Crystallography Open Database

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1545755 CIFC22 H16 N4 O3P 1 21/n 123.507; 6.5815; 25.139
90; 104.31; 90
3768.6Laugeois, Maxime; Ling, Johanne; Férard, Charlène; Michelet, Véronique; Ratovelomanana-Vidal, Virginie; Vitale, Maxime R.
Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3-Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives
Organic Letters, 2017
1545756 CIF
Paper
C14 H11 N O SeP 1 21/c 115.561; 5.9415; 12.471
90; 92.799; 90
1151.6Wang, Liyun; Xu, Ying; Guo, Zhiqiang; Wei, Xuehong
2-(3-Methylphenyl)-1,2-benzoselenazol-3(2<i>H</i>)-one
IUCrData, 2017, 2, x170532
1545757 CIFC19 H10 Br2 OC 1 2/c 117.7623; 7.2919; 23.6434
90; 102.092; 90
2994.4Gu, Xiao; Li, Huiyan; Shan, Bowen; Liu, Zhifeng; Miao, Qian
Synthesis, Structure, and Properties of Tetrabenzo[7]circulene.
Organic letters, 2017, 19, 2246-2249
1545758 CIFC25 H20.5 Cl2.5 N O2C 1 c 113.7789; 14.858; 22.728
90; 98.14; 90
4606.2Zheng, Kai-Lu; You, Min-Qi; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Mediated Intermolecular [3 + 2] Cycloaddition toward Pyrrolo[2,1-a]isoquinolines: Total Synthesis of the Lamellarin Core and Lamellarin G Trimethyl Ether.
Organic letters, 2017, 19, 2262-2265
1545759 CIFC21 H19 N O2P -18.078; 8.37; 12.38
100.58; 101.15; 94.63
801Zheng, Kai-Lu; You, Min-Qi; Shu, Wen-Ming; Wu, Yan-Dong; Wu, An-Xin
Acid-Mediated Intermolecular [3 + 2] Cycloaddition toward Pyrrolo[2,1-a]isoquinolines: Total Synthesis of the Lamellarin Core and Lamellarin G Trimethyl Ether.
Organic letters, 2017, 19, 2262-2265
1545760 CIFC26 H19 N O2P 21 21 217.65703; 9.51508; 26.1253
90; 90; 90
1903.42Kong, Duanyang; Han, Suna; Wang, Rui; Li, Meina; Zi, Guofu; Hou, Gouhua
Kinetic Resolution of 2-Substituted 1,2-Dihydroquinolines via Asymmetric Cu-Catalyzed Borylation Reaction
Chem. Sci., 2017
1545761 CIFC27 H30 B N O4P 21 21 218.52078; 15.6118; 17.52
90; 90; 90
2330.59Kong, Duanyang; Han, Suna; Wang, Rui; Li, Meina; Zi, Guofu; Hou, Gouhua
Kinetic Resolution of 2-Substituted 1,2-Dihydroquinolines via Asymmetric Cu-Catalyzed Borylation Reaction
Chem. Sci., 2017
1545762 CIFC25 H32 B N O6P 21 21 2111.0936; 14.6662; 14.75
90; 90; 90
2399.84Kong, Duanyang; Han, Suna; Wang, Rui; Li, Meina; Zi, Guofu; Hou, Gouhua
Kinetic Resolution of 2-Substituted 1,2-Dihydroquinolines via Asymmetric Cu-Catalyzed Borylation Reaction
Chem. Sci., 2017
1545763 CIFC8.58 H2 Co2 O6.58R -325.8262; 25.8262; 6.8315
90; 90; 120
3946.1Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545764 CIFC8 H2 Co2 N7.55 O6R -325.81; 25.81; 6.901
90; 90; 120
3981Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545765 CIFC8 H2 Co2 O6R -325.892; 25.892; 6.8482
90; 90; 120
3975.9Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545766 CIFC8 H2 Co2 O6 P5.28R -325.7348; 25.7348; 6.8385
90; 90; 120
3922.2Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545767 CIFC8 H2 Ar2 Co2 O6R -325.86; 25.86; 6.8678
90; 90; 120
3977.5Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545768 CIFC8 H2 Co2 O17.92R -325.7599; 25.7599; 6.8766
90; 90; 120
3951.8Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545769 CIFC10 H10 Co2 O6R -325.866; 25.866; 6.8457
90; 90; 120
3966.5Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545770 CIFC9.19 H2 Co2 O7.19R -325.853; 25.853; 6.8494
90; 90; 120
3964.7Gonzalez, Miguel; Mason, Jarad; Bloch, Eric D.; Teat, Simon; Gagnon, Kevin J.; Morrison, Gregory Y.; Queen, Wendy Lee; Long, Jeffrey R.
Structural characterization of framework‒gas interactions in the metal‒organic framework Co2(dobdc) by in situ single-crystal X-ray diffraction
Chem. Sci., 2017
1545771 CIFC72 H83 Cl0 F0 N6 O0 P Pt2 SP 1 21/c 113.7722; 39.9563; 17.7098
90; 97.536; 90
9661.3Leung, Sammual Yu-Lut; Evariste, Sloane; Lescop, Christophe; Hissler, Muriel; Yam, Vivian Wing-Wah
Supramolecular assembly of a phosphole-based moiety into nanostructures dictated by alkynylplatinum(ii) terpyridine complexes through non-covalent Pt⋯Pt and π‒π stacking interactions: synthesis, characterization, photophysics and self-assembly behaviors
Chem. Sci., 2017
1545772 CIFC19 H38 Fe2 N6 O19 P2P n a 2121.3916; 9.4099; 16.1292
90; 90; 90
3246.69Du, Kang; Waters, Emily Alex; Harris, David David
Ratiometric Quantitation of Redox Status with a Molecular Fe2 Magnetic Resonance Probe
Chem. Sci., 2017
1545773 CIFC22 H19 F3 O3P 18.7678; 10.7305; 10.8657
67.757; 88.911; 87.411
945.24Zhang, Junliang; Zhou, Wei; Wang, Hua-Min; Tao, Mengna; Zhu, Chao-Ze; Lin, Tao-Yan
Phosphine-catalyzed Enantioselective [3+2] Cycloadditions of -Substituted Allenoates with β-Perfluoroalkyl Enones
Chem. Sci., 2017
1545774 CIFC30 H37 Au F6 O P SbP 1 21/c 112.9887; 15.9169; 15.3964
90; 106.699; 90
3048.8Rekhroukh, Feriel; Blons, Charlie; Estevez, Laura; Ladeira, Sonia; Miqueu, Karinne; Amgoune, Abderrahmane; Bourissou, Didier
Gold(III)-arene complexes by insertion of olefins into gold-aryl bonds
Chem. Sci., 2017
1545775 CIFC22 H25 Au I PP 1 21 18.429; 10.7662; 11.6292
90; 94.266; 90
1052.41Rekhroukh, Feriel; Blons, Charlie; Estevez, Laura; Ladeira, Sonia; Miqueu, Karinne; Amgoune, Abderrahmane; Bourissou, Didier
Gold(III)-arene complexes by insertion of olefins into gold-aryl bonds
Chem. Sci., 2017
1545776 CIFC64 H82I 1 2/a 116.3409; 9.0662; 35.1804
90; 101.985; 90
5098.4Ivanov, Maxim V.; Thakur, Khushabu; Boddeda, Anitha; Wang, Denan; Rathore, Rajendra
Nodal Arrangement of HOMO Controls the Turning On/Off the Electronic Coupling in Isomeric Polypyrene Wires
The Journal of Physical Chemistry C, 2017, 121, 9202
1545777 CIFBa F6 ZrC m m a7.681; 11.357; 5.511
90; 90; 90
480.742Mehlhorn, Von B; Hoppe, R
Neue Hexafluorozirkonate(IV): BaZrF6, PbZrF6, EuZrF6, SrZrF6
Zeitschrift fur anorganische und allgemeine Chemie, 1976, 425, 180-188
1545778 CIFC14 H12 O2 SeP 1 21/c 17.4743; 17.3909; 10.0665
90; 107.933; 90
1244.92Mandal, Anup; Dana, Suman; Sahoo, Harekrishna; Grandhi, Gowri Sankar; Baidya, Mahiuddin
Ruthenium(II)-Catalyzed ortho-C-H Chalcogenation of Benzoic Acids via Weak O-Coordination: Synthesis of Chalcogenoxanthones.
Organic letters, 2017, 19, 2430-2433
1545779 CIFC19 H14 O2 Se2P -110.126; 12.9083; 13.2893
77.953; 80.076; 82.458
1665.16Mandal, Anup; Dana, Suman; Sahoo, Harekrishna; Grandhi, Gowri Sankar; Baidya, Mahiuddin
Ruthenium(II)-Catalyzed ortho-C-H Chalcogenation of Benzoic Acids via Weak O-Coordination: Synthesis of Chalcogenoxanthones.
Organic letters, 2017, 19, 2430-2433
1545780 CIFC25 H21 Br N2 O3 SP 1 21/c 18.729; 9.996; 25.71
90; 98.72; 90
2217.4Yi, Liang; Zhang, Yuyang; Zhang, Zhao-Fei; Sun, Dequn; Ye, Song
Synthesis of Dihydropyridinone-Fused Indoles and α-Carbolines via N-Heterocyclic Carbene-Catalyzed [3 + 3] Annulation of Indolin-2-imines and Bromoenals.
Organic letters, 2017, 19, 2286-2289
1545781 CIFC14 H21 N O4 SI 1 2 114.811; 5.342; 19.823
90; 99.03; 90
1549Sekiya, Shinji; Okumura, Mao; Kubota, Kei; Nakamura, Tatsuya; Sekine, Daisuke; Hosokawa, Seijiro
Remote Asymmetric Bromination Reaction with Vinylketene Silyl N,O-Acetal and Its Application to Total Synthesis of Pellasoren A.
Organic letters, 2017, 19, 2394-2397
1545782 CIFC12 H18 Br N O3P 1 21 110.006; 6.2513; 10.8417
90; 93.336; 90
677Sekiya, Shinji; Okumura, Mao; Kubota, Kei; Nakamura, Tatsuya; Sekine, Daisuke; Hosokawa, Seijiro
Remote Asymmetric Bromination Reaction with Vinylketene Silyl N,O-Acetal and Its Application to Total Synthesis of Pellasoren A.
Organic letters, 2017, 19, 2394-2397
1545783 CIFC7 H4 Br Cl O2P 1 21/n 17.2271; 8.948; 12.1887
90; 105.819; 90
758.37Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545784 CIFC7 H4 Br Cl O2P 1 21/n 17.2738; 9.0627; 11.7233
90; 102.916; 90
753.25Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545785 CIFC7 H4 Br Cl O2P 1 21/n 17.2577; 9.0397; 11.8561
90; 103.904; 90
755.06Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545786 CIFC7 H4 Br Cl O2P 1 21/n 17.256; 9.0227; 11.9855
90; 104.676; 90
759.07Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545787 CIFC7 H4 Br Cl O2P -13.8949; 8.2939; 11.8408
89.014; 89.991; 78.651
374.97Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545788 CIFC7 H4 Br Cl O2P 1 21/n 17.2385; 8.9976; 12.1313
90; 105.406; 90
761.71Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545789 CIFC7 H4 Br Cl O2P -13.9007; 8.307; 11.9258
88.909; 89.987; 78.731
378.91Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545790 CIFC7 H4 Br Cl O2P 1 21/n 17.2399; 9.0087; 12.0539
90; 105.036; 90
759.26Pramanik, Titas; Srinivas, Pavan Mysore; Tayur, Guru Row N.
FDHALO17: Do halogen bonds dictate the packing preferences in solid solutions?
Faraday Discuss., 2017
1545791 CIFC16 H36 Cl0.07 I4.93 NP 1 21/c 119.948; 28.361; 9.3012
90; 96.59; 90
5227.3Mustoe, Chantal L.; Yu, Darren; Gunabalasingam, Mathusan; Patrick, Brian O.; Kennepohl, Pierre
FDHALO17: Probing covalency in halogen bonds through Donor K-edge X-ray Absorption Spectroscopy: polyhalides as coordination complexes
Faraday Discuss., 2017
1545792 CIFC16 H36 I3 NP -19.463; 15.553; 15.805
83.658; 74.285; 78.5
2190.3Mustoe, Chantal L.; Yu, Darren; Gunabalasingam, Mathusan; Patrick, Brian O.; Kennepohl, Pierre
FDHALO17: Probing covalency in halogen bonds through Donor K-edge X-ray Absorption Spectroscopy: polyhalides as coordination complexes
Faraday Discuss., 2017
1545793 CIFB30 Nd5 O60 Rb15R 3 2 :H13.52363; 13.52363; 31.1617
90; 90; 120
4935.6V.V. Atuchin; A.K. Subanakov; A.S. Aleksandrovsky; B.G. Bazarov; J.G. Bazarova; S.G. Dorzhieva; T.A. Gavrilova; A.S. Krylov; M.S. Molokeev; A.S. Oreshonkov; A.M. Pugachev; Yu.L. Tushinova; A.P. Yelisseyev
Exploration of structural, thermal, vibrational and spectroscopic properties of new noncentrosymmetric double borate Rb3NdB6O12
Advanced Powder Technology, 2017, 28, 1309-1315
1545794 CIFC68 H78 N2 O2 S4P -16.024; 12.4238; 20.231
78.658; 86.669; 78.084
1452.31Ganguly, Anindya; Zhu, Jianfeng; Kelly, Timothy L.
Effect of Cross-Conjugation on Derivatives of Benzoisoindigo, an Isoindigo Analogue with an Extended π-System
The Journal of Physical Chemistry C, 2017, 121, 9110
1545795 CIFLa1.33 Mo4 Na1.33 O16 Sr1.33I 41/a :25.36033; 5.36033; 11.82739
90; 90; 90
339.838Chang Sung Lim; Aleksandr S. Aleksandrovsky; Maxim S. Molokeev; Aleksandr S. Oreshonkov; Victor V. Atuchin
Microwave synthesis and spectroscopic properties of ternary scheelite-type molybdate phosphors NaSrLa(MoO4)3:Er3+,Yb3+
Journal of Alloys and Compounds, 2017, 713, 156-163
1545796 CIFEr0.27 La1.07 Mo4 Na1.33 O16 Sr1.33I 41/a :25.34061; 5.34061; 11.77693
90; 90; 90
335.903Chang Sung Lim; Aleksandr S. Aleksandrovsky; Maxim S. Molokeev; Aleksandr S. Oreshonkov; Victor V. Atuchin
Microwave synthesis and spectroscopic properties of ternary scheelite-type molybdate phosphors NaSrLa(MoO4)3:Er3+,Yb3+
Journal of Alloys and Compounds, 2017, 713, 156-163
1545797 CIFEr0.13 La0.93 Mo4 Na1.33 O16 Sr1.33 Yb0.27I 41/a :25.32926; 5.32926; 11.74788
90; 90; 90
333.652Chang Sung Lim; Aleksandr S. Aleksandrovsky; Maxim S. Molokeev; Aleksandr S. Oreshonkov; Victor V. Atuchin
Microwave synthesis and spectroscopic properties of ternary scheelite-type molybdate phosphors NaSrLa(MoO4)3:Er3+,Yb3+
Journal of Alloys and Compounds, 2017, 713, 156-163
1545798 CIFEr0.07 La0.67 Mo4 Na1.33 O16 Sr1.33 Yb0.6I 41/a :25.30628; 5.30628; 11.68195
90; 90; 90
328.924Chang Sung Lim; Aleksandr S. Aleksandrovsky; Maxim S. Molokeev; Aleksandr S. Oreshonkov; Victor V. Atuchin
Microwave synthesis and spectroscopic properties of ternary scheelite-type molybdate phosphors NaSrLa(MoO4)3:Er3+,Yb3+
Journal of Alloys and Compounds, 2017, 713, 156-163
1545799 CIFC13 H13 N OP 1 21/c 111.2899; 10.188; 8.5203
90; 93.637; 90
978.04Hu, Feng; Nareddy, Pradeep; Lalancette, Roger; Jordan, Frank; Szostak, Michal
σ N-C Bond Difunctionalization in Bridged Twisted Amides: Sew-and-Cut Activation Approach to Functionalized Isoquinolines.
Organic letters, 2017, 19, 2386-2389
1545800 CIFC15 H28 N4 O7 S2P 1 21/c 17.8403; 12.7512; 10.5247
90; 91.486; 90
1051.83Deng, Jie; Xu, Bao-Hua; Wang, Yao-Feng; Mo, Xian-En; Zhang, Rui; Li, You; Zhang, Suo-Jiang
Brønsted acidic ionic liquid-catalyzed dehydrative formation of isosorbide from sorbitol: introduction of a continuous process
Catal. Sci. Technol., 2017
1545801 CIFC8 H24 Br4 N2 PbP b c a8.3343; 8.2225; 27.6171
90; 90; 90
1892.57Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545802 CIFC4 H14 Br4 N2 PbP -18.0135; 8.427; 10.7367
78.957; 69.565; 89.542
665.47Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545803 CIFC5 H11 Br4 N3 PbP 1 21/c 110.6055; 11.6091; 11.9312
90; 110.061; 90
1379.8Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545804 CIFC6 H18 Br4 N2 PbC 1 2/c 124.4632; 8.0039; 8.1963
90; 99.745; 90
1581.69Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545805 CIFC5 H11 Br4 N3 PbP 1 21/c 110.5412; 11.5023; 11.925
90; 109.996; 90
1358.7Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545806 CIFC8 H22 Br4 N2 PbP 1 21/c 113.807; 7.9891; 8.2769
90; 104.34; 90
884.5Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545807 CIFC8 H14 Br4 N2 PbP 1 21/c 17.7688; 8.5108; 24.6314
90; 95.197; 90
1621.9Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545808 CIFC24 H60 Br12 N6 O12 Pb3P 1 21/c 124.7721; 8.0709; 56.964
90; 97.137; 90
11300.7Smith, Matthew D.; Jaffe, Adam; Dohner, Emma R.; Lindenberg, Aaron; Karunadasa, Hemamala I.
Structural Origins of Broadband Emission from Layered Pb‒Br Hybrid Perovskites
Chem. Sci., 2017
1545809 CIFC32 H36 N4 O4P 1 21/n 17.8566; 21.336; 8.3872
90; 90.911; 90
1405.8Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545810 CIFC30 H34 N2 O4 S2P 1 21/n 17.7971; 22.217; 7.9179
90; 91.479; 90
1371.1Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545811 CIFC43 H49 N5 O4P -17.409; 8.781; 15.36
81.63; 86.57; 78.64
969Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545812 CIFC29 H30 N2 O2P 1 21/c 17.5571; 24.125; 12.9363
90; 92.034; 90
2357Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545813 CIFC34 H38 N2 O4P 1 21/n 18.292; 20.615; 8.47
90; 92.435; 90
1446.6Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545814 CIFC44 H46 N6 O4P -17.485; 8.797; 14.171
96.618; 93.306; 91.826
924.6Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545815 CIFC42 H44 N4 O4 S2P -17.492; 9.069; 13.643
98.069; 92.516; 91.428
916.5Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545816 CIFC90 H96 N10 O8P -17.3795; 8.8871; 29.533
89.495; 84.054; 85.281
1919.9Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545817 CIFC75 H73 N8 O6P -17.478; 8.739; 23.37
92.36; 90.29; 93.131
1524Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545818 CIFC46 H48 N4 O4P -17.528; 8.948; 14.11
96.219; 94.61; 90.598
942Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545819 CIFC44 H48 N6 O4P -17.4957; 8.7882; 14.308
97.049; 94.334; 91.781
931.9Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545820 CIFC42 H46 N4 O4 S2P -17.531; 9.026; 13.941
98.18; 92.03; 91.235
937Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545821 CIFC75 H75 N8 O6P -17.4611; 8.7285; 23.6219
92.85; 91.347; 93.317
1533.34Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545822 CIFC77 H79 N8 O5P -17.4709; 8.7326; 23.6381
92.857; 91.317; 93.293
1537.18Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545823 CIFC77 H77 N6 O6P -17.4914; 8.8265; 23.583
92.722; 92.976; 91.626
1554.77Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545824 CIFC46 H50 N4 O4P -17.5407; 8.9198; 14.284
96.506; 96.093; 90.634
948.9Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545825 CIFC27 H38 N2 O2P 1 21/c 18.356; 24.894; 11.744
90; 96.324; 90
2428Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545826 CIFC50 H52 N4 O4P -17.546; 9.4647; 14.8318
85.58; 77.14; 86.77
1028.8Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545827 CIFC42 H48 N6 O4P -17.324; 8.723; 15.107
82.27; 88.73; 78.76
938Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545828 CIFC31 H30 N2 O2P 1 21/c 18.0059; 24.903; 12.0892
90; 91.065; 90
2409.8Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545829 CIFC44 H50 N4 O4P -17.195; 8.865; 15.981
80.52; 84.2; 79.19
985Mir, Niyaz A.; Dubey, Ritesh; Desiraju, Gautam R.
