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Volumn 64, Issue 22, 1999, Pages 8201-8209

Synthesis, structure, and nucleophile-induced rearrangements of spiroketones

Author keywords

[No Author keywords available]

Indexed keywords

KETONE DERIVATIVE;

EID: 0033615497     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990867j     Document Type: Article
Times cited : (26)

References (21)
  • 8
    • 0345597314 scopus 로고    scopus 로고
    • note
    • All orbitals of the "halves" that are antisymmetric vs both molecular planes can interact giving the lower-energy bonding and the higher-energy antibonding combinations that span the entire molecule. The frontier orbitals, and specifically here for the electron acceptors the LUMOs, are of main interest. For the purpose of this discussion, the HOMO-LUMO designation refers only to the π system. The nonbonding electrons are treated separately.
  • 9
    • 0025390935 scopus 로고
    • The semiempirical MNDO-PM3 calculations (Stewart, J. J. P. J. Comp-Aid. Mol. Des. 1990, 4, 1) were carried out using Spartan 5 (Wavefunction Inc.).
    • (1990) J. Comp-Aid. Mol. Des. , vol.4 , pp. 1
    • Stewart, J.J.P.1
  • 10
    • 0012081006 scopus 로고
    • The synthetic strategy followed that used to prepare dione 10 and a related spirosystem: (a) Langer, E.; Lehner, H. Tetrahedron 1973, 29, 375.
    • (1973) Tetrahedron , vol.29 , pp. 375
    • Langer, E.1    Lehner, H.2
  • 13
    • 0344735034 scopus 로고    scopus 로고
    • Manuscript in preparation
    • The details of the crystal structure and the crystal packing of 1 and 2 will be presented elsewhere: Maslak, P.; Varadarajan S.; Rheingold, A. L.; Yap, G. P. Manuscript in preparation.
    • Maslak, P.1    Varadarajan, S.2    Rheingold, A.L.3    Yap, G.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.