메뉴 건너뛰기




Volumn 5, Issue , 2014, Pages

Enolate chemistry with anion-ï interactions

Author keywords

[No Author keywords available]

Indexed keywords

ANION; ANION PI; POLYKETIDE; STEROID; TERPENOID; UNCLASSIFIED DRUG;

EID: 84901297476     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms4911     Document Type: Article
Times cited : (69)

References (42)
  • 1
    • 77954003437 scopus 로고    scopus 로고
    • Experimental evidence for the functional relevance of anion-p interactions
    • Dawson, R. E. et al. Experimental evidence for the functional relevance of anion-p interactions. Nat. Chem. 2, 533-538 (2010).
    • (2010) Nat. Chem. , vol.2 , pp. 533-538
    • Dawson, R.E.1
  • 2
    • 70450202098 scopus 로고    scopus 로고
    • Chiral anion-mediated asymmetric ion pairing chemistry
    • Lacour, J. & Moraleda, D. Chiral anion-mediated asymmetric ion pairing chemistry. Chem. Commun. 45, 7073-7089 (2009).
    • (2009) Chem. Commun. , vol.45 , pp. 7073-7089
    • Lacour, J.1    Moraleda, D.2
  • 3
    • 84872002336 scopus 로고    scopus 로고
    • Asymmetric counteranion-directed catalysis: Concept, definition, and applications
    • Mahlau, M. & List, B. Asymmetric counteranion-directed catalysis: concept, definition, and applications. Angew. Chem. Int. Ed. 52, 518-533 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 518-533
    • Mahlau, M.1    List, B.2
  • 4
    • 84878647209 scopus 로고    scopus 로고
    • Quantification of nitrate-p interactions and selective transport of nitrate using calix[4]pyrroles with two aromatic walls
    • Adriaenssens, L. et al. Quantification of nitrate-p interactions and selective transport of nitrate using calix[4]pyrroles with two aromatic walls. J. Am. Chem. Soc. 135, 8324-8330 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 8324-8330
    • Adriaenssens, L.1
  • 5
    • 84863335373 scopus 로고    scopus 로고
    • Transmembrane anion transport mediated by halogen-bond donors
    • Vargas Jentzsch, A. et al. Transmembrane anion transport mediated by halogen-bond donors. Nat. Commun. 3, 905 (2012).
    • (2012) Nat. Commun. , vol.3 , pp. 905
    • Vargas Jentzsch, A.1
  • 6
    • 84876041833 scopus 로고    scopus 로고
    • Transmembrane halogen-bonding cascades
    • Vargas Jentzsch, A. & Matile, S. Transmembrane halogen-bonding cascades. J. Am. Chem. Soc. 135, 5302-5303 (2013).
    • (2013) J.Am. Chem. Soc. , vol.135 , pp. 5302-5303
    • Vargas Jentzsch, A.1    Matile, S.2
  • 7
    • 0037119776 scopus 로고    scopus 로고
    • Anion-p interactions: Do they exist?
    • Quinonero, D. et al. Anion-p interactions: do they exist? Angew. Chem. Int. Ed. 41, 3389-3392 (2002).
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3389-3392
    • Quinonero, D.1
  • 8
    • 84962408603 scopus 로고    scopus 로고
    • Anion-aromatic bonding: A case for anion recognition by π-acidic rings
    • DOI 10.1021/ja017449s
    • Mascal, M., Armstrong, A. & Bartberger, M. D. Anion-aromatic bonding: a case for anion recognition by p-acidic rings. J. Am. Chem. Soc. 124, 6274-6276 (2002). (Pubitemid 34579378)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.22 , pp. 6274-6276
    • Mascal, M.1    Armstrong, A.2    Bartberger, M.D.3
  • 9
    • 0037167019 scopus 로고    scopus 로고
    • Interaction of anions with perfluoro aromatic compounds
    • DOI 10.1021/ja025693t
    • Alkorta, I., Rozas, I. & Elguero, J. Interaction of anions with perfluoro aromatic compounds. J. Am. Chem. Soc. 124, 8593-8598 (2002). (Pubitemid 34791027)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.29 , pp. 8593-8598
    • Alkorta, I.1    Rozas, I.2    Elguero, J.3
