14.4649
90; 109.83; 90
1730.5Bhausaheb Dhokale; Thaksen Jadhav; Shaikh M. Mobin; Rajneesh Misra
Meso enamine substituted BODIPYs
Chem.Commun., 2014, 50, 9119
7115410 CIFC16 H18 B F2 N3P 1 21/c 17.8218; 23.1144; 8.5337
90; 110.867; 90
1441.66Bhausaheb Dhokale; Thaksen Jadhav; Shaikh M. Mobin; Rajneesh Misra
Meso enamine substituted BODIPYs
Chem.Commun., 2014, 50, 9119
7115411 CIFC31 H30 N2 O2 S2P 1 21 18.9302; 16.065; 9.812
90; 111.616; 90
1308.67Pavol Ondrisek; Rino Schwenk; Jan Cvengros
Synthesis of enantiomerically pure Troger's base derivatives via chiral disulfoxides
Chem.Commun., 2014, 50, 9168
7115412 CIFC32 H32 Cl2 N2 O2 S2P 1 21 112.4612; 9.1606; 13.5717
90; 105.879; 90
1490.12Pavol Ondrisek; Rino Schwenk; Jan Cvengros
Synthesis of enantiomerically pure Troger's base derivatives via chiral disulfoxides
Chem.Commun., 2014, 50, 9168
7115413 CIFC17 H16 Br2 N2P 1 21 17.6662; 8.3832; 12.0468
90; 96.193; 90
769.7Pavol Ondrisek; Rino Schwenk; Jan Cvengros
Synthesis of enantiomerically pure Troger's base derivatives via chiral disulfoxides
Chem.Commun., 2014, 50, 9168
7115414 CIFC57 H69 Cu6 N15 O0P -19.3; 15.907; 20.499
90.581; 92.286; 90.567
3029.8Jun-Hao Wang; Mian Li; Ji Zheng; Xiao-Chun Huang; Dan Li
A dual-emitting Cu6-Cu2-Cu6 cluster as a self-calibrated, wide-range luminescent molecular thermometer
Chem.Commun., 2014, 50, 9115
7115415 CIFC57 H69 Cu7 I N15P -19.1825; 16.4791; 23.3979
102.41; 99.703; 99.9
3327.7Jun-Hao Wang; Mian Li; Ji Zheng; Xiao-Chun Huang; Dan Li
A dual-emitting Cu6-Cu2-Cu6 cluster as a self-calibrated, wide-range luminescent molecular thermometer
Chem.Commun., 2014, 50, 9115
7115416 CIFC57 H69 Cu7 I N15 O0P -19.0947; 16.4229; 23.0642
102.321; 99.053; 100.587
3238.2Jun-Hao Wang; Mian Li; Ji Zheng; Xiao-Chun Huang; Dan Li
A dual-emitting Cu6-Cu2-Cu6 cluster as a self-calibrated, wide-range luminescent molecular thermometer
Chem.Commun., 2014, 50, 9115
7115417 CIFC14 H18 Cu2 I2 N2P 1 21/c 116.35; 7.8394; 15.389
90; 110.453; 90
1848.1Jun-Hao Wang; Mian Li; Ji Zheng; Xiao-Chun Huang; Dan Li
A dual-emitting Cu6-Cu2-Cu6 cluster as a self-calibrated, wide-range luminescent molecular thermometer
Chem.Commun., 2014, 50, 9115
7115418 CIFC57 H69 Cu7 I N15P -19.0869; 16.4643; 23.4304
102.936; 100.45; 99.938
3275.6Jun-Hao Wang; Mian Li; Ji Zheng; Xiao-Chun Huang; Dan Li
A dual-emitting Cu6-Cu2-Cu6 cluster as a self-calibrated, wide-range luminescent molecular thermometer
Chem.Commun., 2014, 50, 9115
7115419 CIFC27 H24 Br N O4P 1 21 112.0177; 6.57341; 15.9929
90; 110.393; 90
1184.21Hong-Ping Deng; Lars Eriksson; Kalman J. Szabo
Allylic sp3 C-H borylation of alkenes via allyl-Pd intermediates: an efficient route to allylboronates
Chem.Commun., 2014, 50, 9207
7115426 CIFC19 H17 F N2 O2P b c a7.512; 16.751; 26.703
90; 90; 90
3360Yuanyuan An; Danqing Zheng; Jie Wu
An unexpected copper(II)-catalyzed three-component reaction of quinazoline 3-oxide, alkylidenecyclopropane, and water
Chem.Commun., 2014, 50, 9165
7115427 CIFC30 H30 N4 Ni4 O17P 1 21/c 112.8539; 14.4578; 30.453
90; 96.497; 90
5623Jia Li; Ying Guo; Hong-Ru Fu; Jian Zhang; Rong-Bin Huang; Lan-Sun Zheng; Jun Tao
A spin-canted NiII4-based metal-organic framework with gas sorption properties and high adsorptive selectivity for light hydrocarbons
Chem.Commun., 2014, 50, 9161
7115428 CIFC12 H56 Be N6 O44 W12C 1 2/c 113.1943; 19.4817; 21.0895
90; 105.218; 90
5230.9Alexander V. Anyushin; Anton I. Smolentsev; Dmitry A. Mainichev; Cristian Vicent; Artem L. Gushchin; Maxim N. Sokolov; Vladimir P. Fedin
Synthesis and characterization of a new Keggin anion: [BeW12O40]^6-^
Chem.Commun., 2014, 50, 9083
7115429 CIFC76 H48 N2 S4P -18.23; 14.22; 14.339
78.34; 76.48; 83.47
1594Harapriya Rath; Abhijit Mallick; Tubai Ghosh; Alok Kalita
Aromatic fused heterocyclic [22] macrocycles with NIR absorption
Chem.Commun., 2014, 50, 9094
7115430 CIFC53 H36 N2P -19.4281; 12.024; 21.1941
75.876; 86.942; 74.587
2246Rajneesh Misra; Thaksen Jadhav; Bhausaheb Dhokale; Shaikh M. Mobin
Reversible mechanochromism and enhanced AIE in tetraphenylethene substituted phenanthroimidazoles
Chem.Commun., 2014, 50, 9076
7115431 CIFC54 H35 N3P 1 21/n 19.0367; 11.565; 38.221
90; 94.875; 90
3980Rajneesh Misra; Thaksen Jadhav; Bhausaheb Dhokale; Shaikh M. Mobin
Reversible mechanochromism and enhanced AIE in tetraphenylethene substituted phenanthroimidazoles
Chem.Commun., 2014, 50, 9076
7115434 CIFC68 H140 Mn24 Ni2 O84P -111.579; 16.538; 20.816
104.53; 105.96; 102.44
3532.4Maria Charalambous; Sotiris M. Zartilas; Eleni E. Moushi; Constantina Papatriantafyllopoulou; Manolis J. Manos; Theocharis C. Stamatatos; Shreya Mukherjee; Vassilios Nastopoulos; George Christou; Anastasios J. Tasiopoulos
Discrete and encapsulated molecular grids: homometallic Mn15 and heterometallic Mn24Ni2 aggregates
Chem.Commun., 2014, 50, 9090
7115435 CIFC121.2 H213.8 Mn15 N9.6 O50P -114.6777; 15.9353; 18.1069
72.5265; 86.1971; 84.1738
4015.93Maria Charalambous; Sotiris M. Zartilas; Eleni E. Moushi; Constantina Papatriantafyllopoulou; Manolis J. Manos; Theocharis C. Stamatatos; Shreya Mukherjee; Vassilios Nastopoulos; George Christou; Anastasios J. Tasiopoulos
Discrete and encapsulated molecular grids: homometallic Mn15 and heterometallic Mn24Ni2 aggregates
Chem.Commun., 2014, 50, 9090
7115436 CIFC22 H12 Cl2 N2 OP -17.7221; 9.0481; 13.843
80.021; 85.86; 73.874
914.8Juanjuan Liu; Lanxiang Zhou; Weijian Ye; Cunde Wang
Formal [3+2] cycloaddition of 1-cyanocyclopropane 1-ester with pyridine, quinoline or isoquinoline: a general and efficient strategy for construction of cyanoindolizine skeletons
Chem.Commun., 2014, 50, 9068
7115437 CIFC24 H17 Br Cl N3 OP 21 21 2110.275; 11.4634; 18.344
90; 90; 90
2160.7Juanjuan Liu; Lanxiang Zhou; Weijian Ye; Cunde Wang
Formal [3+2] cycloaddition of 1-cyanocyclopropane 1-ester with pyridine, quinoline or isoquinoline: a general and efficient strategy for construction of cyanoindolizine skeletons
Chem.Commun., 2014, 50, 9068
7115438 CIFC27 H17 Cl N2 OP -110.4826; 10.6458; 10.96
71.68; 73.572; 67.431
1053.7Juanjuan Liu; Lanxiang Zhou; Weijian Ye; Cunde Wang
Formal [3+2] cycloaddition of 1-cyanocyclopropane 1-ester with pyridine, quinoline or isoquinoline: a general and efficient strategy for construction of cyanoindolizine skeletons
Chem.Commun., 2014, 50, 9068
7115439 CIFC22 H13 Cl N2 OC 1 2/c 123.071; 10.7768; 14.3886
90; 102.951; 90
3486.5Juanjuan Liu; Lanxiang Zhou; Weijian Ye; Cunde Wang
Formal [3+2] cycloaddition of 1-cyanocyclopropane 1-ester with pyridine, quinoline or isoquinoline: a general and efficient strategy for construction of cyanoindolizine skeletons
Chem.Commun., 2014, 50, 9068
7115440 CIFC22 H12 Br Cl N2 OP -17.7273; 8.9408; 14.824
76.526; 80.859; 70.826
936.9Juanjuan Liu; Lanxiang Zhou; Weijian Ye; Cunde Wang
Formal [3+2] cycloaddition of 1-cyanocyclopropane 1-ester with pyridine, quinoline or isoquinoline: a general and efficient strategy for construction of cyanoindolizine skeletons
Chem.Commun., 2014, 50, 9068
7115441 CIFC47 H72 O P2P 1 21/n 115.1477; 18.6492; 16.6712
90; 111.408; 90
4384.6Shigekazu Ito; Shunsuke Okabe; Yasuhiro Ueta; Koichi Mikami
Formation of phosphanoxy-substituted phosphaalkenes via sterically promoted cleavage of the P[double bond, length as m-dash]P diphosphene bond
Chem.Commun., 2014, 50, 9204
7115442 CIFC70 H120 Mn6 N2 O33 Sr2P 21 21 2115.29; 18.205; 36.041
90; 90; 90
10032Changhui Chen; Chunxi Zhang; Hongxing Dong; Jingquan Zhao
A synthetic model for the oxygen-evolving complex in Sr2±containing photosystem II
Chem.Commun., 2014, 50, 9263
7115443 CIFC13.846 H13.846 Cl3.692 N0.923 O3.692P 21 21 2110.2677; 22.1493; 23.3892
90; 90; 90
5319.23Nan Ma; Yiwu Yao; Bing-Xin Zhao; Ying Wang; Wen-Cai Ye; Sheng Jiang
Total synthesis of securinega alkaloids (‒)-norsecurinine, (‒)-niruroidine and (‒)-flueggine A
Chem.Commun., 2014, 50, 9284
7115444 CIFC12 H15 N O3P 21 21 215.80812; 8.2156; 21.4801
90; 90; 90
1024.97Nan Ma; Yiwu Yao; Bing-Xin Zhao; Ying Wang; Wen-Cai Ye; Sheng Jiang
Total synthesis of securinega alkaloids (‒)-norsecurinine, (‒)-niruroidine and (‒)-flueggine A
Chem.Commun., 2014, 50, 9284
7115445 CIFC28 H24 B F4 O2 PP -19.794; 11.579; 12.366
72.176; 86.868; 76.456
1297.7Kyle D. Reichl; Alexander T. Radosevich
A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts
Chem.Commun., 2014, 50, 9302
7115446 CIFC34 H26 B F4 PP c a 2120.732; 19.775; 13.7739
90; 90; 90
5647Kyle D. Reichl; Alexander T. Radosevich
A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts
Chem.Commun., 2014, 50, 9302
7115447 CIFC24 H16P n a 2117.56; 17.03; 5.895
90; 90; 90
1763Kyle D. Reichl; Alexander T. Radosevich
A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts
Chem.Commun., 2014, 50, 9302
7115448 CIFC27 H22P n a 2118.887; 14.683; 7.344
90; 90; 90
2036.6Kyle D. Reichl; Alexander T. Radosevich
A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts
Chem.Commun., 2014, 50, 9302
7115449 CIFC34 H26 B F4 PP 1 21/n 110.743; 10.216; 26.175
90; 94.556; 90
2864Kyle D. Reichl; Alexander T. Radosevich
A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts
Chem.Commun., 2014, 50, 9302
7115450 CIFC15 H12 Br F N2 O4P 15.6907; 7.4227; 9.3653
108.137; 100.781; 90.415
368.39Jacek Kwiatkowski; Yixin Lu
Asymmetric Michael addition of alpha-fluoro-alpha-nitroalkanes to nitroolefins: facile preparation of fluorinated amines and tetrahydropyrimidines
Chem.Commun., 2014, 50, 9313
7115451 CIFC15 H24 Fe2 O5 P2 S2P -110.158; 12.393; 17.576
92.45; 92.727; 95.945
2195.7Dehua Zheng; Mei Wang; Lin Chen; Ning Wang; Minglun Cheng; Licheng Sun
The influence of a S-to-S bridge in diiron dithiolate models on the oxidation reaction: a mimic of the Hairox state of [FeFe]-hydrogenases
Chem.Commun., 2014, 50, 9255
7115452 CIFC13 H15 Fe2 O6 P S2P -18.9553; 10.2137; 11.056
105.403; 93.507; 112.215
887.6Dehua Zheng; Mei Wang; Lin Chen; Ning Wang; Minglun Cheng; Licheng Sun
The influence of a S-to-S bridge in diiron dithiolate models on the oxidation reaction: a mimic of the Hairox state of [FeFe]-hydrogenases
Chem.Commun., 2014, 50, 9255
7115453 CIFC48 H39 B Cl2 F24 Fe2 O6 P2 S2P 1 21/c 112.6932; 18.5417; 25.8275
90; 91.44; 90
6076.7Dehua Zheng; Mei Wang; Lin Chen; Ning Wang; Minglun Cheng; Licheng Sun
The influence of a S-to-S bridge in diiron dithiolate models on the oxidation reaction: a mimic of the Hairox state of [FeFe]-hydrogenases
Chem.Commun., 2014, 50, 9255
7115454 CIFC37 H34 N2 O4P -18.978; 10.664; 15.89
104.914; 94.754; 100.9
1429.6Daobin Yang; Qianqian Yang; Lin Yang; Qian Luo; Yao Chen; Youqin Zhu; Yan Huang; Zhiyun Lu; Suling Zhao
A low bandgap asymmetrical squaraine for high-performance solution-processed small molecule organic solar cells
Chem.Commun., 2014, 50, 9346
7115455 CIFC38 H36 N2 O4P 1 21/c 114.082; 14.0978; 16.5453
90; 112.969; 90
3024.2Daobin Yang; Qianqian Yang; Lin Yang; Qian Luo; Yao Chen; Youqin Zhu; Yan Huang; Zhiyun Lu; Suling Zhao
A low bandgap asymmetrical squaraine for high-performance solution-processed small molecule organic solar cells
Chem.Commun., 2014, 50, 9346
7115456 CIFC60 H44 N6 O RuP -112.84; 13.714; 16.694
110.48; 92.56; 113.89
2457.6Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115457 CIFC53 H34 N4 O RuP -110.203; 13.884; 14.858
77.68; 70.21; 87.94
1933.3Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115458 CIFC67 H39 N3 O10 Ru5P -110.468; 13.376; 22.516
96.81; 100.38; 112.03
2814Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115459 CIFC59 H31 N3 Ni O9 Ru4P -19.461; 12.465; 22.653
98.26; 100.04; 105.21
2487.5Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115460 CIFC59 H31 N3 O9 Pd Ru4P -19.344; 12.595; 22.998
76.21; 79.06; 73.79
2501.9Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115461 CIFC59 H31 N3 O9 Pt Ru4P -110.192; 13.967; 20.939
80.13; 86.41; 68.98
2741.2Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115462 CIFC50 H31 N3 PtP -110.315; 11.935; 14.841
103.07; 97.56; 102.32
1707.4Michal J. Bialek; Lechoslaw Latos-Grazynski
Merging of inner and outer ruthenium organometallic coordination motifs within an azuliporphyrin framework
Chem.Commun., 2014, 50, 9270
7115463 CIFC13 H8 Cl N O3P 21 21 217.9194; 8.8519; 17.343
90; 90; 90
1215.77Amit Kumar; Abhimanyu Yadav; Ajay Verma; Sadhan Jana; Moh. Sattar; Shailesh Kumar; Ch. Durga Prasad; Sangit Kumar
Chemoselective arylation of phenols with bromo-nitroarenes: synthesis of nitro-biaryl-ols and their conversion into benzofurans and carbazoles
Chem.Commun., 2014, 50, 9481
7115464 CIFC13 H10 Br N O3P 21 21 217.9842; 8.9505; 17.463
90; 90; 90
1248Amit Kumar; Abhimanyu Yadav; Ajay Verma; Sadhan Jana; Moh. Sattar; Shailesh Kumar; Ch. Durga Prasad; Sangit Kumar
