Crystallography Open Database

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Searching year of publication is 2015

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1518644 CIFC23 H20 N2 OP -16.345; 11.725; 13.3
67.812; 80.532; 84.005
902.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518645 CIFC24 H35 N3 O2P 1 21 112.8948; 9.7854; 18.3889
90; 94.667; 90
2312.6Li, Xun; Taechalertpaisarn, Jaru; Xin, Dongyue; Burgess, Kevin
Protein-Protein Interface Mimicry by an Oxazoline Piperidine-2,4-dione.
Organic letters, 2015, 17, 632-635
1518646 CIFC34 H56 N2 O7 Si2P 21 21 219.052; 19.871; 22.2031
90; 90; 90
3993.72Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518647 CIFC33 H44 N2 O7 SiP 1 21 118.0919; 10.7097; 18.935
90; 107.979; 90
3489.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518648 CIFC22 H28 N2 O7P 21 21 2111.0538; 12.5835; 15.8359
90; 90; 90
2202.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518649 CIFC17 H17 N O3P 1 21/c 18.9854; 18.5028; 9.4678
90; 109.249; 90
1486.07Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518650 CIFC25 H22 Cl N O4P -18.5929; 9.9207; 13.6227
73.585; 78.745; 86.593
1092.53Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518651 CIFC31 H27 N3 O2P 1 21 17.6192; 12.0803; 14.0233
90; 102.158; 90
1261.8Pertejo, Pablo; Corres, Nazaret; Torroba, Tomás; García-Valverde, María
Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones.
Organic letters, 2015, 17, 612-615
1518652 CIFC30 H38 N2 O7P 1 21 111.3323; 8.5548; 14.1288
90; 92.453; 90
1368.47Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518653 CIFC32 H40 N2 O7P 1 21 113.4499; 7.46; 14.9726
90; 104.948; 90
1451.46Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518654 CIFC42 H59 F3 O10P 1 21 113.4566; 8.18811; 19.1862
90; 100.629; 90
2077.74Inahashi, Yuki; Iwatsuki, Masato; Ishiyama, Aki; Matsumoto, Atsuko; Hirose, Tomoyasu; Oshita, Jun; Sunazuka, Toshiaki; Panbangred, Watanalai; Takahashi, Yoko; Kaiser, Marcel; Otoguro, Kazuhiko; O̅mura, Satoshi
Actinoallolides A-E, New Anti-trypanosomal Macrolides, Produced by an Endophytic Actinomycete, Actinoallomurus fulvus MK10-036.
Organic letters, 2015, 17, 864-867
1518655 CIFC13 H10 N2 O2 SP 1 21/c 111.9124; 7.5041; 14.67
90; 111.533; 90
1219.9Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518656 CIFC13 H10 N4 OP -16.9373; 8.2261; 9.7516
85.814; 78.171; 89.197
543.22Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518657 CIFC14 H11 N5P -17.9667; 8.6666; 9.6847
109.198; 107.554; 92.006
595.36Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518658 CIFC16 H19 N O4P 1 21 18.2102; 6.2167; 14.102
90; 90.69; 90
719.7Lou, Yan-Peng; Zheng, Chang-Wu; Pan, Ren-Ming; Jin, Qiao-Wen; Zhao, Gang; Li, Zhong
Enantioselective Direct Mannich Reactions of Cyclic β-Ketoesters Catalyzed by Chiral Phosphine via a Novel Dual-Reagent Catalysis.