Four- and five-component molecular solids: crystal engineering strategies based on structural inequivalence
IUCrJ, 2016, 3, 96-101
1545830 CIF
Paper
C9 H11 N5 O4 S2P 1 21/n 14.9138; 33.192; 8.3659
90; 99.52; 90
1345.7Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545831 CIF
Paper
C14 H16 N6 O5 S2P -16.8501; 11.3563; 12.3387
82.288; 81.856; 75.804
916.19Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545832 CIF
Paper
C10 H19 N5 O5 S2P -14.9969; 11.6983; 14.6244
70.868; 81.892; 80.262
792.65Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545833 CIF
Paper
C5 H9 N4 O3.5 S2.5C 1 2/c 152.62; 4.816; 17.814
90; 106.785; 90
4322Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545834 CIF
Paper
C10 H13 N5 O4 S2P 1 c 111.3972; 18.1641; 10.338
90; 97.046; 90
2124Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545835 CIF
Paper
C10 H12 N6 O4 S2P -15.1477; 10.8147; 14.2604
69.797; 85.463; 81.889
737.2Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545836 CIF
Paper
C15 H17 N7 O5 S2P -17.0347; 10.2539; 13.7934
81.685; 83.028; 88.283
977.14Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545837 CIF
Paper
C10 H15 N5 O6 S2P -17.7872; 10.213; 10.2464
88.192; 76.587; 77.996
775.22Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545838 CIF
Paper
C14 H24 N6 O5 S2P 1 21/c 19.66166; 23.4685; 8.84352
90; 100.773; 90
1969.88Bolla, Geetha; Nangia, Ashwini
Binary and ternary cocrystals of sulfa drug acetazolamide with pyridine carboxamides and cyclic amides
IUCrJ, 2016, 3, 152-160
1545839 CIFC38 H52 N6 O4P -18.8712; 10.1819; 11.2862
114.633; 93.749; 101
897.56Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545840 CIFC120 H160 N16 O17C 1 2/c 115.533; 8.564; 21.8
90; 93.873; 90
2893Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545841 CIFC36 H48 N6 O6P 1 21/c 115.6084; 13.4786; 17.2209
90; 90.2; 90
3622.9Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545842 CIFC64 H56 N4 O4P -19.0005; 10.0381; 14.4894
108.432; 101.78; 90.484
1212Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545843 CIFC29 H31 N3 O2P -18.9943; 9.5169; 14.927
74.162; 77.589; 89.115
1199.2Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545844 CIFC62 H54 N6 O4P -19.034; 9.889; 14.505
107.761; 101.019; 91.432
1206.5Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545845 CIFC54 H54 N6 O6P -18.6332; 9.0194; 14.869
105.2; 91.263; 91.519
1116.4Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545846 CIFC44 H44 N6 O6P -17.812; 8.763; 14.3
95.009; 95.415; 101.04
950.9Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545847 CIFC56 H56 N6 O8P -110.151; 11.2084; 12.3363
102.012; 105.153; 112.368
1176.1Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545848 CIFC38 H46 N4 O4 S2P -18.662; 10.289; 11.523
65.003; 76.93; 80.277
903.5Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545849 CIFC24 H23 N2 O2P -18.971; 10.078; 11.666
109.665; 94.353; 90.742
989.5Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545850 CIFC42 H58 N4 O4P 1 21/c 111.4579; 11.8325; 14.9792
90; 107.229; 90
1939.7Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545851 CIFC46 H44 N6 O4P -18.983; 12.712; 17.561
89.485; 76.291; 82.933
1933Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545852 CIFC23 H22 N3 O2P -18.778; 10.491; 12.095
66.387; 81.548; 69.631
956.7Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545853 CIFC46 H50 N4 O4P -18.921; 10.723; 10.954
67.417; 81.183; 78.367
944.3Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545854 CIFC40 H48 N6 O6P -18.284; 8.564; 14.6
78.65; 87.26; 64.4
915Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545855 CIFC44 H40 N6 O6P -19.012; 11.241; 18.355
94.296; 93.207; 92.248
1850Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545856 CIFC56 H48 N8 O6P -17.576; 9.081; 16.503
96.651; 90.601; 91.433
1127.3Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545857 CIFC44 H46 N4 O6P 1 21/c 18.876; 11.941; 17.98
90; 97.072; 90
1891.2Dubey, Ritesh; Mir, Niyaz A.; Desiraju, Gautam R.
Quaternary cocrystals: combinatorial synthetic strategies based on long-range synthon Aufbau modules (LSAM)
IUCrJ, 2016, 3, 102-107
1545858 CIFC66 H84 I6 N12 Zn3C 1 2/c 134.376; 15.0832; 29.6413
90; 100.675; 90
15103Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545859 CIFC73.5 H78.76 I6 N12 Zn3C 1 2/c 135.0725; 14.8911; 30.9658
90; 101.956; 90
15821.6Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545860 CIFC285 H317 I24 N48 O15 Zn12P 1 21 132.8072; 14.9123; 34.9062
90; 105.822; 90
16430.2Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545861 CIFC61.47 H64.79 I6.01 N12 O4.06 Zn3C 1 2/c 134.4746; 15.0255; 30.1535
90; 99.681; 90
15397Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545862 CIFC75 H72 I6 N12 O10.5 Zn3C 1 2/c 134.1414; 14.5641; 34.9597
90; 108.633; 90
16472.2Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545863 CIFC67 H66 I6 N12 O9 Zn3C 1 2/c 134.9043; 14.955; 30.3469
90; 100.074; 90
15596.7Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545864 CIFC69.69 H80.8 I6 N14.11 Zn3C 1 2/c 136.8116; 14.6974; 30.6993
90; 103.07; 90
16179.1Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545865 CIFC58.32 H48.8 I6 N14.2 O6.61 Zn3C 1 2/c 132.5791; 15.2458; 29.0346
90; 98.398; 90
14266.7Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545866 CIFC64.44 H65.6 I6 N12 O1.48 Zn3C 1 2/c 135.1288; 14.767; 30.8649
90; 101.432; 90
15693.4Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545867 CIFC120.9 H108 I11.99 N24 O12.59 Zn5.99P -114.8292; 17.9234; 29.9062
96.836; 93.529; 110.142
7364.6Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545868 CIFC123 H113.6 I12 N24 O12.14 Zn6P -114.8303; 17.913; 29.8943
96.803; 93.488; 110.229
7355Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545869 CIFC123 H112.85 I11.99 N24 O12.39 Zn5.99P -114.8303; 17.913; 29.8943
96.803; 93.488; 110.229
7355Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545870 CIFC71.25 H57.96 Br1.92 I6 N12 Zn3C 1 2/c 135.8691; 14.8864; 31.2823
90; 102.711; 90
16294.2Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545871 CIFC60.92 H58.15 I6 N12 O5.89 Zn3C 1 2/c 134.0465; 14.9235; 30.8377
90; 100.629; 90
15399.6Hoshino, Manabu; Khutia, Anupam; Xing, Hongzhu; Inokuma, Yasuhide; Fujita, Makoto
The crystalline sponge method updated
IUCrJ, 2016, 3, 139-151
1545872 CIFF11 Pr Zr2I b a m7.716; 10.006; 10.897
90; 90; 90
841.3Laval, J P; Abaouz, A
Crystal chemistry of anion-excess ReO3-related phases II; Crystal structure of PrZr2F11
Journal of Solid State Chemistry, 1992, 100, 90-100
1545873 CIFC29 H35 N5 O5 S4P 1 21 110.8556; 8.4638; 17.443
90; 96.664; 90
1591.8Antczak, Monika I.; Zhang, Yongyou; Wang, Changguang; Doran, Jennifer; Naidoo, Jacinth; Voruganti, Sukesh; Williams, Noelle S.; Markowitz, Sanford D.; Ready, Joseph M.
Inhibitors of 15-Prostaglandin Dehydrogenase to Potentiate Tissue Repair.
Journal of medicinal chemistry, 2017
1545874 CIFC6 H11 F4 Li N4 O8 S4P 1 21/a 18.9922; 9.6614; 10.2093
90; 105.422; 90
855.02Matsumoto, Kazuhiko; Nishiwaki, Erisa; Hosokawa, Takafumi; Tawa, Shinya; Nohira, Toshiyuki; Hagiwara, Rika
Thermal, Physical, and Electrochemical Properties of Li[N(SO2F)2]-[1-Ethyl-3-methylimidazolium][N(SO2F)2] Ionic Liquid Electrolytes for Li Secondary Batteries Operated at Room and Intermediate Temperatures
The Journal of Physical Chemistry C, 2017, 121, 9209
1545875 CIFC14 H14 S4P 1 21/c 114.0418; 6.1192; 17.399
90; 101.306; 90
1465.99Cerda, Matthew M.; Hammers, Matthew D.; Earp, Mary S.; Zakharov, Lev N.; Pluth, Michael D.
Applications of Synthetic Organic Tetrasulfides as H2S Donors.
Organic letters, 2017, 19, 2314-2317
1545876 CIFC23 H20 N2 O3 SP 1 21/n 110.02; 11.238; 17.984
90; 101.851; 90
1981.9Stefan, Mihaela Corina; Dissanayake, Dushanthi; McCandless, Gregory T.; Biewer, Michael C.
Systematic variation of thiophene substituents in photochromic spiropyrans
Photochem. Photobiol. Sci., 2017
1545877 CIFC23 H19 Br N2 O3 SP 1 21/c 119.967; 11.759; 8.67
90; 94.66; 90
2028.9Stefan, Mihaela Corina; Dissanayake, Dushanthi; McCandless, Gregory T.; Biewer, Michael C.
Systematic variation of thiophene substituents in photochromic spiropyrans
Photochem. Photobiol. Sci., 2017
1545878 CIFBa F11 Na Zr2I 41/a :28.223; 8.223; 23.61
90; 90; 90
1596.5Laval, J. P.; Abaouz, A.
Crystal structure of BaNaZr2F11 : a phase recrystallizing from fluorozirconate glasses
Journal of Solid State Chemistry, 1992, 101, 18-25
1545879 CIFC24 H23 N O6 SP 1 21/n 110.3695; 11.2448; 19.3109
90; 94.823; 90
2243.7Xing, Jiaojiao; Lei, Yu; Gao, Yu-Ning; Shi, Min
PPh3-Catalyzed [3 + 2] Spiroannulation of 1C,3N-Bisnucleophiles Derived from Secondary β-Ketoamides with δ-Acetoxy Allenoate: A Route to Functionalized Spiro N-Heterocyclic Derivatives.
Organic letters, 2017, 19, 2382-2385
1545880 CIFC22 H27 N O6 SP 1 21/c 115.5866; 9.8958; 14.265
90; 98.14; 90
2178.1Xing, Jiaojiao; Lei, Yu; Gao, Yu-Ning; Shi, Min
PPh3-Catalyzed [3 + 2] Spiroannulation of 1C,3N-Bisnucleophiles Derived from Secondary β-Ketoamides with δ-Acetoxy Allenoate: A Route to Functionalized Spiro N-Heterocyclic Derivatives.
Organic letters, 2017, 19, 2382-2385
1545881 CIFC24 H14 Co2 O6P -18.4376; 10.1022; 13.0614
98.593; 92.973; 100.142
1080.1Wang, Gongbao; Lindeboom, Erik-Jan; Heerewaarden, Chris van; Minnaard, Adriaan J.
Synthesis of Ene-yne-enes by Nickel-Catalyzed Double SN2’ substitution of 1,6-Dichlorohexa-2,4-diyne
Catal. Sci. Technol., 2017
1545882 CIFF12 O Tl2 Zr3R -3 m :H7.703; 7.703; 30.017
90; 90; 120
1542.5Mansouri, I.; Avignant, D.
Crystal structure of a new oxyfluoride : Tl2Zr3OF12
Journal of Solid State Chemistry, 1984, 51, 91-99
1545883 CIFC36 H54 O6P 21 21 2110.8783; 11.8013; 26.178
90; 90; 90
3360.68Guo, Yi; Zhang, Na; Chen, Chunmei; Huang, Jinfeng; Li, Xiao-Nian; Liu, Junjun; Zhu, Hucheng; Tong, Qingyi; Zhang, Jinwen; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Tricyclic Polyprenylated Acylphloroglucinols from St John's Wort, Hypericum perforatum.
Journal of natural products, 2017
1545884 CIFC23 H23 N O4 SP 1 21 112.542; 5.445; 15.507
90; 94.578; 90
1055.6Yuan, Xiaoqian; Dong, Shupeng; Liu, Zhen; Wu, Guibing; Zou, Chuncheng; Ye, Jinxing
Enantioselective Michael Addition of Photogenerated o-Quinodimethanes to Enones Catalyzed by Chiral Amino Acid Esters.
Organic letters, 2017, 19, 2322-2325
1545885 CIFC16 H22 O2P 1 21 18.0035; 9.1507; 9.4828
90; 98.897; 90
686.14Schneider, Lisa M.; Schmiedel, Volker M.; Pecchioli, Tommaso; Lentz, Dieter; Merten, Christian; Christmann, Mathias
Asymmetric Synthesis of Carbocyclic Propellanes.
Organic letters, 2017
1545886 CIFC19 H19 Br O3P 21 21 217.3483; 12.121; 18.3918
90; 90; 90
1638.13Schneider, Lisa M.; Schmiedel, Volker M.; Pecchioli, Tommaso; Lentz, Dieter; Merten, Christian; Christmann, Mathias
Asymmetric Synthesis of Carbocyclic Propellanes.
Organic letters, 2017
1545887 CIFC28 H28 N2 O10P 17.3394; 12.4108; 14.7998
107.312; 100.068; 91.14
1263.48Schneider, Lisa M.; Schmiedel, Volker M.; Pecchioli, Tommaso; Lentz, Dieter; Merten, Christian; Christmann, Mathias
Asymmetric Synthesis of Carbocyclic Propellanes.
Organic letters, 2017
1545888 CIFC25 H25 N O2 S2P -18.6354; 9.6432; 14.338
100.662; 96.56; 112.543
1060.91Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1545889 CIFC21 H19 F6 N O3 SP 1 21/c 18.3336; 20.386; 12.286
90; 100.225; 90
2054.1Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1545890 CIFC19 H21 N O3 SP 1 21/c 16.0294; 32.1226; 8.9796
90; 100.835; 90
1708.16Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1545891 CIFC33 H30 N2 O2 SP 1 21/c 112.193; 15.497; 28.3046
90; 93.718; 90
5337Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1545892 CIFC28 H28 N2 O2 SP -18.6014; 15.9764; 18.922
65.929; 81.466; 88.644
2345.9Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1545893 CIFC4 H12 Cu2 I2 N2P 42/n11.7663; 11.7663; 7.5184
90; 90; 90
1040.89Jin, Xiaodong; Davies, Robert P.
Copper-catalysed aromatic-Finkelstein reactions with amine-based ligand systems
Catal. Sci. Technol., 2017
1545894 CIFC20 H65 Cu2 I4 N15P 21 21 219.18796; 12.5494; 35.7355
90; 90; 90
4120.42Jin, Xiaodong; Davies, Robert P.
Copper-catalysed aromatic-Finkelstein reactions with amine-based ligand systems
Catal. Sci. Technol., 2017
1545895 CIFC8 H24 Cu2 I2 N4P 1 21/c 113.3569; 11.5554; 11.4189
90; 95.026; 90
1755.7Jin, Xiaodong; Davies, Robert P.
Copper-catalysed aromatic-Finkelstein reactions with amine-based ligand systems
Catal. Sci. Technol., 2017
1545896 CIFF15 Pr Zr3R 3 m :H12.316; 12.316; 6.115
90; 90; 120
803.3Laval, J. P.; Abaouz, A.
Crystal chemistry of anion-excess ReO3-related phases : crystal structure of beta-PrZr3F15
Journal of Solid State Chemistry, 1992, 96, 324-331
1545897 CIFC4 H15 Ga N2 O8 P2P n a a9.109; 11.021; 11.987
90; 90; 90
1203.4Ann M. Chippindale; Andrew D. Bond; Ashley D. Law; Andrew R. Cowley
Synthesis and Characterization of [NH3(CH2)4NH3][Ga(PO4)(PO3OH)], a One-Dimensional Gallophosphate
Journal of Solid State Chemistry, 1998, 136, 227-232
1545898 CIFC22 H23 N O2 SiP 21 21 219.3782; 11.6315; 17.149
90; 90; 90
1870.7Rodriguez, Kevin X.; Kaltwasser, Nicolai; Toni, Tiffany A.; Ashfeld, Brandon L.
Rearrangement of an Intermediate Cyclopropyl Ketene in a Rh(II)-Catalyzed Formal [4 + 1]-Cycloaddition Employing Vinyl Ketenes as 1,4-Dipoles and Donor-Acceptor Metallocarbenes.
Organic letters, 2017, 19, 2482-2485
1545899 CIFC20 H24 N2P 1 21/n 116.6451; 5.8536; 19.416
90; 113.818; 90
1730.7Zhou, Rong; Liu, Haiwang; Tao, Hairong; Yu, Xingjian; Wu, Jie
Metal-free direct alkylation of unfunctionalized allylic/benzylic sp3 CH bonds via photoredox induced radical cation deprotonation
Chem. Sci., 2017
1545900 CIFC25 H31 N O2P 1 21 15.4583; 10.396; 19.0896
90; 98.026; 90
1072.62Qin, Linlin; Ren, Lei; Wan, Songlin; Liu, Guoliang; Luo, Xinfeng; Liu, Zhenhong; Li, Fangqiong; Yu, Yan; Liu, Jianyu; Wei, Yonggang
Design, Synthesis, and Evaluation of Novel 2,6-Disubstituted Phenol Derivatives as General Anesthetics.
Journal of medicinal chemistry, 2017, 60, 3606-3617
1545901 CIFC22 H28 O4P 21 21 216.1077; 15.287; 21.901
90; 90; 90
2044.9Zhang, Chen; Li, Fangqiong; Yu, Yan; Huang, Anbang; He, Ping; Lei, Ming; Wang, Jianmin; Huang, Longbin; Liu, Zhenhong; Liu, Jianyu; Wei, Yonggang
Design, Synthesis, and Evaluation of a Series of Novel Benzocyclobutene Derivatives as General Anesthetics.
Journal of medicinal chemistry, 2017
1545902 CIFC23 H27 N O4P 1 21 110.0156; 6.613; 15.9543
90; 91.121; 90
1056.5Zhang, Chen; Li, Fangqiong; Yu, Yan; Huang, Anbang; He, Ping; Lei, Ming; Wang, Jianmin; Huang, Longbin; Liu, Zhenhong; Liu, Jianyu; Wei, Yonggang
Design, Synthesis, and Evaluation of a Series of Novel Benzocyclobutene Derivatives as General Anesthetics.
Journal of medicinal chemistry, 2017
1545903 CIFC20 H19 Br N2 O4P 1 21/c 128.3676; 12.0527; 11.4928
90; 91.5907; 90
3927.94Suzuki, Itaru; Tsunoi, Shinji; Shibata, Ikuya
Catalytic Annulation of Diethyl Methylenecyclopropane-1,1-dicarboxylate with 1,1-Dicyanoalkenes.
Organic letters, 2017, 19, 2690-2693
1545904 CIFC50 H81 Li O2P 1 21/n 19.7973; 25.876; 18.478
90; 93.768; 90
4674.3Bukhryakov, Konstantin V.; Schrock, Richard R.; Hoveyda, Amir H.; Müller, Peter; Becker, Jonathan
Synthesis of 2,6-Hexa-tert-butylterphenyl Derivatives, 2,6-(2,4,6-t-Bu3C6H2)2C6H3X, where X = I, Li, OH, SH, N3, or NH2
Organic Letters, 2017
1545905 CIFC126 H183 Cl6 O3 W1.5C 1 2/c 119.931; 65.396; 18.862
90; 90; 90
24585Bukhryakov, Konstantin V.; Schrock, Richard R.; Hoveyda, Amir H.; Müller, Peter; Becker, Jonathan
Synthesis of 2,6-Hexa-tert-butylterphenyl Derivatives, 2,6-(2,4,6-t-Bu3C6H2)2C6H3X, where X = I, Li, OH, SH, N3, or NH2
Organic Letters, 2017
1545906 CIFC28 H31 Br N2 O5 S2P 1 21 113.3441; 6.3849; 16.136
90; 95.366; 90
1368.77Möller, Guido P; Müller, Steffen; Wolfstädter, Bernd T; Wolfrum, Susanne; Schepmann, Dirk; Wünsch, Bernhard; Carreira, Erick M.
Oxetanyl Amino Acids for Peptidomimetics.
Organic letters, 2017, 19, 2510-2513
1545907 CIFC14 H28 N2 O3 SP 21 21 215.4302; 15.9643; 19.0144
90; 90; 90
1648.3Möller, Guido P; Müller, Steffen; Wolfstädter, Bernd T; Wolfrum, Susanne; Schepmann, Dirk; Wünsch, Bernhard; Carreira, Erick M.
Oxetanyl Amino Acids for Peptidomimetics.
Organic letters, 2017, 19, 2510-2513
1545908 CIFC41 H59 Br N6 Ni O Si3P -19.4796; 15.2993; 15.5434
89.381; 78.419; 77.883
2158Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545909 CIFC40 H54 Cu N6 Si3R -3 :H16.4836; 16.4836; 26.069
90; 90; 120
6134.2Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545910 CIFC44 H60 Mg N6 Si3P 1 21/n 112.834; 17.1903; 20.4108
90; 98.1684; 90
4457.4Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545911 CIFC37 H51 Li N6 Si3I 2 320.191; 20.191; 20.191
90; 90; 90
8231.4Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545912 CIFC46 H61 N6 Si3P -110.1605; 15.4631; 15.8502
65.3205; 86.4167; 79.4613
2224.4Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545913 CIFC41 H57 N6 Si3 ZnP -111.1387; 12.298; 17.7675
79.0698; 75.102; 65.8782
2136.8Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545914 CIFC43 H57 Br N6 Ni Si3P 1 21/c 112.702; 18.819; 18.915
90; 105.63; 90
4354.2Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545915 CIFC37 H51 Cu N6 Si3I 2 320.1294; 20.1294; 20.1294
90; 90; 90
8156.3Ruccolo, Serge; Rauch, Michael; Parkin, Gerard
Tris[(1-isopropylbenzimidazol-2-yl)dimethylsilyl]methyl metal complexes, [TismPriBenz]M: a new class of metallacarbatranes, isomerization to a tris(N-heterocyclic carbene) derivative, and evidence for an inverted ligand field
Chem. Sci., 2017
1545916 CIFBa2 F11 Mn3 NaR -3 c :H7.003; 7.003; 35.466
90; 90; 120
1506.3Darriet, J.; Ducau, M.; Feist, M.; Tressaud, A.; Hagenmuller, P.
Crystal structure and magnetic properties of NaBa2Mn3F11 : a new layer-type fluoride compound
Journal of Solid State Chemistry, 1992, 98, 379-385
1545917 CIFCa O10 P2 V2F d d 211.795; 15.784; 7.19
90; 90; 90
1338.6Lii, K. H.; Chueh, B. R.; Kang, H. Y.; Wang, S. L.
