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Volumn 16, Issue 2, 2011, Pages 1603-1624

Synthesis and conformation of substituted chiral binaphthyl-azobenzene cyclic dyads with chiroptical switching capabilities

Author keywords

Axial chirality; Binaphthyl, azobenzene; Chiroptical switch; Circular dichroism; DFT calculation; Helical chirality; Optical rotation

Indexed keywords

AZO COMPOUND; AZOBENZENE; HYDROCARBON;

EID: 79952128092     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16021603     Document Type: Review
Times cited : (23)

References (114)
  • 1
    • 78651506097 scopus 로고    scopus 로고
    • Planar-chiral pillar[5]arene: Chiral switches induced by multiexternal stimulus of temperature, solvents, and addition of achiral guest molecule
    • Ogoshi, T.; Shiga, R.; Yamagishi, T.; Nakamoto, Y. Planar-chiral pillar[5]arene: Chiral switches induced by multiexternal stimulus of temperature, solvents, and addition of achiral guest molecule. J. Org. Chem. 2011, 76, 618-622.
    • (2011) J. Org. Chem. , vol.76 , pp. 618-622
    • Ogoshi, T.1    Shiga, R.2    Yamagishi, T.3    Nakamoto, Y.4
  • 2
    • 77955216855 scopus 로고    scopus 로고
    • A dendrimer chiroptical switch based on the reversible intramolecular photoreaction of anthracene and benzene rings
    • Liu, W.; Cao, D.; Peng, J.; Zhang, H.; Meier, H. A dendrimer chiroptical switch based on the reversible intramolecular photoreaction of anthracene and benzene rings. Chem. Asian J. 2010, 5, 1896-1901.
    • (2010) Chem. Asian J. , vol.5 , pp. 1896-1901
    • Liu, W.1    Cao, D.2    Peng, J.3    Zhang, H.4    Meier, H.5
  • 3
    • 77954606249 scopus 로고    scopus 로고
    • Near-infrared electrochromic and chiroptical switching polymers: Synthesis and characterization of helical poly(N-propargylamides) carrying anthraquinone imide moieties in side chains
    • Zheng, Y.; Cui, J.; Zheng, J.; Wan, X. Near-infrared electrochromic and chiroptical switching polymers: Synthesis and characterization of helical poly(N-propargylamides) carrying anthraquinone imide moieties in side chains. J. Mater. Chem. 2010, 20, 5915-5922.
    • (2010) J. Mater. Chem. , vol.20 , pp. 5915-5922
    • Zheng, Y.1    Cui, J.2    Zheng, J.3    Wan, X.4
  • 4
    • 61849185882 scopus 로고    scopus 로고
    • Electrically-controlled near-infrared chiroptical switching of enantiomeric dinuclear ruthenium complexes
    • Li, D.; Wang, Z.Y.; Ma, D. Electrically-controlled near-infrared chiroptical switching of enantiomeric dinuclear ruthenium complexes. Chem. Commun. 2009, 1529-1531.
    • (2009) Chem. Commun. , pp. 1529-1531
    • Li, D.1    Wang, Z.Y.2    Ma, D.3
  • 5
    • 56549090812 scopus 로고    scopus 로고
    • Synthesis and redox-driven chiroptically switching properties of viologen-containing optically active polymer with main-chain axial chirality
    • Deng, J.; Zhou, C.; Chen, C.; Song, N.; Su, Z. Synthesis and redox-driven chiroptically switching properties of viologen-containing optically active polymer with main-chain axial chirality. Macromolecules 2008, 41, 7805-7811.
    • (2008) Macromolecules , vol.41 , pp. 7805-7811
    • Deng, J.1    Zhou, C.2    Chen, C.3    Song, N.4    Su, Z.5
  • 6
    • 38349172454 scopus 로고    scopus 로고
    • Electrically-driven chiroptical switches based on axially dissymmetric 1,1'-binaphthyl and electrochromic viologens: Synthesis and optical properties
    • Deng, J.; Song, N.; Zhou, Q.; Su, Z. Electrically-driven chiroptical switches based on axially dissymmetric 1,1'-binaphthyl and electrochromic viologens: Synthesis and optical properties. Org. Lett. 2007, 9, 5393-5396.
    • (2007) Org. Lett. , vol.9 , pp. 5393-5396
    • Deng, J.1    Song, N.2    Zhou, Q.3    Su, Z.4
  • 7
    • 34447634913 scopus 로고    scopus 로고
    • Synthesis, complexation, and photoisomerization studies on some chiral monocyclic stilbenophanes and bis-cyclophanes
    • DOI 10.1016/j.tet.2007.06.015, PII S0040402007010423
    • Rajakumar, P.; Selvam, S. Synthesis, complexation, and photoisomerization studies on some chiral monocyclic stilbenophanes and bis-cyclophanes. Tetrahedron 2007, 63, 8891-8901. (Pubitemid 47087862)
    • (2007) Tetrahedron , vol.63 , Issue.36 , pp. 8891-8901
    • Rajakumar, P.1    Selvam, S.2
  • 8
    • 0347719289 scopus 로고    scopus 로고
    • A chiroptical molecular switch with distinct chiral and photochromic entities and its application in optical switching of a cholesteric liquid crystal
    • van Delden, R.A.; Mecca, T.; Rosini, C.; Feringa, B.L. A chiroptical molecular switch with distinct chiral and photochromic entities and its application in optical switching of a cholesteric liquid crystal. Chem. Eur. J. 2004, 10, 61-70.
    • (2004) Chem. Eur. J. , vol.10 , pp. 61-70
    • Van Delden, R.A.1    Mecca, T.2    Rosini, C.3    Feringa, B.L.4
  • 9
    • 0034852829 scopus 로고    scopus 로고
    • In control of motion: From molecular switches to molecular motors
    • DOI 10.1021/ar0001721
    • Feringa, B.L. In control of motion: From molecular switches to molecular motors. Acc. Chem. Res. 2001, 34, 504-513. (Pubitemid 32822171)
    • (2001) Accounts of Chemical Research , vol.34 , Issue.6 , pp. 504-513
    • Feringa, B.L.1
  • 12
    • 17244369977 scopus 로고    scopus 로고
    • BINOL: A versatile chiral reagent
    • DOI 10.1021/cr040079g
    • Brunel, J.M. BINOL: A versatile chiral reagent. Chem. Rev. 2005, 105, 857-897. (Pubitemid 40527378)
    • (2005) Chemical Reviews , vol.105 , Issue.3 , pp. 857-897
    • Brunel, J.M.1
  • 13
    • 0042880939 scopus 로고    scopus 로고
    • Modified BINOL ligands in asymmetric catalysis
    • Chen, Y.; Yekta, S.; Yudin, A. K. Modified BINOL ligands in asymmetric catalysis. Chem. Rev. 2003, 103, 3155-3211.