Organic letters, 2015, 17, 688-691
1518659 CIFC25 H23 Br O S2 SeP 1 21/c 19.5704; 11.7332; 21.056
90; 97.692; 90
2343.1Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518660 CIFC20 H21 F O2 S2P 1 21/c 110.5963; 16.7072; 10.9555
90; 95.184; 90
1931.57Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518661 CIFC64 H48 S4P 1 21/n 120.159; 5.0166; 25.728
90; 109.164; 90
2457.7Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518662 CIFC65 H50 S4P 1 21/n 120.1; 5.1652; 25.159
90; 109.501; 90
2462.2Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518663 CIFC68 H56 Cl2 S4P 1 21/c 17.6706; 17.4871; 20.506
90; 100.272; 90
2706.5Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518664 CIFC66 H52 S4P 1 21/n 121.43; 5.2798; 24.95
90; 111.599; 90
2624.8Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518665 CIFC66 H52 S4P 1 21/n 120.0834; 5.2324; 24.6005
90; 109.019; 90
2444.01Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518666 CIFC8 H16 F7 O6 P2 S2 SbP 1 21/n 114.5029; 8.9034; 14.9927
90; 97.26; 90
1920.41Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518667 CIFC43 H71 F9 N3 O9 P3 S3 Sb4P -111.4789; 11.9874; 26.0864
91.82; 97.564; 112.074
3284.57Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518668 CIFC29 H61.5 F12 N0.5 O12 P4 S4 Sb4P 1 21/c 123.986; 21.83; 22.193
90; 106.57; 90
11138Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518669 CIFC31 H41 F6 N2 O6 S2 SbP 1 21/c 112.3127; 17.4575; 17.0214
90; 91.03; 90
3658.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518670 CIFC4 H9 F4 O3 P SP 1 21/m 110.2147; 8.6511; 11.0323
90; 94.5503; 90
971.83Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518671 CIFC14 H30 F6 O6 P2 S2P 1 21/n 113.4271; 11.8532; 15.7504
90; 110.993; 90
2340.4Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518672 CIFC27 H24 Cl5 F6 N5 O P2 RuP -111.1445; 12.0548; 14.8726
67.197; 84.942; 67.025
1691.09Walden, Andrew G.; Miller, Alexander J. M.
Rapid water oxidation electrocatalysis by a ruthenium complex of the tripodal ligand tris(2-pyridyl)phosphine oxide
Chem. Sci., 2015, 6, 2405
1518673 CIFC33 H48 N2 O9 SP 1 21 113.6507; 10.3032; 13.9805
90; 109.803; 90
1850.02Shen, Hongyun; Shen, Chao; Chen, Chao; Wang, Anming; Zhang, Pengfei
Novel glycosyl pyridyl-triazole@palladium nanoparticles: efficient and recoverable catalysts for C‒C cross-coupling reactions
Catal. Sci. Technol., 2015, 5, 2065
1518674 CIFC75 H71 Cl2 N3 PdP -112.3155; 15.9288; 19.2346
79.609; 87.992; 81.295
3668.5Maluenda, Irene; Chen, Ming-Tsz; Guest, Daniel; Mark Roe, S.; Turner, Michael L.; Navarro, Oscar
Room temperature, solventless telomerization of isoprene with alcohols using (N-heterocyclic carbene)‒palladium catalysts
Catal. Sci. Technol., 2015, 5, 1447
1518675 CIFC27 H39 Cl2 N3 PdC 1 2/c 135.0018; 11.2158; 15.2054
90; 111.789; 90
5542.8Maluenda, Irene; Chen, Ming-Tsz; Guest, Daniel; Mark Roe, S.; Turner, Michael L.; Navarro, Oscar
Room temperature, solventless telomerization of isoprene with alcohols using (N-heterocyclic carbene)‒palladium catalysts
Catal. Sci. Technol., 2015, 5, 1447
1518676 CIFC17 H25 N O2 SiP 1 21/n 17.8451; 10.8055; 41.681
90; 92.188; 90
3530.7Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518677 CIFC19 H19 Cl2 N O SP 1 21/c 19.4678; 22.465; 8.4857
90; 94.892; 90