Chemoselective arylation of phenols with bromo-nitroarenes: synthesis of nitro-biaryl-ols and their conversion into benzofurans and carbazoles
Chem.Commun., 2014, 50, 9481
7115465 CIFC16 H17 N O3P -16.8419; 8.434; 12.6395
82.195; 79.847; 85.04
709.82Amit Kumar; Abhimanyu Yadav; Ajay Verma; Sadhan Jana; Moh. Sattar; Shailesh Kumar; Ch. Durga Prasad; Sangit Kumar
Chemoselective arylation of phenols with bromo-nitroarenes: synthesis of nitro-biaryl-ols and their conversion into benzofurans and carbazoles
Chem.Commun., 2014, 50, 9481
7115466 CIFC13 H11 N O3P c a 2114.4397; 10.6268; 7.2172
90; 90; 90
1107.46Amit Kumar; Abhimanyu Yadav; Ajay Verma; Sadhan Jana; Moh. Sattar; Shailesh Kumar; Ch. Durga Prasad; Sangit Kumar
Chemoselective arylation of phenols with bromo-nitroarenes: synthesis of nitro-biaryl-ols and their conversion into benzofurans and carbazoles
Chem.Commun., 2014, 50, 9481
7115467 CIFC85 H116 Cl2 N12 O3R 3 :H25.629; 25.629; 11.1848
90; 90; 120
6362.4Marc A. Little; Samantha Y. Chong; Marc Schmidtmann; Tom Hasell; Andrew I. Cooper
Guest control of structure in porous organic cages
Chem.Commun., 2014, 50, 9465
7115468 CIFC72 H84 N27P 325.2558; 25.2558; 11.0068
90; 90; 120
6080.1Marc A. Little; Samantha Y. Chong; Marc Schmidtmann; Tom Hasell; Andrew I. Cooper
Guest control of structure in porous organic cages
Chem.Commun., 2014, 50, 9465
7115469 CIFC72 H84 N12P 325.1483; 25.1483; 11.0268
90; 90; 120
6039.5Marc A. Little; Samantha Y. Chong; Marc Schmidtmann; Tom Hasell; Andrew I. Cooper
Guest control of structure in porous organic cages
Chem.Commun., 2014, 50, 9465
7115470 CIFC72 H84 N12P 325.2084; 25.2084; 11.0674
90; 90; 120
6090.7Marc A. Little; Samantha Y. Chong; Marc Schmidtmann; Tom Hasell; Andrew I. Cooper
Guest control of structure in porous organic cages
Chem.Commun., 2014, 50, 9465
7115471 CIFC66 H72 N12F 41 3 224.242; 24.242; 24.242
90; 90; 90
14246Marc A. Little; Samantha Y. Chong; Marc Schmidtmann; Tom Hasell; Andrew I. Cooper
Guest control of structure in porous organic cages
Chem.Commun., 2014, 50, 9465
7115472 CIFC90 H106 N12 O2P 21 21 2116.7488; 19.2538; 25.342
90; 90; 90
8172.2Marc A. Little; Samantha Y. Chong; Marc Schmidtmann; Tom Hasell; Andrew I. Cooper
Guest control of structure in porous organic cages
Chem.Commun., 2014, 50, 9465
7115473 CIFC78 H82 Cl4 Fe O4 P4P 1 21/c 117.1018; 15.8815; 26.2016
90; 90.618; 90
7116Matthieu Beauperin; Radomyr Smaliy; Helene Cattey; Philippe Meunier; Jun Ou; Patrick H. Toy; Jean-Cyrille Hierso
Modular functionalized polyphosphines for supported materials: previously unobserved 31P-NMR 'through-space' ABCD spin systems and heterogeneous palladium-catalysed C-C and C-H arylation
Chem.Commun., 2014, 50, 9505
7115474 CIFC70 H66 Fe P4P 1 21/n 112.146; 26.8418; 19.2035
90; 106.827; 90
5992.67Matthieu Beauperin; Radomyr Smaliy; Helene Cattey; Philippe Meunier; Jun Ou; Patrick H. Toy; Jean-Cyrille Hierso
Modular functionalized polyphosphines for supported materials: previously unobserved 31P-NMR 'through-space' ABCD spin systems and heterogeneous palladium-catalysed C-C and C-H arylation
Chem.Commun., 2014, 50, 9505
7115475 CIFC29 H35 Al F N3P n m a15.11825; 19.66971; 9.20725
90; 90; 90
2737.97Adi E. Nako; Sarah J. Gates; Nicole Schadel; Andrew J. P. White; Mark R. Crimmin
Yttrium-catalysed dehydrocoupling of alanes with amines
Chem.Commun., 2014, 50, 9536
7115476 CIFC33 H44 Al F2 N5P 1 21/c 19.13917; 15.5779; 22.9215
90; 94.3724; 90
3253.82Adi E. Nako; Sarah J. Gates; Nicole Schadel; Andrew J. P. White; Mark R. Crimmin
Yttrium-catalysed dehydrocoupling of alanes with amines
Chem.Commun., 2014, 50, 9536
7115477 CIFC38.5 H52 Al N3P 1 21/c 110.816; 19.4921; 16.6321
90; 90.876; 90
3506.1Adi E. Nako; Sarah J. Gates; Nicole Schadel; Andrew J. P. White; Mark R. Crimmin
Yttrium-catalysed dehydrocoupling of alanes with amines
Chem.Commun., 2014, 50, 9536
7115478 CIFC106 H136 F12 N9 O12.5 P2P -120.542; 23.791; 24.599
91.402; 95.326; 115.533
10773Eleanor A. Wilson; Nicolaas A. Vermeulen; Paul R. McGonigal; Alyssa-Jennifer Avestro; Amy A. Sarjeant; Charlotte L. Stern; J. Fraser Stoddart
Formation of a hetero[3]rotaxane by a dynamic component-swapping strategy
Chem.Commun., 2014, 50, 9665
7115479 CIFC105 H127 F16 N11 O10 P2P -117.5877; 18.0515; 19.1109
73.981; 64.138; 88.09
5221.1Eleanor A. Wilson; Nicolaas A. Vermeulen; Paul R. McGonigal; Alyssa-Jennifer Avestro; Amy A. Sarjeant; Charlotte L. Stern; J. Fraser Stoddart
Formation of a hetero[3]rotaxane by a dynamic component-swapping strategy
Chem.Commun., 2014, 50, 9665
7115480 CIFC15 H17 N3 O2P 1 21 17.0231; 10.3536; 9.2156
90; 93.182; 90
669.07Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115481 CIFC10 H13 N3 O3P 1 21 17.7486; 7.2; 8.8891
90; 98.796; 90
490.09Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115482 CIFC16 H19 N3 O2P 21 21 217.9124; 9.5931; 19.4561
90; 90; 90
1476.8Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115483 CIFC16 H21 N3 O3C 1 2 110.6284; 11.6932; 25.7411
90; 101.369; 90
3136.3Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115484 CIFC18 H22 N4 O6P 21 21 217.9428; 10.4945; 21.4599
90; 90; 90
1788.81Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115485 CIFC17 H22 N4 O5P 1 21 18.3044; 10.8929; 9.6338
90; 90.269; 90
871.45Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115486 CIFC15 H18 N6 O2P 1 21 17.9768; 24.4818; 8.0015
90; 97.823; 90
1548.04Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115487 CIFC16 H18 N4 O2P 21 21 217.6663; 13.8258; 14.6694
90; 90; 90
1554.85Pierre Regenass; Jean-Francois Margathe; Andre Mann; Jean Suffert; Marcel Hibert; Nicolas Girard; Dominique Bonnet
Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process
Chem.Commun., 2014, 50, 9657
7115488 CIFC22 H27 Cl2 O P RuP 1 21/c 18.9441; 14.5843; 16.6608
90; 96.085; 90
2161.05Eder Tomas-Mendivil; Francisco J. Suarez; Josefina Diez; Victorio Cadierno
An efficient ruthenium(IV) catalyst for the selective hydration of nitriles to amides in water under mild conditions
Chem.Commun., 2014, 50, 9661
7115489 CIFC19 H25 N O8P 21 21 219.7254; 9.9683; 20.395
90; 90; 90
1977.2Minghao Feng; Xuefeng Jiang
Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products
Chem.Commun., 2014, 50, 9690
7115490 CIFC19 H25 N O8P 15.0916; 9.9171; 10.6705
81.115; 77.646; 87.407
519.96Minghao Feng; Xuefeng Jiang
Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products
Chem.Commun., 2014, 50, 9690
7115491 CIFC20 H25 N O5P 1 21 19.1672; 7.7813; 12.998
90; 99.487; 90
914.5Minghao Feng; Xuefeng Jiang
Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products
Chem.Commun., 2014, 50, 9690
7115492 CIFC21 H17 N O3P 1 21 110.2758; 8.6059; 10.5383
90; 118.016; 90
822.72Xue-Qiang Chu; Hua Meng; You Zi; Xiao-Ping Xu; Shun-Jun Ji
Metal-free oxidative direct C(sp3)-H bond functionalization of ethers with alpha,alpha-diaryl allylic alcohols
Chem.Commun., 2014, 50, 9718
7115493 CIFC49 H69 Cl3 F6 N6 O9P 21 21 2119.7038; 23.9063; 24.8954
90; 90; 90
11726.9Joonil Cho; Kyohei Sawaki; Shinya Hanashima; Yoshiki Yamaguchi; Motoo Shiro; Kazuhiko Saigo; Yasuhiro Ishida
Stabilization of beta-peptide helices by direct attachment of trifluoromethyl groups to peptide backbones
Chem.Commun., 2014, 50, 9855
7115494 CIFC49.2 H55.8 Cl N4 RhP -112.5336; 13.353; 15.0479
61.684; 87.181; 79.894
2181Eric C. Keske; Brandon D. Moore; Olena V. Zenkina; Ruiyao Wang; Gabriele Schatte; Cathleen M. Crudden
Highly selective directed arylation reactions via back-to-back dehydrogenative C-H borylation/arylation reactions
Chem.Commun., 2014, 50, 9883
7115495 CIFC19 H24 B N O2P 1 21/c 110.0448; 13.1778; 13.6491
90; 96.075; 90
1796.6Eric C. Keske; Brandon D. Moore; Olena V. Zenkina; Ruiyao Wang; Gabriele Schatte; Cathleen M. Crudden
Highly selective directed arylation reactions via back-to-back dehydrogenative C-H borylation/arylation reactions
Chem.Commun., 2014, 50, 9883
7115496 CIFC94.5 H14 Pr S5P 1 21/n 111.325; 21.95; 20.931
90; 101.373; 90
5100.9Qin Zhou; Hui Li; Yongfu Lian; Mitsuaki Suzuki; Lipiao Bao; Wenting Cai,c; Weiwei Wang; Shigeru Nagase; Xing Lu; Takeshi Akasaka
Regioselective synthesis and molecular structure of the first derivative of praseodymium-containing metallofullerenes
Chem.Commun., 2014, 50, 9876
7115497 CIFC19 H15 N3 O3C 1 2/c 118.3707; 6.8494; 24.489
90; 91.718; 90
3080Feng-Cheng Jia; Cheng Xu; Qun Cai; An-Xin Wu
An integration of condensation/Ullmann-type coupling/bicyclization sequences: copper-catalyzed three-component direct synthesis of [1,2,4]triazolo[1,5-b]isoquinolin-5(1H)-ones
Chem.Commun., 2014, 50, 9914
7115498 CIFC130 H130 Cl N10 O4P -114.1468; 14.5133; 16.7542
103.78; 102.619; 99.907
3167.8Brandon E. Hirsch; Semin Lee; Bo Qiao; Chun-Hsing Chen; Kevin P. McDonald; Steven L. Tait; Amar H. Flood
Anion-induced dimerization of 5-fold symmetric cyanostars in 3D crystalline solids and 2D self-assembled crystals
Chem.Commun., 2014, 50, 9827
7115499 CIFC14 H14 N2 O4 SP -17.277; 9.1288; 11.6854
92.665; 97.218; 107.79
730.3Ying-Xiu Li; Lian-Hua Li; Yan-Fang Yang; Hui-Liang Hua; Xiao-Biao Yan; Lian-Biao Zhao; Jin-Bang Zhang; Fa-Jin Ji; Yong-Min Liang
Direct oxidative nitration of aromatic sulfonamides under mild conditions
Chem.Commun., 2014, 50, 9936
7115500 CIFC30 H22 OP 1 21/n 110.7885; 8.7362; 22.4105
90; 91.123; 90
2111.8Seetharaman Manojveer; Rengarajan Balamurugan
A facile access to substituted benzo[a]fluorenes from o-alkynylbenzaldehydes via in situ formed acetals
Chem.Commun., 2014, 50, 9925
7115501 CIFC27 H35 N O SiP 1 21/c 111.569; 9.0333; 46.939
90; 95.9944; 90
4878.6Chao Feng; Daming Feng; Teck-Peng Loh
Rhodium(III)-catalyzed olefinic C-H alkynylation of enamides at room temperature
Chem.Commun., 2014, 50, 9865
7115502 CIFC37 H27 F3 N P PdP 1 21/n 118.5049; 8.9306; 19.6878
90; 111.881; 90
3019.2Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb
[Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)]
Chem.Commun., 2014, 50, 9859
7115503 CIFC36 H26 F3 N2 P PdP -19.9041; 12.3289; 13.1446
92.202; 110.621; 102.448
1455.37Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb
[Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)]
Chem.Commun., 2014, 50, 9859
7115504 CIFC50 H38 F6 O3 P2 Pd2P -111.9714; 12.3041; 16.0441
67.975; 88.863; 86.969
2187.72Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb
[Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)]
Chem.Commun., 2014, 50, 9859
7115505 CIFC42 H32 Cl F3 P2 PdP b c a12.1168; 23.2879; 24.9924
90; 90; 90
7052.2Anant R. Kapdi; Gopal Dhangar; Jose Luis Serrano; Jose Perez; Luis Garcia; Ian J. S. Fairlamb
[Pd(C[logical and]N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C[logical and]N)(2,4,6-F3C6H2)(PPh3)]
Chem.Commun., 2014, 50, 9859
7115506 CIFC16 H12 O2P 1 21/c 114.927; 6.57; 13.515
90; 116.131; 90
1189.9Jianming Liu; Xin Zhang; Lijun Shi; Muwen Liu; Yuanyuan Yue; Fuwei Li; Kelei Zhuo
Base-promoted synthesis of coumarins from salicylaldehydes and aryl-substituted 1,1-dibromo-1-alkenes under transition-metal-free conditions
Chem.Commun., 2014, 50, 9887
7115507 CIFC21 H35 Cr N2 O Si2C 1 2/m 113.073; 15.574; 12.961
90; 118.861; 90
2311.1Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115508 CIFC21 H31 Cl Cr N2P b n a13.5642; 16.8668; 18.294
90; 90; 90
4185.4Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115509 CIFC23 H19 Cl Cr N2P -110.747; 12.676; 16.141
90.42; 107.496; 110.92
1942.6Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115510 CIFC27 H42 Cr N3 Si2P 1 21/n 110.5631; 19.238; 14.5072
90; 111.307; 90
2746.5Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115511 CIFC26 H38 Cr N3 Si2P 1 21/c 19.436; 26.567; 11.327
90; 108.782; 90
2688.3Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115512 CIFC31 H46 Cr N3C 1 2/m 115.964; 13.0182; 14.345
90; 113.436; 90
2735.3Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115513 CIFC34 H48 Cr N4P -112.1837; 12.1849; 12.4184
106.399; 91.635; 113.395
1602.36Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115514 CIFC28 H39 Cr N3 O2 SP b c a19.539; 9.9443; 27.28
90; 90; 90
5300.5Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115515 CIFC32 H51 Cr N3 O2 S Si2P 1 21/n 115.985; 11.686; 19.444
90; 110.836; 90
3394.6Wen Zhou; Brian O. Patrick; Kevin M. Smith
Influence of redox non-innocent phenylenediamido ligands on chromium imido hydrogen-atom abstraction reactivity
Chem.Commun., 2014, 50, 9958
7115516 CIFC44 H41 B F15 O PP 1 21 111.5255; 14.8611; 11.8913
90; 92.265; 90
2035.17Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115517 CIFC28 H34 F3 O3 P SP 1 21/n 112.3858; 10.4816; 21.683
90; 93.545; 90