    • (2003) Chem. Rev. , vol.103 , pp. 3155-3211
    • Chen, Y.1    Yekta, S.2    Yudin, A.K.3
  • 14
    • 20044397048 scopus 로고    scopus 로고
    • Modified BINAP: The how and the why
    • DOI 10.1021/cr040652w
    • Berthod, M.; Mignani, G.; Woodward, G.; Lemaire, M. Modified BINAP: The How and the Why. Chem. Rev. 2005, 105, 1801-1836. (Pubitemid 40773668)
    • (2005) Chemical Reviews , vol.105 , Issue.5 , pp. 1801-1836
    • Berthod, M.1    Mignani, G.2    Woodward, G.3    Lemaire, M.4
  • 15
    • 1542694981 scopus 로고
    • Synthesis of 2,2'-bis(dipheny1phosphino)-1,l'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)- phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of a (acylamino)acrylic acids
    • Miyashita, A.; Yasuda, A.; Takaya, H.; Toriumi, K.; Ito, T.; Souchi, T.; Noyori, R. Synthesis of 2,2'-bis(dipheny1phosphino)-1,l'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)- phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of a (acylamino)acrylic acids. J. Am. Chem. Soc. 1980, 102, 7932-7934.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 7932-7934
    • Miyashita, A.1    Yasuda, A.2    Takaya, H.3    Toriumi, K.4    Ito, T.5    Souchi, T.6    Noyori, R.7
  • 16
    • 77956077305 scopus 로고    scopus 로고
    • Catalytic asymmetric aza-Morita-Baylis-Hillman reaction of methyl acrylate: Role of a bifunctional La(O-iPr)3/linked-BINOL complex
    • Yukawa, T.; Seelig, B.; Xu, Y.; Morimoto, H.; Matsunaga, S.; Berkessel, A.; Shibasaki, M. Catalytic asymmetric aza-Morita-Baylis-Hillman reaction of methyl acrylate: Role of a bifunctional La(O-iPr)3/linked-BINOL complex. J. Am. Chem. Soc. 2010, 132, 11988-11992.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 11988-11992
    • Yukawa, T.1    Seelig, B.2    Xu, Y.3    Morimoto, H.4    Matsunaga, S.5    Berkessel, A.6    Shibasaki, M.7
  • 17
    • 77954303578 scopus 로고    scopus 로고
    • Electrochemical method for the determination of enantiomeric excess of binol using redox-active boronic acids as chiral sensors
    • Mirri, G.; Bull, S.D.; Horton, P.N.; James, T.D.; Male, L.; Tucker, J.H.R. Electrochemical method for the determination of enantiomeric excess of binol using redox-active boronic acids as chiral sensors. J. Am. Chem. Soc. 2010, 132, 8903-8905.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8903-8905
    • Mirri, G.1    Bull, S.D.2    Horton, P.N.3    James, T.D.4    Male, L.5    Tucker, J.H.R.6
  • 18
    • 77956538115 scopus 로고    scopus 로고
    • Phthala phos: Chiral supramolecular ligands for enantioselective rhodium-catalyzed hydrogenation reactions
    • Pignataro, L.; Carboni, S.; Civera, M.; Colombo, R.; Piarulli, U.; Gennari, C. PhthalaPhos: Chiral supramolecular ligands for enantioselective rhodium-catalyzed hydrogenation reactions. Angew. Chem. Int. Ed. 2010, 49, 6633-6637.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 6633-6637
    • Pignataro, L.1    Carboni, S.2    Civera, M.3    Colombo, R.4    Piarulli, U.5    Gennari, C.6
  • 20
    • 77953999411 scopus 로고    scopus 로고
    • Highly enantioselective insertion of carbenoids into N-H bonds catalyzed by copper(I) complexes of binol derivatives
    • Hou, Z.; Wang, J.; He, P.; Wang, J.; Qin, B.; Liu, X.; Lin, L.; Feng, X. Highly enantioselective insertion of carbenoids into N-H bonds catalyzed by copper(I) complexes of binol derivatives. Angew. Chem. Int. Ed. 2010, 49, 4763-4766.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 4763-4766
    • Hou, Z.1    Wang, J.2    He, P.3    Wang, J.4    Qin, B.5    Liu, X.6    Lin, L.7    Feng, X.8
  • 21
    • 77952610990 scopus 로고    scopus 로고
    • Nickel-catalyzed asymmetric addition of alkyne C-H bonds across1,3-dienes using taddol-based chiral phosphoramidite ligands
    • Shirakura, M.; Suginome, M. Nickel-catalyzed asymmetric addition of alkyne C-H bonds across1,3-dienes using taddol-based chiral phosphoramidite ligands. Angew. Chem. Int. Ed. 2010, 49, 3827-3829.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 3827-3829
    • Shirakura, M.1    Suginome, M.2
  • 22
    • 77952666330 scopus 로고    scopus 로고
    • Which is the actual catalyst: Chiral phosphoric acid or chiral calcium phosphate?
    • Hatano, M.; Moriyama, K.; Maki, T.; Ishihara K. Which is the actual catalyst: Chiral phosphoric acid or chiral calcium phosphate? Angew. Chem. Int. Ed. 2010, 49, 3823-3826.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 3823-3826
    • Hatano, M.1    Moriyama, K.2    Maki, T.3    Ishihara, K.4
  • 23
    • 77950202999 scopus 로고    scopus 로고
    • Phosphoramidites: Privileged ligands in asymmetric catalysis
    • Teichert, J.F.; Feringa, B.L. Phosphoramidites: Privileged ligands in asymmetric catalysis. Angew. Chem. Int. Ed. 2010, 49, 2486-2528.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2486-2528
    • Teichert, J.F.1    Feringa, B.L.2
  • 24
    • 78650411624 scopus 로고    scopus 로고
    • Highly enantioselective alkynylation of trifluoropyruvate with alkynylsilanes catalyzed by the BINAP-Pd complex: Access to a-trifluoromethyl- substituted tertiary alcohols
    • Aikawa, K.; Hioki, Y.; Mikami, K. Highly enantioselective alkynylation of trifluoropyruvate with alkynylsilanes catalyzed by the BINAP-Pd complex: Access to a-trifluoromethyl-substituted tertiary alcohols. Org. Lett. 2010, 12, 5716-5719.
    • (2010) Org. Lett. , vol.12 , pp. 5716-5719
    • Aikawa, K.1    Hioki, Y.2    Mikami, K.3
  • 25
    • 77955136606 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of bicyclic ketones catalyzed by BINAP/IPHAN-Ru(II) complex
    • Arai, N.; Akashi, M.; Sugizaki, S.; Ooka, H.; Inoue, T.; Ohkuma, T. Asymmetric hydrogenation of bicyclic ketones catalyzed by BINAP/IPHAN-Ru(II) complex. Org. Lett. 2010, 12, 3380-3383.
    • (2010) Org. Lett. , vol.12 , pp. 3380-3383
    • Arai, N.1    Akashi, M.2    Sugizaki, S.3    Ooka, H.4    Inoue, T.5    Ohkuma, T.6
  • 26
    • 65249154043 scopus 로고    scopus 로고
    • Noncovalent immobilization of enantioselective catalysts
    • Fraile, J.M.; Garcia, J.I.; Mayoral, J.A. Noncovalent Immobilization of Enantioselective Catalysts. Chem. Rev. 2009, 109, 360-417.