Synthesis and crystal structure of Ca(VO)2(PO4)2
Journal of Solid State Chemistry, 1992, 99, 72-77
1545918 CIFBi0.5 Na0.5 O9 TiR 3 c :H5.49; 5.49; 13.387
90; 90; 120
349.429Mahmood, Natheer B.; Al-Shakarchi, Emad K.
Simulation and Experimental data of P-E Hysteresis Loop in BNT and BKT
Journal of Modern Physics, 2017, 8, 844-851
1545919 CIFBi0.5 K0.5 O3 TiP 4 m m3.9071; 3.9071; 3.9571
90; 90; 90
60.407Mahmood, Natheer B.; Al-Shakarchi, Emad K.
Simulation and Experimental data of P-E Hysteresis Loop in BNT and BKT
Journal of Modern Physics, 2017, 8, 844-851
1545920 CIFC181 H119 Cl15 N16 O22 P6 Zr4P -115.402; 17.812; 18.047
87.569; 85.646; 71.376
4677Yagi, Yuma; Masaki, Shuhei; Iwata, Tetsuki; Nakane, Daisuke; Yasui, Takashi; Yuchi, Akio
Triphosphate Ion-Selective Electrode Based on Zr-Porphyrin Complex.
Analytical chemistry, 2017, 89, 3937-3942
1545921 CIFO7 Th V2P n 21 a7.201; 22.771; 6.945
90; 90; 90
1138.8Launay, S.; Mahe, P.; Quarton, M.; Robert, F.
Polymorphisme et structure cristalline de ThV2O7
Journal of Solid State Chemistry, 1992, 97, 305-313
1545922 CIFC37 H39 N O5P 21 21 219.0661; 10.4931; 34.221
90; 90; 90
3255.5Tan, Liang; Tao, Yunliang; Wang, Ting; Zou, Feng; Zhang, Shuhua; Kou, Qunhuan; Niu, Ao; Chen, Qian; Chu, Wenjing; Chen, Xiaoyan; Wang, Haidong; Yang, Yushe
Discovery of Novel Pyridone-Conjugated Monosulfactams as Potent and Broad-Spectrum Antibiotics for Multidrug-Resistant Gram-Negative Infections.
Journal of medicinal chemistry, 2017, 60, 2669-2684
1545923 CIFC37 H60 O11P 1 21 112.5069; 23.641; 25.417
90; 98.788; 90
7427Wang, Luo-Yi; Qin, Jun-Jun; Chen, Zhen-Hua; Zhou, Yu; Tang, Wei; Zuo, Jian-Ping; Zhao, Wei-Min
Absolute Configuration of Periplosides C and F and Isolation of Minor Spiro-orthoester Group-Containing Pregnane-type Steroidal Glycosides from Periploca sepium and Their T-Lymphocyte Proliferation Inhibitory Activities.
Journal of natural products, 2017, 80, 1102-1109
1545924 CIFC20 H24 O5P 1 21 19.7656; 6.1628; 15.4441
90; 101.53; 90
910.72Liu, Ye; Yu, Heng-Yi; Wang, Yan-Mei; Tian, Tian; Wu, Wen-Ming; Zhou, Ming; Meng, Xiang-Gao; Ruan, Han-Li
Neuroprotective Lignans from the Fruits of Schisandra bicolor var. tuberculata.
Journal of natural products, 2017, 80, 1117-1124
1545925 CIFC25 H30 Cl2 O6P 21 21 2111.0269; 13.3801; 16.14
90; 90; 90
2381.31Kong, Fan-Dong; Ma, Qing-Yun; Huang, Sheng-Zhuo; Wang, Pei; Wang, Jun-Feng; Zhou, Li-Man; Yuan, Jing-Zhe; Dai, Hao-Fu; Zhao, You-Xing
Chrodrimanins K-N and Related Meroterpenoids from the Fungus Penicillium sp. SCS-KFD09 Isolated from a Marine Worm, Sipunculus nudus.
Journal of natural products, 2017, 80, 1039-1047
1545926 CIFC32 H42P 1 21/n 17.75029; 34.4156; 9.25694
90; 94.6142; 90
2461.11Ivanov, Maxim V.; Thakur, Khushabu; Boddeda, Anitha; Wang, Denan; Rathore, Rajendra
Nodal Arrangement of HOMO Controls the Turning On/Off the Electronic Coupling in Isomeric Polypyrene Wires
The Journal of Physical Chemistry C, 2017, 121, 9202
1545927 CIFC18 H14 F3 NP 1 21/n 15.9879; 12.983; 18.904
90; 90.542; 90
1469.5Chen, Shuang; Li, Deng-Yuan; Jiang, Liang-Liang; Liu, Kai; Liu, Pei-Nian
Copper-Catalyzed Cascade Transformation of Homopropargyl Azides into Trifluoromethylated Nitriles via C-C Cleavage.
Organic letters, 2017, 19, 2014-2017
1545928 CIFC10 H14 Cl N OP 21 21 214.7337; 6.2908; 33.7597
90; 90; 90
1005.32Wei, Yi; Zhang, Heng-Xia; Zeng, Jun-Liang; Nie, Jing; Ma, Jun-An
Organocatalytic Asymmetric Decarboxylative Amination of β-Keto Acids: Access to Optically Active α-Amino Ketones and 1,2-Amino Alcohols.
Organic letters, 2017, 19, 2162-2165
1545929 CIFC15 H15 Cl O2P 21 21 219.1478; 11.1509; 12.6918
90; 90; 90
1294.64Jia, Zhi-Long; Wang, Yao; Zhao, Chuan-Gang; Zhang, Xiao-Hai; Xu, Peng-Fei
Highly Enantioselective Construction of Hajos-Wiechert Ketone Skeletons via an Organocatalytic Vinylogous Michael/Stetter Relay Sequence.
Organic letters, 2017, 19, 2130-2133
1545930 CIFC29 H25 B N2 OP 1 21/n 113.7906; 11.0012; 15.176
90; 106.407; 90
2208.6Chen, Na; Zhang, Wenjie; Chen, Shun; Wu, Qinghua; Yu, Changjiang; Wei, Yun; Xu, Yuekang; Hao, Erhong; Jiao, Lijuan
Sterically Protected N2O-Type Benzopyrromethene Boron Complexes from Boronic Acids with Intense Red/Near-Infrared Fluorescence.
Organic letters, 2017, 19, 2026-2029
1545931 CIFC33 H27 Br2 Cl3 D N3 O3P 21 21 216.2687; 22.872; 9.2415
90; 90; 90
3438.7Li, Nai-Kai; Zhang, Jun-Qi; Sun, Bing-Bing; Li, Hai-Yan; Wang, Xing-Wang
Chiral Diphosphine-Palladium-Catalyzed Sequential Asymmetric Double-Friedel-Crafts Alkylation and N-Hemiketalization for Spiro-polycyclic Indole Derivatives.
Organic letters, 2017, 19, 1954-1957
1545932 CIFC32 H24 O8P 1 21/n 18.5702; 19.8368; 13.8839
90; 93.903; 90
2354.86Zhang, Ai Hua; Liu, Wen; Jiang, Nan; Wang, Xin Lei; Wang, Gang; Xu, Qiang; Tan, Ren Xiang
Sequestration of Guest Intermediates by Dalesconol Bioassembly Lines in Daldinia eschscholzii.
Organic letters, 2017, 19, 2142-2145
1545933 CIFC31 H22 O7P 1 21/c 113.7367; 8.5632; 19.5622
90; 97.697; 90
2280.37Zhang, Ai Hua; Liu, Wen; Jiang, Nan; Wang, Xin Lei; Wang, Gang; Xu, Qiang; Tan, Ren Xiang
Sequestration of Guest Intermediates by Dalesconol Bioassembly Lines in Daldinia eschscholzii.
Organic letters, 2017, 19, 2142-2145
1545934 CIFC21 H25 B F2 N2 O4P -17.5261; 12.0151; 23.1016
89.001; 85.625; 82.143
2063.31Patalag, Lukas J.; Ulrichs, Jan A.; Jones, Peter G.; Werz, Daniel B.
Decorated BODIPY Fluorophores and Thiol-Reactive Fluorescence Probes by an Aldol Addition.
Organic letters, 2017, 19, 2090-2093
1545935 CIFC21 H22 N2 O6 SC 1 c 126.0091; 6.2157; 15.4618
90; 123.549; 90
2083.22Rajkumar, Sundaram; Clarkson, Guy J.; Shipman, Michael
Regio- and Stereocontrolled Synthesis of 3-Substituted 1,2-Diazetidines by Asymmetric Allylic Amination of Vinyl Epoxide.
Organic letters, 2017, 19, 2058-2061
1545936 CIFC11 H21 N3P 1 21/c 110.4021; 11.1735; 21.729
90; 98; 90
2500.9Jeanbourquin, Loïc N; Scopelliti, Rosario; Fadaei Tirani, Farzaneh; Severin, Kay
Synthesis and Reactivity of 1-Allenyltriazenes.
Organic letters, 2017, 19, 2070-2073
1545937 CIFC16 H23 N3P c a 2110.4082; 7.7785; 19.6994
90; 90; 90
1594.87Jeanbourquin, Loïc N; Scopelliti, Rosario; Fadaei Tirani, Farzaneh; Severin, Kay
Synthesis and Reactivity of 1-Allenyltriazenes.
Organic letters, 2017, 19, 2070-2073
1545938 CIFC26 H48 O2 SiP 1 21/c 127.621; 7.7207; 12.441
90; 91.434; 90
2652.3Werner, Bettina; Kalesse, Markus
Pinacol Coupling Strategy for the Construction of the Bicyclo[6.4.1]tridecane Framework of Schiglautone A.
Organic letters, 2017, 19, 1524-1526
1545939 CIFC20 H23 N O3P 1 21 18.69815; 8.99657; 11.2368
90; 99.4584; 90
867.365Ding, Qiang; Wang, Qiuyan; He, Huan; Cai, Qian
Asymmetric Synthesis of (-)-Pterocarine and (-)-Galeon via Chiral Phase Transfer-Catalyzed Atropselective Formation of Diarylether Cyclophane Skeleton.
Organic letters, 2017, 19, 1804-1807
1545940 CIFC26 H26 N2 O3 SC 1 2/c 118.154; 19.79; 13.725
90; 112.371; 90
4560Bai, Lu; Wang, Yan; Ge, Yicong; Liu, Jingjing; Luan, Xinjun
Diastereoselective Synthesis of Dibenzo[b,d]azepines by Pd(II)-Catalyzed [5 + 2] Annulation of o-Arylanilines with Dienes.
Organic letters, 2017, 19, 1734-1737
1545941 CIFC12 H13 Cl OC 1 2/c 139.96; 11.468; 28.37
90; 134.78; 90
9228Shen, Yangyong; Huang, Bo; Zheng, Jing; Lin, Chen; Liu, Yu; Cui, Sunliang
Csp-Csp(3) Bond Formation via Iron(III)-Promoted Hydroalkynylation of Unactivated Alkenes.
Organic letters, 2017, 19, 1744-1747
1545942 CIFC11 H14 O2P 1 21/c 18.082; 23.635; 5.257
90; 100.75; 90
986.6Liu, Wei; Ren, Wenlong; Li, Jingfu; Shi, Yuan; Chang, Wenju; Shi, Yian
A Ligand-Directed Catalytic Regioselective Hydrocarboxylation of Aryl Olefins with Pd and Formic Acid.
Organic letters, 2017, 19, 1748-1751
1545943 CIFC17 H12 Cl N OP 1 21/c 19.793; 12.819; 11.666
90; 109.278; 90
1382.4Wang, Shun; Guo, Yong-Qiang; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui
K2CO3-Mediated Cyclization and Rearrangement of γ,δ-Alkynyl Oximes To Form Pyridols.
Organic letters, 2017, 19, 1574-1577
1545944 CIFC14 H14 N4 SP 1 21 110.013; 5.4697; 11.876
90; 96.71; 90
646Haidasz, Evan A.; Pratt, Derek A.
Diazaphenoxazines and Diazaphenothiazines: Synthesis of the "Correct" Isomers Reveals They Are Highly Reactive Radical-Trapping Antioxidants.
Organic letters, 2017, 19, 1854-1857
1545945 CIFC60 H56 N4 O4P 1 21/c 116.5759; 13.1086; 12.2124
90; 108.101; 90
2522.27Tominaga, Masahide; Takahashi, Eri; Ukai, Hiroyuki; Ohara, Kazuaki; Itoh, Tsutomu; Yamaguchi, Kentaro
Solvent-Dependent Self-Assembly and Crystal Structures of a Salen-Based Macrocycle.
Organic letters, 2017, 19, 1508-1511
1545946 CIFC19 H16 Cl2 N2 O4P 21 21 216.4551; 13.9906; 19.732
90; 90; 90
1782.01Gammack Yamagata, Adam D.; Dixon, Darren J.
Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids.
Organic letters, 2017, 19, 1894-1897
1545947 CIFC19 H22 N2 O3P 1 21 18.2596; 7.268; 13.7048
90; 102.076; 90
804.5Gammack Yamagata, Adam D.; Dixon, Darren J.
Enantioselective Construction of the ABCDE Pentacyclic Core of the Strychnos Alkaloids.
Organic letters, 2017, 19, 1894-1897
1545948 CIFC12 H14 O5P 1 21/n 114.5321; 4.2646; 17.6646
90; 96.996; 90
1086.6Chan, Chieh-Kai; Tsai, Yu-Lin; Chang, Meng-Yang
CuI Mediated One-Pot Cycloacetalization/Ketalization of o-Carbonyl Allylbenzenes: Synthesis of Benzobicyclo[3.2.1]octane Core.
Organic letters, 2017, 19, 1870-1873
1545949 CIFC15 H20 O5C 1 2/c 136.172; 4.3144; 21.587
90; 125.607; 90
2739Chan, Chieh-Kai; Tsai, Yu-Lin; Chang, Meng-Yang
CuI Mediated One-Pot Cycloacetalization/Ketalization of o-Carbonyl Allylbenzenes: Synthesis of Benzobicyclo[3.2.1]octane Core.
Organic letters, 2017, 19, 1870-1873
1545950 CIFC18 H18 O4P -112.6329; 15.5564; 16.0916
96.072; 105.849; 94.847
3003.75Chan, Chieh-Kai; Tsai, Yu-Lin; Chang, Meng-Yang
CuI Mediated One-Pot Cycloacetalization/Ketalization of o-Carbonyl Allylbenzenes: Synthesis of Benzobicyclo[3.2.1]octane Core.
Organic letters, 2017, 19, 1870-1873
1545951 CIFC7 H7 N O2 SP 1 21/c 19.5486; 14.0756; 5.967
90; 105.349; 90
773.37Reddy, Mallu Kesava; Mallik, Sumitava; Ramakrishna, Isai; Baidya, Mahiuddin
Nitrosocarbonyl-Henry and Denitration Cascade: Synthesis of α-Ketoamides and α-Keto Oximes.
Organic letters, 2017, 19, 1694-1697
1545952 CIFC26 H38 N4 O4 SiC 1 2/c 126.0702; 10.9823; 21.191
90; 108.083; 90
5767.5Wang, Taimin; Duan, Xiaoguang; Zhao, Hua; Zhai, Shengxian; Tao, Cheng; Wang, Huifei; Li, Yun; Cheng, Bin; Zhai, Hongbin
Asymmetric Total Synthesis of (-)-Aspidophylline A.
Organic letters, 2017, 19, 1650-1653
1545953 CIFC27 H26 N2 O4P 21 21 217.9238; 11.0281; 25.0507
90; 90; 90
2189Wang, Dan; Hou, Min; Ji, Yue; Gao, Shuanhu
Total Synthesis of Scholarisine K and Alstolactine A.
Organic letters, 2017, 19, 1922-1925
1545954 CIFC27 H24 F3 N O3 SP 21 21 215.3333; 19.6192; 23.4352
90; 90; 90
2452.1Wang, Huamin; Zhou, Wei; Tao, Mengna; Hu, Anjing; Zhang, Junliang
Functionalized Tetrahydropyridines by Enantioselective Phosphine-Catalyzed Aza-[4 + 2] Cycloaddition of N-Sulfonyl-1-aza-1,3-dienes with Vinyl Ketones.
Organic letters, 2017, 19, 1710-1713
1545955 CIFC22 H22 O6P 1 21 15.521; 17.785; 9.852
90; 91.837; 90
966.9Zhou, Weiping; Ni, Chunjie; Chen, Jiangfei; Wang, Dong; Tong, Xiaofeng
Enantioselective Synthesis of 4H-Pyran via Amine-Catalyzed Formal (3 + 3) Annulation of δ-Acetoxy Allenoate.
Organic letters, 2017, 19, 1890-1893
1545956 CIFC17 H13 N O3 SeP 1 21/c 118.8061; 5.9523; 13.3383
90; 90.605; 90
1493Dana, Suman; Mandal, Anup; Sahoo, Harekrishna; Baidya, Mahiuddin
Ru(II)-Catalyzed C-H Functionalization on Maleimides with Electrophiles: A Demonstration of Umpolung Strategy.
Organic letters, 2017, 19, 1902-1905
1545957 CIFC32 H24 Br N3 O3P 21 21 217.6027; 16.7807; 21.1178
90; 90; 90
2694.18Liu, Jin-Yu; Zhao, Jing; Zhang, Jia-Lu; Xu, Peng-Fei
Quaternary Carbon Center Forming Formal [3 + 3] Cycloaddition Reaction via Bifunctional Catalysis: Asymmetric Synthesis of Spirocyclohexene Pyrazolones.
Organic letters, 2017, 19, 1846-1849
1545958 CIFC23 H13 F3 N2 OP 1 21/c 17.6208; 21.2775; 11.1815
90; 105.554; 90
1746.7Zhang, Ting-Yu; Lin, Jun-Bing; Li, Quan-Zhe; Kang, Jun-Chen; Pan, Jin-Long; Hou, Si-Hua; Chen, Chao; Zhang, Shu-Yu
Copper-Catalyzed Selective ortho-C-H/N-H Annulation of Benzamides with Arynes: Synthesis of Phenanthridinone Alkaloids.
Organic letters, 2017, 19, 1764-1767
1545959 CIFC27 H34 O3P -19.8361; 9.9871; 12.5171
98.404; 92.358; 94.506
1210.9Zhang, Xiang-Zhi; Deng, Yu-Hua; Gan, Kang-Ji; Yan, Xu; Yu, Ke-Yin; Wang, Fang-Xin; Fan, Chun-An
Tandem Spirocyclopropanation/Rearrangement Reaction of Vinyl p-Quinone Methides with Sulfonium Salts: Synthesis of Spirocyclopentenyl p-Dienones.
Organic letters, 2017, 19, 1752-1755
1545960 CIFC39 H24 N12 O7P 1 21/c 127.36; 6.8093; 25.381
90; 112.41; 90
4371.4Lu, Yao; Fu, Zhan-Da; Guo, Qing-Hui; Wang, Mei-Xiang
O6-Corona[6]arenes with Expanded Cavities for Specific Complexation with C70.
Organic letters, 2017, 19, 1590-1593
1545961 CIFC60 H48 Cl6 N6 O6P -111.034; 13.836; 19.748
105.366; 101.194; 101.131
2754.9Lu, Yao; Fu, Zhan-Da; Guo, Qing-Hui; Wang, Mei-Xiang
O6-Corona[6]arenes with Expanded Cavities for Specific Complexation with C70.
Organic letters, 2017, 19, 1590-1593
1545962 CIFC20 H11 Br SP 1 21/n 15.1414; 15.2261; 18.358
90; 97.59; 90
1424.5Ozaki, Kyohei; Matsuoka, Wataru; Ito, Hideto; Itami, Kenichiro
Annulative π-Extension (APEX) of Heteroarenes with Dibenzosiloles and Dibenzogermoles by Palladium/o-Chloranil Catalysis.
Organic letters, 2017, 19, 1930-1933
1545963 CIFC23 H21 Br N2 OP 1 21/n 19.5441; 7.5459; 27.2946
90; 96.595; 90
1952.72Anderson, James C.; Campbell, Ian B.; Campos, Sebastien; Rundell, Christopher D.; Shannon, Jonathan; Tizzard, Graham J.
Base-Controlled Diastereoselective Synthesis of Either anti- or syn-β-Aminonitriles.
Organic letters, 2017, 19, 1918-1921
1545964 CIFC32 H34 O10P 1 21 19.4676; 15.2732; 12.2821
90; 96.493; 90
1764.61Xiao, Zheming; Li, Yayue; Gao, Shuanhu
Total Synthesis and Structural Determination of the Dimeric Tetrahydroxanthone Ascherxanthone A.
Organic letters, 2017, 19, 1834-1837
1545965 CIFC24 H25 N3 O5P 1 21/c 111.0916; 8.5446; 23.4141
90; 95.772; 90
2207.8Wang, Chunyu; Wang, Zhonglei; Xie, Xiaoni; Yao, Xiaotong; Li, Guang; Zu, Liansuo
Total Synthesis of (±)-Grandilodine B.
Organic letters, 2017, 19, 1828-1830
1545966 CIFC16 H17 N O4P 1 21 110.666; 6.294; 11.33
90; 109.47; 90
717.1Li, Jian Long; Shi, Hong Wei; Wang, Qi; Chai, Yong Hai; Yang, Jun
Synthesis of the ABC Tricyclic System of Daphnicyclidin A.
Organic letters, 2017, 19, 1497-1499
1545967 CIFC21 H20 F3 N O2 SP -19.0447; 10.6072; 11.4907
70.444; 89.544; 67.304
949.01Cendón, Borja; Casanova, Noelia; Comanescu, Cezar; García-Fandiño, Rebeca; Seoane, Andrés; Gulías, Moisés; Mascareñas, José L
Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes.
Organic letters, 2017, 19, 1674-1677
1545968 CIFC18 H19 Br F3 N O2 SP n a 217.1072; 23.128; 10.8794
90; 90; 90
1788.3Cendón, Borja; Casanova, Noelia; Comanescu, Cezar; García-Fandiño, Rebeca; Seoane, Andrés; Gulías, Moisés; Mascareñas, José L
Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes.
