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Volumn , Issue 2, 2004, Pages 313-322

Theoretical and Experimental Study of the Regioselectivity of Michael Additions

Author keywords

Density functional calculations; Michael addition; Regioselectivity; Substituent effects; Transition states

Indexed keywords

ACRYLIC ACID; CARBONYL DERIVATIVE; CINNAMIC ACID; ETHYL 3 (2,4 DINITROPHENYL)PROPENOATE; METHYL 3,3 BIS(TRIFLUOROMETHYL)PROPENOATE; UNCLASSIFIED DRUG;

EID: 84962423904     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300523     Document Type: Article
Times cited : (30)

References (30)
  • 2
    • 0002384398 scopus 로고
    • tin enolates in Michael reaction
    • [1b] T. Mukaiyama, S. Kobayashi, Org. React. 1994, 46, 1-104 (tin enolates in Michael reaction).
    • (1994) Org. React. , vol.46 , pp. 1-104
    • Mukaiyama, T.1    Kobayashi, S.2
  • 4
    • 0033936085 scopus 로고    scopus 로고
    • enantioselective Michael reaction
    • [1d] J. S. Johnson, D. A. Evans, Acc. Chem. Res. 2000, 33, 325-335 (enantioselective Michael reaction).
    • (2000) Acc. Chem. Res. , vol.33 , pp. 325-335
    • Johnson, J.S.1    Evans, D.A.2
  • 5
    • 0034986283 scopus 로고    scopus 로고
    • vinylogous Michael reaction
    • [1e] J. Christoffers, Synlett 2001, 723-732 (vinylogous Michael reaction).
    • (2001) Synlett , pp. 723-732
    • Christoffers, J.1
  • 29
    • 84962380997 scopus 로고    scopus 로고
    • note
    • α distance was varied displayed different maxima, depending upon whether the scan was in the forward (decreasing distance) or reverse (increasing distance) direction. The full transition state optimizations for 2 and 4 were initiated with the geometry of the maximum from the forward scan. Selected scans of α- and β-addition to other compounds did not have this problem with hysteresis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.