    • (2009) Chem. Rev. , vol.109 , pp. 360-417
    • Fraile, J.M.1    Garcia, J.I.2    Mayoral, J.A.3
  • 27
    • 49449092482 scopus 로고    scopus 로고
    • Catalytic enantioselective pudovik reaction of aldehydes and aldimines with tethered bis(8-quinolinato) (TBOx) aluminum complex
    • Yamamoto, H.; Abel, J.P. Catalytic enantioselective pudovik reaction of aldehydes and aldimines with tethered bis(8-quinolinato) (TBOx) aluminum complex. J. Am. Chem. Soc. 2008, 130, 10521-10523.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 10521-10523
    • Yamamoto, H.1    Abel, J.P.2
  • 28
    • 53849128905 scopus 로고    scopus 로고
    • Enantioselective organocatalytic direct Michael addition of nitroalkanes to nitroalkenes promoted by a unique bifunctional DMAP-thiourea
    • Rabalakos, C.; Wulff, W.D. Enantioselective organocatalytic direct Michael addition of nitroalkanes to nitroalkenes promoted by a unique bifunctional DMAP-thiourea. J. Am. Chem. Soc. 2008, 130, 13524-13525.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13524-13525
    • Rabalakos, C.1    Wulff, W.D.2
  • 29
    • 77952862479 scopus 로고    scopus 로고
    • Enantioselective gel collapsing: A new means of visual chiral sensing
    • Chen, X.; Huang, Z.; Chen, S.-Y.; Li, K.; Yu, X.-Q.; Pu, L. Enantioselective gel collapsing: A new means of visual chiral sensing. J. Am. Chem. Soc. 2010, 130, 7297-7299.
    • (2010) J. Am. Chem. Soc. , vol.130 , pp. 7297-7299
    • Chen, X.1    Huang, Z.2    Chen, S.-Y.3    Li, K.4    Yu, X.-Q.5    Pu, L.6
  • 30
    • 77956600327 scopus 로고    scopus 로고
    • Highly enantioselective fluorescent recognition of serine and other amino acid derivatives
    • Liu, H.-L.; Zhu, H.-P.; Hou, X.-L.; Lin Pu, L. Highly enantioselective fluorescent recognition of serine and other amino acid derivatives. Org. Lett. 2010, 12, 4172-4175.
    • (2010) Org. Lett. , vol.12 , pp. 4172-4175
    • Liu, H.-L.1    Zhu, H.-P.2    Hou, X.-L.3    Lin Pu, L.4
  • 31
    • 74549124419 scopus 로고    scopus 로고
    • Highly enantioselective recognition of structurally diverse a-hydroxycarboxylic acids using a fluorescent sensor
    • Liu, H.-L.; Peng, Q.; Wu, Y.-D.; Chen, D.; Hou, X.-L.; Sabat, M.; Pu, L. Highly enantioselective recognition of structurally diverse a-hydroxycarboxylic acids using a fluorescent sensor. Angew. Chem. Int. Ed. 2010, 49, 602-606.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 602-606
    • Liu, H.-L.1    Peng, Q.2    Wu, Y.-D.3    Chen, D.4    Hou, X.-L.5    Sabat, M.6    Pu, L.7
  • 32
    • 75149189928 scopus 로고    scopus 로고
    • Chiral discrimination of a-amino acids with a C2-symmetric homoditopic receptor
    • Sambasivan, S.; Kim, D. Ahn, K.H. Chiral discrimination of a-amino acids with a C2-symmetric homoditopic receptor. Chem. Commun. 2010, 46, 541-543.
    • (2010) Chem. Commun. , vol.46 , pp. 541-543
    • Sambasivan, S.1    Kim, D.2    Ahn, K.H.3
  • 33
    • 72949092867 scopus 로고    scopus 로고
    • 1,1'-Binaphthyl-based imidazolium chemosensors for highly selective recognition of tryptophan in aqueous solutions
    • Yang, L.; Qin, S.; Su, X.; Yang, F.; You, J.; Hu, C.; Xie, R.; Lan, J. 1,1'-Binaphthyl-based imidazolium chemosensors for highly selective recognition of tryptophan in aqueous solutions. Org. Biomol. Chem. 2010, 8, 339-348.
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 339-348
    • Yang, L.1    Qin, S.2    Su, X.3    Yang, F.4    You, J.5    Hu, C.6    Xie, R.7    Lan, J.8
  • 34
    • 77954101738 scopus 로고    scopus 로고
    • Synthesis and evaluation of chiral selectors with multiple hydrogen-bonding sites in the macrocyclic cavities
    • Ema, T.; Hamada, K.; Sugita, K.; Nagata, Y.; Sakai, T.; Ohnishi, A. Synthesis and evaluation of chiral selectors with multiple hydrogen-bonding sites in the macrocyclic cavities. J. Org. Chem. 2010, 75, 4492-4500.
    • (2010) J. Org. Chem. , vol.75 , pp. 4492-4500
    • Ema, T.1    Hamada, K.2    Sugita, K.3    Nagata, Y.4    Sakai, T.5    Ohnishi, A.6
  • 35
    • 46149115357 scopus 로고    scopus 로고
    • Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors
    • Nandhakumar, R.; Ryu, J.; Park, H.; Tang, L.; Choi, S.; Kim, K.M. Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors. Tetrahedron 2008, 64, 7704-7708.
    • (2008) Tetrahedron , vol.64 , pp. 7704-7708
    • Nandhakumar, R.1    Ryu, J.2    Park, H.3    Tang, L.4    Choi, S.5    Kim, K.M.6
  • 36
    • 48849105516 scopus 로고    scopus 로고
    • Chiral selector with multiple hydrogen-bonding sites in a macrocyclic cavity
    • Ema, T.; Tanida, D.; Sugita, K.; Sakai, T.; Miyazawa, K.; Ohnishi, A. Chiral selector with multiple hydrogen-bonding sites in a macrocyclic cavity. Org. Lett. 2008, 10, 2365-2368.
    • (2008) Org. Lett. , vol.10 , pp. 2365-2368
    • Ema, T.1    Tanida, D.2    Sugita, K.3    Sakai, T.4    Miyazawa, K.5    Ohnishi, A.6
  • 37
    • 56449128054 scopus 로고    scopus 로고
    • Tuning the chiral cavity of macrocyclic receptor for chiralrecognition and discrimination
    • Ema, T.; Tanida, D.; Hamada, K.; Sakai, T. Tuning the chiral cavity of macrocyclic receptor for chiralrecognition and discrimination. J. Org. Chem. 2008, 73, 9129-9132.
    • (2008) J. Org. Chem. , vol.73 , pp. 9129-9132
    • Ema, T.1    Tanida, D.2    Hamada, K.3    Sakai, T.4
  • 38
    • 55449112158 scopus 로고    scopus 로고
    • Stereoconversion of amino acids and peptides in uryl-pendant binol schiff bases
    • Park, H.; Nandhakumar, R.; Hong, J.; Ham, S.; Chin, J.; Kim, K. M. Stereoconversion of amino acids and peptides in uryl-pendant binol schiff bases. Chem. Eur. J. 2008, 14, 9935-9942.