2809.6Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115518 CIFC34 H38 F5 O3 P SP -18.2485; 9.5183; 22.078
88.372; 86.027; 73.088
1654.37Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115519 CIFC13 H28 F3 O4 P SP 1 21/n 19.0615; 15.507; 13.509
90; 90.58; 90
1898.14Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115520 CIFC23 H32 F3 O4 P SP 21 21 218.9375; 16.5265; 16.7035
90; 90; 90
2467.2Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115521 CIFC13 H26 F3 O4 P SP 21 21 218.1984; 14.7753; 15.114
90; 90; 90
1830.82Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115522 CIFC32 H26 F3 O3 P SC 1 c 110.6205; 16.669; 15.7534
90; 92.271; 90
2786.7Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115523 CIFC32 H38 F3 O3 P SP 1 21/c 19.7033; 17.8716; 16.8564
90; 93.436; 90
2917.87Michael H. Holthausen; Tayseer Mahdi; Christoph Schlepphorst; Lindsay J. Hounjet; Jan J. Weigand; Douglas W. Stephan
Frustrated Lewis pair-mediated C-O or C-H bond activation of ethers
Chem.Commun., 2014, 50, 10038
7115524 CIFC24 H26 Br N3 O2P 21 21 2110.78; 13.453; 15.304
90; 90; 90
2219.4Yu Tan; Han-Lin Luan; Hua Lin; Xing-Wen Sun; Xiao-Di Yang; Han-Qing Dong; Guo-Qiang Lin
One-pot enantioselective construction of indoloquinolizidine derivatives bearing five contiguous stereocenters using aliphatic aldehydes, nitroethylenes, and tryptamine
Chem.Commun., 2014, 50, 10027
7115525 CIFC28 H35 N3 O2P 1 21 19.784; 8.872; 14.497
90; 90; 90
1258.4Yu Tan; Han-Lin Luan; Hua Lin; Xing-Wen Sun; Xiao-Di Yang; Han-Qing Dong; Guo-Qiang Lin
One-pot enantioselective construction of indoloquinolizidine derivatives bearing five contiguous stereocenters using aliphatic aldehydes, nitroethylenes, and tryptamine
Chem.Commun., 2014, 50, 10027
7115526 CIFC23 H13 N O2P 1 21/m 19.638; 7.105; 11.862
90; 95.858; 90
808Shivani Mahajan; Sadhika Khullar; Sanjay K. Mandal; Inder Pal Singh
A one-pot, three-component reaction for the synthesis of novel 7-arylbenzo[c]acridine-5,6-diones
Chem.Commun., 2014, 50, 10078
7115527 CIFC90 H122 N12 O15 SiP 1 21/n 116.9924; 27.8784; 26.0023
90; 97.315; 90
12217.6Mayumi Kudo; Victor Maurizot; Hyuma Masu; Aya Tanatani; Ivan Huc
Structural elucidation of foldamers with no long range conformational order
Chem.Commun., 2014, 50, 10090
7115528 CIFC41 H40 Ga Mo N2 O5P b c n17.1431; 15.7892; 14.4285
90; 90; 90
3905.4Igor L. Fedushkin; Vladimir G. Sokolov; Alexander V. Piskunov; Valentine M. Makarov; Eugeny V. Baranov; Gleb A. Abakumov
Adaptive behavior of a redox-active gallium carbenoid in complexes with molybdenum
Chem.Commun., 2014, 50, 10108
7115529 CIFC44 H45 Ga Mo N2 O3P 1 21 18.82154; 38.0697; 11.69917
90; 97.2432; 90
3897.62Igor L. Fedushkin; Vladimir G. Sokolov; Alexander V. Piskunov; Valentine M. Makarov; Eugeny V. Baranov; Gleb A. Abakumov
Adaptive behavior of a redox-active gallium carbenoid in complexes with molybdenum
Chem.Commun., 2014, 50, 10108
7115530 CIFC104 H118 Ga2 Mo2 N4 Na2 O14P -112.162; 12.7895; 16.926
72.066; 83.271; 85.462
2485Igor L. Fedushkin; Vladimir G. Sokolov; Alexander V. Piskunov; Valentine M. Makarov; Eugeny V. Baranov; Gleb A. Abakumov
Adaptive behavior of a redox-active gallium carbenoid in complexes with molybdenum
Chem.Commun., 2014, 50, 10108
7115531 CIFC25 H33 B O7P -19.5236; 11.7389; 12.5461
62.68; 84.635; 81.559
1232.12Alicia Martos-Redruejo; Ruth Lopez-Duran; Elena Bunuel; Diego J. Cardenas
Ligand-controlled divergent formation of alkenyl- or allylboronates catalyzed by Pd, and synthetic applications
Chem.Commun., 2014, 50, 10094
7115532 CIFC27 H33 B O6 S2P 1 21/c 18.1024; 13.4762; 25.6608
90; 96.518; 90
2783.78Alicia Martos-Redruejo; Ruth Lopez-Duran; Elena Bunuel; Diego J. Cardenas
Ligand-controlled divergent formation of alkenyl- or allylboronates catalyzed by Pd, and synthetic applications
Chem.Commun., 2014, 50, 10094
7115533 CIFC22 H23 N2 O2 SP b c a12.1138; 15.4374; 22.576
90; 90; 90
4221.8Alicia Martos-Redruejo; Ruth Lopez-Duran; Elena Bunuel; Diego J. Cardenas
Ligand-controlled divergent formation of alkenyl- or allylboronates catalyzed by Pd, and synthetic applications
Chem.Commun., 2014, 50, 10094
7115534 CIFC51 H41 F6 N6 O8 Os PP -19.349; 14.949; 20.583
106.442; 90.995; 94.554
2747.9Hai-Jing Nie; Jiang-Yang Shao; Chang-Jiang Yao; Yu-Wu Zhong
Organic-inorganic mixed-valence systems with strongly-coupled triarylamine and cyclometalated osmium
Chem.Commun., 2014, 50, 10082
7115535 CIFC43 H52 O4P -110.0808; 12.8064; 15.1154
89.88; 75.473; 75.26
1822.85Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes
Chem.Commun., 2014, 50, 10112
7115536 CIFC161 H182 Cl2 O16P 1 21/c 113.22632; 25.83704; 20.88126
90; 99.786; 90
7031.9Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes
Chem.Commun., 2014, 50, 10112
7115537 CIFC47 H52 N0 O4P -112.3671; 12.635; 13.8467
77.854; 63.909; 80.759
1894Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes
Chem.Commun., 2014, 50, 10112
7115538 CIFC43 H50 O4P -19.8496; 12.97; 14.9932
89.965; 77.36; 74.04
1793.29Petr Slavik; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes
Chem.Commun., 2014, 50, 10112
7115539 CIFC44 H52 N8 O14 Pd4P 1 21/c 17.9571; 23.6001; 13.0293
90; 92.124; 90
2445.07Marina Juribasic; Krunoslav Uzarevic; Davor Gracin; Manda Curic
Mechanochemical C-H bond activation: rapid and regioselective double cyclopalladation monitored by in situ Raman spectroscopy
Chem.Commun., 2014, 50, 10287
7115540 CIFC36.5 H42.5 N9.5 O9.5 Pd2C 1 c 134.577; 16.50703; 14.29901
90; 97.1631; 90
8097.66Marina Juribasic; Krunoslav Uzarevic; Davor Gracin; Manda Curic
Mechanochemical C-H bond activation: rapid and regioselective double cyclopalladation monitored by in situ Raman spectroscopy
Chem.Commun., 2014, 50, 10287
7115541 CIFC16 H20 N2 O2P 1 21 16.1563; 8.2068; 14.895
90; 100.888; 90
739Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere
Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach
Chem.Commun., 2014, 50, 10218
7115542 CIFC16 H19 Br N2 O2P 1 21 16.137; 8.934; 14.27
90; 99.976; 90
770.6Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere
Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach
Chem.Commun., 2014, 50, 10218
7115543 CIFC14 H16 N2 O2P 1 21 15.8127; 9.5156; 11.5873
90; 103.442; 90
623.35Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere
Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach
Chem.Commun., 2014, 50, 10218
7115544 CIFC20 H19 Br N2 O2P b c a6.56; 16.644; 33.009
90; 90; 90
3604Etienne Pair; Christophe Berini; Romain Noel; Morgane Sanselme; Vincent Levacher; Jean-Francois Briere
Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach
Chem.Commun., 2014, 50, 10218
7115549 CIFC20 H12 N2P 21 21 213.88126; 11.643; 29.5312
90; 90; 90
1334.5Youhei Takeda; Masato Okazaki; Satoshi Minakata
Oxidative skeletal rearrangement of 1,1'-binaphthalene-2,2'-diamines (BINAMs) via C-C bond cleavage and nitrogen migration: a versatile synthesis of U-shaped azaacenes
Chem.Commun., 2014, 50, 10291
7115550 CIFC15 H13 F5 N4 O4 SP 1 21/c 19.459; 22.4257; 9.0101
90; 115.656; 90
1722.83Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115551 CIFC22 H18 Cl F6 N5 O2P b c a21.4875; 20.5465; 21.5438
90; 90; 90
9511.4Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115552 CIFC16 H20 F3 N O4C 1 2/c 121.291; 11.5227; 14.4085
90; 105.162; 90
3411.8Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115553 CIFC10 H6 F3 NP 21 21 214.7643; 12.7324; 13.8685
90; 90; 90
841.28Anton Lishchynskyi; Guillaume Berthon; Vladimir V. Grushin
Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media
Chem.Commun., 2014, 50, 10237
7115554 CIFC87 H88 F12 N4 O18 P2P 1 21/c 114.3256; 36.543; 19.3027
90; 108.61; 90
9576.6Wei-Bo Hu; Hong-Mei Yang; Wen-Jing Hu; Ming-Liang Ma; Xiao-Li Zhao; Xian-Qiang Mi; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen
A pillar[5]arene and crown ether fused bicyclic host: synthesis, guest discrimination and simultaneous binding of two guests with different shapes, sizes and electronic constitutions
Chem.Commun., 2014, 50, 10460
7115555 CIFC16 H18 N2 O3P -16.2955; 9.3559; 12.975
80.69; 89.5; 75.05
728.2Shaoxia Lin; Ling Li; Fushun Liang; Qun Liu
DABCO-catalyzed ring opening of activated cyclopropanes and recyclization leading to gamma-lactams with an all-carbon quaternary center
Chem.Commun., 2014, 50, 10491
7115557 CIFC48 H102 N12 O6 Zr3P 1 21/c 123.4504; 13.3481; 20.7646
90; 103.285; 90
6325.76Adam C. Lamb; Zheng Lu; Zi-Ling Xue
Reactions of zirconium amide amidinates with dioxygen. Observation of an unusual peroxo intermediate in the formation of oxo compounds
Chem.Commun., 2014, 50, 10517
7115558 CIFC16 H18 Br N O4P 1 21 17.96; 6.2115; 17.0041
90; 98.216; 90
832.11Yi-ning Xuan; Zhen-yu Chen; Ming Yan
An organocatalytic cascade reaction of 2-nitrocyclohexanone and alpha,beta-unsaturated aldehydes with unusual regioselectivity
Chem.Commun., 2014, 50, 10471
7115559 CIFC168 H217 F24 N7 O40 P4P -112.6852; 17.3581; 21.7669
104.59; 100.42; 95.616
4509.7Yujuan Zhou; Zhengtao Li; Xiaodong Chi; Connor Thompson; Yong Yao
Formation of a [2]pseudorotaxane based on a pillar[5]arene and a rigid guest in solution and in the solid state
Chem.Commun., 2014, 50, 10482
7115560 CIFC19 H17 N OP -17.5607; 9.6755; 11.352
107.554; 102.789; 103.85
729.07Anupal Gogoi; Anju Modi; Srimanta Guin; Saroj Kumar Rout; Debapratim Das; Bhisma K. Patel
A metal free domino synthesis of 3-aroylindoles via two sp3 C-H activation
Chem.Commun., 2014, 50, 10445
7115561 CIFC22 H20 Eu N5 O10P -19.5509; 11.2004; 12.8518
66.27; 76.414; 80.581
1219.66Jinlei Chen; Fei-Yan Yi; Hong Yu; Shihui Jiao; Guangsheng Pang; Zhong-Ming Sun
Fast response and highly selective sensing of amine vapors using a luminescent coordination polymer
Chem.Commun., 2014, 50, 10506
7115562 CIFC275 H308 Cl6 I10 Ir4 N20 O25P -114.9997; 20.6925; 26.1024
105.607; 100.893; 99.749
7451.9Haohua Huo; Chen Fu; Chuanyong Wang; Klaus Harms; Eric Meggers
Metal-templated enantioselective enamine/H-bonding dual activation catalysis
Chem.Commun., 2014, 50, 10409
7115563 CIFC27 H31 Br2 N O4 S SiP 1 21/a 118.9903; 12.146; 26.2415
90; 108.147; 90
5751.7Tomoya Miura; Takayuki Nakamuro; Kentaro Hiraga; Masahiro Murakami
The stereoselective synthesis of alpha-amino aldols starting from terminal alkynes
Chem.Commun., 2014, 50, 10474
7115564 CIFC98 H20P 42/n c m16.8655; 16.8655; 19.6001
90; 90; 90
5575.2Venkata S. Pavan K. Neti; Maira R. Ceron; A. Duarte-Ruiz; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
High-yield, regiospecific bis-functionalization of C70 using a Diels-Alder reaction in molten anthracene
Chem.Commun., 2014, 50, 10584
7115565 CIFC39 H30 N O4 PP -19.6945; 11.27; 15.8376
92.446; 101.11; 113.846
1538.92Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115566 CIFC39 H23 Cl2 F3 N O4 PP 1 21/n 115.3256; 9.7698; 22.1934
90; 90.145; 90
3322.96Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115567 CIFC40 H24 N O4 PP -19.9693; 10.0382; 17.31
79.783; 89.864; 66.349
1557.1Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115568 CIFC42 H24 N O4 PP -110.2329; 10.298; 17.3524
97.558; 92.475; 116.557
1610.67Jie-Cheng Deng; Chih-Wei Kuo; Shih-Ching Chuang
Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates
Chem.Commun., 2014, 50, 10580
7115569 CIFC88 H100 B Cr F24 N6P 1 21/c 122.049; 17.219; 25.078
90; 114.243; 90
8682Jingmei Shen; Glenn P. A. Yap; William E. Barker IV; William E. Geiger; Klaus H. Theopold
An electron transfer series of octahedral chromium complexes containing a redox non-innocent alpha-diimine ligand
Chem.Commun., 2014, 50, 10626
7115570 CIFC108 H100 B2 Cl4 Cr F48 N6P -113.962; 17.728; 26.214
79.116; 77.828; 70.078
5915Jingmei Shen; Glenn P. A. Yap; William E. Barker IV; William E. Geiger; Klaus H. Theopold
An electron transfer series of octahedral chromium complexes containing a redox non-innocent alpha-diimine ligand
Chem.Commun., 2014, 50, 10626
7115571 CIFC52 H42 N4 O6P 1 21/c 17.8968; 31.81; 16.8438
90; 105.408; 90
4079Lankani P. Wijesinghe; Buddhie S. Lankage; Gearoid M. O Maille; Sarath D. Perera; Deanne Nolan; Longsheng Wang; Sylvia M. Draper
Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes
Chem.Commun., 2014, 50, 10637
7115572 CIFC52 H54 N4 O6P 1 21/n 113.586; 11.951; 31.96
90; 94.14; 90
5176Lankani P. Wijesinghe; Buddhie S. Lankage; Gearoid M. O Maille; Sarath D. Perera; Deanne Nolan; Longsheng Wang; Sylvia M. Draper
Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes
Chem.Commun., 2014, 50, 10637
7115573 CIFC59 H54 Cl0 Fe0 N2 O3P 1 21/c 117.8254; 10.8398; 29.3462
90; 124.42; 90
4677.6Lankani P. Wijesinghe; Buddhie S. Lankage; Gearoid M. O Maille; Sarath D. Perera; Deanne Nolan; Longsheng Wang; Sylvia M. Draper
Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes
Chem.Commun., 2014, 50, 10637
7115574 CIFC4 H4 Br Cu O4 P SP 1 21/c 115.899; 7.627; 7.344
90; 100.075; 90
876.8Wei-Xuan Nie; Song-Song Bao; Dai Zeng; Li-Rong Guo; Li-Min Zheng
Exfoliated layered copper phosphonate showing enhanced adsorption capability towards Pb ions
Chem.Commun., 2014, 50, 10622
7115575 CIFC74 H74 F2 O4 Yb2P 1 21/n 112.994; 12.4469; 18.4353
90; 95.132; 90
2969.68G. B. Deacon; F. Jaroschik; P. C. Junk; R. P. Kelly
A divalent heteroleptic lanthanoid fluoride complex stabilised by the tetraphenylcyclopentadienyl ligand, arising from C-F activation of pentafluorobenzene
Chem.Commun., 2014, 50, 10655
7115576 CIFC62 H50 O YbP 1 21/n 110.272; 40.41; 11.14
90; 105.41; 90
4457.9G. B. Deacon; F. Jaroschik; P. C. Junk; R. P. Kelly
A divalent heteroleptic lanthanoid fluoride complex stabilised by the tetraphenylcyclopentadienyl ligand, arising from C-F activation of pentafluorobenzene
Chem.Commun., 2014, 50, 10655
7115577 CIFC50 H38 B Cl2 N5 O2 PtP 1 21/c 112.2811; 12.5617; 26.9413
90; 100.943; 90
4080.69Ryo Sekiya; Yusuke Tsutsui; Wookjin Choi; Tsuneaki Sakurai; Shu Seki; Yuya Bandoa; Hiromitsu Maeda
Ion-based assemblies of planar anion complexes and cationic PtII complexes
Chem.Commun., 2014, 50, 10615
7115578 CIFC11 H10 N4P 1 21/c 19.1608; 7.6873; 14.6054
90; 103.05; 90
1001.98Li Xu; Xue-Qing Mou; Zhi-Min Chen; Shao-Hua Wang
Copper-catalyzed intermolecular azidocyanation of aryl alkenes
Chem.Commun., 2014, 50, 10676
7115579 CIFC28 H22 N2P 1 21/c 112.208; 9.4997; 19.3
90; 109.62; 90
2108.3Ying Xie; Tengfei Chen; Shaomin Fu; Xing-Shu Li; Yuanfu Deng; Huanfeng Jiang; Wei Zeng
Pd-Catalyzed [3+2] cycloaddition of ketoimines with alkynes via directed sp3 C-H bond activation
Chem.Commun., 2014, 50, 10699
7115580 CIFC H Cl N OP -17.9603; 25.1844; 12.0025
90; 104.539; 90
2329.2Jun-Hui Xu; Jian-Ping Wei; Zheng Hao; Qing-Guo Ma; Xin-Hua Peng
Highly double selective nitration of nitrostilbenes over zeolite
Chem.Commun., 2014, 50, 10710
7115581 CIFC24 H17 N5 O10C 1 2/c 124.48; 8.379; 11.878
90; 106.275; 90
2339Jun-Hui Xu; Jian-Ping Wei; Zheng Hao; Qing-Guo Ma; Xin-Hua Peng
Highly double selective nitration of nitrostilbenes over zeolite
Chem.Commun., 2014, 50, 10710
7115586 CIFC18 H18 Br F2 N O3 S2P 21 21 2118.0666; 21.1169; 22.2584
90; 90; 90
8491.8Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115587 CIFC18 H18 F2 N O SP 21 21 218.7675; 10.5238; 18.173
90; 90; 90
1676.8Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115588 CIFC24 H23 F2 N O3 S2P 21 21 2110.0872; 14.0488; 16.2483
90; 90; 90
2302.6Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115589 CIFC13 H8 Br N O SP 1 21 17.5255; 3.9957; 19.305
90; 95.045; 90
578.2Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115590 CIFC16 H17 F2 N O SP 21 21 219.9519; 10.2705; 15.1165
90; 90; 90
1545.07Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115591 CIFC31 H22 Br F2 N O3 S2P 21 21 218.5124; 14.4301; 22.503
90; 90; 90
2764.2Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115592 CIFC21 H16 Br N O3 SP 1 21/n 19.876; 11.292; 16.818
90; 92.78; 90
1873.3Wenchao Ye; Laijun Zhang; Chuanfa Ni; Jian Rong; Jinbo Hu
Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines
Chem.Commun., 2014, 50, 10596
7115593 CIFC27 H21 N O3 SC 1 c 126.342; 19.322; 18.311
90; 110.59; 90
8725Fei Pan; Shuang Liu; Chao Shu; Rong-Kun Lin; Yong-Fei Yu; Jin-Mei Zhou; Long-Wu Ye
Gold-catalyzed intermolecular oxidation of o-alkynylbiaryls: an easy and practical access to functionalized fluorenes
Chem.Commun., 2014, 50, 10726
7115594 CIFC68 H66 B F24 Ir N PP -113.42933; 18.87158; 27.7213
77.2224; 88.4024; 77.9371
6698.97Nicolas Humbert; Devendra J. Vyas; Celine Besnard; Clement Mazet
An air-stable cationic iridium hydride as a highly active and general catalyst for the isomerization of terminal epoxides
Chem.Commun., 2014, 50, 10592
7115595 CIFC28 H18 N2 S2 SeP -18.0777; 8.1703; 17.9004
83.481; 87.961; 67.919
1087.62Ann Christin Jahnke; Mariana Spulber; Markus Neuburger; Cornelia G. Palivan; Oliver S. Wenger
Electronic coupling mediated by furan, thiophene, selenophene and tellurophene in a homologous series of organic mixed valence compounds
Chem.Commun., 2014, 50, 10883
7115596 CIFC12 H10 F N3 OP 1 21/c 111.785; 5.7638; 16.482
90; 102.47; 90
1093.2Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115597 CIFC12 H9 F2 N3 OP 1 21/n 110.484; 5.4019; 19.491
90; 104.37; 90
1069.3Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115598 CIFC12 H10 N4 O3P -16.9066; 7.942; 11.37
81.16; 87.98; 67.14
567.7Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115599 CIFC12 H10 F N3 OP 1 n 14.5349; 11.591; 10.686
90; 98.22; 90
555.93Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115600 CIFC12 H9 F2 N3 OP 1 21/c 13.7683; 27.238; 10.409
90; 97.29; 90
1059.8Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115601 CIFC12 H10 N4 O3P b c a11.9799; 7.3695; 25.427
90; 90; 90
2244.8Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115602 CIFC12 H11 F2 N3 O2P -18.9104; 9.9683; 13.1855
91.865; 92.788; 91.591
1168.65Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115603 CIFC13 H14 N4 O4P 1 21/c 18.1756; 14.365; 11.375
90; 92.01; 90
1335.1Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115604 CIFC13 H10 F3 N3 OP 1 21/c 114.5029; 12.713; 14.3436
90; 116.799; 90
2360.6Komala Pandurangan; Jonathan A. Kitchen; Salvador Blasco; Francesca Paradisi; Thorfinnur Gunnlaugsson
Supramolecular pyridyl urea gels as soft matter with antibacterial properties against MRSA and/or E. coli
Chem.Commun., 2014, 50, 10819
7115605 CIFC46 H26 Cu F36 N4 O6P -110.3845; 10.7053; 27.4
84.153; 89.737; 64.833
2740Hyung Joon Jeon; Ryotaro Matsuda; Prakash Kanoo; Hiroshi Kajiro; Liangchun Li; Hiroshi Sato; Yongtai Zheng; Susumu Kitagawa
The densely fluorinated nanospace of a porous coordination polymer composed of perfluorobutyl-functionalized ligands
Chem.Commun., 2014, 50, 10861
7115606 CIFC19 H19 N3 OP 1 21/c 115.709; 8.4319; 12.274
90; 96.34; 90
1615.8Zhi-Min Chen; Zhen Zhang; Yong-Qiang Tu; Ming-Hui Xu; Fu-Min Zhang; Chen-Chen Li; Shao-Hua Wang
A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers
Chem.Commun., 2014, 50, 10805
7115607 CIFC21 H26 N6 O2 SiP 1 21/c 18.7189; 9.066; 27.8157
90; 91.003; 90
2198.37Zhi-Min Chen; Zhen Zhang; Yong-Qiang Tu; Ming-Hui Xu; Fu-Min Zhang; Chen-Chen Li; Shao-Hua Wang
A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers
Chem.Commun., 2014, 50, 10805
7115608 CIFC18 H17 N3 O2P -18.6242; 10.2987; 10.3691
61.409; 80.7; 86.903
797.7Zhi-Min Chen; Zhen Zhang; Yong-Qiang Tu; Ming-Hui Xu; Fu-Min Zhang; Chen-Chen Li; Shao-Hua Wang
A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers
Chem.Commun., 2014, 50, 10805
7115609 CIFC24 H25 N O6P 1 21/c 113.637; 13.749; 12.866
90; 111.745; 90
2241Thangavel Selvia; Kannupal Srinivasan
Synthesis of 2,4,5-trisubstituted oxazoles through tin(IV) chloride-mediated reaction of trans-2-aryl-3-nitro-cyclopropane-1,1-dicarboxylates with nitriles
Chem.Commun., 2014, 50, 10845
7115610 CIFC28 H30 N4 PdP -18.25; 14.764; 19.582
88.932; 89.487; 74.757
2300.8M. G. Derry Holaday; Gourav Tarafdar; B. Adinarayana; M. L. P. Reddy; A. Srinivasan
Chemodosimetric cyanide sensing in a 5,15-porphodimethene Pd(II) complex
Chem.Commun., 2014, 50, 10584
7115611 CIFC15 H12 F N O3P -110.1802; 10.4053; 13.1475
90.7253; 108.201; 106.189
1262.93Aditi P. Chavannavar; Allen G. Oliver; Brandon L. Ashfeld
An umpolung approach toward N-aryl nitrone construction: a phosphine-mediated addition of 1,2-dicarbonyls to nitroso electrophiles
Chem.Commun., 2014, 50, 10853
7115612 CIFC19 H30 Cl Ir N O3 PP -18.081; 8.7266; 15.7699
79.849; 79.048; 79.265
1061.23Xiangqing Jia; Lei Zhang; Chuan Qin; Xuebing Leng; Zheng Huang
Iridium complexes of new NCP pincer ligands: catalytic alkane dehydrogenation and alkene isomerization
Chem.Commun., 2014, 50, 11056
7115613 CIFC20 H28 Cl Ir N O PP 1 21/c 110.1303; 13.77; 15.004
90; 105.782; 90
2014.1Xiangqing Jia; Lei Zhang; Chuan Qin; Xuebing Leng; Zheng Huang
Iridium complexes of new NCP pincer ligands: catalytic alkane dehydrogenation and alkene isomerization
Chem.Commun., 2014, 50, 11056
7115614 CIFC26 H37 Cl Ir N O PP 21 21 215.6237; 16.1007; 9.9759
90; 90; 90
2509.5Xiangqing Jia; Lei Zhang; Chuan Qin; Xuebing Leng; Zheng Huang
Iridium complexes of new NCP pincer ligands: catalytic alkane dehydrogenation and alkene isomerization
Chem.Commun., 2014, 50, 11056
7115615 CIFC66 H101 N2 O5 YbP -111.4765; 14.79; 21.9149
93.494; 105.09; 110.393
3318.8Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115616 CIFC66 H101 N2 O5 YP -111.6333; 15.0256; 21.5946
94.787; 104.996; 111.655
3320.8Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115617 CIFC66 H101 N2 O5 SmP 1 21/c 113.8842; 20.6892; 22.5022
90; 91.478; 90
6461.7Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115618 CIFC70 H109 N2 Nd O6P -111.57; 13.0084; 24.217
80.278; 84.826; 74.115
3451.6Jie Qin; Peng Wang; Qingyan Li; Yong Zhang; Dan Yuan; Yingming Yao
Catalytic production of cyclic carbonates mediated by lanthanide phenolates under mild conditions
Chem.Commun., 2014, 50, 10952
7115619 CIFC120 H106 O4P -112.656; 12.875; 16.048
72.271; 84.227; 63.603
2229.2Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115620 CIFC144 H122 O8F d d d :222.3697; 23.8656; 59.021
90; 90; 90
31509Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115621 CIFC92 H74 O4C 1 2/c 142.2144; 8.82075; 23.4233
90; 117.273; 90
7752.3Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115622 CIFC40 H54 B4 O8P 1 21/n 112.2939; 10.7476; 15.7067
90; 109.673; 90
1954.19Akinobu Matsumoto; Mitsuharu Suzuki; Daiki Kuzuhara; Junpei Yuasa; Tsuyoshi Kawai; Naoki Aratani
A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
Chem.Commun., 2014, 50, 10956
7115623 CIFC77 H56 Au2 F10 N2 O2P -111.9116; 12.7221; 21.939
92.367; 90.803; 102.203
3245.9Zhao Chen; Di Wu; Xie Han; Jinhua Liang; Jun Yin; Guang-Ao Yu; Sheng Hua Liu
A novel fluorene-based gold(I) complex with aggregate fluorescence change: a single-component white light-emitting
Chem.Commun., 2014, 50, 11033
7115624 CIFC22 H35 B3 N4 SP 1 21 110.765; 14.567; 14.658
90; 97.11; 90
2281Holger Braunschweig; Christian Horl
Unexpected cluster formation upon hydroboration of a neutral diborene with 9-BBN
Chem.Commun., 2014, 50, 10983
7115625 CIFC25 H43 B3 N4 S SiP 1 21/n 112.667; 14.559; 15.099
90; 94.373; 90
2776Holger Braunschweig; Christian Horl
Unexpected cluster formation upon hydroboration of a neutral diborene with 9-BBN
Chem.Commun., 2014, 50, 10983
7115626 CIFC34 H29 Cl3 N O4 S2P 1 21/c 112.6039; 13.6946; 18.7475
90; 96.73; 90
3213.6Yu Zhang; Ling Pan; Xianxiu Xu; Hongmei Luo; Qun Liu
Tandem Michael addition/imine isomerization/intramolecular [3+2] cycloaddition for the regiospecific synthesis of cyclohepta[b]pyrroles
Chem.Commun., 2014, 50, 11039
7115627 CIFC49.5 H42 Cl4.5 N1.5 O6 S3P -110.069; 13.141; 18.165
110.735; 93.826; 107.061
2109.4Yu Zhang; Ling Pan; Xianxiu Xu; Hongmei Luo; Qun Liu
Tandem Michael addition/imine isomerization/intramolecular [3+2] cycloaddition for the regiospecific synthesis of cyclohepta[b]pyrroles
Chem.Commun., 2014, 50, 11039
7115628 CIFC130 H136 Cu12 P8 S6P 42/n c m :226.081; 26.081; 19.313
90; 90; 90
13137Xiao-Xun Yang; Ibrahim Issac; Sergej Lebedkin; Michael Kuhn; Florian Weigend; Dieter Fensk; Olaf Fuhrac; Andreas Eichhofer
Red-luminescent biphosphine stabilized 'Cu12S6' cluster molecules
Chem.Commun., 2014, 50, 11043
7115629 CIFC152.5 H172 Cu12 P8 S6P -117.803; 18.522; 23.713
83.46; 80.88; 71.93
7322Xiao-Xun Yang; Ibrahim Issac; Sergej Lebedkin; Michael Kuhn; Florian Weigend; Dieter Fensk; Olaf Fuhrac; Andreas Eichhofer
Red-luminescent biphosphine stabilized 'Cu12S6' cluster molecules
Chem.Commun., 2014, 50, 11043
7115630 CIFC23 H36 O4 SiP -18.4432; 10.8187; 12.5225
82.362; 86.419; 85.558
1128.73Zhilong Li; Tsz-Fai Leung; Rongbiao Tong
Total syntheses of +/- -musellarins A-C
Chem.Commun., 2014, 50, 10990
7115631 CIFC42 H58 O2 P2P -16.5471; 10.5962; 14.3323
100.773; 101.934; 107.345
895.07Shanshan Wu; Arnold L. Rheingold; John D. Protasiewicz
Luminescent materials containing multiple benzoxaphosphole units
Chem.Commun., 2014, 50, 11036
7115632 CIFC75 H66 F12 N18 O P2 RuP b c a23.24; 13.2721; 47.443
90; 90; 90
14633.5Alexander J. Metherell; Michael D. Ward
Stepwise assembly of an adamantoid Ru4Ag6 cage by control of metal coordination geometry at specific sites
Chem.Commun., 2014, 50, 10979
7115633 CIFC288 H240 Ag6 F84 N72 P14 Ru4P 1 2/n 124.688; 30.324; 25.247
90; 102.819; 90
18430Alexander J. Metherell; Michael D. Ward