Organic letters, 2017, 19, 1674-1677
1545969 CIFC21 H20 F3 N O2 SP 1 21/c 123.234; 33.003; 7.7417
90; 95.771; 90
5906Cendón, Borja; Casanova, Noelia; Comanescu, Cezar; García-Fandiño, Rebeca; Seoane, Andrés; Gulías, Moisés; Mascareñas, José L
Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes.
Organic letters, 2017, 19, 1674-1677
1545970 CIFC10 H8 F3 N O2 SP -17.4533; 8.8064; 9.0773
74.195; 68.403; 81.369
532.21Cendón, Borja; Casanova, Noelia; Comanescu, Cezar; García-Fandiño, Rebeca; Seoane, Andrés; Gulías, Moisés; Mascareñas, José L
Palladium-Catalyzed Formal (5 + 2) Annulation between ortho-Alkenylanilides and Allenes.
Organic letters, 2017, 19, 1674-1677
1545971 CIFC33 H35 N OP 6121.1037; 21.1037; 10.4985
90; 90; 120
4049.3Sun, Hui; Cui, Bin; Duan, Lili; Li, Yue-Ming
Intramolecular Aminoalkoxylation of Unfunctionalized Olefins via Intramolecular Iodoamination and Aziridinium Ion Ring-Opening Sequence.
Organic letters, 2017, 19, 1520-1523
1545972 CIFC23 H17 Cl N2 O3P 21 21 218.812; 11.495; 19.111
90; 90; 90
1935.83Montesinos-Magraner, Marc; Vila, Carlos; Blay, Gonzalo; Fernández, Isabel; Muñoz, M Carmen; Pedro, José R
Hydroxy-Directed Enantioselective Hydroxyalkylation in the Carbocyclic Ring of Indoles.
Organic letters, 2017, 19, 1546-1549
1545973 CIFC41 H40 Cl2 N2 P2 RuP 1 21/n 111.188; 25.322; 16.401
90; 93.32; 90
4638.6Wang, Zheng; Pan, Bing; Liu, Qingbin; Yue, Erlin; Solan, Gregory A.; Ma, Yanping; Sun, Wen-Hua
Efficient acceptorless dehydrogenation of secondary alcohols to ketones mediated by a PNN-Ru(ii) catalyst
Catal. Sci. Technol., 2017, 7, 1654
1545974 CIFC8 H14 B O3 PP 21 21 216.2846; 11.2864; 14.5243
90; 90; 90
1030.22Markley, Jana L.; Hanson, Paul R.
P-Stereogenic Bicyclo[4.3.1]phosphite Boranes: Synthesis and Utility of Tunable P-Tether Systems for the Desymmetrization of C2-Symmetric 1,3-anti-Diols.
Organic letters, 2017, 19, 2552-2555
1545975 CIFC8 H14 B O3 PP 21 21 216.2929; 11.2901; 14.454
90; 90; 90
1026.9Markley, Jana L.; Hanson, Paul R.
P-Stereogenic Bicyclo[4.3.1]phosphite Boranes: Synthesis and Utility of Tunable P-Tether Systems for the Desymmetrization of C2-Symmetric 1,3-anti-Diols.
Organic letters, 2017, 19, 2552-2555
1545976 CIFC60 H64 I2 N32 O14P 1 21/c 117.0396; 27.7804; 34.0065
90; 90.253; 90
16097.4Jelínková, Kristýna; Surmová, Heda; Matelová, Alena; Rouchal, Michal; Prucková, Zdeňka; Dastychová, Lenka; Nečas, Marek; Vícha, Robert
Cubane Arrives on the Cucurbituril Scene.
Organic letters, 2017, 19, 2698-2701
1545977 CIFC33 H36 N2 O6P 21 21 218.7243; 12.504; 26.5448
90; 90; 90
2895.7Ejima, Hirotaka; Wakita, Fumihiro; Imamura, Ryo; Kato, Takuya; Hosokawa, Seijiro
Stereoselective Synthesis of Tabtoxinine-β-lactam by Using the Vinylogous Mukaiyama Aldol Reaction with Acetate-Type Vinylketene Silyl N,O-Acetal and α-Keto-β-lactam
Organic Letters, 2017
1545978 CIFC36 H72 Cu2.7 Li1.3 N4P 1 21/c 111.6661; 22.7624; 15.2664
90; 108.677; 90
3840.48Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545979 CIFC54 H104 Li6 N6 O6P -111.8638; 12.043; 12.2033
82.499; 66.906; 72.489
1529.35Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545980 CIFC46 H88 Cu0.21 Li5.79 N6 O4P -17.9156; 13.4775; 13.8111
110.986; 94.546; 104.331
1309.7Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545981 CIFC37 H88 Cu Li4 N9 OP -111.9447; 13.7635; 16.4214
80.989; 78.164; 67.824
2437.5Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545982 CIFC46 H88 Cu2 Li4 N6 O4P -18.4118; 11.5807; 13.5645
98.376; 95.058; 94.955
1295.58Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545983 CIFC24 H60 Br Li3 N6P 1 21/c 117.7718; 12.1985; 17.2945
90; 118.237; 90
3303.09Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545984 CIFC24 H60 Br Cu0.09 Li2.91 N6P 1 21/c 117.7591; 12.2389; 17.2889
90; 118.227; 90
3310.9Wheatley, Andrew; Peel, Andrew; Ackroyd, Ryan
Metal exchange in lithiocuprates: implications for our understanding of structure and reactivity
Chem. Sci., 2017
1545985 CIFC24 H28 N4 O6P 1 21/c 116.7641; 11.6113; 14.8749
90; 112.159; 90
2681.6Nikolayevskiy, Herman; Tun, Kyaw Moe; Rablen, Paul R.; Ben Mamoun, Choukri; Herzon, Seth
A complex stereochemical relay approach to the antimalarial alkaloid ocimicide A1. Evidence for a structural revision.
Chem. Sci., 2017
1545986 CIFC30 H44 N4 O6 Pd2 S2P 1 21/n 113.3652; 18.9012; 14.5561
90; 104.314; 90
3563St John-Campbell, Sahra; White, Andrew J. P.; Bull, James A.
Single Operation Palladium Catalysed C(sp3)‒H Functionalisation of Tertiary Aldehydes: Investigations into Transient Imine Directing Groups
Chem. Sci., 2017
1545987 CIFC59 H39 Br4 N7 ZnC 1 2/c 125.037; 9.586; 24.537
90; 120.09; 90
5095Bertini, Federica; Glatz, Mathias; Gorgas, Nikolaus; Stoeger, Berthold; Peruzzini, Maurizio; Veiros, Luis Filipe F.; Kirchner, Karl; Gonsalvi, Luca
Carbon Dioxide Hydrogenation Catalysed by Well-defined Mn(I) PNP Pincer Hydride Complexes
Chem. Sci., 2017
1545988 CIFC39 H50 Au F8 I2 K N4 O12.5P -19.048; 15.1904; 19.1737
73.9435; 78.7765; 88.9763
2482.2Christopherson, Jan-Constantin; Potts, Karlie P.; Bushuyev, Oleksandr S.; Topić, Filip; Huskic, Igor; Rissanen, Kari; Barrett, Christopher J.; Friščić, Tomislav
Assembly and dichroism of a four-component halogen-bonded metal-organic cocrystal salt solvate involving dicyanoaurate(I) acceptors
Faraday Discuss., 2017
1545989 CIFC61 H76 N2 O12P 1 21/n 112.9848; 19.382; 22.2953
90; 99.8421; 90
5528.5Zhu, Kelong; Baggi, Giorgio; Vukotic, V. Nicholas; Loeb, Stephen J.
Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
Chem. Sci., 2017, 8, 3898
1545990 CIFC61 H71 N3 O10P b c a17.819; 17.457; 34.337
90; 90; 90
10681Zhu, Kelong; Baggi, Giorgio; Vukotic, V. Nicholas; Loeb, Stephen J.
Reversible mechanical protection: building a 3D “suit” around a T-shaped benzimidazole axle
Chem. Sci., 2017, 8, 3898
1545991 CIFC31 H48 N4 O10 SP 1 21/c 115.96905; 20.99152; 10.22172
90; 96.6779; 90
3403.22Hu, Ting; Connor, Alan L.; Miller, Daniel P.; Wang, Xiao; Pei, Qiang; Liu, Rui; He, Lan; Zheng, Chong; Zurek, Eva; Lu, Zhong-Lin; Gong, Bing
Helical Folding of Meta-Connected Aromatic Oligoureas.
Organic letters, 2017, 19, 2666-2669
1545992 CIFC46 H70 N6 O17P -111.689; 14.24; 17.345
112.693; 101.236; 97.554
2543.5Hu, Ting; Connor, Alan L.; Miller, Daniel P.; Wang, Xiao; Pei, Qiang; Liu, Rui; He, Lan; Zheng, Chong; Zurek, Eva; Lu, Zhong-Lin; Gong, Bing
Helical Folding of Meta-Connected Aromatic Oligoureas.
Organic letters, 2017, 19, 2666-2669
1545993 CIFC22 H18 O2P -17.689; 10.82; 11.135
100.707; 101.208; 106.471
842.4Liang, Man; Zhang, Shuai; Jia, Jiong; Tung, Chen-Ho; Wang, Jianwu; Xu, Zhenghu
Synthesis of Spiroketals by Synergistic Gold and Scandium Catalysis
Organic Letters, 2017
1545994 CIFC23 H17 Cl N2 O7 SP -19.1593; 11.0566; 12.405
64.95; 76.98; 89.327
1103.85Laws, Stephen W.; Moore, Lucas C.; Di Maso, Michael J.; Nguyen, Q Nhu N; Tantillo, Dean J.; Shaw, Jared T.
Diastereoselective Base-Catalyzed Formal [4 + 2] Cycloadditions of N-Sulfonyl Imines and Cyclic Anhydrides.
Organic letters, 2017, 19, 2466-2469
1545995 CIFC24 H17 N3 O7 SI 1 2/a 113.7214; 9.2266; 34.566
90; 91.593; 90
4374.4Laws, Stephen W.; Moore, Lucas C.; Di Maso, Michael J.; Nguyen, Q Nhu N; Tantillo, Dean J.; Shaw, Jared T.
Diastereoselective Base-Catalyzed Formal [4 + 2] Cycloadditions of N-Sulfonyl Imines and Cyclic Anhydrides.
Organic letters, 2017, 19, 2466-2469
1545996 CIFC25 H27 Cl2 N7 Ni O3P 1 21/c 116.1455; 19.402; 9.224
90; 103.732; 90
2806.9Dai, Zengjin; Luo, Qin; Jiang, Huan; Luo, Qi; Li, Hua; Zhang, Jing; Peng, Tianyou
Ni(II)-N′NN′ Pincer Complexes Catalyzed Dehydrogenation of Primary Alcohols to Carboxylic acids and H2 Accompanied by the Alcohol Etherification
Catal. Sci. Technol., 2017
1545997 CIFC21 H23 N O6P 21 21 218.76; 13.957; 16.322
90; 90; 90
1995.6Chen, Bo; Liu, Xin; Hu, Ya-Jian; Zhang, Dongmei; Deng, Lijuan; Lu, Jieyu; Min, Long; Ye, Wen-Cai; Li, Chuang-Chuang
Enantioselective Total Synthesis of (–)-Colchicine, (+)-Demecolcinone and Metacolchicine: Determination of the Absolute Configurations of the Latter Two Alkaloids
Chem. Sci., 2017
1545998 CIFC40 H36 N3 O14P 1 21 113.869; 9.736; 14.969
90; 105.103; 90
1951Chen, Bo; Liu, Xin; Hu, Ya-Jian; Zhang, Dongmei; Deng, Lijuan; Lu, Jieyu; Min, Long; Ye, Wen-Cai; Li, Chuang-Chuang
Enantioselective Total Synthesis of (‒)-Colchicine, (+)-Demecolcinone and Metacolchicine: Determination of the Absolute Configurations of the Latter Two Alkaloids
Chem. Sci., 2017
1545999 CIFF7 Mn Tl ZrP 1 21/m 16.45; 8.25; 6.459
90; 118; 90
303.5Malika El-Ghozzi; Daniel Avignant; Maurice Guillot
Synthesis, structures, and characterization of MMnZrF7 (M = Tl, Rb, NH4, K) fluorides : an example of 7-coordination of divalent manganese
Journal of Solid State Chemistry, 1994, 108, 51-58
1546000 CIFF7 Mn Rb ZrP 1 21/m 16.439; 8.218; 6.443
90; 117.9; 90
301.3Malika El-Ghozzi; Daniel Avignant; Maurice Guillot
Synthesis, structures, and characterization of MMnZrF7 (M = Tl, Rb, NH4, K) fluorides : an example of 7-coordination of divalent manganese
Journal of Solid State Chemistry, 1994, 108, 51-58
1546001 CIFC15 H16 O3P 1 21/n 17.8742; 12.2573; 13.1272
90; 107.166; 90
1210.55Liu, Xin; Liu, Junyang; Zhao, Jing; Li, Shaoping; Li, Chuang-Chuang
Toward the Total Synthesis of Eurifoloid A.
Organic letters, 2017, 19, 2742-2745
1546002 CIFC28 H30 N2P -110.393; 11.0108; 11.0248
87.324; 66.406; 79.801
1137.5Chi, Yue; Yan, Haihan; Zhang, Wen-Xiong; Xi, Zhenfeng
Synthesis of Quinoline Derivatives via Cu-Catalyzed Cascade Annulation of Heterocumulenes, Alkynes, and Diaryliodonium Salts
Organic Letters, 2017
1546003 CIFC30 H25 N SP 1 21/n 110.3505; 8.6159; 27.293
90; 99.307; 90
2401.9Chi, Yue; Yan, Haihan; Zhang, Wen-Xiong; Xi, Zhenfeng
Synthesis of Quinoline Derivatives via Cu-Catalyzed Cascade Annulation of Heterocumulenes, Alkynes, and Diaryliodonium Salts
Organic Letters, 2017
1546004 CIFC21 H33 N O6P 1 21/c 15.7733; 9.1531; 41.7797
90; 91.716; 90
2206.8Pilsl, Ludwig K. A.; Ertl, Thomas; Reiser, Oliver
Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor-Acceptor Cyclopropane as Key Intermediate.
Organic letters, 2017, 19, 2754-2757
1546005 CIFC15 H23 N O4P 1 21 19.4639; 6.1799; 13.1692
90; 90.131; 90
770.21Pilsl, Ludwig K. A.; Ertl, Thomas; Reiser, Oliver
Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor-Acceptor Cyclopropane as Key Intermediate.
Organic letters, 2017, 19, 2754-2757
1546006 CIFC15 H27 N O4P 2 21 216.02696; 8.5237; 15.8573
90; 90; 90
814.62Pilsl, Ludwig K. A.; Ertl, Thomas; Reiser, Oliver
Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor-Acceptor Cyclopropane as Key Intermediate.
Organic letters, 2017, 19, 2754-2757
1546007 CIFC14 H14 N2 OR -3 :H28.764; 28.764; 7.479
90; 90; 120
5358.9Purkait, Anisha; Roy, Subhra Kanti; Srivastava, Hemant Kumar; Jana, Chandan K.
Metal-Free Sequential C(sp2)–H/OH and C(sp3)–H Aminations of Nitrosoarenes and N-Heterocycles to Ring-Fused Imidazoles
Organic Letters, 2017
1546008 CIFC45 H50 S2C 1 2/c 120.986; 22.422; 7.9388
90; 103.263; 90
3635.9Mitsudo, Koichi; Tanaka, Seiichi; Isobuchi, Ryota; Inada, Tomohiro; Mandai, Hiroki; Korenaga, Toshinobu; Wakamiya, Atsushi; Murata, Yasujiro; Suga, Seiji
Rh-Catalyzed Dehydrogenative Cyclization Leading to Benzosilolothiophene Derivatives via Si–H/C–H Bond Cleavage
Organic Letters, 2017
1546009 CIFC19 H23 N O4P 1 21/n 115.183; 6.7949; 16.513
90; 92.37; 90
1702.1Krieger, Jean-Philippe; Lesuisse, Dominique; Ricci, Gino; Perrin, Marc-Antoine; Meyer, Christophe; Cossy, Janine
Rhodium(III)-Catalyzed C-H Activation/Heterocyclization as a Macrocyclization Strategy. Synthesis of Macrocyclic Pyridones.
Organic letters, 2017
1546010 CIFC25 H27 Br N2 O4P 1 21/c 113.452; 9.374; 19.421
90; 104.972; 90
2365.8Zhang, Kaifan; Xu, Xiaoying; Zheng, Jiuan; Yao, Hequan; Huang, Yue; Lin, Aijun
[3 + 3] Cycloaddition of in Situ Formed Azaoxyallyl Cations with 2-Alkenylindoles: An Approach to Tetrahydro-β-carbolinones.
Organic letters, 2017
1546011 CIFC27 H24 N2 O3P 1 21/c 110.2888; 16.2882; 13.248
90; 91.491; 90
2219.4Meher, Niranjan; Iyer, Parameswar K.
Pendant chain engineering to fine-tune nanomorphology and solid state luminescence in naphthalimide AIEEgens: Application to phenolic nitro-explosive detection in water
Nanoscale, 2017
1546012 CIF
Paper
C12 H10 Cl I O4P 1 21/c 112.232; 12.7073; 17.15
90; 103.5; 90
2592.1Cavallo, Gabriella; Murray, Jane S.; Politzer, Peter; Pilati, Tullio; Ursini, Maurizio; Resnati, Giuseppe
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
IUCrJ, 2017, 4
1546013 CIFC12 H10 F6 I PP 1 21/n 15.9721; 12.9442; 18.387
90; 96.195; 90
1413.1Cavallo, Gabriella; Murray, Jane S.; Politzer, Peter; Pilati, Tullio; Ursini, Maurizio; Resnati, Giuseppe
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
IUCrJ, 2017, 4
1546014 CIFC33 H22 Cl2 F18 I2 O3P -111.7183; 13.4322; 14.8978
113.429; 107.498; 101.366
1913Cavallo, Gabriella; Murray, Jane S.; Politzer, Peter; Pilati, Tullio; Ursini, Maurizio; Resnati, Giuseppe
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
IUCrJ, 2017, 4
1546015 CIFC36 H24 B0.5 Br5.5 F8P 43 3 215.4248; 15.4248; 15.4248
90; 90; 90
3669.9Cavallo, Gabriella; Murray, Jane S.; Politzer, Peter; Pilati, Tullio; Ursini, Maurizio; Resnati, Giuseppe
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
IUCrJ, 2017, 4
1546016 CIFC36 H24 B Br3 Cl2 F10P 41 3 215.2905; 15.2905; 15.2905
90; 90; 90
3574.9Cavallo, Gabriella; Murray, Jane S.; Politzer, Peter; Pilati, Tullio; Ursini, Maurizio; Resnati, Giuseppe
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
IUCrJ, 2017, 4
1546017 CIFC14 H12 B Br F4 O2P -18.1574; 10.0848; 10.157
89.158; 72.819; 66.607
727.64Cavallo, Gabriella; Murray, Jane S.; Politzer, Peter; Pilati, Tullio; Ursini, Maurizio; Resnati, Giuseppe
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
IUCrJ, 2017, 4
1546018 CIFBa F7 Fe ZnP 1 21/c 15.603; 9.971; 9.584
90; 92.8; 90
534.8Von H. Holler; D. Babel
Crystal structure of a high temperature modification of barium-zinc-iron(III) fluoride BaZnFeF7
Zeitschrift fur anorganische und allgemeine Chemie, 1982, 491, 137-144
1546019 CIFC30 H38 O8P 21 21 219.2535; 11.5385; 24.9217
90; 90; 90
2660.93Sriyatep, Teerayut; Andersen, Raymond J.; Patrick, Brian O.; Pyne, Stephen G.; Muanprasat, Chatchai; Seemakhan, Sawinee; Borwornpinyo, Suparerk; Laphookhieo, Surat
Scalemic Caged Xanthones Isolated from the Stem Bark Extract of Garcinia propinqua.
Journal of natural products, 2017, 80, 1658-1667
1546020 CIFC14 H15 N O3P 21 21 215.0478; 14.4096; 16.6991
90; 90; 90
1214.64An, Qianjin; Shen, Jiefeng; Liu, Delong; Liu, Yangang; Zhang, Wanbin
Construction of Chiral-Fused Tricyclic γ-Lactams via a trans-Perhydroindolic Acid-Catalyzed Asymmetric Domino Reaction.
Organic letters, 2017, 19, 2925-2928
1546021 CIFC15 H15 N O3P 1 21/c 17.5525; 19.9782; 8.7575
90; 101.25; 90
1295.99An, Qianjin; Shen, Jiefeng; Liu, Delong; Liu, Yangang; Zhang, Wanbin
Construction of Chiral-Fused Tricyclic γ-Lactams via a trans-Perhydroindolic Acid-Catalyzed Asymmetric Domino Reaction.
Organic letters, 2017, 19, 2925-2928
1546022 CIFC18 H15 Br N2 O4P 1 21 112.578; 22.365; 12.644
90; 107.727; 90
3388Yang, Yu; Ren, Hong-Xia; Chen, Feng; Zhang, Zheng-Bing; Zou, Ying; Chen, Chao; Song, Xiang-Jia; Tian, Fang; Peng, Lin; Wang, Li-Xin
Organocatalytic Asymmetric Annulation between Hydroxymaleimides and Nitrosoarenes: Stereoselective Preparation of Chiral Quaternary N-Hydroxyindolines
Organic Letters, 2017
1546023 CIFC11 H7 F5 N4 OP 1 21/c 110.3109; 16.7247; 7.4603
90; 108.019; 90
1223.4Cheung, Kelvin Pak Shing; Tsui, Gavin Chit
Copper(I)-Catalyzed Interrupted Click Reaction with TMSCF3: Synthesis of 5-Trifluoromethyl 1,2,3-Triazoles
Organic Letters, 2017
1546024 CIFC63 H74 F10 O4 P Pd SP -116.199; 18.065; 23.596
102.7; 107.741; 106.042
5961.7Ingoglia, Bryan T.; Buchwald, Stephen L.
Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands.
Organic letters, 2017, 19, 2853-2856
1546025 CIFCa2 O4 SiP b n m5.0762; 11.2136; 6.7583
90; 90; 90
384.699Mumme, W.G.; Cranswick, L.; Chakoumakos, B.
Rietveld crystal structure refinement from high temperature neutron powder diffraction data for the polymorphs of dicalcium silicate
Neues Jahrbuch fuer Mineralogie. Abhandlungen (Band-Nr) (1950-), 1996, 170, 171-188
1546026 CIFCa2 O4 SiP n a 2120.5266; 9.4963; 5.5897
90; 90; 90
1089.58Mumme, W.G.; Cranswick, L.; Chakoumakos, B.
Rietveld crystal structure refinement from high temperature neutron powder diffraction data for the polymorphs of dicalcium silicate
Neues Jahrbuch fuer Mineralogie. Abhandlungen (Band-Nr) (1950-), 1996, 170, 171-188
1546027 CIFCa2 O4 SiP n m a6.8709; 5.601; 9.5563
90; 90; 90
367.764Mumme, W.G.; Cranswick, L.; Chakoumakos, B.
Rietveld crystal structure refinement from high temperature neutron powder diffraction data for the polymorphs of dicalcium silicate
Neues Jahrbuch fuer Mineralogie. Abhandlungen (Band-Nr) (1950-), 1996, 170, 171-188
1546028 CIFCa2 O4 SiP 63/m m c5.532; 5.532; 7.327
90; 90; 120
194.187Mumme, W.G.; Cranswick, L.; Chakoumakos, B.
Rietveld crystal structure refinement from high temperature neutron powder diffraction data for the polymorphs of dicalcium silicate
Neues Jahrbuch fuer Mineralogie. Abhandlungen (Band-Nr) (1950-), 1996, 170, 171-188
1546029 CIFNb3 O9 PrP 1 21/c 15.3784; 7.602; 16.344
90; 92.21; 90
667.8Torardi, C. C.; Brixner, L. H.; Foris, C. M.
Structure and luminescence of the alpha-LnNb2O9-type rare earth niobates
Journal of Solid State Chemistry, 1985, 58, 204-210
1546030 CIFCr2 F9 K PbP n m a9.812; 5.412; 13.93
90; 90; 90
739.7Vlasse, M.; Chaminade, J. P.; Dance, J. M.; Saux, M.; Hagenmuller, P.
Structural and magnetic properties of KPbCr2F9
Journal of Solid State Chemistry, 1982, 41, 272-276
1546031 CIFC21 H19 N OP 1 21/n 110.0738; 7.7949; 20.89
90; 99.429; 90
1618.2Long, Jinguo; Cao, Xin; Zhu, Longzhi; Qiu, Renhua; Au, Chak-Tong; Yin, Shuang-Feng; Iwasaki, Takanori; Kambe, Nobuaki
Intramolecular, Site-Selective, Iodine-Mediated, Amination of Unactivated (sp(3))C-H Bonds for the Synthesis of Indoline Derivatives.
Organic letters, 2017, 19, 2793-2796
1546032 CIFC26 H26 N2 O4 S2P 1 21/n 112.7471; 12.3553; 15.5929
90; 101.189; 90
2409.1Wu, Zhengxing; Wen, Ke; Zhang, Jingang; Zhang, Wanbin
Pd(II)-Catalyzed Aerobic Intermolecular 1,2-Diamination of Conjugated Dienes: A Regio- and Chemoselective [4 + 2] Annulation for the Synthesis of Tetrahydroquinoxalines.
Organic letters, 2017, 19, 2813-2816
1546033 CIFC27 H28 N2 O4 S2P -18.1304; 12.3569; 12.7925
82.084; 86.551; 72.325
1212.65Wu, Zhengxing; Wen, Ke; Zhang, Jingang; Zhang, Wanbin
Pd(II)-Catalyzed Aerobic Intermolecular 1,2-Diamination of Conjugated Dienes: A Regio- and Chemoselective [4 + 2] Annulation for the Synthesis of Tetrahydroquinoxalines.
Organic letters, 2017, 19, 2813-2816
1546034 CIFCa O4 WI 41/a :25.205; 5.205; 11.275
90; 90; 90
305.46Rodríguez-Hernández, P.; López-Solano, J.; Radescu, S.; Mujica, A.; Muñoz, A.; Errandonea, D.; Pellicer-Porres, J.; Segura, A.; Ferrer-Roca, Ch.; Manjón, F. J.; Kumard, R. S.; Tschaunerd, O.; Aquilantie, G.
Theoretical and experimental study of CaWO~4~ and SrWO~4~ under pressure
Journal of Physics and Chemistry of Solids, 2006, 67, 2164-2171
1546035 CIFCa O4 WI 1 2/a 15.069; 10.851; 5.081
90; 90.091; 90
279.47Rodríguez-Hernández, P.; López-Solano, J.; Radescu, S.; Mujica, A.; Muñoz, A.; Errandonea, D.; Pellicer-Porres, J.; Segura, A.; Ferrer-Roca, Ch.; Manjón, F. J.; Kumard, R. S.; Tschaunerd, O.; Aquilantie, G.
Theoretical and experimental study of CaWO~4~ and SrWO~4~ under pressure
Journal of Physics and Chemistry of Solids, 2006, 67, 2164-2171
1546036 CIFO4 Sr WI 41/a :25.391; 5.391; 11.893
90; 90; 90
345.64Rodríguez-Hernández, P.; López-Solano, J.; Radescu, S.; Mujica, A.; Muñoz, A.; Errandonea, D.; Pellicer-Porres, J.; Segura, A.; Ferrer-Roca, Ch.; Manjón, F. J.; Kumard, R. S.; Tschaunerd, O.; Aquilantie, G.
Theoretical and experimental study of CaWO~4~ and SrWO~4~ under pressure
Journal of Physics and Chemistry of Solids, 2006, 67, 2164-2171
1546037 CIFO4 Sr WI 1 2/a 15.263; 11.182; 5.231
90; 90.35; 90
307.84Rodríguez-Hernández, P.; López-Solano, J.; Radescu, S.; Mujica, A.; Muñoz, A.; Errandonea, D.; Pellicer-Porres, J.; Segura, A.; Ferrer-Roca, Ch.; Manjón, F. J.; Kumard, R. S.; Tschaunerd, O.; Aquilantie, G.
Theoretical and experimental study of CaWO~4~ and SrWO~4~ under pressure
Journal of Physics and Chemistry of Solids, 2006, 67, 2164-2171
1546038 CIFC32 H38 P2 S2P -19.9187; 11.151; 15.866
73.63; 73.24; 67.98
1528Okugawa, Yuto; Hirano, Koji; Miura, Masahiro
Brønsted Base Mediated Stereoselective Diphosphination of Terminal Alkynes with Diphosphanes
Organic Letters, 2017
1546039 CIFC94.67 H110.34 O17.84P 1 21/c 127.6554; 26.5185; 26.1889
90; 94.414; 90
19149.4Hayase, Norihiko; Miyauchi, Yuta; Aida, Yukimasa; Sugiyama, Haruki; Uekusa, Hidehiro; Shibata, Yu; Tanaka, Ken
Synthesis of [8]Cycloparaphenylene-octacarboxylates via Rh-Catalyzed Stepwise Cross-Alkyne Cyclotrimerization
Organic Letters, 2017
1546040 CIFC37 H68 N4 O5 Si2P 21 21 2112.6926; 21.4026; 47.9632
90; 90; 90
13029.4Fanelli, Roberto; Berthomieu, Dorothée; Didierjean, Claude; Doudouh, Abdelatif; Lebrun, Aurélien; Martinez, Jean; Cavelier, Florine
Hydrophobic α,α-Disubstituted Disilylated TESDpg Induces Incipient 310-Helix in Short Tripeptide Sequence
Organic Letters, 2017
1546041 CIFC18 H18 Cl N3 OP 1 21 111.6963; 7.8375; 18.213
90; 96.443; 90
1659Tang, Wenjun; Liu, Jiawang; Nie, Ming; Zhou, Qing-Hai; Gao, Shen; Jiang, Wenhao; Chung, Lung Wa; Ding, Kuiling
Enantioselective Palladium-Catalyzed Diboration of 1,1-Disubstituted Allenes
Chem. Sci., 2017
1546042 CIFC22 H31 B2 Br O4P 1 21 111.1006; 6.9951; 30.827
90; 94.93; 90
2384.9Tang, Wenjun; Liu, Jiawang; Nie, Ming; Zhou, Qing-Hai; Gao, Shen; Jiang, Wenhao; Chung, Lung Wa; Ding, Kuiling
Enantioselective Palladium-Catalyzed Diboration of 1,1-Disubstituted Allenes
Chem. Sci., 2017
1546043 CIFC9 H6 O2P 21 21 2124.72245; 5.994222; 14.31013
90; 90; 90
2120.64Shtukenberg, Alexander G.; Zhu, Qiang; Carter, Damien J.; Vogt, Leslie; Hoja, Johannes; Schneider, Elia; Song, Hongxing; Pokroy, Boaz; Polishchuk, Iryna; Tkatchenko, Alexandre; Oganov, Artem R.; Rohl, Andrew L.; Tuckerman, Mark E.; Kahr, Bart
Powder diffraction and crystal structure prediction identify four new coumarin polymorphs
Chem. Sci., 2017
1546044 CIFC9 H6 O2P 21 21 2116.78223; 5.92141; 13.85224
90; 90; 90
1376.56Shtukenberg, Alexander G.; Zhu, Qiang; Carter, Damien J.; Vogt, Leslie; Hoja, Johannes; Schneider, Elia; Song, Hongxing; Pokroy, Boaz; Polishchuk, Iryna; Tkatchenko, Alexandre; Oganov, Artem R.; Rohl, Andrew L.; Tuckerman, Mark E.; Kahr, Bart
Powder diffraction and crystal structure prediction identify four new coumarin polymorphs
Chem. Sci., 2017
1546045 CIFC9 H6 O2P 21 21 2117.06176; 6.03613; 13.9083
90; 90; 90
1432.4Shtukenberg, Alexander G.; Zhu, Qiang; Carter, Damien J.; Vogt, Leslie; Hoja, Johannes; Schneider, Elia; Song, Hongxing; Pokroy, Boaz; Polishchuk, Iryna; Tkatchenko, Alexandre; Oganov, Artem R.; Rohl, Andrew L.; Tuckerman, Mark E.; Kahr, Bart
Powder diffraction and crystal structure prediction identify four new coumarin polymorphs
Chem. Sci., 2017
1546046 CIFC9 H6 O2P 21 21 2124.27024; 5.92062; 14.18934
90; 90; 90
2038.94Shtukenberg, Alexander G.; Zhu, Qiang; Carter, Damien J.; Vogt, Leslie; Hoja, Johannes; Schneider, Elia; Song, Hongxing; Pokroy, Boaz; Polishchuk, Iryna; Tkatchenko, Alexandre; Oganov, Artem R.; Rohl, Andrew L.; Tuckerman, Mark E.; Kahr, Bart
Powder diffraction and crystal structure prediction identify four new coumarin polymorphs
Chem. Sci., 2017
1546047 CIFC9 H6 O2P 21 21 214.86771; 6.88178; 20.8508
90; 90; 90
698.47Shtukenberg, Alexander G.; Zhu, Qiang; Carter, Damien J.; Vogt, Leslie; Hoja, Johannes; Schneider, Elia; Song, Hongxing; Pokroy, Boaz; Polishchuk, Iryna; Tkatchenko, Alexandre; Oganov, Artem R.; Rohl, Andrew L.; Tuckerman, Mark E.; Kahr, Bart
Powder diffraction and crystal structure prediction identify four new coumarin polymorphs
Chem. Sci., 2017
1546048 CIFC9 H6 O2P 1 21 13.97954; 15.2907; 5.8583
90; 94.237; 90
355.5Shtukenberg, Alexander G.; Zhu, Qiang; Carter, Damien J.; Vogt, Leslie; Hoja, Johannes; Schneider, Elia; Song, Hongxing; Pokroy, Boaz; Polishchuk, Iryna; Tkatchenko, Alexandre; Oganov, Artem R.; Rohl, Andrew L.; Tuckerman, Mark E.; Kahr, Bart
Powder diffraction and crystal structure prediction identify four new coumarin polymorphs
Chem. Sci., 2017
1546049 CIFC9 H12 Cl N O3P 1 21 113.5539; 5.4096; 15.0157
90; 108.421; 90
1044.56Ramalhete, Susana; Foster, Jamie S.; Green, Hayley R.; Nartowski, Karol P.; Heinrich, Margaux; Martin, Peter; Khimyak, Yaroslav Z.; Lloyd, Gareth O.
FDHALO17: Halogen effects on the solid-state packing of phenylalanine derivatives and the resultant gelation properties
Faraday Discuss., 2017
1546050 CIFC9 H11 F2 N O3P 1 21 113.1; 5.4019; 14.423
90; 100.712; 90
1002.9Ramalhete, Susana; Foster, Jamie S.; Green, Hayley R.; Nartowski, Karol P.; Heinrich, Margaux; Martin, Peter; Khimyak, Yaroslav Z.; Lloyd, Gareth O.
FDHALO17: Halogen effects on the solid-state packing of phenylalanine derivatives and the resultant gelation properties
Faraday Discuss., 2017
1546051 CIFC9 H12 Br N O3P 1 21 16.3036; 5.3042; 15.9161
90; 97.947; 90
527.05Ramalhete, Susana; Foster, Jamie S.; Green, Hayley R.; Nartowski, Karol P.; Heinrich, Margaux; Martin, Peter; Khimyak, Yaroslav Z.; Lloyd, Gareth O.
FDHALO17: Halogen effects on the solid-state packing of phenylalanine derivatives and the resultant gelation properties
Faraday Discuss., 2017
1546052 CIFC9 H12 F N O3P 1 21 113.3028; 5.4628; 14.0151
90; 104.048; 90
988.02Ramalhete, Susana; Foster, Jamie S.; Green, Hayley R.; Nartowski, Karol P.; Heinrich, Margaux; Martin, Peter; Khimyak, Yaroslav Z.; Lloyd, Gareth O.
FDHALO17: Halogen effects on the solid-state packing of phenylalanine derivatives and the resultant gelation properties
Faraday Discuss., 2017
1546053 CIFC9 H12 I N O3P 21 21 215.3139; 6.3152; 32.741
90; 90; 90
1098.73Ramalhete, Susana; Foster, Jamie S.; Green, Hayley R.; Nartowski, Karol P.; Heinrich, Margaux; Martin, Peter; Khimyak, Yaroslav Z.; Lloyd, Gareth O.
FDHALO17: Halogen effects on the solid-state packing of phenylalanine derivatives and the resultant gelation properties
Faraday Discuss., 2017
1546054 CIFC20 H36 Br2 I6 N4 RuP 1 21/n 19.2035; 11.3936; 18.5083
90; 103.339; 90
1888.4Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546055 CIFC36 H36 Cl2 N4 RuP 4 n c13.906; 13.906; 8.6877
90; 90; 90
1680Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546056 CIFC36 H36 Br2 I2 N4 RuP -19.563; 10.473; 10.744
67.46; 79.07; 74.903
954.7Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546057 CIFC36 H36 Br4 N4 RuP -19.789; 11.319; 17.303
89.362; 76.377; 85.007
1856.1Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546058 CIFC20 H36 Br6 N4 RuP 42/m n m11.3121; 11.3121; 13.6918
90; 90; 90
1752.1Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546059 CIFC36 H36 I4 N4 RuP -19.616; 10.4083; 11.1012
68.06; 78.128; 72.29
976.42Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546060 CIFC36 H36 Cl2.17 I3.83 N4 RuP -17.918; 10.314; 13.411
92.609; 100.426; 102.641
1046.89Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546061 CIFC36 H36 Cl2 I2 N4 RuP -19.5548; 10.4967; 10.5869
67.342; 80.018; 75.957
946.8Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546062 CIFC36 H36 Br2 Cl2 N4 RuP -19.567; 10.4897; 10.691
67.358; 79.414; 75.292
953.31Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546063 CIFC36 H38 Br2 N4 O RuC 1 2/c 116.5219; 13.6105; 17.4958
90; 116.603; 90
3517.8Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546064 CIFC20 H36 I8 N4 RuP 1 21/n 110.8205; 10.0771; 18.3892
90; 104.044; 90
1945.2Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546065 CIFC20 H36 Br2 N4 RuC 1 2/c 116.6612; 9.776; 18.368
90; 115.466; 90
2701.1Mosquera, Marta Elena Gonzalez; Gomez-Sal, Pilar; Egido, Irene; López López, María; Hortelano, Carlos
FDHALO17: Comparison of Halogen Bonding networks with Ru(II) complexes and analysis of the influence of the XB interaction on their reactivity
Faraday Discuss., 2017
1546066 CIFC25 H24 B Cl2 Cu F4 N6P 1 21/n 111.15632; 11.63305; 22.483
90; 102.758; 90
2845.85Lalevée, Jacques; Dietlin, Céline; Morlet-Savary, Fabrice; Fouassier, Jean Pierre; Gigmes, Didier; Dumur, Frederic; Kermagoret, Anthony; Garra, Patxi; Mousawi, Assi
New copper (I) complex based initiating systems in redox polymerization and comparison with amine/benzoyl peroxide reference
Polym. Chem., 2017
1546067 CIFC52 H49 B Cu F4 N3 O2 P2P 1 21/c 112.3268; 21.2128; 19.3122
90; 104.764; 90
4883.1Lalevée, Jacques; Dietlin, Céline; Morlet-Savary, Fabrice; Fouassier, Jean Pierre; Gigmes, Didier; Dumur, Frederic; Kermagoret, Anthony; Garra, Patxi; Mousawi, Assi
New copper (I) complex based initiating systems in redox polymerization and comparison with amine/benzoyl peroxide reference
Polym. Chem., 2017
1546068 CIFC109 H90 B Cl6 O Os P3P -113.8163; 18.0472; 18.3229
79.946; 89.601; 82.37
4458.1He, Xumin; He, Xiehua; Li, Shenyan; Zhuo, Kaiyue; Qin, Weixiang; Dong, Shuyu; Chen, Jiangxi; Ren, Lei; Liu, Gang; Xia, Haiping
Amphipathic Metal-Containing Macromolecules with Photothermal Properties
Polym. Chem., 2017
1546069 CIFC24 H47 N11 O13P 1 21/c 19.11756; 21.6446; 17.9917
90; 98.128; 90
3514.92Marafon, Giulia; Menegazzo, Ileana; De Zotti, Marta; Crisma, Marco; Toniolo, Claudio; Moretto, Alessandro
Tuning morphological architectures generated through living supramolecular assembly of a helical foldamer end-capped with two complementary nucleobases.
Soft matter, 2017
1546070 CIFC31 H46 N6 O8P 1 21/n 110.7942; 18.8139; 16.8871
90; 98.486; 90
3391.9Marafon, Giulia; Menegazzo, Ileana; De Zotti, Marta; Crisma, Marco; Toniolo, Claudio; Moretto, Alessandro
Tuning morphological architectures generated through living supramolecular assembly of a helical foldamer end-capped with two complementary nucleobases.
Soft matter, 2017
1546071 CIFAl2 F12 Pb3P 1 21/n 19.435; 9.61; 10.1
90; 90.59; 90
915.7Decap, G.; Retoux, R.; Calage, Y.
Pb3Al2F12 : Crystal structure of a cyclo-fluoroaluminate related to Ba3Al2F12
Zeitschrift fur Anorganische und Allgemeine Chemie, 1994, 620, 1449-1454
1546072 CIFC23 H18 O4 SP 1 21/c 113.939; 11.8628; 12.342
90; 105.579; 90
1965.8Wu, Wanqing; Yi, Songjian; Huang, Wei; Luo, Di; Jiang, Huanfeng
Ag-Catalyzed Oxidative Cyclization Reaction of 1,6-Enynes and Sodium Sulfinate: Access to Sulfonylated Benzofurans.
Organic letters, 2017, 19, 2825-2828
1546073 CIFC24 H23 N O6P 1 21/c 19.6711; 19.4443; 11.2024
90; 95.091; 90
2098.3Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546074 CIFC24 H25 N O4C 1 2/c 125.91; 11.234; 17.776
90; 126.13; 90
4179Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546075 CIFC19 H21 N O5P 1 21/c 18.4092; 18.977; 21.008
90; 92.133; 90
3350.2Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546076 CIFC24 H25 N O5P -17.5258; 11.7781; 12.4974
80.639; 77.851; 78.666
1053.3Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546077 CIFC24 H22 Br N O5P 1 21/n 110.1412; 18.601; 11.3292
90; 91.857; 90
2136Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546078 CIFC38 H30 N2 O2 SP 1 21/c 111.0551; 16.7135; 16.0419
90; 90.679; 90
2963.8Shin, Jinhwan; Lee, Jiyoun; Ko, Donguk; De, Nirupam; Yoo, Eun Jeong
Synthesis of Fused Polycyclic 1,4-Benzodiazepines via Metal-Free Cascade [5 + 2]/[2 + 2] Cycloadditions.
Organic letters, 2017
1546079 CIFC25 H24 O2P -17.611; 11.49; 11.506
105.352; 94.19; 109.278
901.5Xie, Jiaxin; Wang, Jianchun; Dong, Guangbin
Synthetic Study of Phainanoids. Highly Diastereoselective Construction of the 4,5-Spirocycle via Palladium-Catalyzed Intramolecular Alkenylation.
Organic letters, 2017, 19, 3017-3020
1546080 CIFC56 H48 Br6 Fe2 N8 O16 Zn3P 32 2 112.8153; 12.8153; 38.817
90; 90; 120
5520.9Brechin, Euan K.; Sanz, Sergio; O'Connor, Helen; Martí-Centelles, Vicente; Comar, Priyanka; Pitak, Mateusz; Coles, Simon; Lorusso, Giulia; Palacios, Elias; Evangelisti, Marco; Baldansuren, Amgalanbaatar; Chilton, Nicholas F.; Weihe, Høgni; McInnes, Eric J. L.; Lusby, Paul; Piligkos, Stergios
[MIII2MII3]n+ trigonal bipyramidal cages based on diamagnetic and paramagnetic metalloligands.
