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Volumn 43, Issue 23, 2010, Pages 9583-9587

Chiroptical induction and molecular recognition in optically active hyperbranched polyethers with inherently chiral benzophenone core

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EID: 78651318730     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma101660s     Document Type: Letter
Times cited : (9)

References (33)
  • 5
    • 1842430722 scopus 로고    scopus 로고
    • (b) Pu, L. Chem. Rev. 2004,104, 1687.
    • (2004) Chem. Rev. , vol.104 , pp. 1687
    • Pu, L.1
  • 20
    • 0032479816 scopus 로고    scopus 로고
    • It has been reported that enantiomerically pure glycidol does not easily racemize under basic conditions. In fact, it can be produced from 3-chloro-1,2-propanediol by treatment with a base without racemization. Glycidol has been used as starting material for the synthesis of chiral oxathiazolidines under basic conditions and long times of heating
    • It has been reported that enantiomerically pure glycidol does not easily racemize under basic conditions. In fact, it can be produced from 3-chloro-1,2-propanediol by treatment with a base without racemization. Glycidol has been used as starting material for the synthesis of chiral oxathiazolidines under basic conditions and long times of heating. Kasai, N.; Suzuki, T.; Furukawa, Y. J. Mol. Catal. B: Enzym. 1998, 4, 237.
    • (1998) J. Mol. Catal. B: Enzym. , vol.4 , pp. 237
    • Kasai, N.1    Suzuki, T.2    Furukawa, Y.3
  • 21
    • 0029099084 scopus 로고
    • Racemization of enantiomerically pure glycidol is not expected under the ROMBP polymerization conditions
    • Racemization of enantiomerically pure glycidol is not expected under the ROMBP polymerization conditions. See: Gautun, H. S. H.; Carlsen, P. H. J. Tetrahedron: Asymmetry 1995, 6, 1667.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1667
    • Gautun, H.S.H.1    Carlsen, P.H.J.2
  • 23
    • 78651271057 scopus 로고    scopus 로고
    • The spectrum was compared with that of 1,3-dimethoxybenzene
    • The spectrum was compared with that of 1,3-dimethoxybenzene.
  • 26
    • 84981751013 scopus 로고
    • Racemization has been reported even in poly-substituted benzophenones
    • (b) Racemization has been reported even in poly-substituted benzophenones. See: Lauer, D.; Staab, H. A. Chem. Ber. 1969, 102, 1631.
    • (1969) Chem. Ber. , vol.102 , pp. 1631
    • Lauer, D.1    Staab, H.A.2
  • 29
    • 85163172201 scopus 로고
    • The "Pfeiffer effect" is the change in optical rotation of an optically active substance in solution upon addition of a racemic mixture of certain other compound
    • The "Pfeiffer effect" is the change in optical rotation of an optically active substance in solution upon addition of a racemic mixture of certain other compound. Pfeiffer, P.; Quehl, K. Ber. 1931,64,2667.
    • (1931) Ber. , vol.64 , pp. 2667
    • Pfeiffer, P.1    Quehl, K.2
  • 31
    • 33845184268 scopus 로고
    • The phenomenon observed for our systems does not fit into the "sergeant and soldiers" concept, which has been coined to indicate chiral amplification arising from the presence of only a small ratio of chiral units versus achiral units in linear polymers
    • The phenomenon observed for our systems does not fit into the "sergeant and soldiers" concept, which has been coined to indicate chiral amplification arising from the presence of only a small ratio of chiral units versus achiral units in linear polymers: (a) Green, M. M.; Reidy, M. P. J. Am. Chem. Soc. 1989,111,6452.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 6452
    • Green, M.M.1    Reidy, M.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.