| Year |
Citation |
Score |
| 2022 |
King D, Wilson CR, Herron L, Deng CL, Mehdi S, Tiwary P, Hof F, Isaacs L. Molecular recognition of methylated amino acids and peptides by Pillar[6]MaxQ. Organic & Biomolecular Chemistry. PMID 36097881 DOI: 10.1039/d2ob01487d |
0.571 |
|
| 2021 |
Warmerdam Z, Kamba BE, Le MH, Schrader T, Isaacs L, Bayer P, Hof F. Binding Methylarginines and Methyllysines as Free Amino Acids: A Comparative Study of Multiple Host Classes. Chembiochem : a European Journal of Chemical Biology. 23: e202100502. PMID 34758178 DOI: 10.1002/cbic.202100502 |
0.604 |
|
| 2020 |
Ndendjio SZ, Liu W, Yvanez N, Meng Z, Zavalij PY, Isaacs LD. Triptycene walled glycoluril trimer: synthesis and recognition properties New Journal of Chemistry. 44: 338-345. PMID 33867799 DOI: 10.1039/C9Nj05336K |
0.385 |
|
| 2020 |
Brady KG, Gilberg L, Sigwalt D, Bistany-Riebman J, Murkli S, Klemm J, Kulhánek P, Šindelář V, Isaacs L. Conformationally Mobile Acyclic Cucurbit[n]uril-Type Receptors Derived from an S-shaped Methylene Bridged Glycoluril Pentamer. Supramolecular Chemistry. 32: 479-494. PMID 33731981 DOI: 10.1080/10610278.2020.1795173 |
0.34 |
|
| 2020 |
Lu X, Zebaze Ndendjio SA, Zavalij PY, Isaacs L. Acyclic Cucurbit[]uril-Type Receptors: Optimization of Electrostatic Interactions for Dicationic Guests. Organic Letters. PMID 32520574 DOI: 10.1021/Acs.Orglett.0C01637 |
0.318 |
|
| 2020 |
Xue W, Zavalij PY, Isaacs L. Pillar[n]MaxQ: A New High Affinity Host Family for Sequestration in Water. Angewandte Chemie (International Ed. in English). PMID 32413198 DOI: 10.1002/Anie.202005902 |
0.342 |
|
| 2020 |
Xue W, Zavalij PY, Isaacs L. Back Cover: Pillar[n]MaxQ: A New High Affinity Host Family for Sequestration in Water (Angew. Chem. Int. Ed. 32/2020) Angewandte Chemie. 59: 13664-13664. DOI: 10.1002/Anie.202007682 |
0.322 |
|
| 2020 |
Xue W, Zavalij PY, Isaacs L. Rücktitelbild: Pillar[n]MaxQ: A New High Affinity Host Family for Sequestration in Water (Angew. Chem. 32/2020) Angewandte Chemie. 132: 13768-13768. DOI: 10.1002/Ange.202007682 |
0.322 |
|
| 2019 |
Xue W, Zavalij PY, Isaacs L. Acyclic cucurbit[n]uril type receptors: secondary versus tertiary amide arms Supramolecular Chemistry. 31: 685-694. PMID 33013149 DOI: 10.1080/10610278.2019.1646425 |
0.326 |
|
| 2019 |
Shaya D, Isaacs L. Acyclic Cucurbit[n]uril-Type Containers as Receptors for Neuromuscular Blocking Agents: Structure-Binding Affinity Relationships. Croatica Chemica Acta. 92: 163-171. PMID 32855560 DOI: 10.5562/Cca3507 |
0.389 |
|
| 2019 |
Pandey S, Kankanamalage DVDW, Zhou X, Hu C, Isaacs L, Jayawickramarajah J, Mao H. Chaperone Assisted Host-Guest Interactions Revealed by Single-Molecule Force Spectroscopy. Journal of the American Chemical Society. PMID 31679339 DOI: 10.1021/Jacs.9B09019 |
0.358 |
|
| 2019 |
Liu W, Ai H, Meng Z, Isaacs L, Xu Z, Xue M, Yan Q. Interactions between acyclic CB[n]-type receptors and nitrated explosive materials. Chemical Communications (Cambridge, England). PMID 31429448 DOI: 10.1039/C9Cc05117A |
0.327 |
|
| 2019 |
Xue W, Zavalij PY, Isaacs L. Triazole functionalized acyclic cucurbit[n]uril-type receptors: host·guest recognition properties Organic and Biomolecular Chemistry. 17: 5561-5569. PMID 31112196 DOI: 10.1039/C9Ob00906J |
0.376 |
|
| 2019 |
Ndendjio SAZ, Isaacs L. Molecular recognition properties of acyclic cucurbiturils toward amino acids, peptides, and a protein Supramolecular Chemistry. 31: 432-441. DOI: 10.1080/10610278.2019.1619737 |
0.319 |
|
| 2019 |
Ganapati S, Isaacs L. Acyclic cucurbit[n]urils capped with alkylene linkers: synthesis and molecular recognition properties Supramolecular Chemistry. 31: 114-126. DOI: 10.1080/10610278.2018.1539228 |
0.383 |
|
| 2019 |
Murkli S, McNeill JN, Isaacs L. Cucurbit[8]uril•guest complexes: blinded dataset for the SAMPL6 challenge Supramolecular Chemistry. 31: 150-158. DOI: 10.1080/10610278.2018.1516885 |
0.356 |
|
| 2018 |
Samanta SK, Moncelet D, Vinciguerra B, Briken V, Isaacs L. Metal Organic Polyhedra: A Click-and-Clack Approach Toward Targeted Delivery. Helvetica Chimica Acta. 101. PMID 31231137 DOI: 10.1002/Hlca.201800057 |
0.324 |
|
| 2018 |
Rizzi A, Murkli S, McNeill JN, Yao W, Sullivan M, Gilson MK, Chiu MW, Isaacs L, Gibb BC, Mobley DL, Chodera JD. Overview of the SAMPL6 host-guest binding affinity prediction challenge. Journal of Computer-Aided Molecular Design. PMID 30415285 DOI: 10.1007/S10822-018-0170-6 |
0.324 |
|
| 2018 |
Liu W, Lu X, Meng Z, Isaacs L. A glycoluril dimer-triptycene hybrid receptor: synthesis and molecular recognition properties. Organic & Biomolecular Chemistry. PMID 30155536 DOI: 10.1039/C8Ob01575A |
0.371 |
|
| 2018 |
