메뉴 건너뛰기




Volumn 298, Issue , 2011, Pages 99-128

Recent theoretical and experimental advances in the electronic circular dichroisms of planar chiral cyclophanes

Author keywords

Chiroptical properties; Cyclophane; Electronic circular dichroisms; Planar chirality; Quantum chemical calculations

Indexed keywords

AROMATIC HYDROCARBON;

EID: 79951816202     PISSN: 03401022     EISSN: None     Source Type: Book Series    
DOI: 10.1007/128_2010_59     Document Type: Article
Times cited : (21)

References (63)
  • 1
    • 34249686052 scopus 로고    scopus 로고
    • Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
    • Berova N, Bari LD, Pescitelli G (2007) Application of electronic circular dichroism in configurational and conformational analysis of organic compounds. Chem Soc Rev 36: 914-931
    • (2007) Chem Soc Rev , vol.36 , pp. 914-931
    • Berova, N.1    Bari, L.D.2    Pescitelli, G.3
  • 2
    • 0000700630 scopus 로고
    • Macro rings XII. Stereochemical consequences of steric compression in the smallest paracyclophane
    • Cram DJ, Allinger NL (1955) Macro rings XII. Stereochemical consequences of steric compression in the smallest paracyclophane. J Am Chem Soc 77:6289-6294
    • (1955) J Am Chem Soc , vol.77 , pp. 6289-6294
    • Cram, D.J.1    Allinger, N.L.2
  • 3
    • 0000436875 scopus 로고
    • [2.2] Paracyclophane system optical activity. II. Circular dichroism of ring-substituted paracyclophanes
    • Nugent MJ, Weigang OE Jr (1969) [2.2]Paracyclophane system optical activity. II. Circular dichroism of ring-substituted paracyclophanes. J Am Chem Soc 91:4556-4558
    • (1969) J Am Chem Soc , vol.91 , pp. 4556-4558
    • Nugent, M.J.1    Weigang Jr., O.E.2
  • 4
    • 0000018043 scopus 로고
    • Absolute Konfiguration Unt Circulardichroismus von Aktiven [2.2]. Paracyclophan-derivaten
    • Falk H, Rbich-Rohrwig P, Schlögl K (1970) Absolute Konfiguration Unt Circulardichroismus von Aktiven [2.2]Paracyclophan-derivaten. Tetrahedron 26:511-527
    • (1970) Tetrahedron , vol.26 , pp. 511-527
    • Falk, H.1    Rbich-Rohrwig, P.2    Schlögl, K.3
  • 5
    • 0142009578 scopus 로고    scopus 로고
    • [2.2] Paracyclophane derivatives in asymmetric catalysis
    • Gibson SE, Knight JD (2003) [2.2]Paracyclophane derivatives in asymmetric catalysis. Org Biomol Chem 1:1256-1269
    • (2003) Org Biomol Chem , vol.1 , pp. 1256-1269
    • Gibson, S.E.1    Knight, J.D.2
  • 6
    • 11844252995 scopus 로고    scopus 로고
    • Cyclophanes as templates in stereoselective synthesis
    • Gleiter R, Hopf H (eds) Wiley-VCH, Weinheim
    • Rozenberg V, Sergeeva E, Hopf H (2004) Cyclophanes as templates in stereoselective synthesis. In: Gleiter R, Hopf H (eds) Modern cyclophane chemistry. Wiley-VCH, Weinheim, pp 435-462
    • (2004) Modern Cyclophane Chemistry , pp. 435-462
    • Rozenberg, V.1    Sergeeva, E.2    Hopf, H.3
  • 7
    • 69049117258 scopus 로고    scopus 로고
    • Asymmetric and fused heterocycles based on [2.2]paracyclo-phane
    • Aly AA, Brown AB (2009) Asymmetric and fused heterocycles based on [2.2]paracyclo-phane. Tetrahedron 65:8055-8089
    • (2009) Tetrahedron , vol.65 , pp. 8055-8089
    • Aly, A.A.1    Brown, A.B.2
  • 8
    • 20444432448 scopus 로고    scopus 로고
    • Electronic circular dichroism of cyclophanes
    • Gleiter R, Hopf H (eds) Wiley-VCH, Weinheim
    • Grimme S, Bahlmann A (2004) Electronic circular dichroism of cyclophanes. In: Gleiter R, Hopf H (eds) Modern cyclophane chemistry. Wiley-VCH, Weinheim, pp 311-336
    • (2004) Modern Cyclophane Chemistry , pp. 311-336
