Crystallography Open Database

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4515459 CIFC32 H26 Mn N2 O3 PP 1 21/c 19.7663; 16.9042; 16.0896
90; 97.951; 90		2630.72Das, Uttam Kumar; Ben-David, Yehoshoa; Leitus, Gregory; Diskin-Posner, Yael; Milstein, David
Dehydrogenative Cross-Coupling of Primary Alcohols To Form Cross-Esters Catalyzed by a Manganese Pincer Complex
ACS Catalysis, 2018, 9, 479
4515460 CIFC18 H23 N3 O2P 1 21/c 18.3986; 10.167; 18.964
90; 101.38; 90		1587.5van der Puyl, Vincent A.; Derosa, Joseph; Engle, Keary M.
Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds
ACS Catalysis, 2018, 9, 224
4515461 CIFC20 H27 N3 O2P -19.4368; 11.2965; 18.1549
81.081; 81.652; 73.77		1825.2van der Puyl, Vincent A.; Derosa, Joseph; Engle, Keary M.
Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds
ACS Catalysis, 2018, 9, 224
4515462 CIFC22 H33 B F2 O4 SiP 21 21 217.4443; 10.4007; 31.5827
90; 90; 90		2445.32Guo, Wen-Hao; Zhao, Hai-Yang; Luo, Zhi-Ji; Zhang, Shu; Zhang, Xingang
Fluoroalkylation–Borylation of Alkynes: An Efficient Method To Obtain (Z)-Tri- and Tetrasubstituted Fluoroalkylated Alkenylboronates
ACS Catalysis, 2018, 9, 38
4515463 CIFC28 H47 B O8 P2 PdC 1 2/c 126.0162; 11.1134; 23.2857
90; 108.358; 90		6389.9Espinosa, Matthew R.; Charboneau, David J.; Garcia de Oliveira, André; Hazari, Nilay
Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels
ACS Catalysis, 2018, 9, 301
4515464 CIFC9 H15 B O2I 41/a c d :213.2301; 13.2301; 38.893
90; 90; 90		6807.7Espinosa, Matthew R.; Charboneau, David J.; Garcia de Oliveira, André; Hazari, Nilay
Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels
ACS Catalysis, 2018, 9, 301
4515465 CIFC15 H15 Cl N2P 1 21/n 18.473; 17.4446; 9.0374
90; 94.072; 90		1332.43Fu, Niankai; Shen, Yifan; Allen, Anthony R.; Song, Lu; Ozaki, Atsushi; Lin, Song
Mn-Catalyzed Electrochemical Chloroalkylation of Alkenes.
ACS catalysis, 2019, 9, 746-754
4515466 CIFC18 H14 F3 N O4P 1 21 111.8498; 9.5906; 14.708
90; 96.008; 90		1662.33Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515467 CIFC17 H15 N O4P 1 21 113.5517; 9.2461; 11.8061
90; 106.796; 90		1416.2Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515468 CIFC60 H79 N6 O15 PP 21 21 219.8665; 19.0145; 31.36
90; 90; 90		5883.3Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515469 CIFC17 H14 Br N O4I 1 2 122.7393; 5.2121; 14.2943
90; 93.045; 90		1691.76Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515470 CIFC17 H15 N O4P 1 21 110.8042; 8.4963; 15.825
90; 103.232; 90		1414.1Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515471 CIFC18 H17 N O4P -19.806; 14.9855; 21.2136
89.141; 86.664; 88.303		3110.4Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515472 CIFC36 H57 N7 O7C 1 2 126.466; 17.7566; 22.8328
90; 124.789; 90		8812.3Featherston, Aaron L.; Shugrue, Christopher R.; Mercado, Brandon Q.; Miller, Scott J.
Phosphothreonine (pThr)-Based Multifunctional Peptide Catalysis for Asymmetric Baeyer-Villiger Oxidations of Cyclobutanones.
ACS catalysis, 2019, 9, 242-252
4515473 CIFC20 H23 N O2P b c a13.76; 7.1297; 34.2631
90; 90; 90		3361.37Ho, Hon Eong; Stephens, Thomas C.; Payne, Thomas J.; O’Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics
ACS Catalysis, 2018, 9, 504
4515474 CIFC45.67 H35.35 Cl3.35 N2 O2I 1 2/a 17.38319; 26.3138; 19.6731
90; 93.6518; 90		3814.33Ho, Hon Eong; Stephens, Thomas C.; Payne, Thomas J.; O’Brien, Peter; Taylor, Richard J. K.; Unsworth, William P.
Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics
ACS Catalysis, 2018, 9, 504
4515475 CIFC22 H40 Mn N3 O5 P2 SP b c a11.5; 14.765; 34.41
90; 90; 90		5843Bertini, Federica; Glatz, Mathias; Stöger, Berthold; Peruzzini, Maurizio; Veiros, Luis F.; Kirchner, Karl; Gonsalvi, Luca
Carbon Dioxide Reduction to Methanol Catalyzed by Mn(I) PNP Pincer Complexes under Mild Reaction Conditions
ACS Catalysis, 2018, 9, 632
4515476 CIFC27 H29 NP -18.9763; 10.84; 11.572
109.84; 99.23; 93.29		1037.8Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui
Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C–H Activation
ACS Catalysis, 2018, 9, 599
4515477 CIFC23 H40 N Sc Si2P -19.616; 10.433; 13.436
100.936; 95.927; 95.808		1306.3Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui
Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C‒H Activation
ACS Catalysis, 2018, 9, 599
4515478 CIFC15 H24 F6 N PC 1 c 119.003; 10.452; 8.8763
90; 96.73; 90		1750.9Tang, Bin; Hu, Xiaoyan; Liu, Chunli; Jiang, Tao; Alam, Fakhre; Chen, Yanhui
Tandem Cyclization/Hydroarylation of α,ω-Dienes Triggered by Scandium-Catalyzed C–H Activation
ACS Catalysis, 2018, 9, 599
4515479 CIFC29 H20 B F18 N6 RhP 1 21/c 118.0106; 9.0679; 19.7109
90; 96.859; 90		3196.1Avullala, Thirupataiah; Asgari, Parham; Hua, Yuanda; Bokka, Apparao; Ridlen, Shawn G.; Yum, Kyungsuk; Dias, H. V. Rasika; Jeon, Junha
Umpolung <i>α</i>-Silylation of Cyclopropyl Acetates via Low-Temperature Catalytic C-C Activation.
ACS catalysis, 2019, 9, 402-408
4515480 CIFC36 H48 Cl2 N2 O RuP 1 21/c 119.3364; 10.43031; 16.58648
90; 95.7369; 90		3328.48Małecki, Paweł; Gajda, Katarzyna; Gajda, Roman; Woźniak, Krzysztof; Trzaskowski, Bartosz; Kajetanowicz, Anna; Grela, Karol
Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application
ACS Catalysis, 2018, 9, 587
4515481 CIFC53 H50 Cl2 N2 O RuP 1 21/n 113.16; 10.12687; 37.8176
90; 98.1376; 90		4989.19Małecki, Paweł; Gajda, Katarzyna; Gajda, Roman; Woźniak, Krzysztof; Trzaskowski, Bartosz; Kajetanowicz, Anna; Grela, Karol
Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application
ACS Catalysis, 2018, 9, 587
4515482 CIFC41 H48 Br N3 O7P 21 21 2111.6704; 12.4895; 24.8148
90; 90; 90		3616.94Paria, Suva; Kang, Qi-Kai; Hatanaka, Miho; Maruoka, Keiji
Design of Efficient Chiral Bifunctional Phase-Transfer Catalysts Possessing an Amino Functionality for Asymmetric Aminations
ACS Catalysis, 2018, 9, 78
4515483 CIFC71 H72 N2 NiP 21 21 2114.9159; 18.747; 20.4012
90; 90; 90		5704.8Cai, Yuan; Zhang, Jia-Wen; Li, Feng; Liu, Jia-Ming; Shi, Shi-Liang
Nickel/N-Heterocyclic Carbene Complex-Catalyzed Enantioselective Redox-Neutral Coupling of Benzyl Alcohols and Alkynes to Allylic Alcohols
ACS Catalysis, 2018, 9, 1
4515484 CIFC23 H22 N2 O4 S2P 19.0036; 10.9036; 11.9944
103.063; 98.741; 91.068		1132Yang, Shengbiao; Wang, Lihong; Zhang, Hongwei; Liu, Chunyang; Zhang, Linli; Wang, Xiaomin; Zhang, Ge; Li, Yan; Zhang, Qian
Copper-Catalyzed Asymmetric Aminocyanation of Arylcyclopropanes for Synthesis of γ-Amino Nitriles
ACS Catalysis, 2018, 9, 716
4515485 CIFC37 H31 F2 I P2 PdC 1 2/c 112.09; 15.2246; 20.0614
90; 91.35; 90		3691.6Hori, Kaishi; Motohashi, Hirotaka; Saito, Daichi; Mikami, Koichi
Precatalyst Effects on Pd-Catalyzed Cross-Coupling Difluoromethylation of Aryl Boronic Acids
ACS Catalysis, 2018, 9, 417
4515486 CIFC56 H34 F16 Ir N4 PC 1 2/c 116.49; 22.606; 13.5064
90; 90.007; 90		5034.8Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François
Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
ACS Catalysis, 2018, 9, 1320
4515487 CIFC49 H32 Cl2 F16 Ir N4 PP -111.7565; 12.8586; 18.657
81.314; 80.238; 73.409		2648.1Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François
Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
ACS Catalysis, 2018, 9, 1320
4515488 CIFC56 H34 F16 Ir N4 PR -3 :H26.5472; 26.5472; 38.495
90; 90; 120		23494.8Boyaala, Rabab; Touzani, Rachid; Roisnel, Thierry; Dorcet, Vincent; Caytan, Elsa; Jacquemin, Denis; Boixel, Julien; Guerchais, Véronique; Doucet, Henri; Soulé, Jean-François
Catalyst-Controlled Regiodivergent C‒H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
ACS Catalysis, 2018, 9, 1320
4515489 CIFC27 H43 Al Cl N3 Si3P -19.6279; 10.9013; 17.0857
98.271; 102.568; 108.408		1616.39Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515490 CIFC24 H24 Al N3P 21 21 217.3795; 13.4511; 21.1096
90; 90; 90		2095.39Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515491 CIFC18 H19 Al Cl N3P 1 21/c 18.9033; 22.602; 8.763
90; 100.967; 90		1731.2Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515492 CIFC35 H44 Al N4P -19.0364; 10.9957; 16.5417
91.033; 97.953; 107.345		1550.72Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515493 CIFC29 H33 Al N3P 1 21/n 19.6204; 24.1661; 10.8834
90; 94.131; 90		2523.68Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515494 CIFC33 H48 Al N3 Si3P -19.2076; 12.1268; 16.763
98.513; 98.865; 103.694		1763.3Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515495 CIFC15 H24 Al Cl4 N3 O7P 1 21/n 17.0617; 25.6486; 13.413
90; 105.218; 90		2344.2Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515496 CIFC27 H37 Al Cl N3P 1 21/n 19.2525; 15.9339; 17.4939
90; 95.425; 90		2567.5Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515497 CIFC27 H38 Al N3P -18.9098; 9.0012; 17.5788
89.93; 76.945; 69.158		1278.64Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515498 CIFC33 H42 Al N3P 1 21/c 116.055; 10.4568; 35.146
90; 98.496; 90		5835.7Zhang, Guoqi; Wu, Jing; Zeng, Haisu; Neary, Michelle C.; Devany, Matthew; Zheng, Shengping; Dub, Pavel A.
Dearomatization and Functionalization of Terpyridine Ligands Leading to Unprecedented Zwitterionic Meisenheimer Aluminum Complexes and Their Use in Catalytic Hydroboration
ACS Catalysis, 2018, 9, 874
4515499 CIFC57 H34 B2 F30 Nd Si3C 1 2/c 139.687; 12.1443; 26.344
90; 98.409; 90		12561Schmidt, Bradley M.; Pindwal, Aradhana; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Zwitterionic Trivalent (Alkyl)lanthanide Complexes in Ziegler-Type Butadiene Polymerization
ACS Catalysis, 2018, 9, 827
4515500 CIFC20 H16 O4I 1 a 16.101; 7.1857; 36.046
90; 94.848; 90		1574.6Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515501 CIFC23 H31 Cl Fe N2P 1 2/c 114.4785; 9.0523; 16.7522
90; 92.179; 90		2194Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515502 CIFC29 H35 Cl Fe N2P b c a16.5485; 10.4399; 31.246
90; 90; 90		5398.2Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515503 CIFC26 H38 Cl Fe N3P b c a11.9206; 15.6644; 27.735
90; 90; 90		5178.93Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515504 CIFC37 H40 Fe N2P 1 21/c 112.631; 15.5444; 16.5595
90; 105.365; 90		3135.1Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515505 CIFC25 H35 Cl Fe N2P 1 21/c 117.827; 15.8552; 11.0869
90; 104.133; 90		3038.9Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515506 CIFC24 H20 Fe2P 1 21/n 111.736; 10.478; 14.979
90; 102.775; 90		1796.4Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515507 CIFC28 H41 Cl Fe N2P 21 21 218.6146; 17.039; 19.7629
90; 90; 90		2900.9Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515508 CIFC32 H41 Cl Fe N2P 1 21/c 18.4344; 22.681; 15.3166
90; 90.017; 90		2930.1Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515509 CIFC26 H37 Cl Fe N2P 1 21/c 18.5309; 16.6841; 17.0048
90; 91.196; 90		2419.8Liang, Qiuming; Sheng, Kai; Salmon, Andrew; Zhou, Vivian Yue; Song, Datong
Active Iron(II) Catalysts toward gem-Specific Dimerization of Terminal Alkynes
ACS Catalysis, 2018, 9, 810
4515510 CIFC19 H13 N O4 SP -17.0423; 9.2936; 12.8025
89.117; 75.476; 77.243		790.39Shu, Chao; Shi, Chong-Yang; Sun, Qing; Zhou, Bo; Li, Tian-You; He, Qiao; Lu, Xin; Liu, Rai-Shung; Ye, Long-Wu
Generation of Endocyclic Vinyl Carbene Complexes via Gold-Catalyzed Oxidative Cyclization of Terminal Diynes: Toward Naphthoquinones and Carbazolequinones
ACS Catalysis, 2018, 9, 1019
4515511 CIFC30 H29 Al N4 OP -19.633; 11.189; 12.051
89.56; 71.1; 83.22		1220Mandal, Mukunda; Luke, Anna M.; Dereli, Büşra; Elwell, Courtney E.; Reineke, Theresa M.; Tolman, William B.; Cramer, Christopher J.