    • (2008) Chem. Eur. J. , vol.14 , pp. 9935-9942
    • Park, H.1    Nandhakumar, R.2    Hong, J.3    Ham, S.4    Chin, J.5    Kim, K.M.6
  • 39
    • 33846044312 scopus 로고    scopus 로고
    • Enantioselective fluorescent recognition of amino alcohols by a chiral tetrahydroxyl 1,1′-binaphthyl compound
    • DOI 10.1021/jo061769i
    • Wang, Q.; Chen, X.; Tao, L.; Wang, L.; Xiao, D.; Yu, X.-Q.; Pu, L. Enantioselective fluorescent recognition of amino alcohols by a chiral tetrahydroxyl 1,1'-binaphthyl compound. J. Org. Chem. 2007, 72, 97-101. (Pubitemid 46068208)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.1 , pp. 97-101
    • Wang, Q.1    Chen, X.2    Tao, L.3    Wang, L.4    Xiao, D.5    Yu, X.-Q.6    Pu, L.7
  • 41
    • 0037471533 scopus 로고    scopus 로고
    • Synthesis and recognition of amino acids by binaphthyl-crown receptors
    • DOI 10.1016/S0040-4020(03)00478-2
    • Tsubaki, K.; Tanaka, H.; Morikawa, H.; Fuji, K. Synthesis and recognition of amino acids by binaphthyl-crown receptors. Tetrahedron 2003, 59, 3195-3199. (Pubitemid 36513608)
    • (2003) Tetrahedron , vol.59 , Issue.18 , pp. 3195-3199
    • Tsubaki, K.1    Tanaka, H.2    Morikawa, H.3    Fuji, K.4
  • 42
    • 78650602117 scopus 로고    scopus 로고
    • Light-driven reversible handedness inversion in self-organized helical superstructures
    • Mathews, M.; Zola, R.S.; Hurley, S.; Yang, D.-K.; White, T.J.; Bunning, T.J.; Li, Q. Light-driven reversible handedness inversion in self-organized helical superstructures. J. Am. Chem. Soc. 2010, 132, 18361-18366.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 18361-18366
    • Mathews, M.1    Zola, R.S.2    Hurley, S.3    Yang, D.-K.4    White, T.J.5    Bunning, T.J.6    Li, Q.7
  • 44
    • 73249150081 scopus 로고    scopus 로고
    • Helical polyacetylene: Asymmetric polymerization in a chiral liquid-crystal field
    • Akagi, K. Helical polyacetylene: Asymmetric polymerization in a chiral liquid-crystal field. Chem. Rev. 2009, 109, 5354-5361.
    • (2009) Chem. Rev. , vol.109 , pp. 5354-5361
    • Akagi, K.1
  • 46
    • 34447525379 scopus 로고    scopus 로고
    • Highly twisted helical polyacetylene with morphology free from the bundle of fibrils synthesized in chiral nematic liquid crystal reaction field
    • DOI 10.1021/ja070701x
    • Goh, M.; Kyotani, M.; Akagi, K. Highly twisted helical polyacetylene with morphology free from the bundle of fibrils synthesized in chiral nematic liquid crystal reaction field. J. Am. Chem. Soc. 2007, 129, 8519-8527. (Pubitemid 47066514)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.27 , pp. 8519-8527
    • Goh, M.1    Kyotani, M.2    Akagi, K.3
  • 47
    • 33845973715 scopus 로고    scopus 로고
    • Host-guest effect on chirality transfer from a binaphthyl derivative to a host nematic liquid crystal
    • DOI 10.1039/b611538a
    • Yoshizawa, A.; Kobayashi, K.; Sato, M. Host-guest effect on chirality transfer from a binaphthyl derivative to a host nematic liquid crystal. Chem. Commun. 2007, 257-259. (Pubitemid 46052675)
    • (2007) Chemical Communications , Issue.3 , pp. 257-259
    • Yoshizawa, A.1    Kobayashi, K.2    Sato, M.3
  • 49
    • 33749579465 scopus 로고    scopus 로고
    • Amplification of chirality in liquid crystals
    • DOI 10.1039/b608749c
    • Eelkema, R.; Feringa, B.L. Amplification of chirality in liquid crystals. Org. Biomol. Chem. 2006, 4, 3729-3745. (Pubitemid 44536083)
    • (2006) Organic and Biomolecular Chemistry , vol.4 , Issue.20 , pp. 3729-3745
    • Eelkema, R.1    Feringa, B.L.2
  • 51
    • 27144549231 scopus 로고    scopus 로고
    • Synthesis of helical polyacetylene in chiral nematic liquid crystals using crown ether type binaphthyl derivatives as chiral dopants
    • DOI 10.1021/ja051548e
    • Akagi, K.; Guo, S.; Mori, T.; Goh, M.; Piao, G.; Kyotan, M. Synthesis of helical polyacetylene in chiral nematic liquid crystals using crown ether type binaphthyl derivatives as chiral dopants. J. Am. Chem. Soc. 2005, 127, 14647-14654. (Pubitemid 41511002)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.42 , pp. 14647-14654
    • Akagi, K.1    Quo, S.2    Mori, T.3    Goh, M.4    Piao, G.5    Kyotani, M.6
  • 52
    • 4444300394 scopus 로고    scopus 로고
    • New 2,2'-substituted 4,4'-dimethoxy-6,6'- dimethyl[1,1'-biphenyls], inducing a strong helical twisting power in liquid crystals
    • Holzwarth, R.; Bartsch, R.; Cherkaoui, Z.; Solladié, G. New 2,2'-substituted 4,4'-dimethoxy-6,6'- dimethyl[1,1'-biphenyls], inducing a strong helical twisting power in liquid crystals. Chem. Eur. J. 2004, 10, 3931-3935.
    • (2004) Chem. Eur. J. , vol.10 , pp. 3931-3935
    • Holzwarth, R.1    Bartsch, R.2    Cherkaoui, Z.3    Solladié, G.4
  • 53
    • 0031025810 scopus 로고    scopus 로고
    • Conformational analysis of some trans- 4,5-Diaryl-1,3-dioxolanes by CD spectroscopy and induction of cholesteric mesophases in nematic solvents: A correlation between twisting power and structure of the dopant
    • Carlo, R.; Piero, S.G.; Gloria, P.; Stefano, M.; Simone, S. Conformational analysis of some trans- 4,5-Diaryl-1,3-dioxolanes by CD spectroscopy and induction of cholesteric mesophases in nematic solvents: A correlation between twisting power and structure of the dopant. J. Am. Chem. Soc. 1997, 119, 506-512.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 506-512
    • Carlo, R.1    Piero, S.G.2    Gloria, P.3    Stefano, M.4    Simone, S.5
  • 54
    • 33845373434 scopus 로고
    • Induction of the cholesteric mesophase in nematic liquid crystals: Correlation between the conformation of open-chain chiral 1,l'-binaphthyls and their twisting powers
    • Gottarelli, G.; Spada, G.P. Induction of the cholesteric mesophase in nematic liquid crystals: Correlation between the conformation of open-chain chiral 1,l'-binaphthyls and their twisting powers. J. Org. Chem. 1986, 51, 589-592.
    • (1986) J. Org. Chem. , vol.51 , pp. 589-592
    • Gottarelli, G.1    Spada, G.P.2
  • 56
    • 77957977330 scopus 로고    scopus 로고
    • BINAP adsorption on palladium: A combined infrared spectroscopy and theoretical study
    • Reimann, S.; Urakawa, A.; Baiker, A. BINAP adsorption on palladium: A combined infrared spectroscopy and theoretical study. J. Phys. Chem. C 2010, 114, 17836-17844.