    • Grimme, S.1    Bahlmann, A.2
  • 9
    • 79951817708 scopus 로고    scopus 로고
    • Cyclophanes: From planar chirality and helicity to cyclochir-ality
    • Takemura H (ed Research Signpost, Kerala
    • Vögtle F, Pawlitzki G (2002) Cyclophanes: from planar chirality and helicity to cyclochir-ality. In: Takemura H (ed) Cyclophane chemistry for the 21st century. Research Signpost, Kerala, pp 55-90
    • (2002) Cyclophane Chemistry for the 21st Century , pp. 55-90
    • Vögtle, F.1    Pawlitzki, G.2
  • 11
    • 67649183444 scopus 로고    scopus 로고
    • Optical signatures of molecular dissymmetry: Combining theory with experiments to address stereochemical puzzles
    • Mukhopadhyay P, Wipf P, Beratan DN (2009) Optical signatures of molecular dissymmetry: combining theory with experiments to address stereochemical puzzles. Acc Chem Res 42:809-819
    • (2009) Acc Chem Res , vol.42 , pp. 809-819
    • Mukhopadhyay, P.1    Wipf, P.2    Beratan, D.N.3
  • 12
    • 43249097508 scopus 로고    scopus 로고
    • The determination of the absolute configurations of chiral molecules using Vibrational Circular Dichroism (VCD) spectroscopy
    • DOI 10.1002/chir.20477
    • Stephens PJ, Devlin FJ, Pan J-J (2008) The determination of the absolute configurations of chiral molecules using vibrational circular dichroism (VCD) spectroscopy. Chirality 20:643-663 (Pubitemid 351656169)
    • (2008) Chirality , vol.20 , Issue.5 , pp. 643-663
    • Stephens, P.J.1    Devlin, F.J.2    Pan, J.-J.3
  • 13
    • 0242322522 scopus 로고    scopus 로고
    • Absolute configuration determination of chiral molecules in the solution state using vibrational circular dichroism
    • DOI 10.1002/chir.10287
    • Freedman TB, Cao X, Dukor RK, Nafie LA (2003) Absolute configuration determination of chiral molecules in the solution state using vibrational circular dichroism. Chirality 15:743-758 (Pubitemid 37356644)
    • (2003) Chirality , vol.15 , Issue.9 , pp. 743-758
    • Freedman, T.B.1    Cao, X.2    Dukor, R.3    Nafie, L.A.4
  • 14
    • 33644691370 scopus 로고    scopus 로고
    • Absolute configuration determination of donor-acceptor [2.2]paracyclophanes by comparison of theoretical and experimental vibrational circular dichroism spectra
    • DOI 10.1002/chir.20233
    • Furo T, Mori T, Origane Y, Wada T, Izumi H, Inoue Y (2006) Absolute configuration determination of donor-acceptor [2.2]paracyclophanes by comparison of theoretical and experimental vibrational circular dichroism spectra. Chirality 18:205-211 (Pubitemid 43334163)
    • (2006) Chirality , vol.18 , Issue.3 , pp. 205-211
    • Furo, T.1    Mori, T.2    Origane, Y.3    Wada, T.4    Izumi, H.5    Inoue, Y.6
  • 16
    • 0001156729 scopus 로고
    • Conformational analysis. CIV. Structures, energies, and electronic absorption spectra of the [n]paracyclophanes
    • Allinger NL, Sprague JT, Liljefors T (1974) Conformational analysis. CIV. Structures, energies, and electronic absorption spectra of the [n]paracyclophanes. J Am Chem Soc 96:5100-5104
    • (1974) J Am Chem Soc , vol.96 , pp. 5100-5104
    • Allinger, N.L.1    Sprague, J.T.2    Liljefors, T.3
  • 17
    • 0344995715 scopus 로고
    • Synthese mittlerer und groaer Ringe, X. (+)- und (-)-[6]Paracyclophan-8- carbonsaure aus (+)- und (-)-3,6-Hexanooxepin-4-carbonsaure
    • Tochtermann W, Vagt W, Snatzke G (1985) Synthese mittlerer und groaer Ringe, X. (+)- und (-)-[6]Paracyclophan-8-carbonsaure aus (+)- und (-)-3,6-Hexanooxepin-4-carbonsaure. Chem Ber 118:1996-2010
    • (1985) Chem Ber , vol.118 , pp. 1996-2010
