Crystallography Open Database

Result: there are 27369 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Searching year of publication is 2015

Blue left arrow Blue left arrow First | Blue left arrow Previous 300 | of 92 | Next 300 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1520454 CIFC32 H26 N4 OP 1 21/c 17.474; 9.2641; 35.865
90; 91.227; 90		2482.7Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520455 CIFC36 H28 N4 OP 1 21/c 111.2158; 10.0647; 24.8459
90; 97.414; 90		2781.25Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520456 CIFC21 H17 Br F3 N O2P 21 21 219.1964; 13.4028; 15.611
90; 90; 90		1924.2Zhang, Xiao; Liu, Wen-Bo; Tu, Hang-Fei; You, Shu-Li
Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles
Chem. Sci., 2015, 6, 4525
1520484 CIFC42 H59 N2 O5 YP 1 21/n 111.5994; 17.3406; 20.277
90; 101.616; 90		3995Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520485 CIFC42 H59 N2 O5 YbP 1 21/n 111.6286; 17.386; 20.275
90; 101.788; 90		4012.6Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520486 CIFC42 H55 Cl4 N2 O5 YP 1 21/n 111.801; 20.57; 18.885
90; 104.53; 90		4437.6Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520487 CIFC45 H55 Cl4 N2 O4 YbC 1 2/c 124.1809; 15.0796; 25.3731
90; 102.719; 90		9025Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520488 CIFC50 H75 N2 O3 YP -110.5853; 12.7151; 19.2574
89.476; 76.593; 74.104		2420.77Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520489 CIFC36 H43 Cl4 N2 O4 YbP -111.1518; 14.3086; 14.3249
110.668; 112.05; 101.601		1829.7Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520490 CIFC101 H141 N4 O6 Y2P -115.7733; 17.1095; 20.0984
93.832; 99.873; 110.235		4967Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520491 CIFC60 H74 N4 O4P -111.2497; 12.373; 20.0241
95.185; 106.067; 94.622		2651.1Xia, Debin; Marszalek, Tomasz; Li, Mengmeng; Guo, Xin; Baumgarten, Martin; Pisula, Wojciech; Müllen, Klaus
Solution-Processable n-Type Organic Semiconductors Based on Angular-Shaped 2-(12H-Dibenzofluoren-12-ylidene)malononitrilediimide.
Organic letters, 2015, 17, 3074-3077
1520492 CIFC13 H10 Cl N3 O2P b c a7.24; 11.439; 29.79
90; 90; 90		2467Xia, Guomin; Ruan, Chengyan; Wang, Hongming
Highly sensitive detection of carbon dioxide by a pyrimido[1,2-a]benzimidazole derivative: combining experimental and theoretical studies.
The Analyst, 2015, 140, 5099-5104
1520493 CIFC30 H26 Co F6 N6 O7 S2P -111.0341; 12.5779; 13.0044
82.865; 88.796; 66.687		1643.85Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520494 CIFC29 H35 F6 N7 O12 S2 ZnP 1 21/n 113.0156; 12.7488; 22.3963
90; 92.294; 90		3713.3Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520495 CIFC36 H42 Co F6 N6 O11 S2P 1 21/n 112.4657; 15.6171; 21.316
90; 91.047; 90		4149.1Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520496 CIFC30 H30 F6 N6 O11 S2 ZnP -114.707; 21.388; 25.657
67.683; 75.282; 89.683		7184Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520497 CIFC30 H32.5 F6 N6 O10 S2 ZnP -111.0677; 13.3087; 13.5558
71.591; 78.668; 67.235		1740.65Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520498 CIFC29 H27.5 Co F6 N7 O9.25 S2P -113.2461; 20.9848; 26.9609
111.361; 96.713; 94.455		6872.7Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520499 CIFC37.35 H42.46 Cl2 N6 O3.88 RuP -110.4996; 13.3012; 13.4802
80.434; 82.981; 86.221		1840.52Tong, Lianpeng; Zong, Ruifa; Zhou, Rongwei; Kaveevivitchai, Nattawut; Zhang, Gang; Thummel, Randolph P.
Ruthenium catalysts for water oxidation involving tetradentate polypyridine-type ligands.
Faraday discussions, 2015, 185, 87-104
1520502 CIFC37 H20 F4 N4 O4P 1 21/c 122.674; 10.0584; 13.4593
90; 99.514; 90		3027.4Zhang, Jian; Jin, Jianyong; Cooney, Ralph; Fu, Qiang; Qiao, Greg G.; Thomas, Sylvie; Merkel, Tim C.
Synthesis of perfectly alternating copolymers for polymers of intrinsic microporosity
Polym. Chem., 2015, 6, 5003
1520504 CIFC20 H16 I N OP -110.699; 11.726; 22.2683
94.284; 101.795; 109.369		2549Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520505 CIFC20 H16 I N OP b c a7.2355; 20.9295; 23.0167
90; 90; 90		3485.5Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520506 CIFC30 H24 Cl4 N2 O2 ZnC 1 2/c 121.692; 4.8468; 28.611
90; 111.442; 90		2799.9Men, Guangwen; Chen, Chunrong; Liang, Chunshuang; Han, Wenkun; Jiang, Shimei
A novel cascade strategy with supramolecular and chemodosimetric methods for designing a fluorescent ratiometric detector hypersensitive to trace water.
The Analyst, 2015, 140, 5454-5458
1520507 CIFC42 H86 N4 O6P -14.7746; 5.4698; 44.772
91.162; 91.821; 96.985		1159.66Zhong, Di-Chang; Liao, Lie-Qiang; Wang, Ke-Jun; Liu, Hui-Jin; Luo, Xu-Zhong
Heat-set gels formed from easily accessible gelators of a succinamic acid derivative (SAD) and a primary alkyl amine (R-NH2).
Soft matter, 2015, 11, 6386-6392
1520513 CIFC24 H24P 1 21/n 17.4014; 30.606; 7.739
90; 100.806; 90		1722Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520514 CIFC20 H24 O4 SP 1 n 111.2988; 5.7063; 14.045
90; 102.129; 90		885.3Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520515 CIFC25 H29 N O5 SF d d 222.419; 52.094; 7.523
90; 90; 90		8786Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520516 CIFC25 H29 N O5 SC 1 2/c 130.166; 11.6914; 14.2065
90; 113.297; 90		4601.9Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520517 CIFC19 H19 F OP 21 21 218.4903; 9.6656; 18.663
90; 90; 90		1531.6Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520518 CIFC43 H41 N3 O4P 1 21/c 131.617; 15.428; 14.478
90; 101.899; 90		6910Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke
Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols
Organic Letters, 2015, 17, 3138-3141
1520519 CIFC13 H12 Cl N O4P 21 21 217.9023; 12.49; 12.9
90; 90; 90		1273.2Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo
Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones.
Organic letters, 2015, 17, 3026-3029
1520520 CIFC39 H40 B F2 N3 O4P -18.745; 10.225; 20.19
89.48; 86.38; 65.669		1641.4Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520521 CIFC37.5 H36.5 B Cl1.5 F2 N3 O4P -18.776; 10.567; 19.225
84.193; 82.204; 69.585		1652.6Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520522 CIFC46 H44 B2 N2 O2P 1 21/c 17.274; 17.864; 15.322
90; 100.332; 90		1958.7Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520523 CIFC42 H36 B2 N2 O2P 1 21/c 17.054; 17.672; 13.751
90; 96.406; 90		1703.5Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520524 CIFC53 H69 N6 O25 P2 RuP n n a21.3561; 19.4016; 14.9635
90; 90; 90		6200.01Fielden, John; Sumliner, Jordan M.; Han, Nannan; Geletii, Yurii V.; Xiang, Xu; Musaev, Djamaladdin G.; Lian, Tianquan; Hill, Craig L.
Water splitting with polyoxometalate-treated photoanodes: enhancing performance through sensitizer design
Chem. Sci., 2015, 6, 5531
1520525 CIFC34 H20 Co2 N2 O8P -112.956; 13.122; 13.752
84.973; 67.595; 83.245		2144.1Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520526 CIFC17 H10 Co N O4P -17.7116; 10.2889; 11.0085
71.43; 86.282; 82.265		820.22Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520527 CIFC34 H20 Co2 N2 O8P -112.9698; 13.1304; 13.7579
85.041; 68.014; 83.544		2156.3Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520528 CIFC17 H10 Co N O4P -17.6397; 10.4311; 10.9968
71.121; 87.061; 83.361		823.5Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520529 CIFC51 H30 Co3 N3 O12C 1 2 117.173; 19.784; 13.887
90; 95.771; 90		4694Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520530 CIFC51 H30 Co3 N3 O12C 1 2 117.0391; 20.0278; 13.8334
90; 96.243; 90		4692.7Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520531 CIFC13 H8 Br Mn N2 O5P 1 21/c 115.1341; 13.1528; 7.0537
90; 98.591; 90		1388.33Walsh, James J.; Smith, Charlotte L.; Neri, Gaia; Whitehead, George F. S.; Robertson, Craig M.; Cowan, Alexander J.