Stepwise assembly of an adamantoid Ru4Ag6 cage by control of metal coordination geometry at specific sites
Chem.Commun., 2014, 50, 10979
7115634 CIFC51 H34 N5 PtP -19.5314; 12.4762; 16.9813
111.157; 97.191; 90.47
1865.3Abraham B. Alemayehu; Hugo Vazquez-Lima; Christine M. Beavers; Kevin J. Gagnon; Jesper Bendix; Abhik Ghosh
Platinum corroles
Chem.Commun., 2014, 50, 11093
7115635 CIFC56.23 H45.24 Cl0.31 N4.96 PtP -110.4746; 11.6239; 18.2464
87.752; 83.482; 77.657
2156Abraham B. Alemayehu; Hugo Vazquez-Lima; Christine M. Beavers; Kevin J. Gagnon; Jesper Bendix; Abhik Ghosh
Platinum corroles
Chem.Commun., 2014, 50, 11093
7115636 CIFC54 H40 N5 PtP -19.5493; 12.9707; 17.3628
106.105; 96.859; 93.679
2040.7Abraham B. Alemayehu; Hugo Vazquez-Lima; Christine M. Beavers; Kevin J. Gagnon; Jesper Bendix; Abhik Ghosh
Platinum corroles
Chem.Commun., 2014, 50, 11093
7115638 CIFC24 H18 Ba2 N2 O13P -17.8709; 8.8711; 19.835
100.55; 92.53; 92.59
1358.2Chan Song; Guan-Yao Wang; Ya-Ling Wang; De-Ming Kong; Yong-Jian Wang; Yue Li; Wen-Juan Ruan
A barium based coordination polymer for the activity assay of deoxyribonuclease I
Chem.Commun., 2014, 50, 11177
7115639 CIFC32 H32 F6 N2 O4 P2 RuP -112.66; 13.268; 13.386
119.526; 92.516; 115.846
1662Yusuke Kita; Takafumi Higuchi; Kazushi Mashima
Hydrogenation of amides catalyzed by a combined catalytic system of a Ru complex with a zinc salt
Chem.Commun., 2014, 50, 11211
7115640 CIFC20 H22 N2 O5P -112.199; 12.84; 14.621
100.605; 114.357; 104.026
1916.8Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115641 CIFC20 H22 N2 O5P 1 21/c 115.2319; 7.8737; 15.4675
90; 90.233; 90
1855Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115642 CIFC20 H22 N2 O5P 1 21/c 19.6837; 9.5017; 20.5631
90; 92.044; 90
1890.8Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115643 CIFC20 H22 N2 O6P 1 21/c 19.3854; 18.319; 11.434
90; 109.579; 90
1852.2Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115644 CIFC20 H22 N2 O6P 1 21/c 19.6391; 27.15; 8.0064
90; 111.845; 90
1944.8Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115645 CIFC20 H22 N2 O6P 1 21/c 111.626; 10.168; 15.862
90; 97.357; 90
1859.7Xue Zhong; You Li; Jing Zhang; Wu-Xia Zhang; Shi-Xue Wang; Fu-She Han
Formal [3+3] cycloaddition of indol-2-yl carbinol with azadiene and the oxidative ring expansion reaction for the synthesis of indole azepinones
Chem.Commun., 2014, 50, 11181
7115647 CIFC118.79 H92.79 Cl26.38 N18 Zn2P 1 21/n 118.058; 17.549; 21.217
90; 100.9; 90
6602Huimin Ding; Xiangshi Meng; Xu Cui; Yihui Yang; Tailin Zhou; Caixing Wang; Matthias Zeller; Cheng Wang
Highly-efficient synthesis of covalent porphyrinic cages via DABCO-templated imine condensation reactions
Chem.Commun., 2014, 50, 11162
7115648 CIFC56.5 H70 Fe2 N6P 1 21/n 115.9655; 14.7809; 21.7126
90; 104.422; 90
4962.4Richard A. Lewis; K. Cory MacLeod; Brandon Q. Mercado; Patrick L. Holland
Geometric and redox flexibility of pyridine as a redox-active ligand that can reversibly accept one or two electrons
Chem.Commun., 2014, 50, 11114
7115649 CIFC145 H183 Fe4 N17 O3P c a 2127.6897; 11.5655; 42.052
90; 90; 90
13467Richard A. Lewis; K. Cory MacLeod; Brandon Q. Mercado; Patrick L. Holland
Geometric and redox flexibility of pyridine as a redox-active ligand that can reversibly accept one or two electrons
Chem.Commun., 2014, 50, 11114
7115650 CIFC12 H18 Al3 Cl12 DyP -19.5626; 9.6465; 17.8181
93.3339; 97.4937; 119.608
1402.42Shan-Shan Liu; Joseph W. Ziller; Yi-Quan Zhang; Bing-Wu Wang; William J. Evans; Song Gao
A half-sandwich organometallic single-ion magnet with hexamethylbenzene coordinated to the Dy(III) ion
Chem.Commun., 2014, 50, 11418
7115651 CIFC12 H18 Al3 Cl12 TbP -19.5934; 9.6912; 17.8558
93.2661; 97.3859; 119.652
1416.64Shan-Shan Liu; Joseph W. Ziller; Yi-Quan Zhang; Bing-Wu Wang; William J. Evans; Song Gao
A half-sandwich organometallic single-ion magnet with hexamethylbenzene coordinated to the Dy(III) ion
Chem.Commun., 2014, 50, 11418
7115652 CIFC23 H24 N2 O10 SeP -110.0929; 11.5641; 11.7886
67.928; 77.776; 67.513
1174.4Mohammad S. Afzal; Jean-Philippe Pitteloud; Daniela Buccella
Enhanced ratiometric fluorescent indicators for magnesium based on azoles of the heavier chalcogens
Chem.Commun., 2014, 50, 11358
7115653 CIFC23 H24 N2 O10 SP -110.094; 11.5565; 11.7894
67.376; 77.489; 67.165
1166.3Mohammad S. Afzal; Jean-Philippe Pitteloud; Daniela Buccella
Enhanced ratiometric fluorescent indicators for magnesium based on azoles of the heavier chalcogens
Chem.Commun., 2014, 50, 11358
7115654 CIFC35 H53 Cl N2 Si ZnP 1 21/n 111.089; 17.537; 17.947
90; 98.91; 90
3448Sebastian Schafer; Ralf Koppe; Michael T. Gamer; Peter W. Roesky
Zinc-silylene complexes
Chem.Commun., 2014, 50, 11401
7115655 CIFC54 H66 Cl2 N4 Si2 Zn2P 1 21/n 112.479; 14.937; 14.85
90; 104.21; 90
2683.3Sebastian Schafer; Ralf Koppe; Michael T. Gamer; Peter W. Roesky
Zinc-silylene complexes
Chem.Commun., 2014, 50, 11401
7115656 CIFC34 H56 Cl2 N4 Si2 ZnP 1 21/c 111.432; 23.618; 16.42
90; 105.97; 90
4262.3Sebastian Schafer; Ralf Koppe; Michael T. Gamer; Peter W. Roesky
Zinc-silylene complexes
Chem.Commun., 2014, 50, 11401
7115657 CIFC14 H26 B7 N2P -19.6172; 9.7108; 10.0025
96.336; 109.264; 102.874
842.34Marc-Andre Legare; Marc-Andre Courtemanche; Frederic-Georges Fontaine
Lewis base activation of borane-dimethylsulfide into strongly reducing ion pairs for the transformation of carbon dioxide to methoxyboranes
Chem.Commun., 2014, 50, 11362
7115658 CIFC35 H42 N5 O P ZnP 1 21/c 110.6521; 14.2354; 21.9063
90; 95.875; 90
3304.4Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115659 CIFC31 H46 N5 P ZnP 1 21/n 113.017; 17.0162; 14.0147
90; 90.091; 90
3104.3Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115660 CIFC33 H37 Cl K0 Li0 N5 O P ZnP 1 21/n 114.4797; 10.8889; 20.9293
90; 100.088; 90
3248.9Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115661 CIFC37 H48 N5 O P Si ZnP -19.9691; 11.3621; 17.9387
102.22; 98.414; 109.478
1819.61Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115662 CIFC35 H47 N6 P Si2 ZnP 1 21/c 118.0474; 12.0098; 17.5841
90; 102.768; 90
3717Zehuai Mou; Bo Liu; Meiyan Wang; Hongyan Xie; Ping Li; Lei Li; Shihui Li; Dongmei Cui
Isoselective ring-opening polymerization of rac-lactide initiated by achiral heteroscorpionate zwitterionic zinc complexes
Chem.Commun., 2014, 50, 11411
7115663 CIFC10 H15 N O5P 21 21 215.598; 13.2848; 14.6114
90; 90; 90
1086.63William P. Unsworth; Nicola Clark; Thomas O. Ronson; Kiri Stevens; Amber L. Thompson; Scott G. Lamont; Jeremy Robertson
Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans
Chem.Commun., 2014, 50, 11393
7115664 CIFC10 H15 N O5P 21 21 215.8112; 7.6935; 23.7155
90; 90; 90
1060.28William P. Unsworth; Nicola Clark; Thomas O. Ronson; Kiri Stevens; Amber L. Thompson; Scott G. Lamont; Jeremy Robertson
Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans
Chem.Commun., 2014, 50, 11393
7115665 CIFC10 H15 N O5P 21 21 215.7625; 8.6145; 21.3435
90; 90; 90
1059.51William P. Unsworth; Nicola Clark; Thomas O. Ronson; Kiri Stevens; Amber L. Thompson; Scott G. Lamont; Jeremy Robertson
Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans
Chem.Commun., 2014, 50, 11393
7115666 CIFC36.5 H31 Cl O2P -19.1923; 9.5033; 17.017
75.35; 77.27; 84.99
1402.1Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115667 CIFC88 H92 O4P -110.871; 11.053; 15.84
81.772; 77.584; 68.14
1720.9Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115668 CIFC44 H40 O4P 21 21 219.6016; 14.338; 24.574
90; 90; 90
3383Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115669 CIFC60 H56 OP -19.6111; 9.8047; 12.6063
75.516; 79.934; 88.667
1132.2Jin-Hua Wang; Hai-Tao Feng; Yan-Song Zheng
Synthesis of tetraphenylethylene pillar[6]arenes and the selective fast quenching of their AIE fluorescence by TNT
Chem.Commun., 2014, 50, 11407
7115670 CIFC6 H18 S Si2C 1 2/c 118.407; 5.7619; 11.61
90; 113.848; 90
1126.2Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115671 CIFC64 H82 Cl10 Cu2 O4 P2 S8 Sn6P -112.6985; 13.1259; 15.4384
115.138; 101.519; 101.37
2164.23Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115672 CIFC84 H118 Cl2 Cu2 O8 P2 S14 Sn10P -112.4911; 15.09; 15.4207
91.029; 102.416; 101.294
2778.2Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115673 CIFC84 H118 Ag2 Cl2 O8 P2 S14 Sn10P -112.528; 15.2617; 15.4195
91.365; 102.845; 100.328
2821.6Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115674 CIFC63.5 H127 Ag10 Cl7 N20 S20 Sn10I 41/a :230.8293; 30.8293; 54.2835
90; 90; 90
51593.5Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115675 CIFC48 H52 Au2 O2 P2 S4 Sn2P 1 21/c 114.5079; 12.1592; 15.0025
90; 103.39; 90
2574.57Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115676 CIFC53 H66 Au2 Cl10 N4 P2 S4 Sn2P -18.522; 12.3547; 17.3906
77.566; 83.985; 71.477
1694.12Jens P. Eussner; Stefanie Dehnen
Bronze, silver and gold: functionalized group 11 organotin sulfide clusters
Chem.Commun., 2014, 50, 11385
7115677 CIFC164.5 H217 Au6 B2 Cl F8 N12 O6P -118.436; 18.589; 30.244
99.0625; 91.888; 117.078
9048.7Alba Collado; Adrian Gomez-Suarez; Paul B. Webb; Hedi Kruger; Michael Buhl; David B. Cordes; Alexandra M. Z. Slawin; Steven P. Nolan
Trapping atmospheric CO2 with gold
Chem.Commun., 2014, 50, 11321
7115678 CIFC31 H24 Cl O PP -110.1588; 13.9351; 18.4004
78.641; 75.556; 73.465
2395.8Anup Bhunia; Trinadh Kaicharla; Digvijay Porwal; Rajesh G. Gonnade; Akkattu T. Biju
Multicomponent reactions involving phosphines, arynes and aldehydes
Chem.Commun., 2014, 50, 11389
7115679 CIFC32 H25 As Cl F3 O4 SP 1 21/c 19.6419; 14.7407; 20.9802
90; 91.849; 90
2980.33Anup Bhunia; Trinadh Kaicharla; Digvijay Porwal; Rajesh G. Gonnade; Akkattu T. Biju
Multicomponent reactions involving phosphines, arynes and aldehydes
Chem.Commun., 2014, 50, 11389
7115680 CIFC31 H23 Cl2 O1.25 PP 1 21/c 114.2166; 28.5677; 12.5338
90; 97.179; 90
5050.5Anup Bhunia; Trinadh Kaicharla; Digvijay Porwal; Rajesh G. Gonnade; Akkattu T. Biju
Multicomponent reactions involving phosphines, arynes and aldehydes
Chem.Commun., 2014, 50, 11389
7115681 CIFC17.85 H111 Br N O41.69I m m a21.0197; 25.2728; 12.0096
90; 90; 90
6379.8S. Muromachi; K. A. Udachin; K. Shin; S. Alavi; I. L. Moudrakovski; R. Ohmura; J. A. Ripmeester
Guest-induced symmetry lowering of an ionic clathrate material for carbon capture
Chem.Commun., 2014, 50, 11476
7115682 CIFC130 H97 Co6.5 Mo24 N26 O88 P2P 1 21/c 129.607; 26.66; 24.133
90; 108.178; 90
18098C. Zhang; X. Lin; Z. Zhang; L.-S. Long; C. Wang; W. Lin
A hybrid polyoxometalate-organic molecular catalyst for visible light driven water oxidation
Chem.Commun., 2014, 50, 11591
7115683 CIFC44 H44 B2 F4 N6 O2P -111.4702; 13.147; 14.9642
113.625; 95.348; 105.167
1944.7Yafei Wang; Long Chen; Reda M. El-Shishtawy; Saadullah G. Aziz; Klaus Mullen
Synthesis and optophysical properties of dimeric aza-BODIPY dyes with a push-pull benzodipyrrolidone core
Chem.Commun., 2014, 50, 11540
7115684 CIFC46 H46 B2 Cl4 F6 N6 O2P 1 21/c 14.7273; 19.711; 25.1808
90; 97.316; 90
2327.2Yafei Wang; Long Chen; Reda M. El-Shishtawy; Saadullah G. Aziz; Klaus Mullen
Synthesis and optophysical properties of dimeric aza-BODIPY dyes with a push-pull benzodipyrrolidone core
Chem.Commun., 2014, 50, 11540
7115685 CIFC36 H27.5 N0.5 O4P 1 21 111.7738; 12.39402; 19.49664
90; 106.917; 90
2721.92Weiliang Chen; Xuan Fu; Lili Lin; Xiao Yuan; Weiwei Luo; Juhua Feng; Xiaohua Liu; Xiaoming Feng
An asymmetric [3+2] cycloaddition of alkynes with oxiranes by selective C-C bond cleavage of epoxides: highly efficient synthesis of chiral furan derivatives
Chem.Commun., 2014, 50, 11480
7115686 CIFC60 H80 N2 O4P -19.93781; 15.1528; 17.8125
69.7564; 88.9555; 87.1772
2513.57Kamil Kotwica; Piotr Bujak; Damian Wamil; Mariusz Materna; Lukasz Skorka; Piotr A. Gunka; Robert Nowakowski; Barbara Golec; Beata Luszczynska; Malgorzata Zagorska; Adam Pron
Indanthrone dye revisited after sixty years
Chem.Commun., 2014, 50, 11543
7115687 CIFC26 H39 Ni O2 P3P 1 21/n 111.4995; 14.7887; 16.1942
90; 98.174; 90
2726.1Yeong-Eun Kim; Jin Kim; Yunho Lee
Formation of a nickel carbon dioxide adduct and its transformation mediated by a Lewis acid
Chem.Commun., 2014, 50, 11458
7115688 CIFC65 H63 B F15 Ni O2 P3P -113.7796; 15.3191; 15.8751
97.002; 95.9; 111.372
3057.8Yeong-Eun Kim; Jin Kim; Yunho Lee
Formation of a nickel carbon dioxide adduct and its transformation mediated by a Lewis acid
Chem.Commun., 2014, 50, 11458
7115689 CIFC50 H78 N2 Ni2 P6I b c a18.508; 19.9088; 28.5632
90; 90; 90
10524.7Yeong-Eun Kim; Jin Kim; Yunho Lee
Formation of a nickel carbon dioxide adduct and its transformation mediated by a Lewis acid