Computational Prediction and Experimental Verification of ε-Caprolactone Ring-Opening Polymerization Activity by an Aluminum Complex of an Indolide/Schiff-Base Ligand
ACS Catalysis, 2018, 9, 885
4515512 CIFC26 H30 N2 O3P 21 21 219.1036; 13.3256; 36.2038
90; 90; 90		4391.92Shen, Hong-Cheng; Zhang, Ling; Chen, Shu-Sen; Feng, Jiajie; Zhang, Bo-Wen; Zhang, Ying; Zhang, Xinhao; Wu, Yun-Dong; Gong, Liu-Zhu
Enantioselective Addition of Cyclic Ketones to Unactivated Alkenes Enabled by Amine/Pd(II) Cooperative Catalysis
ACS Catalysis, 2018, 9, 791
4515513 CIFC25 H27 Br N2 O2P 21 21 219.0909; 13.2501; 36.0908
90; 90; 90		4347.3Shen, Hong-Cheng; Zhang, Ling; Chen, Shu-Sen; Feng, Jiajie; Zhang, Bo-Wen; Zhang, Ying; Zhang, Xinhao; Wu, Yun-Dong; Gong, Liu-Zhu
Enantioselective Addition of Cyclic Ketones to Unactivated Alkenes Enabled by Amine/Pd(II) Cooperative Catalysis
ACS Catalysis, 2018, 9, 791
4516631 CIFC15 H12 Co2 N4 O7C 1 2/c 134.882; 10.203; 13.579
90; 112.867; 90		4453Wang, Hai-Hua; Hou, Lei; Li, Yong-Zhi; Jiang, Chen-Yu; Wang, Yao-Yu; Zhu, Zhonghua
Porous MOF with Highly Efficient Selectivity and Chemical Conversion for CO<sub>2</sub>.
ACS applied materials & interfaces, 2017, 9, 17969-17976
4516632 CIFC36 H24 Cl2 Cu12 N36 Na2 O24P -110.5333; 12.8234; 13.1215
84.199; 82.718; 67.584		1622.5Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516633 CIFC36 H24 Br2 Cu12 N36 Na2 O24P -110.327; 13.165; 13.182
89.986; 81.289; 68.559		1645.9Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516634 CIFC36 H24 Cu12 I2 N36 Na2 O24P -110.397; 13.176; 13.196
89.966; 81.245; 69.982		1676.1Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516635 CIFC18 H12 Cl Cu6 K N18 O12P -110.602; 12.725; 13.11
83.607; 81.991; 67.784		1618Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516636 CIFC18 H12 Br Cu6 K N18 O12P -110.2886; 13.1326; 13.1248
89.9; 68.551; 81.119		1627.88Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516637 CIFC18 H12 Cu6 I K N18 O12P -110.336; 13.12; 13.11
89.928; 69.412; 81.047		1641.3Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516638 CIFC45 H64 Cu6 F N33 O27P -112.9723; 15.0889; 17.921
90.4389; 90.3035; 93.3656		3501.6Guo, Ling-Yu; Su, Hai-Feng; Kurmoo, Mohamedally; Wang, Xing-Po; Zhao, Quan-Qin; Lin, Shui-Chao; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
Multifunctional Triple-Decker Inverse 12-Metallacrown-4 Sandwiching Halides.
ACS applied materials & interfaces, 2017, 9, 19980-19987
4516639 CIFC36 H34 B NP 1 21/c 113.112; 13.4058; 16.2914
90; 101.021; 90		2810.84Lee, Young Hoon; Park, Sunghee; Oh, Jihun; Shin, Jong Won; Jung, Jaehoon; Yoo, Seunghyup; Lee, Min Hyung
Rigidity-Induced Delayed Fluorescence by Ortho Donor-Appended Triarylboron Compounds: Record-High Efficiency in Pure Blue Fluorescent Organic Light-Emitting Diodes.
ACS applied materials & interfaces, 2017, 9, 24035-24042
4516640 CIFC36 H34 B N OP 1 21/c 115.361; 12.176; 14.9
90; 90.95; 90		2786.4Lee, Young Hoon; Park, Sunghee; Oh, Jihun; Shin, Jong Won; Jung, Jaehoon; Yoo, Seunghyup; Lee, Min Hyung
Rigidity-Induced Delayed Fluorescence by Ortho Donor-Appended Triarylboron Compounds: Record-High Efficiency in Pure Blue Fluorescent Organic Light-Emitting Diodes.
ACS applied materials & interfaces, 2017, 9, 24035-24042
4516641 CIFC36 H34 B NP 1 21/n 18.346; 18.245; 17.714
90; 93.04; 90		2693.6Lee, Young Hoon; Park, Sunghee; Oh, Jihun; Shin, Jong Won; Jung, Jaehoon; Yoo, Seunghyup; Lee, Min Hyung
Rigidity-Induced Delayed Fluorescence by Ortho Donor-Appended Triarylboron Compounds: Record-High Efficiency in Pure Blue Fluorescent Organic Light-Emitting Diodes.
ACS applied materials & interfaces, 2017, 9, 24035-24042
4516642 CIFC26 H18 Co4 N20 O10P -17.988; 9.978; 11.035
104.884; 98.534; 103.807		804.6Gong, Teng; Lou, Xiaobing; Gao, En-Qing; Hu, Bingwen
Pillared-Layer Metal-Organic Frameworks for Improved Lithium-Ion Storage Performance.
ACS applied materials & interfaces, 2017, 9, 21839-21847
4516643 CIFC22 H36 N2 O6P 21 21 215.6365; 7.316; 54.623
90; 90; 90		2252.5Nuthanakanti, Ashok; Srivatsan, Seergazhi G.
Surface-Tuned and Metal-Ion-Responsive Supramolecular Gels Based on Nucleolipids.
ACS applied materials & interfaces, 2017, 9, 22864-22874
4516644 CIFC26 H44 N2 O6P 21 21 215.5928; 7.2712; 63.511
90; 90; 90		2582.8Nuthanakanti, Ashok; Srivatsan, Seergazhi G.
Surface-Tuned and Metal-Ion-Responsive Supramolecular Gels Based on Nucleolipids.
ACS applied materials & interfaces, 2017, 9, 22864-22874
4516645 CIFC24 H40 N2 O6P 21 21 215.6059; 7.3036; 59.161
90; 90; 90		2422.24Nuthanakanti, Ashok; Srivatsan, Seergazhi G.
Surface-Tuned and Metal-Ion-Responsive Supramolecular Gels Based on Nucleolipids.
ACS applied materials & interfaces, 2017, 9, 22864-22874
4516646 CIFC45 H28 N10 Ni3 O18R -3 :H22.3712; 22.3712; 95.1715
90; 90; 120		41249.3Yu, Mei-Hui; Zhang, Ping; Feng, Rui; Yao, Zhao-Quan; Yu, Yi-Chen; Hu, Tong-Liang; Bu, Xian-He
Construction of a Multi-Cage-Based MOF with a Unique Network for Efficient CO<sub>2</sub> Capture.
ACS applied materials & interfaces, 2017, 9, 26177-26183
4516647 CIFC54 H24 Br6 Fe2 N6 O26P -3 1 m13.7841; 13.7841; 9.2424
90; 90; 120		1520.8Benmansour, Samia; Abhervé, Alexandre; Gómez-Claramunt, Patricia; Vallés-García, Cristina; Gómez-García, Carlos J
Nanosheets of Two-Dimensional Magnetic and Conducting Fe(II)/Fe(III) Mixed-Valence Metal-Organic Frameworks.
ACS applied materials & interfaces, 2017, 9, 26210-26218
4516648 CIFC54 H24 Cl6 Fe2 N6 O26P -3 1 m13.6909; 13.6909; 9.1968
90; 90; 120		1492.9Benmansour, Samia; Abhervé, Alexandre; Gómez-Claramunt, Patricia; Vallés-García, Cristina; Gómez-García, Carlos J
Nanosheets of Two-Dimensional Magnetic and Conducting Fe(II)/Fe(III) Mixed-Valence Metal-Organic Frameworks.
ACS applied materials & interfaces, 2017, 9, 26210-26218
4516649 CIFC27 H30 B3 N3 O9P -115.255; 15.812; 16.019
61.29; 71.61; 83		3214Gontarczyk, Krzysztof; Bury, Wojciech; Serwatowski, Janusz; Wieciński, Piotr; Woźniak, Krzysztof; Durka, Krzysztof; Luliński, Sergiusz
Hybrid Triazine-Boron Two-Dimensional Covalent Organic Frameworks: Synthesis, Characterization, and DFT Approach to Layer Interaction Energies.
ACS applied materials & interfaces, 2017, 9, 31129-31141
4516650 CIFC42 H33 In3 N0 O20 P2C 1 2/c 128.825; 11.472; 18.905
90; 106.62; 90		5990Du, Xi; Fan, Ruiqing; Qiang, Liangsheng; Xing, Kai; Ye, Haoxin; Ran, Xinya; Song, Yang; Wang, Ping; Yang, Yulin
Controlled Zn<sup>2+</sup>-Triggered Drug Release by Preferred Coordination of Open Active Sites within Functionalization Indium Metal Organic Frameworks.
ACS applied materials & interfaces, 2017, 9, 28939-28948
4516651 CIFC21 H12 In N0 O7 PR 3 :H14.1755; 14.1755; 9.5058
90; 90; 120		1654.2Du, Xi; Fan, Ruiqing; Qiang, Liangsheng; Xing, Kai; Ye, Haoxin; Ran, Xinya; Song, Yang; Wang, Ping; Yang, Yulin
Controlled Zn<sup>2+</sup>-Triggered Drug Release by Preferred Coordination of Open Active Sites within Functionalization Indium Metal Organic Frameworks.
ACS applied materials & interfaces, 2017, 9, 28939-28948
4516652 CIFC52 H36 Cd5 N8 O28I 1 2/a 116.039; 13.034; 42.157
90; 100.927; 90		8653Hong, Xu-Jia; Wei, Qin; Cai, Yue-Peng; Wu, Bing-Bing; Feng, Hai-Xing; Yu, Ying; Dong, Ren-Feng
Pillar-Layered Metal-Organic Framework with Sieving Effect and Pore Space Partition for Effective Separation of Mixed Gas C<sub>2</sub>H<sub>2</sub>/C<sub>2</sub>H<sub>4</sub>.
ACS applied materials & interfaces, 2017, 9, 29374-29379
4516742 CIFC78 H60 Cu3 N8 O15R -3 :H15.598; 15.598; 59.01
90; 90; 120		12434Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian
Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction
ACS Catalysis, 2019, 9, 1726
4516743 CIFC78 H66 Co3 N8 O18R -3 :H15.7439; 15.7439; 61.146
90; 90; 120		13125.7Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian
Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction
ACS Catalysis, 2019, 9, 1726
4516744 CIFC468 H450 N48 Ni18 O135R -3 :H15.7128; 15.7128; 60.539
90; 90; 120		12944.1Wang, Xiao-Kun; Liu, Jiang; Zhang, Lei; Dong, Long-Zhang; Li, Shun-Li; Kan, Yu-He; Li, Dong-Sheng; Lan, Ya-Qian
Monometallic Catalytic Models Hosted in Stable Metal‒Organic Frameworks for Tunable CO2 Photoreduction
ACS Catalysis, 2019, 9, 1726
4516815 CIFC11 H6 Br NP -14.7861; 5.9851; 7.9546
83.224; 75.23; 84.63		218.31Ossowski, Jakub; Wächter, Tobias; Silies, Laura; Kind, Martin; Noworolska, Agnieszka; Blobner, Florian; Gnatek, Dominika; Rysz, Jakub; Bolte, Michael; Feulner, Peter; Terfort, Andreas; Cyganik, Piotr; Zharnikov, Michael
Thiolate versus Selenolate: Structure, Stability, and Charge Transfer Properties.
ACS nano, 2015, 9, 4508-4526
4516816 CIFC11 H8 Br N OP 1 21/c 118.518; 6.151; 8.6436
90; 90.291; 90		984.53Ossowski, Jakub; Wächter, Tobias; Silies, Laura; Kind, Martin; Noworolska, Agnieszka; Blobner, Florian; Gnatek, Dominika; Rysz, Jakub; Bolte, Michael; Feulner, Peter; Terfort, Andreas; Cyganik, Piotr; Zharnikov, Michael
Thiolate versus Selenolate: Structure, Stability, and Charge Transfer Properties.
ACS nano, 2015, 9, 4508-4526
4518011 CIFC39 H72 N15 P3P 1 21/c 119.771; 13.978; 16.975
90; 90.001; 90		4691Wang, Lebin; Zhang, Jinbo; Zhao, Na; Ren, Chuanli; Liu, Shaofeng; Li, Zhibo
Synthesis of Tris-Phosphazene Bases with Triazine as Core and Their Applications for Efficient Ring-Opening Alternating Copolymerization of Epoxide and Anhydride: Notable Effect of Basicity and Molecular Size
ACS Macro Letters, 2020, 9, 1398-1402
4518012 CIFC21 H54 N15 P3P 1 2/c 123.6761; 7.0053; 22.401
90; 117.192; 90		3304.8Wang, Lebin; Zhang, Jinbo; Zhao, Na; Ren, Chuanli; Liu, Shaofeng; Li, Zhibo
Synthesis of Tris-Phosphazene Bases with Triazine as Core and Their Applications for Efficient Ring-Opening Alternating Copolymerization of Epoxide and Anhydride: Notable Effect of Basicity and Molecular Size
ACS Macro Letters, 2020, 9, 1398-1402
4518408 CIFC164 H312 N16 O19 Zn8P 1 21/c 117.095; 14.339; 38.364
90; 106.233; 90		9029.1Krupiński, Piotr; Grala, Agnieszka; Wolska-Pietkiewicz, Małgorzata; Danowski, Wojciech; Justyniak, Iwona; Lewiński, Janusz
From Uncommon Ethylzinc Complexes Supported by Ureate Ligands to Water-Soluble ZnO Nanocrystals: A Mechanochemical Approach
ACS Sustainable Chemistry & Engineering, 2021, 9, 1540-1549
4518484 CIFC26 H45 N8 O30 Zn3.5P -17.272; 11.453; 12.792
105.317; 97.72; 94.62		1010.7Li, Yixing; Zhang, Xiao; Lan, Jianwen; Li, Dazhi; Wang, Zhijiang; Xu, Ping; Sun, Jianmin
A High-Performance Zinc-Organic Framework with Accessible Open Metal Sites Catalyzes CO2 and Styrene Oxide into Styrene Carbonate under Mild Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 2795-2803
4518547 CIFC20 H27 N O2P -17.9105; 10.1433; 12.1778
68.787; 73.015; 71.871		847.74Zhou, Kun; Hao, Hong-Yan; Mao, Yang-Jie; Wu, Qiu-Zi; Chen, Lei; Wang, Shuang; Jin, Wu; Xu, Zhen-Yuan; Lou, Shao-Jie; Xu, Dan-Qian
Solvent-less Dehydrogenative C–H Etherification with Alcohols Using Mechanochemistry
ACS Sustainable Chemistry & Engineering, 2021, 9, 4433-4439
4518570 CIFC14 H14 N4 O6 V2 ZnP 1 21/c 18.0272; 10.3866; 21.6398
90; 95.314; 90		1796.5Tian, Hongrui; Liu, Shumei; Zhang, Zhong; Dang, Tianyi; Lu, Ying; Liu, Shuxia
Highly Stable Polyoxovanadate-Based Zn‒MOF with Dual Active Sites as a Solvent-free Catalyst for C‒C Bond Formation
ACS Sustainable Chemistry & Engineering, 2021, 9, 4660-4667
4518716 CIFC12 H8 Br N O2 S2P -17.3124; 8.0674; 11.1844
90.429; 96.849; 93.54		653.76Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518717 CIFC12 H8 Br N O2 S2P -17.5012; 7.6684; 12.37
77.306; 82.115; 74.588		666.8Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518718 CIFC12 H8 Cl N O2 S2P -17.4862; 7.6173; 12.26
77.313; 81.768; 74.085		653.34Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518719 CIFC13 H11 N O2 S2P 1 21/c 16.637; 24.4347; 7.9539
90; 93.577; 90		1287.4Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518720 CIFC13 H9 Cl O2 S2P 1 21/c 15.4415; 7.9266; 30.427
90; 94.695; 90		1308Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518721 CIFC13 H9 Br O2 S2P 1 21/c 15.4811; 7.9282; 30.7236
90; 95.134; 90		1329.75Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518722 CIFC14 H14 O2 S2P 21 21 215.9037; 12.98; 17.9041
90; 90; 90		1371.99Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518723 CIFC12 H8 F2 S2P 21 21 215.7416; 13.0516; 14.497
90; 90; 90		1086.36Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4518724 CIFC12 H8 Br2 S2C c c 27.7242; 28.033; 5.9565
90; 90; 90		1289.8Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej
Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides
ACS Sustainable Chemistry & Engineering, 2021, 9, 7171-7178
4519018 CIFC19 H15 F N O2 PP -18.6254; 8.9016; 10.8499
80.225; 85.954; 77.248		800.24Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519019 CIFC21 H20 N O4 PP -111.1796; 12.4375; 14.5087
102.974; 93.417; 104.758		1886.37Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519020 CIFC15 H16 N O2 PP -18.7838; 8.7951; 20.4442
90.45; 93.891; 117.301		1398.88Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519021 CIFC16 H18 N O2 PP -113.2516; 14.607; 17.427
108.164; 109.21; 94.747		2961.45Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519022 CIFC47.01 H44.01 N2 O4 P2P -18.7408; 10.399; 11.263
82.043; 85.124; 82.282		1002.41Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519023 CIFC18 H16 N O3 PP -18.4872; 11.6741; 16.8354
108.405; 96.291; 90.405		1571.67Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519024 CIFC19 H15 Cl N O P SP 1 21/n 112.1934; 10.7695; 13.8808
90; 105.735; 90		1754.48Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519025 CIFC20 H18 N O2 P SP 1 21/n 112.1983; 10.781; 13.9142
90; 104.72; 90		1769.8Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519026 CIFC19 H15 N2 O3 P SC 1 2/c 118.8671; 11.7269; 16.0554
90; 95.579; 90		3535.47Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519027 CIFC16 H16 N O P SP 1 21/c 19.0779; 16.1069; 10.5344
90; 102.06; 90		1506.31Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.
Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions
ACS Sustainable Chemistry & Engineering, 2021, 9, 10704-10709
4519080 CIFC18 H33 B F4 N2 O2P 1 21/c 117.223; 8.252; 15.149
90; 99.137; 90		2125.7del Río, Enrique; Vidil, Thomas; Gati, Wafa; Grau, Étienne; Taton, Daniel; Cramail, Henri
Ester-Containing Imidazolium-Type Ionic Liquid Crystals Derived from Bio-based Fatty Alcohols
ACS Sustainable Chemistry & Engineering, 2021, 9, 12687-12698
4519192 CIFC40 H70 Mo24 N8 O96 P2 Zn8P 1 2/c 112.4443; 12.4258; 18.7974
90; 108.271; 90		2760.1Chen, Yanhong; Chang, Shenzhen; An, Haiyan; Li, Yanqin; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui
Two Polymorphic Polyoxometalate-Based Metal–Organic Frameworks for the Efficient Synthesis of Functionalized Sulfoxides and Detoxification of Mustard Gas Simulants
ACS Sustainable Chemistry & Engineering, 2021, 9, 15683-15693
4519193 CIFC40 H70 Mo24 N8 O96 P2 Zn8P 1 2/n 112.398; 12.41; 18.721
90; 109.145; 90		2721.1Chen, Yanhong; Chang, Shenzhen; An, Haiyan; Li, Yanqin; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui
Two Polymorphic Polyoxometalate-Based Metal–Organic Frameworks for the Efficient Synthesis of Functionalized Sulfoxides and Detoxification of Mustard Gas Simulants
ACS Sustainable Chemistry & Engineering, 2021, 9, 15683-15693
4519267 CIFC22 H15 Cl N2 OC 1 2/c 131.3976; 6.9692; 19.2078
90; 125.086; 90		3439.25Cai, Chen; Lu, Yi; Yuan, Chengcheng; Fang, Zheng; Yang, Xiaobing; Liu, Chengkou; Guo, Kai
Organocatalytic Electrosynthesis of Cinnolines through Cascade Radical Cyclization and Migration
ACS Sustainable Chemistry & Engineering, 2021, 9, 16989-16996
4519268 CIFC19 H20 F2 N2 OP 1 21/c 111.1841; 11.7671; 12.2739
90; 105.7; 90		1555.04Niu, Kaikai; Zhou, Pan; Ding, Ling; Hao, Yanke; Liu, Yuxiu; Song, Hongjian; Wang, Qingmin
Photoelectrochemical Decarboxylative C–H Alkylation of Quinoxalin-2(1H)-ones
ACS Sustainable Chemistry & Engineering, 2021, 9, 16820-16828
5000076 CIFC10 H16 I2 N2P 21 21 217.61; 11.01; 17.27
90; 90; 90		1446.99Koo, Chung Hoe; Kim, Hoon Sup
The Crystal Structure of Nicotine Dihydroiodide
Journal of the Korean Chemical Society, 1965, 9, 134-141
5000224 CIFO2 SnP 42/m n m4.737; 4.737; 3.185
90; 90; 90		71.5Baur, W. H.
Über die Verfeinerung der Kristallstrukturbestimmung einiger Vertreter des Rutiltyps: TiO~2~, SnO~2~, GeO~2~ und MgF~2~
Acta Crystallographica, 1956, 9, 515-520
6000270 CIFMn3 O8 Ta2I 41/a11.2728; 11.2728; 9.803
90; 90; 90		1245.73Grins, J.; Esmaeilzadeh, S.; Berastegui, P.; Eriksson, S.
Determination of the magnetic structure at 10 k of Mn3Ta2O8, and refinement of the crystal structure at 295 K, using neutron powder diffraction data
Journal of Materials Chemistry, 1999, 9, 1575-1578
6000355 CIFC2 H10 F4 N2 O8 P2 Ti2P 1 21/c 17.508; 8.881; 8.961
90; 107.22; 90		570.72Serre, C.; Ferey, G.
Hydrothermal synthesis and ab initio structural approach of two new layered oxyfluorinated titanium(IV) phosphates: Ti2(PO4)(2)F4.N2C2H10(MIL-6) and Ti2(PO4)(2)F4.N2C3H12.H2O
Journal of Materials Chemistry, 1999, 9, 579-584
6000356 CIFC3 H14 F4 N2 O9 P2 Ti2C 1 2 116.82; 6.333; 6.331
90; 106.2; 90		647.61Serre, C.; Ferey, G.
Hydrothermal synthesis and ab initio structural approach of two new layered oxyfluorinated titanium(IV) phosphates: Ti2(PO4)(2)F4.N2C2H10(MIL-6) and Ti2(PO4)(2)F4.N2C3H12.H2O
Journal of Materials Chemistry, 1999, 9, 579-584
6000680 CIFC2 H16 Al2 N2 O12 P2P -110.3749; 6.6077; 9.9094
90.762; 115.265; 90.162		614.27Kongshaug, K. O.; Fjellvag, H.; Lillerud, K. P.
Layered aluminophosphates II. Crystal structure and thermal behaviour of the layered aluminophosphate UiO-15 and its high temperature variants
Journal of Materials Chemistry, 1999, 9, 1591-1598
6000681 CIFC2 H12 Al2 N2 O10 P2P 1 21/c 110.289; 6.7508; 9.6253
90; 116.124; 90		600.26Kongshaug, K. O.; Fjellvag, H.; Lillerud, K. P.
Layered aluminophosphates II. Crystal structure and thermal behaviour of the layered aluminophosphate UiO-15 and its high temperature variants
Journal of Materials Chemistry, 1999, 9, 1591-1598
6000682 CIFC2 H10 Al2 N2 O9 P2P 1 21/c 19.4218; 6.9137; 9.4082
90; 113.002; 90		564.12Kongshaug, K. O.; Fjellvag, H.; Lillerud, K. P.
Layered aluminophosphates II. Crystal structure and thermal behaviour of the layered aluminophosphate UiO-15 and its high temperature variants
Journal of Materials Chemistry, 1999, 9, 1591-1598
7120919 CIFC36 H33 N8 Ni O10I 1 a 117.435; 19.1274; 22.985
90; 110.64; 90		7173.2Yang, Jing-Mei; Zhu, Yan-Hong; Chen, Sheng; Lu, Xing; Wu, Yi-Ming; Ma, Feng-E; Li, Liang-Ping; Yang, Yang; Shi, Zhen-Hao; Huang, Kun-Yuan; Hong, Xue; Jiang, Ping; Peng, Yan
A β-carboline derivative-based nickel(ii) complex as a potential antitumor agent: synthesis, characterization, and cytotoxicity.
MedChemComm, 2018, 9, 100-107
7121054 CIFC21 H18 Cl Cu N4 O SP -19.4142; 10.2389; 11.9095
87.064; 67.901; 71.422		1005.13Hu, Jiyong; Liao, Chunli; Mao, Ruina; Zhang, Junshuai; Zhao, Jin'an; Gu, Zhenzhen
DNA interactions and <i>in vitro</i> anticancer evaluations of pyridine-benzimidazole-based Cu complexes.
MedChemComm, 2018, 9, 337-343
7121055 CIFC38 H28 Br3 Cu2 N6 OP 1 21/m 19.7938; 19.0133; 14.1848
90; 103.517; 90		2568.2Hu, Jiyong; Liao, Chunli; Mao, Ruina; Zhang, Junshuai; Zhao, Jin'an; Gu, Zhenzhen
DNA interactions and <i>in vitro</i> anticancer evaluations of pyridine-benzimidazole-based Cu complexes.
MedChemComm, 2018, 9, 337-343
7121167 CIFC9 H14 N6 O2 SiP -16.0637; 6.3295; 17.0569
82.559; 81.097; 72.642		614.89Cousin, David; Hummersone, Marc G.; Bradshaw, Tracey D.; Zhang, Jihong; Moody, Christopher J.; Foreiter, Magdalena B.; Summers, Helen S.; Lewis, William; Wheelhouse, Richard T.; Stevens, Malcolm F. G.
Synthesis and growth-inhibitory activities of imidazo[5,1-<i>d</i>]-1,2,3,5-tetrazine-8-carboxamides related to the anti-tumour drug temozolomide, with appended silicon, benzyl and heteromethyl groups at the 3-position.
MedChemComm, 2018, 9, 545-553
7121168 CIFC11 H18 N6 O3 SiP -17.5168; 9.0109; 11.412
88.485; 78.814; 86.275		756.61Cousin, David; Hummersone, Marc G.; Bradshaw, Tracey D.; Zhang, Jihong; Moody, Christopher J.; Foreiter, Magdalena B.; Summers, Helen S.; Lewis, William; Wheelhouse, Richard T.; Stevens, Malcolm F. G.
Synthesis and growth-inhibitory activities of imidazo[5,1-<i>d</i>]-1,2,3,5-tetrazine-8-carboxamides related to the anti-tumour drug temozolomide, with appended silicon, benzyl and heteromethyl groups at the 3-position.
MedChemComm, 2018, 9, 545-553
7121233 CIFC58.5 H60 Cl4 N6 O5.5 Ru2 S4P 1 21/c 111.5669; 22.0229; 24.962
90; 98.749; 90		6284.7Qin, Qi-Pin; Meng, Ting; Tan, Ming-Xiong; Liu, Yan-Cheng; Wang, Shu-Long; Zou, Bi-Qun; Liang, Hong
Synthesis, characterization and biological evaluation of six highly cytotoxic ruthenium(ii) complexes with 4'-substituted-2,2':6',2''-terpyridine.
MedChemComm, 2018, 9, 525-533
7121289 CIFC19 H20 F N O3 S SiP -17.6192; 10.3601; 13.1271
102.578; 92.847; 101.855		984.91Roscales, Silvia; Bechmann, Nicole; Weiss, Daniel Holger; Köckerling, Martin; Pietzsch, Jens; Kniess, Torsten
Novel valdecoxib derivatives by ruthenium(ii)-promoted 1,3-dipolar cycloaddition of nitrile oxides with alkynes - synthesis and COX-2 inhibition activity.
MedChemComm, 2018, 9, 534-544
7121290 CIFC18 H19 F N2 O3 S SiP -19.705; 9.854; 11.726
65.43; 68.51; 76.92		945.3Roscales, Silvia; Bechmann, Nicole; Weiss, Daniel Holger; Köckerling, Martin; Pietzsch, Jens; Kniess, Torsten
Novel valdecoxib derivatives by ruthenium(ii)-promoted 1,3-dipolar cycloaddition of nitrile oxides with alkynes - synthesis and COX-2 inhibition activity.
MedChemComm, 2018, 9, 534-544
7121489 CIFC15 H14 N3 O6 Re S2P 1 21/c 126.3056; 9.4798; 16.1346
90; 106.786; 90		3852.1Mašković, Jelena M; Hatzidimitriou, Antonios; Damjanović, Ana; Stanojković, Tatjana P; Trifunović, Srećko R; Geronikaki, Athina A.; Papagiannopoulou, Dionysia
Synthesis, characterization and biological evaluation of Pd(ii), Cu(ii), Re(i) and <sup>99m</sup>Tc(i) thiazole-based complexes.
MedChemComm, 2018, 9, 831-842
7121490 CIFC24 H28 Cl2 Cu N4 S4P 1 21/c 119.911; 8.771; 8.088
90; 93.416; 90		1410Mašković, Jelena M; Hatzidimitriou, Antonios; Damjanović, Ana; Stanojković, Tatjana P; Trifunović, Srećko R; Geronikaki, Athina A.; Papagiannopoulou, Dionysia
Synthesis, characterization and biological evaluation of Pd(ii), Cu(ii), Re(i) and <sup>99m</sup>Tc(i) thiazole-based complexes.
MedChemComm, 2018, 9, 831-842
7121580 CIFC22 H29 N O2P 21 21 216.8428; 12.319; 21.388
90; 90; 90		1802.93Savić, Marina P; Ajduković, Jovana J; Plavša, Jovana J; Bekić, Sofija S; Ćelić, Andjelka S; Klisurić, Olivera R; Jakimov, Dimitar S.; Petri, Edward T.; Djurendić, Evgenija A
Evaluation of A-ring fused pyridine d-modified androstane derivatives for antiproliferative and aldo-keto reductase 1C3 inhibitory activity.
