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Volumn , Issue 6, 2001, Pages 1033-1043

Stereoselection in reactions of chiral allyl ethers: The case of 1,3-dipolar cycloaddition

Author keywords

Asymmetric synthesis; Chirality; Cycloadditions; Transition states

Indexed keywords

ETHER DERIVATIVE; NITRONE DERIVATIVE;

EID: 0035078009     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200103)2001:6<1033::aid-ejoc1033>3.0.co;2-w     Document Type: Short Survey
Times cited : (19)

References (68)
  • 14
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    • note
    • We refer in all cases to a concerted mechanism for 1,3-dipolar cycloadditions:
  • 24
    • 0000617968 scopus 로고
    • [10b] Electrostatic interactions with the 1,3-dipole were invoked in the explanation of cycloadditions to Oppolzer's chiral sultams: K. S. Kim, B. H. Kim, W. M. Park, S. J. Cho, B. J. Mhin, J. Am. Chem. Soc. 1993, 115, 7472-7477.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 7472-7477
    • Kim, K.S.1    Kim, B.H.2    Park, W.M.3    Cho, S.J.4    Mhin, B.J.5
  • 31
    • 33847579013 scopus 로고    scopus 로고
    • (CD-ROM included in Chem. Commun. 1997, no. 6).
    • (1997) Chem. Commun. , Issue.6
  • 34
    • 85088882686 scopus 로고    scopus 로고
    • note
    • [2,8,9]
  • 45
    • 33847604731 scopus 로고    scopus 로고
    • (CD-ROM included in Chem. Commun. 1997, no. 6). -
    • (1997) Chem. Commun. , Issue.6
  • 48
    • 85088882873 scopus 로고    scopus 로고
    • note
    • [2,8,9]
  • 57
    • 0029987159 scopus 로고    scopus 로고
    • Nitrile imines also react with (E)-γ-oxygenated-α,β-unsaturated esters and enones: The regioselectivity is generally high, but syn selectivity only modest (≤ 70:30). The results, however, fit perfectly within the framework of the "outside alkoxy" theory: L. Grubert, G. Galley, M. Pätzel, Tetrahedron: Asymmetry 1996, 7, 1137-1148.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 1137-1148
    • Grubert, L.1    Galley, G.2    Pätzel, M.3
  • 60
    • 33847579586 scopus 로고    scopus 로고
    • note
    • For some recent applications of chiral Lewis acids in the stereocontrol of 1,3-dipolar cycloadditions (although to achiral alkenes):
  • 68
    • 33847597730 scopus 로고    scopus 로고
    • note
    • Extension of the force field parameters to nonoxygenated 1,3-dipoles, such as diazoalkanes and azomethyne ylides, is in progress in our laboratories: Preliminary results are quite encouraging.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.