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Volumn 61, Issue 12, 1996, Pages 697-702

Steroids 54. Amino acylamidosteroids

Author keywords

aminoalkyl carboxamidosteroid; cyclosteroid; epoxysteroid; Ritter reaction

Indexed keywords

AMINO ACYLAMIDOSTEROID; ANTIARRHYTHMIC AGENT; EPOXYSTEROID; IMMUNOMODULATING AGENT; STEROID; UNCLASSIFIED DRUG;

EID: 0030474376     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(96)00202-4     Document Type: Article
Times cited : (12)

References (22)
  • 2
    • 0011339308 scopus 로고
    • Corticosteroids as immunoregulatory agents
    • 2. Djordjevic J (1983). Corticosteroids as immunoregulatory agents. Acta Med Medianae 22:95-99.
    • (1983) Acta Med Medianae , vol.22 , pp. 95-99
    • Djordjevic, J.1
  • 3
    • 4243559624 scopus 로고
    • Nouveau dérivés du 5α-pregnan-20-o1 et ses sels avec les acides, leur préparation, leur application comme médicament, et les compositions les enfermant
    • Belg. Patent 884.794
    • 3. Roussel-Uclaf (1981). Nouveau dérivés du 5α-pregnan-20-o1 et ses sels avec les acides, leur préparation, leur application comme médicament, et les compositions les enfermant. Belg. Patent 884.794. Chem Abstr (1982) 96:20373j.
    • (1981) Chem Abstr , vol.96
    • Roussel-Uclaf1
  • 4
    • 85013541724 scopus 로고
    • Nouveaux dérivés stéroids 3-amino substitué et leur sels, procédé de préparation, application a titre médicaments et compositions les enfermant
    • Belg. Patent 891.201 (1982)
    • 4. Roussel-Uctaf (1982). Nouveaux dérivés stéroids 3-amino substitué et leur sels, procédé de préparation, application a titre médicaments et compositions les enfermant. Belg. Patent 891.201. Chem Abstr (1982)97:110287j.
    • (1982) Chem Abstr , vol.97
    • Roussel-Uctaf1
  • 7
    • 0346002251 scopus 로고
    • Reduction von oximen mit natriumboranat in gegenwart von übergangsmetallverbindungen
    • 7. Ipaktschi J (1984). Reduction von Oximen mit Natriumboranat in Gegenwart von Übergangsmetallverbindungen. Chem Ber 117:856-858.
    • (1984) Chem Ber , vol.117 , pp. 856-858
    • Ipaktschi, J.1
  • 8
    • 0011375008 scopus 로고
    • Structural biochemistry. II. Synthesis of 3β-hydroxy-17β-(L-prolyl-L-prolyl)amino-5α-androstane
    • 8. Pettit GR, DasGupta AK, Smith RL (1966). Structural biochemistry. II. Synthesis of 3β-hydroxy-17β-(L-prolyl-L-prolyl)amino-5α-androstane. Can J Chem 44:2023-2029.
    • (1966) Can J Chem , vol.44 , pp. 2023-2029
    • Pettit, G.R.1    DasGupta, A.K.2    Smith, R.L.3
  • 9
    • 0014311186 scopus 로고
    • 17-Aminoacylamido-5-androsten-3β-ols
    • 9. Flouret G, Cole W (1968). 17-Aminoacylamido-5-androsten-3β-ols. J Med Chem 11:880-882.
    • (1968) J Med Chem , vol.11 , pp. 880-882
    • Flouret, G.1    Cole, W.2
  • 10
    • 0011283540 scopus 로고
    • Structural biochemistry. IV. 3β-Hydroxy-17β-(L-prolyl)amino-androst-5-ene
    • 10. Pettit GR, Smith RL, DasGupta AK, Occolowitz JL (1967). Structural biochemistry. IV. 3β-Hydroxy-17β-(L-prolyl)amino-androst-5-ene. Can J Chem 45:501-507.
    • (1967) Can J Chem , vol.45 , pp. 501-507
    • Pettit, G.R.1    Smith, R.L.2    DasGupta, A.K.3    Occolowitz, J.L.4
  • 11
    • 0011289630 scopus 로고
    • Molecular rearrangements in the sterols, VII. The chemistry of the epi-i-sterols and their rearrangement products
    • 11. Wagner AF, Wolff NE, Wallis ES (1952). Molecular rearrangements in the sterols, VII. The chemistry of the epi-i-sterols and their rearrangement products. J Org Chem 17:529-541.
    • (1952) J Org Chem , vol.17 , pp. 529-541
    • Wagner, A.F.1    Wolff, N.E.2    Wallis, E.S.3
  • 12
    • 4243559623 scopus 로고
    • 6β-Hydroxy-3:5-cyclopregnan-20-one and related compounds
    • 12. Patel DK, Petrov V, Stuart-Webb IA (1957). 6β-Hydroxy-3:5-cyclopregnan-20-one and related compounds. J Chem Soc 665-668.
    • (1957) J Chem Soc , pp. 665-668
    • Patel, D.K.1    Petrov, V.2    Stuart-Webb, I.A.3
  • 13
    • 37049154481 scopus 로고