    • Tochtermann, W.1    Vagt, W.2    Snatzke, G.3
  • 18
    • 84985653972 scopus 로고
    • Synthese mittlerer und grober Ringe, XXVII. Chromatographische Enantiomerentrennung von 3,6-Hepta-nophthalid - Ein Beitrag zur Frage der absoluten Konfiguration von [n]Paracyclophancarbon-säuren
    • Tochtermann W, Olsson G, Mannschreck A, Stühler G, Snatzke G (1990) Synthese mittlerer und grober Ringe, XXVII. Chromatographische Enantiomerentrennung von 3,6-Hepta-nophthalid - ein Beitrag zur Frage der absoluten Konfiguration von [n]Paracyclophancarbon-säuren. Chem Ber 123:1437-1439
    • (1990) Chem Ber , vol.123 , pp. 1437-1439
    • Tochtermann, W.1    Olsson, G.2    Mannschreck, A.3    Stühler, G.4    Snatzke, G.5
  • 19
    • 0031881716 scopus 로고    scopus 로고
    • Synthesis, structure, and chiroptical properties of the first 4- oxa[7]paracyclophane
    • Grimme S, Pischel I, Laufenberg S, Vögtle F (1998) Synthesis, structure, and chiroptical properties of the first 4-oxa[7]paracyclophane. Chirality 10:147-153 (Pubitemid 28084114)
    • (1998) Chirality , vol.10 , Issue.1-2 , pp. 147-153
    • Grimme, S.1    Pischel, I.2    Laufenberg, S.3    Vogtle, F.4
  • 20
    • 0034026464 scopus 로고    scopus 로고
    • Circular dichroism and absolute stereochemistry of [8]paracyclophane-10- carbonitrile and related compounds
    • Nehira T, Soutome T, Harada N (2000) Circular dichroism and absolute stereochemistry of [8] paracyclophane-10-carbonitrile and related compounds. Enantiomer 5:139-144 (Pubitemid 30192941)
    • (2000) Enantiomer , vol.5 , Issue.1 , pp. 139-144
    • Nehira, T.1    Soutome, T.2    Harada, N.3
  • 21
    • 84987334313 scopus 로고
    • Darstellung, chiroptische Eigenschaften und absolute Konfi-guration von Derivaten des [10] Paracyclophans
    • Eberhardt H, Schlögl K (1972) Darstellung, chiroptische Eigenschaften und absolute Konfi-guration von Derivaten des [10]Paracyclophans. Liebigs Ann Chem 760:157-170
    • (1972) Liebigs Ann Chem , vol.760 , pp. 157-170
    • Eberhardt, H.1    Schlögl, K.2
  • 22
    • 68049121761 scopus 로고    scopus 로고
    • An enantiopure cyclophane-type imidazole with no central but planar chirality
    • Ishida Y, Iwasa E, Matsuoka Y, Miyauchi H, Saigo K (2009) An enantiopure cyclophane-type imidazole with no central but planar chirality. Chem Commun 3401-3403
    • (2009) Chem Commun , pp. 3401-3403
    • Ishida, Y.1    Iwasa, E.2    Matsuoka, Y.3    Miyauchi, H.4    Saigo, K.5
  • 23
    • 0035808866 scopus 로고    scopus 로고
    • Stereocontrol of molecular jump-rope: Crystallization-induced asymmetric transformation of planar-chiral cyclophanes
    • DOI 10.1016/S0040-4039(00)02043-8, PII S0040403900020438
    • Kanomata N, Ochiai Y (2001) Stereocontrol of molecular jump-rope: crystallization-induced asymmetric transformation of planar-chiral cyclophanes. Tetrahedron Lett 42:1045-1048 (Pubitemid 32149840)
    • (2001) Tetrahedron Letters , vol.42 , Issue.6 , pp. 1045-1048
    • Kanomata, N.1    Ochiai, Y.2
  • 24
    • 79951829549 scopus 로고
    • The absolute configuration of [8][8], [8][10]paracyclo-phanes and related paracyclophane compounds
    • Yamamoto K, Nakazaki M (1974) The absolute configuration of [8][8], [8][10]paracyclo-phanes and related paracyclophane compounds. Chem Lett 1051-1054
    • (1974) Chem Lett , pp. 1051-1054
    • Yamamoto, K.1    Nakazaki, M.2
  • 25
    • 15844429133 scopus 로고    scopus 로고
    • Chiral dithia[n]paracyclophanes - Synthesis, crystal structure, and chiroptical properties
