메뉴 건너뛰기




Volumn 74, Issue 8, 2009, Pages 715-720

Synthesis of spiroannulated oligopyrrole macrocycles derived from lithocholic acid

Author keywords

Calix 4 pyrrole; Chiral receptor; Microwave synthesis; Pyrrole macrocycle; Steroidal heterocycle; Supramolecular synthon

Indexed keywords

3,3 BIS(PYRROL 2 YL) 5BETA CHOLAN 24 OATE; BILE ACID; CARBONYL DERIVATIVE; LITHOCHOLIC ACID; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 65549124926     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2009.04.004     Document Type: Article
Times cited : (8)

References (23)
  • 1
    • 4544234923 scopus 로고    scopus 로고
    • Use of bile acids in pharmacological and supramolecular applications
    • Virtanen E., and Kolehmainen E. Use of bile acids in pharmacological and supramolecular applications. Eur J Org Chem (2004) 3385-3399
    • (2004) Eur J Org Chem , pp. 3385-3399
    • Virtanen, E.1    Kolehmainen, E.2
  • 2
    • 0002503177 scopus 로고    scopus 로고
    • Bile acids as building blocks of supramolecular hosts
    • Tamminen J., and Kolehmainen E. Bile acids as building blocks of supramolecular hosts. Molecules 6 (2001) 21-46
    • (2001) Molecules , vol.6 , pp. 21-46
    • Tamminen, J.1    Kolehmainen, E.2
  • 3
    • 0029740419 scopus 로고    scopus 로고
    • Steroidal oxazoles, oxazolines, and oxazolidines
    • Camoutsis C. Steroidal oxazoles, oxazolines, and oxazolidines. J Heterocycl Chem 33 (1996) 539-557
    • (1996) J Heterocycl Chem , vol.33 , pp. 539-557
    • Camoutsis, C.1
  • 4
    • 0036218671 scopus 로고    scopus 로고
    • Molecular imprinting of biologically active steroidal systems
    • Davidson L., and Hayes W. Molecular imprinting of biologically active steroidal systems. Curr Org Chem 6 (2002) 265-281
    • (2002) Curr Org Chem , vol.6 , pp. 265-281
    • Davidson, L.1    Hayes, W.2
  • 5
    • 57049095166 scopus 로고    scopus 로고
    • Study of the supramolecular chiral assembly of meso-"C-glucoside"-porphyrin derivatives in aqueous media
    • Monti D., Venanzi M., Gatto E., Mancini G., Sorrenti A., Štěpánek P., and Drašar P. Study of the supramolecular chiral assembly of meso-"C-glucoside"-porphyrin derivatives in aqueous media. N J Chem 32 (2008) 2127-2133
    • (2008) N J Chem , vol.32 , pp. 2127-2133
    • Monti, D.1    Venanzi, M.2    Gatto, E.3    Mancini, G.4    Sorrenti, A.5    Štěpánek, P.6    Drašar, P.7
  • 7
    • 0036336922 scopus 로고    scopus 로고
    • An estradiol-porphyrin conjugate selectively localizes into estrogen receptor-positive breast cancer cells
    • Swamy N., James D.A., Mohr S.C., Hanson R.N., and Ray R. An estradiol-porphyrin conjugate selectively localizes into estrogen receptor-positive breast cancer cells. Bioorg Med Chem 10 (2002) 3237-3243
    • (2002) Bioorg Med Chem , vol.10 , pp. 3237-3243
    • Swamy, N.1    James, D.A.2    Mohr, S.C.3    Hanson, R.N.4    Ray, R.5
  • 8
    • 0023239984 scopus 로고
    • Steroids and related natural-products. 104. Synthesis of bufalitoxin and bufotoxin. 36. Bufadienolides
    • Pettit G.R., Kamano Y., Drašar P., Inoue M., and Knight J.C. Steroids and related natural-products. 104. Synthesis of bufalitoxin and bufotoxin. 36. Bufadienolides. J Org Chem 52 (1987) 3573-3578
    • (1987) J Org Chem , vol.52 , pp. 3573-3578
    • Pettit, G.R.1    Kamano, Y.2    Drašar, P.3    Inoue, M.4    Knight, J.C.5
  • 9
    • 34248545237 scopus 로고    scopus 로고
    • A review on synthetic and natural steroid dimers: 1997-2006
    • Nahar L., Sarker S.D., and Turner A.B. A review on synthetic and natural steroid dimers: 1997-2006. Curr Med Chem 14 (2007) 1349-1370
    • (2007) Curr Med Chem , vol.14 , pp. 1349-1370
    • Nahar, L.1    Sarker, S.D.2    Turner, A.B.3
  • 10
    • 33645993920 scopus 로고    scopus 로고
    • Steroidal conjugates and their pharmacological applications
    • Salunke D.B., Hazra B.G., and Pore V.S. Steroidal conjugates and their pharmacological applications. Curr Med Chem 13 (2006) 813-847
    • (2006) Curr Med Chem , vol.13 , pp. 813-847
    • Salunke, D.B.1    Hazra, B.G.2    Pore, V.S.3
  • 11
    • 65549125715 scopus 로고    scopus 로고
    • Drašar P, Huong NTT, Klímková P. Syntéza methyl (5β)-3,3-di-1H-pyrrol-2-ylcholan-24-oátu. Czech 300167, Czech Pat Appl PV 2007;868
    • Drašar P, Huong NTT, Klímková P. Syntéza methyl (5β)-3,3-di-1H-pyrrol-2-ylcholan-24-oátu. Czech 300167, Czech Pat Appl PV 2007;868.