Liu W, Lu X, Xue W, Samanta SK, Zavalij PY, Meng Z, Isaacs L. Hybrid molecular container based on glycoluril and triptycene: synthesis, binding properties, and triggered release. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30044903 DOI: 10.1002/Chem.201802981 |
0.395 |
|
| 2018 |
Lu X, Samanta SK, Zavalij PY, Isaacs L. Blurring the Lines Between Host and Guest: A Chimeric Receptor Derived from Cucurbituril and Triptycene. Angewandte Chemie (International Ed. in English). PMID 29749674 DOI: 10.1002/Anie.201803132 |
0.363 |
|
| 2018 |
Liu W, Lu X, Xue W, Samanta SK, Zavalij PY, Meng Z, Isaacs L. Front Cover: Hybrid Molecular Container Based on Glycoluril and Triptycene: Synthesis, Binding Properties, and Triggered Release (Chem. Eur. J. 53/2018) Chemistry – a European Journal. 24: 13983-13983. DOI: 10.1002/Chem.201804178 |
0.304 |
|
| 2017 |
Ganapati S, Isaacs L. Acyclic Cucurbit[n]uril-type Receptors: Preparation, Molecular Recognition Properties and Biological Applications. Israel Journal of Chemistry. 58: 250-263. PMID 29805180 DOI: 10.1002/Ijch.201700098 |
0.443 |
|
| 2017 |
Li Y, Dong Y, Miao X, Ren Y, Zhang B, Wang P, Yu Y, Li B, Isaacs L, Cao L. Shape-Controllable and Fluorescent Supramolecular Organic Frameworks Through Aqueous Host-Guest Complexation. Angewandte Chemie (International Ed. in English). PMID 29193530 DOI: 10.1002/Anie.201710553 |
0.309 |
|
| 2017 |
Zhou X, Su X, Pathak P, Vik R, Vinciguerra B, Isaacs L, Jayawickramarajah J. Host-Guest Tethered DNA Transducer: ATP Fueled Release of a Protein Inhibitor from Cucurbit[7]uril. Journal of the American Chemical Society. PMID 28882044 DOI: 10.1021/Jacs.7B07977 |
0.345 |
|
| 2017 |
Samanta S, Quigley J, Vinciguerra B, Briken V, Isaacs L. Cucurbit[7]uril Enables Multistimuli Responsive Release from the Self-Assembled Hydrophobic Phase of a Metal Organic Polyhedron. Journal of the American Chemical Society. PMID 28621947 DOI: 10.1021/Jacs.7B05154 |
0.327 |
|
| 2017 |
Ganapati S, Grabitz SD, Murkli S, Scheffenbichler F, Rudolph MI, Zavalij PY, Eikermann M, Isaacs L. Molecular Containers Bind Drugs of Abuse in Vitro and Reverse the Hyperlocomotive Effect of Methamphetamine in Rats. Chembiochem : a European Journal of Chemical Biology. 18: 1583-1588. PMID 28586110 DOI: 10.1002/Cbic.201700289 |
0.325 |
|
| 2017 |
Samanta SK, Brady KG, Isaacs L. Self-assembly of cucurbit[7]uril based triangular [4]molecular necklaces and their fluorescence properties. Chemical Communications (Cambridge, England). PMID 28210729 DOI: 10.1039/C6Cc10328F |
0.371 |
|
| 2017 |
Liu W, Samanta SK, Smith BD, Isaacs L. Synthetic mimics of biotin/(strept)avidin. Chemical Society Reviews. PMID 28191579 DOI: 10.1039/C7Cs00011A |
0.329 |
|
| 2017 |
Sigwalt D, Šekutor M, Cao L, Zavalij PY, Hostaš J, Ajani H, Hobza P, Mlinarić-Majerski K, Glaser R, Isaacs L. Unraveling the Structure-Affinity Relationship Between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids. Journal of the American Chemical Society. PMID 28182422 DOI: 10.1021/Jacs.7B00056 |
0.403 |
|
| 2016 |
Bockus AT, Smith LC, Grice AG, Ali OA, Young CC, Mobley W, Leek A, Roberts JL, Vinciguerra B, Isaacs L, Urbach AR. Cucurbit[7]uril-Tetramethylrhodamine Conjugate for Direct Sensing and Cellular Imaging. Journal of the American Chemical Society. 138: 16549-16552. PMID 27998093 DOI: 10.1021/Jacs.6B11140 |
0.682 |
|
| 2016 |
Webber MJ, Appel EA, Vinciguerra B, Cortinas AB, Thapa LS, Jhunjhunwala S, Isaacs L, Langer R, Anderson DG. Supramolecular PEGylation of biopharmaceuticals. Proceedings of the National Academy of Sciences of the United States of America. PMID 27911829 DOI: 10.1073/Pnas.1616639113 |
0.312 |
|
| 2016 |
Gong W, Yang X, Zavalij PY, Isaacs L, Zhao Z, Liu S. From Packed "Sandwich" to "Russian Doll": Assembly by Charge-Transfer Interactions in Cucurbit[10]uril. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27862408 DOI: 10.1002/Chem.201604149 |
0.382 |
|
| 2016 |
Sigwalt D, Zavalij PY, Isaacs L. Cationic acyclic cucurbit[n]uril-type containers: synthesis and molecular recognition toward nucleotides. Supramolecular Chemistry. 28: 825-834. PMID 27746668 DOI: 10.1080/10610278.2016.1167893 |
0.398 |
|
| 2016 |
Samanta SK, Moncelet D, Briken V, Isaacs L. Metal Organic Polyhedron Capped with Cucurbit[8]uril Delivers Doxorubicin to Cancer Cells. Journal of the American Chemical Society. PMID 27723965 DOI: 10.1021/Jacs.6B09504 |
0.368 |
|
| 2016 |
Hostaš J, Sigwalt D, Šekutor M, Ajani H, Dubecký M, Řezáč J, Zavalij PY, Cao L, Wohlschlager C, Mlinarić-Majerski K, Isaacs L, Glaser R, Hobza P. A Nexus between Theory and Experiment: Non-Empirical Quantum Mechanical Computational Methodology Applied to Cucurbit[n]uril⋅Guest Binding Interactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27723181 DOI: 10.1002/Chem.201601833 |