    • (2010) J. Phys. Chem. C , vol.114 , pp. 17836-17844
    • Reimann, S.1    Urakawa, A.2    Baiker, A.3
  • 57
    • 77953799021 scopus 로고    scopus 로고
    • Experimental and theoretical studies on the chiroptical properties of donor-acceptor binaphthyls. Effects of dynamic conformer population on circular dichroism
    • Nishizaka, M.; Mori, T.; Inoue, Y. Experimental and theoretical studies on the chiroptical properties of donor-acceptor binaphthyls. Effects of dynamic conformer population on circular dichroism. J. Phys. Chem. Lett. 2010, 1, 1809-1812.
    • (2010) J. Phys. Chem. Lett. , vol.1 , pp. 1809-1812
    • Nishizaka, M.1    Mori, T.2    Inoue, Y.3
  • 58
    • 68049104704 scopus 로고    scopus 로고
    • Synthesis and helicate formation of a new family of BINOL-based bis(bipyridine) ligands
    • Bunzen, J.; Bruhn, T.; Bringmann, G.; Lutzen, A. Synthesis and helicate formation of a new family of BINOL-based bis(bipyridine) ligands. J. Am. Chem. Soc. 2009, 131, 3621-3630.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3621-3630
    • Bunzen, J.1    Bruhn, T.2    Bringmann, G.3    Lutzen, A.4
  • 59
    • 33644925316 scopus 로고    scopus 로고
    • Density functional theoretical study on enantiomerization of 2,2'-biphenol
    • Sahnoun, R.; Koseki, S.; Fujimura, Y. Density functional theoretical study on enantiomerization of 2,2'-biphenol. J. Phys. Chem. A 2006, 110, 2440-2447.
    • (2006) J. Phys. Chem. A , vol.110 , pp. 2440-2447
    • Sahnoun, R.1    Koseki, S.2    Fujimura, Y.3
  • 60
    • 1842588432 scopus 로고    scopus 로고
    • Synthesis of an octahydro-1,1′-binaphthyl thioether ligand and comparison with unhydrogenated binaphthyl analogues
    • DOI 10.1016/S0957-4166(03)00583-4, PII S0957416603005834
    • Albrow, V.; Biswas, K.; Crane, A.; Chaplin, N.; Easun, T.; Gladiali, S.; Lygo, B.; Woodward, S. Synthesis of an octahydro-1,1'-binaphthyl thioether ligand and comparison with unhydrogenated binaphthyl analogues. Tetrahedron Asymmetry 2003, 14, 2813-2819. (Pubitemid 38435362)
    • (2003) Tetrahedron Asymmetry , vol.14 , Issue.18 , pp. 2813-2819
    • Albrow, V.1    Biswas, K.2    Crane, A.3    Chaplin, N.4    Easun, T.5    Gladiali, S.6    Lygo, B.7    Woodward, S.8
  • 61
    • 0035807679 scopus 로고    scopus 로고
    • Vibrational circular dichroism of 1,1′-binaphthyl derivatives: Experimental and theoretical study
    • DOI 10.1021/jp011485w
    • Setnicka, V.; Urbanová, M.; Bour, P.; Král, V.; Volka, K. Vibrational circular dichroism of 1,1'- binaphthyl derivatives: Experimental and theoretical study. J. Phys. Chem. A 2001, 105, 8931-8938. (Pubitemid 35378320)
    • (2001) Journal of Physical Chemistry A , vol.105 , Issue.39 , pp. 8931-8938
    • Setnicka, V.1    Urbanova, M.2    Bour, P.3    Kral, V.4    Volka, K.5
  • 62
    • 1542730287 scopus 로고
    • Rotational barriers of 1,1'-binaphthyls: A computational study
    • Kranz, M.; Clark, T.; Schleyer, P.v.R. Rotational barriers of 1,1'-binaphthyls: A computational study. J. Org. Chem. 1993, 58, 3317-3325.
    • (1993) J. Org. Chem. , vol.58 , pp. 3317-3325
    • Kranz, M.1    Clark, T.2    Schleyer, P.V.R.3
  • 63
    • 77955836958 scopus 로고    scopus 로고
    • Supramolecular control of fluorescence through reversible encapsulation
    • Dube, H.; Ams, M.R.; Rebek, J., Jr. Supramolecular control of fluorescence through reversible encapsulation. J. Am. Chem. Soc. 2010, 132, 9984-9985.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 9984-9985
    • Dube, H.1    Ams, M.R.2    Rebek Jr., J.3
  • 64
    • 77951824188 scopus 로고    scopus 로고
    • Layer-by-layer ultrathin films of azobenzene-containing polymer/layered double hydroxides with reversible photoresponsive behavior
    • Han, J.; Yan, D.; Shi, W.; Ma, J.; Yan, H.; Wei, M.; Evans, D.G.; Duan, X. Layer-by-layer ultrathin films of azobenzene-containing polymer/layered double hydroxides with reversible photoresponsive behavior. J. Phys. Chem. B 2010, 114, 5678-5685.
    • (2010) J. Phys. Chem. B , vol.114 , pp. 5678-5685
    • Han, J.1    Yan, D.2    Shi, W.3    Ma, J.4    Yan, H.5    Wei, M.6    Evans, D.G.7    Duan, X.8
  • 65
    • 77952975061 scopus 로고    scopus 로고
    • Photoresponsive host-guest systems based on a new azobenzene-containing crytpand
    • Liu, M.; Yan, X.; Hu, M.; Chen, X.; Zhang, M.; Zheng, B.; Hu, X.; Shao, S.; Huang, F. Photoresponsive host-guest systems based on a new azobenzene-containing crytpand. Org. Lett. 2010, 12, 2558-2561.
    • (2010) Org. Lett. , vol.12 , pp. 2558-2561
    • Liu, M.1    Yan, X.2    Hu, M.3    Chen, X.4    Zhang, M.5    Zheng, B.6    Hu, X.7    Shao, S.8    Huang, F.9
  • 66
    • 77953046105 scopus 로고    scopus 로고
    • Structure of silver(I) complex prepared from azobenzenonaphthalenophane, photochemical coordination change of silver(I) and silver(I)-induced acceleration of Z-E thermal isomerization of azobenzene unit
    • Oka, Y.; Tamaoki, N. Structure of silver(I) complex prepared from azobenzenonaphthalenophane, photochemical coordination change of silver(I) and silver(I)-induced acceleration of Z-E thermal isomerization of azobenzene unit. Inorg. Chem. 2010, 49, 4765-4767.
    • (2010) Inorg. Chem. , vol.49 , pp. 4765-4767
    • Oka, Y.1    Tamaoki, N.2
  • 67
    • 76249087074 scopus 로고    scopus 로고
    • Photoinduced control over the self-organized orientation of amorphous molecular materials using polarized light
    • Kawamoto, M.; Sassa, T.; Wada, T. Photoinduced control over the self-organized orientation of amorphous molecular materials using polarized light. J. Phys. Chem. B, 2010, 114, 1227-1232.
    • (2010) J. Phys. Chem. B , vol.114 , pp. 1227-1232
    • Kawamoto, M.1    Sassa, T.2    Wada, T.3
  • 68
    • 77950248976 scopus 로고    scopus 로고
    • Diastereoselective synergistic dual-mode optical switch with integrated chirochromic helicene and photochromic bis-azobenzene moieties
    • Chen, W.-C.; Lee, Y.-W.; Chen, C.-T. Diastereoselective, synergistic dual-mode optical switch with integrated chirochromic helicene and photochromic bis-azobenzene moieties. Org. Lett. 2010, 12, 1472-1475.
