메뉴 건너뛰기




Volumn 61, Issue 11, 1996, Pages 664-669

Synthesis of 3α- and 3β-dimers from selected bile acids

Author keywords

bile acid dimer; cholic acid; lithocholic acid; regioselective hydrolysis

Indexed keywords

BILE ACID;

EID: 0030298529     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(96)00187-0     Document Type: Article
Times cited : (47)

References (25)
  • 2
    • 37049078126 scopus 로고
    • Design and synthesis of new bile acid-based macrocycles
    • 2. Maitra U, Balasubramanian S (1995). Design and synthesis of new bile acid-based macrocycles. J Chem Soc Perkin Trans 1:83-87.
    • (1995) J Chem Soc Perkin Trans , vol.1 , pp. 83-87
    • Maitra, U.1    Balasubramanian, S.2
  • 3
    • 0027485707 scopus 로고
    • Cholic acid as an architectural component in biomimetic/molecular recognition chemistry. Synthesis of the first "colaphanes."
    • 3. Bonar-Law RP, Davis AP (1993). Cholic acid as an architectural component in biomimetic/molecular recognition chemistry. Synthesis of the first "colaphanes." Tetrahedron 49:9829-9844.
    • (1993) Tetrahedron , vol.49 , pp. 9829-9844
    • Bonar-Law, R.P.1    Davis, A.P.2
  • 4
    • 0027520178 scopus 로고
    • Cholic acid as an architectural component in biomimetic/molecular recognition chemistry: NMR and molecular mechanics study of a "tetra-acetoxycholophane."
    • 4. Bonar-Law RP, Davis AP (1993). Cholic acid as an architectural component in biomimetic/molecular recognition chemistry: NMR and molecular mechanics study of a "tetra-acetoxycholophane." Tetrahedron 49:9845-9854.
    • (1993) Tetrahedron , vol.49 , pp. 9845-9854
    • Bonar-Law, R.P.1    Davis, A.P.2
  • 5
    • 0027370867 scopus 로고
    • Cholic acid as an architectural component in biomimetic/molecular recognition chemistry. Synthesis of "colaphanes" with facial differentiation of functionality
    • 5. Bonar-Law RP, Davis AP (1993). Cholic acid as an architectural component in biomimetic/molecular recognition chemistry. Synthesis of "colaphanes" with facial differentiation of functionality. Tetrahedron 49:9855-9866.
    • (1993) Tetrahedron , vol.49 , pp. 9855-9866
    • Bonar-Law, R.P.1    Davis, A.P.2
  • 6
    • 0000976353 scopus 로고
    • Oligomeric derivatives of 3α,7β-dihydroxy-5β-cholan-24-oic acid (ursodeoxycholic acid)
    • 6. Ghedini N, Ferruti P (1983). Oligomeric derivatives of 3α,7β-dihydroxy-5β-cholan-24-oic acid (ursodeoxycholic acid). Synth Commun 13:701-706.
    • (1983) Synth Commun , vol.13 , pp. 701-706
    • Ghedini, N.1    Ferruti, P.2
  • 7
  • 9
    • 0000878905 scopus 로고
    • Radikalisch Polymerisierbare Gallensäuren in Monoschichten, Mizellen and Vesikeln
    • 9. Ahlheim M, Hallensleben ML (1992). Radikalisch Polymerisierbare Gallensäuren in Monoschichten, Mizellen and Vesikeln. Makromol Chem 193:779-797.
    • (1992) Makromol Chem , vol.193 , pp. 779-797
    • Ahlheim, M.1    Hallensleben, M.L.2
  • 10
    • 0002914673 scopus 로고
    • Steroids. IX. Facile inversion of unhindered sterol configuration
    • 10. Bose AK, Lai B, Hoffman WA, Manhas MS (1973). Steroids. IX. Facile inversion of unhindered sterol configuration. Tetrahedron Lett 18:1619-1622.
    • (1973) Tetrahedron Lett , vol.18 , pp. 1619-1622
    • Bose, A.K.1    Lai, B.2    Hoffman, W.A.3    Manhas, M.S.4
  • 11
    • 0001188751 scopus 로고
    • Potential bile acid metabolites. 8. 7,12-Dihydroxy- and 7β-hydroxy-5β-cholanic acids
    • 11. Iida T, Chang FC (1983). Potential bile acid metabolites. 8. 7,12-Dihydroxy- and 7β-hydroxy-5β-cholanic acids. J Org Chem 48: 1194-1197.
    • (1983) J Org Chem , vol.48 , pp. 1194-1197
    • Iida, T.1    Chang, F.C.2
  • 12
    • 0029049423 scopus 로고
    • Stereoselective synthesis of 3β-bile acid derivatives from the 3α-analog
    • 12. Denike JK, Moskova M, Zhu XX (1995). Stereoselective synthesis of 3β-bile acid derivatives from the 3α-analog. Chem Phys Lipids 77:261-267.
    • (1995) Chem Phys Lipids , vol.77 , pp. 261-267
    • Denike, J.K.1    Moskova, M.2    Zhu, X.X.3
  • 13
    • 84986808811 scopus 로고
    • Preparation of new polymers from bile acid derivatives
    • 13. Denike JK, Zhu XX (1994). Preparation of new polymers from bile acid derivatives. Macromol Rapid Commun 15:459-465.
    • (1994) Macromol Rapid Commun , vol.15 , pp. 459-465
