메뉴 건너뛰기




Volumn 33, Issue 10, 2003, Pages 1695-1706

The first syntheses of 16β-chloro- and 16β-bromo-cyproterone acetate

Author keywords

16 Bromo cyproterone acetate; 16 Chloro cyproterone acetate; 16 Dehydropregnenolone acetate; Synthesis

Indexed keywords

16BETA BROMOCYPROTERONE ACETATE; 16BETA CHLOROCYPROTERONE ACETATE; CYPROTERONE ACETATE; DEHYDROPREGNENOLONE ACETATE; PREGNENOLONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037569253     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120018931     Document Type: Article
Times cited : (4)

References (11)
  • 1
    • 0036365198 scopus 로고    scopus 로고
    • Synthesis and phamocological evaluation of new 16-methyl pregnane derivatives
    • Ramirez, E.; Cabeza, M.; Heuze, I.; Gutierrez, E.; Bratoeff, E. Synthesis and phamocological evaluation of new 16-methyl pregnane derivatives. Chem. Pharm. Bull. 2002, 50 (1), 15-20.
    • (2002) Chem. Pharm. Bull. , vol.50 , Issue.1 , pp. 15-20
    • Ramirez, E.1    Cabeza, M.2    Heuze, I.3    Gutierrez, E.4    Bratoeff, E.5
  • 2
    • 0030917903 scopus 로고    scopus 로고
    • Synthesis and progestational activity of 16-methylene-17α-hydroxy-19-norpregn-4-ene-3,20-dione and its derivative
    • Li, F.; Kumar, N.; Tsong, Y.; Monder, C.; Wayne Bardin, C. Synthesis and progestational activity of 16-methylene-17α-hydroxy-19-norpregn-4-ene-3,20-dione and its derivative. Steroids 1997, 62, 403-408.
    • (1997) Steroids , vol.62 , pp. 403-408
    • Li, F.1    Kumar, N.2    Tsong, Y.3    Monder, C.4    Wayne Bardin, C.5
  • 3
    • 0038565993 scopus 로고    scopus 로고
    • 6-17α-Hydroxy- Progesterone Compound and Compositions. US Patent 3,234,093, February 8, 1966
    • 6-17α-Hydroxy- Progesterone Compound and Compositions. US Patent 3,234,093, February 8, 1966.
    • Wiechert, R.1
  • 4
    • 0015375068 scopus 로고
    • Synthesis and biological activity of 17-esters of 6-dehydro-16-methylene-17α-hydroxyprogesterones
    • Shapiro, E.L.; Weber, L.; Harris, H.; Miskowicz, C.; Neri, R.; Herzog, H.L. Synthesis and biological activity of 17-esters of 6-dehydro-16-methylene-17α-hydroxyprogesterones. J. Med. Chem. 1972, 15, 716-720.
    • (1972) J. Med. Chem. , vol.15 , pp. 716-720
    • Shapiro, E.L.1    Weber, L.2    Harris, H.3    Miskowicz, C.4    Neri, R.5    Herzog, H.L.6
  • 5
    • 37049174781 scopus 로고
    • Hydrogen tranfer part IV. The use of quinones of high potential as dehydrogenation reagent
    • Braude, E.A.; Brook, A.G.; Linstead, R.P. Hydrogen tranfer part IV. The use of quinones of high potential as dehydrogenation reagent. J. Chem. Soc. 1954, 3569-3574.
    • (1954) J. Chem. Soc. , pp. 3569-3574
    • Braude, E.A.1    Brook, A.G.2    Linstead, R.P.3
  • 6
    • 0020341632 scopus 로고
    • Synthesis of 1-hydroxylated bile acid: Methyl 1α,3α-dihydroxy 5β-cholan-24-oate
    • Herz, J.E.; Ocampo, R. Synthesis of 1-hydroxylated bile acid: methyl 1α,3α-dihydroxy 5β-cholan-24-oate. Steroids 1982, 40, 661.
    • (1982) Steroids , vol.40 , pp. 661
    • Herz, J.E.1    Ocampo, R.2
  • 7
    • 0037889699 scopus 로고    scopus 로고
    • Process for the production of 17α-Acetoxy-1,2-Methylene-4,6-Pregnadiene-3,20-Dione. US Patent 4,599,200, July 8, 1986
    • Hanfried, A. Process for the production of 17α-Acetoxy-1,2-Methylene-4,6-Pregnadiene-3,20-Dione. US Patent 4,599,200, July 8, 1986.
    • Hanfried, A.1
  • 8
    • 0014543976 scopus 로고
    • The synthesis and progestational activity of some 1,2α-cyclomethylene-16-methylene progesterone derivatives
    • Shapiro, E.L.; Popper, T.L.; Weber, L.; Neri, R.; Herzog, H.L. The synthesis and progestational activity of some 1,2α-cyclomethylene-16-methylene progesterone derivatives. J. Med. Chem. 1969, 12, 631-636.
    • (1969) J. Med. Chem. , vol.12 , pp. 631-636
    • Shapiro, E.L.1    Popper, T.L.2    Weber, L.3    Neri, R.4    Herzog, H.L.5
  • 9
    • 0038565989 scopus 로고    scopus 로고
    • Novel Process for Preparing Steroid Halohydrins and Vinyl Halides. US Patent 3,766,225, October 16, 1973
    • Harris, H.E.; Miskowicz, J. Novel Process for Preparing Steroid Halohydrins and Vinyl Halides. US Patent 3,766,225, October 16, 1973.
    • Harris, H.E.1    Miskowicz, J.2
  • 10
    • 0033935074 scopus 로고    scopus 로고
    • A practical large-scale synthesis of 17α- acetoxy-11α-(4-N,N-dimethylaminophenyl)-19-norpregna-4,9-dione (CDB-2914)
    • Rao, P.N.; Kirk Acosta, C.; Bahr, M.L.; Burdett, J.E.; Cessac, J.W.; Morrison, P.A.; Kim, H.K. A practical large-scale synthesis of 17α- acetoxy-11α-(4-N,N-dimethylaminophenyl)-19-norpregna-4,9-dione (CDB-2914). Steroids 2000, 65, 395-400.
    • (2000) Steroids , vol.65 , pp. 395-400
    • Rao, P.N.1    Kirk Acosta, C.2    Bahr, M.L.3    Burdett, J.E.4    Cessac, J.W.5    Morrison, P.A.6    Kim, H.K.7
  • 11
    • 0037551905 scopus 로고
    • Rapid chromatographic technique for preparative separations with moderate resolution
    • Still, C.W.; Kahn, M.; Mitra, A. Rapid chromatographic technique for preparative separations with moderate resolution. J. Org. Chem. 1973, 43, 293-295.
    • (1973) J. Org. Chem. , vol.43 , pp. 293-295
    • Still, C.W.1    Kahn, M.2    Mitra, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.