Chem. Sci., 2017
1546081 CIFC56 H48 Br6 Cr2 N6 O14 Zn3P 32 2 113.2429; 13.2429; 38.38
90; 90; 120
5829.1Brechin, Euan K.; Sanz, Sergio; O'Connor, Helen; Martí-Centelles, Vicente; Comar, Priyanka; Pitak, Mateusz; Coles, Simon; Lorusso, Giulia; Palacios, Elias; Evangelisti, Marco; Baldansuren, Amgalanbaatar; Chilton, Nicholas F.; Weihe, Høgni; McInnes, Eric J. L.; Lusby, Paul; Piligkos, Stergios
[MIII2MII3]n+ trigonal bipyramidal cages based on diamagnetic and paramagnetic metalloligands.
Chem. Sci., 2017
1546082 CIFC54 H48 Cl6 Co3 Fe2 N6 O12P 32 2 112.7708; 12.7708; 39.0709
90; 90; 120
5518.5Brechin, Euan K.; Sanz, Sergio; O'Connor, Helen; Martí-Centelles, Vicente; Comar, Priyanka; Pitak, Mateusz; Coles, Simon; Lorusso, Giulia; Palacios, Elias; Evangelisti, Marco; Baldansuren, Amgalanbaatar; Chilton, Nicholas F.; Weihe, Høgni; McInnes, Eric J. L.; Lusby, Paul; Piligkos, Stergios
[MIII2MII3]n+ trigonal bipyramidal cages based on diamagnetic and paramagnetic metalloligands.
Chem. Sci., 2017
1546083 CIFC158 H194 Cr2 F18 N6 O47 P6 Pd3 S6P -118.4407; 22.0037; 27.1925
104.146; 109.298; 95.522
9907.3Brechin, Euan K.; Sanz, Sergio; O'Connor, Helen; Martí-Centelles, Vicente; Comar, Priyanka; Pitak, Mateusz; Coles, Simon; Lorusso, Giulia; Palacios, Elias; Evangelisti, Marco; Baldansuren, Amgalanbaatar; Chilton, Nicholas F.; Weihe, Høgni; McInnes, Eric J. L.; Lusby, Paul; Piligkos, Stergios
[MIII2MII3]n+ trigonal bipyramidal cages based on diamagnetic and paramagnetic metalloligands.
Chem. Sci., 2017
1546084 CIFC23 H32 O4P 21 21 2111.014; 13.291; 13.869
90; 90; 90
2030.2Zhao, Jinlian; Feng, Jiamin; Tan, Zhen; Liu, Jimei; Zhao, Jianyuan; Chen, Ridao; Xie, Kebo; Zhang, Dewu; Li, Yan; Yu, Liyan; Chen, Xiaoguang; Dai, Jungui
Stachybotrysins A–G, Phenylspirodrimane Derivatives from the Fungus Stachybotrys chartarum
Journal of Natural Products, 2017
1546085 CIFC21 H25 N O4 SP 1 21/n 17.0338; 11.9216; 24.1813
90; 91.725; 90
2026.78Zheng, Nan; Zhang, Lijie; Gong, Jianxian; Yang, Zhen
Formal Total Synthesis of (±)-Lycojaponicumin C
Organic Letters, 2017
1546086 CIFC15 H11 Cl OP 21 21 215.8858; 13.567; 15.5282
90; 90; 90
1239.97Xiang, Jia-Chen; Cheng, Yan; Wang, Zi-Xuan; Ma, Jin-Tian; Wang, Miao; Tang, Bo-Cheng; Wu, Yan-Dong; Wu, An-Xin
Oxidative Trimerization of Amino Acids: Selective Synthesis of 2,3,5-Trisubstituted Pyridines.
Organic letters, 2017, 19, 2997-3000
1546087 CIFC22 H24 Br N O3 SP 21 21 219.73; 10.167; 21.994
90; 90; 90
2175.8Ueda, Hiroki; Masutomi, Koji; Shibata, Yu; Tanaka, Ken
Rhodium-Catalyzed Asymmetric [2 + 2 + 2] Cyclization of 1,6-Enynes with Aliphatic and Aromatic Alkenes.
Organic letters, 2017, 19, 2913-2916
1546088 CIFC53 H43 B Cl3 F2 N3 O8P -18.332; 16.762; 18.465
114.14; 92.762; 92.985
2343.3Sheng, Wanle; Zheng, Yu-Qing; Wu, Qinghua; Wu, Yayang; Yu, Changjiang; Jiao, Lijuan; Hao, Erhong; Wang, Jie-Yu; Pei, Jian
Synthesis, Properties, and Semiconducting Characteristics of BF2 Complexes of β,β-Bisphenanthrene-Fused Azadipyrromethenes.
Organic letters, 2017, 19, 2893-2896
1546089 CIFC52.5 H47 B Cl F2 N3 O8P 1 2/c 112.926; 11.204; 19.694
90; 123; 90
2392Sheng, Wanle; Zheng, Yu-Qing; Wu, Qinghua; Wu, Yayang; Yu, Changjiang; Jiao, Lijuan; Hao, Erhong; Wang, Jie-Yu; Pei, Jian
Synthesis, Properties, and Semiconducting Characteristics of BF2 Complexes of β,β-Bisphenanthrene-Fused Azadipyrromethenes.
Organic letters, 2017, 19, 2893-2896
1546090 CIFC130 H56 N4 Ni S0 UC 1 2/m 125.0308; 15.3288; 19.941
90; 93.983; 90
7632.7Cai, Wenting; Morales-Martínez, Roser; Zhang, Xingxing; Najera, Daniel; Romero, Elkin; Metta Magana, Alejandro Jose; Rodriguez-Fortea, Antonio; Fortier, Skye; Chen, Ning; Poblet, Josep M.; Echegoyen, Luis
Single Crystal Structures and Theoretical Calculations of Uranium Endohedral Metallofullerenes (U@C2n, 2n=74, 82) Show Cage Isomer Dependent Oxidation States for U
Chem. Sci., 2017
1546091 CIFC122 H56 N4 Ni UC 1 2/c 125.102; 14.9208; 38.636
90; 94.044; 90
14435Cai, Wenting; Morales-Martínez, Roser; Zhang, Xingxing; Najera, Daniel; Romero, Elkin; Metta Magana, Alejandro Jose; Rodriguez-Fortea, Antonio; Fortier, Skye; Chen, Ning; Poblet, Josep M.; Echegoyen, Luis
Single Crystal Structures and Theoretical Calculations of Uranium Endohedral Metallofullerenes (U@C2n, 2n=74, 82) Show Cage Isomer Dependent Oxidation States for U
Chem. Sci., 2017
1546092 CIFC128 H53 N4 Ni S2 UP 1 21/c 117.7846; 17.2807; 26.6533
90; 107.376; 90
7817.6Cai, Wenting; Morales-Martínez, Roser; Zhang, Xingxing; Najera, Daniel; Romero, Elkin; Metta Magana, Alejandro Jose; Rodriguez-Fortea, Antonio; Fortier, Skye; Chen, Ning; Poblet, Josep M.; Echegoyen, Luis
Single Crystal Structures and Theoretical Calculations of Uranium Endohedral Metallofullerenes (U@C2n, 2n=74, 82) Show Cage Isomer Dependent Oxidation States for U
Chem. Sci., 2017
1546093 CIFC15 H10 O2P c a 2124.2286; 5.6429; 7.6125
90; 90; 90
1040.78Jhun, Byung Hak; Yi, Seung Yeon; Jeong, Donghyun; Cho, Jaeheung; Park, Soo Young; You, Youngmin
Aggregation of an n–π* Molecule Induces Fluorescence Turn-on
The Journal of Physical Chemistry C, 2017, 121, 11907
1546094 CIFC21 H21 N O3 SP 1 21 19.8947; 8.25; 12.8004
90; 110.44; 90
979.12Lin, Tao-Yan; Wu, Hai-Hong; Feng, Jian-Jun; Zhang, Junliang
Transfer of Chirality in the Rhodium-Catalyzed Chemoselective and Regioselective Allylic Alkylation of Hydroxyarenes with Vinyl Aziridines.
Organic letters, 2017, 19, 2897-2900
1546095 CIFC42 H49 N O4P 1 21 19.9619; 24.0179; 15.5925
90; 101.3; 90
3658.4Tlustý, Martin; Slavík, Petr; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Inherently Chiral Upper-Rim-Bridged Calix[4]arenes Possessing a Seven Membered Ring.
Organic letters, 2017
1546096 CIFC21 H19 N O4P 1 21 18.3201; 7.3604; 14.5839
90; 105.938; 90
858.78Kumar, Mukesh; Chauhan, Pankaj; Valkonen, Arto; Rissanen, Kari; Enders, Dieter
Asymmetric Synthesis of Functionalized Tricyclic Chromanes via an Organocatalytic Triple Domino Reaction.
Organic letters, 2017, 19, 3025-3028
1546097 CIFC14 H13 F6 N O2P 1 21/c 115.0424; 9.1167; 42.181
90; 96.995; 90
5741.5Gietter-Burch, Amber A S; Devannah, Vijayarajan; Watson, Donald A.
Trifluoromethylation of Secondary Nitroalkanes.
Organic letters, 2017, 19, 2957-2960
1546098 CIFC20 H30 O9P 6518.6492; 18.6492; 12.5645
90; 90; 120
3784.4Zhou, Lei; Tuo, Yali; Hao, Yi; Guo, Xiaoman; Tang, Wei; Xue, Yongbo; Zeng, Junfen; Zhou, Yu; Xiang, Ming; Zuo, Jianping; Yao, Guangmin; Zhang, Yonghui
Cinnamomols A and B, Immunostimulative Diterpenoids with a New Carbon Skeleton from the Leaves of Cinnamomum cassia.
Organic letters, 2017, 19, 3029-3032
1546099 CIFC20 H36 O11P 32 2 117.1874; 17.1874; 42.085
90; 90; 120
10766.6Zhou, Lei; Tuo, Yali; Hao, Yi; Guo, Xiaoman; Tang, Wei; Xue, Yongbo; Zeng, Junfen; Zhou, Yu; Xiang, Ming; Zuo, Jianping; Yao, Guangmin; Zhang, Yonghui
Cinnamomols A and B, Immunostimulative Diterpenoids with a New Carbon Skeleton from the Leaves of Cinnamomum cassia.
Organic letters, 2017, 19, 3029-3032
1546100 CIFC21 H16 N2 O5 ZnP 1 21/c 111.3928; 15.6359; 16.3018
90; 96.451; 90
2885.56Schneemann, Andreas; Rudolf, Robin; Henke, Sebastian; Takahashi, Yukiko; Banh, Hung; Hante, Inke; Schneider, Christian; Noro, Shin-ichiro; Fischer, Roland A.
Linker functionalisation triggers an alternative 3D-topology for Zn-isophthalate-4,4′-bipyridine frameworks
Dalton Transactions, 2017, 46, 8198-8203
1546101 CIFC21 H18 N2 O5 ZnP b a m16.496; 15.8918; 11.4039
90; 90; 90
2989.5Schneemann, Andreas; Rudolf, Robin; Henke, Sebastian; Takahashi, Yukiko; Banh, Hung; Hante, Inke; Schneider, Christian; Noro, Shin-ichiro; Fischer, Roland A.
Linker functionalisation triggers an alternative 3D-topology for Zn-isophthalate-4,4′-bipyridine frameworks
Dalton Transactions, 2017, 46, 8198-8203
1546102 CIFC21 H18 N2 O5 ZnP -19.9902; 11.4259; 12.1064
109.285; 108.208; 97.69
1194.98Schneemann, Andreas; Rudolf, Robin; Henke, Sebastian; Takahashi, Yukiko; Banh, Hung; Hante, Inke; Schneider, Christian; Noro, Shin-ichiro; Fischer, Roland A.
Linker functionalisation triggers an alternative 3D-topology for Zn-isophthalate-4,4′-bipyridine frameworks
Dalton Transactions, 2017, 46, 8198-8203
1546103 CIFC20 H16 N2 O5 ZnP -110.0944; 10.3898; 10.493
65.925; 75.649; 76.069
961.2Schneemann, Andreas; Rudolf, Robin; Henke, Sebastian; Takahashi, Yukiko; Banh, Hung; Hante, Inke; Schneider, Christian; Noro, Shin-ichiro; Fischer, Roland A.
Linker functionalisation triggers an alternative 3D-topology for Zn-isophthalate-4,4′-bipyridine frameworks
Dalton Transactions, 2017, 46, 8198-8203
1546104 CIFC21 H51.5 La N3 O19.75P -110.8019; 11.2323; 15.296
73.963; 79.565; 73.194
1697.1Weekes, David M.; Cawthray, Jacqueline F.; Rieder, Meghanne; Syeda, Jaweria; Ali, Munawar; Wasan, Ellen; Kostelnik, Tom Kostelnik; Patrick, Brian O.; Panahifar, A.; Cooper, David M.L.; Al-Dissi, Ahmad; Wasan, Kishor; Orvig, Chris
La(III) biodistribution profiles from intravenous and oral dosing of two lanthanum complexes, La(dpp)3 and La(XT), and evaluation as treatments for bone resorption disorders
Metallomics, 2017
1546105 CIFCu3 H4 O8 SeP n m a8.382; 6.087; 12.285
90; 90; 90
626.8Gerald Giester
Crystal structure of synthetic Cu3SeO4(OH)4
Monatshefte fur Chemie, 1991, 122, 229-234
1546106 CIFC17 H27 N O3.5P -4 21 c21.2016; 21.2016; 7.9468
90; 90; 90
3572.1Shymanska, Nataliia V.; Pierce, Joshua G.
Stereoselective Synthesis of Quaternary Pyrrolidine-2,3-diones and β-Amino Acids.
Organic letters, 2017, 19, 2961-2964
1546107 CIFC32 H42 O5P 21 21 219.3051; 12.8967; 23.172
90; 90; 90
2780.76Zhang, Ya-Long; Zhou, Xu-Wei; Wang, Xiao-Bing; Wu, Lin; Yang, Ming-Hua; Luo, Jun; Yin, Yong; Luo, Jian-Guang; Kong, Ling-Yi
Xylopiana A, a Dimeric Guaiane with a Case-Shaped Core from Xylopia vielana: Structural Elucidation and Biomimetic Conversion.
Organic letters, 2017, 19, 3013-3016
1546108 CIFC26 H28 N2 O3P -110.294; 10.7033; 12.376
69.312; 79.586; 66.46
1168.2Liu, Rai-Shung; Liu, Jinxian; Skaria, Manisha; Sharma, Pankaj; Chiang, Yun-Wei
Ground-State Dioxygen Undergoes Metal-Free [3+2]-Annulations with Allenes and Nitrosoarenes Under Ambient Conditions
Chem. Sci., 2017
1546109 CIFC16 H15 N O3P 3213.9065; 13.9065; 6.0548
90; 90; 120
1014.07Liu, Rai-Shung; Liu, Jinxian; Skaria, Manisha; Sharma, Pankaj; Chiang, Yun-Wei
Ground-State Dioxygen Undergoes Metal-Free [3+2]-Annulations with Allenes and Nitrosoarenes Under Ambient Conditions
Chem. Sci., 2017
1546110 CIFC28 H24 Cl2 N2 O2P 1 21 116.42; 5.9044; 25.212
90; 90.487; 90
2444.2Liu, Rai-Shung; Liu, Jinxian; Skaria, Manisha; Sharma, Pankaj; Chiang, Yun-Wei
Ground-State Dioxygen Undergoes Metal-Free [3+2]-Annulations with Allenes and Nitrosoarenes Under Ambient Conditions
Chem. Sci., 2017
1546111 CIFC17 H17 N O4P 1 21 18.48; 5.698; 15.656
90; 93.2; 90
755.3Liu, Rai-Shung; Liu, Jinxian; Skaria, Manisha; Sharma, Pankaj; Chiang, Yun-Wei
Ground-State Dioxygen Undergoes Metal-Free [3+2]-Annulations with Allenes and Nitrosoarenes Under Ambient Conditions
Chem. Sci., 2017
1546112 CIFC27 H24 N4 O2C 1 c 133.1101; 8.5492; 16.653
90; 99.906; 90
4643.6Basu Roy, Sohini; Prodhan, Chandraday; Chaudhuri, Keya; Rajak, Kajal Krishna
A benzimidazole-based chemodosimeter for the fluorometric detection of Zn and Cu via 1,5 proton shifts and C‒N bond cleavage
Photochem. Photobiol. Sci., 2017
1546113 CIFC24 H18 B F10 NP -4 21 c22.206; 22.206; 8.692
90; 90; 90
4286.1Krause, Lennard; Niepötter, Benedikt; Schürmann, Christian J.; Stalke, Dietmar; Herbst-Irmer, Regine
Validation of experimental charge-density refinement strategies: when do we overfit?
IUCrJ, 2017, 4
1546114 CIFC24 H18 B F10 NP -4 21 c22.206; 22.206; 8.692
90; 90; 90
4286.1Krause, Lennard; Niepötter, Benedikt; Schürmann, Christian J.; Stalke, Dietmar; Herbst-Irmer, Regine
Validation of experimental charge-density refinement strategies: when do we overfit?
IUCrJ, 2017, 4
1546115 CIFC20 H23 P SP b c a10.9323; 14.5698; 21.091
90; 90; 90
3359.4Krause, Lennard; Niepötter, Benedikt; Schürmann, Christian J.; Stalke, Dietmar; Herbst-Irmer, Regine
Validation of experimental charge-density refinement strategies: when do we overfit?
IUCrJ, 2017, 4
1546116 CIFC20 H23 P SP b c a10.932; 14.57; 21.091
90; 90; 90
3359.4Krause, Lennard; Niepötter, Benedikt; Schürmann, Christian J.; Stalke, Dietmar; Herbst-Irmer, Regine
Validation of experimental charge-density refinement strategies: when do we overfit?
IUCrJ, 2017, 4
1546117 CIFC32 H53 B10 O2 P3 RuP -112.5744; 15.5222; 19.5052
88.259; 81.988; 89.388
3768.1Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
Rapid Reversible Borane to Boryl Hydride Exchange by Metal Shuttling on the Carborane Cluster Surface
Chem. Sci., 2017
1546118 CIFC32 H52 B10 Cl O2 P3 RuP 1 21/n 112.4465; 23.0308; 13.2665
90; 96.239; 90
3780.4Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
Rapid Reversible Borane to Boryl Hydride Exchange by Metal Shuttling on the Carborane Cluster Surface
Chem. Sci., 2017
1546119 CIFC67.59 H76.99 N12P 21 21 2111.1553; 19.49; 30.332
90; 90; 90
6595Hasell, T.; Little, M. A.; Chong, S. Y.; Schmidtmann, M.; Briggs, M. E.; Santolini, V.; Jelfs, K. E.; Cooper, A. I.
Chirality as a tool for function in porous organic cages.
Nanoscale, 2017, 9, 6783-6790
1546120 CIFC142.09 H188.18 Cl5.5 N24 O9.92P 3 2 117.5575; 17.5575; 28.6921
90; 90; 120
7659.8Hasell, T.; Little, M. A.; Chong, S. Y.; Schmidtmann, M.; Briggs, M. E.; Santolini, V.; Jelfs, K. E.; Cooper, A. I.
Chirality as a tool for function in porous organic cages.
Nanoscale, 2017, 9, 6783-6790
1546121 CIFC130 H160.5 N24 O15.25P 21 324.318; 24.318; 24.318
90; 90; 90
14381Hasell, T.; Little, M. A.; Chong, S. Y.; Schmidtmann, M.; Briggs, M. E.; Santolini, V.; Jelfs, K. E.; Cooper, A. I.
Chirality as a tool for function in porous organic cages.
Nanoscale, 2017, 9, 6783-6790
1546122 CIFC151 H214 Cl2 N24 O10P 6317.5938; 17.5938; 32.2344
90; 90; 120
8641.1Hasell, T.; Little, M. A.; Chong, S. Y.; Schmidtmann, M.; Briggs, M. E.; Santolini, V.; Jelfs, K. E.; Cooper, A. I.
Chirality as a tool for function in porous organic cages.
Nanoscale, 2017, 9, 6783-6790
1546123 CIFC10 H18 O4P 21 21 219.296; 8.0943; 6.9478
90; 90; 90
1085.16Wang, Ling-Yan; Chen, Ming-Hua; Wu, Jiang; Sun, Hua; Liu, Wei; Qu, Yu-Hong; Li, Yan-Cheng; Wu, Yu-Zhuo; Li, Rui; Zhang, Dan; Wang, Su-Juan; Lin, Sheng
Bioactive Glycosides from the Twigs of Litsea cubeba.
Journal of natural products, 2017, 80, 1808-1818
1546124 CIFC24 H23 N3 O3 SP b c a15.862; 15.219; 18.723
90; 90; 90
4519.8Xu, Wei; Wang, Gaonan; Sun, Ning; Liu, Yuanhong
Gold-Catalyzed Formal [3 + 2] Cycloaddition of Ynamides with 4,5-Dihydro-1,2,4-oxadiazoles: Synthesis of Functionalized 4-Aminoimidazoles.
Organic letters, 2017, 19, 3307-3310
1546125 CIFC21 H22 Cl5 Mg N3 OC 1 2/c 124.0022; 8.6136; 25.556
90; 116.047; 90
4747Rosen, Tomer; Goldberg, I.; Navarra, Wanda; Venditto, Vincenzo; Kol, Moshe
Divergent [{ONNN}Mg-Cl] complexes in the highly active and living lactide polymerization
Chem. Sci., 2017
1546126 CIFC47 H54 Cl12 Mg2 N6 O2C 1 2/c 127.298; 14.9001; 16.8775
90; 124.63; 90
5648.6Rosen, Tomer; Goldberg, I.; Navarra, Wanda; Venditto, Vincenzo; Kol, Moshe
Divergent [{ONNN}Mg-Cl] complexes in the highly active and living lactide polymerization
Chem. Sci., 2017
1546127 CIFF19 Fe3 Sr5I 4/m14.294; 14.294; 7.307
90; 90; 90
1493Graulich, J.; Babel, D.