    • (2010) Org. Lett. , vol.12 , pp. 1472-1475
    • Chen, W.-C.1    Lee, Y.-W.2    Chen, C.-T.3
  • 69
    • 77949280344 scopus 로고    scopus 로고
    • A light-controlled molecular brake with complete ON-OFF rotation
    • Basheer, M.C.; Oka, Y.; Mathews, M.; Tamaoki, N. A light-controlled molecular brake with complete ON-OFF rotation. Chem. Eur. J. 2010, 16, 3489-3496.
    • (2010) Chem. Eur. J. , vol.16 , pp. 3489-3496
    • Basheer, M.C.1    Oka, Y.2    Mathews, M.3    Tamaoki, N.4
  • 70
    • 78049413958 scopus 로고    scopus 로고
    • Non-destructive erasable molecular switches and memory using light-driven twisting motions
    • Kawamoto, M.; Shiga, N.; Takaishi, K.; Yamashita, T. Non-destructive erasable molecular switches and memory using light-driven twisting motions. Chem. Commun. 2010, 46, 8344-8346.
    • (2010) Chem. Commun. , vol.46 , pp. 8344-8346
    • Kawamoto, M.1    Shiga, N.2    Takaishi, K.3    Yamashita, T.4
  • 71
    • 60149097223 scopus 로고    scopus 로고
    • Spectral tuning of azobenzene photoswitches for biological applications
    • Sadovski, O.; Beharry, A.A.; Zhang, F.; Woolley, G.A. Spectral tuning of azobenzene photoswitches for biological applications. Angew. Chem. Int. Ed. 2009, 48, 1484-1486.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1484-1486
    • Sadovski, O.1    Beharry, A.A.2    Zhang, F.3    Woolley, G.A.4
  • 72
    • 70349300001 scopus 로고    scopus 로고
    • Control and modulation of chirality for azobenzene-substituted polydiacetylene LB films with circularly polarized light
    • Zou, G.; Jiang, H.; Kohn, H.; Manaka, T.; Iwamoto, M. Control and modulation of chirality for azobenzene-substituted polydiacetylene LB films with circularly polarized light. Chem. Commun. 2009, 5627-5629.
    • (2009) Chem. Commun. , pp. 5627-5629
    • Zou, G.1    Jiang, H.2    Kohn, H.3    Manaka, T.4    Iwamoto, M.5
  • 73
    • 70350637502 scopus 로고    scopus 로고
    • Highly efficient reversible Z-E photoisomerization of a bridged azobenzene with visible light through resolved S1(np) absorption bands
    • Siewertsen, R.; Neumann, H.; Buchheim-Stehn, B.; Herges, R.; Näther, C.; Renth, F.; Temps, F. Highly efficient reversible Z-E photoisomerization of a bridged azobenzene with visible light through resolved S1(np) absorption bands. J. Am. Chem. Soc. 2009, 131, 15594-15595.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 15594-15595
    • Siewertsen, R.1    Neumann, H.2    Buchheim-Stehn, B.3    Herges, R.4    Näther, C.5    Renth, F.6    Temps, F.7
  • 75
  • 76
    • 40349108730 scopus 로고    scopus 로고
    • A fluorescent guest encapsulated by a photoreactive azobenzene dendrimer
    • DOI 10.1039/b718095k
    • Puntoriero, F.; Bergamini, G.; Ceroni, P.; Balzania, V.; Vögtle, F. A fluorescent guest encapsulated by a photoreactive azobenzene dendrimer. New J. Chem. 2008, 32, 401-406. (Pubitemid 351342286)
    • (2008) New Journal of Chemistry , vol.32 , Issue.3 , pp. 401-406
    • Puntoriero, F.1    Bergamini, G.2    Ceroni, P.3    Balzani, V.4    Vogtle, F.5
  • 77
    • 50249099319 scopus 로고    scopus 로고
    • Planar chiral azobenzenophanes as chiroptic switches for photon mode reversible reflection color control in induced chiral nematic liquid crystals
    • Tamaoki, N.; Mathews, M. Planar chiral azobenzenophanes as chiroptic switches for photon mode reversible reflection color control in induced chiral nematic liquid crystals. J. Am. Chem. Soc. 2008, 130, 11409-11416.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11409-11416
    • Tamaoki, N.1    Mathews, M.2
  • 78
    • 48849102219 scopus 로고    scopus 로고
    • Photomodulated chiral induction in helical azobenzene oligomers
    • King, E.D.; Tao, P.; Sanan, T.T.; Hadad, C.M.; Parquetted, J.R. Photomodulated chiral induction in helical azobenzene oligomers. Org. Lett. 2008, 10, 1671-1674.
    • (2008) Org. Lett. , vol.10 , pp. 1671-1674
    • King, E.D.1    Tao, P.2    Sanan, T.T.3    Hadad, C.M.4    Parquetted, J.R.5
  • 80
    • 34249701962 scopus 로고    scopus 로고
    • Light-driven supramolecular chirality in propeller-like hydrogen-bonded complexes that show columnar mesomorphism
    • DOI 10.1002/anie.200603796
    • Vera, F.; Tejedor, R.M.; Romero, P.; Barberá, J.; Ros, M.B.; Serrano, J.L.; Sierra, T. Light-driven supramolecular chirality in propeller-like hydrogen-bonded complexes that show columnar mesomorphism. Angew. Chem. Int. Ed. 2007, 46, 1873-1877. (Pubitemid 46981325)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.11 , pp. 1873-1877
    • Vera, F.1    Tejedor, R.M.2    Romero, P.3    Barbera, J.4    Ros, M.B.5    Serrano, J.L.6    Sierra, T.7
  • 81
    • 34250782789 scopus 로고    scopus 로고
    • Influence of helical twisting power on the photoswitching behavior of chiral azobenzene compounds: Applications to high-performance switching devices
    • DOI 10.1002/chem.200600954
    • Alam, M.Z.; Yoshioka, T.; Ogata, T.; Nonaka, T.; Kurihara, S. Influence of helical twisting poweron the photoswitching behavior of chiral azobenzene compounds: Applications to highperformance switching devices. Chem. Eur. J. 2007, 13, 2641-2647. (Pubitemid 46953338)
    • (2007) Chemistry - A European Journal , vol.13 , Issue.9 , pp. 2641-2647
    • Alam, Md.Z.1    Yoshioka, T.2    Ogata, T.3    Nonaka, T.4    Kurihara, S.5
  • 82
    • 34447343572 scopus 로고    scopus 로고
    • Photoinduced chirality in azobenzenecontaining polymer systems
    • Choi, S.-W.; Kawauchi, S.; Ha, N.Y.; Takezoe, H. Photoinduced chirality in azobenzenecontaining polymer systems. Phys. Chem. Chem. Phys. 2007, 9, 3671-3681.
    • (2007) Phys. Chem. Chem. Phys. , vol.9 , pp. 3671-3681
    • Choi, S.-W.1    Kawauchi, S.2    Ha, N.Y.3    Takezoe, H.4
  • 83
    • 33645303805 scopus 로고    scopus 로고
    • Mechanical twisting of a guest by a photoresponsive host
    • Muraoka, T.; Kinbara, K.; Aida, T. Mechanical twisting of a guest by a photoresponsive host Nature 2006, 440, 512-515.