    • DOI 10.1016/0040-4020(96)00540-6
    • Pischel I, Nieger M, Archut A, Vögtle F (1996) Chiral dithia[n]paracyclophanes - synthesis, crystal structure, and chiroptical properties. Tetrahedron 52:10043-10052 (Pubitemid 26233618)
    • (1996) Tetrahedron , vol.52 , Issue.30 , pp. 10043-10052
    • Pischel, I.1    Nieger, M.2    Archut, A.3    Vogtle, F.4
  • 26
    • 0001556409 scopus 로고
    • Experimental and theoretical study of dithia [n]metacyclophanes: Syntheses, chiroptical properties, and conformational analysis
    • Grimme S, Pischel I, Vögtle F, Niegers M (1995) Experimental and theoretical study of dithia [n]metacyclophanes: syntheses, chiroptical properties, and conformational analysis. J Am Chem Soc 117:157-162
    • (1995) J Am Chem Soc , vol.117 , pp. 157-162
    • Grimme, S.1    Pischel, I.2    Vögtle, F.3    Niegers, M.4
  • 27
    • 27744499841 scopus 로고    scopus 로고
    • UV/Vis spectra of cyclophanes
    • Gleiter R, Hopf H (eds Wiley-VCH, Weinheim
    • Rademacher P (2004) UV/Vis spectra of cyclophanes. In: Gleiter R, Hopf H (eds) Modern cyclophane chemistry. Wiley-VCH, Weinheim, pp 275-310
    • (2004) Modern Cyclophane Chemistry , pp. 275-310
    • Rademacher, P.1
  • 28
    • 0002012744 scopus 로고
    • Consequences of s-p-interaction in [2.2]-paracyclophane
    • Gleiter R (1969) Consequences of s-p-interaction in [2.2]-paracyclophane. Tetrahedron Lett 10:4453-4456
    • (1969) Tetrahedron Lett , vol.10 , pp. 4453-4456
    • Gleiter, R.1
  • 29
    • 0032535961 scopus 로고    scopus 로고
    • Circular dichroism spectra (350-185 nm) of a new series of 4- substituted [2.2]paracyclophanes: A quantitative analysis within the devoe polarizability model
    • DOI 10.1016/S0957-4166(97)00522-3, PII S0957416697005223
    • Rosini C, Ruzziconi R, Superchi S, Fringuelli F, Piermatti O (1998) Circular dichroism spectra (350-185 nm) of a new series of 4-substituted [2.2]paracyclophanes: a quantitative analysis within the DeVoe polarizability model. Tetrahedron Assymetry 9:55-62 (Pubitemid 28096374)
    • (1998) Tetrahedron Asymmetry , vol.9 , Issue.1 , pp. 55-62
    • Rosini, C.1    Ruzziconi, R.2    Superchi, S.3    Fringuelli, F.4    Piermatti, O.5
  • 30
    • 73949109316 scopus 로고    scopus 로고
    • Electronic and vibrational circular dichroism spectra of chiral 4-X-[2.2]paracyclophanes with X containing fluorine atoms
    • Abbate S, Lebon F, Gangemi R, Longhi G, Spizzichino S, Ruzziconi R (2009) Electronic and vibrational circular dichroism spectra of chiral 4-X-[2.2]paracyclophanes with X containing fluorine atoms. J Phys Chem A 113:14851-14859
    • (2009) J Phys Chem A , vol.113 , pp. 14851-14859
    • Abbate, S.1    Lebon, F.2    Gangemi, R.3    Longhi, G.4    Spizzichino, S.5    Ruzziconi, R.6
  • 32
    • 0006012227 scopus 로고
    • [2.2] Paracyclophane system optical activity. I. Theory
    • Weigang OE Jr, Nugent MJ (1969) [2.2]Paracyclophane system optical activity. I. Theory. J Am Chem Soc 91:4555-4556
    • (1969) J Am Chem Soc , vol.91 , pp. 4555-4556
    • Weigang Jr., O.E.1    Nugent, M.J.2
  • 33
    • 34548174438 scopus 로고    scopus 로고
    • Quantum chemical study on the circular dichroism spectra and specific rotation of donor-acceptor cyclophanes
    • DOI 10.1021/jp073596m
    • Mori T, Inoue Y, Grimme S (2007) Quantum chemical study on the circular dichroism spectra and specific rotation of donor-acceptor cyclophanes. J Phys Chem A 111:7995-8006 (Pubitemid 47310943)
    • (2007) Journal of Physical Chemistry A , vol.111 , Issue.32 , pp. 7995-8006