  • 12
    • 79955766939 scopus 로고    scopus 로고
    • Aromatic rings in chemical and biological recognition: Energetics and structures
    • Salonen, L. M., Ellermann, M. & Diederich, F. Aromatic rings in chemical and biological recognition: energetics and structures. Angew. Chem. Int. Ed. 50, 4808-4842 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4808-4842
    • Salonen, L.M.1    Ellermann, M.2    Diederich, F.3
  • 13
    • 84876259430 scopus 로고    scopus 로고
    • Anion-p interactions in supramolecular architectures
    • Chifotides, H. T. & Dunbar, K. R. Anion-p interactions in supramolecular architectures. Acc. Chem. Res. 46, 894-906 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 894-906
    • Chifotides, H.T.1    Dunbar, K.R.2
  • 14
    • 84876245830 scopus 로고    scopus 로고
    • Experimental quantification of anion-p interactions in solution using neutral host-guest model systems
    • Ballester, P. Experimental quantification of anion-p interactions in solution using neutral host-guest model systems. Acc. Chem. Res. 46, 874-884 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 874-884
    • Ballester, P.1
  • 15
    • 84870203103 scopus 로고    scopus 로고
    • Understanding substituent effects in noncovalent interactions involving aromatic rings
    • Wheeler, S. E. Understanding substituent effects in noncovalent interactions involving aromatic rings. Acc. Chem. Res. 46, 1029-1038 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 1029-1038
    • Wheeler, S.E.1
  • 16
    • 84875720198 scopus 로고    scopus 로고
    • Ion-p interactions in ligand design for anions and main group cations
    • Watt, M. M., Collins, M. S. & Johnson, D. W. Ion-p interactions in ligand design for anions and main group cations. Acc. Chem. Res. 46, 955-966 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 955-966
    • Watt, M.M.1    Collins, M.S.2    Johnson, D.W.3
  • 17
    • 84888602598 scopus 로고    scopus 로고
    • Synthetic ion transporters that work with anion-p interactions, halogen bonds and anion-macrodipole interactions
    • Vargas Jentzsch, A., Hennig, A., Mareda, J. & Matile, S. Synthetic ion transporters that work with anion-p interactions, halogen bonds and anion-macrodipole interactions. Acc. Chem. Res. 46, 2791-2800 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 2791-2800
    • Vargas Jentzsch, A.1    Hennig, A.2    Mareda, J.3    Matile, S.4
  • 18
    • 84872515650 scopus 로고    scopus 로고
    • Anion-p interactions: Generality, binding strength, and structure
    • Wang, D. -X. & Wang, M. -X. Anion-p interactions: generality, binding strength, and structure. J. Am. Chem. Soc. 135, 892-897 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 892-897
    • Wang, D.-X.1    Wang, M.-X.2
  • 19
    • 84884882444 scopus 로고    scopus 로고
    • Selective nitrate binding in competitive hydrogen bonding solvents: Do anion-p interactions facilitate nitrate selectivity? Angew
    • Watt, M. M., Zakharov, L. N., Haley, M. M. & Johnson, D. W. Selective nitrate binding in competitive hydrogen bonding solvents: do anion-p interactions facilitate nitrate selectivity? Angew. Chem. Int. Ed. 52, 10275-10280 (2013).
    • (2013) Chem. Int. Ed. , vol.52 , pp. 10275-10280
    • Watt, M.M.1    Zakharov, L.N.2    Haley, M.M.3    Johnson, D.W.4
  • 20
    • 84862224291 scopus 로고    scopus 로고
    • Weak intermolecular anion-p interactions in pentafluorobenzylsubstituted ammonium betaines
    • Giese, M. et al. Weak intermolecular anion-p interactions in pentafluorobenzylsubstituted ammonium betaines. Eur. J. Inorg. Chem. 2012, 2995-2999 (2012).