FDCDU15 - Carbon Dioxide Utilisation: Improving the efficiency of electrochemical CO2 reduction using immobilized manganese complexes
Faraday Discuss., 2015
1520532 CIFC23 H26 Br Mn N2 O10P -16.52291; 13.1864; 16.0537
102.912; 95.846; 98.607		1317.59Walsh, James J.; Smith, Charlotte L.; Neri, Gaia; Whitehead, George F. S.; Robertson, Craig M.; Cowan, Alexander J.
FDCDU15 - Carbon Dioxide Utilisation: Improving the efficiency of electrochemical CO2 reduction using immobilized manganese complexes
Faraday Discuss., 2015
1520533 CIFC15 H16 O2P -17.5962; 8.0111; 10.4017
111.355; 93.168; 90.2112		588.43Park, Jung-Woo; Kou, Kevin G. M.; Kim, Daniel K.; Dong, Vy M.
Rh-Catalyzed Desymmetrization of α-Quaternary Centers by Isomerization-Hydroacylation.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 4479-4483
1520534 CIFC20 H20 N4 O4P 17.9466; 14.9541; 16.2556
78.9198; 79.5663; 82.7612		1856Park, Jung-Woo; Kou, Kevin G. M.; Kim, Daniel K.; Dong, Vy M.
Rh-Catalyzed Desymmetrization of α-Quaternary Centers by Isomerization-Hydroacylation.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 4479-4483
1520535 CIFC41 H46 N4 S2C 1 2/c 124.1082; 18.137; 16.7624
90; 106.002; 90		7045.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520536 CIFC65 H64 B2 N4 S2I 41/a :241.594; 41.594; 13.1413
90; 90; 90		22735.2Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520537 CIFC71 H56 B2 F20 N4 O2 S2P 1 21/c 114.5445; 22.7136; 19.7133
90; 98.039; 90		6448.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520538 CIFC42 H49 B N2 S3P -16.3487; 16.1168; 19.3671
74.649; 85.857; 83.373		1896.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520539 CIFC32 H45 B N2 S3P -16.524; 13.6675; 18.0034
98.64; 95.792; 101.67		1539.9Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520540 CIFC30 H39 B Br2 N2 S3P -110.2773; 12.1331; 14.8059
65.908; 79.793; 68.09		1563Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520542 CIFC32 H25 N O4P 1 21 16.62144; 20.1343; 9.362
90; 100.915; 90		1225.54Zhao, Shuai; Zhao, Yuan-Yuan; Lin, Jun-Bing; Xie, Ting; Liang, Yong-Min; Xu, Peng-Fei
Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives.
Organic letters, 2015, 17, 3206-3209
1520543 CIFC25 H20 Au Br F3 PP 21 21 218.3781; 14.3827; 19.3153
90; 90; 90		2327.49Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520544 CIFC27 H22 Au2 Br Cl2 F6 PP 1 21/n 111.2208; 16.168; 17.031
90; 108.049; 90		2937.7Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520545 CIFC56 H40 Au6 Br2 F18 O2 P2C 1 2/m 111.61; 23.9064; 11.1568
90; 97.975; 90		3066.66Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520546 CIFS3 TiP 1 21/m 14.9476; 3.3787; 8.7479
90; 97.617; 90		144.944Lipatov, Alexey; Wilson, Peter M.; Shekhirev, Mikhail; Teeter, Jacob D.; Netusil, Ross; Sinitskii, Alexander
Few-layered titanium trisulfide (TiS3) field-effect transistors.
Nanoscale, 2015, 7, 12291-12296
1520547 CIFC25 H24 SP -19.4128; 9.6074; 12.0794
97.999; 97.992; 108.357		1007.08Zhang, Hang; Wang, Bo; Yi, Heng; Zhang, Yan; Wang, Jianbo
Rh(II)-Catalyzed [2,3]-Sigmatropic Rearrangement of Sulfur Ylides Derived from Cyclopropenes and Sulfides.
Organic letters, 2015, 17, 3322-3325
1520552 CIFC36 H22 N12P 1 21/n 115.3809; 11.5149; 17.7975
90; 90.677; 90		3151.9Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520553 CIFC35 H19 F4 N6 O2 PI b a 221.689; 29.869; 10.7143
90; 90; 90		6941Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520554 CIFC51 H33 Co F4 N8P 1 21/c 112.3996; 15.4999; 21.5037
90; 97.248; 90		4099.8Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520555 CIFC24 H20 Br2 N2C 1 2/c 116.3504; 14.9527; 9.2389
90; 92.387; 90		2256.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520556 CIFC24 H18 N2P -19.4274; 12.3411; 15.5934
83.302; 82.714; 79.24		1759.9Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520557 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.33; 10.8862; 17.8919
90; 110.048; 90		2622Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520558 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.3809; 10.9748; 11.0438
109.43; 98.185; 97.328		1153.7Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520559 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.4495; 11.0503; 11.0576
109.671; 96.586; 97.962		1172.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520560 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.369; 10.925; 18.106
90; 110.574; 90		2661Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520561 CIFC51 H58 F6 O14 S2P -111.2709; 11.7647; 20.1194
88.271; 83.035; 86.352		2642.1Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520562 CIFC46 H46 Cl2 F6 O14 S2P 1 n 111.616; 18.2419; 11.617
90; 94.1589; 90		2455.14Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520563 CIFC48.75 H55.04 Cl2.25 F3 O12 SP n a 2135.9931; 12.0648; 11.369
90; 90; 90		4937Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520564 CIFC51 H58 F6 O14 S2P 21 21 2111.3045; 12.1357; 37.187
90; 90; 90		5101.6Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520565 CIFC51 H55 F9 O16 S3P 1 21/c 122.0373; 11.9982; 22.7155
90; 110.288; 90		5633.5Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520566 CIFC51 H55 F9 O16 S3P b c a20.6289; 22.2856; 24.1696
90; 90; 90		11111.4Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520572 CIFC43 H56 O19P -18.6734; 11.1397; 11.8133
92.575; 96.635; 108.711		1069.74Lai, Yongji; Liu, Tingting; Sa, Rongjian; Wei, Xialan; Xue, Yongbo; Wu, Zhaodi; Luo, Zengwei; Xiang, Ming; Zhang, Yonghui; Yao, Guangmin
Neolignans with a Rare 2-Oxaspiro[4.5]deca-6,9-dien-8-one Motif from the Stem Bark of Cinnamomum subavenium.
Journal of natural products, 2015, 78, 1740-1744
1520573 CIFC17 H15 N SP 21 21 216.1669; 12.182; 17.8605
90; 90; 90		1341.77Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520574 CIFC19 H17 N OP b c a7.4565; 18.3137; 20.6855
90; 90; 90		2824.73Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520575 CIFC16 H15 N3P 1 21/m 19.7773; 6.90436; 9.79548
90; 98.985; 90		653.14Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520576 CIFC21 H15 N3P 1 21/c 114.0946; 11.4421; 9.74761
90; 99.2056; 90		1551.77Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520577 CIFC20 H20 O6P 21 21 2110.1756; 12.2477; 13.4918
90; 90; 90		1681.45Bautista, Elihú; Fragoso-Serrano, Mabel; Toscano, Rubén A; García-Peña, María Del Rosario; Ortega, Alfredo
Teotihuacanin, a Diterpene with an Unusual Spiro-10/6 System from Salvia amarissima with Potent Modulatory Activity of Multidrug Resistance in Cancer Cells.
Organic letters, 2015, 17, 3280-3282
1520578 CIFC56 H57 Cu3 N38 O22.5P -114.1016; 14.4022; 20.4554
94.939; 95.386; 119.157		3570.2Palomas, David; Kalamaras, Christos; Haycock, Peter; White, Andrew J. P.; Hellgardt, Klaus; Horton, Andrew; Crimmin, Mark R.
Re-evaluating selectivity as a determining factor in peroxidative methane oxidation by multimetallic copper complexes
Catal. Sci. Technol., 2015, 5, 4108
1520579 CIFC24 H52 B6 Cu4 F8 N4 O17C 1 2/c 114.4651; 19.3815; 14.1054
90; 90.991; 90		3953.9Palomas, David; Kalamaras, Christos; Haycock, Peter; White, Andrew J. P.; Hellgardt, Klaus; Horton, Andrew; Crimmin, Mark R.