    • Mori, T.1    Inoue, Y.2    Grimme, S.3
  • 34
    • 2342621883 scopus 로고
    • New aspects of organic charge-transfer compounds: Syntheses, structures and solid-state properties
    • Yoshida Z, Shiba T, Oshiro Y (eds VCH, Weinheim
    • Staab HA (1989) New aspects of organic charge-transfer compounds: syntheses, structures and solid-state properties. In: Yoshida Z, Shiba T, Oshiro Y (eds) New aspects of organic chemistry I. VCH, Weinheim, pp 227-236
    • (1989) New Aspects of Organic Chemistry i , pp. 227-236
    • Staab, H.A.1
  • 35
    • 20444449263 scopus 로고    scopus 로고
    • Absolute configuration of Chiral [2.2]paracyclo-phanes with intramolecular charge-transfer interaction. Failure of the exciton chirality method and use of the sector rule applied to the cotton effect of the CT transition
    • and 1638
    • Furo T, Mori T, Wada T, Inoue Y (2005) Absolute configuration of Chiral [2.2]paracyclo-phanes with intramolecular charge-transfer interaction. Failure of the exciton chirality method and use of the sector rule applied to the cotton effect of the CT transition. J Am Chem Soc 127:7995-8006 and 1638
    • (2005) J Am Chem Soc , vol.127 , pp. 7995-8006
    • Furo, T.1    Mori, T.2    Wada, T.3    Inoue, Y.4
  • 36
    • 67549093105 scopus 로고    scopus 로고
    • Chiral cooperativity and solvent-induced tautom-erism effects in electronic circular dichroism spectra of [2.2]paracyclophane ketimines
    • Warnke I, Ay S, Bräse S, Furche F (2009) Chiral cooperativity and solvent-induced tautom-erism effects in electronic circular dichroism spectra of [2.2]paracyclophane ketimines. J Phys Chem A 113:6987-6993
    • (2009) J Phys Chem A , vol.113 , pp. 6987-6993
    • Warnke, I.1    Ay, S.2    Bräse, S.3    Furche, F.4
  • 37
    • 33745344132 scopus 로고
    • Circulardiehroismus und Elektronenanregungsspektren chiraler [2,2]Metacyclophane
    • Langer E, Lehner H (1973) Circulardiehroismus und Elektronenanregungsspektren chiraler [2, 2]Metacyclophane. Monatsh Chem 104:644-653
    • (1973) Monatsh Chem , vol.104 , pp. 644-653
    • Langer, E.1    Lehner, H.2
  • 38
    • 0002243567 scopus 로고
    • Experimental and theoretical study of the circular dichroism spectra of oxa- and thia-[2.2]metacyclophane
    • Grimme S, Peyerimhoff SD, Bartram S, Vögtle F, Breest A, Hormes J (1993) Experimental and theoretical study of the circular dichroism spectra of oxa- and thia-[2.2]metacyclophane. Chem Phys Lett 213:32-40
    • (1993) Chem Phys Lett , vol.213 , pp. 32-40
    • Grimme, S.1    Peyerimhoff, S.D.2    Bartram, S.3    Vögtle, F.4    Breest, A.5    Hormes, J.6
  • 39
    • 37049079217 scopus 로고
    • The first [2.2]cyclophane with free N-H in the bridge
    • Muller D, Nieger M, Vögtle F (1994) The first [2.2]cyclophane with free N-H in the bridge. J Chem Soc Chem Commun 1361-1362
    • (1994) J Chem Soc Chem Commun , pp. 1361-1362
    • Muller, D.1    Nieger, M.2    Vögtle, F.3
  • 40
    • 37049086963 scopus 로고
    • A study of the N-inversion barrier and the circular dichroism spectra of 1-thia-10-aza[2.2]metacyclophane
    • Wortmann-Saleh D, Grimme S, Engels B, Müller D, Vögtle F (1995) A study of the N-inversion barrier and the circular dichroism spectra of 1-thia-10-aza[2.2]metacyclophane. J Chem Soc Perkin Trans 2 1185-1189
    • (1995) J Chem Soc Perkin Trans , vol.2 , pp. 1185-1189
    • Wortmann-Saleh, D.1    Grimme, S.2    Engels, B.3    Müller, D.4    Vögtle, F.5
  • 41
    • 84984355893 scopus 로고
    • Chirale dreilagige und kondensierte [2.2]Cyclophane. Synthese, Struktur, Chiroptik