MedChemComm, 2018, 9, 969-981
7121581 CIFC28 H36 N2 O2P 1 21 111.4355; 7.2184; 14.3262
90; 92.092; 90		1181.8Savić, Marina P; Ajduković, Jovana J; Plavša, Jovana J; Bekić, Sofija S; Ćelić, Andjelka S; Klisurić, Olivera R; Jakimov, Dimitar S.; Petri, Edward T.; Djurendić, Evgenija A
Evaluation of A-ring fused pyridine d-modified androstane derivatives for antiproliferative and aldo-keto reductase 1C3 inhibitory activity.
MedChemComm, 2018, 9, 969-981
7121582 CIFC28 H32 N2P 21 21 217.8675; 12.2525; 23.0556
90; 90; 90		2222.48Savić, Marina P; Ajduković, Jovana J; Plavša, Jovana J; Bekić, Sofija S; Ćelić, Andjelka S; Klisurić, Olivera R; Jakimov, Dimitar S.; Petri, Edward T.; Djurendić, Evgenija A
Evaluation of A-ring fused pyridine d-modified androstane derivatives for antiproliferative and aldo-keto reductase 1C3 inhibitory activity.
MedChemComm, 2018, 9, 969-981
7121616 CIFC23 H27 Cl0 F N4 O3P 1 21/c 117.423; 6.0728; 20.2071
90; 103.62; 90		2077.92Kucwaj-Brysz, Katarzyna; Kurczab, Rafał; Żesławska, Ewa; Lubelska, Annamaria; Marć, Małgorzata Anna; Latacz, Gniewomir; Satała, Grzegorz; Nitek, Wojciech; Kieć-Kononowicz, Katarzyna; Handzlik, Jadwiga
The role of aryl-topology in balancing between selective and dual 5-HT<sub>7</sub>R/5-HT<sub>1A</sub> actions of 3,5-substituted hydantoins.
MedChemComm, 2018, 9, 1033-1044
7121694 CIFC43 H39 N6 O12 S2P -15.097; 11.161; 20.474
76.969; 86.696; 84.67		1129Chen, Cheng; Xiang, Yang; Liu, Ya; Hu, Xiangdong; Yang, Ke-Wu
Mercaptoacetate thioesters and their hydrolysate mercaptoacetic acids jointly inhibit metallo-β-lactamase L1.
MedChemComm, 2018, 9, 1172-1177
7121719 CIFC20 H17 N3 O2P 1 21/n 19.949; 15.604; 11.098
90; 104.703; 90		1666.5Sun, Wuji; Fang, Shubiao; Yan, Hong
Discovery of novel picolinamide-based derivatives as novel VEGFR-2 kinase inhibitors: synthesis, <i>in vitro</i> biological evaluation and molecular docking.
MedChemComm, 2018, 9, 1054-1058
7121720 CIFC25 H19 N3 O2P 21 21 215.4568; 7.5939; 45.622
90; 90; 90		1890.5Sun, Wuji; Fang, Shubiao; Yan, Hong
Discovery of novel picolinamide-based derivatives as novel VEGFR-2 kinase inhibitors: synthesis, <i>in vitro</i> biological evaluation and molecular docking.
MedChemComm, 2018, 9, 1054-1058
7121827 CIFC27 H29 N7 O2P 1 21/n 19.814; 9.916; 25.156
90; 90.477; 90		2448Karvande, Anirudha; Khan, Shahnawaz; Khan, Irfan; Singh, Deepti; Khedgikar, Vikram; Kushwaha, Priyanka; Ahmad, Naseer; Kothari, Priyanka; Dhasmana, Anupam; Kant, Ruchir; Trivedi, Ritu; Chauhan, Prem M. S.
Discovery of a tetrazolyl β-carboline with <i>in vitro</i> and <i>in vivo</i> osteoprotective activity under estrogen-deficient conditions.
MedChemComm, 2018, 9, 1213-1225
7121917 CIFC18 H22 Cl N3 OP c a 2137.512; 7.28; 12.978
90; 90; 90		3544Castriconi, Federica; Paolino, Marco; Grisci, Giorgio; Francini, Cinzia Maria; Reale, Annalisa; Giuliani, Germano; Anzini, Maurizio; Giorgi, Gianluca; Mennuni, Laura; Sabatini, Chiara; Lanza, Marco; Caselli, Gianfranco; Cappelli, Andrea
Development of subnanomolar-affinity serotonin 5-HT<sub>4</sub> receptor ligands based on quinoline structures.
MedChemComm, 2018, 9, 1466-1471
7121918 CIFC20 H29 N3 O3P 1 21/c 111.3833; 11.7128; 15.0977
90; 103.83; 90		1954.62Castriconi, Federica; Paolino, Marco; Grisci, Giorgio; Francini, Cinzia Maria; Reale, Annalisa; Giuliani, Germano; Anzini, Maurizio; Giorgi, Gianluca; Mennuni, Laura; Sabatini, Chiara; Lanza, Marco; Caselli, Gianfranco; Cappelli, Andrea
Development of subnanomolar-affinity serotonin 5-HT<sub>4</sub> receptor ligands based on quinoline structures.
MedChemComm, 2018, 9, 1466-1471
7122121 CIFC20 H18 Cl2 N3 O2 Pt SP 1 21/n 111.425; 15.9927; 11.939
90; 105.051; 90		2106.62Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122122 CIFC17 H14 Cl2 N2 O3 Pt SP -18.5196; 9.9538; 10.8961
95.033; 90.166; 98.338		910.61Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122123 CIFC17 H13 Cl2 I N2 O3 Pt SP 1 21/c 18.594; 11.5135; 21.0202
90; 108.188; 90		1975.97Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122124 CIFC18 H17 Br Cl2 N2 O4 Pt SC 1 2/c 123.8724; 7.916; 23.4616
90; 106.984; 90		4240.26Qin, Qi-Pin; Zou, Bi-Qun; Hu, Fei-Long; Huang, Guo-Bao; Wang, Shu-Long; Gu, Yun-Qiong; Tan, Ming-Xiong
Platinum(ii) complexes with rutaecarpine and tryptanthrin derivatives induce apoptosis by inhibiting telomerase activity and disrupting mitochondrial function.
MedChemComm, 2018, 9, 1639-1648
7122205 CIFC24 H18 Cl F N2 O3P 1 21/c 110.474; 11.271; 17.518
90; 96.136; 90		2056.2Umar, Tarana; Shalini, Shruti; Raza, Md Kausar; Gusain, Siddharth; Kumar, Jitendra; Ahmed, Waqar; Tiwari, Manisha; Hoda, Nasimul
New amyloid beta-disaggregating agents: synthesis, pharmacological evaluation, crystal structure and molecular docking of <i>N</i>-(4-((7-chloroquinolin-4-yl)oxy)-3-ethoxybenzyl)amines.
MedChemComm, 2018, 9, 1891-1904
7122206 CIFC25 H23 Cl N2 O2P -15.35; 14.08; 14.717
101; 90.44; 97.24		1079Umar, Tarana; Shalini, Shruti; Raza, Md Kausar; Gusain, Siddharth; Kumar, Jitendra; Ahmed, Waqar; Tiwari, Manisha; Hoda, Nasimul
New amyloid beta-disaggregating agents: synthesis, pharmacological evaluation, crystal structure and molecular docking of <i>N</i>-(4-((7-chloroquinolin-4-yl)oxy)-3-ethoxybenzyl)amines.
MedChemComm, 2018, 9, 1891-1904
7122245 CIFC21 H22 O6C 1 2/c 156.225; 4.6615; 14.0454
90; 101.729; 90		3604.3Maguire, Casey J.; Chen, Zhi; Mocharla, Vani P.; Sriram, Madhavi; Strecker, Tracy E.; Hamel, Ernest; Zhou, Heling; Lopez, Ramona; Wang, Yifan; Mason, Ralph P.; Chaplin, David J.; Trawick, Mary Lynn; Pinney, Kevin G.
Synthesis of dihydronaphthalene analogues inspired by combretastatin A-4 and their biological evaluation as anticancer agents.
MedChemComm, 2018, 9, 1649-1662
7122246 CIFC20 H22 O5P 1 21/n 112.1996; 6.7253; 20.3499
90; 94.1342; 90		1665.28Maguire, Casey J.; Chen, Zhi; Mocharla, Vani P.; Sriram, Madhavi; Strecker, Tracy E.; Hamel, Ernest; Zhou, Heling; Lopez, Ramona; Wang, Yifan; Mason, Ralph P.; Chaplin, David J.; Trawick, Mary Lynn; Pinney, Kevin G.
Synthesis of dihydronaphthalene analogues inspired by combretastatin A-4 and their biological evaluation as anticancer agents.
MedChemComm, 2018, 9, 1649-1662
7122375 CIFC9 H11 N3 SP 1 21/c 113.2482; 8.2243; 10.2827
90; 111.265; 90		1044.09Mathew, Bijo; Baek, Seung Cheol; Grace Thomas Parambi, Della; Pil Lee, Jae; Joy, Monu; Annie Rilda, P. R.; Randev, Rugma V.; Nithyamol, P.; Vijayan, Vijitha; Inasu, Sini T.; Mathew, Githa Elizabeth; Lohidakshan, Krishnakumar K.; Kumar Krishnan, Girish; Kim, Hoon
Selected aryl thiosemicarbazones as a new class of multi-targeted monoamine oxidase inhibitors.
MedChemComm, 2018, 9, 1871-1881
7122487 CIFC13 H19 N O3P 21 21 217.3307; 20.5418; 8.597
90; 90; 90		1294.59Pańczyk, Katarzyna; Żelaszczyk, Dorota; Koczurkiewicz, Paulina; Słoczyńska, Karolina; Pękala, Elżbieta; Żesławska, Ewa; Nitek, Wojciech; Żmudzki, Paweł; Marona, Henryk; Waszkielewicz, Anna
Synthesis and anticonvulsant activity of phenoxyacetyl derivatives of amines, including aminoalkanols and amino acids.
MedChemComm, 2018, 9, 1933-1948
7122488 CIFC14 H20 N O3P n a 2121.431; 8.483; 7.516
90; 90; 90		1366.4Pańczyk, Katarzyna; Żelaszczyk, Dorota; Koczurkiewicz, Paulina; Słoczyńska, Karolina; Pękala, Elżbieta; Żesławska, Ewa; Nitek, Wojciech; Żmudzki, Paweł; Marona, Henryk; Waszkielewicz, Anna
Synthesis and anticonvulsant activity of phenoxyacetyl derivatives of amines, including aminoalkanols and amino acids.
MedChemComm, 2018, 9, 1933-1948
7122489 CIFC13 H19 N O3P 21 21 217.3182; 20.524; 8.5965
90; 90; 90		1291.2Pańczyk, Katarzyna; Żelaszczyk, Dorota; Koczurkiewicz, Paulina; Słoczyńska, Karolina; Pękala, Elżbieta; Żesławska, Ewa; Nitek, Wojciech; Żmudzki, Paweł; Marona, Henryk; Waszkielewicz, Anna
Synthesis and anticonvulsant activity of phenoxyacetyl derivatives of amines, including aminoalkanols and amino acids.
MedChemComm, 2018, 9, 1933-1948
7122519 CIFC15 H18 O5P 21 21 218.2861; 9.8316; 18.092
90; 90; 90		1473.9Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122520 CIFC15 H18 O5P 21 21 218.1993; 9.5498; 18.6176
90; 90; 90		1457.79Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122521 CIFC14 H14 O5P 21 21 214.674; 12.9175; 21.3349
90; 90; 90		1288.12Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122522 CIFC15 H20 O5P 21 21 218.8306; 10.0761; 17.1204
90; 90; 90		1523.34Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122523 CIFC14 H16 O5P 1 21 17.6832; 7.5202; 11.6492
90; 91.533; 90		672.84Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122524 CIFC15 H20 O5P 21 21 2111.0585; 11.4256; 11.8876
90; 90; 90		1502Francuz, Jovana; Popsavin, Mirjana; Djokić, Sanja; Kojić, Vesna; Srdić-Rajić, Tatjana; Rodić, Marko V; Jakimov, Dimitar; Popsavin, Velimir
Novel <i>O</i>-methyl goniofufurone and 7-<i>epi</i>-goniofufurone derivatives: synthesis, <i>in vitro</i> cytotoxicity and SAR analysis.
MedChemComm, 2018, 9, 2017-2027
7122525 CIFC48 H70 N6 O10P 1 21 110.819; 14.713; 30.167
90; 96.24; 90		4773.5Kovaleva, Kseniya S.; Zubkov, Fedor I.; Bormotov, Nikolay I.; Novikov, Roman A.; Dorovatovskii, Pavel V.; Khrustalev, Victor N.; Gatilov, Yuriy V.; Zarubaev, Vladimir V.; Yarovaya, Olga I.; Shishkina, Larisa N.; Salakhutdinov, Nariman F.
Synthesis of d-(+)-camphor-based <i>N</i>-acylhydrazones and their antiviral activity.
MedChemComm, 2018, 9, 2072-2082
7122526 CIFC15 H20 N2 O2P 1 21 110.6401; 13.1077; 11.089
90; 111.31; 90		1440.8Kovaleva, Kseniya S.; Zubkov, Fedor I.; Bormotov, Nikolay I.; Novikov, Roman A.; Dorovatovskii, Pavel V.; Khrustalev, Victor N.; Gatilov, Yuriy V.; Zarubaev, Vladimir V.; Yarovaya, Olga I.; Shishkina, Larisa N.; Salakhutdinov, Nariman F.
Synthesis of d-(+)-camphor-based <i>N</i>-acylhydrazones and their antiviral activity.
MedChemComm, 2018, 9, 2072-2082
7122527 CIFC58 H74 N6 O8P 1 21 110.949; 15.752; 31.273
90; 98.92; 90		5328.4Kovaleva, Kseniya S.; Zubkov, Fedor I.; Bormotov, Nikolay I.; Novikov, Roman A.; Dorovatovskii, Pavel V.; Khrustalev, Victor N.; Gatilov, Yuriy V.; Zarubaev, Vladimir V.; Yarovaya, Olga I.; Shishkina, Larisa N.; Salakhutdinov, Nariman F.
Synthesis of d-(+)-camphor-based <i>N</i>-acylhydrazones and their antiviral activity.
MedChemComm, 2018, 9, 2072-2082
7122579 CIFC H N OP 1 21 16.9872; 15.5151; 19.425
90; 98.467; 90		2082.9Zhao, Fengyi; Lu, Wen; Su, Fan; Xu, Li; Jiang, Dong; Sun, Xu; Shi, Jiuzhou; Zhou, Mengyi; Lin, Feng; Cao, Fuliang
Synthesis and potential antineoplastic activity of dehydroabietylamine imidazole derivatives.
MedChemComm, 2018, 9, 2091-2099
7122580 CIFC25 H37 N3 O5P 1 21 110.3659; 7.0531; 16.9815
90; 92.543; 90		1240.32Zhao, Fengyi; Lu, Wen; Su, Fan; Xu, Li; Jiang, Dong; Sun, Xu; Shi, Jiuzhou; Zhou, Mengyi; Lin, Feng; Cao, Fuliang
Synthesis and potential antineoplastic activity of dehydroabietylamine imidazole derivatives.
