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Volumn 73, Issue 19, 2008, Pages 7756-7763

Structure-directed reversion in the π-facial stereoselective alkylation of chiral bicyclic lactams

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; AMIDES; ARSENIC COMPOUNDS; BENZENE; CHLORINE COMPOUNDS; COMPLEXATION; FLOW INTERACTIONS; HYDROCARBONS; HYDROGEN; HYDROGEN BONDS; NONMETALS;

EID: 53049106312     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801665k     Document Type: Article
Times cited : (13)

References (69)
  • 1
    • 53049098814 scopus 로고    scopus 로고
    • Högberg, H.-E. In Stereoselective Synthesis, Methods of Organic Chemistry (Houben-Weyl); Helmchen, G., Hoffman, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: Stuttgart, 1996; E21, 2, pp 791-915.
    • Högberg, H.-E. In Stereoselective Synthesis, Methods of Organic Chemistry (Houben-Weyl); Helmchen, G., Hoffman, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: Stuttgart, 1996; E21, Vol. 2, pp 791-915.
  • 2
    • 0025992651 scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Romo, D.; Meyers, A. I. Tetrahedron 1991, 47, 9503.
    • (1991) Tetrahedron , vol.47 , pp. 9503
    • Romo, D.1    Meyers, A.I.2
  • 3
    • 0004157026 scopus 로고
    • Blackwell Scientific Publications: Oxford
    • (b) Meyers, A. I. In Stereocontrolled Organic Synthesis; Blackwell Scientific Publications: Oxford, 1994; pp 145-175.
    • (1994) Stereocontrolled Organic Synthesis , pp. 145-175
    • Meyers, A.I.1
  • 31
    • 53049105591 scopus 로고    scopus 로고
    • For a recent review on chiral oxazolopiperidone lactams, see
    • (b) For a recent review on chiral oxazolopiperidone lactams, see: Escolano, C.; Amat, M.; Bosch, J. Chem. Eur. J. 2007, 72, 4431.
    • (2007) Chem. Eur. J , vol.72 , pp. 4431
    • Escolano, C.1    Amat, M.2    Bosch, J.3
  • 36
    • 2342483687 scopus 로고    scopus 로고
    • Brewster, A. G.; Broady, S.; Davies, C. E.; Heightman, T. D.; Hermitage, S. A.; Hughes, M.; Moloney, M. G.; Woods, G. Org. Biomol. Chem. 2004, 2, 1031. See also refs 3d and 5e.
    • (d) Brewster, A. G.; Broady, S.; Davies, C. E.; Heightman, T. D.; Hermitage, S. A.; Hughes, M.; Moloney, M. G.; Woods, G. Org. Biomol. Chem. 2004, 2, 1031. See also refs 3d and 5e.
  • 55
    • 53049087640 scopus 로고    scopus 로고
    • Since the MST model was parametrized from experimental free energies of solvation at 298 K, the gas phase free energy difference was also determined at this temperature for the sake of internal consistency.
    • Since the MST model was parametrized from experimental free energies of solvation at 298 K, the gas phase free energy difference was also determined at this temperature for the sake of internal consistency.
  • 64
    • 53049087183 scopus 로고    scopus 로고
    • The dielectric permittivity is 7.5 at 295 K. Data taken from Handbook of Chemistry and Physics, 80th ed.; Lide, D. R., Ed.; CRC: Boca Raton, 1999.
    • The dielectric permittivity is 7.5 at 295 K. Data taken from Handbook of Chemistry and Physics, 80th ed.; Lide, D. R., Ed.; CRC: Boca Raton, 1999.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.