1798.3Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518680 CIFC21 H31 Ni O3 P SP 1 21/n 19.5684; 16.352; 13.9609
90; 95.255; 90
2175.18Chen, Min; Zou, Wenping; Cai, Zhengguo; Chen, Changle
Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts
Polym. Chem., 2015, 6, 2669
1518681 CIFC46 H39 B F15 Ni O3 P SP n a 2124.5629; 15.6599; 11.5597
90; 90; 90
4446.47Chen, Min; Zou, Wenping; Cai, Zhengguo; Chen, Changle
Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts
Polym. Chem., 2015, 6, 2669
1518682 CIFH18 N8 Ni O6F m -3 m10.8738; 10.8738; 10.8738
90; 90; 90
1285.71Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518683 CIFH12 N2 Ni O12P -15.7531; 7.6604; 11.4876
106.347; 98.45; 101.538
464.73Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518684 CIFH12 N2 Ni O12P -15.8056; 7.7023; 11.6864
105.841; 98.451; 102.203
479.59Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518685 CIFC52 H48 N4 O4P n a 2118.809; 10.08; 20.725
90; 90; 90
3929Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518686 CIFC62 H66 Cl6 N4 O12P -19.8315; 14.743; 21.249
101.193; 91.334; 94.028
3011.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518687 CIFC63 H70 N4 O16P -111.12; 14.029; 20.02
108.726; 98.537; 94.981
2894.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518711 CIFC15 H22 O5P 1 21/c 113.3435; 7.2491; 15.3576
90; 92.261; 90
1484.36Peng, Jin-Bao; Qi, Yue; Jing, Ze-Ran; Wang, Shao-Hua; Tu, Yong-Qiang; Zhu, Dao-Yong; Zhang, Fu-Min
Efficient Oxa-Diels‒Alder/Semipinacol Rearrangement/Aldol Cascade Reaction: Short Approach to Polycyclic Architectures
Organic Letters, 2015, 150209135056006
1518712 CIFC21 H28 O3P 21 21 216.0078; 15.1366; 20.0221
90; 90; 90
1820.76Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518713 CIFC23 H27 F3 O3P 21 21 216.2097; 14.9142; 23.193
90; 90; 90
2147.97Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518714 CIFC14 H26 Cl3 N4 O P RuP 1 21/n 16.9163; 23.66; 11.8396
90; 97.078; 90
1922.7Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518715 CIFC15 H23 Cl2 N4 O P RuP -110.5379; 12.8283; 13.7451
100.766; 97.279; 91.491
1808.34Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518716 CIFC42 H55 Cl2 N5 O10C 1 2 125.187; 8.1556; 21.154
90; 99.308; 90
4288.1Rose, Tristan E.; Lawson, Kenneth V.; Harran, Patrick. G.
Large ring-forming alkylations provide facile access to composite macrocycles
Chem. Sci., 2015, 6, 2219
1518717 CIFC18 H27 B Br N O5 SP -19.483; 13.115; 17.336
90.88; 99.38; 91.32
2126.3Carrillo, Josué Ayuso; Ingleson, Michael J.; Turner, Michael L.
Thienyl MIDA Boronate Esters as Highly Effective Monomers for Suzuki‒Miyaura Polymerization Reactions
Macromolecules, 2015, 48, 979
1518718 CIFC18 H26 O4 SiP b c a16.759; 7.4334; 30.141
90; 90; 90
3754.9Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518719 CIFC18 H26 O4 SiP -16.1239; 16.8945; 17.8873
91.468; 95.3024; 90.184
1842.1Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518720 CIFC166 H366 Ag62 F6 Mo38 N2 O129 S42P -118.4308; 19.5522; 35.0688
93.065; 95.734; 112.904
11523.9Huang, Ren-Wu; Xu, Qing-Qing; Lu, Hong-Lin; Guo, Xiao-Kang; Zang, Shuang-Quan; Gao, Guang-Gang; Tang, Ming-Sheng; Mak, Thomas C. W.
Self-assembly of an unprecedented polyoxomolybdate anion [Mo20O66](12-) in a giant peanut-like 62-core silver-thiolate nanocluster.