Re-evaluating selectivity as a determining factor in peroxidative methane oxidation by multimetallic copper complexes
Catal. Sci. Technol., 2015, 5, 4108
1520580 CIFC84 H118 Al3 N6 O6P 1 21/n 113.8521; 24.7127; 22.886
90; 93.263; 90		7821.7Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520581 CIFC27 H37 Al N2 O2P 1 21 19.9462; 10.3018; 12.8708
90; 108.547; 90		1250.3Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520582 CIFC29 H41 Al N2 O3P 21 21 218.0191; 13.4769; 25.379
90; 90; 90		2742.77Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520583 CIFC41 H65 Al N2 O3P 1 21/c 116.6845; 19.6643; 12.0401
90; 99.106; 90		3900.4Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520584 CIFC32 H48 Hf N2 O4P 1 21/c 114.0484; 13.4118; 16.8344
90; 101.404; 90		3109.22Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520585 CIFC32 H48 Hf N2 O4P 4310.3884; 10.3884; 28.732
90; 90; 90		3100.72Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520586 CIFC32 H48 Hf N2 O4P 4110.39461; 10.39461; 28.7569
90; 90; 90		3107.12Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520587 CIFC31 H45.67 Al N2 O3P a -326.2561; 26.2561; 26.2561
90; 90; 90		18100.5Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520588 CIFC32 H48 N2 O4 TiP 1 21/c 113.7916; 12.9946; 17.548
90; 102.79; 90		3066.86Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520589 CIFC45 H70 ThP 1 c 112.658; 10.48; 18.889
90; 127; 90		2001Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520590 CIFC48 H74 ThP 1 21/n 110.699; 26.148; 17.831
90; 98.273; 90		4936Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520591 CIFC49 H72 ThP -110.468; 11.297; 18.569
80.098; 82.085; 78.986		2110.8Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520592 CIFC53 H73 N ThP -111.109; 21.888; 21.958
97.052; 90.196; 90.925		5298Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520593 CIFC53 H73 N O ThP 1 21/c 115.278; 12.306; 25.718
90; 90.308; 90		4835.2Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520594 CIFC52 H77 N O ThP -110.9616; 11.0914; 20.157
77.206; 84.115; 75.93		2315.1Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520595 CIFC15 H20 N2 O3P 1 21 17.9384; 7.0246; 12.9394
90; 98.464; 90		713.7Mercado-Marin, Eduardo V; Sarpong, Richmond
Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 5048-5052
1520596 CIFC26 H29 N3 O3P 21 21 218.7961; 9.7026; 35.0914
90; 90; 90		2994.9Mercado-Marin, Eduardo V; Sarpong, Richmond
Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 5048-5052
1520597 CIFC16 H12 Cl N OP 21 21 219.3918; 13.5329; 51.624
90; 90; 90		6561.3Pedroni, J.; Saget, T.; Donets, P. A.; Cramer, N.
Enantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system
Chem. Sci., 2015, 6, 5164
1520598 CIFC40 H62 N2 Si2P -19.4109; 10.1841; 11.6538
91.036; 102.694; 116.006		970.92Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520599 CIFC20 H31 N OP 1 21/n 19.269; 17.342; 11.775
90; 96.71; 90		1880Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520600 CIFC46 H70 N2 Si2P -112.8; 13.86; 14.36
66.45; 79.9; 67.84		2162Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520601 CIFC46 H70 N2 Si2P -112.79; 13.783; 14.433
66.35; 79.58; 67.48		2152Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520602 CIFC24 H39 N O Se2 SiP 1 21/n 114.6952; 10.08; 17.7472
90; 109.567; 90		2477.04Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520611 CIFC22 H23 F N6 O5P 1 21/c 113.8135; 13.3386; 14.0876
90; 114.496; 90		2362.04Tsou, Nancy; Shultz, C. Scott; Andreani, Teresa; Ball, Richard G.; Brunskill, Andrew; Balsells, Jaume; Cohen, Ryan D.; DaSilva, Jimmy; Li, Jing; Reamer, Robert A.; de Lera Ruiz, Manuel; Variankaval, Narayan; Varsolona, Richard J.; Yasuda, Nobuyoshi; York, Gregory
Careful Navigation of the Crystallographic Landscape of MK-8970: A Racemic Acetal Carbonate Prodrug of Raltegravir
Organic Process Research & Development, 2015, 19, 1882
1520612 CIFC25 H29 F N6 O8P 21 21 219.4933; 11.2461; 24.486
90; 90; 90		2614.2Tsou, Nancy; Shultz, C. Scott; Andreani, Teresa; Ball, Richard G.; Brunskill, Andrew; Balsells, Jaume; Cohen, Ryan D.; DaSilva, Jimmy; Li, Jing; Reamer, Robert A.; de Lera Ruiz, Manuel; Variankaval, Narayan; Varsolona, Richard J.; Yasuda, Nobuyoshi; York, Gregory
Careful Navigation of the Crystallographic Landscape of MK-8970: A Racemic Acetal Carbonate Prodrug of Raltegravir
Organic Process Research & Development, 2015, 19, 1882
1520613 CIFC25 H29 F N6 O8P 1 21/n 111.2744; 9.4324; 25.6466
90; 102.205; 90		2665.73Tsou, Nancy; Shultz, C. Scott; Andreani, Teresa; Ball, Richard G.; Brunskill, Andrew; Balsells, Jaume; Cohen, Ryan D.; DaSilva, Jimmy; Li, Jing; Reamer, Robert A.; de Lera Ruiz, Manuel; Variankaval, Narayan; Varsolona, Richard J.; Yasuda, Nobuyoshi; York, Gregory
Careful Navigation of the Crystallographic Landscape of MK-8970: A Racemic Acetal Carbonate Prodrug of Raltegravir
Organic Process Research & Development, 2015, 19, 1882
1520614 CIFC25 H23 N O3P 1 21/c 19.4141; 23.293; 9.0609
90; 92.942; 90		1984.3Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520615 CIFC18 H17 N O2P 1 21/c 18.0166; 15.8594; 11.2674
90; 98.788; 90		1415.7Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520616 CIFC37 H31 N O5P 1 21/n 111.364; 10.93; 24.447
90; 96.564; 90		3017Mo, Lei; Wu, Lin-Lin; Wang, Shaozhong; Yao, Zhu-Jun
Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes.
Organic letters, 2015, 17, 3314-3317
1520617 CIFC41 H48 Br N7 O3P -111.7286; 15.6534; 22.6519
93.311; 99.266; 107.5		3889.5Nair, Ratish R.; Raju, M.; Patel, Neha P.; Raval, Ishan H.; Suresh, E.; Haldar, Soumya; Chatterjee, Pabitra B.
Naked eye instant reversible sensing of Cu(2+) and its in situ imaging in live brine shrimp Artemia.
The Analyst, 2015, 140, 5464-5468
1520618 CIFC56 H100 F N O4P -415.6111; 15.6111; 10.505
90; 90; 90		2560.14Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520619 CIFC22 H50 Cl2 F N O4P 1 21/c 19.9446; 18.0891; 15.7361
90; 103.523; 90		2752.27Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520620 CIFC26 H60 F N O6P b c n9.9133; 17.3454; 18.3631
90; 90; 90		3157.54Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520621 CIFC26 H60 F N O4C 1 2/c 122.5166; 14.2863; 19.8783
90; 103.626; 90		6214.47Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520622 CIFC38.39 H77.58 F N O12P 21 21 218.978; 24.2645; 10.3218
90; 90; 90		4753.1Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520623 CIFC22 H44 F0.5 N0.5 O7C 1 2 125.1923; 9.6565; 10.6715
90; 92.2457; 90		2594.06Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520624 CIFC28 H64 F N O4P b c a18.6017; 18.6158; 19.1084
90; 90; 90		6616.96Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520625 CIFC56 H64 F N O4P 21 21 2110.6859; 12.6528; 34.797
90; 90; 90		4704.78Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520626 CIFC49 H80 F N O7P 1 c 18.7551; 12.7463; 22.1115
90; 92.0698; 90		2465.93Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520627 CIFC73 H78 F N O3P -114.5683; 19.9837; 20.7534
91.2454; 94.4191; 103.901		5842.46Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520628 CIFC55 H72 F N O3P -19.4953; 12.1501; 21.4618
81.8444; 89.1604; 78.5486		2401.96Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520629 CIFC54 H68 F N O2P 1 21/n 111.2887; 17.6025; 24.966
90; 98.4318; 90		4907.35Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520630 CIFC60 H80 F N O2P -113.4717; 17.5643; 24.8506
78.8655; 80.5422; 69.645		5379Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520631 CIFC76 H96 F N3 O5C 1 2/c 127.7157; 9.7374; 25.2072
90; 105.664; 90		6550.2Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520633 CIFC22 H21 Br N2 O3 S2P b c a11.7745; 15.3391; 24.3582
90; 90; 90		4399.34Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520634 CIFC22 H20 N2 O4 S2P -19.0038; 10.66; 11.8108
75.2664; 76.0323; 75.5364		1042.26Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520635 CIFC30 H29 N O3P 21 21 217.37176; 14.7771; 21.8173
90; 90; 90		2376.63Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520636 CIFC29 H32 N2 S2P 1 21 110.39896; 9.11807; 13.7409
90; 108.291; 90		1237.06Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520637 CIFC21 H15 F O2P 1 21/c 112.0845; 5.9453; 22.597
90; 103.246; 90		1580.3Du, Xiang-Wei; Stanley, Levi M.
Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives.
Organic letters, 2015, 17, 3276-3279
1520638 CIFC29 H24 Au Fe O2 P SP -19.187; 9.964; 15.554
108.411; 96.805; 95.38		1328.34Fernández-Gallardo, Jacob; Elie, Benelita T.; Sadhukha, Tanmoy; Prabha, Swayam; Sanaú, Mercedes; Rotenberg, Susan A.; Ramos, Joe W.; Contel, María
Heterometallic titanium‒gold complexes inhibit renal cancer cells in vitro and in vivo
Chem. Sci., 2015, 6, 5269
1520639 CIFC33 H29 Cl N2 O2 SP 1 21 110.1227; 25.116; 11.547
90; 97.553; 90		2910.3Wang, Yidong; Zhang, Peichao; Liu, Yuan; Xia, Fei; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2+2] versus [4+2]-cycloadditions of 3-styrylindoles with N-allenamides: observation of interesting substituent effects
Chem. Sci., 2015, 6, 5564
1520640 CIFC35 H32 N2 O4 SP 21 21 216.0633; 11.5428; 42.4729
90; 90; 90		2972.57Wang, Yidong; Zhang, Peichao; Liu, Yuan; Xia, Fei; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2+2] versus [4+2]-cycloadditions of 3-styrylindoles with N-allenamides: observation of interesting substituent effects
Chem. Sci., 2015, 6, 5564
1520655 CIFC32 H38 O5 Si2P 1 21/c 19.2692; 9.7098; 34.752
90; 92.266; 90		3125.3Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520656 CIFC16 H17 Cl O5P -16.9648; 7.7685; 14.728
76.228; 76.658; 84.002		752.04Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520657 CIFC18 H17 Br O5P 1 21 15.6762; 10.5443; 14.1611
90; 100.294; 90		833.92Sinha, Debarshi; Biswas, Arnab; Singh, Vinod K.
Chiral Phosphine-Silver(I) Complex Catalyzed Enantioselective Interrupted Feist-Bénary Reaction with Ynones: The Aldol-Cycloisomerization Cascade.
Organic letters, 2015, 17, 3302-3305
1520658 CIFC19 H20 N2 O6P 21 21 215.8624; 9.6327; 31.868
90; 90; 90		1799.61Chen, Shi; Ibrahim, Ahmad A.; Mondal, Mukulesh; Magee, Anthony J.; Cruz, Adam J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene Heterodimers.
Organic letters, 2015, 17, 3248-3251
1520659 CIFC22 H32 Cl2 I2 Si2P 1 21/n 113.1915; 9.4009; 22.0383
90; 106.275; 90		2623.49Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520660 CIFC16 H10 Cl2 I2P b c a9.0806; 15.5457; 23.2185
90; 90; 90		3277.6Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520661 CIFC20 H16 Br2 OP -17.1574; 11.25; 22.434
84.231; 84.177; 89.834		1787.9Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520662 CIFC25 H36 OP 1 21/c 114.4666; 10.0707; 16.4037
90; 109.508; 90		2252.65Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520663 CIFC28 H34 OC 1 2/c 123.302; 11.4445; 18.904
90; 104.415; 90		4882.6Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520664 CIFC20 H16 Br2 OP -16.0698; 11.4589; 13.8421
67.027; 85.348; 76.337		861.26Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520665 CIFC62 H138 Ge2 Si14C 1 2/c 138.0616; 9.3192; 48.0059
90; 92.3498; 90		17013.6Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520666 CIFC80 H162 Ge2 Si14P 1 21/a 112.7486; 20.8969; 18.9393
90; 103.248; 90		4911.28Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520667 CIFC64 H142 Ge2 Si14P b c a21.4391; 21.7284; 36.5231
90; 90; 90		17013.8Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520670 CIFC44 H28 O14P 1 21/c 119.7826; 11.0872; 30.0405
90; 95.85; 90		6554.6Cheuk, Dominic; Khamar, Dikshitkumar; McArdle, Patrick; Rasmuson, Åke C.
Solid Forms, Crystal Habits, and Solubility of Danthron
Journal of Chemical & Engineering Data, 2015, 60, 2110
1520671 CIFC15 H16 O3P 41 21 29.6557; 9.6557; 26.319
90; 90; 90		2453.8Shi, Yu-Sheng; Liu, Yun-Bao; Ma, Shuang-Gang; Li, Yong; Qu, Jing; Li, Li; Yuan, Shao-Peng; Hou, Qi; Li, Yu-Huan; Jiang, Jian-Dong; Yu, Shi-Shan
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum.
Journal of natural products, 2015, 78, 1526-1535
1520672 CIFC11 H14 O3P 21 21 216.1491; 8.0979; 20.2092
90; 90; 90		1006.31Shi, Yu-Sheng; Liu, Yun-Bao; Ma, Shuang-Gang; Li, Yong; Qu, Jing; Li, Li; Yuan, Shao-Peng; Hou, Qi; Li, Yu-Huan; Jiang, Jian-Dong; Yu, Shi-Shan
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum.
Journal of natural products, 2015, 78, 1526-1535
1520673 CIFC20 H30 O4P 21 21 217.587; 9.6985; 25.106
90; 90; 90		1847.4Xu, Jing; Sun, Yihang; Wang, Meicheng; Ren, Quanhui; Li, Shen; Wang, Hao; Sun, Xiaocong; Jin, Da-Qing; Sun, Hongwei; Ohizumi, Yasushi; Guo, Yuanqiang
Bioactive Diterpenoids from the Leaves of Callicarpa macrophylla.
Journal of natural products, 2015, 78, 1563-1569
1520674 CIFC28 H33 N3 Na O10 Re SP 1 21/c 131.609; 10.4939; 9.2829
90; 96.146; 90		3061.5Jia, Jianhua; Cui, Mengchao; Dai, Jiapei; Liu, Boli
(99m)Tc(CO)3-Labeled Benzothiazole Derivatives Preferentially Bind Cerebrovascular Amyloid: Potential Use as Imaging Agents for Cerebral Amyloid Angiopathy.
Molecular pharmaceutics, 2015, 12, 2937-2946
1520675 CIFC16 H14 N2 OP 1 21/n 113.4616; 4.959; 19.7696
90; 93.71; 90		1316.98Li, Shangda; Ji, Huafang; Cai, Lei; Li, Gang
Pd(ii)-catalyzed remote regiodivergent ortho- and meta-C‒H functionalizations of phenylethylamines
Chem. Sci., 2015, 6, 5595
1520676 CIFC20 H18 N2 O3C 1 2/c 133.97; 6.299; 16.431
90; 92.257; 90		3513Li, Shangda; Ji, Huafang; Cai, Lei; Li, Gang
Pd(ii)-catalyzed remote regiodivergent ortho- and meta-C‒H functionalizations of phenylethylamines
Chem. Sci., 2015, 6, 5595
1520682 CIFC26 H19 N3 O5 SP -110.4761; 10.8361; 11.3358
76.911; 61.867; 86.563		1103.68Rao, Wei-Hao; Zhan, Bei-Bei; Chen, Kai; Ling, Peng-Xiang; Zhang, Zhuo-Zhuo; Shi, Bing-Feng
Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp(3))-H Bonds with Sodium Sulfinates.
Organic letters, 2015, 17, 3552-3555
1520683 CIFC20 H24 Cl N3 OP 1 21 110.868; 6.8325; 12.6102
90; 103.793; 90		909.38Johnson, Rebecca E.; de Rond, Tristan; Lindsay, Vincent N. G.; Keasling, Jay D.; Sarpong, Richmond
Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.
