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Volumn 82, Issue 8, 2010, Pages 1569-1574

Mechanostereochemistry

Author keywords

Catenanes; Mechanical bonds; Mechanically interlocked molecules; Molecular recognition; Molecular switches; Rotaxanes; Self assembly; Template directed synthesis

Indexed keywords

CATENANES; INTERLOCKED MOLECULES; MECHANICAL BONDS; MOLECULAR SWITCHES; ROTAXANES; TEMPLATE-DIRECTED SYNTHESIS;

EID: 77956160607     PISSN: 00334545     EISSN: 13653075     Source Type: Journal    
DOI: 10.1351/PAC-CON-10-02-09     Document Type: Article
Times cited : (52)

References (50)
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    • 0003570337 scopus 로고    scopus 로고
    • F. Diederich, P. J. Stang (Eds.)., Wiley-VCH, Weinheim
    • F. Diederich, P. J. Stang (Eds.). Templated Organic Synthesis, Wiley-VCH, Weinheim (1999).
    • (1999) Templated Organic Synthesis
  • 13
    • 0003542983 scopus 로고    scopus 로고
    • J.-P. Sauvage, C. O. Dietrich-Buchecker (Eds.)., Wiley- VCH, Weinheim
    • J.-P. Sauvage, C. O. Dietrich-Buchecker (Eds.). Molecular Catenanes, Rotaxanes and Knots, Wiley- VCH, Weinheim (1999).
    • (1999) Molecular Catenanes, Rotaxanes and Knots
  • 14
    • 67849124458 scopus 로고    scopus 로고
    • th American Chemical Society National Meeting in Philadelphia on 17 August 2008, one (J. F. S.) of the authors proposed the use of the term " mechanostereochemistry" to encompass all aspects of the "mechanical bond" in chemistry. The term mechanostereochemistry has been employed recently in another context. See
    • th American Chemical Society National Meeting in Philadelphia on 17 August 2008, one (J. F. S.) of the authors proposed the use of the term " mechanostereochemistry" to encompass all aspects of the "mechanical bond" in chemistry. The term mechanostereochemistry has been employed recently in another context. See: I. Frank, U. Friedrichs. Nat. Chem. 1, 264 (2009).
    • (2009) Nat. Chem. , vol.1 , pp. 264
    • Frank, I.1    Friedrichs, U.2
  • 40
    • 0030727412 scopus 로고    scopus 로고
    • Previously, we had advocated, the use of the term "co- conformation" to designate the different three-dimensional spatial arrangements of the components of mechanically interlocked molecules
    • Previously, we had advocated (M. C. T. Fyfe, P. T. Glink, S. Menzer, J. F. Stoddart, A. J. P. White, D. J. Williams. Angew. Chem., Int. Ed. 36, 2068 (1997)) the use of the term "co-conformation" to designate the different three-dimensional spatial arrangements of the components of mechanically interlocked molecules.
    • (1997) Angew. Chem., Int. Ed. , vol.36 , pp. 2068
    • Fyfe, M.C.T.1    Glink, P.T.2    Menzer, S.3    Stoddart, J.F.4    White, A.J.P.5    Williams, D.J.6
  • 41
    • 37049107485 scopus 로고
    • While conformational diastereoisomerism is now commonplace throughout the reaches of organic chemistry (for an example at the top end of the scale of energy barriers to interconversion, consider the trianthranilides-see, configurational diastereoisomerism dominates organic chemistry across a wide spectrum of different compound types from those where it is displayed around carbon-carbon double bonds in the cis and trans sense (e.g. the TTF unit in the structural formula in Fig. 4a, bottom) to the more conventional situations that exist as soon as two or more chiral elements coexist in the same molecule. Even epimers abound
    • While conformational diastereoisomerism is now commonplace throughout the reaches of organic chemistry (for an example at the top end of the scale of energy barriers to interconversion, consider the trianthranilides-see: A. Hoorfar, W. D. Ollis, J. A. Price, J. S. Stephanatou, J. F. Stoddart. J. Chem. Soc., Perkin Trans. 1 1649 (1982)), configurational diastereoisomerism dominates organic chemistry across a wide spectrum of different compound types from those where it is displayed around carbon-carbon double bonds in the cis and trans sense (e.g., the TTF unit in the structural formula in Fig. 4a, bottom) to the more conventional situations that exist as soon as two or more chiral elements coexist in the same molecule. Even epimers abound.
    • (1982) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1649
    • Hoorfar, A.1    Ollis, W.D.2    Price, J.A.3    Stephanatou, J.S.4    Stoddart, J.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.