MedChemComm, 2018, 9, 2091-2099
7124502 CIFC18 H14 Cu N4 O8P -110.093; 10.384; 10.818
78.634; 65.151; 71.085		970.8Hu, Kun; Liu, Chensi; Li, Jingui; Liang, Fupei
Copper(ii) complexes based on quinoline-derived Schiff-base ligands: synthesis, characterization, HSA/DNA binding ability, and anticancer activity.
MedChemComm, 2018, 9, 1663-1672
7124503 CIFC19 H16 Cl2 Cu N2 O2P 1 21/n 19.784; 12.52; 15.403
90; 101.907; 90		1846Hu, Kun; Liu, Chensi; Li, Jingui; Liang, Fupei
Copper(ii) complexes based on quinoline-derived Schiff-base ligands: synthesis, characterization, HSA/DNA binding ability, and anticancer activity.
MedChemComm, 2018, 9, 1663-1672
7124504 CIFC38 H32 Cu2 N4 O14 S2P -18.818; 9.995; 13.151
99.756; 104.779; 103.63		1056.2Hu, Kun; Liu, Chensi; Li, Jingui; Liang, Fupei
Copper(ii) complexes based on quinoline-derived Schiff-base ligands: synthesis, characterization, HSA/DNA binding ability, and anticancer activity.
MedChemComm, 2018, 9, 1663-1672
7124505 CIFC19 H22 N2 O3P 21 21 217.24927; 12.5565; 19.2992
90; 90; 90		1756.72Ang, M Trisha C; Gumbau-Brisa, Roger; Allan, David S.; McDonald, Robert; Ferguson, Michael J.; Holbein, Bruce E.; Bierenstiel, Matthias
DIBI, a 3-hydroxypyridin-4-one chelator iron-binding polymer with enhanced antimicrobial activity.
MedChemComm, 2018, 9, 1206-1212
7124506 CIFC12 H18 N2 O4P 1 21/n 17.1337; 25.555; 7.1778
90; 101.331; 90		1283.02Ang, M Trisha C; Gumbau-Brisa, Roger; Allan, David S.; McDonald, Robert; Ferguson, Michael J.; Holbein, Bruce E.; Bierenstiel, Matthias
DIBI, a 3-hydroxypyridin-4-one chelator iron-binding polymer with enhanced antimicrobial activity.
MedChemComm, 2018, 9, 1206-1212
7151626 CIFC16 H18 O4 Se2I 41/a :218.124; 18.124; 9.8424
90; 90; 90		3233Tripathi, Santosh K.; Sharma, Sagar; Singh, Harkesh B.; Butcher, Ray J.
2-Phenoxyethanol derived diselenide and related compounds; synthesis of a seven-membered seleninate ester.
Organic & biomolecular chemistry, 2011, 9, 581-587
7151627 CIFC20 H26 O6 Se2C 1 2/c 115.814; 15.1093; 18.2919
90; 93.682; 90		4361.6Tripathi, Santosh K.; Sharma, Sagar; Singh, Harkesh B.; Butcher, Ray J.
2-Phenoxyethanol derived diselenide and related compounds; synthesis of a seven-membered seleninate ester.
Organic & biomolecular chemistry, 2011, 9, 581-587
7151628 CIFC22 H16 N2 O2 SP 1 21/n 110.8591; 10.0425; 17.0542
90; 100.888; 90		1826.32Bhurruth-Alcor, Yushma; Røst, Therese; Jorgensen, Michael R.; Kontogiorgis, Christos; Skorve, Jon; Cooper, Robert G.; Sheridan, Joseph M.; Hamilton, William D. O.; Heal, Jonathan R.; Berge, Rolf K.; Miller, Andrew D.
Synthesis of novel PPARα/γ dual agonists as potential drugs for the treatment of the metabolic syndrome and diabetes type II designed using a new de novo design program PROTOBUILD.
Organic & biomolecular chemistry, 2011, 9, 1169-1188
7151629 CIFC26 H18 N2 O2 SP 1 21/n 118.0309; 5.88641; 19.522
90; 98.636; 90		2048.52Bhurruth-Alcor, Yushma; Røst, Therese; Jorgensen, Michael R.; Kontogiorgis, Christos; Skorve, Jon; Cooper, Robert G.; Sheridan, Joseph M.; Hamilton, William D. O.; Heal, Jonathan R.; Berge, Rolf K.; Miller, Andrew D.
Synthesis of novel PPARα/γ dual agonists as potential drugs for the treatment of the metabolic syndrome and diabetes type II designed using a new de novo design program PROTOBUILD.
Organic & biomolecular chemistry, 2011, 9, 1169-1188
7151630 CIFC33 H36 Cl3 N3 Ni O5P 1 21 18.565; 12.029; 16.76
90; 91.239; 90		1726.4Luo, Xiaoyan; Jin, Zhichao; Li, Pengfei; Gao, Jiabin; Yue, Weimin; Liang, Xinmiao; Ye, Jinxing
Catalytic asymmetric Michael addition of α,β-unsaturated aldehydes to Ni(II) complexes of the Schiff base of glycine.
Organic & biomolecular chemistry, 2011, 9, 793-801
7151631 CIFC19 H23 Br2 N2 O3 PP 1 21 17.529; 13.009; 23.237
90; 90.36; 90		2275.9Cheng, Ge; Slawin, Alexandra M. Z.; Vautravers, Nicolas R.; André, Pascal; Morris, Russell E.; Samuel, Ifor D. W.; Cole-Hamilton, David
Synthesis of hybrid dendritic molecules with diazaphospholidine oxide grafted at the surface of octavinylsilsesquioxane (OVS).
Organic & biomolecular chemistry, 2011, 9, 1189-1200
7151632 CIFC25 H26 I N2 O3 PP 1 21/n 114.786; 9.781; 16.323
90; 101.211; 90		2315.6Cheng, Ge; Slawin, Alexandra M. Z.; Vautravers, Nicolas R.; André, Pascal; Morris, Russell E.; Samuel, Ifor D. W.; Cole-Hamilton, David
Synthesis of hybrid dendritic molecules with diazaphospholidine oxide grafted at the surface of octavinylsilsesquioxane (OVS).
Organic & biomolecular chemistry, 2011, 9, 1189-1200
7151633 CIFC18 H20 Br N2 O2 PP 1 21/n 19.3517; 16.96; 11.251
90; 103.824; 90		1732.8Cheng, Ge; Slawin, Alexandra M. Z.; Vautravers, Nicolas R.; André, Pascal; Morris, Russell E.; Samuel, Ifor D. W.; Cole-Hamilton, David
Synthesis of hybrid dendritic molecules with diazaphospholidine oxide grafted at the surface of octavinylsilsesquioxane (OVS).
Organic & biomolecular chemistry, 2011, 9, 1189-1200
7151634 CIFC21 H32 N2 O6P 1 21 15.1216; 10.4652; 21.3646
90; 95.373; 90		1140.08Bouillère, Francelin; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie
Access to β,γ-diamino acids. Application to the synthesis of 3-deoxyaminostatine.
Organic & biomolecular chemistry, 2011, 9, 394-399
7151635 CIFC20 H20 Cl2 N2 PdP 6118.7436; 18.7436; 13.3951
90; 90; 120		4075.5Grach, Guillaume; Dinut, Aurelia; Marque, Sylvain; Marrot, Jérôme; Gil, Richard; Prim, Damien
Enantioselective Friedel-Crafts alkylation of indole derivatives catalyzed by new Yb(OTf)3-pyridylalkylamine complexes as chiral Lewis acids.
Organic & biomolecular chemistry, 2011, 9, 497-503
7151636 CIFC9 H6 Cl N O SP b c a13.912; 5.9518; 21.173
90; 90; 90		1753.2Wisastra, Rosalina; Ghizzoni, Massimo; Maarsingh, Harm; Minnaard, Adriaan J.; Haisma, Hidde J.; Dekker, Frank J.
Isothiazolones; thiol-reactive inhibitors of cysteine protease cathepsin B and histone acetyltransferase PCAF.
Organic & biomolecular chemistry, 2011, 9, 1817-1822
7151637 CIFC9 H7 N O SP 1 21/c 117.363; 6.389; 7.471
90; 95.868; 90		824.4Wisastra, Rosalina; Ghizzoni, Massimo; Maarsingh, Harm; Minnaard, Adriaan J.; Haisma, Hidde J.; Dekker, Frank J.
Isothiazolones; thiol-reactive inhibitors of cysteine protease cathepsin B and histone acetyltransferase PCAF.
Organic & biomolecular chemistry, 2011, 9, 1817-1822
7151638 CIFC15 H11 N S2P n a 2116.771; 7.1231; 21.515
90; 90; 90		2570.2Galindo, Miguel A.; Hannant, Jennifer; Harrington, Ross W.; Clegg, William; Horrocks, Benjamin R.; Pike, Andrew R.; Houlton, Andrew
Pyrrolyl-, 2-(2-thienyl)pyrrolyl- and 2,5-bis(2-thienyl)pyrrolyl-nucleosides: synthesis, molecular and electronic structure, and redox behaviour of C5-thymidine derivatives.
Organic & biomolecular chemistry, 2011, 9, 1555-1564
7151639 CIFC16 H13 N S2P 1 21/c 118.3919; 16.7137; 9.28
90; 103.914; 90		2768.94Galindo, Miguel A.; Hannant, Jennifer; Harrington, Ross W.; Clegg, William; Horrocks, Benjamin R.; Pike, Andrew R.; Houlton, Andrew
Pyrrolyl-, 2-(2-thienyl)pyrrolyl- and 2,5-bis(2-thienyl)pyrrolyl-nucleosides: synthesis, molecular and electronic structure, and redox behaviour of C5-thymidine derivatives.
Organic & biomolecular chemistry, 2011, 9, 1555-1564
7151640 CIFC17 H15 N S2P c a 2118.2767; 5.6221; 14.5289
90; 90; 90		1492.89Galindo, Miguel A.; Hannant, Jennifer; Harrington, Ross W.; Clegg, William; Horrocks, Benjamin R.; Pike, Andrew R.; Houlton, Andrew
Pyrrolyl-, 2-(2-thienyl)pyrrolyl- and 2,5-bis(2-thienyl)pyrrolyl-nucleosides: synthesis, molecular and electronic structure, and redox behaviour of C5-thymidine derivatives.
Organic & biomolecular chemistry, 2011, 9, 1555-1564
7151641 CIFC22 H23 N3 O5 SP 1 21 18.0959; 5.7246; 22.417
90; 95.369; 90		1034.38Galindo, Miguel A.; Hannant, Jennifer; Harrington, Ross W.; Clegg, William; Horrocks, Benjamin R.; Pike, Andrew R.; Houlton, Andrew
Pyrrolyl-, 2-(2-thienyl)pyrrolyl- and 2,5-bis(2-thienyl)pyrrolyl-nucleosides: synthesis, molecular and electronic structure, and redox behaviour of C5-thymidine derivatives.
Organic & biomolecular chemistry, 2011, 9, 1555-1564
7151642 CIFC4 H8 Cl NP 1 21/n 110.158; 5.7057; 11.3236
90; 111.933; 90		608.8Galindo, Miguel A.; Hannant, Jennifer; Harrington, Ross W.; Clegg, William; Horrocks, Benjamin R.; Pike, Andrew R.; Houlton, Andrew
Pyrrolyl-, 2-(2-thienyl)pyrrolyl- and 2,5-bis(2-thienyl)pyrrolyl-nucleosides: synthesis, molecular and electronic structure, and redox behaviour of C5-thymidine derivatives.
Organic & biomolecular chemistry, 2011, 9, 1555-1564
7151643 CIFC13 H15 Cl N4 O4P 1 21 110.019; 6.5258; 22.94
90; 101.39; 90		1470.3Yang, Hao-Zhe; Pan, Mei-Ying; Jiang, Da-Wei; He, Yang
Synthesis of Janus type nucleoside analogues and their preliminary bioactivity.
Organic & biomolecular chemistry, 2011, 9, 1516-1522
7151644 CIFC19 H16 F3 N O3 SP 1 21/c 17.4866; 14.3369; 17.3851
90; 100.017; 90		1837.58Čížková, Martina; Kolivoška, Viliam; Císařová, Ivana; Šaman, David; Pospíšil, Lubomír; Teplý, Filip
Nitrogen heteroaromatic cations by [2+2+2] cycloaddition.
Organic & biomolecular chemistry, 2011, 9, 450-462
7151645 CIFC18 H18 F3 N O3 S2P c a 2112.175; 10.9843; 14.5988
90; 90; 90		1952.35Čížková, Martina; Kolivoška, Viliam; Císařová, Ivana; Šaman, David; Pospíšil, Lubomír; Teplý, Filip
Nitrogen heteroaromatic cations by [2+2+2] cycloaddition.
Organic & biomolecular chemistry, 2011, 9, 450-462
7151646 CIFC21 H18 F3 N O3 SC 1 2/c 123.1671; 10.5994; 15.6896
90; 92.516; 90		3848.98Čížková, Martina; Kolivoška, Viliam; Císařová, Ivana; Šaman, David; Pospíšil, Lubomír; Teplý, Filip
Nitrogen heteroaromatic cations by [2+2+2] cycloaddition.
Organic & biomolecular chemistry, 2011, 9, 450-462
7151647 CIFC12 H8 N2P n a 2123.3925; 6.2169; 13.0456
90; 90; 90		1897.21Čížková, Martina; Kolivoška, Viliam; Císařová, Ivana; Šaman, David; Pospíšil, Lubomír; Teplý, Filip
Nitrogen heteroaromatic cations by [2+2+2] cycloaddition.
Organic & biomolecular chemistry, 2011, 9, 450-462
7151648 CIFC17 H13 F3 N2 O3 SP -17.4977; 10.5242; 11.7581
81.4639; 79.5813; 75.5501		878.42Čížková, Martina; Kolivoška, Viliam; Císařová, Ivana; Šaman, David; Pospíšil, Lubomír; Teplý, Filip
Nitrogen heteroaromatic cations by [2+2+2] cycloaddition.
Organic & biomolecular chemistry, 2011, 9, 450-462
7151649 CIFC18 H30 N2 O6 SiC 2 2 2110.9379; 12.55; 31.289
90; 90; 90		4295.1Luo, Qun; Wu, Dayong; Liu, Shixiong; Tang, Daihua; Huang, Yong; Liu, Xinhou; Wang, Fuyi; Wang, Ruiyao; Wu, Gang
The formation of thymidine-based T-tetramers with remarkable structural and metal ion size effects.
Organic & biomolecular chemistry, 2011, 9, 1030-1033
7151650 CIFC28 H26 N4 O3P 1 21/c 111.2213; 11.0837; 18.7917
90; 100.181; 90		2300.39Chanda, Kaushik; Maiti, Barnali; Yellol, Gorakh S.; Chien, Ming-Hsien; Kuo, Min-Liang; Sun, Chung-Ming
Polymer supported synthesis of novel benzoxazole linked benzimidazoles under microwave conditions: In vitro evaluation of VEGFR-3 kinase inhibition activity.