Nanoscale, 2015, 7, 7151-7154
1518723 CIFC32 H28 O4 SiP -17.0418; 10.4998; 17.4226
93.591; 96.204; 103.663
1239.21Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518724 CIFC31 H28 O4 SiP 1 21/n 114.0146; 10.5314; 16.6752
90; 100.775; 90
2417.8Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.
Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.
Organic letters, 2015, 17, 856-859
1518725 CIFC18 H12 F N O3P 1 21/c 13.798; 11.416; 31.2
90; 90.82; 90
1353Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518726 CIFC22 H16 F4 O3P -17.668; 11.45; 11.497
97.96; 98.584; 103.944
952.6Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei
One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.
Organic letters, 2015, 17, 1090-1093
1518727 CIFC53 H53 F3 N4 O3 P2 SC 1 c 124.05898; 12.60445; 17.26646
90; 109.899; 90
4923.42Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518728 CIFC67 H72 Cl Ir N4 P2P -111.53121; 15.09347; 16.48026
91.4726; 100.955; 90.9436
2814.45Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518729 CIFC54 H52 Cl Ir N4 O2 P2R -330.1754; 30.1754; 27.5094
90; 90; 120
21692.9Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518730 CIFC71.5 H80 Cl2 Ir2 N4 P2P -113.28816; 15.4534; 18.6095
66.4438; 87.7181; 64.8361
3131.28Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518731 CIFC55.5 H62 Au2 Cl3 Ir N4 P2P 1 21/c 112.88426; 13.46559; 30.9781
90; 99.5872; 90
5299.46Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518732 CIFC48.63 H73.25 Cl3.25 N6 O10P 21 21 2110.3987; 18.7734; 27.849
90; 90; 90
5436.7Pettit, George R.; Smith, Thomas H.; Arce, Pablo M.; Flahive, Erik J.; Anderson, Collin R.; Chapuis, Jean-Charles; Xu, Jun-Ping; Groy, Thomas L.; Belcher, Paul E.; Macdonald, Christian B.
Antineoplastic agents. 599. Total synthesis of dolastatin 16.
Journal of natural products, 2015, 78, 476-485
1518733 CIFC20 H22 O7P c a 2128.5983; 8.3343; 7.7428
90; 90; 90
1845.47Kim, Hiyoung; Yang, Inho; Ryu, Shin-Young; Won, Dong Hwan; Giri, Awadut G.; Wang, Weihong; Choi, Hyukjae; Chin, Jungwook; Hahn, Dongyup; Kim, Eunhee; Han, Chulkyeong; Lee, Jihye; Nam, Sang-Jip; Ho, Won-Kyung; Kang, Heonjoong
Acredinones A and B, Voltage-Dependent Potassium Channel Inhibitors from the Sponge-Derived Fungus Acremonium sp. F9A015.
Journal of natural products, 2015, 78, 363-367
1518734 CIFC20 H18 O2P 1 21/c 18.7862; 16.6613; 11.1995
90; 112.702; 90
1512.47Sun, Qiu; Yao, Chang Jiang; König, Burkhard
A triphenylphosphine mediated photo-rearrangement and methanol addition of aryl chalcones to 1-propanones.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2015, 14, 948-952
1518735 CIFC46 H34 N4 O4P b c a10.981; 16.009; 19.987
90; 90; 90
3513.6Nielsen, Christian Benedikt Orea; Sørensen, Henning Osholm; Kongsted, Jacob
Comparison between Theoretically and Experimentally Determined Electronic Properties: Applications to Two-Photon Singlet Oxygen Sensitizers.
The journal of physical chemistry. A, 2015, 119, 1906-1916
1518736 CIFC55 H48 N2 O3P -110.069; 13.876; 16.5
109.803; 94.46; 103.692
2075.7Nielsen, Christian Benedikt Orea; Sørensen, Henning Osholm; Kongsted, Jacob
Comparison between Theoretically and Experimentally Determined Electronic Properties: Applications to Two-Photon Singlet Oxygen Sensitizers.