Zweikernige aniongruppen [Fe2F10]4- in der kristallstruktur von Sr5Fe3F19
Zeitschrift fur anorganische und allgemeine Chemie, 1991, 597, 51-59
1546128 CIFC117.06 H104.25 I12 N25.11 O10.05 Zn6C 1 2 134.9084; 14.9228; 29.6669
90; 101.028; 90
15169Sairenji, Shiho; Kikuchi, Takashi; Abozeid, Mohamed Ahmed; Takizawa, Shinobu; Sasai, Hiroaki; Ando, Yuichiro; Ohmatsu, Kohsuke; Ooi, Takashi; Fujita, Makoto
Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method
Chem. Sci., 2017
1546129 CIFC132.77 H138.74 I12 N24 O9.74 Zn6C 1 2 136.0217; 14.6919; 30.6728
90; 101.672; 90
15897.2Sairenji, Shiho; Kikuchi, Takashi; Abozeid, Mohamed Ahmed; Takizawa, Shinobu; Sasai, Hiroaki; Ando, Yuichiro; Ohmatsu, Kohsuke; Ooi, Takashi; Fujita, Makoto
Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method
Chem. Sci., 2017
1546130 CIFC100.85 H95.62 Cl11.35 I12.03 N24.48 O2.88 S0.48 Zn6C 1 2 133.9973; 14.9225; 31.1158
90; 101.047; 90
15493.3Sairenji, Shiho; Kikuchi, Takashi; Abozeid, Mohamed Ahmed; Takizawa, Shinobu; Sasai, Hiroaki; Ando, Yuichiro; Ohmatsu, Kohsuke; Ooi, Takashi; Fujita, Makoto
Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method
Chem. Sci., 2017
1546131 CIFC122.98 H117.96 I12 N28 Zn6C 1 2 134.869; 14.9135; 31.5649
90; 102.275; 90
16039.1Sairenji, Shiho; Kikuchi, Takashi; Abozeid, Mohamed Ahmed; Takizawa, Shinobu; Sasai, Hiroaki; Ando, Yuichiro; Ohmatsu, Kohsuke; Ooi, Takashi; Fujita, Makoto
Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method
Chem. Sci., 2017
1546132 CIFC136.11 H131.89 I12 N27.41 Zn6C 1 2 136.1897; 14.6874; 34.7427
90; 109.742; 90
17381.5Sairenji, Shiho; Kikuchi, Takashi; Abozeid, Mohamed Ahmed; Takizawa, Shinobu; Sasai, Hiroaki; Ando, Yuichiro; Ohmatsu, Kohsuke; Ooi, Takashi; Fujita, Makoto
Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method
Chem. Sci., 2017
1546133 CIFC18 H22 B10 N2P b c a12.0727; 12.564; 26.304
90; 90; 90
3989.8Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546134 CIFC38 H38 B10 Cl2 F10 Ir N4 PC 1 2/c 141.094; 11.9824; 19.1819
90; 108.189; 90
8973.3Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546135 CIFC14 H28 B20 N2C 1 2/c 130.853; 6.836; 12.622
90; 106.229; 90
2556Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546136 CIFC40 H34 B10 Cl0 F10 Ir N4 PP -110.4515; 13.4143; 18.7342
96.628; 97.799; 105.863
2470.87Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546137 CIFC40 H42 B10 Cl4 F10 Ir N4 PP 1 21/n 110.3413; 19.9619; 23.794
90; 94.892; 90
4894Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546138 CIFC35 H27 Cl2 F10 Ir N4 O0.5 PP 21 21 219.6791; 12.7772; 28.988
90; 90; 90
3585Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546139 CIFC34 H29 B10 F10 Ir N4 O0 PP 1 21/c 119.439; 11.727; 19.346
90; 100.293; 90
4339.2Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546140 CIFC36 H34 B10 Cl2 F10 Ir N4 PP 1 2/c 117.3958; 12.1322; 24.263
90; 106.755; 90
4903.3Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546141 CIFC35 H32 B10 F10 Ir N4 PP 1 21/c 119.3966; 11.8557; 19.0311
90; 99.693; 90
4313.9Yan, Hong; Li, Xiang; Yin, Yongheng; Lu, Changsheng; Tong, Xiao; Zhao, Qiang
Using highly emissive and environmentally sensitive o-carborane-functionalized metallophosphors to monitor mitochondrial polarity
Chem. Sci., 2017
1546142 CIFC20 H30 N4 O5P 21 21 219.8604; 12.364; 15.752
90; 90; 90
1920.4Zheng, Yongbiao; Zhang, Jiyan; Wei, Liufeng; Shi, Mianmian; Wang, Jifeng; Huang, Jianzhong
Gunnilactams A-C, Macrocyclic Tetralactams from the Mycelial Culture of the Entomogenous Fungus Paecilomyces gunnii.
Journal of natural products, 2017, 80, 1935-1938
1546143 CIFC20 H24 N4 O5P 21 21 219.4557; 12.8247; 15.429
90; 90; 90
1871Zheng, Yongbiao; Zhang, Jiyan; Wei, Liufeng; Shi, Mianmian; Wang, Jifeng; Huang, Jianzhong
Gunnilactams A-C, Macrocyclic Tetralactams from the Mycelial Culture of the Entomogenous Fungus Paecilomyces gunnii.
Journal of natural products, 2017, 80, 1935-1938
1546144 CIFC20 H20 Br2 Mn N3 O5P -18.794; 10.086; 12.604
76.44; 78.13; 79.99
1054.2Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546145 CIFC20 H22 Mn N3 O5P 1 21/c 18.7051; 15.844; 14.3082
90; 111.219; 90
1839.6Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546146 CIFC21 H20 Cl2 Mn N3 O2 SP 1 21/n 17.8995; 19.6273; 14.075
90; 103.223; 90
2124.4Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546147 CIFC22 H28 Cl Mn N2 O9P 1 21/n 17.3227; 16.417; 20.421
90; 107.009; 90
2347.6Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546148 CIFC22 H26 Mn N2 O6 ReP b c a14.2637; 17.4799; 17.7014
90; 90; 90
4413.5Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546149 CIFC21 H20 Br2 Mn N3 O2 SP 1 21/n 18.428; 14.1; 19.038
90; 97.917; 90
2241Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546150 CIFC22 H28 F6 Mn N2 O5 PP 1 21/c 17.3187; 20.537; 16.1889
90; 95.132; 90
2423.5Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546151 CIFC20 H20 Br2 Mn N5 O2P -18.1; 11.44; 12.45
71.154; 73.375; 86.565
1045.5Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546152 CIFC22 H26 Mn N3 O7P 1 21/c 19.223; 13.875; 16.951
90; 101.021; 90
2129.2Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546153 CIFC22 H28 Cl Mn N2 O7P 1 21/c 17.3962; 15.437; 19.592
90; 90; 90
2236.9Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546154 CIFC23 H26 Mn N3 O2 SP b c a15.9799; 15.253; 17.7327
90; 90; 90
4322.2Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546155 CIFC20 H20 Cl2 Mn N5 O2P -18.08; 11.412; 12.082
71.822; 73.52; 86.773
1014.4Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546156 CIFC23 H28 F3 Mn N2 O8 SP 1 21/c 17.416; 17.927; 18.623
90; 93.457; 90
2471Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546157 CIFC22 H26 Mn N2 O8 ReP b c a14.7377; 16.7073; 18.4223
90; 90; 90
4536.1Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546158 CIFC23 H26 Mn N3 O4 SP 1 21/n 18.7807; 14.932; 17.271
90; 102.122; 90
2214Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546159 CIFC20 H22 Cl3 Mn N2 O7P 1 21/c 17.324; 15.433; 19.273
90; 90.0406; 90
2178.5Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546160 CIFC20 H20 Cl2 Mn N2 O6 ReP 1 21/c 18.741; 18.116; 13.841
90; 100.912; 90
2152Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546161 CIFC44 H52 Mn2 N10 O8P 1 21/n 116.719; 14.5578; 17.9507
90; 104.338; 90
4233Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546162 CIFC22 H26 Mn N3 O5P -18.813; 14.3852; 16.9362
81.336; 75.607; 84.498
2052.16Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546163 CIFC20 H20 Br2 Mn N2 O6 ReP 1 21/a 113.849; 18.445; 8.901
90; 100.56; 90
2235.2Kachi-Terajima, Chihiro; Ishii, Rikako; Tojo, Yoshiaki; Fukuda, Masato; Kitagawa, Yasutaka; Asaoka, Mizuki; Miyasaka, Hitoshi
Ferromagnetic Exchange Coupling in a Family of MnIII Salen-Type Schiff-Base Out-of-Plane Dimers
The Journal of Physical Chemistry C, 2017
1546164 CIFC17 H24 O3P 1 21 110.927; 5.4369; 13.378
90; 100.686; 90
781Liu, Yun-Ting; Chen, Ji-Qiang; Li, Lin-Ping; Shao, Xin-Yang; Xie, Jian-Hua; Zhou, Qi-Lin
Asymmetric Hydrogenation of Tetrasubstituted Cyclic Enones to Chiral Cycloalkanols with Three Contiguous Stereocenters.
Organic letters, 2017, 19, 3231-3234
1546165 CIFC16 H24 O7P -110.8731; 11.2643; 14.1668
92.003; 93.9208; 101.502
1694.2Giarrusso, James; Do, Dung T.; Johnson, Jeffrey S.
Chemoselective and Diastereoconvergent Cu(II)-Catalyzed Aerobic Endoperoxidation of Polycarbonyls.
Organic letters, 2017, 19, 3107-3110
1546166 CIFC15 H22 O6P 1 21/c 18.999; 9.833; 17.8989
90; 101.692; 90
1550.96Giarrusso, James; Do, Dung T.; Johnson, Jeffrey S.
Chemoselective and Diastereoconvergent Cu(II)-Catalyzed Aerobic Endoperoxidation of Polycarbonyls.
Organic letters, 2017, 19, 3107-3110
1546167 CIFC19 H28 O7P -19.945; 10.1542; 10.9266
73.626; 65.348; 74.857
949.02Giarrusso, James; Do, Dung T.; Johnson, Jeffrey S.
Chemoselective and Diastereoconvergent Cu(II)-Catalyzed Aerobic Endoperoxidation of Polycarbonyls.
Organic letters, 2017, 19, 3107-3110
1546168 CIFC26 H30 F2 N2 O2P -18.4306; 11.7839; 12.6627
96.816; 105.872; 103.544
1153.69Maity, Soham; Dolui, Pravas; Kancherla, Rajesh; Maiti, Debabrata
Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
Chem. Sci., 2017
1546169 CIFC20 H40 Al Si3 TiP 1 21/c 118.6834; 9.2143; 15.3519
90; 108.428; 90
2507.4Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546170 CIFC30 H47 Al F4 Si3 Ti2P -112.149; 16.6519; 18.1791
105.807; 102.06; 91.054
3449.4Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546171 CIFC21.5 H41.5 Al Si3 TiP 1 21/c 113.804; 20.5426; 18.7994
90; 105.291; 90
5142.2Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546172 CIFC18 H46 Al K O2 Si3P -113.5985; 13.6009; 16.6858
106.549; 107.02; 98.4556
2737.85Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546173 CIFC30 H58 Al Si3 TiP 1 21/c 117.5367; 11.3812; 18.6758
90; 115.366; 90
3368.11Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546174 CIFC30 H47 Al Si3 Ti2P 1 21/c 113.9593; 26.812; 9.5669
90; 90.391; 90
3580.6Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546175 CIFC30 H51 Al Si3 Ti2P -111.8167; 16.7464; 18.0477
105.953; 103.15; 90.965
3331.8Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546176 CIFC21 H39 Al F3 O3 S Si3 TiP 1 21/n 115.9334; 8.8807; 41.2358
90; 92.756; 90
5828.1Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium–aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546177 CIFC30 H56 Al N2 O3 Si3 TiP n a 2112.528; 18.992; 15.352
90; 90; 90
3653Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546178 CIFC27 H54 Al N2 Si3 TiP 1 21/n 111.686; 15.497; 18.639
90; 107.884; 90
3212Brown, Alexandra C.; Altman, Alison B.; Lohrey, Trevor D.; Hohloch, Stephan; Arnold, John
Hydride oxidation from a titanium‒aluminum bimetallic complex: insertion, thermal and electrochemical reactivity
Chem. Sci., 2017
1546179 CIFC18 H17 F N2 O2P -17.1689; 9.283; 11.8655
95.669; 91.769; 107.117
749.5Robertson, Craig. C.; Wright, James S.; Carrington, Elliot J.; Perutz, Robin N.; Hunter, Christopher A.; Brammer, Lee
Hydrogen bonding vs. halogen bonding: the solvent decides
Chem. Sci., 2017
1546180 CIFC18 H14 F4 N2 O2P -16.1939; 7.4692; 9.0672
86.863; 75.722; 71.755
385.97Robertson, Craig. C.; Wright, James S.; Carrington, Elliot J.; Perutz, Robin N.; Hunter, Christopher A.; Brammer, Lee
Hydrogen bonding vs. halogen bonding: the solvent decides
Chem. Sci., 2017
1546181 CIFC65 H74 B N9 O4.28 S ZnP 1 21/c 113.6329; 14.5215; 63.8849
90; 91.6616; 90
12642Kirk, Martin L.; Shultz, David A.; Zhang, Jinyuan; Dangi, Ranjana; Ingersol, Laura; Yang, Jing; Finney, Nathaniel S.; Sommer, Roger D.; Wojtas, Lukasz
Heterospin biradicals provide insight into molecular conductance and rectification
Chem. Sci., 2017
1546182 CIFC65 H74 B N9 O4 S ZnP 1 21/c 122.0024; 16.5492; 21.1852
90; 112.792; 90
7111.7Kirk, Martin L.; Shultz, David A.; Zhang, Jinyuan; Dangi, Ranjana; Ingersol, Laura; Yang, Jing; Finney, Nathaniel S.; Sommer, Roger D.; Wojtas, Lukasz
Heterospin biradicals provide insight into molecular conductance and rectification
Chem. Sci., 2017
1546183 CIFC13 H15 Cl O5 SP 21 21 216.853; 9.6726; 21.2802
90; 90; 90
1410.59Espina, Marta; Corte-Rodríguez, Mario; Aguado, Leticia; Montes-Bayón, María; Sierra, Marta I.; Martínez-Camblor, Pablo; Blanco-González, Elisa; Sierra, L María
Cisplatin resistance in cell models: evaluation of metallomic and biological predictive biomarkers to address early therapy failure.
Metallomics : integrated biometal science, 2017, 9, 564-574
1546184 CIFC14 H16 O4 SP 1 21/c 121.102; 10.963; 5.929
90; 92.57; 90
1370.2Espina, Marta; Corte-Rodríguez, Mario; Aguado, Leticia; Montes-Bayón, María; Sierra, Marta I.; Martínez-Camblor, Pablo; Blanco-González, Elisa; Sierra, L María
Cisplatin resistance in cell models: evaluation of metallomic and biological predictive biomarkers to address early therapy failure.
Metallomics : integrated biometal science, 2017, 9, 564-574
1546185 CIFAg Cl6 Cs2 SbF m -3 m10.664; 10.664; 10.664
90; 90; 90
1213Tran, T. Thao; Panella, Jessica R.; Chamorro, Juan R.; Morey, Jennifer R.; McQueen, Tyrel M.
Designing Indirect-Direct Bandgap Transitions in Double Perovskites
Mater. Horiz., 2017
1546186 CIFAg Cl6 Cs2 InF m -3 m10.469; 10.469; 10.469
90; 90; 90
1147Tran, T. Thao; Panella, Jessica R.; Chamorro, Juan R.; Morey, Jennifer R.; McQueen, Tyrel M.
Designing Indirect-Direct Bandgap Transitions in Double Perovskites
Mater. Horiz., 2017
1546187 CIFC20 H26 F16 I2 N2 O4I 1 2/a 131.169; 5.462; 19.627
90; 102.81; 90
3258.2Zavala, Jose; Greenan, Rebecca; Krantz, Q. Todd; DeMarini, David M.; Higuchi, Mark; Gilmour, M. Ian; White, Paul A.
Regulating temperature and relative humidity in air‒liquid interface in vitro systems eliminates cytotoxicity resulting from control air exposures
Toxicol. Res., 2017
1546188 CIFC25 H19 N OP 1 21/c 110.4008; 19.8632; 8.9591
90; 91.71; 90
1850.1Yao, Tuanli; Ren, Beige; Wang, Bo; Zhao, Yanna
Highly Selective Synthesis of Dihydrobenzo[d]isoxazoles and Dihydrobenzo[d]oxazoles from Oximes and Arynes via in Situ Generation of Nitrones.
Organic letters, 2017, 19, 3135-3138
1546189 CIFC21 H19 N OP 1 21/c 19.4297; 9.7758; 18.503
90; 103.717; 90
1657Yao, Tuanli; Ren, Beige; Wang, Bo; Zhao, Yanna
Highly Selective Synthesis of Dihydrobenzo[d]isoxazoles and Dihydrobenzo[d]oxazoles from Oximes and Arynes via in Situ Generation of Nitrones.
Organic letters, 2017, 19, 3135-3138
1546190 CIFC17 H13 N O2P 1 21/c 18.098; 14.164; 11.844
90; 98.751; 90
1342.7Samineni, Ramesh; Madapa, Jaipal; Srihari, Pabbaraja; Mehta, Goverdhan
Spiroannulation of Oxindoles via Aryne and Alkyne Incorporation: Substituent-Diverted, Transition-Metal-Free, One-Pot Access to Spirooxindoles.
Organic letters, 2017, 19, 3119-3122
1546191 CIFC26 H19 N O3P 1 21/n 19.593; 16.282; 12.782
90; 100.516; 90
1963Samineni, Ramesh; Madapa, Jaipal; Srihari, Pabbaraja; Mehta, Goverdhan
Spiroannulation of Oxindoles via Aryne and Alkyne Incorporation: Substituent-Diverted, Transition-Metal-Free, One-Pot Access to Spirooxindoles.
Organic letters, 2017, 19, 3119-3122
1546192 CIFC19 H26 N2P 21 21 2111.1357; 12.5468; 22.93
90; 90; 90
3203.7Wang, Nengzhong; Du, Shuo; Li, Dong; Jiang, Xuefeng
Divergent Asymmetric Total Synthesis of (+)-Vincadifformine, (-)-Quebrachamine, (+)-Aspidospermidine, (-)-Aspidospermine, (-)-Pyrifolidine, and Related Natural Products.
Organic letters, 2017, 19, 3167-3170
1546193 CIFC13 H12 F3 N O6 RuP -18.558; 9.278; 11.548
89.047; 68.729; 70.014
796.9Fan, Zhoulong; Li, Jie; Lu, Heng; Wang, Dong-Yu; Wang, Chao; Uchiyama, Masanobu; Zhang, Ao
Monomeric Octahedral Ruthenium(II) Complex Enabled meta-C‒H Nitration of Arenes with Removable Auxiliaries
Organic Letters, 2017
1546194 CIFC18 H33 N O3P 1 21 110.7535; 6.972; 12.657
90; 110.71; 90
887.62Novaes, Luiz F. T.; Pastre, Julio C.
Formal Total Synthesis of Actinoranone and Asymmetric Synthesis of Labda-7,13-(E)-dien-15-ol.
Organic letters, 2017
1546195 CIFC28 H23 Br2 N5 O4P -18.5342; 8.687; 18.025
88.68; 84.146; 78.769
1303.9Wang, Xiao; Wu, Lin; Yang, Peng; Song, Xiang-Jia; Ren, Hong-Xia; Peng, Lin; Wang, Li-Xin
Isatin N,N'-Cyclic Azomethine Imine 1,3-Dipole and Base Catalyzed Michael Addition with β-Nitrostyrene via C3 Umpolung of Oxindole.
Organic letters, 2017, 19, 3051-3054
1546196 CIFC16 H34 F N O4 S SiP -114.494; 15.866; 18.793
96.478; 90.043; 90.052
4294Liu, Lu; Gerstner, Nels C.; Oxtoby, Lucas J.; Guzei, Ilia A.; Schomaker, Jennifer M.
Fluorinated Amine Stereotriads via Allene Amination
Organic Letters, 2017
1546197 CIFC81.02 H72.05 Cl4.05 F12 N4 O8 Sb2P 1 21/c 113.5017; 18.3754; 16.0677
90; 104.555; 90
3858.45Kurata, Ryohei; Sakamaki, Daisuke; Ito, Akihiro
Tetraaza[1.1.1.1]m,p,m,p-cyclophane Diradical Dications Revisited: Tuning Spin States by Confronted Arenes.
Organic letters, 2017, 19, 3115-3118
1546198 CIFC67 H38 B F20 N2 O4P 1 21/c 112.556; 18.88; 24.126
90; 91.189; 90
5718Kurata, Ryohei; Sakamaki, Daisuke; Ito, Akihiro
Tetraaza[1.1.1.1]m,p,m,p-cyclophane Diradical Dications Revisited: Tuning Spin States by Confronted Arenes.
Organic letters, 2017, 19, 3115-3118
1546199 CIFC25 H24 N2 O3P 21 21 2112.237; 12.4525; 13.7714
90; 90; 90
2098.5Tabata, Hidetsugu; Yoneda, Tetsuya; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
Tolvaptan-Type Vasopressin Receptor Ligands: Important Role of Axial Chirality in the Active Form.