0.386 |
|
| 2016 |
She N, Moncelet D, Gilberg L, Lu X, Sindelar V, Briken V, Isaacs L. Glycoluril-Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27492252 DOI: 10.1002/Chem.201601796 |
0.407 |
|
| 2016 |
Li W, Bockus AT, Vinciguerra B, Isaacs L, Urbach AR. Predictive recognition of native proteins by cucurbit[7]uril in a complex mixture. Chemical Communications (Cambridge, England). PMID 27311878 DOI: 10.1039/C6Cc03193E |
0.678 |
|
| 2016 |
Lu X, Isaacs L. Uptake of Hydrocarbons in Aqueous Solution by Encapsulation in Acyclic Cucurbit[n]uril-Type Molecular Containers. Angewandte Chemie (International Ed. in English). PMID 27169688 DOI: 10.1002/Anie.201602671 |
0.37 |
|
| 2016 |
Carroy G, Lemaur V, De Winter J, Isaacs L, De Pauw E, Cornil J, Gerbaux P. Energy-resolved collision-induced dissociation of non-covalent ions: charge- and guest-dependence of decomplexation reaction efficiencies. Physical Chemistry Chemical Physics : Pccp. PMID 27086657 DOI: 10.1039/C6Cp01026A |
0.303 |
|
| 2016 |
Sigwalt D, Moncelet D, Falcinelli S, Mandadapu V, Zavalij PY, Day A, Briken V, Isaacs L. Acyclic Cucurbit[n]uril-Type Molecular Containers: Influence of Linker Length on Their Function as Solubilizing Agents. Chemmedchem. PMID 26990780 DOI: 10.1002/Cmdc.201600090 |
0.31 |
|
| 2016 |
Ganapati S, Zavalij PY, Eikermann M, Isaacs L. In Vitro selectivity of an acyclic cucurbit[n]uril molecular container towards neuromuscular blocking agents relative to commonly used drugs Organic and Biomolecular Chemistry. 14: 1277-1287. PMID 26648135 DOI: 10.1039/C5Ob02356D |
0.338 |
|
| 2016 |
Škalamera D, Cao L, Isaacs L, Glaser R, Mlinarić-Majerski K. Steric hindrance to the syntheses and stabilities of 1,5- and 2,6-naphthalene N-permethylated diammonium salts Tetrahedron. 72: 1541-1546. DOI: 10.1016/J.Tet.2016.02.002 |
0.354 |
|
| 2015 |
Vinciguerra B, Zavalij PY, Isaacs L. Synthesis and Recognition Properties of Cucurbit[8]uril Derivatives. Organic Letters. 17: 5068-71. PMID 26405845 DOI: 10.1021/Acs.Orglett.5B02558 |
0.376 |
|
| 2015 |
Zhang M, Sigwalt D, Isaacs L. Differentially functionalized acyclic cucurbiturils: synthesis, self-assembly and CB[6]-induced allosteric guest binding. Chemical Communications (Cambridge, England). 51: 14620-3. PMID 26288859 DOI: 10.1039/C5Cc05803A |
0.4 |
|
| 2015 |
Lu X, Isaacs L. Synthesis and Recognition Properties of Enantiomerically Pure Acyclic Cucurbit[n]uril-Type Molecular Containers. Organic Letters. 17: 4038-41. PMID 26251172 DOI: 10.1021/Acs.Orglett.5B01948 |
0.41 |
|
| 2015 |
Cao L, Škalamera Đ, Zavalij PY, Hostaš J, Hobza P, Mlinarić-Majerski K, Glaser R, Isaacs L. Influence of hydrophobic residues on the binding of CB[7] toward diammonium ions of common ammonium···ammonium distance. Organic & Biomolecular Chemistry. 13: 6249-54. PMID 25962667 DOI: 10.1039/C5Ob00784D |
0.336 |
|
| 2015 |
Robinson EL, Zavalij PY, Isaacs L. Synthesis of a Disulfonated Derivative of Cucurbit[7]uril and Investigations of its Ability to Solubilize Insoluble Drugs. Supramolecular Chemistry. 27: 288-297. PMID 25937787 DOI: 10.1080/10610278.2014.940952 |
0.349 |
|
| 2015 |
Gilberg L, Zhang B, Zavalij PY, Sindelar V, Isaacs L. Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents. Organic & Biomolecular Chemistry. 13: 4041-50. PMID 25731639 DOI: 10.1039/C5Ob00184F |
0.399 |
|
| 2015 |
Yu Y, Li J, Zhang M, Cao L, Isaacs L. Hydrophobic monofunctionalized cucurbit[7]uril undergoes self-inclusion complexation and forms vesicle-type assemblies. Chemical Communications (Cambridge, England). 51: 3762-5. PMID 25647163 DOI: 10.1039/C5Cc00236B |
0.356 |
|
| 2015 |
Wang J, Wang M, Xiang J, Cao L, Wu A, Isaacs L. Dimeric packing of molecular clips induced by interactions between π-systems Crystengcomm. 17: 2486-2495. DOI: 10.1039/C4Ce02447H |
0.352 |
|
| 2014 |
Zhang M, Cao L, Isaacs L. Cucurbit[6]uril-cucurbit[7]uril heterodimer promotes controlled self-assembly of supramolecular networks and supramolecular micelles by self-sorting of amphiphilic guests. Chemical Communications (Cambridge, England). 50: 14756-9. PMID 25318021 DOI: 10.1039/C4Cc07268E |
0.337 |
|
| 2014 |
Isaacs L. Stimuli Responsive Systems Constructed Using Cucurbit[n]uril-Type Molecular Containers Accounts of Chemical Research. 47: 2052-2062. PMID 24785941 DOI: 10.1021/Ar500075G |
0.401 |
|
| 2014 |
Zhang B, Zavalij PY, Isaacs L. Acyclic CB[n]-type molecular containers: effect of solubilizing group on their function as solubilizing excipients Organic and Biomolecular Chemistry. 12: 2413-2422. PMID 24595500 DOI: 10.1039/C3Ob42603C |