Organic & biomolecular chemistry, 2011, 9, 1917-1926
7151651 CIFC17 H13 N O3P 1 21/c 16.4285; 31.4664; 7.0702
90; 106.517; 90		1371.16Chen, Guofei; Fu, Chunling; Ma, Shengming
A novel synthesis of oxazolidine-2,4-diones via an efficient fixation of CO2 with 3-aryl-2-alkynamides.
Organic & biomolecular chemistry, 2011, 9, 105-110
7151652 CIFC104 H86 N4 Nd2 O20 Zn2C 1 c 123.576; 16.388; 24.599
90; 91.441; 90		9501Chen, Guofei; Fu, Chunling; Ma, Shengming
A novel synthesis of oxazolidine-2,4-diones via an efficient fixation of CO2 with 3-aryl-2-alkynamides.
Organic & biomolecular chemistry, 2011, 9, 105-110
7151653 CIFC53 H45 N2 O11 Tb ZnP -113.028; 13.163; 15.397
75.58; 82.38; 83.32		2525.1Chen, Guofei; Fu, Chunling; Ma, Shengming
A novel synthesis of oxazolidine-2,4-diones via an efficient fixation of CO2 with 3-aryl-2-alkynamides.
Organic & biomolecular chemistry, 2011, 9, 105-110
7151654 CIFC53 H45 Ho N2 O11 ZnP -113.056; 13.146; 15.367
75.54; 82.406; 83.166		2521.4Chen, Guofei; Fu, Chunling; Ma, Shengming
A novel synthesis of oxazolidine-2,4-diones via an efficient fixation of CO2 with 3-aryl-2-alkynamides.
Organic & biomolecular chemistry, 2011, 9, 105-110
7151655 CIFC68 H57 N4 O14 Pr Zn2P 1 21/n 110.719; 21.494; 26.116
90; 90.83; 90		6016Chen, Guofei; Fu, Chunling; Ma, Shengming
A novel synthesis of oxazolidine-2,4-diones via an efficient fixation of CO2 with 3-aryl-2-alkynamides.
Organic & biomolecular chemistry, 2011, 9, 105-110
7151656 CIFC14 H15 Br2 N OP -15.6309; 8.4895; 14.66
88.759; 84.82; 73.866		670.4King, Frank D.; Aliev, Abil E.; Caddick, Stephen; Tocher, D. A.
A novel synthesis of (di)-benzazocinones via an endocyclic N-acyliminium ion cyclisation.
Organic & biomolecular chemistry, 2011, 9, 1547-1554
7151657 CIFC14 H18 F3 N O2 SP 21 21 2110.9351; 11.7459; 24.978
90; 90; 90		3208.2Mei, Haibo; Xiong, Yiwen; Han, Jianlin; Pan, Yi
A facile process for the asymmetric synthesis of β-trifluoromethylated β-amino ketones via addition of ketone enolates to sulfinylimine.
Organic & biomolecular chemistry, 2011, 9, 1402-1406
7151658 CIFC24 H29 N O4P 1 21/n 110.881; 17.932; 11.015
90; 104.754; 90		2078Ramesh, Veera V. E.; Roy, Arup; Vijayadas, Kuruppanthara N.; Kendhale, Amol M.; Prabhakaran, Panchami; Gonnade, Rajesh; Puranik, Vedavati G.; Sanjayan, Gangadhar J.
Conformationally rigid aromatic amino acids as potential building blocks for abiotic foldamers.
Organic & biomolecular chemistry, 2011, 9, 367-369
7151659 CIFC21 H14 N2 O7P b c a11.8387; 16.585; 19.535
90; 90; 90		3835.6Ramesh, Veera V. E.; Roy, Arup; Vijayadas, Kuruppanthara N.; Kendhale, Amol M.; Prabhakaran, Panchami; Gonnade, Rajesh; Puranik, Vedavati G.; Sanjayan, Gangadhar J.
Conformationally rigid aromatic amino acids as potential building blocks for abiotic foldamers.
Organic & biomolecular chemistry, 2011, 9, 367-369
7151660 CIFC96 H96 N16 O24P -112.27; 19.6334; 20.4221
75.23; 72.675; 75.364		4457.3Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151661 CIFC99 H102 N16 O25P -111.8003; 20.6248; 21.2868
110.363; 97.492; 99.82		4683.8Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151662 CIFC103 H110 N16 O25P -111.1398; 22.0112; 22.5117
113.189; 100.427; 99.965		4804.5Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151663 CIFC103 H110 N16 O25P -111.8347; 20.5903; 22.5132
113.258; 95.992; 100.282		4865.6Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151664 CIFC100 H104 N16 O24P -111.9965; 20.2594; 22.8564
114.695; 96.967; 99.77		4857.9Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151665 CIFC102 H107 N17 O24P -112.0137; 20.275; 22.8339
115.072; 96.578; 99.681		4857.3Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151666 CIFC132 H163 N16 O25.5P -112.6739; 20.5874; 25.8506
77.841; 77.976; 74.025		6257.4Helttunen, Kaisa; Nauha, Elisa; Kurronen, Anni; Shahgaldian, Patrick; Nissinen, Maija
Conformational polymorphism and amphiphilic properties of resorcinarene octapodands.
Organic & biomolecular chemistry, 2011, 9, 906-914
7151667 CIFC16 H10 Cl2 N2 O2P -17.753; 8.285; 11.93
84.628; 76.938; 84.323		740.8Crespo, Abel; Coelho, Alberto; Diz, Paula M.; Fernández, Franco; Novoa de Armas, Hector; Sotelo, Eddy
Convergent assembly of structurally diverse quinazolines.
Organic & biomolecular chemistry, 2011, 9, 351-357
7151668 CIFC56 H60 F12 N2 O10 P2P 1 21/c 112.789; 26.622; 20.717
90; 127.862; 90		5569Xu, Zhikai; Jiang, Lasheng; Feng, Yahui; Zhang, Suhui; Liang, Jidong; Pan, Shaowu; Yang, Yu; Yang, Dengke; Cai, Yuepeng
One-pot synthesis of donor-acceptor [2]rotaxanes based on cryptand-paraquat recognition motif.
Organic & biomolecular chemistry, 2011, 9, 1237-1243
7151669 CIFC56 H68 F12 N2 O10 P2P -113.672; 14.541; 16.402
112.152; 92.063; 104.255		2897Xu, Zhikai; Jiang, Lasheng; Feng, Yahui; Zhang, Suhui; Liang, Jidong; Pan, Shaowu; Yang, Yu; Yang, Dengke; Cai, Yuepeng
One-pot synthesis of donor-acceptor [2]rotaxanes based on cryptand-paraquat recognition motif.
Organic & biomolecular chemistry, 2011, 9, 1237-1243
7151670 CIFC72 H94 F12 N2 O11 P2P 1 21/c 113.677; 17.347; 34.994
90; 106.807; 90		7948Xu, Zhikai; Jiang, Lasheng; Feng, Yahui; Zhang, Suhui; Liang, Jidong; Pan, Shaowu; Yang, Yu; Yang, Dengke; Cai, Yuepeng
One-pot synthesis of donor-acceptor [2]rotaxanes based on cryptand-paraquat recognition motif.
Organic & biomolecular chemistry, 2011, 9, 1237-1243
7151671 CIFC72 H92 F12 N2 O11 P2P 1 21/c 113.666; 17.343; 34.9
90; 106.726; 90		7922Xu, Zhikai; Jiang, Lasheng; Feng, Yahui; Zhang, Suhui; Liang, Jidong; Pan, Shaowu; Yang, Yu; Yang, Dengke; Cai, Yuepeng
One-pot synthesis of donor-acceptor [2]rotaxanes based on cryptand-paraquat recognition motif.
Organic & biomolecular chemistry, 2011, 9, 1237-1243
7151672 CIFC11 H11 Br2 N O5P -16.5189; 10.7194; 11.0482
65.732; 77.573; 80.693		684.99Shearman, James W.; Myers, Rebecca M.; Brenton, James D.; Ley, Steven V.
Total syntheses of subereamollines A and B.
Organic & biomolecular chemistry, 2011, 9, 62-65
7151673 CIFC11 H11 Br2 N O5P 1 21/c 110.9772; 25.2605; 10.1567
90; 104.6; 90		2725.4Shearman, James W.; Myers, Rebecca M.; Brenton, James D.; Ley, Steven V.
Total syntheses of subereamollines A and B.
Organic & biomolecular chemistry, 2011, 9, 62-65
7151674 CIFC10 H6 Br2 O4P n a 218.971; 10.6189; 22.6185
90; 90; 90		2154.69Shearman, James W.; Myers, Rebecca M.; Brenton, James D.; Ley, Steven V.
Total syntheses of subereamollines A and B.
Organic & biomolecular chemistry, 2011, 9, 62-65
7151675 CIFC13 H20 N2 O5C 1 2/c 120.618; 4.6216; 16.874
90; 117.449; 90		1426.9Zhang, Yagang; Song, Di; Brown, Julius C.; Shimizu, Ken D.
Suppression of background sites in molecularly imprinted polymers via urea-urea monomer aggregation.
Organic & biomolecular chemistry, 2011, 9, 120-126
7151676 CIFC20 H14 F3 N O3P 1 21/n 18.779; 15.427; 12.67
90; 94.858; 90		1709.78Wang, De-Wei; Syu, Siang-en; Hung, Yi-Ting; Chen, Pei-yi; Lee, Chia-Jui; Chen, Ko-Wei; Chen, Yu-Jhang; Lin, Wenwei
Organocatalytic tandem three-component reaction of aldehyde, alkyl vinyl ketone, and amide: one-pot syntheses of highly functional alkenes.
Organic & biomolecular chemistry, 2011, 9, 363-366
7151677 CIFC15 H15 Br N2 O3P -17.811; 8.3322; 12.4088
70.775; 89.288; 78.72		746.65Wang, De-Wei; Syu, Siang-en; Hung, Yi-Ting; Chen, Pei-yi; Lee, Chia-Jui; Chen, Ko-Wei; Chen, Yu-Jhang; Lin, Wenwei
Organocatalytic tandem three-component reaction of aldehyde, alkyl vinyl ketone, and amide: one-pot syntheses of highly functional alkenes.
Organic & biomolecular chemistry, 2011, 9, 363-366
7151678 CIFC21 H20 N2 O3P 1 21/n 19.8444; 10.7537; 17.1394
90; 100.088; 90		1786.39Wang, De-Wei; Syu, Siang-en; Hung, Yi-Ting; Chen, Pei-yi; Lee, Chia-Jui; Chen, Ko-Wei; Chen, Yu-Jhang; Lin, Wenwei
Organocatalytic tandem three-component reaction of aldehyde, alkyl vinyl ketone, and amide: one-pot syntheses of highly functional alkenes.
Organic & biomolecular chemistry, 2011, 9, 363-366
7151679 CIFC19 H16 N2 O6P c a b11.2975; 15.8036; 20.145
90; 90; 90		3596.71Wang, De-Wei; Syu, Siang-en; Hung, Yi-Ting; Chen, Pei-yi; Lee, Chia-Jui; Chen, Ko-Wei; Chen, Yu-Jhang; Lin, Wenwei
Organocatalytic tandem three-component reaction of aldehyde, alkyl vinyl ketone, and amide: one-pot syntheses of highly functional alkenes.
Organic & biomolecular chemistry, 2011, 9, 363-366
7151680 CIFC19 H16 Cl N O4P 1 21/c 17.8329; 16.6085; 13.2043
90; 101.014; 90		1686.14Wang, De-Wei; Syu, Siang-en; Hung, Yi-Ting; Chen, Pei-yi; Lee, Chia-Jui; Chen, Ko-Wei; Chen, Yu-Jhang; Lin, Wenwei
Organocatalytic tandem three-component reaction of aldehyde, alkyl vinyl ketone, and amide: one-pot syntheses of highly functional alkenes.
Organic & biomolecular chemistry, 2011, 9, 363-366
7151681 CIFC38 H36 N O7P -19.851; 11.303; 15.868
82.36; 76.88; 64.54		1552.4Liu, Jia; Wang, Xi; Sun, Chang-Liang; Li, Bi-Jie; Shi, Zhang-Jie; Wang, Min
New strategy to construct fused/bridged/spiro carbocyclic scaffolds based on the design of novel 6-C synthon precursor.
Organic & biomolecular chemistry, 2011, 9, 1572-1577
7151682 CIFC31 H34 O13P 1 21/n 112.624; 10.895; 21.852
90; 104.9; 90		2904.4Liu, Jia; Wang, Xi; Sun, Chang-Liang; Li, Bi-Jie; Shi, Zhang-Jie; Wang, Min
New strategy to construct fused/bridged/spiro carbocyclic scaffolds based on the design of novel 6-C synthon precursor.
Organic & biomolecular chemistry, 2011, 9, 1572-1577
7151683 CIFC20 H17 N3 O8P 21 21 219.7745; 9.7915; 20.5118
90; 90; 90		1963.12Sen, Subhabrata; Potti, Venkata R.; Surakanti, Ramu; Murthy, Y. L. N.; Pallepogu, Raghavaiah
Enantioselective synthesis of spirooxoindoles via chiral auxiliary (bicyclic lactam) controlled SNAr reactions.
Organic & biomolecular chemistry, 2011, 9, 358-360
7151684 CIFC16 H12 N2 O3P 21 21 217.471; 8.305; 21.194
90; 90; 90		1315.02Sunderland, Peter T.; Dhami, Archana; Mahon, Mary F.; Jones, Louise A.; Tully, Sophie R.; Lloyd, Matthew D.; Thompson, Andrew S.; Javaid, Hashim; Martin, Niall M. B.; Threadgill, Michael D.
Synthesis of 4-alkyl-, 4-aryl- and 4-arylamino-5-aminoisoquinolin-1-ones and identification of a new PARP-2 selective inhibitor.
Organic & biomolecular chemistry, 2011, 9, 881-891
7151685 CIFC16 H11 Br N2 O3P -18.618; 9.912; 10.226
114.347; 108.553; 100.738		701.65Sunderland, Peter T.; Dhami, Archana; Mahon, Mary F.; Jones, Louise A.; Tully, Sophie R.; Lloyd, Matthew D.; Thompson, Andrew S.; Javaid, Hashim; Martin, Niall M. B.; Threadgill, Michael D.
Synthesis of 4-alkyl-, 4-aryl- and 4-arylamino-5-aminoisoquinolin-1-ones and identification of a new PARP-2 selective inhibitor.
Organic & biomolecular chemistry, 2011, 9, 881-891
7151686 CIFC32 H24 N2 O4P 1 2/c 113.988; 10.997; 16.197
90; 95.645; 90		2479.44Sunderland, Peter T.; Dhami, Archana; Mahon, Mary F.; Jones, Louise A.; Tully, Sophie R.; Lloyd, Matthew D.; Thompson, Andrew S.; Javaid, Hashim; Martin, Niall M. B.; Threadgill, Michael D.
