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Volumn 49, Issue 35, 2010, Pages 6028-6030

Erratum: Reconfiguration of Stereoisomers under Sonomechanical Activation (Angewandte Chemie - International Edition (2010) (49) DOI: 10.1002/anie.201001360);Reconfiguration of stereoisomers under sonomechanical activation

Author keywords

Atropisomers; Configurational inversion; Mechanochemistry; Sonochemistry; mechanochemistry; atropisomers; sonochemistry; configurational inversion

Indexed keywords

CHEMICAL ENGINEERING; CHEMICAL REACTIONS; CHEMISTRY; SONOCHEMISTRY;

EID: 77956013889     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201504650     Document Type: Erratum
Times cited : (8)

References (26)
  • 2
    • 84889615363 scopus 로고    scopus 로고
    • (Eds.: D. Braga, F. Grepioni), Wiley-VCH
    • G. Kaupp, Making Crystals by Design (Eds.: D. Braga, F. Grepioni), Wiley-VCH, 2007, pp. 87-148.
    • (2007) Making Crystals by Design , pp. 87-148
    • Kaupp, G.1
  • 4
    • 60849090780 scopus 로고    scopus 로고
    • A clear-cut distinction between mechanochemistry and mechanophysics, and their misleading association with solid-state processes in general, is lacking. Although the conflict may be largely semantic, for an illuminating perspective, see
    • A clear-cut distinction between mechanochemistry and mechanophysics, and their misleading association with solid-state processes in general, is lacking. Although the conflict may be largely semantic, for an illuminating perspective, see: G. Kaupp, CrystEngComm 2009, 11, 388-403.
    • (2009) CrystEngComm , vol.11 , pp. 388-403
    • Kaupp, G.1
  • 6
    • 0003942864 scopus 로고
    • Even though the R/S notation can be utilized for atropisomers, these substances are devoid of chiral centers and therefore, their axial chirality is best denoted by M and P descriptors (or alternatively aR, aS); see, Wiley, New York, 1200
    • Even though the R/S notation can be utilized for atropisomers, these substances are devoid of chiral centers and therefore, their axial chirality is best denoted by M and P descriptors (or alternatively aR, aS); see: E. L. Eliel, S. H. Wilen, Stereochemistry of Organic Compounds, Wiley, New York, 1994, pp. 1119-1121, 1200.
    • (1994) Stereochemistry of Organic Compounds , pp. 1119-1121
    • Eliel, E.L.1    Wilen, S.H.2
  • 8
    • 33745458078 scopus 로고    scopus 로고
    • For representative examples of mechanotransduction of physical forces into chemical systems, see
    • For representative examples of mechanotransduction of physical forces into chemical systems, see: a) J. M. J. Paulusse, R. P. Sijbesma, Angew. Chem. 2004, 116, 4560-4562;
    • (2004) Angew. Chem. , vol.116 , pp. 4560-4562
    • Paulusse, J.M.J.1    Sijbesma, R.P.2
  • 21
    • 38849205997 scopus 로고    scopus 로고
    • for an extended commentary, see
    • for an extended commentary, see: G. Cravotto, P. Cintas, Angew. Chem. 2007, 119, 5573-5575;
    • (2007) Angew. Chem. , vol.119 , pp. 5573-5575
    • Cravotto, G.1    Cintas, P.2
  • 23
    • 0001259843 scopus 로고    scopus 로고
    • For a review, see, (Ed.: T. J. Mason), JAI, London, and references therein
    • For a review, see: J.-L. Luche, P. Cintas, Advances in Sonochemistry, Vol. 5 (Ed.: T. J. Mason), JAI, London, 1999, pp. 147-174, and references therein.
    • (1999) Advances in Sonochemistry , vol.5 , pp. 147-174
    • Luche, J.-L.1    Cintas, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.