Organic letters, 2015, 17, 3474-3477
1520684 CIFC13 H17 Cl O3P n a 2128.508; 5.4891; 8.1976
90; 90; 90		1282.79Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520685 CIFC21 H21 Cl O4P b c a15.5081; 11.7102; 20.245
90; 90; 90		3676.6Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520686 CIFC33 H30 N2 O6 S2P -110.7946; 12.4093; 13.1553
76.627; 68.739; 81.216		1593.12Yan, Xiaonan; Ling, Fei; Zhang, Yuchen; Ma, Cheng
Three-Component Functionalized Dihydropyridine Synthesis via a Formal Inverse Electron-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3536-3539
1520694 CIFC33 H27 N3 O13P -111.319; 12.665; 14.597
86.284; 86.306; 68.207		1937.1Chen, Ji-Peng; He, Wei; Yang, Zhen-Yu; Yao, Zhu-Jun
Synthesis of Tricyclo[4,3,1,0(1,5)]decane Core of Plumisclerin A Using Pauson-Khand Annulation and SmI2-Mediated Radical Cyclization.
Organic letters, 2015, 17, 3379-3381
1520695 CIFC41 H29 N2 OP 21 21 219.7022; 14.1065; 22.5755
90; 90; 90		3089.78Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520696 CIFC41 H32 N2 OP b c a9.7137; 21.2283; 30.357
90; 90; 90		6259.8Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520697 CIFC28 H19 F3 N2 OP -19.7447; 10.0599; 12.2374
103.037; 100.267; 97.73		1130.75Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520698 CIFC27 H21 N O SP 1 21/n 111.5129; 21.7914; 17.1772
90; 98.718; 90		4259.66Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520699 CIFC42 H34 N2 OP 1 21/n 17.8222; 19.2845; 21.7791
90; 100.329; 90		3232.1Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520700 CIFC21 H23 N2 O RhP 1 21/n 17.9626; 12.2907; 18.1403
90; 102.579; 90		1732.7Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520702 CIFC41 H60 N8 O3 Ti2P 1 21/n 119.8643; 9.0349; 24.8875
90; 106.793; 90		4276.1Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520703 CIFC163 H221 N28 O13 Ti4P -119.976; 20.518; 21.236
89.583; 78.919; 76.303		8292Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520704 CIFC22 H20 N2 O3P -111.7148; 11.8534; 14.1205
110; 95.83; 100.677		1781.51Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520705 CIFC22 H22 N2 O3P c a 2117.651; 15.5231; 13.7865
90; 90; 90		3777.48Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520706 CIFC22 H20 N2 O3P 1 21/n 115.2406; 5.6664; 20.6863
90; 94.254; 90		1781.53Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520707 CIFC20 H23 N O8P 21 21 218.7215; 11.3257; 19.217
90; 90; 90		1898.2Paladino, Marco; Zaifman, Joshua; Ciufolini, Marco A.
Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol.
Organic letters, 2015, 17, 3422-3425
1520708 CIFC15 H15 N3 O4P 1 21/n 111.4762; 7.95324; 16.5869
90; 107.894; 90		1440.7Wang, Qi; Tang, Xuli; Luo, Xiangchao; de Voogd, Nicole J.; Li, Pinglin; Li, Guoqiang
(+)- and (-)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata.
Organic letters, 2015, 17, 3458-3461
1520709 CIFC324.95 H223.55 Cu4 N97.65 Na11.5 O115.55 S16 Zn12P 1 n 121.91216; 32.64068; 35.0386
90; 98.2694; 90		24800Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520710 CIFC326.45 H230.05 Cu10 N98.15 O119.55 S16 Zn6.4P -124.6339; 26.2771; 38.566
71.189; 77.8; 87.75		23086Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520711 CIFC325.25 H227.25 Cu16 N97.75 O116.25 S16P -124.6594; 26.1086; 38.5294
71.7131; 78.2731; 87.7169		23054.1Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520712 CIFC80 H52 N24 O20 S4 Zn4I 41/a16.4641; 16.4641; 53.397
90; 90; 90		14474.1Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520713 CIFC25 H24 N4 O4P 1 21/c 120.3743; 5.7348; 19.2424
90; 102.342; 90		2196.4Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520714 CIFC28 H28 N2 O4 S4P 1 21/c 16.5498; 20.4037; 11.0725
90; 100.469; 90		1455.1Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520715 CIFC28 H28 N2 O4 S4I 1 2/a 115.181; 15.559; 23.696
90; 105.016; 90		5406Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520716 CIFC25 H45 N O2 SP 1 21/c 137.479; 7.292; 9.0925
90; 93.702; 90		2479.8Bhat, R.; Patel, H.; Tsai, P.-C.; Sun, X.-L.; Daoud, D.; Lalancette, R. A.; Michniak-Kohn, B.; Pietrangelo, A.
Effect of residue structure on the thermal and thermoresponsive properties of γ-substituted poly(N-acryloyl-2-pyrrolidones)
Polym. Chem., 2015, 6, 5993
1520720 CIFC21 H31 Cl3 O2C 1 2 122.6971; 11.6034; 19.6097
90; 124.027; 90		4280.19Wang, Li-Jun; Xiong, Juan; Liu, Shu-Ting; Pan, Li-Long; Yang, Guo-Xun; Hu, Jin-Feng
ent-Abietane-Type and Related Seco-/Nor-diterpenoids from the Rare Chloranthaceae Plant Chloranthus sessilifolius and Their Antineuroinflammatory Activities.
Journal of natural products, 2015, 78, 1635-1646
1520721 CIFC20 H32 O3P 1 21 16.1311; 17.3576; 8.5062
90; 98.395; 90		895.54Wang, Li-Jun; Xiong, Juan; Liu, Shu-Ting; Pan, Li-Long; Yang, Guo-Xun; Hu, Jin-Feng
ent-Abietane-Type and Related Seco-/Nor-diterpenoids from the Rare Chloranthaceae Plant Chloranthus sessilifolius and Their Antineuroinflammatory Activities.
Journal of natural products, 2015, 78, 1635-1646
1520722 CIFC20 H30 O4P 21 21 217.0352; 9.6018; 26.5701
90; 90; 90		1794.83Wang, Li-Jun; Xiong, Juan; Liu, Shu-Ting; Pan, Li-Long; Yang, Guo-Xun; Hu, Jin-Feng
ent-Abietane-Type and Related Seco-/Nor-diterpenoids from the Rare Chloranthaceae Plant Chloranthus sessilifolius and Their Antineuroinflammatory Activities.
Journal of natural products, 2015, 78, 1635-1646
1520723 CIFC22 H29 N3 O5P 1 21/c 113.212; 9.1505; 18.16
90; 105.195; 90		2118.7Braun, Doris E.; Koztecki, Lien H.; McMahon, Jennifer A.; Price, Sarah L.; Reutzel-Edens, Susan M
Navigating the Waters of Unconventional Crystalline Hydrates.
Molecular pharmaceutics, 2015, 12, 3069-3088
1520724 CIFC22 H28.46 N3 O4.73C 1 2/c 126.498; 9.6469; 20.342
90; 128.706; 90		4057.8Braun, Doris E.; Koztecki, Lien H.; McMahon, Jennifer A.; Price, Sarah L.; Reutzel-Edens, Susan M
Navigating the Waters of Unconventional Crystalline Hydrates.
Molecular pharmaceutics, 2015, 12, 3069-3088
1520725 CIFC22 H28.9 N3 O4.95C 1 2/c 126.663; 9.634; 20.863
90; 128.322; 90		4204Braun, Doris E.; Koztecki, Lien H.; McMahon, Jennifer A.; Price, Sarah L.; Reutzel-Edens, Susan M
Navigating the Waters of Unconventional Crystalline Hydrates.
Molecular pharmaceutics, 2015, 12, 3069-3088
1520726 CIFC44 H42 F6 N6 O7 S2P b c a21.512; 10.424; 40.881
90; 90; 90		9167Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520727 CIFC28 H23 F3 N2 O3P -18.882; 10.743; 14.629
87; 76.43; 65.66		1234.8Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520728 CIFC25 H34 N2 O9 SiP b c a10.3059; 20.6482; 25.5756
90; 90; 90		5442.4Cheng, Qing-Qing; Qian, Yu; Zavalij, Peter Y.; Doyle, Michael P.
Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor Cyclopropanes.
Organic letters, 2015, 17, 3568-3571
1520729 CIFC25 H31 N O3 S2P 1 21 16.6067; 19.709; 9.7407
90; 109.22; 90		1197.65Fernández-Valparís, Javier; Romo, Juan Manuel; Romea, Pedro; Urpí, Fèlix; Kowalski, Hubert; Font-Bardia, Mercè
Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2.
Organic letters, 2015, 17, 3540-3543
1520734 CIFC15 H24 N2 O3P 21 21 217.9518; 12.143; 14.869
90; 90; 90		1435.7Pan, Qi-Ming; Li, Yu-Huan; Hua, Jing; Huang, Fu-Ping; Wang, Heng-Shan; Liang, Dong
Antiviral Matrine-Type Alkaloids from the Rhizomes of Sophora tonkinensis.