Synthesis of 4-alkyl-, 4-aryl- and 4-arylamino-5-aminoisoquinolin-1-ones and identification of a new PARP-2 selective inhibitor.
Organic & biomolecular chemistry, 2011, 9, 881-891
7151687 CIFC20 H16 Br N O5P 1 21 18.2259; 12.3386; 9.1136
90; 97.552; 90		917Jin, Zhichao; Yu, Feng; Wang, Xiao; Huang, Huicai; Luo, Xiaoyan; Liang, Xinmiao; Ye, Jinxing
A one-pot asymmetric organocatalytic tandem reaction for the synthesis of oxazine derivatives.
Organic & biomolecular chemistry, 2011, 9, 1809-1816
7151688 CIFC24 H25 F3 N2 O2 SP 21 21 219.6263; 14.1765; 16.473
90; 90; 90		2248Grellepois, Fabienne; Nonnenmacher, Jean; Lachaud, Fabien; Portella, Charles
Enantiomerically pure 2-aryl(alkyl)-2-trifluoromethylaziridines: synthesis and ring opening with selected O- and N-nucleophiles.
Organic & biomolecular chemistry, 2011, 9, 1160-1168
7151689 CIFC21 H20 F5 N O2 SP 43 21 29.7065; 9.7065; 45.227
90; 90; 90		4261.1Li, Peng; Liu, Li-Juan; Liu, Jin-Tao
Per(poly)fluoroalkanesulfinamides assisted diastereoselective three-component inverse-electron-demand aza Diels-Alder reaction.
Organic & biomolecular chemistry, 2011, 9, 74-77
7151690 CIFC14 H11 Cl F7 N O2 SP 1 21/c 112.1841; 5.7816; 24.406
90; 99.492; 90		1695.7Li, Peng; Liu, Li-Juan; Liu, Jin-Tao
Per(poly)fluoroalkanesulfinamides assisted diastereoselective three-component inverse-electron-demand aza Diels-Alder reaction.
Organic & biomolecular chemistry, 2011, 9, 74-77
7151691 CIFC25 H33 N O9P 21 21 2110.7328; 12.0282; 19.7768
90; 90; 90		2553.1Kurhade, Suresh E.; Mengawade, Tanaji; Bhuniya, Debnath; Palle, Venkata P.; Reddy, D. Srinivasa
Synthesis of novel sugar-lactam conjugates using the Aubé reaction.
Organic & biomolecular chemistry, 2011, 9, 744-747
7151692 CIFC14 H12 N2 O4 SP 1 21 16.771; 26.804; 7.448
90; 89.867; 90		1351.73Jeffs, Laura; Arquier, Damien; Kariuki, Benson; Bethell, Donald; Page, Philip C Bulman; Hutchings, Graham J.
On the enantioselectivity of aziridination of styrene catalysed by copper triflate and copper-exchanged zeolite Y: consequences of the phase behaviour of enantiomeric mixtures of N-arene-sulfonyl-2-phenylaziridines.
Organic & biomolecular chemistry, 2011, 9, 1079-1084
7151693 CIFC14 H12 N2 O4 SP 1 21/a 113.483; 7.543; 14.765
90; 114.997; 90		1360.98Jeffs, Laura; Arquier, Damien; Kariuki, Benson; Bethell, Donald; Page, Philip C Bulman; Hutchings, Graham J.
On the enantioselectivity of aziridination of styrene catalysed by copper triflate and copper-exchanged zeolite Y: consequences of the phase behaviour of enantiomeric mixtures of N-arene-sulfonyl-2-phenylaziridines.
Organic & biomolecular chemistry, 2011, 9, 1079-1084
7151694 CIFC21 H31 N3 O7P 1 21/c 110.158; 14.069; 17.637
90; 99.962; 90		2482.6Desmarchelier, Alaric; Marrot, Jérôme; Moreau, Xavier; Greck, Christine
Asymmetric organocatalytic Michael-α-amination sequence for the construction of a quaternary stereocenter.
Organic & biomolecular chemistry, 2011, 9, 994-997
7151695 CIFC20 H16 N2 OC 1 2/c 123.0916; 7.3204; 38.0041
90; 97.32; 90		6371.8Wu, Hung-Chou; Hwang, Long-Chih; Wu, Ming-Jung
A copper-mediated cyclization reaction of hydrazine with enediynones providing pyrazolo[1,5-a]pyridines.
Organic & biomolecular chemistry, 2011, 9, 670-672
7151696 CIFC38 H42 Cu2 N4P 1 21/a 114.2593; 12.1166; 19.4748
90; 101.738; 90		3294.38Wu, Hung-Chou; Hwang, Long-Chih; Wu, Ming-Jung
A copper-mediated cyclization reaction of hydrazine with enediynones providing pyrazolo[1,5-a]pyridines.
Organic & biomolecular chemistry, 2011, 9, 670-672
7151697 CIFC17 H19 Cl Cu N2 OP -19.3101; 9.2508; 11.242
69.333; 84.453; 76.764		881.72Wu, Hung-Chou; Hwang, Long-Chih; Wu, Ming-Jung
A copper-mediated cyclization reaction of hydrazine with enediynones providing pyrazolo[1,5-a]pyridines.
Organic & biomolecular chemistry, 2011, 9, 670-672
7151698 CIFC22 H22 O4P -16.0102; 10.0194; 15.9053
81.28; 83.245; 75.899		914.94Sada, Mutsumi; Nomura, Kenichi; Matsubara, Seijiro
A tandem reaction of organozinc reagent prepared from palladium-catalyzed umpolung method: diastereoselective formation of cyclohexene derivatives bearing three adjacent stereocenters.
Organic & biomolecular chemistry, 2011, 9, 1389-1393
7151699 CIFC13 H13 N O2P c a 218.894; 8.467; 15.2509
90; 90; 90		1148.48Smith, Catherine J.; Smith, Christopher D.; Nikbin, Nikzad; Ley, Steven V.; Baxendale, Ian R.
Flow synthesis of organic azides and the multistep synthesis of imines and amines using a new monolithic triphenylphosphine reagent.
Organic & biomolecular chemistry, 2011, 9, 1927-1937
7151700 CIFC7 H3 Br N4P -17.4355; 8.5948; 13.7214
88.715; 89.784; 68.818		817.43Smith, Catherine J.; Smith, Christopher D.; Nikbin, Nikzad; Ley, Steven V.; Baxendale, Ian R.
Flow synthesis of organic azides and the multistep synthesis of imines and amines using a new monolithic triphenylphosphine reagent.
Organic & biomolecular chemistry, 2011, 9, 1927-1937
7151701 CIFC10 H9 N5 OC 1 2/c 127.8326; 6.2301; 11.8916
90; 94.99; 90		2054.19Smith, Catherine J.; Nikbin, Nikzad; Ley, Steven V.; Lange, Heiko; Baxendale, Ian R.
A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles.
Organic & biomolecular chemistry, 2011, 9, 1938-1947
7151702 CIFC11 H7 N5C 1 c 110.1129; 14.736; 7.3628
90; 118.152; 90		967.43Smith, Catherine J.; Nikbin, Nikzad; Ley, Steven V.; Lange, Heiko; Baxendale, Ian R.
A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles.
Organic & biomolecular chemistry, 2011, 9, 1938-1947
7151703 CIFC12 H13 N5C 1 2/c 133.4277; 6.1102; 12.4082
90; 106.375; 90		2431.57Smith, Catherine J.; Nikbin, Nikzad; Ley, Steven V.; Lange, Heiko; Baxendale, Ian R.
A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles.
Organic & biomolecular chemistry, 2011, 9, 1938-1947
7151704 CIFC10 H5 Br N6P -17.2576; 8.4262; 8.8405
97.305; 110.101; 90.585		502.74Smith, Catherine J.; Nikbin, Nikzad; Ley, Steven V.; Lange, Heiko; Baxendale, Ian R.
A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles.
Organic & biomolecular chemistry, 2011, 9, 1938-1947
7151705 CIFC18 H28 N2 O6 Se2P 1 21 16.9783; 11.2514; 14.4801
90; 91.389; 90		1136.58Bhuyan, Bhaskar J.; Mugesh, Govindasamy
Synthesis, characterization and antioxidant activity of angiotensin converting enzyme inhibitors.
Organic & biomolecular chemistry, 2011, 9, 1356-1365
7151706 CIFC21 H36 Br N2 O3P 15.3658; 10.1748; 10.905
82.918; 88.385; 78.119		578.17Bhuyan, Bhaskar J.; Mugesh, Govindasamy
Synthesis, characterization and antioxidant activity of angiotensin converting enzyme inhibitors.
Organic & biomolecular chemistry, 2011, 9, 1356-1365
7151707 CIFC10 H12 O3 SeP 21 a b5.7334; 7.899; 47.642
90; 90; 90		2157.6Bhuyan, Bhaskar J.; Mugesh, Govindasamy
Synthesis, characterization and antioxidant activity of angiotensin converting enzyme inhibitors.
Organic & biomolecular chemistry, 2011, 9, 1356-1365
7151708 CIFC12 H13 N O4P 1 21 15.654; 7.4586; 13.1
90; 99.649; 90		544.62Hong, Bor-Cherng; Kotame, Prakash; Liao, Ju-Hsiou
Enantioselective organocatalytic domino Michael-acetalization-Henry reactions of 2-hydroxynitrostyrene and aldehyde for the synthesis of tetrahydro-6H-benzo[c]chromenones.
Organic & biomolecular chemistry, 2011, 9, 382-386
7151709 CIFC12 H12 Br N O4P 21 21 216.8992; 6.9979; 24.978
90; 90; 90		1205.9Hong, Bor-Cherng; Kotame, Prakash; Liao, Ju-Hsiou
Enantioselective organocatalytic domino Michael-acetalization-Henry reactions of 2-hydroxynitrostyrene and aldehyde for the synthesis of tetrahydro-6H-benzo[c]chromenones.
Organic & biomolecular chemistry, 2011, 9, 382-386
7151710 CIFC13 H15 N O6P 1 21 15.331; 7.848; 14.735
90; 95.877; 90		613.2Hong, Bor-Cherng; Kotame, Prakash; Liao, Ju-Hsiou
Enantioselective organocatalytic domino Michael-acetalization-Henry reactions of 2-hydroxynitrostyrene and aldehyde for the synthesis of tetrahydro-6H-benzo[c]chromenones.
Organic & biomolecular chemistry, 2011, 9, 382-386
7151711 CIFC27 H26 Cl N3 O2P -19.7651; 11.2401; 11.3429
76.03; 81.135; 73.662		1154.42He, Ping; Nie, Yi-Bo; Wu, Jing; Ding, Ming-Wu
Unexpected synthesis of indolo[1,2-c]quinazolines by a sequential Ugi 4CC-Staudinger-aza-Wittig-nucleophilic addition reaction.
Organic & biomolecular chemistry, 2011, 9, 1429-1436
7151712 CIFC25 H25 N O2P 1 21/c 19.4053; 9.7021; 21.9587
90; 92.978; 90		2001.05Cheetham, Caroline A.; Massey, Richard S.; Pira, Silvain L.; Pritchard, Robin G.; Wallace, Timothy W.
Atroposelective formation of dibenz[c,e]azepines via intramolecular direct arylation with centre-axis chirality transfer.
Organic & biomolecular chemistry, 2011, 9, 1831-1838
7151713 CIFC16 H18 N2 O2P 1 21/c 113.333; 10.094; 11.308
90; 109.94; 90		1430.6Pozharskii, Alexander F.; Povalyakhina, Maria A.; Degtyarev, Alexander V.; Ryabtsova, Oxana V.; Ozeryanskii, Valery A.; Dyablo, Olga V.; Tkachuk, Anna V.; Kazheva, Olga N.; Chekhlov, Anatolii N.; Dyachenko, Oleg A.
Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect.
Organic & biomolecular chemistry, 2011, 9, 1887-1900
7151714 CIFC24 H22 N7P -16.6455; 12.928; 12.943
101.997; 90.461; 94.532		1083.94Pozharskii, Alexander F.; Povalyakhina, Maria A.; Degtyarev, Alexander V.; Ryabtsova, Oxana V.; Ozeryanskii, Valery A.; Dyablo, Olga V.; Tkachuk, Anna V.; Kazheva, Olga N.; Chekhlov, Anatolii N.; Dyachenko, Oleg A.
Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect.
Organic & biomolecular chemistry, 2011, 9, 1887-1900
7151715 CIFC20 H32 N4P 1 c 134.582; 10.1577; 8.339
90; 92.891; 90		2925.5Pozharskii, Alexander F.; Povalyakhina, Maria A.; Degtyarev, Alexander V.; Ryabtsova, Oxana V.; Ozeryanskii, Valery A.; Dyablo, Olga V.; Tkachuk, Anna V.; Kazheva, Olga N.; Chekhlov, Anatolii N.; Dyachenko, Oleg A.
Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect.
Organic & biomolecular chemistry, 2011, 9, 1887-1900
7151716 CIFC24 H22 N5P 1 21/c 110.247; 11.52; 34.634
90; 102.208; 90		3996Pozharskii, Alexander F.; Povalyakhina, Maria A.; Degtyarev, Alexander V.; Ryabtsova, Oxana V.; Ozeryanskii, Valery A.; Dyablo, Olga V.; Tkachuk, Anna V.; Kazheva, Olga N.; Chekhlov, Anatolii N.; Dyachenko, Oleg A.
Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect.
Organic & biomolecular chemistry, 2011, 9, 1887-1900
7151717 CIFC17 H9 I O3P 1 21/c 112.173; 14.445; 8.223
90; 103.46; 90		1406.2Raffa, Guillaume; Belot, Sébastien; Balme, Geneviève; Monteiro, Nuno
Iodocyclization versus diiodination in the reaction of 3-alkynyl-4-methoxycoumarins with iodine: Synthesis of 3-iodofuro[2,3-b]chromones.
Organic & biomolecular chemistry, 2011, 9, 1474-1478
7151718 CIFC18 H12 I2 O3P 1 21/c 118.6185; 14.0017; 14.1965
90; 107.82; 90		3523.34Raffa, Guillaume; Belot, Sébastien; Balme, Geneviève; Monteiro, Nuno
Iodocyclization versus diiodination in the reaction of 3-alkynyl-4-methoxycoumarins with iodine: Synthesis of 3-iodofuro[2,3-b]chromones.
Organic & biomolecular chemistry, 2011, 9, 1474-1478
7151719 CIFC25 H21 Cl N2 O3P 21 21 2110.27; 11.202; 18.897
90; 90; 90		2174Liu, Tang-Lin; Xue, Zhi-Yong; Tao, Hai-Yan; Wang, Chun-Jiang
Catalytic asymmetric 1,3-dipolar cycloaddition of N-unprotected 2-oxoindolin-3-ylidene derivatives and azomethine ylides for the construction of spirooxindole-pyrrolidines.
