Sinnokrot, Valeev et Sherrill, « Estimates of the ab initio limit for pi–pi interactions: The benzene dimer », J. Am. Chem. Soc., vol. 124, no 36, , p. 10887–10893 (PMID12207544, DOI10.1021/ja025896h)
Huber, Margreiter, Fuchs et von Grafenstein, « Heteroaromatic π-Stacking Energy Landscapes », Journal of Chemical Information and Modeling, vol. 54, no 5, , p. 1371–1379 (PMID24773380, DOI10.1021/ci500183u)
McGaughey, Gagné et Rappé, « Pi-Stacking interactions. Alive and well in proteins », J. Biol. Chem., vol. 273, no 25, , p. 15458–15463 (PMID9624131, DOI10.1074/jbc.273.25.15458)
Riley et Hobza, « On the Importance and Origin of Aromatic Interactions in Chemistry and Biodisciplines », Acc. Chem. Res., vol. 46, no 4, , p. 927–936 (DOI10.1021/ar300083h)
Hunter et Sanders, « The nature of π–π Interactions », J. Am. Chem. Soc., vol. 112, no 14, , p. 5525–5534 (DOI10.1021/ja00170a016)
Cozzi, Cinquini, Annuziata et Siegel, « Dominance of polar/.pi. Over charge-transfer effects in stacked phenyl interactions », J. Am. Chem. Soc., vol. 115, no 12, , p. 5330–5331 (DOI10.1021/ja00065a069)
Cockroft, Hunter, Lawson et Perkins, « Electrostatic control of aromatic stacking interactions », J. Am. Chem. Soc., vol. 127, no 24, , p. 8594–8595 (PMID15954755, DOI10.1021/ja050880n)
Cockroft, Perkins, Zonta et Adams, « Substituent effects on aromatic stacking interactions », Org. Biomol. Chem., vol. 5, no 7, , p. 1062–1080 (PMID17377660, DOI10.1039/b617576g, lire en ligne)
Rashkin et Waters, « Unexpected substituent effects in offset pi–pi stacked interactions in water », J. Am. Chem. Soc., vol. 124, no 9, , p. 1860–1861 (PMID11866592, DOI10.1021/ja016508z)
Sinnokrot et Sherrill, « Unexpected Substituent Effects in Face-to-Face π-Stacking Interactions », J. Phys. Chem. A, vol. 107, no 41, , p. 8377–8379 (DOI10.1021/jp030880e, Bibcode2003JPCA..107.8377S)
Ringer, Sinnokrot, Lively et Sherrill, « The effect of multiple substituents on sandwich and T-shaped pi–pi interactions », Chem. Eur. J., vol. 12, no 14, , p. 3821–8 (PMID16514687, DOI10.1002/chem.200501316)
Wheeler et Houk, « Substituent effects in the benzene dimer are due to direct interactions of the substituents with the unsubstituted benzene », J. Am. Chem. Soc., vol. 130, no 33, , p. 10854–10855 (PMID18652453, PMCID2655233, DOI10.1021/ja802849j)
Paliwal, Geib et Wilcox, « Molecular Torsion Balance for Weak Molecular Recognition Forces. Effects of "Tilted-T" Edge-to-Face Aromatic Interactions on Conformational Selection and Solid-State Structure », J. Am. Chem. Soc., vol. 116, no 10, , p. 4497–4498 (DOI10.1021/ja00089a057)
Bloom et Wheeler, « Taking the Aromaticity out of Aromatic Interactions », Angew. Chem., vol. 123, no 34, , p. 7993–7995 (DOI10.1002/ange.201102982)
Grimme, « Do Special Noncovalent π–π Stacking Interactions Really Exist? », Angew. Chem. Int. Ed., vol. 47, no 18, , p. 3430–3434 (DOI10.1002/anie.200705157)
A. Sygula, F. R. Fronczek, R. Sygula, P. W. Rabideau and M. M. Olmstead, « A Double Concave Hydrocarbon Buckycatcher », J. Am. Chem. Soc., vol. 129, no 13, , p. 3842–3843 (PMID17348661, DOI10.1021/ja070616p)
Babine et Bender, « Molecular Recognition of Proteinminus signLigand Complexes: Applications to Drug Design », Chem. Rev., vol. 97, no 5, , p. 1359–1472 (PMID11851455, DOI10.1021/cr960370z)