The journal of physical chemistry. A, 2015, 119, 1906-1916
1518737 CIFC55 H44 N2 O2P -18.5037; 9.8109; 13.1211
92.898; 97.615; 107.974
1027.2Nielsen, Christian Benedikt Orea; Sørensen, Henning Osholm; Kongsted, Jacob
Comparison between Theoretically and Experimentally Determined Electronic Properties: Applications to Two-Photon Singlet Oxygen Sensitizers.
The journal of physical chemistry. A, 2015, 119, 1906-1916
1518738 CIFC19.5 H18.5 As3 Cl6.5 S6P n m a20.703; 9.885; 14.702
90; 90; 90
3008.8Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518739 CIFC24 H24 Cl3 S6 Sb3R -3 c :H14.2066; 14.2066; 33.41
90; 90; 120
5839.7Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518740 CIFC36 H42 As3 Cl3 S6P -110.0055; 12.424; 16.522
81.285; 88.456; 84.579
2020.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518741 CIFC30 H42 As3 Cl3 S6R -3 :H16.413; 16.413; 23.8
90; 90; 120
5552.4Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518742 CIFC24 H30 Cl3 S6 Sb3P 1 21/n 116.0971; 11.4604; 16.3368
90; 91.867; 90
3012.2Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518743 CIFC30 H42 Cl3 S6 Sb3R -3 :H16.458; 16.458; 23.9449
90; 90; 120
5616.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518744 CIFC32 H30 N8 O5 Zn4P 42/m c m11.5382; 11.5382; 25.813
90; 90; 90
3436.5Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518745 CIFC34 H32 N8 O5 Zn4P 42/m c m11.517; 11.517; 34.474
90; 90; 90
4573Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518747 CIFC14 H9 Cl N4 O2P -111.31; 13.792; 13.982
93.902; 90.56; 112.233
2012.7Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518748 CIFC15 H11 Br N4 O2P b c a10.784; 9.6655; 28.858
90; 90; 90
3007.9Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan
Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.
Organic letters, 2015, 17, 1118-1121
1518753 CIFC37 H31 Cu F12 N4P -112.1667; 12.1867; 13.5954
81.549; 77.873; 65.444
1788.5Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions
Chem. Sci., 2015, 6, 2474
1518754 CIFC16 H6 F12 N2I 41/a :236.71; 36.71; 4.9148
90; 90; 90
6623.3Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions
Chem. Sci., 2015, 6, 2474
1518755 CIFC18 H27 Au B Cl N2 O2P 1 21/n 111.295; 10.512; 16.9583
90; 102.328; 90
1967.1Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518756 CIFC53 H79 Au B Cl N4 O4P 1 21/c 115.396; 14.4925; 24.966
90; 100.935; 90
5469.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518757 CIFC19 H27 B F3 Li N2 O5 SP -15.9513; 10.9562; 17.3953
96.176; 93.242; 97.646
1114.73Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518758 CIFC26 H39 B Cl N2 O2 RhP 1 21/c 116.46; 13.8072; 11.9483
90; 104.628; 90
2627.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518759 CIFC33 H47 B Cl Ir N2 O2C 1 2/c 135.4699; 10.667; 18.1337
90; 115.404; 90
6197.6Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518760 CIFC193.98 H267.94 N41 O29 Ru2C 1 2/c 129.8268; 17.7117; 38.0786
90; 96.79; 90
19975.2Anderson, Bryce L.; Maher, Andrew G.; Nava, Matthew; Lopez, Nazario; Cummins, Christopher C.; Nocera, Daniel G.
Ultrafast Photoinduced Electron Transfer from Peroxide Dianion.