0.378 |
|
| 2014 |
Cao L, Śekutor M, Zavalij PY, Mlinarić-Majerski K, Glaser R, Isaacs L. Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant. Angewandte Chemie (International Ed. in English). 53: 988-93. PMID 24382654 DOI: 10.1002/Anie.201309635 |
0.361 |
|
| 2014 |
Hoffman U, Grosse-Sundrup M, Eikermann-Haerter K, Zaremba S, Ayata C, Zhang B, Ma D, Isaacs L, Eikermann M. Calabadion: A New Agent to Reverse the Effects of Benzylisoquinoline and Steroidal Neuromuscular-Blocking Agents Survey of Anesthesiology. 58: 47. DOI: 10.1097/Sa.0000000000000028 |
0.4 |
|
| 2014 |
Cao L, Isaacs L. Absolute and relative binding affinity of cucurbit[7]uril towards a series of cationic guests Supramolecular Chemistry. 26: 251-258. DOI: 10.1080/10610278.2013.852674 |
0.351 |
|
| 2014 |
Wittenberg JB, Isaacs L. Cucurbit[6]uril dimer induces supramolecular polymerisation of a cationic polyethylene glycol derivative Supramolecular Chemistry. 26: 157-167. DOI: 10.1080/10610278.2013.842642 |
0.636 |
|
| 2014 |
Šekutor M, Molčanov K, Cao L, Isaacs L, Glaser R, Mlinaric̈-Majerski K. Design, synthesis, and X-ray structural analyses of diamantane diammonium salts: Guests for cucurbit[n]uril (CB[n]) hosts European Journal of Organic Chemistry. 2014: 2533-2542. DOI: 10.1002/Ejoc.201301844 |
0.397 |
|
| 2013 |
Lemaur V, Carroy G, Poussigue F, Chirot F, De Winter J, Isaacs L, Dugourd P, Cornil J, Gerbaux P. Homotropic Allosterism: In-Depth Structural Analysis of the Gas-Phase Noncovalent Complexes Associating a Double-Cavity Cucurbit[n]uril-Type Host and Size-Selected Protonated Amino Compounds. Chempluschem. 78: 959-969. PMID 31986725 DOI: 10.1002/Cplu.201300208 |
0.337 |
|
| 2013 |
Hoffmann U, Grosse-Sundrup M, Eikermann-Haerter K, Zaremba S, Ayata C, Zhang B, Ma D, Isaacs L, Eikermann M. Calabadion: A new agent to reverse the effects of benzylisoquinoline and steroidal neuromuscular-blocking agents. Anesthesiology. 119: 317-25. PMID 23549405 DOI: 10.1097/Aln.0B013E3182910213 |
0.414 |
|
| 2013 |
Wittenberg JB, Zavalij PY, Isaacs L. Supramolecular ladders from dimeric cucurbit[6]uril. Angewandte Chemie (International Ed. in English). 52: 3690-4. PMID 23417996 DOI: 10.1002/Anie.201300404 |
0.611 |
|
| 2013 |
Ghosh S, Mukhopadhyay P, Isaacs L. Deconvolution of a multi-component interaction network using systems chemistry Journal of Systems Chemistry. 1. DOI: 10.1186/1759-2208-1-6 |
0.703 |
|
| 2013 |
Hettiarachchi G, Ma D, Nguyen D, Isaacs L, Briken V. Abstract 4347: Toxicology and drug delivery by novel Cucurbit[n]uril-type molecular containers. Cancer Research. 73: 4347-4347. DOI: 10.1158/1538-7445.Am2013-4347 |
0.501 |
|
| 2013 |
Lemaur V, Carroy G, Poussigue F, Chirot F, De Winter J, Isaacs L, Dugourd P, Cornil J, Gerbaux P. Back Cover: Homotropic Allosterism: In-Depth Structural Analysis of the Gas-Phase Noncovalent Complexes Associating a Double-Cavity Cucurbit[n
]uril-Type Host and Size-Selected Protonated Amino Compounds (ChemPlusChem 9/2013) Chempluschem. 78: 1208-1208. DOI: 10.1002/Cplu.201300279 |
0.325 |
|
| 2012 |
Ma D, Zhang B, Hoffmann U, Sundrup MG, Eikermann M, Isaacs L. Acyclic cucurbit[n]uril-type molecular containers bind neuromuscular blocking agents in vitro and reverse neuromuscular block in vivo. Angewandte Chemie (International Ed. in English). 51: 11358-62. PMID 23047893 DOI: 10.1002/Anie.201206031 |
0.504 |
|
| 2012 |
Vinciguerra B, Cao L, Cannon JR, Zavalij PY, Fenselau C, Isaacs L. Synthesis and self-assembly processes of monofunctionalized cucurbit[7]uril. Journal of the American Chemical Society. 134: 13133-40. PMID 22799491 DOI: 10.1021/Ja3058502 |
0.401 |
|
| 2012 |
Chernikova E, Berdnikova D, Fedorov Y, Fedorova O, Peregudov A, Isaacs L. Self-assembly of a ternary architecture driven by cooperative Hg2+ ion binding between cucurbit[7]uril and crown ether macrocyclic hosts Chemical Communications. 48: 7256-7258. PMID 22710743 DOI: 10.1039/C2Cc33243D |
0.365 |
|
| 2012 |
Cao L, Isaacs L. Daisy chain assembly formed from a cucurbit[6]uril derivative. Organic Letters. 14: 3072-5. PMID 22650758 DOI: 10.1021/Ol3011425 |
0.387 |
|
| 2012 |
Ma D, Hettiarachchi G, Nguyen D, Zhang B, Wittenberg JB, Zavalij PY, Briken V, Isaacs L. Acyclic cucurbit[n]uril molecular containers enhance the solubility and bioactivity of poorly soluble pharmaceuticals. Nature Chemistry. 4: 503-10. PMID 22614387 DOI: 10.1038/Nchem.1326 |
0.65 |
|
| 2012 |
Shen C, Ma D, Meany B, Isaacs L, Wang Y. Acyclic cucurbit[n]uril molecular containers selectively solubilize single-walled carbon nanotubes in water. Journal of the American Chemical Society. 134: 7254-7. PMID 22512431 DOI: 10.1021/Ja301462E |