  • 12
    • 65549112427 scopus 로고    scopus 로고
    • Syntéza spiroanelovaných oligopyrrolových makrocyklů odvozených od lithocholové kyseliny
    • Drašar P., Huong N.T.T., and Klímková P. Syntéza spiroanelovaných oligopyrrolových makrocyklů odvozených od lithocholové kyseliny. Czech Pat Appl PV (2007) 2007-2869
    • (2007) Czech Pat Appl PV , pp. 2007-2869
    • Drašar, P.1    Huong, N.T.T.2    Klímková, P.3
  • 13
    • 65549106245 scopus 로고    scopus 로고
    • Mono-spiroanelované oligopyrrolové makrocykly odvozené od lithocholové kyseliny a způsob jejich přípravy
    • Drašar P., Huong N.T.T., and Klímková P. Mono-spiroanelované oligopyrrolové makrocykly odvozené od lithocholové kyseliny a způsob jejich přípravy. Czech 300168, Czech Pat Appl PV (2008) 2008-2367
    • (2008) Czech 300168, Czech Pat Appl PV , pp. 2008-2367
    • Drašar, P.1    Huong, N.T.T.2    Klímková, P.3
  • 14
    • 65549097493 scopus 로고    scopus 로고
    • Syntéza spiroanelovaných oligopyrrolových macrocyklů odvozených od lithocholové kyseliny
    • Drašar P., Klímková P., and Huong N.T.T. Syntéza spiroanelovaných oligopyrrolových macrocyklů odvozených od lithocholové kyseliny. Chem Listy 101 (2007) 960. http://www.chemicke-listy.cz/docs/full/2007_11_927-985.pdf
    • (2007) Chem Listy , vol.101 , pp. 960
    • Drašar, P.1    Klímková, P.2    Huong, N.T.T.3
  • 15
    • 65549104112 scopus 로고    scopus 로고
    • Syntéza spiroanelovaného oligopyrrolového macrocyklu odvozeného od lithocholové kyseliny.
    • Available from
    • Klímková P, Huong NTT, Šauliová J, Drašar P. Syntéza spiroanelovaného oligopyrrolového macrocyklu odvozeného od lithocholové kyseliny. Chem Listy 2006;100:649. Available from: http://www.chemicke-listy.cz/docs/full/2006_08_646-655.pdf.
    • (2006) Chem Listy , vol.100 , pp. 649
    • Klímková, P.1    Huong, N.T.T.2    Šauliová, J.3    Drašar, P.4
  • 16
    • 41549106170 scopus 로고    scopus 로고
    • A microwave promoted and Lewis acid catalysed solventless approach to 4-azasteroids
    • Borthakur M., and Boruah R.C. A microwave promoted and Lewis acid catalysed solventless approach to 4-azasteroids. Steroids 73 (2008) 637-641
    • (2008) Steroids , vol.73 , pp. 637-641
    • Borthakur, M.1    Boruah, R.C.2
  • 17
    • 84982071924 scopus 로고
    • Polyterpenes and polyterpenoids. XCVII. Correspondence of the steric configuration of the 3-hydroxy group in lithocholic acid and epicoprosterol
    • Ruzicka L., and Goldberg M.W. Polyterpenes and polyterpenoids. XCVII. Correspondence of the steric configuration of the 3-hydroxy group in lithocholic acid and epicoprosterol. Helv Chim Acta 18 (1935) 668-675
    • (1935) Helv Chim Acta , vol.18 , pp. 668-675
    • Ruzicka, L.1    Goldberg, M.W.2
  • 18
    • 0018613003 scopus 로고
    • Potential bile-acid metabolites. 2. 3,7,12-Trisubstituted 5 beta-cholanic acids
    • Chang F.C. Potential bile-acid metabolites. 2. 3,7,12-Trisubstituted 5 beta-cholanic acids. J Org Chem 44 (1979) 4567-4572
    • (1979) J Org Chem , vol.44 , pp. 4567-4572
    • Chang, F.C.1
  • 19
    • 2342582711 scopus 로고    scopus 로고
    • The remote-oxyfunctionalization of unactivated carbons in (5 beta)-3-oxobile acids by 2,6-dichloropyridine N-oxide catalyzed by ruthenium-porphyrin and HBr: a direct lactonization at C-20
    • Ogawa S., Iida T., Goto T., Mano N., Goto J., and Nambara T. The remote-oxyfunctionalization of unactivated carbons in (5 beta)-3-oxobile acids by 2,6-dichloropyridine N-oxide catalyzed by ruthenium-porphyrin and HBr: a direct lactonization at C-20. Org Biomol Chem 2 (2004) 1013-1018
    • (2004) Org Biomol Chem , vol.2 , pp. 1013-1018
    • Ogawa, S.1    Iida, T.2    Goto, T.3    Mano, N.4    Goto, J.5    Nambara, T.6
  • 20
    • 1942486430 scopus 로고    scopus 로고
    • Synthesis and characterization of lithocholic acid derived dipyrromethanes: precursors for pyrrole-steroidal macrocycles
    • Koivukorpi J., Valkonen A., and Kolehmainen E. Synthesis and characterization of lithocholic acid derived dipyrromethanes: precursors for pyrrole-steroidal macrocycles. J Mol Struct 693 (2004) 81-86
    • (2004) J Mol Struct , vol.693 , pp. 81-86
    • Koivukorpi, J.1    Valkonen, A.2    Kolehmainen, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.