The journal of physical chemistry. B, 2015, 119, 7422-7429
1518761 CIFC25 H23 F12 Fe2 O10P -19.507; 11.729; 16.605
102.703; 96.771; 112.595
1625Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518762 CIFC35 H25 F24 Fe3 O14P 1 21 19.7834; 20.8414; 12.0955
90; 102.57; 90
2407.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518763 CIFC35 H25 F24 Fe3 O14P 1 21 19.7979; 20.819; 12.0998
90; 102.659; 90
2408.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518764 CIFC35 H19 F30 Fe3 O14C 1 2/c 120.934; 13.481; 17.739
90; 92.848; 90
5000Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518765 CIFC25 H23 F12 Fe Mn O10P -19.464; 11.8255; 16.508
102.022; 97.859; 112.682
1618.3Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518766 CIFC35 H25 F24 Fe Ni2 O14P 1 21 19.7682; 20.7583; 12.0575
90; 103.126; 90
2381Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518767 CIFC16 H11 Br N6 O3P 1 21/c 117.554; 6.445; 15.846
90; 111.672; 90
1666Okamoto, Noriko; Sueda, Takuya; Minami, Hideki; Miwa, Yoshihisa; Yanada, Reiko
Regioselective Iodoazidation of Alkynes: Synthesis of α,α-Diazidoketones
Organic Letters, 2015, 150226085504000
1518768 CIFC15 H18 Cl2 N4 O3 PtP 1 21/c 119.113; 8.7386; 12.407
90; 107.31; 90
1978.4Tabatabaei Rezaei, Seyed Jamal; Amani, Vahid; Nabid, Mohammad Reza; Safari, Nasser; Niknejad, Hassan
Folate-decorated polymeric Pt(ii) prodrug micelles for targeted intracellular delivery and cytosolic glutathione-triggered release of platinum anticancer drugs
Polym. Chem., 2015, 6, 2844
1518769 CIFC25 H33 N3 O4P 21 21 216.0367; 19.1261; 20.5025
90; 90; 90
2367.2Meng, Ling-Hong; Du, Feng-Yu; Li, Xiao-Ming; Pedpradab, Patchara; Xu, Gang-Ming; Wang, Bin-Gui
Rubrumazines A-C, Indolediketopiperazines of the Isoechinulin Class from Eurotium rubrum MA-150, a Fungus Obtained from Marine Mangrove-Derived Rhizospheric Soil.
Journal of natural products, 2015, 78, 909-913
1518770 CIFC20 H16 Cl4 N2P b c a11.2813; 14.1148; 24.5832
90; 90; 90
3914.5Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518771 CIFC18 H26 Cl2 N2P -19.3474; 9.8657; 12.3923
66.695; 69.579; 62.115
908.59Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng
Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.
Organic letters, 2015, 17, 1026-1029
1518772 CIFC28 H23 Br Cl3 N O2P 21 21 219.6557; 10.7366; 25.0366
90; 90; 90
2595.53Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518773 CIFC26 H21 N O2 SP 21 21 217.3516; 9.5635; 29.4896
90; 90; 90
2073.33Saha, Satyajit; Schneider, Christoph
Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.
Organic letters, 2015, 17, 648-651
1518774 CIFC17 H24 O6C 1 2 119.391; 6.455; 15.383
90; 115.322; 90
1740Gao, Chun; Han, Li; Zheng, Dan; Jin, Hongwei; Gai, Chunyan; Wang, Jianbin; Zhang, Hao; Zhang, Liangren; Fu, Hongzheng
Dimeric Abietane Diterpenoids and Sesquiterpenoid Lactones from Teucrium viscidum.
Journal of natural products, 2015, 78, 630-638
1518775 CIFC20 H28 O4P 21 21 2110.734; 12.344; 13.282
90; 90; 90
1759.9Gao, Chun; Han, Li; Zheng, Dan; Jin, Hongwei; Gai, Chunyan; Wang, Jianbin; Zhang, Hao; Zhang, Liangren; Fu, Hongzheng
Dimeric Abietane Diterpenoids and Sesquiterpenoid Lactones from Teucrium viscidum.
Journal of natural products, 2015, 78, 630-638

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