Da Silva et al., « Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease », J. Mol. Graphics Modell., vol. 25, no 2, , p. 169–175 (PMID16413803, DOI10.1016/j.jmgm.2005.12.002)
Singh et al., « Chemistry, Design, and Structure-Activity Relationship of Cocaine Antagonists », Chem. Rev., vol. 100, no 3, , p. 925–1024 (PMID11749256, DOI10.1021/cr9700538, lire en ligne)
Ashton, Goodnow, Kaifer et Reddington, « A [2] Catenane Made to Order », J. Angew. Chem. Int. Ed., vol. 28, no 10, , p. 1396–1399 (DOI10.1002/anie.198913961)
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Singh et al., « Chemistry, Design, and Structure-Activity Relationship of Cocaine Antagonists », Chem. Rev., vol. 100, no 3, , p. 925–1024 (PMID11749256, DOI10.1021/cr9700538, lire en ligne)
Sinnokrot et Sherrill, « Unexpected Substituent Effects in Face-to-Face π-Stacking Interactions », J. Phys. Chem. A, vol. 107, no 41, , p. 8377–8379 (DOI10.1021/jp030880e, Bibcode2003JPCA..107.8377S)
Sinnokrot, Valeev et Sherrill, « Estimates of the ab initio limit for pi–pi interactions: The benzene dimer », J. Am. Chem. Soc., vol. 124, no 36, , p. 10887–10893 (PMID12207544, DOI10.1021/ja025896h)
Huber, Margreiter, Fuchs et von Grafenstein, « Heteroaromatic π-Stacking Energy Landscapes », Journal of Chemical Information and Modeling, vol. 54, no 5, , p. 1371–1379 (PMID24773380, DOI10.1021/ci500183u)
McGaughey, Gagné et Rappé, « Pi-Stacking interactions. Alive and well in proteins », J. Biol. Chem., vol. 273, no 25, , p. 15458–15463 (PMID9624131, DOI10.1074/jbc.273.25.15458)
Cockroft, Hunter, Lawson et Perkins, « Electrostatic control of aromatic stacking interactions », J. Am. Chem. Soc., vol. 127, no 24, , p. 8594–8595 (PMID15954755, DOI10.1021/ja050880n)
Cockroft, Perkins, Zonta et Adams, « Substituent effects on aromatic stacking interactions », Org. Biomol. Chem., vol. 5, no 7, , p. 1062–1080 (PMID17377660, DOI10.1039/b617576g, lire en ligne)
Rashkin et Waters, « Unexpected substituent effects in offset pi–pi stacked interactions in water », J. Am. Chem. Soc., vol. 124, no 9, , p. 1860–1861 (PMID11866592, DOI10.1021/ja016508z)
Ringer, Sinnokrot, Lively et Sherrill, « The effect of multiple substituents on sandwich and T-shaped pi–pi interactions », Chem. Eur. J., vol. 12, no 14, , p. 3821–8 (PMID16514687, DOI10.1002/chem.200501316)
Wheeler et Houk, « Substituent effects in the benzene dimer are due to direct interactions of the substituents with the unsubstituted benzene », J. Am. Chem. Soc., vol. 130, no 33, , p. 10854–10855 (PMID18652453, PMCID2655233, DOI10.1021/ja802849j)
A. Sygula, F. R. Fronczek, R. Sygula, P. W. Rabideau and M. M. Olmstead, « A Double Concave Hydrocarbon Buckycatcher », J. Am. Chem. Soc., vol. 129, no 13, , p. 3842–3843 (PMID17348661, DOI10.1021/ja070616p)
Babine et Bender, « Molecular Recognition of Proteinminus signLigand Complexes: Applications to Drug Design », Chem. Rev., vol. 97, no 5, , p. 1359–1472 (PMID11851455, DOI10.1021/cr960370z)
Da Silva et al., « Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease », J. Mol. Graphics Modell., vol. 25, no 2, , p. 169–175 (PMID16413803, DOI10.1016/j.jmgm.2005.12.002)
Singh et al., « Chemistry, Design, and Structure-Activity Relationship of Cocaine Antagonists », Chem. Rev., vol. 100, no 3, , p. 925–1024 (PMID11749256, DOI10.1021/cr9700538, lire en ligne)