Journal of natural products, 2015, 78, 1683-1688
1520735 CIFC15 H22 N2 O3P 21 21 219.052; 10.577; 14.128
90; 90; 90		1352.7Pan, Qi-Ming; Li, Yu-Huan; Hua, Jing; Huang, Fu-Ping; Wang, Heng-Shan; Liang, Dong
Antiviral Matrine-Type Alkaloids from the Rhizomes of Sophora tonkinensis.
Journal of natural products, 2015, 78, 1683-1688
1520736 CIFC16 H16 N2 O SP 21 21 217.2412; 10.1066; 19.681
90; 90; 90		1440.33Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520737 CIFC14 H14 N2 O S2P 21 21 217.1805; 9.8395; 19.6096
90; 90; 90		1385.47Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520738 CIFC24 H25 Cl2 N3 O Ru SP 21 21 2110.0568; 14.9314; 16.7695
90; 90; 90		2518.1Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520739 CIFC20 H20 Cl2 N2 O Ru S2P 21 21 216.6174; 17.1016; 19.4048
90; 90; 90		2196Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520740 CIFC20 H20 Cl2 N2 O2 Ru SP 21 21 216.503; 10.2867; 31.8305
90; 90; 90		2129.28Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520741 CIFC39 H69 Ga N2 Si3P -110.5026; 11.3327; 19.4036
85.025; 85.154; 71.124		2173.1Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520742 CIFC43 H80 Ga Li N2 Si4P 1 21/m 111.519; 20.858; 11.942
90; 117.73; 90		2539.7Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520743 CIFC47 H84 Ga Li N2 O2 Si3P 1 21/n 111.5267; 18.7832; 24.68
90; 90.988; 90		5342.6Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520744 CIFC43 H77 Ga N2 O Si3P -111.3181; 13.8704; 17.8645
69.483; 71.891; 67.251		2371.9Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520745 CIFC40 H71 Ga N2 Si3P 1 21/c 121.8907; 11.0318; 20.6366
90; 117.951; 90		4402.3Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520746 CIFC35 H58 N2 Si2 ZnC 1 2/c 110.6838; 19.4876; 18.4437
90; 102.692; 90		3746.18Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520747 CIFC42 H69 Al N2 Rh SiP 1 21/n 110.8994; 20.7161; 18.9857
90; 92.16; 90		4283.79Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520748 CIFC45 H73 N2 Rh Si ZnP -110.3195; 11.6531; 19.8109
77.86; 75.973; 73.269		2188Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520749 CIFC45 H73 Mg N2 Rh SiP -110.3775; 11.6602; 19.854
77.684; 75.691; 73.192		2202.2Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520750 CIFC72 H98 Al2 N4 Rh2C 1 2/c 117.4233; 16.5193; 23.4839
90; 104.958; 90		6530.1Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520751 CIFC22 H16 N2P 1 21/c 111.9993; 4.2453; 29.803
90; 100.261; 90		1493.9Suh, Sung-Eun; Barros, Stephanie A.; Chenoweth, David M.
Triple Aryne-Tetrazine Reaction Enabling Rapid Access to a New Class of Polyaromatic Heterocycles.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 5128-5132
1520752 CIFC20 H12 Cu2 N2 O10R -3 m :H18.7387; 18.7387; 37.4863
90; 90; 120		11399.4Li, Bin; Wen, Hui-Min; Wang, Hailong; Wu, Hui; Yildirim, Taner; Zhou, Wei; Chen, Banglin
Porous metal‒organic frameworks with Lewis basic nitrogen sites for high-capacity methane storage
Energy Environ. Sci., 2015, 8, 2504
1520753 CIFC13 H13 Cl N2 O2 SP 1 21/c 115.767; 5.759; 15.721
90; 112.32; 90		1320.5Lu, Lei; Ma, Juan; Qu, Panpan; Li, Feng
Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols.
Organic letters, 2015, 17, 2350-2353
1520754 CIFC23 H21 N O3 S2P -17.667; 8.7269; 17.0497
88.1161; 89.15; 62.1966		1008.54Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro
Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters.
Organic letters, 2015, 17, 2454-2457
1520755 CIFC270 H372 B6 N8 O30C 1 2/c 152.579; 21.835; 29.598
90; 117.54; 90		30130Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1520756 CIFC28 H44 O4 Si2P 21 21 217.702; 13.1321; 27.4999
90; 90; 90		2781.4Shi, Hang; Tan, Ceheng; Zhang, Weibin; Zhang, Zichun; Long, Rong; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2342-2345
1520757 CIFC24 H20 O3P 1 21/c 117.7328; 8.7774; 13.0228
90; 110.419; 90		1899.61Li, Mingliang; Yang, Yudong; Zhou, Danni; Wan, Danyang; You, Jingsong
Nickel-Catalyzed Addition-Type Alkenylation of Unactivated, Aliphatic C-H Bonds with Alkynes: A Concise Route to Polysubstituted γ-Butyrolactones.
Organic letters, 2015, 17, 2546-2549
1520758 CIFC22 H33 N O9P -19.9044; 11.8847; 11.9608
60.57; 81.21; 75.803		1187.9Xu, Sanjia; Ciufolini, Marco A.
Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.
Organic letters, 2015, 17, 2424-2427
1520759 CIFC19 H27 N O10P -110.5221; 10.6666; 10.7161
74.105; 73.746; 61.845		1003.6Xu, Sanjia; Ciufolini, Marco A.
Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.
Organic letters, 2015, 17, 2424-2427
1520760 CIFC22 H36 O3P 21 21 218.1087; 11.9482; 20.232
90; 90; 90		1960.2Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng
Concise synthesis of the core structures of saundersiosides.
Organic letters, 2015, 17, 2346-2349
1520761 CIFC26 H40 O5P 21 21 217.3909; 12.9276; 25.254
90; 90; 90		2412.9Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng
Concise synthesis of the core structures of saundersiosides.
Organic letters, 2015, 17, 2346-2349
1520762 CIFC18 H23 N O4P 21 21 215.2667; 15.2534; 20.3019
90; 90; 90		1630.95Lin, Cheng-Wei; Hong, Bor-Cherng; Chang, Wan-Chen; Lee, Gene-Hsiang
A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis.
Organic letters, 2015, 17, 2314-2317
1520763 CIFC20 H30 Mo6 N4 Na4 O48 P4P -19.024; 19.4282; 21.1568
103.992; 95.5616; 103.407		3454.8Oms, Olivier; Benali, Tarik; Marrot, Jérome; Mialane, Pierre; Puget, Marin; Serier-Brault, Hélène; Deniard, Philippe; Dessapt, Rémi; Dolbecq, Anne
Fully Oxidized and Mixed-Valent Polyoxomolybdates Structured by Bisphosphonates with Pendant Pyridine Groups: Synthesis, Structure and Photochromic Properties
Inorganics, 2015, 3, 279
1520764 CIFC20 H30 K3.5 Mo6 N4 Na0.5 O45.5 P4P -117.9501; 19.4745; 19.8487
76.188; 69.59; 76.669		6231.6Oms, Olivier; Benali, Tarik; Marrot, Jérome; Mialane, Pierre; Puget, Marin; Serier-Brault, Hélène; Deniard, Philippe; Dessapt, Rémi; Dolbecq, Anne
Fully Oxidized and Mixed-Valent Polyoxomolybdates Structured by Bisphosphonates with Pendant Pyridine Groups: Synthesis, Structure and Photochromic Properties
Inorganics, 2015, 3, 279
1520765 CIFC32 H102.5 Mo8 N14 O53.25 P4P -117.6023; 22.134; 28.323
97.443; 95.464; 107.43		10334.2Oms, Olivier; Benali, Tarik; Marrot, Jérome; Mialane, Pierre; Puget, Marin; Serier-Brault, Hélène; Deniard, Philippe; Dessapt, Rémi; Dolbecq, Anne
Fully Oxidized and Mixed-Valent Polyoxomolybdates Structured by Bisphosphonates with Pendant Pyridine Groups: Synthesis, Structure and Photochromic Properties
Inorganics, 2015, 3, 279
1520766 CIFC2 H499 As8 Cs8.5 Na34.5 O538 W81 Y8P -121.7759; 32.0368; 33.0799
94.172; 107.537; 90.561		21934.4Ibrahim, Masooma; Bassil, Bassem; Kortz, Ulrich
Synthesis and Characterization of 8-Yttrium(III)-Containing 81-Tungsto-8-Arsenate(III), [Y8(CH3COO)(H2O)18(As2W19O68)4(W2O6)2(WO4)]43−
Inorganics, 2015, 3, 267
1520954 CIFC48 H64 Cl In N2 O2P -111.7715; 12.7462; 15.4167
105.421; 96.436; 103.43		2131.3Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520955 CIFC73 H103.5 In2 N8.5 O6P 21 21 2115.0752; 22.4148; 23.2893
90; 90; 90		7869.6Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520956 CIFC34 H46 Cl In N4 O2C 1 2 136.78; 8.3688; 24.188
90; 115.26; 90		6733.3Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520957 CIFC42 H58 In N3 O3P 21 21 219.192; 16.465; 25.858
90; 90; 90		3913.5Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520958 CIFC64 H58 In N3 O3 Si2P 21 21 2112.019; 20.066; 23.278
90; 90; 90		5614Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520959 CIFC25 H40 O2P 1 21 114.07; 10.406; 14.8885
90; 103.249; 90		2121.84Challinor, Victoria L.; Johnston, Ryne C.; Bernhardt, Paul V.; Lehmann, Reginald P.; Krenske, Elizabeth H.; De Voss, James J.
Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa
Chem. Sci., 2015, 6, 5740
1520960 CIFC34 H30 Br N2 O5 P PdP 1 21 19.566; 10.649; 17.115
90; 95.18; 90		1736.4Xie, Lan-Gui; Bagutski, Viktor; Audisio, Davide; Wolf, Larry M.; Schmidts, Volker; Hofmann, Kathrin; Wirtz, Cornelia; Thiel, Walter; Thiele, Christina M.; Maulide, Nuno
Dynamic behaviour of monohaptoallylpalladium species: internal coordination as a driving force in allylic alkylation chemistry
Chem. Sci., 2015, 6, 5734
1520961 CIFC45 H27 B Cl8 F8 Ir N4P 1 21/n 19.2828; 22.6451; 24.351
90; 97.192; 90		5078.5Monti, Filippo; Baschieri, Andrea; Matteucci, Elia; Mazzanti, Andrea; Sambri, Letizia; Barbieri, Andrea; Armaroli, Nicola
A chelating diisocyanide ligand for cyclometalated Ir(iii) complexes with strong and tunable luminescence.
Faraday discussions, 2015, 185, 233-248
1521275 CIFC24 H43 Ir O2 P2P -18.5336; 11.7835; 13.3762
100.381; 95.958; 103.944		1268.7Rimoldi, M.; Fodor, D.; van Bokhoven, J. A.; Mezzetti, A.
Catalytic hydrogenation of liquid alkenes with a silica-grafted hydride pincer iridium(iii) complex: support for a heterogeneous mechanism
Catal. Sci. Technol., 2015, 5, 4575
1521276 CIFC25 H45 Ir O2 P2P 1 21/c 116.2181; 10.735; 15.8712
90; 107.894; 90		2629.5Rimoldi, M.; Fodor, D.; van Bokhoven, J. A.; Mezzetti, A.
Catalytic hydrogenation of liquid alkenes with a silica-grafted hydride pincer iridium(iii) complex: support for a heterogeneous mechanism
Catal. Sci. Technol., 2015, 5, 4575
1521277 CIFC20 H27 Br N4 OP 1 21 18.9698; 18.4284; 12.3981
90; 98.31; 90		2027.88Zaretsky, Serge; Hickey, Jennifer L.; Tan, Joanne; Pichugin, Dmitry; St. Denis, Megan A.; Ler, Spencer; Chung, Benjamin K. W.; Scully, Conor C. G.; Yudin, Andrei K.
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Chem. Sci., 2015, 6, 5446
1521278 CIFC33 H53 N7 O7P 1 21 110.0804; 9.9982; 19.7575
90; 103.299; 90		1937.88Zaretsky, Serge; Hickey, Jennifer L.; Tan, Joanne; Pichugin, Dmitry; St. Denis, Megan A.; Ler, Spencer; Chung, Benjamin K. W.; Scully, Conor C. G.; Yudin, Andrei K.
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Chem. Sci., 2015, 6, 5446
1521279 CIFC43 H72 Cl7 N P2 Pt RuP -19.6223; 14.2389; 18.6464
85.8029; 78.4958; 76.9593		2437.81Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521280 CIFC73 H96 Cl5 N P4 Pd RuP -111.5671; 13.5147; 24.091
76.202; 88.744; 72.724		3487.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521281 CIFC81 H144 Cl11 Ir O2 P4 Ru2C 1 2/c 113.811; 40.893; 16.343
90; 97.877; 90		9143Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521282 CIFC51 H92 Cl3 Ir P2 RuP -110.9458; 15.8362; 16.7533
111.788; 96.293; 99.958		2607.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521283 CIFC63 H88 As Cl7 O2 P2 Pt RuP -111.307; 13.305; 24.398
75.582; 88.059; 71.085		3358.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521284 CIFC46 H80 Cl5 P2 Rh RuP -110.935; 12.995; 18.693
78.174; 75.183; 75.241		2455.3Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521285 CIFC40 H74 Cl6 O P2 Pt Ru SP -110.432; 12.713; 19.025
77.214; 80.085; 82.926		2414.3Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521286 CIFC61 H83 Ag Cl8 F3 N3 O3 P2 Ru SP -113.297; 14.55; 18.906
111.639; 93.007; 92.517		3387.4Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521287 CIFC81.47 H144.4 Cl8.53 O3.16 P4 Rh2 Ru2C 1 2/c 132.65; 13.4; 23.89
90; 109.79; 90		9835Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521288 CIFC55 H79 Ag Cl8 F3 N3 O3 P2 Ru SP -114.248; 15.814; 16.607
70.503; 74.933; 68.534		3241.9Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521289 CIFC76 H134 Au B Cl10 F4 P4 Ru2P 1 2/c 119.988; 16.619; 27.233
90; 100.779; 90		8887Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521290 CIFC37 H66 Au Cl3 P2 RuP 1 21/c 113.392; 17.683; 20.172
90; 121.735; 90		4062.7Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1523614 CIFC16 H13 N O4C 1 2/c 124.4884; 7.9625; 18.5286
90; 131.954; 90		2686.8Verma, Akhilesh K.; Danodia, Abhinandan K.; Saunthwal, Rakesh K.; Patel, Monika; Choudhary, Deepak
Palladium-Catalyzed Triple Successive C-H Functionalization: Direct Synthesis of Functionalized Carbazoles from Indoles.
Organic letters, 2015, 17, 3658-3661
1523944 CIFC32 H30 N2 O4 S4P -111.2966; 12.1022; 12.7036
85.244; 70.619; 77.661		1600.36Yadagiri, Dongari; Anbarasan, Pazhamalai
Tandem 1,2-sulfur migration and (aza)-Diels‒Alder reaction of β-thio-α-diazoimines: rhodium catalyzed synthesis of (fused)-polyhydropyridines, and cyclohexenes
Chem. Sci., 2015, 6, 5847
1523945 CIFC24 H40 N4 O4 SiP n a 2118.1083; 17.6737; 7.671
90; 90; 90		2455.03Kaßner, L.; Nagel, K.; Grützner, R.-E.; Korb, M.; Rüffer, T.; Lang, H.; Spange, S.
Polyamide 6/silica hybrid materials by a coupled polymerization reaction
Polym. Chem., 2015, 6, 6297
1523946 CIFC24 H40 N4 O4 SiI -4 2 d13.9688; 13.9688; 13.3347
90; 90; 90		2601.96Kaßner, L.; Nagel, K.; Grützner, R.-E.; Korb, M.; Rüffer, T.; Lang, H.; Spange, S.
