메뉴 건너뛰기




Volumn 68, Issue 9, 2003, Pages 739-749

Hydrolytic behavior of 5α-hydroxy-11β- and 5β-hydroxy- 11α-substituted 19-norsteroids

Author keywords

11 Substituted 5(10),9(11) steroids; 11 Substituted steroids; 11 Substituted steroids; Hydrolysis; Steroid

Indexed keywords

19 NORSTEROID; 3 ETHYLENEDIOXY 5ALPHA,10ALPHA EPOXYESTR 9(11) EN 17 ONE; 3 ETHYLENEDIOXY 5BETA,10BETA EPOXYESTR 9(11) EN 17 ONE; COPPER ION; ESTRANE DERIVATIVE; NORSTEROID; UNCLASSIFIED DRUG; COPPER;

EID: 0242708674     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2003.07.003     Document Type: Article
Times cited : (7)

References (14)
  • 1
    • 0019443088 scopus 로고
    • Regio and stereospecific synthesis of 11β-substituted 19-norsteroids
    • Bélanger A., Philibert D., Teutsch G. Regio and stereospecific synthesis of 11β-substituted 19-norsteroids. Steroids. 37:1981;361-382.
    • (1981) Steroids , vol.37 , pp. 361-382
    • Bélanger, A.1    Philibert, D.2    Teutsch, G.3
  • 2
    • 0028335832 scopus 로고
    • History and perspectives of antiprogestins from the chemist's point of view
    • Teutsch G., Philibert D. History and perspectives of antiprogestins from the chemist's point of view. Human. Reprod. 9:1994;12-31.
    • (1994) Human. Reprod. , vol.9 , pp. 12-31
    • Teutsch, G.1    Philibert, D.2
  • 3
    • 0028318803 scopus 로고
    • Effects of D-ring substituents on antiprogestational (antagonist) and progestational (agonist) activity of 11β-aryl steroids
    • Cook C.E., Lee Y.W., Wani M.C., Fail P.A., Petrow V. Effects of D-ring substituents on antiprogestational (antagonist) and progestational (agonist) activity of 11β-aryl steroids. Human Reprod. 9:1994;32-39.
    • (1994) Human Reprod. , vol.9 , pp. 32-39
    • Cook, C.E.1    Lee, Y.W.2    Wani, M.C.3    Fail, P.A.4    Petrow, V.5
  • 4
    • 0031963453 scopus 로고    scopus 로고
    • 11β-Substituted 13β-ethyl gonane derivatives exhibit reversal of antiprogestational activity
    • Rao P.N., Cessac J.W., Blye R.P., Kim H.K. 11β-Substituted 13β-ethyl gonane derivatives exhibit reversal of antiprogestational activity. Steroids. 63:1998;50-57.
    • (1998) Steroids , vol.63 , pp. 50-57
    • Rao, P.N.1    Cessac, J.W.2    Blye, R.P.3    Kim, H.K.4
  • 5
    • 0031667026 scopus 로고    scopus 로고
    • New 11β-aryl substituted steroids exhibit both progestational and antiprogestational activity
    • Rao P.N., Wang Z., Cessac J.W., Rosenberg R.S., Jenkins D.J.A., Diamandis E.P. New 11β-aryl substituted steroids exhibit both progestational and antiprogestational activity. Steroids. 63:1998;523-530.
    • (1998) Steroids , vol.63 , pp. 523-530
    • Rao, P.N.1    Wang, Z.2    Cessac, J.W.3    Rosenberg, R.S.4    Jenkins, D.J.A.5    Diamandis, E.P.6
  • 6
    • 0018385755 scopus 로고
    • Regio and stereospecific synthesis of 11β-substituted 19 norsteroids
    • Teutsch G., Bélanger A. Regio and stereospecific synthesis of 11β-substituted 19 norsteroids. Tetrahedron Lett. 22:1979;2051-2054.
    • (1979) Tetrahedron Lett. , vol.22 , pp. 2051-2054
    • Teutsch, G.1    Bélanger, A.2
  • 7
    • 0000220487 scopus 로고
    • New methods of synthesis of β-aminoethylpyrazoles
    • Jones R.G., Mann M.J. New methods of synthesis of β- aminoethylpyrazoles. J. Am. Chem. Soc. 75:1953;4048-4052.
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 4048-4052
    • Jones, R.G.1    Mann, M.J.2
  • 8
    • 0242455442 scopus 로고
    • Synthesis of 4-acetylphenylmethylsilanes using 2-(4-bromophenyl)-2- methyl-1,3-dioxolane
    • Neville R.G. Synthesis of 4-acetylphenylmethylsilanes using 2-(4-bromophenyl)-2-methyl-1,3-dioxolane. J. Org. Chem. 24:1959;111-112.
    • (1959) J. Org. Chem. , vol.24 , pp. 111-112
    • Neville, R.G.1
  • 9
    • 33744586503 scopus 로고
    • Pyridinium p-toluenesulfonate. A mild and efficient catalyst for tetrahydropyranylation of alcohols
    • Miyashita M., Yoshikoshi A., Grisco P.A. Pyridinium p-toluenesulfonate. A mild and efficient catalyst for tetrahydropyranylation of alcohols. J. Org. Chem. 42:1977;3772-3774.
    • (1977) J. Org. Chem. , vol.42 , pp. 3772-3774
    • Miyashita, M.1    Yoshikoshi, A.2    Grisco, P.A.3
  • 11
    • 0027398673 scopus 로고
    • Synthesis of oxygen-bridged antigestagens
    • Cleve A., Ottow E., Neef G., Wiechert R. Synthesis of oxygen-bridged antigestagens. Tetrahedron. 49:1993;2217-2226.
    • (1993) Tetrahedron , vol.49 , pp. 2217-2226
    • Cleve, A.1    Ottow, E.2    Neef, G.3    Wiechert, R.4
  • 13
    • 0024284705 scopus 로고
    • Preliminary applications of cross-axis syncronous flow-through coil planet centrifuge for large-scale preparative counter-current chromatography
    • Zhang T.Y., Lee Y.W., Fang Q.C., Xiao R., Ito Y. Preliminary applications of cross-axis syncronous flow-through coil planet centrifuge for large-scale preparative counter-current chromatography. J. Chromatogr. 454:1988;185-193.
    • (1988) J. Chromatogr. , vol.454 , pp. 185-193
    • Zhang, T.Y.1    Lee, Y.W.2    Fang, Q.C.3    Xiao, R.4    Ito, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.