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Volumn 69, Issue 5, 2004, Pages 1646-1651

Origin of Chiral Induction in Radical Reactions with the Diastereoisomers (5R)- and (5S)-5-l-Menthyloxyfuran-2[5H]-one

Author keywords

[No Author keywords available]

Indexed keywords

CRYSTAL STRUCTURE; CRYSTALLIZATION; X RAY CRYSTALLOGRAPHY;

EID: 1442348934     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo030292x     Document Type: Article
Times cited : (47)

References (89)
  • 11
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    • 1442291999 scopus 로고
    • Ph.D. Dissertation, RWTH Aachen
    • (d) Hoffmann, N. Ph.D. Dissertation, RWTH Aachen, 1992.
    • (1992)
    • Hoffmann, N.1
  • 68
    • 1442292000 scopus 로고
    • (BASF) German Offen. 2111119
    • Bolz, G.; Wiersdorff, W.-W. (BASF) German Offen. 2111119, 1972.
    • (1972)
    • Bolz, G.1    Wiersdorff, W.-W.2
  • 69
    • 1442340996 scopus 로고    scopus 로고
    • note
    • The diastereoismer ent-1 possessing the S configuration at the acetal center can be obtained via the same procedure using d-menthol as chiral substrate.
  • 70
    • 1442267465 scopus 로고    scopus 로고
    • note
    • These crystalline-induced dynamic resolutions are also named asymmetric transformation of second order or second kind while the corresponding reactions in solution are called asymmetric transformation of first order or first kind.
  • 73
    • 0004219526 scopus 로고
    • Collins, A. N., Sheldrake, G. N., Crosby, J., Eds.; J. Wiley & Sons: Chichester
    • (c) Chirality in Industry I; Collins, A. N., Sheldrake, G. N., Crosby, J., Eds.; J. Wiley & Sons: Chichester, 1992.
    • (1992) Chirality in Industry I
  • 74
    • 0004219524 scopus 로고    scopus 로고
    • Collins, A. N., Sheldrake, G. N., Crosby, J., Eds.; J. Wiley & Sons: Chichester
    • (d) Bruggink, A. Chirality in Industry II; Collins, A. N., Sheldrake, G. N., Crosby, J., Eds.; J. Wiley & Sons: Chichester, 1997.
    • (1997) Chirality in Industry II
    • Bruggink, A.1
  • 81
    • 0025364262 scopus 로고
    • It should be noted that the concept of double induction was mainly developed for cases where chiral information is localized on the two reaction partners. Nevertheless, the concept should be applicable for cases where the two elements of chiral induction are located only on one substrate as far as the two corresponding diastereomers are investigated. For corresponding examples, see: Evans, D. A.; Clark, J. S.; Metternich, R.; Novack, V. J.; Sheppard, G. S. J. Am. Chem. Soc. 1990, 112, 866.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 866
    • Evans, D.A.1    Clark, J.S.2    Metternich, R.3    Novack, V.J.4    Sheppard, G.S.5
  • 85


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.