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Volumn 13, Issue 9, 2007, Pages 2473-2479

Inherently chiral molecular clips: Synthesis, chiroptical properties, and application to chiral discrimination

Author keywords

Chirality; Circular dichroism; Exciton coupling; Host guest systems; Molecular clips

Indexed keywords

CHEMICAL BONDS; DICHROISM; ENANTIOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL);

EID: 34250745339     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200601585     Document Type: Article
Times cited : (20)

References (93)
  • 43
    • 0034632783 scopus 로고    scopus 로고
    • B. Yurke, A. J. Turberfield, A. P. Jills. Jr., F. C. Simmel. J. L. Neumann, Nature 2000, 406, 605-608:
    • g) B. Yurke, A. J. Turberfield, A. P. Jills. Jr., F. C. Simmel. J. L. Neumann, Nature 2000, 406, 605-608:
  • 45
  • 48
    • 23744480691 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4844-4870. and references therein.
    • Angew. Chem. Int. Ed. 2005, 44, 4844-4870. and references therein.
  • 53
    • 0037091002 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 1355-1358:
    • (2002) Chem. Int. Ed , vol.41 , pp. 1355-1358
    • Angew1
  • 61
    • 34250778484 scopus 로고    scopus 로고
    • Ph.D. thesis, University of Duisburg-Essen, October
    • d) S. Madenci. Ph.D. thesis, University of Duisburg-Essen, October 2006:
    • (2006)
    • Madenci, S.1
  • 63
    • 0035804387 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 717-720.
    • (2001) Chem. Int. Ed , vol.40 , pp. 717-720
    • Angew1
  • 75
    • 34250743278 scopus 로고    scopus 로고
    • COSY and HMQC spectra are given in the Supporting Information
    • COSY and HMQC spectra are given in the Supporting Information.
  • 76
    • 20444449263 scopus 로고    scopus 로고
    • We demonstrated recently that rigid, inherently chiral [2.2]paracyclophanes possess similarly high g factors: see. T. Furo, T. Mori, T. Wada, Y. Inoue, J. Am. Chem. Soc. 2005, 127, 8242-8243.
    • We demonstrated recently that rigid, inherently chiral [2.2]paracyclophanes possess similarly high g factors: see. T. Furo, T. Mori, T. Wada, Y. Inoue, J. Am. Chem. Soc. 2005, 127, 8242-8243.
  • 79
    • 34250787185 scopus 로고    scopus 로고
    • See the Experimental Section for the absolute configurations of anti-1 and aini-2.
    • See the Experimental Section for the absolute configurations of anti-1 and aini-2.
  • 88
    • 34250761549 scopus 로고    scopus 로고
    • Macromodel. version 7.1. Schrödinger, Portland. OR
    • Macromodel. version 7.1. Schrödinger, Portland. OR.
  • 89
    • 0001013736 scopus 로고
    • a) Y. Inoue. Chem. Rev. 1992, 92, 741-770;
    • (1992) Chem. Rev , vol.92 , pp. 741-770
    • Inoue, Y.1
  • 91
    • 0037008974 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 3147-3154;
    • (2002) Chem. Int. Ed , vol.41 , pp. 3147-3154
    • Angew1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.