Polyamide 6/silica hybrid materials by a coupled polymerization reaction
Polym. Chem., 2015, 6, 6297
1529061 CIFC37 H22 B F9P -110.1241; 10.1353; 17.3058
84.1092; 73.833; 63.9157		1531.42Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529062 CIFC28 H18 B F9P -19.7736; 16.1049; 16.4046
76.766; 74.775; 75.51		2375.1Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529063 CIFC28 H20 B F9 OP 1 21/n 18.6666; 35.693; 15.69
90; 91.689; 90		4851.4Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529064 CIFC37 H56 N8 O9P 1 21 19.2715; 36.7577; 11.3129
90; 90.098; 90		3855.4Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529065 CIFC40 H68 N8 O13P 1 21 113.3658; 9.4864; 17.7634
90; 104.204; 90		2183.42Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529066 CIFC36 H52 N8 O9I 1 2 116.9971; 9.2681; 25.8496
90; 99.408; 90		4017.3Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529067 CIFC39 H64 N8 O12P 1 21 117.7309; 9.6245; 26.236
90; 107.755; 90		4263.9Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529068 CIFC39 H64 N8 O12P 1 21 19.769; 13.318; 17.543
90; 103.191; 90		2222.2Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529074 CIFC18 H18 F2 N O4 VP 1 21/n 117.7691; 7.9596; 25.4492
90; 107.241; 90		3437.67Choing, Stephanie N.; Francis, Aaron J.; Clendenning, Graham; Schuurman, Michael S.; Sommer, Roger D.; Tamblyn, Isaac; Weare, Walter W.; Cuk, Tanja
Long-Lived LMCT in a d0Vanadium(V) Complex by Internal Conversion to a State of 3dxyCharacter
The Journal of Physical Chemistry C, 2015, 119, 17029
1529075 CIFC28.52 H21.52 F6 N0.48 O2 S2P 1 21/c 118.2529; 6.5741; 21.2658
90; 100.998; 90		2504.95Ohshima, Satoko; Morimoto, Masakazu; Irie, Masahiro
Light-driven bending of diarylethene mixed crystals
Chem. Sci., 2015, 6, 5746
1529076 CIFC27 H20 F6 N2 O2 S2P -115.141; 18.267; 19.761
72.453; 86.674; 77.582		5089Ohshima, Satoko; Morimoto, Masakazu; Irie, Masahiro
Light-driven bending of diarylethene mixed crystals
Chem. Sci., 2015, 6, 5746
1529077 CIFC113.3 H88.95 Cl2 Cu2 F24 N15.65 O14 S2P 32 2 129.93; 29.93; 28.878
90; 90; 120		22403Mortezaei, Shahab; Catarineu, Noelle R.; Duan, Xueyou; Hu, Chunhua; Canary, James W.
Redox-configurable ambidextrous catalysis: structural and mechanistic insight
Chem. Sci., 2015, 6, 5904
1529078 CIFC65.36 H70.72 N4 O2.68C 1 2/c 134.794; 5.836; 28.131
90; 97.862; 90		5659Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529079 CIFC66 H67 N4 O2C 1 2/c 134.89; 5.8074; 28.103
90; 98.31; 90		5634.4Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529080 CIFC68 H71 N4 O4.5C 1 2/c 134.814; 5.8498; 27.956
90; 98.517; 90		5630.6Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529081 CIFC63 H69 N4 O3C 1 2/c 134.994; 5.7712; 28.005
90; 97.696; 90		5604.9Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529082 CIFC63 H69 N7 O6C 1 2/c 134.875; 5.794; 28.028
90; 98.453; 90		5602Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529083 CIFC68 H68 N4 O2C 1 2/c 135.119; 5.8515; 28.129
90; 96.944; 90		5738Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529084 CIFC68 H70 N4P -15.8032; 17.6171; 28.095
82.852; 89.95; 81.848		2820.8Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529085 CIFC70 H76 N4C 1 2 134.833; 5.8219; 28.205
90; 98.49; 90		5657.1Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529086 CIFC74 H72 N4P -15.8111; 17.553; 28.328
82.08; 89.417; 83.086		2841.1Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529087 CIFC70 H74 N6C 1 2 135.689; 5.9481; 28.84
90; 97.562; 90		6069Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529088 CIFC133 H99 Cu5.5 N17 O31R -3 :H29.5994; 29.5994; 52.255
90; 90; 120		39648Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529089 CIFC168 H156 Cu3 F0 N12 O27 S0C 1 2/c 157.029; 34.131; 24.4704
90; 95.496; 90		47412Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529090 CIFC128 H126 Br4 Cu2 N6 O17 S4P 1 21/n 111.0753; 32.119; 47.079
90; 92.659; 90		16729Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529091 CIFC108 H102 Cu2 F12 N10 O36 S4P -114.4856; 18.0721; 30.4166
96.787; 93.193; 102.088		7704.9Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529092 CIFC47 H44.5 B Cu F4 N5.5 O11P b c a9.459; 29.785; 34.465
90; 90; 90		9710Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529093 CIFC149 H187 B4 Cu2 F16 N19 O34.5P 1 21/c 128.9123; 20.7706; 29.7284
90; 101.224; 90		17511.2Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529094 CIFC93 H105 Br3 Cu2 N6 O16.5 S4.5P -115.4223; 19.5085; 28.1607
100.656; 105.671; 102.75		7682Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529193 CIFC23 H20 Br N O2P -19.823; 10.177; 11.186
92.48; 113.89; 100.8		995.5Sha, Qiang; Arman, Hadi; Doyle, Michael P.
Three-Component Cascade Reactions with 2,3-Diketoesters: A Novel Metal-Free Synthesis of 5-Vinyl-pyrrole and 4-Hydroxy-indole Derivatives.
Organic letters, 2015, 17, 3876-3879
1529194 CIFC94 H120 N6 O2 Y2P 1 21/n 113.16; 16.367; 19.701
90; 103.837; 90		4120Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529195 CIFC98 H128 N6 O2 Y2P 1 21/n 113.324; 16.849; 19.59
90; 104.35; 90		4261Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529196 CIFC98 H128 N6 O4 Y2P 1 21/n 113.2137; 17.8164; 18.8346
90; 102.372; 90		4331.1Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529197 CIFC70 H100 N6 O2 Y2C 1 2/c 116.313; 20.362; 20.231
90; 92.019; 90		6716Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529198 CIFC94 H120 N6 O2 Y2P 1 21/n 115.639; 17.514; 16.24
90; 104.711; 90		4302Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529199 CIFC72 H104 N6 O4 Y2P 1 21/n 113.492; 13.673; 19.028
90; 101.334; 90		3442Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529200 CIFC47 H62 N3 O2 YP 1 21/n 112.902; 21.925; 16.088
90; 106.222; 90		4370Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529201 CIFC71.5 H54 Al Cl5 N4 O3P 1 21/c 115.72; 14.2236; 28.919
90; 96.12; 90		6429.3Gao, Bo; Li, Dongni; Li, Xiang; Duan, Ranlong; Pang, Xuan; Cui, Yuan; Duan, Qian; Chen, Xuesi
Preparation of biocompatible, biodegradable and sustainable polylactides catalyzed by aluminum complexes bearing unsymmetrical dinaphthalene-imine derivatives via ring-opening polymerization of lactides
Catal. Sci. Technol., 2015, 5, 4644
1529202 CIFC68 H50 Al Cl3 N4 O2P 1 21/n 114.265; 20.847; 18.412
90; 97.691; 90		5426.2Gao, Bo; Li, Dongni; Li, Xiang; Duan, Ranlong; Pang, Xuan; Cui, Yuan; Duan, Qian; Chen, Xuesi
Preparation of biocompatible, biodegradable and sustainable polylactides catalyzed by aluminum complexes bearing unsymmetrical dinaphthalene-imine derivatives via ring-opening polymerization of lactides
Catal. Sci. Technol., 2015, 5, 4644
1529203 CIFC43.5 H73 N6 O P Si6 UP -111.5703; 11.7055; 21.152
86.747; 83.81; 75.03		2750.1Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529204 CIFC40 H69 N6 O P Si6 ThP -111.4301; 21.3302; 24.614
99.881; 90.073; 95.606		5882.8Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529205 CIFC40 H69 N7 O Si6 UC 1 2/c 115.5201; 17.9868; 37.3806
90; 97.783; 90		10338.9Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529206 CIFC43.5 H73 N7 O Si6 ThP -111.2966; 23.057; 23.27
66.405; 87.39; 77.614		5419.5Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529207 CIFC43.5 H73 N7 S Si6 UP -111.581; 11.6278; 21.115
86.775; 83.982; 75.259		2733.3Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529208 CIFC43.5 H73 N7 S Si6 ThP -111.6047; 11.6602; 21.204
86.479; 83.836; 75.464		2759.5Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529209 CIFC52.5 H91.5 N6 Ni O P Si6 ThP -114.8598; 19.6824; 24.2681
105.87; 101.321; 96.5472		6587.8Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529210 CIFC114 H143 Cl N14 O5P 1 21/n 110.9481; 39.559; 24.446
90; 92.404; 90		10578Galán, Albano; Valderrey, Virginia; Ballester, Pablo
Ordered co-encapsulation of chloride with polar neutral guests in a tetraurea calix[4]pyrrole dimeric capsule
Chem. Sci., 2015, 6, 6325
1529211 CIFC16 H11 N O2P 1 21/c 115.281; 3.8302; 24.754
90; 125.705; 90		1176.5Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529212 CIFC16 H12 O3P 1 21/n 16.0914; 8.5177; 23.947
90; 90.598; 90		1242.4Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964

Blue left arrow Blue left arrow First | Blue left arrow Previous 300 | of 92 | Next 300 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.