    • Steroids and related compounds. Part VIII. Some transformation products of 5-methyl-10-norandrost-8(9)-ene-3:6-diol-17-one
    • 13. Davis M, Petrov V (1950). Steroids and related compounds. Part VIII. Some transformation products of 5-methyl-10-norandrost-8(9)-ene-3:6-diol-17-one. J Chem Soc 1185-1188.
    • (1950) J Chem Soc , pp. 1185-1188
    • Davis, M.1    Petrov, V.2
  • 14
    • 0014003744 scopus 로고
    • Steroid amines. Part II. 17α-Aminoaandrostane derivatives
    • 14. Davis M, Parnell EW, Warburton D (1966). Steroid amines. Part II. 17α-Aminoaandrostane derivatives. J Chem Soc Perkin I 1698-1700.
    • (1966) J Chem Soc Perkin I , pp. 1698-1700
    • Davis, M.1    Parnell, E.W.2    Warburton, D.3
  • 15
    • 0011283899 scopus 로고
    • Methoden zur herstellung und umwandlungen von aminosäuren und derivaten
    • Houben-Weyl, Müller E (ed). Band XI/2. Stickstoffverbindungen II/III. Thieme G, 1958. Stuttgart
    • 15. Wieland T, Mueller R, Niemann E, Birkofer L, Schöberl A, Wagner A, Söil A (1958). Methoden zur Herstellung und Umwandlungen von Aminosäuren und Derivaten. In: Houben-Weyl, Methoden der Organischen Chemie. Müller E (ed). Band XI/2. Stickstoffverbindungen II/III. Thieme G, 1958. Stuttgart pp. 367-368.
    • (1958) Methoden der Organischen Chemie , pp. 367-368
    • Wieland, T.1    Mueller, R.2    Niemann, E.3    Birkofer, L.4    Schöberl, A.5    Wagner, A.6    Söil, A.7
  • 16
    • 33947488929 scopus 로고
    • The use of esters of N-hydroxysuccinirnide in peptide synthesis
    • 16. Anderson GW, Zimmerman JE, Callahan FM (1964). The use of esters of N-hydroxysuccinirnide in peptide synthesis. J Am Chem Soc 86:1839-1842.
    • (1964) J Am Chem Soc , vol.86 , pp. 1839-1842
    • Anderson, G.W.1    Zimmerman, J.E.2    Callahan, F.M.3
  • 17
    • 0013819125 scopus 로고
    • The synthesis of 17α amino-androsten-3β-ol: NMR spectra of 17-substituted androstanes
    • 17. Robinson CH, Ermann C, Hollis DP (1965). The synthesis of 17α amino-androsten-3β-ol: NMR spectra of 17-substituted androstanes. Steroids 6:509-518.
    • (1965) Steroids , vol.6 , pp. 509-518
    • Robinson, C.H.1    Ermann, C.2    Hollis, D.P.3
  • 18
    • 18844460949 scopus 로고
    • A new reaction of nitriles. I. Amides from alkenes and mononitriles
    • 18. Ritter JJ, Minieri PP (1948). A new reaction of nitriles. I. Amides from alkenes and mononitriles. J Am Chem Soc 70:4045-4048.
    • (1948) J Am Chem Soc , vol.70 , pp. 4045-4048
    • Ritter, J.J.1    Minieri, P.P.2
  • 20
    • 0011283228 scopus 로고
    • Applications de la réaction de ritter en série stéroide. III. Ouverture d'epoxy-4,5β-cholestanes par l'acetonitrile. Conformation du groupe amide
    • 20. Ryan RJ, Julia S (1973). Applications de la réaction de Ritter en série stéroide. III. Ouverture d'epoxy-4,5β-cholestanes par l'acetonitrile. Conformation du groupe amide. Tetrahedron 29: 3649-3654.
    • (1973) Tetrahedron , vol.29 , pp. 3649-3654
    • Ryan, R.J.1    Julia, S.2
  • 21
    • 0011376451 scopus 로고
    • Application de la reaction de ritter en série stéroide. I. Préparation d'acetaminoalcools trans a partir d'epoxydes-5,6. Conformation du groupe amide
    • 21. Bourgery G, Frankel JJ, Julia S, Ryan RJ (1972). Application de la reaction de Ritter en série stéroide. I. Préparation d'acetaminoalcools trans a partir d'epoxydes-5,6. Conformation du groupe amide. Tetrahedron 28:1377-1390.
    • (1972) Tetrahedron , vol.28 , pp. 1377-1390
    • Bourgery, G.1    Frankel, J.J.2    Julia, S.3    Ryan, R.J.4
  • 22
    • 0000080942 scopus 로고
    • Ritter reaction on steroids. Ring expansion of steroid oxethanes into dihydrooxazines
    • 22. Schneider Gy, Hackler L, Sohár P (1985). Ritter reaction on steroids. Ring expansion of steroid oxethanes into dihydrooxazines. Tetrahedron 41:3377-3386.
    • (1985) Tetrahedron , vol.41 , pp. 3377-3386
    • Schneider, Gy.1    Hackler, L.2    Sohár, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.