    • Vögtle F, Ostrowicki A, Begcmann B, Jansen M, Nieger M, Niecke E (1990) Chirale dreilagige und kondensierte [2.2]Cyclophane. Synthese, Struktur, Chiroptik. Chem Ber 123:169-176
    • (1990) Chem Ber , vol.123 , pp. 169-176
    • Vögtle, F.1    Ostrowicki, A.2    Begcmann, B.3    Jansen, M.4    Nieger, M.5    Niecke, E.6
  • 42
    • 3743094833 scopus 로고
    • Tricarbonylchrom-Komplexe von chiralen [2.2]Metacyclophanen: Darstellung, Struktur und chiroptische Eigenschaften
    • Schulz J, Bartram S, Nieger M, Vögtle F (1992) Tricarbonylchrom- Komplexe von chiralen [2.2]Metacyclophanen: Darstellung, Struktur und chiroptische Eigenschaften. Chem Ber 125:2553-2569
    • (1992) Chem Ber , vol.125 , pp. 2553-2569
    • Schulz, J.1    Bartram, S.2    Nieger, M.3    Vögtle, F.4
  • 43
    • 0042635418 scopus 로고    scopus 로고
    • Experimental and theoretical studies of a chiral azulenophane: Synthesis, structure and circular dichroism spectra of 14,17-dimethyl [2] 1,3)azuleno[2]paracyclophane
    • Grimme S, Mennicke W, Vögtle F, Nieger M (1999) Experimental and theoretical studies of a chiral azulenophane: synthesis, structure and circular dichroism spectra of 14,17-dimethyl[2] (1,3)azuleno[2]paracyclophane. J Chem Soc Perkin Trans 2:521-528
    • (1999) J Chem Soc Perkin Trans , vol.2 , pp. 521-528
    • Grimme, S.1    Mennicke, W.2    Vögtle, F.3    Nieger, M.4
  • 44
    • 60549097752 scopus 로고    scopus 로고
    • Calculation of electronic circular dichroism spectra with time-dependent double-hybrid density functional theory
    • Goerigk L, Grimme S (2009) Calculation of electronic circular dichroism spectra with time-dependent double-hybrid density functional theory. J Phys Chem A 113:767-776
    • (2009) J Phys Chem A , vol.113 , pp. 767-776
    • Goerigk, L.1    Grimme, S.2
  • 45
    • 0033522723 scopus 로고    scopus 로고
    • Chiroptical properties of 12,15-dichloro[3.0]orthometacyclophane- correlations between molecular structure and circular dichroism spectra of a biphenylophane
    • DOI 10.1016/S0957-4166(99)00220-7, PII S0957416699002207
    • Niederalt C, Grimme S, Peyerimhoff SD, Sobanski A, Vögtle A, Lutz M, Spek AL, Eis MJ, Wolf WH, Bickelhaupt F (1999) Chiroptical properties of 12,15-dichloro[3.0]orthometacy-clophane - correlations between molecular structure and circular dichroism spectra of a biphenylophane. Tetrahedron Asymmetry 10:2153-2164 (Pubitemid 29386772)
    • (1999) Tetrahedron Asymmetry , vol.10 , Issue.11 , pp. 2153-2164
    • Niederalt, C.1    Grimme, S.2    Peyerimhoff, S.D.3    Sobanski, A.4    Vogtle, F.5    Lutz, M.6    Spek, A.L.7    Van Eis, M.J.8    De Wolf, W.H.9    Bickelhaupt, F.10
  • 46
    • 34250313660 scopus 로고    scopus 로고
    • Experimental and theoretical study of the CD spectra and conformational properties of axially chiral 2,2′-, 3,3′-, and 4,4′-biphenol ethers
    • DOI 10.1021/jp071709w
    • 0 -biphenol ethers. J Phys Chem A 111:4222-4234 (Pubitemid 46910770)
    • (2007) Journal of Physical Chemistry A , vol.111 , Issue.20 , pp. 4222-4234
    • Mori, T.1    Inoue, Y.2    Grimme, S.3
  • 47
    • 84982066726 scopus 로고
    • Transanuiare Wechselwirkungen bei [2.2]Phanen, III. [2,2] (2,6)Naphthalinophan und [2.2](2,6)Naphthalinophan-1,11-dien
    • Haenel MW, Staab HA (1973) Transanuiare Wechselwirkungen bei [2.2]Phanen, III. [2,2] (2,6)Naphthalinophan und [2.2](2,6)Naphthalinophan-1,11-dien. Chem Ber 106:2203-2216
    • (1973) Chem Ber , vol.106 , pp. 2203-2216
    • Haenel, M.W.1    Staab, H.A.2
  • 48