Chem.Commun., 2014, 50, 11458
7115690 CIFC180 H132 K2 O26 Yb2P -114.1075; 14.4693; 17.9695
102.772; 90.083; 91.038
3576.6Brodie L. Reid; Stefano Stagni; Joanna M. Malicka; Massimo Cocchi; Garry S. Hanan; Mark I. Ogden; Massimiliano Massi
Lanthanoid beta-triketonates: a new class of highly efficient NIR emitters for bright NIR-OLEDs
Chem.Commun., 2014, 50, 11580
7115691 CIFC35 H76 Cl N13 O9 P4 Ru2P -114.5313; 17.5256; 18.3097
66.927; 73.12; 76.513
4067.1Manuel Serrano-Ruiz; Silvia Imberti; Leonardo Bernasconi; Nazira Jadagayeva; Franco Scalambra; Antonio Romerosa
Study of the interaction of water with the aqua-soluble dimeric complex [RuCp(PTA)2-mu-CN-1 kappa C:2 kappa^2^ N-RuCp(PTA)2](CF3SO3) (PTA = 1,3,5-triaza-7-phosphaadamantane) by neutron and X-ray diffraction in solution
Chem.Commun., 2014, 50, 11587
7115692 CIFC186 H102 In9 N30 O72 Ru2P 3 2 115.778; 15.778; 28.032
90; 90; 120
6043.5Lei Wang; Weiting Yang; Yangxue Li; Zhigang Xie; Wei Zhu; Zhong-Ming Sun
Dynamically controlled one-pot synthesis of heterogeneous core-shell MOF single crystals using guest molecules
Chem.Commun., 2014, 50, 11653
7115693 CIFC14 H6 In N2 O8R -3 c :H15.7069; 15.7069; 52.887
90; 90; 120
11300Lei Wang; Weiting Yang; Yangxue Li; Zhigang Xie; Wei Zhu; Zhong-Ming Sun
Dynamically controlled one-pot synthesis of heterogeneous core-shell MOF single crystals using guest molecules
Chem.Commun., 2014, 50, 11653
7115694 CIFC21.5 H19 Cl N2 O2 SP n n a14.6631; 22.9825; 13.3003
90; 90; 90
4482.13Wenyan Hao; Jiangbo Zeng; Mingzhong Cai
The copper(I)-catalyzed tandem reaction of o-alkynylphenyl isothiocyanates with isocyanides: a rapid synthesis of 5H-benzo[d]imidazo[5,1-b][1,3]thiazines
Chem.Commun., 2014, 50, 11686
7115695 CIFC194 H156 N O24 Sc3P -117.8883; 18.2158; 28.6383
72.268; 88.036; 63.205
7875.6Min-Yen Ku; Shing-Jong Huang; Shou-Ling Huang; Yi-Hung Liu; Chien-Chen Lai; Shie-Ming Peng; Sheng-Hsien Chiu
Hemicarceplex formation allows ready identification of the isomers of the metallofullerene Sc3N@C80 using 1H and 13C NMR spectroscopy
Chem.Commun., 2014, 50, 11709
7115696 CIFC68 H40 Cu2 N8 O17 Zn4I b c a28.1305; 26.1877; 28.1745
90; 90; 90
20755.4Alexandre Burgun; Rachel S. Crees; Marcus L. Cole; Christian J. Doonan; Christopher J. Sumby
A 3-D diamondoid MOF catalyst based on in situ generated [Cu(L)2] N-heterocyclic carbene (NHC) linkers: hydroboration of CO2
Chem.Commun., 2014, 50, 11760
7115697 CIFC27 H30.88 Cl2 N4.5 O1.25 P PdC 1 2/c 117.6807; 21.7456; 15.1674
90; 103.312; 90
5674.8Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115698 CIFC52 H56 Cl2 N8 O2 P2 Pd2P 1 21/c 113.5981; 17.4517; 10.9141
90; 100.235; 90
2548.8Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115699 CIFC26 H28 N4 O PP 1 21/c 118.7336; 10.702; 11.7743
90; 94.201; 90
2354.3Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115700 CIFC26 H30 Cl2 N4 O2 P PdP -18.972; 9.771; 16.661
101.704; 100.03; 94.767
1397.7Corey A. Sanz; Michael J. Ferguson; Robert McDonald; Brian O. Patrick; Robin G. Hicks
Classical and non-classical redox reactions of Pd(II) complexes containing redox-active ligands
Chem.Commun., 2014, 50, 11676
7115701 CIFC154 H148 B4 N6 O3 Si2P 1 21/n 111.8934; 26.2175; 20.3647
90; 101.101; 90
6231.2Shannon A. Couchman; Trevor K. Thompson; David J. D. Wilson; Jason L. Dutton; Caleb D. Martin
Investigating the ring expansion reaction of pentaphenylborole and an azide
Chem.Commun., 2014, 50, 11724
7115702 CIFC23 H19 N3 O5 SP -18.6842; 10.9725; 11.2956
100.974; 95.529; 99.687
1032.37Xianyu Meng; Peiqiu Liao; Jianquan Liu; Xihe Bi
Silver-catalyzed cyclization of 2-pyridyl alkynyl carbinols with isocyanides: divergent synthesis of indolizines and pyrroles
Chem.Commun., 2014, 50, 11837
7115703 CIFC H Br N O SP 17.1457; 9.8623; 11.5311
96.212; 94.459; 97.061
798.31Xianyu Meng; Peiqiu Liao; Jianquan Liu; Xihe Bi
Silver-catalyzed cyclization of 2-pyridyl alkynyl carbinols with isocyanides: divergent synthesis of indolizines and pyrroles
Chem.Commun., 2014, 50, 11837
7115704 CIFC17 H13 N3 OP 1 21/c 117.916; 4.643; 20.248
90; 124.13; 90
1394.2Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115705 CIFC11 H12 N2 O2P -17.423; 8.934; 9.001
118.77; 97.71; 93.62
512.87Sascha Wiechmann; Tyll Freese; Martin H. H. Drafz; Eike G. Hubner; Jan C. Namyslo; Martin Nieger; Andreas Schmidt
Sydnone anions and abnormal N-heterocyclic carbenes of O-ethylsydnones. Characterizations, calculations and catalyses
Chem.Commun., 2014, 50, 11822
7115706 CIFC44 H35 Br N2 O2 P2 PdP 1 21/c 111.8099; 17.9947; 17.1796
90; 100.544; 90
3589.3Sascha Wiechmann; Tyll Freese; Martin H. H. Drafz; Eike G. Hubner; Jan C. Namyslo; Martin Nieger; Andreas Schmidt
Sydnone anions and abnormal N-heterocyclic carbenes of O-ethylsydnones. Characterizations, calculations and catalyses
Chem.Commun., 2014, 50, 11822
7115707 CIFC27 H36 Br N O3P -17.548; 8.2091; 20.886
92.198; 95.579; 101.425
1260.3Peiyi Wang; Yuan Lin; Mark Smith; Sheng Feng; Baoan Song; Song Yang; Jun Hu
Host-guest interaction manipulated self-assembly of pyridinium-tailored naphthalene
Chem.Commun., 2014, 50, 11950
7115708 CIFC180 H270 Ag55 Mo6 O60R -3 :H22.261; 22.261; 47.421
90; 90; 120
20351.2Kun Zhou; Yun Geng; Li-Kai Yan; Xin-Long Wang; Xian-Chun Liu; Guo-Gang Shan; Kui-Zhan Shao; Zhong-Min Su; Ying-Ning Yu
An ultrastable {Ag55Mo6} nanocluster with a Ag-centered multishell structure
Chem.Commun., 2014, 50, 11934
7115709 CIFC34 H38 N4 O6 S2C 1 2/c 122.6373; 9.557; 16.0764
90; 105.708; 90
3348.15Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115710 CIFC36 H40 N6 O6P b c a15.1665; 17.7506; 24.997
90; 90; 90
6729.6Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115711 CIFC36 H40 N6 O6P 1 21/c 18.387; 14.2432; 14.6816
90; 104.354; 90
1699.08Murat K. Deliomeroglu; Vincent M. Lynch; Jonathan L. Sessler
Conformationally switchable non-cyclic tetrapyrrole receptors: synthesis of tetrakis(1H-pyrrole-2-carbaldehyde) derivatives and their anion binding properties
Chem.Commun., 2014, 50, 11863
7115712 CIFC33 H27 Br N2 O2P 21 21 218.9032; 11.1649; 27.772
90; 90; 90
2760.6Yan Liu; Hong-Hao Zhang; Yu-Chen Zhang; Yan Jiang; Feng Shi; Shu-Jiang Tu
Organocatalytic enantioselective and (Z)-selective allylation of 3-indolylmethanol via hydrogen-bond activation
Chem.Commun., 2014, 50, 12054
7115713 CIFC26 H20P 1 21 19.8251; 9.502; 10.709
90; 107.096; 90
955.6Guo-Feng Zhang; Ze-Qiang Chen; Matthew P. Aldred; Zhe Hu; Tao Chen; Zhenli Huang; Xianggao Meng; Ming-Qiang Zhu
Direct validation of the restriction of intramolecular rotation hypothesis via the synthesis of novel ortho-methyl substituted tetraphenylethenes and their application in cell imaging
Chem.Commun., 2014, 50, 12058
7115714 CIFC28 H24P -19.036; 9.48; 12.9
111.14; 98.54; 98.34
995Guo-Feng Zhang; Ze-Qiang Chen; Matthew P. Aldred; Zhe Hu; Tao Chen; Zhenli Huang; Xianggao Meng; Ming-Qiang Zhu
Direct validation of the restriction of intramolecular rotation hypothesis via the synthesis of novel ortho-methyl substituted tetraphenylethenes and their application in cell imaging
Chem.Commun., 2014, 50, 12058
7115715 CIFC30 H28P 4/n :212.9991; 12.9991; 6.573
90; 90; 90
1110.7Guo-Feng Zhang; Ze-Qiang Chen; Matthew P. Aldred; Zhe Hu; Tao Chen; Zhenli Huang; Xianggao Meng; Ming-Qiang Zhu
Direct validation of the restriction of intramolecular rotation hypothesis via the synthesis of novel ortho-methyl substituted tetraphenylethenes and their application in cell imaging
Chem.Commun., 2014, 50, 12058
7115716 CIFC9 H4 N4 ZnI -4 3 m16.9615; 16.9615; 16.9615
90; 90; 90
4879.7Fei Wang; Hong-Ru Fu; Yao Kang; Jian Zhang
A new approach towards zeolitic tetrazolate-imidazolate frameworks (ZTIFs) with uncoordinated N-heteroatom sites for high CO2 uptake
Chem.Commun., 2014, 50, 12065
7115717 CIFC8 H12 N6 ZnI m -3 m29.3187; 29.3187; 29.3187
90; 90; 90
25201.9Fei Wang; Hong-Ru Fu; Yao Kang; Jian Zhang
A new approach towards zeolitic tetrazolate-imidazolate frameworks (ZTIFs) with uncoordinated N-heteroatom sites for high CO2 uptake
Chem.Commun., 2014, 50, 12065
7115718 CIFC29.5 H18 B2 Cl F20 N OP 1 21 18.8098; 21.0038; 17.4138
90; 98.837; 90
3183.99Owen J. Metters; Andy M. Chapman; Alasdair P. M. Robertson; Christopher H. Woodall; Paul J. Gates; Duncan F. Wass; Ian Manners
Generation of aminoborane monomers RR'N[double bond, length as m-dash]BH2 from amine-boronium cations [RR'NH-BH2L]^+^: metal catalyst-free formation of polyaminoboranes at ambient temperature
Chem.Commun., 2014, 50, 12146
7115719 CIFC H7 B Cl NP n m a12.7715; 6.5471; 5.2055
90; 90; 90
435.26Owen J. Metters; Andy M. Chapman; Alasdair P. M. Robertson; Christopher H. Woodall; Paul J. Gates; Duncan F. Wass; Ian Manners
Generation of aminoborane monomers RR'N[double bond, length as m-dash]BH2 from amine-boronium cations [RR'NH-BH2L]^+^: metal catalyst-free formation of polyaminoboranes at ambient temperature
Chem.Commun., 2014, 50, 12146
7115720 CIFC26 H30 N4 O10 Pd3R -3 :H27.371; 27.371; 10.3756
90; 90; 120
6731.7Sandeep Pimparkar; Masilamani Jeganmohan
Palladium-catalyzed cyclization of benzamides with arynes: application to the synthesis of phenaglydon and N-methylcrinasiadine
Chem.Commun., 2014, 50, 12116
7115727 CIFC130 H118 Cl4 Cu2 F12 Fe4 N8 O P2P -113.306; 15.0432; 16.3418
105.93; 93.409; 112.27
2861.3Manik Lal Saha; Nikita Mittal; Jan W. Bats; Michael Schmittel
A six-component metallosupramolecular pentagon via self-sorting
Chem.Commun., 2014, 50, 12189
7115728 CIFC88 H78 N3 S5P -18.9864; 14.484; 40.078
90.144; 90.062; 107.934
4963Ganesan Karthik; A. Srinivasan; C. H. Suresh; Tavarekere K. Chandrashekar
Fused core-modified planar antiaromatic 32pi heptaphyrins: unusual synthesis and structural diversity
Chem.Commun., 2014, 50, 12127
7115729 CIFC88 H79 N3 S3 Se2P -18.933; 14.5081; 40.1827
90.036; 89.997; 107.971
4953.6Ganesan Karthik; A. Srinivasan; C. H. Suresh; Tavarekere K. Chandrashekar
Fused core-modified planar antiaromatic 32pi heptaphyrins: unusual synthesis and structural diversity
Chem.Commun., 2014, 50, 12127
7115730 CIFC11 H13 N O3P c a 2113.1081; 9.6334; 8.0059
90; 90; 90
1010.95Pingping Duan; Xia Lan; Ying Chen; Shao-Song Qian; Jie Jack Li; Liang Lu; Yanbo Lu; Bo Chen,; Mei Hong; Jing Zhao
Rhodium(III)-catalyzed C-H activation/[4+3] annulation of N-phenoxyacetamides and alpha,beta-unsaturated aldehydes: an efficient route to 1,2-oxazepines at room temperature
Chem.Commun., 2014, 50, 12135
7115731 CIFC11 H17 N O3P 1 21/c 111.9758; 6.7; 14.3713
90; 110.07; 90
1083.1Pingping Duan; Xia Lan; Ying Chen; Shao-Song Qian; Jie Jack Li; Liang Lu; Yanbo Lu; Bo Chen,; Mei Hong; Jing Zhao
Rhodium(III)-catalyzed C-H activation/[4+3] annulation of N-phenoxyacetamides and alpha,beta-unsaturated aldehydes: an efficient route to 1,2-oxazepines at room temperature
Chem.Commun., 2014, 50, 12135
7115732 CIFC18 H24 N O4P 1 c 112.7071; 4.847; 14.6978
90; 98.347; 90
895.67Pingping Duan; Xia Lan; Ying Chen; Shao-Song Qian; Jie Jack Li; Liang Lu; Yanbo Lu; Bo Chen,; Mei Hong; Jing Zhao
Rhodium(III)-catalyzed C-H activation/[4+3] annulation of N-phenoxyacetamides and alpha,beta-unsaturated aldehydes: an efficient route to 1,2-oxazepines at room temperature
Chem.Commun., 2014, 50, 12135
7115733 CIFC11 H13 N O2P 1 21/c 120.667; 5.2935; 9.2989
90; 94.551; 90
1014.1Pingping Duan; Xia Lan; Ying Chen; Shao-Song Qian; Jie Jack Li; Liang Lu; Yanbo Lu; Bo Chen,; Mei Hong; Jing Zhao
Rhodium(III)-catalyzed C-H activation/[4+3] annulation of N-phenoxyacetamides and alpha,beta-unsaturated aldehydes: an efficient route to 1,2-oxazepines at room temperature
Chem.Commun., 2014, 50, 12135
7115734 CIFC29 H46 Cl F10 N3 O S2P b c a26.1622; 17.7752; 15.1251
90; 90; 90
7033.8Louise E. Karagiannidis; Cally J. E. Haynes; Katie J. Holder; Isabelle L. Kirby; Stephen J. Moore; Neil J. Wells; Philip A. Gale
Highly effective yet simple transmembrane anion transporters based upon ortho-phenylenediamine bis-ureas
Chem.Commun., 2014, 50, 12050
7115735 CIFC74 H110 Cl2 F20 N10 O5 S5P -115.6225; 17.683; 18.4051
71.341; 69.884; 67.95
4317.4Louise E. Karagiannidis; Cally J. E. Haynes; Katie J. Holder; Isabelle L. Kirby; Stephen J. Moore; Neil J. Wells; Philip A. Gale
Highly effective yet simple transmembrane anion transporters based upon ortho-phenylenediamine bis-ureas
Chem.Commun., 2014, 50, 12050
7115736 CIFC24 H26 Cl F2 N7 O6P 1 21/c 17.3305; 23.581; 15.409
90; 97.282; 90
2642.1Louise E. Karagiannidis; Cally J. E. Haynes; Katie J. Holder; Isabelle L. Kirby; Stephen J. Moore; Neil J. Wells; Philip A. Gale
Highly effective yet simple transmembrane anion transporters based upon ortho-phenylenediamine bis-ureas
Chem.Commun., 2014, 50, 12050