0.487 |
|
| 2012 |
Muddana HS, Varnado CD, Bielawski CW, Urbach AR, Isaacs L, Geballe MT, Gilson MK. Blind prediction of host-guest binding affinities: a new SAMPL3 challenge. Journal of Computer-Aided Molecular Design. 26: 475-87. PMID 22366955 DOI: 10.1007/S10822-012-9554-1 |
0.67 |
|
| 2012 |
Ma D, Glassenberg R, Ghosh S, Zavalij PY, Isaacs L. Acyclic cucurbituril congener binds to local anaesthetics Supramolecular Chemistry. 24: 325-332. DOI: 10.1080/10610278.2012.658394 |
0.648 |
|
| 2011 |
Lucas D, Minami T, Iannuzzi G, Cao L, Wittenberg JB, Anzenbacher P, Isaacs L. Templated synthesis of glycoluril hexamer and monofunctionalized cucurbit[6]uril derivatives. Journal of the American Chemical Society. 133: 17966-76. PMID 21970313 DOI: 10.1021/Ja208229D |
0.707 |
|
| 2011 |
Wittenberg JB, Costales MG, Zavalij PY, Isaacs L. A clipped [3]rotaxane derived from bis-nor-seco-cucurbit[10]uril. Chemical Communications (Cambridge, England). 47: 9420-2. PMID 21776502 DOI: 10.1039/C1Cc13358F |
0.621 |
|
| 2011 |
Lucas D, Isaacs L. Recognition properties of acyclic glycoluril oligomers. Organic Letters. 13: 4112-5. PMID 21739945 DOI: 10.1021/Ol201636Q |
0.616 |
|
| 2011 |
Hettiarachchi G, Ma D, Nguyen D, Isaacs L, Briken V. Abstract 4429: Toxicology and drug delivery by novel cucurbit[n]uril-type nanocontainers Cancer Research. 71: 4429-4429. DOI: 10.1158/1538-7445.Am2011-4429 |
0.483 |
|
| 2011 |
Isaacs L. The Mechanism of Cucurbituril Formation Israel Journal of Chemistry. 51: 578-591. DOI: 10.1002/Ijch.201100022 |
0.391 |
|
| 2010 |
Ma D, Zavalij PY, Isaacs L. Acyclic cucurbit[n]uril congeners are high affinity hosts. The Journal of Organic Chemistry. 75: 4786-95. PMID 20540586 DOI: 10.1021/Jo100760G |
0.561 |
|
| 2010 |
Cao LP, Meng XG, Ding JY, Chen YF, Gao M, Wu YD, Li YT, Wu AX, Isaacs L. Nanotubular non-covalent macrocycle within non-covalent macrocycle assembly: (MeOH)(12) encapsulated in a molecular clip cyclododecamer. Chemical Communications (Cambridge, England). 46: 4508-10. PMID 20485785 DOI: 10.1039/C0Cc00677G |
0.324 |
|
| 2010 |
Hettiarachchi G, Nguyen D, Wu J, Lucas D, Ma D, Isaacs L, Briken V. Toxicology and drug delivery by cucurbit[n]uril type molecular containers. Plos One. 5: e10514. PMID 20463906 DOI: 10.1371/Journal.Pone.0010514 |
0.646 |
|
| 2010 |
Ma D, Gargulakova Z, Zavalij PY, Sindelar V, Isaacs L. Reasons why aldehydes do not generally participate in cucurbit[n]uril forming reactions. The Journal of Organic Chemistry. 75: 2934-41. PMID 20345157 DOI: 10.1021/Jo100186Q |
0.497 |
|
| 2010 |
Ghosh S, Isaacs L. Biological catalysis regulated by cucurbit[7]uril molecular containers. Journal of the American Chemical Society. 132: 4445-54. PMID 20210325 DOI: 10.1021/Ja910915K |
0.527 |
|
| 2010 |
Wu J, Isaacs L. Cucurbit[7]uril complexation drives thermal trans-cis-azobenzene isomerization and enables colorimetric amine detection. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11675-80. PMID 19774569 DOI: 10.1002/Chem.200901522 |
0.338 |
|
| 2010 |
Hettiarachchi G, Nguyen D, Wu J, Lucas D, Ma D, Isaacs L, Briken V. Abstract 5528: Toxicology and drug delivery by Cucurbit[n]urils and derivatives Cancer Research. 70: 5528-5528. DOI: 10.1158/1538-7445.Am10-5528 |
0.626 |
|
| 2010 |
Nally R, Scherman OA, Isaacs L. Polymer deaggregation and assembly controlled by a double cavity cucurbituril Supramolecular Chemistry. 22: 683-690. DOI: 10.1080/10610278.2010.497213 |
0.763 |
|
| 2009 |
Fedorova OA, Chernikova EY, Fedorov YV, Gulakova EN, Peregudov AS, Lyssenko KA, Jonusauskas G, Isaacs L. Cucurbit[7]uril complexes of crown-ether derived styryl and (bis)styryl dyes. The Journal of Physical Chemistry. B. 113: 10149-58. PMID 19719283 DOI: 10.1021/Jp903289Q |
0.362 |
|
| 2009 |
Huang WH, Zavalij PY, Isaacs L. Metal-ion-induced folding and dimerization of a glycoluril decamer in water. Organic Letters. 11: 3918-21. PMID 19655803 DOI: 10.1021/Ol901539Q |
0.478 |
|
| 2009 |
She N, Gao M, Cao L, Wu A, Isaacs L. Sensor for nitrophenol based on a fluorescent molecular clip. Organic Letters. 11: 2603-6. PMID 19449886 DOI: 10.1021/Ol900858D |
0.314 |
|
| 2009 |
Fang X, Kögerler P, Isaacs L, Uchida S, Mizuno N. Cucurbit[n]uril-polyoxoanion hybrids. Journal of the American Chemical Society. 131: 432-3. PMID 19113849 DOI: 10.1021/Ja807751B |
0.331 |
|
| 2009 |
Nally R, Isaacs L. Toward supramolecular polymers incorporating double cavity cucurbituril hosts Tetrahedron. 65: 7249-7258. DOI: 10.1016/J.Tet.2009.02.055 |
0.789 |
|
| 2008 |
Huang WH, Zavalij PY, Isaacs L. Cucurbit[6]uril p-xylylenediammonium diiodide deca-hydrate inclusion complex. Acta Crystallographica. Section E, Structure Reports Online. 64: o1321-2. PMID 21202946 DOI: 10.1107/S1600536808018412 |