Organic & biomolecular chemistry, 2011, 9, 1980-1986
7151720 CIFC16 H9 F10 N5 OP 1 21/n 116.012; 11.932; 19.682
90; 104.571; 90		3639Bose, Purnandhu; Ahamed, B. Nisar; Ghosh, Pradyut
Functionalized guanidinium chloride based colourimetric sensors for fluoride and acetate: single crystal X-ray structural evidence of -NH deprotonation and complexation.
Organic & biomolecular chemistry, 2011, 9, 1972-1979
7151721 CIFC37 H31 N5 O4P b c a14.5032; 9.6882; 44.522
90; 90; 90		6255.8Bose, Purnandhu; Ahamed, B. Nisar; Ghosh, Pradyut
Functionalized guanidinium chloride based colourimetric sensors for fluoride and acetate: single crystal X-ray structural evidence of -NH deprotonation and complexation.
Organic & biomolecular chemistry, 2011, 9, 1972-1979
7151722 CIFC36 H22 F10 N5 O6P 1 21/m 16.8654; 34.567; 7.138
90; 98.565; 90		1675.1Bose, Purnandhu; Ahamed, B. Nisar; Ghosh, Pradyut
Functionalized guanidinium chloride based colourimetric sensors for fluoride and acetate: single crystal X-ray structural evidence of -NH deprotonation and complexation.
Organic & biomolecular chemistry, 2011, 9, 1972-1979
7151723 CIFC18 H14 OP 1 21/c 14.7615; 11.9406; 21.373
90; 93.296; 90		1213.2Böß, Esther; Hillringhaus, Tim; Nitsch, Jacqueline; Klussmann, Martin
Lewis acid-catalysed one pot synthesis of substituted xanthenes.
Organic & biomolecular chemistry, 2011, 9, 1744-1748
7151724 CIFC16 H16 O2P -17.3745; 8.763; 10.395
99.79; 110.27; 98.47		605.3Böß, Esther; Hillringhaus, Tim; Nitsch, Jacqueline; Klussmann, Martin
Lewis acid-catalysed one pot synthesis of substituted xanthenes.
Organic & biomolecular chemistry, 2011, 9, 1744-1748
7151725 CIFC20 H16 SiP 21 21 218.3831; 11.7677; 15.012
90; 90; 90		1480.9Tanikawa, Tomoharu; Saito, Masaichi; Guo, Jing Dong; Nagase, Shigeru
Synthesis, structures and optical properties of trisilasumanene and its related compounds.
Organic & biomolecular chemistry, 2011, 9, 1731-1735
7151726 CIFC8 H13 N O3P 1 21 16.0046; 6.104; 12.099
90; 103.144; 90		431.84Franklin, Andrew I.; Bensa, David; Adams, Harry; Coldham, Iain
Transannular dipolar cycloaddition as an approach towards the synthesis of the core ring system of the sarain alkaloids.
Organic & biomolecular chemistry, 2011, 9, 1901-1907
7151727 CIFC30 H30 Br2 N2 O4P 21 21 219.5861; 14.757; 19.402
90; 90; 90		2744.6Franklin, Andrew I.; Bensa, David; Adams, Harry; Coldham, Iain
Transannular dipolar cycloaddition as an approach towards the synthesis of the core ring system of the sarain alkaloids.
Organic & biomolecular chemistry, 2011, 9, 1901-1907
7151728 CIFC37 H52 Cl N O11P 1 21 19.772; 17.25; 11.937
90; 97.6; 90		1994.5Yu, Jipan; Miao, Zhiwei; Chen, Ruyu
Highly efficient asymmetric vinylogous Mannich reaction induced by O-pivaloylated d-galactosylamine as the chiral auxiliary.
Organic & biomolecular chemistry, 2011, 9, 1756-1762
7151729 CIFC32 H18 N4P b c a7.5239; 13.8384; 22.5279
90; 90; 90		2345.6Lin, Yi-Chun; Lin, Chih-Hsiu; Chen, Chan-Yu; Sun, Shih-Sheng; Pal, Bikash
Synthesis of electron deficient acene derivatives via a bidirectional iterative elongation reaction
Organic & Biomolecular Chemistry, 2011, 9, 4507
7151730 CIFC8 H11 Cl3 I N O2P 1 21 18.0678; 16.6957; 9.6537
90; 99.437; 90		1282.73Ahmad, Sajjad; Thomas, Lynne H.; Sutherland, Andrew
Stereoselective synthesis of polyhydroxylated aminocyclohexanes.
Organic & biomolecular chemistry, 2011, 9, 2801-2808
7151731 CIFC8 H12 Cl3 N O4C 1 2 139.705; 5.8312; 20.2162
90; 91.296; 90		4679.4Ahmad, Sajjad; Thomas, Lynne H.; Sutherland, Andrew
Stereoselective synthesis of polyhydroxylated aminocyclohexanes.
Organic & biomolecular chemistry, 2011, 9, 2801-2808
7151732 CIFC34 H30 N2 OP -19.4283; 10.252; 14.872
77.695; 79.25; 71.711		1322.4He, Yong; Krishnamoorthy, Pasupathy; Lima, Heather M.; Chen, Yingzhong; Wu, Haiyan; Sivappa, Rasapalli; Dias, H. V. Rasika; Lovely, Carl J.
Intramolecular Diels-Alder chemistry of 4-vinylimidazoles.
Organic & biomolecular chemistry, 2011, 9, 2685-2701
7151733 CIFC24 H26 N4 O3 SP c a 2110.5806; 10.1271; 40.3707
90; 90; 90		4325.8He, Yong; Krishnamoorthy, Pasupathy; Lima, Heather M.; Chen, Yingzhong; Wu, Haiyan; Sivappa, Rasapalli; Dias, H. V. Rasika; Lovely, Carl J.
Intramolecular Diels-Alder chemistry of 4-vinylimidazoles.
Organic & biomolecular chemistry, 2011, 9, 2685-2701
7151734 CIFC30 H35 Cl2 N7 O5 S2P 1 21/n 116.9209; 10.9678; 19.3539
90; 114.309; 90		3273.3He, Yong; Krishnamoorthy, Pasupathy; Lima, Heather M.; Chen, Yingzhong; Wu, Haiyan; Sivappa, Rasapalli; Dias, H. V. Rasika; Lovely, Carl J.
Intramolecular Diels-Alder chemistry of 4-vinylimidazoles.
Organic & biomolecular chemistry, 2011, 9, 2685-2701
7151735 CIFC11 H10 O3P 1 21/c 18.3372; 10.931; 9.7141
90; 94.165; 90		882.95Malik, Heetika; Kohlen, Wouter; Jamil, Muhammad; Rutjes, Floris P. J. T.; Zwanenburg, Binne
Aromatic A-ring analogues of orobanchol, new germination stimulants for seeds of parasitic weeds.
Organic & biomolecular chemistry, 2011, 9, 2286-2293
7151736 CIFC17 H14 O6P -16.8264; 8.0831; 12.8838
91.219; 96.917; 94.85		702.85Malik, Heetika; Kohlen, Wouter; Jamil, Muhammad; Rutjes, Floris P. J. T.; Zwanenburg, Binne
Aromatic A-ring analogues of orobanchol, new germination stimulants for seeds of parasitic weeds.
Organic & biomolecular chemistry, 2011, 9, 2286-2293
7151737 CIFC17 H14 O6P 1 c 18.1223; 7.04; 13.0388
90; 107.502; 90		711.06Malik, Heetika; Kohlen, Wouter; Jamil, Muhammad; Rutjes, Floris P. J. T.; Zwanenburg, Binne
Aromatic A-ring analogues of orobanchol, new germination stimulants for seeds of parasitic weeds.
Organic & biomolecular chemistry, 2011, 9, 2286-2293
7151738 CIFC17 H14 O6P 1 21/c 16.6845; 7.9964; 26.937
90; 94.935; 90		1434.5Malik, Heetika; Kohlen, Wouter; Jamil, Muhammad; Rutjes, Floris P. J. T.; Zwanenburg, Binne
Aromatic A-ring analogues of orobanchol, new germination stimulants for seeds of parasitic weeds.
Organic & biomolecular chemistry, 2011, 9, 2286-2293
7151739 CIFC24 H23 Br N2 O6P 1 21/n 18.558; 15.813; 16.673
90; 98.473; 90		2231.7Pan, Huan-Rui; Wang, Xiao-Rong; Yan, Cai-Xia; Sun, Zhong-Xin; Cheng, Ying
The multicomponent reaction of imidazo[1,5-a]pyridine carbenes with phthalaldehydes and dimethyl acetylenedicarboxylate: a facile construction of benzo[d]furo[3,2-b]azepines.
Organic & biomolecular chemistry, 2011, 9, 2166-2174
7151740 CIFC24 H23 Br N2 O6P -429.508; 29.508; 12.139
90; 90; 90		10569.7Pan, Huan-Rui; Wang, Xiao-Rong; Yan, Cai-Xia; Sun, Zhong-Xin; Cheng, Ying
The multicomponent reaction of imidazo[1,5-a]pyridine carbenes with phthalaldehydes and dimethyl acetylenedicarboxylate: a facile construction of benzo[d]furo[3,2-b]azepines.
Organic & biomolecular chemistry, 2011, 9, 2166-2174
7151741 CIFC24 H23 Br N2 O6P -17.9953; 12.083; 13.275
65.855; 88.718; 84.251		1164.1Pan, Huan-Rui; Wang, Xiao-Rong; Yan, Cai-Xia; Sun, Zhong-Xin; Cheng, Ying
The multicomponent reaction of imidazo[1,5-a]pyridine carbenes with phthalaldehydes and dimethyl acetylenedicarboxylate: a facile construction of benzo[d]furo[3,2-b]azepines.
Organic & biomolecular chemistry, 2011, 9, 2166-2174
7151742 CIFC14 H16 O4P 21 21 215.4822; 8.8469; 24.9538
90; 90; 90		1210.27Nesbitt, Caroline L.; McErlean, Christopher S. P.
Total synthesis of C19 lipid diols containing a 2,5-disubstituted-3-oxygenated tetrahydrofuran.
Organic & biomolecular chemistry, 2011, 9, 2198-2208
7151743 CIFC27 H22 Br N O4P 1 21 15.4962; 14.702; 14.657
90; 100.037; 90		1166.2Li, Wenjun; Wu, Wenbin; Yu, Feng; Huang, Huicai; Liang, Xinmiao; Ye, Jinxing
Catalytic asymmetric Michael addition with curcumin derivative.
Organic & biomolecular chemistry, 2011, 9, 2505-2511
7151744 CIFC4 H9 Cl O2 SP 1 21/n 17.0225; 7.3868; 13.8536
90; 100.912; 90		705.65Yoo, Ellie Jung-Hwa; Feketeová, Linda; Khairallah, George N.; White, Jonathan M.; O'Hair, Richard A J
Structure and unimolecular chemistry of protonated sulfur betaines, (CH3)2S(+)(CH2)(n)CO2H (n = 1 and 2).
Organic & biomolecular chemistry, 2011, 9, 2751-2759
7151745 CIFC11 H13 N3 O9 SP -17.3627; 9.589; 11.7822
69.895; 73.702; 79.988		746.99Yoo, Ellie Jung-Hwa; Feketeová, Linda; Khairallah, George N.; White, Jonathan M.; O'Hair, Richard A J
Structure and unimolecular chemistry of protonated sulfur betaines, (CH3)2S(+)(CH2)(n)CO2H (n = 1 and 2).
Organic & biomolecular chemistry, 2011, 9, 2751-2759
7151746 CIFC24 H17 N2 O3P n a 2116.927; 12.667; 18.063
90; 90; 90		3873Qi, Hengzhen; Li, Xinyao; Xu, Jiaxi
Stereoselective control in the Staudinger reactions involving monosubstituted ketenes with electron acceptor substituents: experimental investigation and theoretical rationalization.
Organic & biomolecular chemistry, 2011, 9, 2702-2714
7151747 CIFC16 H12 N2 OP 1 21/c 112.294; 4.9467; 20.381
90; 101.322; 90		1215.3Qi, Hengzhen; Li, Xinyao; Xu, Jiaxi
Stereoselective control in the Staudinger reactions involving monosubstituted ketenes with electron acceptor substituents: experimental investigation and theoretical rationalization.
Organic & biomolecular chemistry, 2011, 9, 2702-2714
7151748 CIFC11 H5 F4 N OI 41 c d13.0912; 13.0912; 23.1759
90; 90; 90		3971.9Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151749 CIFC26.5 H16 Br3 F2 N S3P -17.0016; 10.9436; 17.466
92.675; 99.643; 90.003		1317.9Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151750 CIFC11 H4 F3 N SP -17.223; 7.9584; 9.1866
100.979; 97.143; 113.863		462.01Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151751 CIFC18 H8 F2 O2P 1 21/n 16.198; 6.525; 15.416
90; 97.211; 90		618.5Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151752 CIFC18 H8 Br F3 S2P 1 21/c 19.8845; 15.668; 10.3729
90; 92.2845; 90		1605.18Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151753 CIFC18 H8 Br F3 S2P 1 21/c 115.1514; 12.9717; 8.1916
90; 103.522; 90		1565.34Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151754 CIFC18 H8 F2 S2P 1 21/c 17.823; 3.911; 21.623
90; 92.499; 90		660.9Ponce González, Julia; Edgar, Mark; Elsegood, Mark R. J.; Weaver, George W.
Synthesis of fluorinated fused benzofurans and benzothiophenes: Smiles-type rearrangement and cyclisation of perfluoro(het)aryl ethers and sulfides.
Organic & biomolecular chemistry, 2011, 9, 2294-2305
7151755 CIFC14 H18 N2 O4 SP -15.6949; 9.6545; 13.611
73.2; 83.98; 80.88		706Kissane, Marie; Murphy, Maureen; O'Brien, Elisabeth; Chopra, Jay; Murphy, Linda; Collins, Stuart G.; Lawrence, Simon E.; Maguire, Anita R.
Addition-substitution reactions of 2-thio-3-chloroacrylamides with carbon, nitrogen, oxygen, sulfur and selenium nucleophiles.
Organic & biomolecular chemistry, 2011, 9, 2452-2472
7151756 CIFC20 H25 N O4 SP 21 21 215.3188; 12.594; 29.209
90; 90; 90		1956.6Kissane, Marie; Murphy, Maureen; O'Brien, Elisabeth; Chopra, Jay; Murphy, Linda; Collins, Stuart G.; Lawrence, Simon E.; Maguire, Anita R.
Addition-substitution reactions of 2-thio-3-chloroacrylamides with carbon, nitrogen, oxygen, sulfur and selenium nucleophiles.
Organic & biomolecular chemistry, 2011, 9, 2452-2472
7151757 CIFC9 H14 N2 O2 SeP n a 218.37; 11; 12.192
90; 90; 90		1122.5Hodage, Ananda S.; Phadnis, Prasad P.; Wadawale, Amey; Priyadarsini, K. I.; Jain, Vimal K.
Synthesis, characterization and structures of 2-(3,5-dimethylpyrazol-1-yl)ethylseleno derivatives and their probable glutathione peroxidase (GPx) like activity.
Organic & biomolecular chemistry, 2011, 9, 2992-2998

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