메뉴 건너뛰기




Volumn 11, Issue 1, 2006, Pages 121-129

Synthetic studies on erythromycin derivatives: Reactivity of the C12-21 Alkene

Author keywords

Alkene; Cycloaddition; Epoxidation; Erythromycin; Pyrazoline

Indexed keywords

ALKENE; DRUG DERIVATIVE; EPOXIDE; ERYTHROMYCIN; PYRAZOLE DERIVATIVE;

EID: 33644794481     PISSN: 14203049     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/11010121     Document Type: Article
Times cited : (4)

References (14)
  • 3
    • 0023620518 scopus 로고
    • Aglycon modifications of erythromycin A: Regiospecific and stereospecific elaboration of the C-12 position
    • Hauske, J. R.; Guardliana, M.; Kostek, G.; Schulte, G. Aglycon modifications of erythromycin A: regiospecific and stereospecific elaboration of the C-12 position. J. Org. Chem. 1987, 52, 4622-4625.
    • (1987) J. Org. Chem. , vol.52 , pp. 4622-4625
    • Hauske, J.R.1    Guardliana, M.2    Kostek, G.3    Schulte, G.4
  • 5
    • 0042659225 scopus 로고    scopus 로고
    • Synthetic studies of erythromycin derivatives: 6-O-methylation of (9S)-12,21-anhydro-9-dihydroerythromycin A derivatives
    • Chen, W. M.; Wong, H. N. C.; Chu, D. T. W.; Lin, X. D. Synthetic studies of erythromycin derivatives: 6-O-methylation of (9S)-12,21-anhydro-9- dihydroerythromycin A derivatives. Tetrahedron, 2003, 59, 7033-7045.
    • (2003) Tetrahedron , vol.59 , pp. 7033-7045
    • Chen, W.M.1    Wong, H.N.C.2    Chu, D.T.W.3    Lin, X.D.4
  • 7
    • 4544246197 scopus 로고    scopus 로고
    • Zirconium-catalyzed enantioselective [3+2] cycloaddition of hydrazones to olefins leading to optically active pyrazolidine, pyrazoline, and 1,3-diamine derivatives
    • Yamashita, Y.; Kobayashi, S. Zirconium-catalyzed enantioselective [3+2] cycloaddition of hydrazones to olefins leading to optically active pyrazolidine, pyrazoline, and 1,3-diamine derivatives. J. Am. Chem. Soc. 2004, 126, 11279-11282.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 11279-11282
    • Yamashita, Y.1    Kobayashi, S.2
  • 8
    • 0141782720 scopus 로고    scopus 로고
    • Convergent synthesis and antibacterial activity of pyrazole and pyrazoline derivatives of diazepam
    • Berghot, M.A.; Moawad, E.B. Convergent synthesis and antibacterial activity of pyrazole and pyrazoline derivatives of diazepam. Eur. J. Pharm. Sci. 2003, 20, 173-179
    • (2003) Eur. J. Pharm. Sci. , vol.20 , pp. 173-179
    • Berghot, M.A.1    Moawad, E.B.2
  • 9
    • 17444449069 scopus 로고    scopus 로고
    • 1-N-substituted thiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: Synthesis and evaluation as MAO inhibitors
    • Gokhan, N.; Yesilada, A.; Ucar, G.; Erol, K.; Bilgin, A. A. 1-N-substituted thiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: synthesis and evaluation as MAO inhibitors. Arch. Pharm. (Weinheim) 2003, 336, 362-371.
    • (2003) Arch. Pharm. (Weinheim) , vol.336 , pp. 362-371
    • Gokhan, N.1    Yesilada, A.2    Ucar, G.3    Erol, K.4    Bilgin, A.A.5
  • 10
    • 0000436578 scopus 로고
    • Enantioselective preparation of functionalized cyclopentanoids via a common chiral (π-allyl)palladium complex
    • Deardorff, D. R.; Linde, R. G.; Martin, A. M.; Shulman, M. J. Enantioselective preparation of functionalized cyclopentanoids via a common chiral (π-allyl)palladium complex. J. Org. Chem. 1989, 54, 2759-2762.
    • (1989) J. Org. Chem. , vol.54 , pp. 2759-2762
    • Deardorff, D.R.1    Linde, R.G.2    Martin, A.M.3    Shulman, M.J.4
  • 11
    • 9844232015 scopus 로고
    • The endocyclic restriction test: An experimental evalution of the geometry at oxygen in the transition structure for epoxidation of an alkene by a peroxy acid
    • Woods, K. W.; Beak, P. The endocyclic restriction test: an experimental evalution of the geometry at oxygen in the transition structure for epoxidation of an alkene by a peroxy acid. J. Am. Chem. Soc. 1991, 113, 6281-6283.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6281-6283
    • Woods, K.W.1    Beak, P.2
  • 13
    • 33947332136 scopus 로고
    • Observations regarding the mechanism of olefin epoxidation with per acids
    • Kwart, H.; Hoffman, D.M. Observations regarding the mechanism of olefin epoxidation with per acids J. Org. Chem. 1966, 37, 419-425.
    • (1966) J. Org. Chem. , vol.37 , pp. 419-425
    • Kwart, H.1    Hoffman, D.M.2
  • 14
    • 33644809653 scopus 로고    scopus 로고
    • CCDC 289455 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.