    • (2006) Nature , vol.440 , pp. 512-515
    • Muraoka, T.1    Kinbara, K.2    Aida, T.3
  • 84
    • 33645523191 scopus 로고    scopus 로고
    • Structural control of the electronic properties of photodynamic azobenzene-derivatized p-conjugated oligothiophenes
    • Jousselme, B.; Blanchard, P.; Allain, M.; Levillain, E.; Dias, M.; Roncali, J. Structural control of the electronic properties of photodynamic azobenzene-derivatized p-conjugated oligothiophenes. J. Phys. Chem. A 2006, 110, 3488-3494.
    • (2006) J. Phys. Chem. A , vol.110 , pp. 3488-3494
    • Jousselme, B.1    Blanchard, P.2    Allain, M.3    Levillain, E.4    Dias, M.5    Roncali, J.6
  • 87
    • 33847139421 scopus 로고    scopus 로고
    • Light-driven twisting behaviour of chiral cyclic compounds
    • DOI 10.1039/b616320c
    • Kawamoto, M.; Aoki, T.; Wada, T. Light-driven twisting behaviour of chiral cyclic compounds. Chem. Commun. 2007, 930-932. (Pubitemid 46295395)
    • (2007) Chemical Communications , Issue.9 , pp. 930-932
    • Kawamoto, M.1    Aoki, T.2    Wada, T.3
  • 88
    • 68049097188 scopus 로고    scopus 로고
    • Photoswitching of dextro/levo rotation with axially chiral binaphthyls linked to an azobenzene
    • Takaishi, K.; Kawamoto, M.; Tsubaki, K.; Wada, T. Photoswitching of dextro/levo rotation with axially chiral binaphthyls linked to an azobenzene. J. Org. Chem. 2009, 74, 5723-5726.
    • (2009) J. Org. Chem. , vol.74 , pp. 5723-5726
    • Takaishi, K.1    Kawamoto, M.2    Tsubaki, K.3    Wada, T.4
  • 89
    • 79551477299 scopus 로고    scopus 로고
    • Helical chirality of azobenzenes induced by an intramolecular chiral axis and potential as chiroptical switches
    • Takaishi, K.; Kawamoto, M.; Tsubaki, K.; Furuyama, T.; Muranaka, A.; Uchiyama, M. Helical chirality of azobenzenes induced by an intramolecular chiral axis and potential as chiroptical switches. Chem. Eur. J. 2011, 17, 1778-1782.
    • (2011) Chem. Eur. J. , vol.17 , pp. 1778-1782
    • Takaishi, K.1    Kawamoto, M.2    Tsubaki, K.3    Furuyama, T.4    Muranaka, A.5    Uchiyama, M.6
  • 90
    • 77953485620 scopus 로고    scopus 로고
    • A bridged azobenzene derivative as a reversible, light-induced chirality switch
    • Haberhauer, G.; Kallweit, C. A bridged azobenzene derivative as a reversible, light-induced chirality switch. Angew. Chem. Int. Ed. 2010, 49, 2418-2421.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2418-2421
    • Haberhauer, G.1    Kallweit, C.2
  • 91
    • 0038448217 scopus 로고    scopus 로고
    • Convenient synthesis and efficient resolution of 3,3′- bis(benzyloxy)-1,1′-binaphthalene-2,2′-diol
    • DOI 10.1016/S0957-4166(03)00219-2
    • Tsubaki, K.; Morikawa, H.; Tanaka, H.; Fuji, K. Convenient synthesis and efficient resolution of 3,3'-bis(benzyloxy)-1,1'-binaphthalene-2,2'-diol. Tetrahedron Asymmetry 2003, 14, 1393-1396. (Pubitemid 36859713)
    • (2003) Tetrahedron Asymmetry , vol.14 , Issue.10 , pp. 1393-1396
    • Tsubaki, K.1    Morikawa, H.2    Tanaka, H.3    Fuji, K.4
  • 92
    • 40649107591 scopus 로고    scopus 로고
    • Total synthesis of demethylwedelolactone and wedelolactone by Cu-mediated/Pd(0)-catalysis and oxidativecyclization
    • Chang, C.-F.; Yang, L.-Y.; Chang, S.-W. Fang, Y.-T.; Lee, Y.-J. Total synthesis of demethylwedelolactone and wedelolactone by Cu-mediated/Pd(0)- catalysis and oxidativecyclization. Tetrahedron 2008, 68, 3661-3666.
    • (2008) Tetrahedron , vol.68 , pp. 3661-3666
    • Chang, C.-F.1    Yang, L.-Y.2    Chang, S.-W.3    Fang, Y.-T.4    Lee, Y.-J.5
  • 93
    • 0032564640 scopus 로고    scopus 로고
    • First total synthesis of (-)-8-epi-9-deoxygoniopypyrone
    • DOI 10.1016/S0040-4039(98)02269-2, PII S0040403998022692
    • Surivet, J.-P.; Vatèle, J.-M. First total synthesis of (-)-8-epi-9-deoxygoniopypyrone. Tetrahedron Lett. 1998, 39, 9681-9682. (Pubitemid 28551719)
    • (1998) Tetrahedron Letters , vol.39 , Issue.52 , pp. 9681-9682
    • Surivet, J.-P.1    Vatele, J.-M.2
  • 94
    • 0000753770 scopus 로고
    • Regioselective de-O-benzylation with lewis acids
    • Hori, H.; Nishida, Y.; Ohrui, H.; Meguro, H. Regioselective de-O-benzylation with lewis acids. J. Org. Chem. 1989, 54, 1346-1353.
    • (1989) J. Org. Chem. , vol.54 , pp. 1346-1353
    • Hori, H.1    Nishida, Y.2    Ohrui, H.3    Meguro, H.4
  • 95
    • 0033950175 scopus 로고    scopus 로고
    • Synthesis and characterization of new enantiopure 7,7'-disubstituted 2,2'- dihydroxy-1,1'-binaphthyls: Useful ligands for the asymmetric allylation reaction of aldehydes
    • Bandin, M.; Casolari, S.; Cozzi, P.G.; Proni, G.; Schmohel, E.; Spada, G.P.; Tagliavini, E.; Umani-Ronchi, A. Synthesis and characterization of new enantiopure 7,7'-disubstituted 2,2'- dihydroxy-1,1'-binaphthyls: Useful ligands for the asymmetric allylation reaction of aldehydes. Eur. J. Org. Chem. 2000, 491-497.
    • (2000) Eur. J. Org. Chem. , pp. 491-497
    • Bandin, M.1    Casolari, S.2    Cozzi, P.G.3    Proni, G.4    Schmohel, E.5    Spada, G.P.6    Tagliavini, E.7    Umani-Ronchi, A.8
  • 96
    • 0001693102 scopus 로고
    • Auf 2,2',7,7'-Tetrahydroxy-1,1'-binaphthyl basierende neuartige chirale mono- und ditope cyclophanartige wirtverbindungen mit einer unpolaren bindungsstelle
    • Diederich, F.; Hester, M.R.; Uyeki, M.A. Auf 2,2',7,7'-Tetrahydroxy-1,1'- binaphthyl basierende neuartige chirale mono- und ditope cyclophanartige wirtverbindungen mit einer unpolaren bindungsstelle. Angew. Chem. 1988, 100, 1775-1777.