    • 0006410712 scopus 로고
    • Transanulare Wechselwirkungen bei [2.2]Phanen, XI. Chirales und achirales [ 2,2](1,5)Naphthalinophan
    • Haenel MW (1978) Transanulare Wechselwirkungen bei [2.2]Phanen, XI. Chirales und achirales [2,2](1,5)Naphthalinophan. Chem Ber 111:1789-1797
    • (1978) Chem Ber , vol.111 , pp. 1789-1797
    • Haenel, M.W.1
  • 49
    • 3042882455 scopus 로고    scopus 로고
    • New biphenylenophanes and biphenylophanes - 1,8-dimethylbiphenylene by continuous vacuum pyrolysis
    • Laufenberg S, Feuerbacher N, Pischel S, Borsch O, Nieger M, Vögtle F (1997) New biphe-nylenophanes and biphenylophanes - 1,8-dimethylbiphenylene by continuous vacuum pyrol-ysis. Liebigs Ann 1901-1906 (Pubitemid 127787974)
    • (1997) Liebigs Annales , Issue.9 , pp. 1901-1906
    • Laufenberg, S.1    Feuerbacher, N.2    Pischel, I.3    Borsch, O.4    Nieger, M.5    Vogtle, F.6
  • 50
    • 0041742165 scopus 로고
    • Preparation of (-)-M)-[2.2]paracyclophano-hexahelicene from (-)-(M)-1,4-dimethylhexahelicenea and the absolute configuration of 4-substituted [2.2]paracyclophanes
    • Nakazaki M, Yamamoto K, Maeda M (1981) Preparation of (-)-(M)-[2.2]paracyclophano-hexahelicene from (-)-(M)-1,4-dimethylhexahelicenea and the absolute configuration of 4-substituted [2.2]paracyclophanes. J Org Chem 46:1985-1987
    • (1981) J Org Chem , vol.46 , pp. 1985-1987
    • Nakazaki, M.1    Yamamoto, K.2    Maeda, M.3
  • 51
    • 68149170815 scopus 로고    scopus 로고
    • Planar chiral asymmetric naphthalenediimide cyclophanes: Synthesis, characterization and tunable FRET properties
    • Gabutti S, Schaffner S, Neuburger M, Fischer M, Schäfer G, Mayor M (2009) Planar chiral asymmetric naphthalenediimide cyclophanes: synthesis, characterization and tunable FRET properties. Org Biomol Chem 7:3222-3229
    • (2009) Org Biomol Chem , vol.7 , pp. 3222-3229
    • Gabutti, S.1    Schaffner, S.2    Neuburger, M.3    Fischer, M.4    Schäfer, G.5    Mayor, M.6
  • 52
    • 1542792629 scopus 로고
    • Chemistry of multilayered cyclophanes
    • Misumi S, Otsubo T (1978) Chemistry of multilayered cyclophanes. Acc Chem Res 11: 251-256
    • (1978) Acc Chem Res , vol.11 , pp. 251-256
    • Misumi, S.1    Otsubo, T.2
  • 54
    • 0001149892 scopus 로고
    • Syntheses of the optically active multilayered [2.2]paracyclophanes with known absolute configurations
    • Nakazaki M, Yamamoto K, Tanaka S, Kametani H (1977) Syntheses of the optically active multilayered [2.2]paracyclophanes with known absolute configurations. J Org Chem 42: 287-291
    • (1977) J Org Chem , vol.42 , pp. 287-291
    • Nakazaki, M.1    Yamamoto, K.2    Tanaka, S.3    Kametani, H.4
  • 55
    • 56449105132 scopus 로고    scopus 로고
    • Optical resolution, absolute configuration, and chiroptical properties of three-layered [3.3] paracyclophane
    • Muranaka A, Shibahara M, Watanabe M, Matsumoto T, Shinmyozu T, Kobayashi N (2008) Optical resolution, absolute configuration, and chiroptical properties of three-layered [3.3] paracyclophane. J Org Chem 73:9125-9128
    • (2008) J Org Chem , vol.73 , pp. 9125-9128
    • Muranaka, A.1    Shibahara, M.2    Watanabe, M.3    Matsumoto, T.4    Shinmyozu, T.5    Kobayashi, N.6
  • 56
    • 0032562564 scopus 로고    scopus 로고
    • A triple layered helical chiral cyclophane-one-pot synthesis, enantiomer separation and chiroptical properties
    • DOI 10.1016/S0957-4166(98)00115-3, PII S0957416698001153