    • (2012) Eur. J. Inorg. Chem. , vol.2012 , pp. 2995-2999
    • Giese, M.1
  • 21
    • 84888581674 scopus 로고    scopus 로고
    • Electron sharing and anion-p recognition in molecular triangular prisms
    • Schneebeli, S. T. et al. Electron sharing and anion-p recognition in molecular triangular prisms. Angew. Chem. Int. Ed. 52, 13100-13104 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 13100-13104
    • Schneebeli, S.T.1
  • 22
    • 78650913510 scopus 로고    scopus 로고
    • Relevant anion-p interactions in biological systems: The case of urate oxidase
    • Estarellas, C., Frontera, A., Quiñonero, D. & Deyà, P. M. Relevant anion-p interactions in biological systems: the case of urate oxidase. Angew. Chem. Int. Ed. 50, 415-418 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 415-418
    • Estarellas, C.1    Frontera, A.2    Quiñonero, D.3    Deya, P.M.4
  • 23
    • 84884218160 scopus 로고    scopus 로고
    • Catalysis with anion-p interactions
    • Zhao, Y. et al. Catalysis with anion-p interactions. Angew. Chem. Int. Ed. 52, 9940-9943 (2013).
    • (2013) Angew. Chem Int. Ed. , vol.52 , pp. 9940-9943
    • Zhao, Y.1
  • 24
    • 84893757590 scopus 로고    scopus 로고
    • Anion-p catalysis
    • Zhao, Y. et al. Anion-p catalysis. J. Am. Chem. Soc. 136, 2101-2111 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 2101-2111
    • Zhao, Y.1
  • 25
    • 84876275836 scopus 로고    scopus 로고
    • The cation-p interaction
    • Dougherty, D. A. The cation-p interaction. Acc. Chem. Res. 46, 885-893 (2013).
    • (2013) Acc. Chem. Res. , vol.46 , pp. 885-893
    • Dougherty, D.A.1
  • 27
    • 80052935221 scopus 로고    scopus 로고
    • Nitrogen cation-p interactions in asymmetric organocatalytic synthesis
    • Yamada, S. & Fossey, J. S. Nitrogen cation-p interactions in asymmetric organocatalytic synthesis. Org. Biomol. Chem. 9, 7275-7281 (2011).
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 7275-7281
    • Yamada, S.1    Fossey, J.S.2
  • 28
    • 77950805314 scopus 로고    scopus 로고
    • Enantioselective thiourea-catalyzed cationic polycyclizations
    • Knowles, R. R., Lin, S. & Jacobsen, E. N. Enantioselective thiourea-catalyzed cationic polycyclizations. J. Am. Chem. Soc. 132, 5030-5032 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 5030-5032
    • Knowles, R.R.1    Lin, S.2    Jacobsen, E.N.3
  • 29
    • 84879969716 scopus 로고    scopus 로고
    • Use of anion-aromatic interactions to position the general base in the ketosteroid isomerase active site
    • Schwans, J. P. et al. Use of anion-aromatic interactions to position the general base in the ketosteroid isomerase active site. Proc. Natl Acad. Sci. USA 110, 11308-11313 (2013).
    • (2013) Proc. Natl Acad. Sci. USA , vol.110 , pp. 11308-11313
    • Schwans, J.P.1
  • 30
    • 84865434436 scopus 로고    scopus 로고
    • Boundaries of anion/ naphthalenediimide interactions: From anion-p interactions to anion-induced charge-transfer and electron-transfer phenomena
    • Guha, S., Goodson, F. S., Corson, L. J. & Saha, S. Boundaries of anion/ naphthalenediimide interactions: from anion-p interactions to anion-induced charge-transfer and electron-transfer phenomena. J. Am. Chem. Soc. 134, 13679-13691 (2012).
    • (2012) J.Am. Chem. Soc. , vol.134 , pp. 13679-13691
    • Guha, S.1    Goodson, F.S.2    Corson, L.J.3    Saha, S.4
  • 32
    • 34548771245 scopus 로고    scopus 로고
    • Mimicry of polyketide synthases - Enantioselective 1,4-addition reactions of malonic acid half-thioesters to nitroolefins
    • DOI 10.1002/anie.200702187