7115737 CIFC23 H25 N O5 SP 1 21/c 111.074; 12.584; 15.635
90; 98.076; 90
2157.2Shuo Zhang; Zhengliang Xu; Jiong Jia; Chen-Ho Tung; Zhenghu Xu
Synthesis of spiroaminals by bimetallic Au/Sc relay catalysis: TMS as a traceless controlling group
Chem.Commun., 2014, 50, 12084
7115738 CIFC16 H24 N32 O0 Zn4P 1 c 119.2148; 13.3436; 10.6713
90; 95.038; 90
2725.5Shunshun Xiong; Youjin Gong; Hongxia Wang; Hailong Wang; Qiang Liu; Mei Gu; Xiaolin Wang; Banglin Chen; Zhiyong Wang
A new tetrazolate zeolite-like framework for highly selective CO2/CH4 and CO2/N2 separation
Chem.Commun., 2014, 50, 12101
7115739 CIFC66 H24 Cu6 N6 O32 S3R -3 m :H18.819; 18.819; 38.603
90; 90; 120
11840Chengling Song; Yabing He; Bin Li; Yajing Ling; Hailong Wang; Yunlong Feng; Rajamani Krishna; Banglin Chen
Enhanced CO2 sorption and selectivity by functionalization of a NbO-type metal-organic framework with polarized benzothiadiazole moieties
Chem.Commun., 2014, 50, 12105
7115740 CIFC62 H44 Al2 N4 O16P -111.8503; 12.3444; 14.6936
104.263; 90.576; 105.922
1996.31Virginie Bereau; Carine Duhayon; Jean-Pascal Sutter
Supramolecular control over recognition and efficient detection of picric acid
Chem.Commun., 2014, 50, 12061
7115741 CIFC78 H58 Al2 N10 O30P -111.8132; 15.0997; 25.2353
96.757; 96.333; 108.853
4177.3Virginie Bereau; Carine Duhayon; Jean-Pascal Sutter
Supramolecular control over recognition and efficient detection of picric acid
Chem.Commun., 2014, 50, 12061
7115742 CIFC40 H54 Al2 N6 O20P -19.3142; 11.313; 11.6842
74.397; 88.276; 70.465
1115.1Virginie Bereau; Carine Duhayon; Jean-Pascal Sutter
Supramolecular control over recognition and efficient detection of picric acid
Chem.Commun., 2014, 50, 12061
7115743 CIFC42 H40 N6P -19.8125; 14.2149; 14.358
81.339; 71.164; 86.24
1873.53Mohamed El Garah; Artur Ciesielski; Nicolas Marets; Veronique Bulach; Mir Wais Hosseini; Paolo Samori
Molecular tectonics based nanopatterning of interfaces with 2D metal-organic frameworks (MOFs)
Chem.Commun., 2014, 50, 12250
7115744 CIFC9 H13 Cu Fe0.5 I N O PI -4 3 m29.2489; 29.2489; 29.2489
90; 90; 90
25022.4Mujahuddin M. Siddiqui; Shaikh M. Mobin; Irena Senkovska; Stefan Kaskel; Maravanji S. Balakrishna
Novel zeotype frameworks with soft cyclodiphosphazane linkers and soft Cu4X4 clusters as nodes
Chem.Commun., 2014, 50, 12273
7115745 CIFC18 H26 Br2 Cu2 Fe N2 P2I -4 3 m28.8993; 28.8993; 28.8993
90; 90; 90
24135.8Mujahuddin M. Siddiqui; Shaikh M. Mobin; Irena Senkovska; Stefan Kaskel; Maravanji S. Balakrishna
Novel zeotype frameworks with soft cyclodiphosphazane linkers and soft Cu4X4 clusters as nodes
Chem.Commun., 2014, 50, 12273
7115746 CIFC35 H56 Bi In N2P 1 21/n 18.741; 21.4064; 19.0397
90; 99.26; 90
3516.2C. Ganesamoorthy; D. Blaser; C. Wolper; S. Schulz
Sequential Bi-C bond activation reactions of BiEt3via insertion reactions of RE {R = HC[C(Me)N(2,6-i-Pr2C6H3)]2; E = Al, Ga, In}
Chem.Commun., 2014, 50, 12382
7115747 CIFC33 H51 Ga N2P -110.3656; 12.119; 13.7
71.293; 75.982; 73.618
1541.9C. Ganesamoorthy; D. Blaser; C. Wolper; S. Schulz
Sequential Bi-C bond activation reactions of BiEt3via insertion reactions of RE {R = HC[C(Me)N(2,6-i-Pr2C6H3)]2; E = Al, Ga, In}
Chem.Commun., 2014, 50, 12382
7115748 CIFC35 H56 Bi Ga N2P -19.0994; 12.0444; 16.5176
74.379; 79.774; 85.921
1715.2C. Ganesamoorthy; D. Blaser; C. Wolper; S. Schulz
Sequential Bi-C bond activation reactions of BiEt3via insertion reactions of RE {R = HC[C(Me)N(2,6-i-Pr2C6H3)]2; E = Al, Ga, In}
Chem.Commun., 2014, 50, 12382
7115749 CIFC35 H56 Al Bi N2P -111.594; 12.2244; 12.6546
72.804; 88.915; 89.682
1713.1C. Ganesamoorthy; D. Blaser; C. Wolper; S. Schulz
Sequential Bi-C bond activation reactions of BiEt3via insertion reactions of RE {R = HC[C(Me)N(2,6-i-Pr2C6H3)]2; E = Al, Ga, In}
Chem.Commun., 2014, 50, 12382
7115750 CIFC24 H36 Bi N7 O9P b c n13.9796; 15.2329; 13.2072
90; 90; 90
2812.47Luis M. P. Lima; Maryline Beyler; Fatima Oukhatar; Patricia Le Saec; Alain Faivre-Chauvet; Carlos Platas-Iglesias; Rita Delgado; Raphael Tripier
H2Me-do2pa: an attractive chelator with fast, stable and inert natBi3+ and 213Bi3+ complexation for potential alpha-radioimmunotherapy applications
Chem.Commun., 2014, 50, 12371
7115751 CIFC18 H14 Co I2 N2P 1 21/n 17.9139; 15.284; 14.611
90; 90.99; 90
1767Mohamed R. Saber; Kim R. Dunbar
Ligands effects on the magnetic anisotropy of tetrahedral cobalt complexes
Chem.Commun., 2014, 50, 12266
7115752 CIFC36 H30 Co I2 P2P 1 21/c 119.165; 10.198; 17.929
90; 112.23; 90
3243.7Mohamed R. Saber; Kim R. Dunbar
Ligands effects on the magnetic anisotropy of tetrahedral cobalt complexes
Chem.Commun., 2014, 50, 12266
7115753 CIFC36 H30 As2 Co I2P 1 21/c 119.117; 10.215; 18.245
90; 111.72; 90
3309.9Mohamed R. Saber; Kim R. Dunbar
Ligands effects on the magnetic anisotropy of tetrahedral cobalt complexes
Chem.Commun., 2014, 50, 12266
7115754 CIFC30 H28 N2P 1 21/n 110.9355; 18.231; 12.2805
90; 109.896; 90
2302.2Di Wu; Yongxin Li; Rakesh Ganguly; Rei Kinjo
Synthesis and structural characterization of a C4 cumulene including 4-pyridylidene units, and its reactivity towards ammonia-borane
Chem.Commun., 2014, 50, 12378
7115755 CIFC32 H34 N2R -323.567; 23.567; 12.095
90; 90; 120
5817.6Di Wu; Yongxin Li; Rakesh Ganguly; Rei Kinjo
Synthesis and structural characterization of a C4 cumulene including 4-pyridylidene units, and its reactivity towards ammonia-borane
Chem.Commun., 2014, 50, 12378
7115756 CIFC32 H36 N2R -323.7045; 23.7045; 11.91
90; 90; 120
5795.7Di Wu; Yongxin Li; Rakesh Ganguly; Rei Kinjo
Synthesis and structural characterization of a C4 cumulene including 4-pyridylidene units, and its reactivity towards ammonia-borane
Chem.Commun., 2014, 50, 12378
7115757 CIFC25 H22 N2 O2 SP 1 21/n 113.247; 11.312; 14.218
90; 109.78; 90
2004.9Hui Li; Xiaoxun Li; Hao-Yuan Wang; Gabrielle N. Winston-McPherson; Hao-miao Julie Geng; Ilia A. Guzei; Weiping Tang
Copper-catalyzed tandem annulation/arylation for the synthesis of diindolylmethanes from propargylic alcohols
Chem.Commun., 2014, 50, 12293
7115758 CIFC31 H26 N2 O2 SP 1 21/c 114.1262; 9.3818; 20.2526
90; 108.247; 90
2549.1Hui Li; Xiaoxun Li; Hao-Yuan Wang; Gabrielle N. Winston-McPherson; Hao-miao Julie Geng; Ilia A. Guzei; Weiping Tang
Copper-catalyzed tandem annulation/arylation for the synthesis of diindolylmethanes from propargylic alcohols
Chem.Commun., 2014, 50, 12293
7115759 CIFC6 H8 Mo N2 O6 P2P 1 21/n 17.1284; 9.7853; 18.2084
90; 94.13; 90
1266.8M. B. Geeson; A. R. Jupp; J. E. McGrady; J. M. Goicoechea
On the coordination chemistry of phosphinecarboxamide: assessing ligand basicity
Chem.Commun., 2014, 50, 12281
7115760 CIFC12 H12 N2P 1 21/c 17.7787; 8.3955; 15.691
90; 93.859; 90
1022.4Jia Meng; Yi-Jin Li; Yu-Long Zhao; Xiu-Bin Bu; Qun Liu
A base-catalyzed cycloisomerization of 5-cyano-pentyne derivatives: an efficient synthesis of 3-cyano-4,5-dihydro-1H-pyrroles
Chem.Commun., 2014, 50, 12490
7115761 CIFC88 H15 N2 O2 Sc3P 1 21/c 111.156; 21.026; 21.582
90; 96.297; 90
5032Yutaka Maeda; Masato Kimura; Chihiro Ueda; Michio Yamada; Toru Kikuchi; Mitsuaki Suzuki; Wei-Wei Wang; Naomi Mizorogi; Nikolaos Karousis; Nikos Tagmatarchis; Tadashi Hasegawa; Marilyn M. Olmstead; Alan L. Balch; Shigeru Nagase; Takeshi Akasaka
Isolation and characterization of [5,6]-pyrrolidino-Sc3N@Ih-C80 diastereomers
Chem.Commun., 2014, 50, 12552
7115762 CIFC16 H27 F N O2 P SP 21 21 234.891; 6.7332; 7.8957
90; 90; 90
1854.9Toshiaki Murai; Takae Hayashi; Kyohei Yamada; Yuuki Maekawa; Mao Minoura
Fluorinative hydrolysis of phosphorothioic acid esters with a binaphthyl group through axis-to-center chirality transfer leading to the formation of P-chiral phosphorothioic monofluoridic acid salts
Chem.Commun., 2014, 50, 12473
7115763 CIFC16 H12 Cl N O S2P -17.4568; 10.4808; 10.804
110.442; 98.772; 103.159
745.1Fei Huang; Ping Wu; Liandi Wang; Jiping Chen; Chenglin Sun; Zhengkun Yu
Copper-mediated intramolecular oxidative C-H/N-H cross-coupling of alpha-alkenoyl ketene N,S-acetals to synthesize pyrrolone derivatives
Chem.Commun., 2014, 50, 12479
7115764 CIFC40 H8 Cl4 F30 N2 O4P 1 21/c 120.971; 20.21; 10.319
90; 95.733; 90
4352Chunming Liu; Chengyi Xiao; Yan Li; Wenping Hu; Zhibo Li; Zhaohui Wang
High performance, air stable n-type single crystal transistors based on core-tetrachlorinated perylene diimides
Chem.Commun., 2014, 50, 12462
7115765 CIFC22 H24 Br N OP 1 21 18.705; 9.823; 11.361
90; 97.49; 90
963.2Mu-Wang Chen; Xian-Feng Cai; Zhang-Pei Chen; Lei Shi; Yong-Gui Zhou
Facile construction of three contiguous stereogenic centers via dynamic kinetic resolution in asymmetric transfer hydrogenation of quinolines
Chem.Commun., 2014, 50, 12526
7115766 CIFC21 H37 F N O6 P Si2 WP -113.1797; 14.2791; 15.1502
96.4947; 90.2543; 93.9588
2825.91Vitaly Nesterov; Zheng-Wang Qu; Gregor Schnakenburg; Stefan Grimme; Rainer Streubel
Selective phosphanyl complex trapping using TEMPO. Synthesis and reactivity of P-functional P-nitroxyl phosphane complexes
Chem.Commun., 2014, 50, 12508
7115767 CIFC21 H39 N O6 P Si2 WP 1 21/c 114.7971; 15.3781; 12.4122
90; 95.438; 90
2811.7Vitaly Nesterov; Zheng-Wang Qu; Gregor Schnakenburg; Stefan Grimme; Rainer Streubel
Selective phosphanyl complex trapping using TEMPO. Synthesis and reactivity of P-functional P-nitroxyl phosphane complexes
Chem.Commun., 2014, 50, 12508
7115768 CIFC21 H39 F N O6 P Si2 WP -19.1438; 12.6924; 13.4939
80.702; 85.6; 71.974
1469Vitaly Nesterov; Zheng-Wang Qu; Gregor Schnakenburg; Stefan Grimme; Rainer Streubel
Selective phosphanyl complex trapping using TEMPO. Synthesis and reactivity of P-functional P-nitroxyl phosphane complexes
Chem.Commun., 2014, 50, 12508
7115769 CIFC20 H25 N5 OP 1 21/c 110.0802; 9.8139; 19.8569
90; 90.1493; 90
1964.4Cooper W. Johnston; Travis R. Schwantje; Michael J. Ferguson; Robert McDonald; Robin G. Hicks
Metal coordination, and metal-ligand redox non-innocence, modulates allosteric C-N bond homolysis in an N-benzyl tetrazine
Chem.Commun., 2014, 50, 12542
7115770 CIFC30 H27 F12 N5 O5 RuP 1 21/n 120.7821; 7.8915; 23.1429
90; 115.71; 90
3419.73Cooper W. Johnston; Travis R. Schwantje; Michael J. Ferguson; Robert McDonald; Robin G. Hicks
Metal coordination, and metal-ligand redox non-innocence, modulates allosteric C-N bond homolysis in an N-benzyl tetrazine
Chem.Commun., 2014, 50, 12542
7115771 CIFC5 H8 N6 O2P b c a9.9861; 9.1996; 16.6035
90; 90; 90
1525.33Steven P. Kelley; Patrick S. Barber; Peter H. K. Mullins; Robin D. Rogers
Structural clues to UO2^2+^/VO^2+^ competition in seawater extraction using amidoxime-based extractants
Chem.Commun., 2014, 50, 12504
7115772 CIFC10 H18 N12 O10 V2C 1 2/c 116.9496; 7.4133; 16.5253
90; 111.845; 90
1927.34Steven P. Kelley; Patrick S. Barber; Peter H. K. Mullins; Robin D. Rogers
Structural clues to UO2^2+^/VO^2+^ competition in seawater extraction using amidoxime-based extractants
Chem.Commun., 2014, 50, 12504
7115773 CIFC5 H16 N6 O9 UP 1 21/c 112.738; 21.4891; 10.819
90; 67.784; 90
2741.6Steven P. Kelley; Patrick S. Barber; Peter H. K. Mullins; Robin D. Rogers
Structural clues to UO2^2+^/VO^2+^ competition in seawater extraction using amidoxime-based extractants
Chem.Commun., 2014, 50, 12504
7115774 CIFC17 H21 N O3P 6511.2648; 11.2648; 21.2304
90; 90; 120
2333.1Dilip V. Patil; Hyun-Sub Park; Jaeyoung Koo; Jin Wook Han; Seunghoon Shin
Aerobic oxygenative cleavage of electron deficient C-C triple bonds in the gold-catalyzed cyclization of 1,6-enynes
Chem.Commun., 2014, 50, 12722
7115775 CIFC32 H30 N2 O5 S2P -111.7659; 13.1216; 19.8185
103.757; 92.1867; 107.097
2821.3Takuya Yokosaka; Tetsuhiro Nemoto; Hiroki Nakayama; Naoki Shiga; Yasumasa Hamada
Synthesis of nitrogen-containing fused-polycyclic compounds from tyramine derivatives using phenol dearomatization and cascade cyclization
Chem.Commun., 2014, 50, 12775
7115776 CIFC32 H30 N2 O5 S2P 1 21/c 110.76675; 17.892; 14.4006
90; 92.0238; 90
2772.38Takuya Yokosaka; Tetsuhiro Nemoto; Hiroki Nakayama; Naoki Shiga; Yasumasa Hamada
Synthesis of nitrogen-containing fused-polycyclic compounds from tyramine derivatives using phenol dearomatization and cascade cyclization
Chem.Commun., 2014, 50, 12775
7115777 CIFC38 H49 Cl N4 SiP 1 21/c 115.3901; 14.1529; 16.9834
90; 110.025; 90
3475.59Syed Usman Ahmad; Tibor Szilvasi; Shigeyoshi Inoue
A facile access to a novel NHC-stabilized silyliumylidene ion and C-H activation of phenylacetylene
Chem.Commun., 2014, 50, 12619
7115778 CIFC48 H42 SiC 1 2/c 126.3057; 8.3377; 34.2192
90; 99.146; 90
7409.85Syed Usman Ahmad; Tibor Szilvasi; Shigeyoshi Inoue
A facile access to a novel NHC-stabilized silyliumylidene ion and C-H activation of phenylacetylene