0.525 |
|
| 2008 |
Isaacs L. Cucurbit[n]urils: from mechanism to structure and function. Chemical Communications (Cambridge, England). 619-29. PMID 19322405 DOI: 10.1039/B814897J |
0.376 |
|
| 2008 |
She N, Meng X, Gao M, Wu A, Isaacs L. Tetrameric molecular bowl assembled from glycoluril building blocks Chemical Communications. 3133-3135. PMID 18594719 DOI: 10.1039/B800785C |
0.314 |
|
| 2008 |
Ghosh S, Wu A, Fettinger JC, Zavalij PY, Isaacs L. Self-sorting molecular clips. The Journal of Organic Chemistry. 73: 5915-25. PMID 18588344 DOI: 10.1021/Jo8009424 |
0.54 |
|
| 2008 |
Huang WH, Zavalij PY, Isaacs L. Cucurbit[n]uril formation proceeds by step-growth cyclo-oligomerization. Journal of the American Chemical Society. 130: 8446-54. PMID 18529059 DOI: 10.1021/Ja8013693 |
0.58 |
|
| 2008 |
Huang WH, Zavalij PY, Isaacs L. Folding of long-chain alkanediammonium ions promoted by a cucurbituril derivative. Organic Letters. 10: 2577-80. PMID 18503277 DOI: 10.1021/Ol800893N |
0.513 |
|
| 2008 |
Nichols JM, Liu Y, Zavalij P, Isaacs L, Doyle MP. Diphenylglycoluril as a novel ligand architecture for dirhodium(II) carboxamidates Inorganica Chimica Acta. 361: 3309-3314. DOI: 10.1016/J.Ica.2007.12.001 |
0.307 |
|
| 2007 |
Rekharsky MV, Mori T, Yang C, Ko YH, Selvapalam N, Kim H, Sobransingh D, Kaifer AE, Liu S, Isaacs L, Chen W, Moghaddam S, Gilson MK, Kim K, Inoue Y. A synthetic host-guest system achieves avidin-biotin affinity by overcoming enthalpy-entropy compensation. Proceedings of the National Academy of Sciences of the United States of America. 104: 20737-42. PMID 18093926 DOI: 10.1073/Pnas.0706407105 |
0.352 |
|
| 2007 |
Liu S, Zavalij PY, Lam Y, Isaacs L. Refolding Foldamers: Triazene-Arylene Oligomers That Change Shape with Chemical Stimuli Journal of the American Chemical Society. 129: 11232-11241. PMID 17696539 DOI: 10.1021/Ja073320S |
0.348 |
|
| 2007 |
Huang WH, Zavalij PY, Isaacs L. Chiral recognition inside a chiral cucurbituril. Angewandte Chemie (International Ed. in English). 46: 7425-7. PMID 17694587 DOI: 10.1002/Anie.200702189 |
0.46 |
|
| 2007 |
Liu S, Kim K, Isaacs L. Mechanism of the conversion of inverted CB[6] to CB[6]. The Journal of Organic Chemistry. 72: 6840-7. PMID 17676913 DOI: 10.1021/Jo071034T |
0.371 |
|
| 2007 |
Chakrabarti S, Mukhopadhyay P, Lin S, Isaacs L. Reconfigurable four-component molecular switch based on pH-controlled guest swapping. Organic Letters. 9: 2349-52. PMID 17500562 DOI: 10.1021/Ol070730C |
0.628 |
|
| 2007 |
Huang W, Zavalij PY, Isaacs L. Cucurbit[6]uril p-phenylenediammonium diiodide decahydrate inclusion complex Acta Crystallographica Section E: Crystallographic Communications. 63. DOI: 10.1107/S160053680700387X |
0.49 |
|
| 2007 |
Isaacs L, Chin DN, Bowden N, Xia Y, Whitesides GM. Self-Assembling Systems on Scales from Nanometers to Millimeters: Design and Discovery Supramolecular Materials and Technologies. 4: 1-46. DOI: 10.1002/9780470511497.ch1 |
0.604 |
|
| 2006 |
Huang WH, Liu S, Zavalij PY, Isaacs L. Nor-seco-cucurbit[10]uril exhibits homotropic allosterism. Journal of the American Chemical Society. 128: 14744-5. PMID 17105250 DOI: 10.1021/Ja064776X |
0.536 |
|
| 2006 |
Mukhopadhyay P, Zavalij PY, Isaacs L. High fidelity kinetic self-sorting in multi-component systems based on guests with multiple binding epitopes. Journal of the American Chemical Society. 128: 14093-102. PMID 17061892 DOI: 10.1021/Ja063390J |
0.672 |
|
| 2006 |
Wang ZG, Zhou BH, Chen YF, Yin GD, Li YT, Wu AX, Isaacs L. Substituent effects control the self-association of molecular clips in the crystalline state. The Journal of Organic Chemistry. 71: 4502-8. PMID 16749780 DOI: 10.1021/Jo0603375 |
0.313 |
|
| 2006 |
Lagona J, Wagner BD, Isaacs L. Molecular-recognition properties of a water-soluble cucurbit[6]uril analogue Journal of Organic Chemistry. 71: 1181-1190. PMID 16438536 DOI: 10.1021/Jo052294I |
0.795 |
|
| 2006 |
Lagona J, Fettinger JC, Isaacs L. Cucurbit[n]uril analogues: synthetic and mechanistic studies. The Journal of Organic Chemistry. 70: 10381-92. PMID 16323848 DOI: 10.1021/Jo051655R |
0.795 |
|
| 2005 |
Wagner BD, Roland PG, Lagona J, Isaacs L. A Cucurbit[6]uril analogue: Host properties monitored by fluorescence spectroscopy Journal of Physical Chemistry B. 109: 7686-7691. PMID 16851892 DOI: 10.1021/Jp044369C |
0.783 |
|
| 2005 |
Isaacs L, Park SK, Liu S, Ko YH, Selvapalam N, Kim Y, Kim H, Zavalij PY, Kim GH, Lee HS, Kim K. The inverted cucurbit[n]uril family. Journal of the American Chemical Society. 127: 18000-1. PMID 16366540 DOI: 10.1021/Ja056988K |
0.36 |
|
| 2005 |