    • Lubkoll, J. & Wennemers, H. Mimicry of polyketide synthases? enantioselective 1,4-addition reactions of malonic acid half-thioesters to nitroolefins. Angew. Chem. Int. Ed. 46, 6841-6844 (2007). (Pubitemid 47425800)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.36 , pp. 6841-6844
    • Lubkoll, J.1    Wennemers, H.2
  • 33
    • 84883484875 scopus 로고    scopus 로고
    • Expanding the fluorine chemistry of living systems using engineered polyketide synthase pathways
    • Walker, M. C. et al. Expanding the fluorine chemistry of living systems using engineered polyketide synthase pathways. Science 341, 1089-1094 (2013).
    • (2013) Science , vol.341 , pp. 1089-1094
    • Walker, M.C.1
  • 35
    • 0000859989 scopus 로고
    • Convergent functional groups. 15. Synthetic and structural studies of large and rigid molecular clefts
    • Shimizu, K. D., Dewey, T. M. & Rebek, Jr. J. Convergent functional groups. 15. Synthetic and structural studies of large and rigid molecular clefts. J. Am. Chem. Soc. 116, 5145-5149 (1994). (Pubitemid 24981092)
    • (1994) Journal of the American Chemical Society , vol.116 , Issue.12 , pp. 5145-5149
    • Shimizu, K.D.1    Dewey, T.M.2    Rebek Jr., J.3
  • 36
    • 33745697770 scopus 로고    scopus 로고
    • Rapid screening of a receptor with molecular memory
    • DOI 10.1021/ol060706j
    • Lavin, J. M. & Shimizu, K. D. Rapid screening of a receptor with molecular memory. Org. Lett. 8, 2389-2392 (2006). (Pubitemid 43998264)
    • (2006) Organic Letters , vol.8 , Issue.11 , pp. 2389-2392
    • Lavin, J.M.1    Shimizu, K.D.2
  • 37
    • 51049122142 scopus 로고    scopus 로고
    • Enantioselective copper-catalyzed conjugate addition and allylic substitution reactions
    • Alexakis, A., Bäckvall, J. E., Krause, N., Pàmies, O. & Diéguez, M. Enantioselective copper-catalyzed conjugate addition and allylic substitution reactions. Chem. Rev. 108, 2796-2823 (2008).
    • (2008) Chem. Rev. , vol.108 , pp. 2796-2823
    • Alexakis, A.1    Bäckvall, J.E.2    Krause, N.3    Pàmies, O.4    Diéguez, M.5
  • 38
    • 77749298554 scopus 로고    scopus 로고
    • Emil Knoevenagel and the roots of aminocatalysis
    • List, B. Emil Knoevenagel and the roots of aminocatalysis. Angew. Chem. Int. Ed. 49, 1730-1734 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1730-1734
    • List, B.1
  • 39
    • 0035543093 scopus 로고    scopus 로고
    • The depth of chemical time and the power of enzymes as catalysts
    • Wolfenden, R. & Snider, M. J. The depth of chemical time and the power of enzymes as catalysts. Acc. Chem. Res. 34, 938-945 (2001).
    • (2001) Acc. Chem. Res. , vol.34 , pp. 938-945
    • Wolfenden, R.1    Snider, M.J.2
  • 40
    • 33746204093 scopus 로고    scopus 로고
    • Enzyme mechanisms, models, and mimics
    • Kirby, A. J. Enzyme mechanisms, models, and mimics. Angew. Chem. Int. Ed. 35, 707-724 (1996).
    • (1996) Angew. Chem. Int. Ed. , vol.35 , pp. 707-724
    • Kirby, A.J.1
  • 41
    • 0038736789 scopus 로고
    • Camphor derivatives as chiral auxiliaries in asymmetric synthesis
    • Oppolzer, W. Camphor derivatives as chiral auxiliaries in asymmetric synthesis. Tetrahedron 43, 1969-2004 (1987).
    • (1987) Tetrahedron , vol.43 , pp. 1969-2004
    • Oppolzer, W.1
  • 42
    • 84858016905 scopus 로고    scopus 로고
    • Enantioselective self-sorting on planar, p-acidic surfaces of anion-p transporters
    • Lin, N.-T. et al. Enantioselective self-sorting on planar, p-acidic surfaces of anion-p transporters. Chem. Sci. 3, 1121-1127 (2012).
    • (2012) Chem. Sci. , vol.3 , pp. 1121-1127
    • Lin, N.-T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.