    • Denike, J.K.1    Zhu, X.X.2
  • 14
    • 0000216596 scopus 로고    scopus 로고
    • Preparation and characterization of copolymers of new monomers from bile acid derivatives with methacrylic monomers and selective hydrolysis of the homopolymers
    • 14. Zhu XX, Moskova M, Denike JK (1996). Preparation and characterization of copolymers of new monomers from bile acid derivatives with methacrylic monomers and selective hydrolysis of the homopolymers. Polymer 37:493-498.
    • (1996) Polymer , vol.37 , pp. 493-498
    • Zhu, X.X.1    Moskova, M.2    Denike, J.K.3
  • 16
    • 0024819109 scopus 로고
    • Isolation and structure of the unusual Indian Ocean Cephalodiscus gilchristi components, cephalostatins 5 and 6
    • 16. Pettit GR, Kamano Y, Dufresne G, Inoue M, Christie N, Schmidt JM, Doubek DL (1989). Isolation and structure of the unusual Indian Ocean Cephalodiscus gilchristi components, cephalostatins 5 and 6. Can J Chem 67:1509-1513.
    • (1989) Can J Chem , vol.67 , pp. 1509-1513
    • Pettit, G.R.1    Kamano, Y.2    Dufresne, G.3    Inoue, M.4    Christie, N.5    Schmidt, J.M.6    Doubek, D.L.7
  • 17
    • 0001420768 scopus 로고    scopus 로고
    • Syntheses of α- and β-dimers of lithocholic acid esters
    • 17. Li Y, Dias JR (1996). Syntheses of α- and β-dimers of lithocholic acid esters. Org Prep Proc Int 28:203-209.
    • (1996) Org Prep Proc Int , vol.28 , pp. 203-209
    • Li, Y.1    Dias, J.R.2
  • 18
    • 0000591172 scopus 로고
    • A water-soluble dimeric steroid with catalytic properties; rate enhancements from hydrophobic binding
    • 18. Guthrie JP, Cossar J, Dawson A (1986). A water-soluble dimeric steroid with catalytic properties; rate enhancements from hydrophobic binding. Can J Chem 64:2456-2469.
    • (1986) Can J Chem , vol.64 , pp. 2456-2469
    • Guthrie, J.P.1    Cossar, J.2    Dawson, A.3
  • 19
    • 0026735902 scopus 로고
    • Simple procedure for reductive coupling of steroids with a cross conjugated dienone system
    • 19. Schmidt A, Beckert R, Weiss D (1992). Simple procedure for reductive coupling of steroids with a cross conjugated dienone system. Tetrahedron Lett 33:4299-4300.
    • (1992) Tetrahedron Lett , vol.33 , pp. 4299-4300
    • Schmidt, A.1    Beckert, R.2    Weiss, D.3
  • 22
    • 0020789485 scopus 로고
    • Photolabile derivatives of bile salts. Synthesis and suitability for photoaffinity labeling
    • 22. Kramer W, Kurz G (1983). Photolabile derivatives of bile salts. Synthesis and suitability for photoaffinity labeling. Steroids 24:910-923.
    • (1983) Steroids , vol.24 , pp. 910-923
    • Kramer, W.1    Kurz, G.2
  • 23
    • 0011957698 scopus 로고
    • Glucoronides of monohydroxylated bile acids: Specificity of microsomal glucuronyl transferase for the glucuronidation site, C-3 configuration, and side chain length
    • 23. Radominska-Pyrek A, Zimniak P, Chari M, Golunski E, Lester R, St Pyrek J (1986). Glucoronides of monohydroxylated bile acids: specificity of microsomal glucuronyl transferase for the glucuronidation site, C-3 configuration, and side chain length. J Lipid Res 32:17755-17767.
    • (1986) J Lipid Res , vol.32 , pp. 17755-17767
    • Radominska-Pyrek, A.1    Zimniak, P.2    Chari, M.3    Golunski, E.4    Lester, R.5    St Pyrek, J.6
  • 24
    • 0026502608 scopus 로고
    • Modified bile acids: Preparation of 7α,12α-dihydroxy-3β- and 7α, 12α-dihydroxy-3α-(2-hydroxyethoxy)-5β-cholanic acid and their biological activity
    • 24. Wess G, Kramer W, Bartmann W, Enhsen A, Glombik H, Müllner S, Bock K, Dries A, Kleine H, Schmitt W (1992). Modified bile acids: preparation of 7α,12α-dihydroxy-3β- and 7α, 12α-dihydroxy-3α-(2-hydroxyethoxy)-5β-cholanic acid and their biological activity. Tetrahedron Lett 33:195-198.
    • (1992) Tetrahedron Lett , vol.33 , pp. 195-198
    • Wess, G.1    Kramer, W.2    Bartmann, W.3    Enhsen, A.4    Glombik, H.5    Müllner, S.6    Bock, K.7    Dries, A.8    Kleine, H.9    Schmitt, W.10
  • 25
    • 33745356391 scopus 로고
    • Contact electron-spin coupling of nuclear magnetic moments
    • 25. Karplus M (1959), Contact electron-spin coupling of nuclear magnetic moments. J Chem Phys 30:11-15.
    • (1959) J Chem Phys , vol.30 , pp. 11-15
    • Karplus, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.