Liu S, Zavalij PY, Isaacs L. Cucurbit[10]uril Journal of the American Chemical Society. 127: 16798-16799. PMID 16316221 DOI: 10.1021/Ja056287N |
0.331 |
|
| 2005 |
Liu S, Ruspic C, Mukhopadhyay P, Chakrabarti S, Zavalij PY, Isaacs L. The cucurbit[n]uril family: prime components for self-sorting systems. Journal of the American Chemical Society. 127: 15959-67. PMID 16277540 DOI: 10.1021/Ja055013X |
0.699 |
|
| 2005 |
Lagona J, Mukhopadhyay P, Chakrabarti S, Isaacs L. The cucurbit[n]uril family. Angewandte Chemie (International Ed. in English). 44: 4844-70. PMID 16052668 DOI: 10.1002/Anie.200460675 |
0.784 |
|
| 2005 |
Isaacs L, Lagona J. Chapter 3 From methylene bridged glycoluril dimers to cucurbit[n]uril analogs with some detours along the way Strategies and Tactics in Organic Synthesis. 6: 71-99. DOI: 10.1016/S1874-6004(05)80026-7 |
0.797 |
|
| 2005 |
Lagona J, Mukhopadhyay P, Chakrabarti S, Isaacs L. Die Cucurbit[n]uril‐Familie Angewandte Chemie. 117: 4922-4949. DOI: 10.1002/Ange.200460675 |
0.757 |
|
| 2004 |
Mukhopadhyay P, Wu A, Isaacs L. Social self-sorting in aqueous solution. The Journal of Organic Chemistry. 69: 6157-64. PMID 15357573 DOI: 10.1021/Jo049976A |
0.664 |
|
| 2004 |
Wu A, Mukhopadhyay P, Chakraborty A, Fettinger JC, Isaacs L. Molecular clips form isostructural dimeric aggregates from benzene to water. Journal of the American Chemical Society. 126: 10035-43. PMID 15303878 DOI: 10.1021/Ja0486972 |
0.673 |
|
| 2004 |
Lagona J, Fettinger JC, Isaacs L. Cucurbit[n]uril analogues. Organic Letters. 5: 3745-7. PMID 14507220 DOI: 10.1021/Ol035468W |
0.781 |
|
| 2003 |
Burnett CA, Witt D, Fettinger JC, Isaacs L. Acyclic congener of cucurbituril: synthesis and recognition properties. The Journal of Organic Chemistry. 68: 6184-91. PMID 12895048 DOI: 10.1021/Jo034399W |
0.415 |
|
| 2003 |
Wu A, Isaacs L. Self-Sorting: The Exception or the Rule? Journal of the American Chemical Society. 125: 4831-4835. PMID 12696902 DOI: 10.1021/Ja028913B |
0.303 |
|
| 2003 |
Burnett CA, Lagona J, Wu A, Shaw JA, Coady D, Fettinger JC, Day AI, Isaacs L. Preparation of glycoluril monomers for expanded cucurbit[n]uril synthesis Tetrahedron. 59: 1961-1970. DOI: 10.1016/S0040-4020(03)00150-9 |
0.777 |
|
| 2002 |
Wu A, Chakraborty A, Witt D, Lagona J, Damkaci F, Ofori MA, Chiles JK, Fettinger JC, Isaacs L. Methylene-bridged glycoluril dimers: synthetic methods. The Journal of Organic Chemistry. 67: 5817-30. PMID 12153286 DOI: 10.1021/Jo0258958 |
0.785 |
|
| 2002 |
Chakraborty A, Wu A, Witt D, Lagona J, Fettinger JC, Isaacs L. Diastereoselective formation of glycoluril dimers: isomerization mechanism and implications for cucurbit[n]uril synthesis. Journal of the American Chemical Society. 124: 8297-306. PMID 12105910 DOI: 10.1021/Ja025876F |
0.801 |
|
| 2002 |
Wu A, Fettinger JC, Isaacs L. Glycoluril derivatives form hydrogen bonded tapes rather than cucurbit[ n ]uril congeners Tetrahedron. 58: 9769-9777. DOI: 10.1016/S0040-4020(02)01307-8 |
0.326 |
|
| 2001 |
Isaacs L, Witt D, Lagona J. Self-association of facially amphiphilic methylene bridged glycoluril dimers. Organic Letters. 3: 3221-4. PMID 11574036 DOI: 10.1021/Ol016561S |
0.772 |
|
| 2000 |
Witt D, Lagona J, Damkaci F, Fettinger JC, Isaacs L. Diastereoselective Formation of Methylene-Bridged Glycoluril Dimers. Organic Letters. 2: 755-758. PMID 10814425 DOI: 10.1021/Ol991382K |
0.789 |
|
| 1999 |
Lahiri J, Isaacs L, Tien J, Whitesides GM. A strategy for the generation of surfaces presenting ligands for studies of binding based on an active ester as a common reactive intermediate: a surface plasmon resonance study. Analytical Chemistry. 71: 777-90. PMID 10051846 DOI: 10.1021/Ac980959T |
0.685 |
|
| 1999 |
Lahiri J, Isaacs L, Grzybowski B, Carbeck JD, Whitesides GM. Biospecific Binding of Carbonic Anhydrase to Mixed SAMs Presenting Benzenesulfonamide Ligands: A Model System for Studying Lateral Steric Effects Langmuir. 15: 7186-7198. DOI: 10.1021/La9815650 |
0.739 |
|
| 1998 |
Rao J, Lahiri J, Isaacs L, Weis RM, Whitesides GM. A trivalent system from vancomycin.D-ala-D-Ala with higher affinity than avidin.biotin. Science (New York, N.Y.). 280: 708-11. PMID 9563940 DOI: 10.1126/Science.280.5364.708 |
0.576 |
|
| 1998 |
Boudon C, Gisselbrecht J, Gross M, Thiel W, Cardullo F, Seiler P, Isaacs L, Nierengarten J, Haldimann RF, Diederich F, Mordasini-Denti T. Propriétés rédox de fullerènes fonctionnalisés The Canadian Journal of Chemical Engineering. 76: 1008-1012. DOI: 10.1002/Cjce.5450760606 |
0.376 |
|
| 1997 |
Simanek EE, Isaacs L, Li X, Wang CCC, Whitesides GM. Self-Assembly of Zinc Porphyrins around the Periphery of Hydrogen-Bonded Aggregates That Bear Imidazole Groups The Journal of Organic Chemistry. 62: 8994-9000. DOI: 10.1021/Jo9615458 |