Chem.Commun., 2014, 50, 12619
7115779 CIFC20 H29 N3 OP 1 21/c 15.925; 21.571; 14.937
90; 98.009; 90
1890.45Merle Arrowsmith; William M. S. Shepherd; Michael S. Hill; Gabriele Kociok-Kohn
Alkaline earth catalysis for the 100% atom-efficient three component assembly of imidazolidin-2-ones
Chem.Commun., 2014, 50, 12676
7115780 CIFC28 H37 N3 OP -19.6521; 10.7206; 12.8289
101.305; 99.6262; 97.8647
1263.5Merle Arrowsmith; William M. S. Shepherd; Michael S. Hill; Gabriele Kociok-Kohn
Alkaline earth catalysis for the 100% atom-efficient three component assembly of imidazolidin-2-ones
Chem.Commun., 2014, 50, 12676
7115781 CIFC60 H80 Mg N6 O3P -110.1968; 10.6378; 25.6421
89.1862; 87.2201; 87.8363
2775.97Merle Arrowsmith; William M. S. Shepherd; Michael S. Hill; Gabriele Kociok-Kohn
Alkaline earth catalysis for the 100% atom-efficient three component assembly of imidazolidin-2-ones
Chem.Commun., 2014, 50, 12676
7115782 CIFC11 H10 B Br F2 N2P n m a12.4626; 6.6321; 13.828
90; 90; 90
1142.93Marcel Wirtz; Andreas Gruter; Philipp Rebmann; Tobias Dier; Dietrich A. Volmer; Volker Huch; Gregor Jung
Two-color emissive probes for click reactions
Chem.Commun., 2014, 50, 12694
7115783 CIFC11 H10 B F2 I N2P -17.3108; 8.5603; 10.3487
93.027; 95.908; 113.336
588.4Marcel Wirtz; Andreas Gruter; Philipp Rebmann; Tobias Dier; Dietrich A. Volmer; Volker Huch; Gregor Jung
Two-color emissive probes for click reactions
Chem.Commun., 2014, 50, 12694
7115784 CIFC16 H19 B F2 N2 SiP c a 2123.5959; 11.5341; 12.3552
90; 90; 90
3362.56Marcel Wirtz; Andreas Gruter; Philipp Rebmann; Tobias Dier; Dietrich A. Volmer; Volker Huch; Gregor Jung
Two-color emissive probes for click reactions
Chem.Commun., 2014, 50, 12694
7115785 CIFC16 H19 B F2 N2 SiP -17.0599; 9.2121; 13.9179
88.475; 76.337; 72.777
839.2Marcel Wirtz; Andreas Gruter; Philipp Rebmann; Tobias Dier; Dietrich A. Volmer; Volker Huch; Gregor Jung
Two-color emissive probes for click reactions
Chem.Commun., 2014, 50, 12694
7115786 CIFC28 H20 N4 Ni2 O2 S8 ZnP 3 1 c27.525; 27.525; 24.215
90; 90; 120
15888Thomas B. Faust; Pavel M. Usov; Deanna M. D'Alessandro; Cameron J. Kepert
Highly unusual interpenetration isomers of electroactive nickel bis(dithiolene) coordination frameworks
Chem.Commun., 2014, 50, 12772
7115787 CIFC40 H48 N8 Ni2 O4 S8 ZnC 1 2/c 115.35; 22.346; 15.4658
90; 107.269; 90
5065.8Thomas B. Faust; Pavel M. Usov; Deanna M. D'Alessandro; Cameron J. Kepert
Highly unusual interpenetration isomers of electroactive nickel bis(dithiolene) coordination frameworks
Chem.Commun., 2014, 50, 12772
7115788 CIFC15 H29 F15 Ga N4 Na P2C 1 2/c 131.23; 10.037; 18.142
90; 116.85; 90
5074Rajiv Bhalla; William Levason; Sajinder K. Luthra; Graeme McRobbie; Gillian Reid; George Sanderson; Wenjian Zhang
[GaF3(BzMe2-tacn)] - a neutral 'metalloligand' towards alkali metal and ammonium cations in water
Chem.Commun., 2014, 50, 12673
7115789 CIFC15 H25 B F7 Ga N3 NaP 1 21/c 110.967; 15.793; 22.313
90; 90.057; 90
3864.7Rajiv Bhalla; William Levason; Sajinder K. Luthra; Graeme McRobbie; Gillian Reid; George Sanderson; Wenjian Zhang
[GaF3(BzMe2-tacn)] - a neutral 'metalloligand' towards alkali metal and ammonium cations in water
Chem.Commun., 2014, 50, 12673
7115790 CIFC30 H62 F18 Ga2 K2 N6 O6 P2P -19.5708; 10.2233; 13.1728
95.498; 91.765; 112.97
1178Rajiv Bhalla; William Levason; Sajinder K. Luthra; Graeme McRobbie; Gillian Reid; George Sanderson; Wenjian Zhang
[GaF3(BzMe2-tacn)] - a neutral 'metalloligand' towards alkali metal and ammonium cations in water
Chem.Commun., 2014, 50, 12673
7115791 CIFC14 H14 O2 S2P 1 21/c 15.7235; 7.5497; 15.671
90; 97.432; 90
671.47Jose A. Souto; Willian Lewis; Robert A. Stockman
Isolation of stable non cyclic 1,2-disulfoxides. Revisiting the thermolysis of S-aryl sulfinimines
Chem.Commun., 2014, 50, 12630
7115792 CIFC18 H22 O2 S2P -17.5624; 8.0233; 8.1209
84.776; 69.822; 61.946
406.65Jose A. Souto; Willian Lewis; Robert A. Stockman
Isolation of stable non cyclic 1,2-disulfoxides. Revisiting the thermolysis of S-aryl sulfinimines
Chem.Commun., 2014, 50, 12630
7115793 CIFC14 H14 S2P 1 21 17.5701; 5.7018; 14.6979
90; 94.682; 90
632.29Jose A. Souto; Willian Lewis; Robert A. Stockman
Isolation of stable non cyclic 1,2-disulfoxides. Revisiting the thermolysis of S-aryl sulfinimines
Chem.Commun., 2014, 50, 12630
7115794 CIFC45 H48 B F20 P SiP -111.6772; 12.5736; 17.0286
79.442; 75.102; 77.292
2335.61Thomas J. Herrington; Bryan J. Ward; Laurence R. Doyle; Joe McDermott; Andrew J. P. White; Patricia A. Hunt; Andrew E. Ashley
Bypassing a highly unstable frustrated Lewis pair: dihydrogen cleavage by a thermally robust silylium-phosphine adduct
Chem.Commun., 2014, 50, 12753
7115795 CIFC189 H20 N6 S6 Sc6P -110.9934; 13.7404; 17.238
91.347; 101.124; 105.539
2453.8Bin Liu; Hailin Cong; Xiaofang Li; Bing Yu; Lipiao Bao; Wenting Cai; Yunpeng Xie; Xing Lu
Highly regioselective 1,3-dipolar cycloaddition of diphenylnitrilimine to Sc3N@Ih-C80 affording a very stable, unprecedented pyrazole-ring fused derivative of endohedral metallofullerenes
Chem.Commun., 2014, 50, 12710
7115796 CIFC52 H40 O3 Si3P -110.688; 14.471; 17.002
104.62; 103.75; 103.5
2348Yuanjing Cai; Kerim Samedov; Haley Albright; Brian S. Dolinar; Ilia A. Guzei; Rongrong Hu; Chaocan Zhang; Ben Zhong Tang; Robert West
High solid-state fluorescence in ring-shaped AEE-active tetraphenylsilole derivatives
Chem.Commun., 2014, 50, 12714
7115797 CIFC60 H52 O4 Si4C 1 2/c 119.956; 28.804; 10.023
90; 102.117; 90
5633Yuanjing Cai; Kerim Samedov; Haley Albright; Brian S. Dolinar; Ilia A. Guzei; Rongrong Hu; Chaocan Zhang; Ben Zhong Tang; Robert West
High solid-state fluorescence in ring-shaped AEE-active tetraphenylsilole derivatives
Chem.Commun., 2014, 50, 12714
7115798 CIFC80 H60 O4 Si4P -111.226; 12.704; 13.186
115.699; 103.433; 101.434
1549.3Yuanjing Cai; Kerim Samedov; Haley Albright; Brian S. Dolinar; Ilia A. Guzei; Rongrong Hu; Chaocan Zhang; Ben Zhong Tang; Robert West
High solid-state fluorescence in ring-shaped AEE-active tetraphenylsilole derivatives
Chem.Commun., 2014, 50, 12714
7115799 CIFC60 H52 O4 Si4P -112.373; 12.616; 18.679
75.714; 73.48; 66.738
2538Yuanjing Cai; Kerim Samedov; Haley Albright; Brian S. Dolinar; Ilia A. Guzei; Rongrong Hu; Chaocan Zhang; Ben Zhong Tang; Robert West
High solid-state fluorescence in ring-shaped AEE-active tetraphenylsilole derivatives
Chem.Commun., 2014, 50, 12714
7115800 CIFC28 H22P 1 21/c 17.86; 5.7022; 22.413
90; 103.09; 90
978.4Yuanjing Cai; Kerim Samedov; Haley Albright; Brian S. Dolinar; Ilia A. Guzei; Rongrong Hu; Chaocan Zhang; Ben Zhong Tang; Robert West
High solid-state fluorescence in ring-shaped AEE-active tetraphenylsilole derivatives
Chem.Commun., 2014, 50, 12714
7115801 CIFC49 H68 F4 N2 P4 Pd2 S2P 1 21/n 117.9352; 15.2259; 19.6389
90; 102.132; 90
5243.2Chandra Mouli Palit; Daniel J. Graham; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Reduction of CO2 to free CO by a Pd(I)-Pd(I) dimer
Chem.Commun., 2014, 50, 12840
7115802 CIFC40 H52 Si2P 21 21 2114.4346; 15.1821; 17.0101
90; 90; 90
3727.7Xiaomin Xu; Bowen Shan; Sergii Kalytchuk; Minghua Xie; Shuaijun Yang; Danqing Liu; Stephen V. Kershaw; Qian Miao
Synthesis, solution-processed thin film transistors and solid solutions of silylethynylated diazatetracenes
Chem.Commun., 2014, 50, 12828
7115803 CIFC38 H46 Cl4 N2 Si2C 1 2/c 135.551; 15.1706; 14.9907
90; 104.265; 90
7835.6Xiaomin Xu; Bowen Shan; Sergii Kalytchuk; Minghua Xie; Shuaijun Yang; Danqing Liu; Stephen V. Kershaw; Qian Miao
Synthesis, solution-processed thin film transistors and solid solutions of silylethynylated diazatetracenes
Chem.Commun., 2014, 50, 12828
7115804 CIFC78 H102 N2 Si4P 21 21 2114.4307; 15.1331; 16.975
90; 90; 90
3707Xiaomin Xu; Bowen Shan; Sergii Kalytchuk; Minghua Xie; Shuaijun Yang; Danqing Liu; Stephen V. Kershaw; Qian Miao
Synthesis, solution-processed thin film transistors and solid solutions of silylethynylated diazatetracenes
Chem.Commun., 2014, 50, 12828
7115805 CIFC38 H46 Cl4 N2 Si2C 1 2/c 135.4482; 15.1828; 14.9575
90; 103.908; 90
7814.2Xiaomin Xu; Bowen Shan; Sergii Kalytchuk; Minghua Xie; Shuaijun Yang; Danqing Liu; Stephen V. Kershaw; Qian Miao
Synthesis, solution-processed thin film transistors and solid solutions of silylethynylated diazatetracenes
Chem.Commun., 2014, 50, 12828
7115806 CIFC38 H46 Cl4 N2 Si2C 1 2/c 135.3907; 15.1394; 14.9478
90; 104.143; 90
7766.2Xiaomin Xu; Bowen Shan; Sergii Kalytchuk; Minghua Xie; Shuaijun Yang; Danqing Liu; Stephen V. Kershaw; Qian Miao
Synthesis, solution-processed thin film transistors and solid solutions of silylethynylated diazatetracenes
Chem.Commun., 2014, 50, 12828
7115807 CIFC36 H78 K2 Mg2 Si6P 1 21/c 112.0299; 10.6135; 19.818
90; 95.26; 90
2519.7Sharon E. Baillie; Tobias D. Bluemke; William Clegg; Alan R. Kennedy; Jan Klett; Luca Russo; Marco de Tullio; Eva Hevia
Potassium-alkyl magnesiates: synthesis, structures and Mg-H exchange applications of aromatic and heterocyclic substrates
Chem.Commun., 2014, 50, 12859
7115808 CIFC34 H90 K2 Mg N6 Si4P 21 21 2112.2327; 17.0823; 25.0444
90; 90; 90
5233.3Sharon E. Baillie; Tobias D. Bluemke; William Clegg; Alan R. Kennedy; Jan Klett; Luca Russo; Marco de Tullio; Eva Hevia
Potassium-alkyl magnesiates: synthesis, structures and Mg-H exchange applications of aromatic and heterocyclic substrates
Chem.Commun., 2014, 50, 12859
7115809 CIFC28 H76 K2 Mg N4 Si4P -111.0105; 14.4843; 14.9162
85.542; 75.58; 82.035
2279.34Sharon E. Baillie; Tobias D. Bluemke; William Clegg; Alan R. Kennedy; Jan Klett; Luca Russo; Marco de Tullio; Eva Hevia
Potassium-alkyl magnesiates: synthesis, structures and Mg-H exchange applications of aromatic and heterocyclic substrates
Chem.Commun., 2014, 50, 12859
7115810 CIFC18 H16 F N O3P 1 21/c 111.2895; 10.3789; 13.6515
90; 112.765; 90
1474.97Jia-Jia Cao; Xiang Wang; Shun-Yi Wang; Shun-Jun Ji
Mn(III)-mediated reactions of 2-isocyanobiaryl with 1,3-dicarbonyl compounds: efficient synthesis of 6-alkylated and 6-monofluoro-alkylated phenanthridines
Chem.Commun., 2014, 50, 12892
7115811 CIFC26 H33 Br O2P -111.0845; 12.9326; 15.6251
91.858; 97.458; 94.863
2210.8Irem Yalavac; Sarah E. Lyons; Michael R. Webb; David J. Procter
SmI2-H2O-mediated 5-exo/6-exo lactone radical cyclisation cascades
Chem.Commun., 2014, 50, 12863
7115812 CIFC18 H15 F3 OF d d 238.6451; 18.5006; 8.3788
90; 90; 90
5990.5Jun Xu; Yun-Long Wang; Tian-Jun Gong; Bin Xiao; Yao Fu
Copper-catalyzed endo-type trifluoromethylarylation of alkynes
Chem.Commun., 2014, 50, 12915
7115813 CIFC13 H16 N4 OP n 21 a9.252; 10.1218; 13.0422
90; 90; 90
1221.36Samuel J. James; Andrea Perrin; Christopher D. Jones; Dmitry S. Yufit; Jonathan W. Steed
Highly interlocked anion-bridged supramolecular networks from interrupted imidazole-urea gels
Chem.Commun., 2014, 50, 12851
7115814 CIFC52 H64 Cl2 Cu N16 O4P 4/n19.9812; 19.9812; 6.9508
90; 90; 90
2775.1Samuel J. James; Andrea Perrin; Christopher D. Jones; Dmitry S. Yufit; Jonathan W. Steed
Highly interlocked anion-bridged supramolecular networks from interrupted imidazole-urea gels
Chem.Commun., 2014, 50, 12851
7115815 CIFC80 H104 Cu N26 O14P -113.1; 13.3909; 13.441
75.123; 77.751; 74.712
2171.6Samuel J. James; Andrea Perrin; Christopher D. Jones; Dmitry S. Yufit; Jonathan W. Steed
Highly interlocked anion-bridged supramolecular networks from interrupted imidazole-urea gels
Chem.Commun., 2014, 50, 12851
7115816 CIFC18 H22 Au Cl N4 O2 P2 SP -17.2892; 10.5717; 13.9822
98.495; 90.191; 91.103
1065.42Maria J. Rodriguez-Alvarez; Cristian Vidal; Josefina Diez; Joaquin Garcia-Alvarez
Introducing deep eutectic solvents as biorenewable media for Au(I)-catalysed cycloisomerisation of upsilon-alkynoic acids: an unprecedented catalytic system
Chem.Commun., 2014, 50, 12927
7115817 CIFC42 H26 B F2 N5 S2P -18.2448; 13.187; 19.061
100.053; 95.703; 95.546
2016.7Xiaolin Zhu; Rui Liu; Yuhao Li; Hai Huang; Qiang Wang; Danfeng Wang; Xuan Zhu; Shishen Liu; Hongjun Zhu
An AIE-active boron-difluoride complex: multi-stimuli-responsive fluorescence and application in data security protection
Chem.Commun., 2014, 50, 12951
7115818 CIFC66 H74 Cr2 N4 O2P -110.547; 11.953; 13.565
65.131; 88.615; 67.984
1420.2Awal Noor; Sadaf Qayyum; Tobias Bauer; Stefan Schwarz; Birgit Weber; Rhett Kempe
CO2 and SO2 activation by a Cr-Cr quintuple bond
Chem.Commun., 2014, 50, 13127
7115819 CIFC50 H58 Cr2 N4 O4 S2P 1 21/n 110.829; 19.623; 23.199
90; 93.411; 90
4921Awal Noor; Sadaf Qayyum; Tobias Bauer; Stefan Schwarz; Birgit Weber; Rhett Kempe
CO2 and SO2 activation by a Cr-Cr quintuple bond
Chem.Commun., 2014, 50, 13127

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