    • Harren J, Sobanski A, Nieger M, Yamamoto C, Okamoto Y, Vögtle F (1998) A triple layered helical chiral cyclophane - one-pot synthesis, enantiomer separation and chiroptical properties. Tetrahedron Asymmetry 9:1369-1375 (Pubitemid 28218577)
    • (1998) Tetrahedron Asymmetry , vol.9 , Issue.8 , pp. 1369-1375
    • Harren, J.1    Sobanski, A.2    Nieger, M.3    Yamamoto, C.4    Okamoto, Y.5    Vogtle, F.6
  • 57
    • 0042334835 scopus 로고    scopus 로고
    • Bridged bioxepines and bi[10]paracyclophanes - Synthesis and absolute configuration of a bi[10]paracyclophane with two chiral planes and one chiral axis
    • DOI 10.1016/j.tet.2003.07.009
    • Tochtermann W, Kuckling D, Meints C, Kraus J, Bringmann G (2003) Bridged bioxepines and bi[10]paracyclophanes - synthesis and absolute configuration of a bi[10]paracyclophane with two chiral planes and one chiral axis. Tetrahedron 59:7791-7801 (Pubitemid 37103099)
    • (2003) Tetrahedron , vol.59 , Issue.39 , pp. 7791-7801
    • Tochtermann, W.1    Kuckling, D.2    Meints, C.3    Kraus, J.4    Bringmann, G.5
  • 58
    • 57149140845 scopus 로고    scopus 로고
    • Synchronized stereocontrol of planar chirality by crystallization-induced asymmetric transformation
    • Kanomata N, Mishima G, Onozato J (2009) Synchronized stereocontrol of planar chirality by crystallization-induced asymmetric transformation. Tetrahedron Lett 50:409-412
    • (2009) Tetrahedron Lett , vol.50 , pp. 409-412
    • Kanomata, N.1    Mishima, G.2    Onozato, J.3
  • 59
    • 64549111258 scopus 로고    scopus 로고
    • Synthesis of planar-chiral bridged bipyridines and terpyridines by metal-mediated coupling reactions of pyridinophanes
    • Kanomata N, Suzuki J, Kubota H, Nishimura K, Enomoto T (2009) Synthesis of planar-chiral bridged bipyridines and terpyridines by metal-mediated coupling reactions of pyridinophanes. Tetrahedron Lett 50:2740-2743
    • (2009) Tetrahedron Lett , vol.50 , pp. 2740-2743
    • Kanomata, N.1    Suzuki, J.2    Kubota, H.3    Nishimura, K.4    Enomoto, T.5
  • 60
    • 13244298302 scopus 로고    scopus 로고
    • 0 -bi([2]paracyclo[2](5,8) isoquinolinophane): Synthesis, structural analysis, and chiroptical properties
    • 0 -bi([2]paracyclo[2](5,8)isoquinolinophane): synthesis, structural analysis, and chiroptical properties. J Org Chem 70:1011-1018
    • (2005) J Org Chem , vol.70 , pp. 1011-1018
    • Ricci, G.1    Ruzziconi, R.2    Giorgio, E.3
  • 61
    • 73949108686 scopus 로고    scopus 로고
    • Study of the photobeha-vior of a newly synthesized chiroptical molecule: (E)-(Rp,Rp)-1,2-Bis{4-methyl-[2]paracyclo [2] 5,8)quinolinophan-2-yl}ethane
    • Gentili PL, Bussotti L, Ruzziconi R, Spizzichino S, Foggi P (2009) Study of the photobeha-vior of a newly synthesized chiroptical molecule: (E)-(Rp,Rp)-1,2-Bis{4-methyl-[2]paracyclo [2](5,8)quinolinophan-2-yl}ethane. J Phys Chem A 113:14650-14656
    • (2009) J Phys Chem A , vol.113 , pp. 14650-14656
    • Gentili, P.L.1    Bussotti, L.2    Ruzziconi, R.3    Spizzichino, S.4    Foggi, P.5
  • 63
    • 0030221367 scopus 로고    scopus 로고
    • Poly(amine/imine) dendrimers bearing planar chiral terminal groups - Synthesis and chiroptical properties
    • DOI 10.1016/0957-4166(96)00277-7
    • Issberner J, Böhme M, Grimme S, Neiger M, Paulus W, Vögtle F (1996) Dendrimers bearing planar chiral terminal groups - synthesis and chiroptical properties. Tetrahedron Asymmetry 7:2223-2232 (Pubitemid 26287896)
    • (1996) Tetrahedron Asymmetry , vol.7 , Issue.8 , pp. 2223-2232
    • Issberner, J.1    Bohme, M.2    Grimme, S.3    Nieger, M.4    Paulus, W.5    Vogtle, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.