0.633 |
|
| 1997 |
Colton IJ, Anderson JR, Gao J, Chapman RG, Isaacs L, Whitesides GM. Formation of Protein Charge Ladders by Acylation of Amino Groups on Proteins Journal of the American Chemical Society. 119: 12701-12709. DOI: 10.1021/Ja9723491 |
0.551 |
|
| 1997 |
Cardullo F, Seiler P, Isaacs L, Nierengarten J, Haldimann RF, Diederich F, Mordasini-Denti T, Thiel W, Boudon C, Gisselhrccht J, Gross M. Bis- through Tetrakis-Adducts of C60 by Reversible Tether-Directed Remote Functionalization and systematic investigation of the changes in fullerene properties as a function of degree, pattern, and nature of functionalization Helvetica Chimica Acta. 80: 343-371. DOI: 10.1002/Hlca.19970800203 |
0.506 |
|
| 1997 |
Isaacs L, Diederich F, Haldimann RF. Multiple Adducts of C60 by Tether-Directed Remote Functionalization and synthesis of soluble derivatives of new carbon allotropes Cn(60+5) Helvetica Chimica Acta. 80: 317-342. DOI: 10.1002/Hlca.19970800202 |
0.47 |
|
| 1997 |
Rüttimann M, Haldimann RF, Isaacs L, Diederich F, Khong A, Jiménez-Vázquez H, Cross RJ, Saunders M. π-Electron Ring-Current Effects in Multiple Adducts of3He@C60 and3He@C70: A3He NMR Study Chemistry - a European Journal. 3: 1071-1076. DOI: 10.1002/Chem.19970030714 |
0.447 |
|
| 1996 |
Cardullo F, Isaacs L, Diederich F, Gisselbrecht J, Boudon C, Gross M. Regiospecific templated synthesis of D2h-symmetrical tetrakis-adduct C64(COOEt)8 by reversible tether-directed remote functionalization of C60 Chemical Communications. 797-799. DOI: 10.1039/Cc9960000797 |
0.469 |
|
| 1996 |
Seiler P, Isaacs L, Diederich F. The X-Ray Crystal Structure and Packing of a Hexakis-adduct of C60: Temperature dependence of weak C?H?O interactions Helvetica Chimica Acta. 79: 1047-1058. DOI: 10.1002/Hlca.19960790413 |
0.426 |
|
| 1995 |
Boudon C, Gisselbrecht J, Gross M, Isaacs L, Anderson HL, Faust R, Diederich F. Electrochemistry of Mono- through Hexakis-adducts of C60 Helvetica Chimica Acta. 78: 1334-1344. DOI: 10.1002/Hlca.19950780523 |
0.728 |
|
| 1995 |
Jonas U, Cardullo F, Belik P, Diederich F, Gügel A, Harth E, Herrmann A, Isaacs L, Müllen K, Ringsdorf H, Thilgen C, Uhlmann P, Vasella A, Waldraff CAA, Walter M. Synthesis of a Fullerene[60] Cryptate and Systematic Langmuir-Blodgett and Thin-Film Investigations of Amphiphilic Fullerene Derivatives Chemistry - a European Journal. 1: 243-251. DOI: 10.1002/Chem.19950010408 |
0.677 |
|
| 1995 |
Isaacs L, Seiler P, Diederich F. Solubilized Derivatives of C195 and C260: The First Members of a New Class of Carbon Allotropes Cn(60+ 5) Angewandte Chemie International Edition in English. 34: 1466-1469. DOI: 10.1002/Anie.199514661 |
0.414 |
|
| 1995 |
Isaacs L, Seiler P, Diederich F. Lösliche Derivate von C195 und C260: die ersten Verbindungen einer neuen Klasse von Kohlenstoffallotropen Cn(60 + 5) Angewandte Chemie. 107: 1636-1639. DOI: 10.1002/Ange.19951071336 |
0.406 |
|
| 1994 |
Diederich F, Isaacs L, Philp D. Valence isomerism and rearrangements in methanofullerenes Journal of the Chemical Society-Perkin Transactions 1. 391-394. DOI: 10.1039/P29940000391 |
0.42 |
|
| 1994 |
Diederich F, Isaacs L, Philp D. Syntheses, structures, and properties of methanofullerenes Chemical Society Reviews. 23: 243. DOI: 10.1039/Cs9942300243 |
0.42 |
|
| 1994 |
Isaacs L, Haldimann RF, Diederich F. Tether-Directed Remote Functionalization of Buckminsterfullerene: Regiospecific Hexaadduct Formation Angewandte Chemie International Edition in English. 33: 2339-2342. DOI: 10.1002/Anie.199423391 |
0.401 |
|
| 1994 |
Isaacs L, Haldimann RF, Diederich F. Spacer-kontrollierte Fernfunktionalisierung von Buckminsterfulleren: regiospezifische Bildung eines Hexaadduktes Angewandte Chemie. 106: 2434-2437. DOI: 10.1002/Ange.19941062237 |
0.393 |
|
| 1993 |
Isaacs L, Diederich F. Structures and Chemistry of Methanofullerenes: A Versatile Route intoN-[(Methanofullerene)carbonyl]-Substituted Amino Acids Helvetica Chimica Acta. 76: 2454-2464. DOI: 10.1002/Hlca.19930760705 |
0.449 |
|
| 1993 |
Isaacs L, Wehrsig A, Diederich F. Improved Purification of C60 and Formation of ?- and ?-Homoaromatic methano-bridged fullerenes by reaction with alkyl diazoacetates Helvetica Chimica Acta. 76: 1231-1250. DOI: 10.1002/Hlca.19930760310 |
0.428 |
|
| 1992 |
Bunshah RF, Jou S, Prakash S, Doerr HJ, Isaacs L, Wehrsig A, Yeretzian C, Cynn H, Diederich F. Fullerene formation in sputtering and electron beam evaporation processes The Journal of Physical Chemistry. 96: 6866-6869. DOI: 10.1021/J100196A005 |
0.424 |
|
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