    • (1988) Angew. Chem. , vol.100 , pp. 1775-1777
    • Diederich, F.1    Hester, M.R.2    Uyeki, M.A.3
  • 97
    • 0028198270 scopus 로고
    • Synthesis of (R)- and (S)-7,7'-bis(diphenylphosphino)-2,2'-dimethoxy-1, 1'-binaphthyl, a new axially dissymmetric bis(triarylphosphine)
    • DOI 10.1016/S0957-4166(00)86197-2
    • Horiuchi, T.; Ohta, T.; Stephan, M.; Takaya, H. Synthesis of (R)- and (S)-7,7'- bis(diphenylphosphino)-2,2'-dimethoxy-l,l'-binaphthyl, a new axially dissymmetric bis(triarylphosphine). Tetrahedron Asymmetry 1994, 5, 325-328. (Pubitemid 24117555)
    • (1994) Tetrahedron Asymmetry , vol.5 , Issue.3 , pp. 325-328
    • Horiuchi, T.1    Ohta, T.2    Stephan, M.3    Takaya, H.4
  • 100
    • 65949112025 scopus 로고    scopus 로고
    • Synthesis of chiral dotriacontanaphthalenes: How many naphthalene units are we able to elaborately connect?
    • Sue, D.; Takaishi, K.; Harada, T.; Kuroda, R.; Kawabata, T.; Tsubaki, K. Synthesis of chiral dotriacontanaphthalenes: How many naphthalene units are we able to elaborately connect? J. Org. Chem. 2009, 74, 3940-3943.
    • (2009) J. Org. Chem. , vol.74 , pp. 3940-3943
    • Sue, D.1    Takaishi, K.2    Harada, T.3    Kuroda, R.4    Kawabata, T.5    Tsubaki, K.6
  • 101
    • 0034641234 scopus 로고    scopus 로고
    • Anomalous CD/UV exciton splitting of a binaphthyl derivative: The case of 2,2'-diiodo-1,1'-binaphthalene
    • DOI 10.1021/ja000114a
    • Bari, L.D.; Pescitelli, G.; Marchetti, F.; Salvadori, P. Anomalous CD/UV exciton splitting of a binaphthyl derivative: The case of 2,2'-diiodo-1,1'- binaphthalene. J. Am. Chem. Soc. 2000, 122, 6395-6398. (Pubitemid 30481738)
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.27 , pp. 6395-6398
    • Di Bari, L.1    Pescitelli, G.2    Marchetti, F.3    Salvadori, P.4
  • 102
    • 0008731726 scopus 로고
    • The exciton chirality method and its application to configurational and conformational studies of natural products
    • Harada, N.; Nakanishi, K. The exciton chirality method and its application to configurational and conformational studies of natural products. Acc. Chem. Res. 1972, 5, 257-263.
    • (1972) Acc. Chem. Res. , vol.5 , pp. 257-263
    • Harada, N.1    Nakanishi, K.2
  • 104
    • 67749135571 scopus 로고    scopus 로고
    • Metal-bis(helicene) assemblies incorporating p-conjugated phosphole-azahelicene ligands: Impacting chiroptical properties by metal variation
    • Graule, S.; Rudolph, M.; Vanthuyne, N.; Autschbach, J.; Roussel, C.; Crassous, J.; Réau, R. Metal-bis(helicene) assemblies incorporating p-conjugated phosphole-azahelicene ligands: Impacting chiroptical properties by metal variation. J. Am. Chem. Soc. 2009, 131, 3183-3185.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3183-3185
    • Graule, S.1    Rudolph, M.2    Vanthuyne, N.3    Autschbach, J.4    Roussel, C.5    Crassous, J.6    Réau, R.7
  • 105
    • 67650314382 scopus 로고    scopus 로고
    • The chiro-optical properties of a lemniscular octaphyrin
    • Rzepa, H.S. The chiro-optical properties of a lemniscular octaphyrin. Org. Lett. 2009, 11, 3088-3091.
    • (2009) Org. Lett. , vol.11 , pp. 3088-3091
    • Rzepa, H.S.1
  • 106
    • 0034647806 scopus 로고    scopus 로고
    • Quantitative chirality of helicenes
    • DOI 10.1016/S0957-4166(00)00235-4, PII S0957416600002354
    • Katzenelson, O.; Edelstein, J.; Avnir, D. Quantitative chirality of helicenes. Tetrahedron Asymmetry 2000, 11, 2695-2704. (Pubitemid 30484085)
    • (2000) Tetrahedron Asymmetry , vol.11 , Issue.13 , pp. 2695-2704
    • Katzenelson, O.1    Edelstein, J.2    Avnir, D.3
  • 107
    • 33847649249 scopus 로고    scopus 로고
    • Chiral helicenoid diarylethene with large change in specific optical rotation by photochromism
    • DOI 10.1021/jo0620213
    • Okumura, T.; Tani, Y.; Miyake, K.; Yokoyama, Y. Chiral helicenoid diarylethene with large change in specific optical rotation by photochromism. J. Org. Chem. 2007, 72, 1634-1638. (Pubitemid 46355459)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.5 , pp. 1634-1638
    • Okuyama, T.1    Tani, Y.2    Miyake, K.3    Yokoyama, Y.4
  • 109
    • 23944519407 scopus 로고    scopus 로고
    • Dual modulation of a molecular switch with exceptional chiroptical properties
    • DOI 10.1021/ja0526721
    • Wang, Z.Y.; Todd, E.K.; Meng, X.S.; Gao, J.P. Dual modulation of a molecular switch with exceptional chiroptical properties. J. Am. Chem. Soc. 2005, 127, 11552-11553. (Pubitemid 41208714)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.33 , pp. 11552-11553
    • Wang, Z.Y.1    Todd, E.K.2    Meng, X.S.3    Gao, J.P.4
  • 110
    • 1342296307 scopus 로고
    • The activated complex and the absolute rate of chemical reactions
    • Eyring, H. The activated complex and the absolute rate of chemical reactions. Chem. Rev. 1935, 17, 65-77.
    • (1935) Chem. Rev. , vol.17 , pp. 65-77
    • Eyring, H.1
  • 112
    • 34147103394 scopus 로고    scopus 로고
    • A light-driven pseudo[4]rotaxane encoded by induced circular dichroism in a hydrogel
    • DOI 10.1002/adfm.200600981
    • Ma, X.; Wang, Q.; Qu, D.; Xu, Y.; Ji, F.; Tian, H. A light-driven pseudo[4]rotaxane encoded by induced circular dichroism in a hydrogel. Adv. Funct. Mater. 2007, 17, 829-837. (Pubitemid 46571650)
    • (2007) Advanced Functional Materials , vol.17 , Issue.5 , pp. 829-837
    • Ma, X.1    Wang, Q.2    Qu, D.3    Xu, Y.4    Ji, F.5    Tian, H.6
  • 114
    • 43049141516 scopus 로고    scopus 로고
    • The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: Two new functionals and systematic testing of four M06-class functionals and 12 other functionals
    • Zhao, Y.; Truhlar, D.G. The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: Two new functionals and systematic testing of four M06-class functionals and 12 other functionals. Theor. Chem. Account. 2008, 120, 215-241.
    • (2008) Theor. Chem. Account. , vol.120 , pp. 215-241
    • Zhao, Y.1    Truhlar, D.G.2


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