Journal of medicinal chemistry, 2017, 60, 4503-4509
1546200 CIFC30.5 H60.33333 O5.83333P 114.9136; 14.9888; 22.7918
97.926; 93.125; 114.454
4558.1Niu, Biao; Ke, Chang-Qiang; Li, Bo-Han; Li, Yuanyuan; Yi, Yongji; Luo, Yongwei; Shuai, Lin; Yao, Sheng; Lin, Li-Gen; Li, Jia; Ye, Yang
Cucurbitane Glucosides from the Crude Extract of Siraitia grosvenorii with Moderate Effects on PGC-1α Promoter Activity.
Journal of natural products, 2017, 80, 1428-1435
1546201 CIFC21 H32 N2 OP 21 21 217.45094; 9.21543; 26.7264
90; 90; 90
1835.13Luo, Pan; Xia, Wenjuan; Morris-Natschke, Susan L; Lee, Kuo-Hsiung; Zhao, Yu; Gu, Qiong; Xu, Jun
Vitepyrroloids A-D, 2-Cyanopyrrole-Containing Labdane Diterpenoid Alkaloids from the Leaves of Vitex trifolia.
Journal of natural products, 2017, 80, 1679-1683
1546202 CIFC14 H26 O5 SiP 1 21 16.209; 7.0974; 19.3995
90; 90.588; 90
854.85Markovič, Martin; Koóš, Peter; Čarný, Tomáš; Sokoliová, Saskia; Boháčiková, Nikola; Moncol, Ján; Gracza, Tibor
Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A.
Journal of natural products, 2017, 80, 1631-1638
1546203 CIFC14 H26 O5 SiP 1 21 15.9878; 7.3276; 18.7222
90; 97.466; 90
814.49Markovič, Martin; Koóš, Peter; Čarný, Tomáš; Sokoliová, Saskia; Boháčiková, Nikola; Moncol, Ján; Gracza, Tibor
Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A.
Journal of natural products, 2017, 80, 1631-1638
1546204 CIFC14 H26 O5 SiP 1 21 16.2011; 7.0991; 19.423
90; 90.899; 90
854.94Markovič, Martin; Koóš, Peter; Čarný, Tomáš; Sokoliová, Saskia; Boháčiková, Nikola; Moncol, Ján; Gracza, Tibor
Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A.
Journal of natural products, 2017, 80, 1631-1638
1546205 CIFC14 H26 O5 SiP 1 21 15.9893; 7.3207; 18.7356
90; 97.532; 90
814.39Markovič, Martin; Koóš, Peter; Čarný, Tomáš; Sokoliová, Saskia; Boháčiková, Nikola; Moncol, Ján; Gracza, Tibor
Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A.
Journal of natural products, 2017, 80, 1631-1638
1546206 CIFC23 H28 O7P 1 21 124.3633; 9.12727; 31.0898
90; 109.128; 90
6531.8Hong, Min Jee; Kim, Jinwoong
Determination of the Absolute Configuration of Khellactone Esters from Peucedanum japonicum Roots.
Journal of natural products, 2017, 80, 1354-1360
1546207 CIFC30 H33 Cl3 N2 O2 SiP 1 21/c 111.2706; 28.0835; 10.5737
90; 116.053; 90
3006.69Rodriguez, Kevin X.; Kaltwasser, Nicolai; Toni, Tiffany A.; Ashfeld, Brandon L.
Rearrangement of an Intermediate Cyclopropyl Ketene in a Rh(II)-Catalyzed Formal [4 + 1]-Cycloaddition Employing Vinyl Ketenes as 1,4-Dipoles and Donor-Acceptor Metallocarbenes.
Organic letters, 2017, 19, 2482-2485
1546208 CIFC66 H70 I2 N36 O16R -3 :H28.8798; 28.8798; 25.2097
90; 90; 120
18209Jelínková, Kristýna; Surmová, Heda; Matelová, Alena; Rouchal, Michal; Prucková, Zdeňka; Dastychová, Lenka; Nečas, Marek; Vícha, Robert
Cubane Arrives on the Cucurbituril Scene.
Organic letters, 2017, 19, 2698-2701
1546209 CIFC16 H20 N4 O2P 1 21/c 15.4544; 18.7828; 14.6592
90; 92.914; 90
1499.88Jelínková, Kristýna; Surmová, Heda; Matelová, Alena; Rouchal, Michal; Prucková, Zdeňka; Dastychová, Lenka; Nečas, Marek; Vícha, Robert
Cubane Arrives on the Cucurbituril Scene.
Organic letters, 2017, 19, 2698-2701
1546210 CIFC15 H20 O3P 1 c 19.198; 9.442; 15.292
90; 104.995; 90
1282.8Liu, Xin; Liu, Junyang; Zhao, Jing; Li, Shaoping; Li, Chuang-Chuang
Toward the Total Synthesis of Eurifoloid A.
Organic letters, 2017, 19, 2742-2745
1546211 CIFC16 H12 Br NP -14.4612; 11.7056; 13.0331
67.332; 89.169; 81.812
621.02Kumar, Gangam Srikanth; Kumar, Pravin; Kapur, Manmohan
Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines.
Organic letters, 2017, 19, 2494-2497
1546212 CIFC21 H23 N3 O3P 1 21 18.0393; 8.6325; 13.2604
90; 90.9524; 90
920.13Tooriyama, Shino; Mimori, Yuji; Wu, Yuqiu; Kogure, Noriyuki; Kitajima, Mariko; Takayama, Hiromitsu
Asymmetric Total Synthesis of Pentacyclic Indole Alkaloid Andranginine and Absolute Configuration of Natural Product Isolated from Kopsia arborea.
Organic letters, 2017, 19, 2722-2725
1546213 CIFC25 H29 Br N2 O6P 21 21 2110.0435; 10.7709; 24.399
90; 90; 90
2639.4Möller, Guido P; Müller, Steffen; Wolfstädter, Bernd T; Wolfrum, Susanne; Schepmann, Dirk; Wünsch, Bernhard; Carreira, Erick M.
Oxetanyl Amino Acids for Peptidomimetics.
Organic letters, 2017, 19, 2510-2513
1546214 CIFC24 H30 Br N3 O5P 21 21 219.6689; 13.7338; 17.9303
90; 90; 90
2381Möller, Guido P; Müller, Steffen; Wolfstädter, Bernd T; Wolfrum, Susanne; Schepmann, Dirk; Wünsch, Bernhard; Carreira, Erick M.
Oxetanyl Amino Acids for Peptidomimetics.
Organic letters, 2017, 19, 2510-2513
1546215 CIFC14 H15 N O3P n m a25.771; 6.8258; 7.1894
90; 90; 90
1264.7Lv, Ningning; Chen, Zhengkai; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong
Synthesis of Functionalized Indenones via Rh-Catalyzed C-H Activation Cascade Reaction.
Organic letters, 2017, 19, 2588-2591
1546216 CIFC12 H8 F3 N O3P n a 2118.3137; 12.486; 4.8092
90; 90; 90
1099.7Lv, Ningning; Chen, Zhengkai; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong
Synthesis of Functionalized Indenones via Rh-Catalyzed C-H Activation Cascade Reaction.
Organic letters, 2017, 19, 2588-2591
1546217 CIFC21 H15 F O2P 1 21 16.2656; 15.4462; 8.1799
90; 94.209; 90
789.51Zhang, Zong-Feng; Zhu, Dong-Xing; Chen, Wen-Wen; Xu, Bin; Xu, Ming-Hua
Enantioselective Synthesis of gem-Diaryl Benzofuran-3(2H)-ones via One-Pot Asymmetric Rhodium/Palladium Relay Catalysis.
Organic letters, 2017, 19, 2726-2729
1546218 CIFC23 H15 N3 O2P -4 21 c21.6276; 21.6276; 8.1936
90; 90; 90
3832.6Barve, Indrajeet J.; Thikekar, Tushar Ulhas; Sun, Chung-Ming
Silver(I)-Catalyzed Regioselective Synthesis of Triazole Fused-1,5-Benzoxazocinones.
Organic letters, 2017, 19, 2370-2373
1546219 CIFC28 H41 N O11P 21 21 2110.77; 15.109; 17.72
90; 90; 90
2883Ma, Guo-Zhen; Li, Peng-Fei; Liu, Lu; Li, Wei-Dong Z; Chen, Li
Diastereoselective Synthesis of Cephalotaxus Esters via Asymmetric Mukaiyama Aldol Reaction.
Organic letters, 2017, 19, 2250-2253
1546220 CIFC11 H19 N O3P 21 21 217.784; 9.7886; 14.7958
90; 90; 90
1127.36Sekita, Hiroko; Adachi, Kyohei; Kobayashi, Ippei; Sato, Yusuke; Nakada, Masahisa
Enantio- and Stereoselective Construction of Atisane Scaffold via Organocatalytic Intramolecular Michael Reaction and Diels-Alder Reaction.
Organic letters, 2017, 19, 2390-2393
1546221 CIFC27 H36 Br N O2P 21 21 2110.5792; 12.2534; 20.4903
90; 90; 90
2656.2Roiser, Lukas; Waser, Mario
Enantioselective Spirocyclopropanation of para-Quinone Methides Using Ammonium Ylides.
Organic letters, 2017, 19, 2338-2341
1546222 CIFC20 H17 Br OP 1 21 19.4386; 11.6291; 14.6798
90; 93.296; 90
1608.6Yuan, Xiaoqian; Dong, Shupeng; Liu, Zhen; Wu, Guibing; Zou, Chuncheng; Ye, Jinxing
Enantioselective Michael Addition of Photogenerated o-Quinodimethanes to Enones Catalyzed by Chiral Amino Acid Esters.
Organic letters, 2017, 19, 2322-2325
1546223 CIFC26 H20 Cl2 OP 21 21 2110.6637; 10.7733; 18.111
90; 90; 90
2080.7Yuan, Xiaoqian; Dong, Shupeng; Liu, Zhen; Wu, Guibing; Zou, Chuncheng; Ye, Jinxing
Enantioselective Michael Addition of Photogenerated o-Quinodimethanes to Enones Catalyzed by Chiral Amino Acid Esters.
Organic letters, 2017, 19, 2322-2325
1546224 CIFC25 H23 N O2 SP 1 21 19.717; 11.448; 10.196
90; 112.48; 90
1048Najib, Atifah; Hirano, Koji; Miura, Masahiro
Palladium-Catalyzed Asymmetric Benzylic Substitution of Secondary Benzyl Carbonates with Nitrogen and Oxygen Nucleophiles.
Organic letters, 2017, 19, 2438-2441
1546225 CIFC29 H38 N2 O2 SP 1 21/c 119.884; 8.5199; 15.7656
90; 99.117; 90
2637.1Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1546226 CIFC27 H26 N2 O2 SP 1 21/c 113.1459; 11.374; 15.2985
90; 92.322; 90
2285.58Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1546227 CIFC25 H31 N O3 SP -19.2471; 10.0565; 12.1074
83.941; 76.636; 83.733
1085.11Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1546228 CIFC29 H30 Cl2 N2 O3 SP n a 2120.5163; 16.682; 7.9278
90; 90; 90
2713.3Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1546229 CIFC27 H27 N O3 SP 1 21/c 112.3798; 23.4215; 8.3687
90; 109.349; 90
2289.5Saputra, Mirza A.; Dange, Nitin S.; Cleveland, Alexander H.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations.
Organic letters, 2017, 19, 2414-2417
1546230 CIFC25 H27 N O2 SP -15.9068; 13.7441; 14.5687
109.313; 100.073; 97.026
1078.12Maiti, Saikat; Mal, Prasenjit
Dehydrogenative Aromatic Ring Fusion for Carbazole Synthesis via C-C/C-N Bond Formation and Alkyl Migration.
Organic letters, 2017, 19, 2454-2457
1546231 CIFC34 H28 N2 O2P -19.9922; 19.11; 21.951
89.352; 86.158; 85.402
4168.6Zheng, Jiuan; Li, Panpan; Gu, Meng; Lin, Aijun; Yao, Hequan
Synthesis of Spiropentadiene Pyrazolones by Rh(III)-Catalyzed Formal sp(3) C-H Activation/Annulation.
Organic letters, 2017, 19, 2829-2832
1546232 CIFC24 H14 F3 N OP 1 21/c 110.4652; 10.8048; 17.209
90; 105.635; 90
1873.9Xiang, Jia-Chen; Cheng, Yan; Wang, Zi-Xuan; Ma, Jin-Tian; Wang, Miao; Tang, Bo-Cheng; Wu, Yan-Dong; Wu, An-Xin
Oxidative Trimerization of Amino Acids: Selective Synthesis of 2,3,5-Trisubstituted Pyridines.
Organic letters, 2017, 19, 2997-3000
1546233 CIFC20 H20 F3 N O4P 1 21/n 110.6016; 6.4032; 27.3243
90; 91.4282; 90
1854.31Gietter-Burch, Amber A S; Devannah, Vijayarajan; Watson, Donald A.
Trifluoromethylation of Secondary Nitroalkanes.
Organic letters, 2017, 19, 2957-2960
1546234 CIFC22 H20 N4 O5P -17.3583; 8.6653; 15.7812
94.049; 95.948; 105.631
958.7Xie, Jiaxin; Wang, Jianchun; Dong, Guangbin
Synthetic Study of Phainanoids. Highly Diastereoselective Construction of the 4,5-Spirocycle via Palladium-Catalyzed Intramolecular Alkenylation.
Organic letters, 2017, 19, 3017-3020
1546235 CIFC26 H25 N3 O6 S2P 1 21/n 111.9761; 12.0471; 17.418
90; 98.702; 90
2484.1Wu, Zhengxing; Wen, Ke; Zhang, Jingang; Zhang, Wanbin
Pd(II)-Catalyzed Aerobic Intermolecular 1,2-Diamination of Conjugated Dienes: A Regio- and Chemoselective [4 + 2] Annulation for the Synthesis of Tetrahydroquinoxalines.
Organic letters, 2017, 19, 2813-2816
1546236 CIFC22 H24 Cl N2 O RhP 1 21/n 17.58618; 16.9757; 15.6843
90; 93.0656; 90
2016.94Long, Zhen; Wang, Zhigang; Zhou, Danni; Wan, Danyang; You, Jingsong
Rh(III)-Catalyzed Regio- and Chemoselective [4 + 1]-Annulation of Azoxy Compounds with Diazoesters for the Synthesis of 2H-Indazoles: Roles of the Azoxy Oxygen Atom.
Organic letters, 2017, 19, 2777-2780
1546237 CIFC28 H25 N O4P c a 2114.8441; 10.42006; 14.7439
90; 90; 90
2280.53Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546238 CIFC17 H19 N O5P -18.1791; 8.4632; 11.3125
70.672; 84.194; 80.842
728.52Ma, Xiao-Yan; An, Xian-Tao; Zhao, Xian-He; Du, Ji-Yuan; Deng, Yu-Hua; Zhang, Xiang-Zhi; Fan, Chun-An
Au-Catalyzed [2 + 3] Annulation of Enamides with Propargyl Esters: Total Synthesis of Cephalotaxine and Cephalezomine H.
Organic letters, 2017, 19, 2965-2968
1546239 CIFC21 H20 N2P 3 1 c18.6655; 18.6655; 8.1126
90; 90; 120
2447.8Zhu, Zhengbo; Seidel, Daniel
Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization.
Organic letters, 2017, 19, 2841-2844
1546240 CIFC19 H25 O8P 21 21 216.4987; 6.9114; 41.4349
90; 90; 90
1861.05Nur-E-Alam, Mohammad; Yousaf, Muhammad; Ahmed, Sarfaraz; Al-Sheddi, Ebtesam S; Parveen, Ifat; Fazakerley, David M.; Bari, Ahmed; Ghabbour, Hazem A.; Threadgill, Michael D.; Whatley, Kezia C. L.; Hoffmann, Karl F.; Al-Rehaily, Adnan J
Neoclerodane Diterpenoids from Reehal Fatima, Teucrium yemense.
Journal of natural products, 2017, 80, 1900-1908
1546241 CIFC41 H34 F3 N3 O2P -19.5081; 13.6271; 14.3689
105.485; 106.87; 99.403
1657.4Ye, Tzuen-Yang; Selvaraju, Manikandan; Sun, Chung-Ming
Cascade Synthesis of Benzimidazole-Linked Pyrroles via Copper Catalyzed Oxidative Cyclization and Ketonization.
Organic letters, 2017, 19, 3103-3106
1546242 CIFC33 H27 N3 O4 SP -19.4864; 9.9158; 15.8741
82.816; 79.911; 71.445
1389.8Ye, Tzuen-Yang; Selvaraju, Manikandan; Sun, Chung-Ming
Cascade Synthesis of Benzimidazole-Linked Pyrroles via Copper Catalyzed Oxidative Cyclization and Ketonization.
Organic letters, 2017, 19, 3103-3106
1546243 CIFC61.5 H59 Al Cl8 N4 NiP 1 21 116.975; 15.547; 24.68
90; 101.91; 90
6373Gomes, Pedro T.; Gomes, Clara S. B.; Ribeiro, Alejandro F. G.; Fernandes, Anabela C.; Bento, Artur; do Rosário Ribeiro, Maria; Pascu, Sofia I.; Kociok-Kohn, Gabriele; Duarte, Maria Teresa Teresa
Reactivity of cationic α-diimine cyclopentadienyl nickel complexes towards AlEt2Cl: Synthesis, characterisation and ethylene polymerisation
Catal. Sci. Technol., 2017
1546244 CIFC90 H84 Al Cl9 N6 Ni3P -114.507; 16.966; 19.647
112.115; 101.465; 100.432
4212.5Gomes, Pedro T.; Gomes, Clara S. B.; Ribeiro, Alejandro F. G.; Fernandes, Anabela C.; Bento, Artur; do Rosário Ribeiro, Maria; Pascu, Sofia I.; Kociok-Kohn, Gabriele; Duarte, Maria Teresa Teresa
Reactivity of cationic α-diimine cyclopentadienyl nickel complexes towards AlEt2Cl: Synthesis, characterisation and ethylene polymerisation
Catal. Sci. Technol., 2017
1546245 CIFC34.25 H41.5 Al Cl4.75 N2 NiP 1 21 112.652; 23.843; 12.739
90; 100.858; 90
3774.07Gomes, Pedro T.; Gomes, Clara S. B.; Ribeiro, Alejandro F. G.; Fernandes, Anabela C.; Bento, Artur; do Rosário Ribeiro, Maria; Pascu, Sofia I.; Kociok-Kohn, Gabriele; Duarte, Maria Teresa Teresa
Reactivity of cationic α-diimine cyclopentadienyl nickel complexes towards AlEt2Cl: Synthesis, characterisation and ethylene polymerisation
Catal. Sci. Technol., 2017
1546246 CIFC123 H254 K2 N2 O32 Si8 U2F d d 292.6284; 24.32104; 13.71515
90; 90; 90
30897.8Kelly, Rory P.; Falcone, Marta; Lamsfus, Carlos Alvarez; Scopelliti, Rosario; Maron, Laurent; Meyer, Karsten; Mazzanti, Marinella
Metathesis of a UV imido complex: a route to a terminal UV sulfide
Chem. Sci., 2017
1546247 CIFC66 H144 K N2 O22 Si4 UP 21 21 2125.92909; 26.18261; 26.16679
90; 90; 90
17764.4Kelly, Rory P.; Falcone, Marta; Lamsfus, Carlos Alvarez; Scopelliti, Rosario; Maron, Laurent; Meyer, Karsten; Mazzanti, Marinella
Metathesis of a UV imido complex: a route to a terminal UV sulfide
Chem. Sci., 2017
1546248 CIFC73 H152 K N2 O22 S Si4 UP -114.4445; 14.4565; 47.0418
82.352; 84.245; 78.583
9515.4Kelly, Rory P.; Falcone, Marta; Lamsfus, Carlos Alvarez; Scopelliti, Rosario; Maron, Laurent; Meyer, Karsten; Mazzanti, Marinella
Metathesis of a UV imido complex: a route to a terminal UV sulfide
Chem. Sci., 2017
1546249 CIFC26 H48 K2 O12 S6P 1 21/c 119.133; 9.457; 22.775
90; 111.465; 90
3835.1Kelly, Rory P.; Falcone, Marta; Lamsfus, Carlos Alvarez; Scopelliti, Rosario; Maron, Laurent; Meyer, Karsten; Mazzanti, Marinella
Metathesis of a UV imido complex: a route to a terminal UV sulfide
Chem. Sci., 2017
1546250 CIFC74 H152 K N2 O22 S3 Si4 UP 1 21 113.827; 24.6484; 14.3945
90; 99.042; 90
4844.9Kelly, Rory P.; Falcone, Marta; Lamsfus, Carlos Alvarez; Scopelliti, Rosario; Maron, Laurent; Meyer, Karsten; Mazzanti, Marinella
Metathesis of a UV imido complex: a route to a terminal UV sulfide
Chem. Sci., 2017
1546251 CIFC39 H30 Cl6 F2 N P PtP 1 21/n 111.49295; 22.2749; 14.299
90; 91.1028; 90
3659.93Shaw, Paul Anthony; Clarkson, Guy James; Rourke, Jonathan P.
Reversible C-C bond formation at a triply cyclometallated platinum(IV) centre
Chem. Sci., 2017
1546252 CIFC38 H30 F2 N P PtP -112.1213; 12.1909; 12.2729
68.816; 69.917; 64.636
1489.24Shaw, Paul Anthony; Clarkson, Guy James; Rourke, Jonathan P.
Reversible C-C bond formation at a triply cyclometallated platinum(IV) centre
Chem. Sci., 2017
1546253 CIFC38 H29 Cl F2 N P PtP -111.3911; 11.7933; 12.863
100.845; 97.595; 117.163
1462.19Shaw, Paul Anthony; Clarkson, Guy James; Rourke, Jonathan P.
Reversible C-C bond formation at a triply cyclometallated platinum(IV) centre
Chem. Sci., 2017
1546254 CIFC42 H34 Cl10 F2 N O P PtI 1 2/a 123.6952; 14.2502; 27.6824
90; 103.199; 90
9100.3Shaw, Paul Anthony; Clarkson, Guy James; Rourke, Jonathan P.
Reversible C-C bond formation at a triply cyclometallated platinum(IV) centre
Chem. Sci., 2017

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