메뉴 건너뛰기




Volumn 69, Issue 5, 2004, Pages 301-312

Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and D-homosteroids by intramolecular cyclization reactions

Author keywords

Cycloaddition; D Homosteroids; Hetero Diels Alder reaction; Intramolecular Prins reaction; Quinolines

Indexed keywords

1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 6' BROMO 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 6' BROMO 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 6' METHOXY 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 6' METHOXY 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 1' ACETYL 6' NITRO 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA ACETOXY 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 6' BROMO 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 6' BROMO 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 6' METHOXY 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 6' METHOXY 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 1' ACETYL 6' NITRO 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 6' BROMO 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 6' BROMO 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 6' METHOXY 4' METHYL(16ALPHA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 6' METHOXY 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 1',4',16,17 TETRAHYDRO 3BETA HYDROXY 6' NITRO 4' METHYL(16BETA,17ALPHA)ANDROSTA 5,16 DIENO[17,16 B]QUINOLINE; 3BETA ACETOXY N ACETYL 16BETA [N (4' NITRO)PHENYL]AMINO 17ABETA FLUORO 17ALPHA METHYL DEXTRO HOMOANDROST 5 ENE; 3BETA HYDROXY 16BETA [N (4' NITRO)PHENYL]AMINO 17ABETA FLUORO 17ALPHA METHYL DEXTRO HOMOANDROST 5 ENE; 3BETA HYDROXY N ACETYL 16BETA [N (4' NITRO)PHENYL]AMINO 17ABETA FLUORO 17ALPHA METHYL DEXTRO HOMOANDROST 5 ENE; 4 NITROANILINE; ANDROSTANE DERIVATIVE; QUINOLINE DERIVATIVE; STEROID; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 3042534884     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2004.01.004     Document Type: Article
Times cited : (19)

References (14)
  • 2
    • 0034675633 scopus 로고    scopus 로고
    • A novel approach in drug discovery: Synthesis of estrone-talaromycin natural product hybrids
    • Tietze L.F., Schneider G., Wölfling J., Fecher A., Nöbel T., Petersen S., et al. A novel approach in drug discovery: synthesis of estrone-talaromycin natural product hybrids. Chem. Eur. J. 6:2000;3755-3760
    • (2000) Chem. Eur. J. , vol.6 , pp. 3755-3760
    • Tietze, L.F.1    Schneider, G.2    Wölfling, J.3    Fecher, A.4    Nöbel, T.5    Petersen, S.6
  • 4
    • 0030602266 scopus 로고    scopus 로고
    • Recent progress in the synthesis of 1,2,3,4-tetrahydroquinolines
    • Katritzky A.R., Rachwal S., Rachwal B. Recent progress in the synthesis of 1, 2, 3, 4-tetrahydroquinolines. Tetrahedron. 52:1996;15031-15070
    • (1996) Tetrahedron , vol.52 , pp. 15031-15070
    • Katritzky, A.R.1    Rachwal, S.2    Rachwal, B.3
  • 5
    • 0030848359 scopus 로고    scopus 로고
    • A convergent synthetic route to (+)-dynemicin a and analogs of wide structural variability
    • Myers A.G., Tom N.J., Fraley M.E., Cohen S.B., Madar D.J. A convergent synthetic route to (+)-dynemicin A and analogs of wide structural variability. J. Am. Chem. Soc. 119:1997;6072-6094
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6072-6094
    • Myers, A.G.1    Tom, N.J.2    Fraley, M.E.3    Cohen, S.B.4    Madar, D.J.5
  • 8
    • 0141554100 scopus 로고    scopus 로고
    • Synthesis of novel steroid alkaloids by cyclization of arylimines from estrone
    • Wölfling J, Frank É, Schneider G, Tietze LF. Synthesis of novel steroid alkaloids by cyclization of arylimines from estrone. Eur J Org Chem 1999;3013-20.
    • (1999) Eur J Org Chem , pp. 3013-3020
    • Wölfling, J.1    Frank, É.2    Schneider, G.3    Tietze, L.F.4
  • 9
    • 0000069896 scopus 로고    scopus 로고
    • Synthesis of azasteroids and D-homosteroids by intramolecular cyclisation reactions of steroid arylimines
    • Wölfling J, Frank É, Schneider G, Bes MT, Tietze LF. Synthesis of azasteroids and D-homosteroids by intramolecular cyclisation reactions of steroid arylimines. Synlett 1998;1205-6.
    • (1998) Synlett , pp. 1205-1206
    • Wölfling, J.1    Frank, É.2    Schneider, G.3    Bes, M.T.4    Tietze, L.F.5
  • 10
    • 0036176964 scopus 로고    scopus 로고
    • Bismuth(III) chloride: An efficient catalyst for the one-pot stereoselective synthesis of octahydroacridines
    • Sabitha G, Reddy EV, Yadav JS. Bismuth(III) chloride: an efficient catalyst for the one-pot stereoselective synthesis of octahydroacridines. Synthesis 2002;409-12.
    • (2002) Synthesis , pp. 409-412
    • Sabitha, G.1    Reddy, E.V.2    Yadav, J.S.3
  • 11
    • 0034175538 scopus 로고    scopus 로고
    • Intramolecular cyclisation of aromatic imines: An approach to tetrahydrochromano[4,3-b]quinolines
    • Jones W., Kiselyov A.S. Intramolecular cyclisation of aromatic imines: an approach to tetrahydrochromano[4, 3-b]quinolines. Tetrahedron Lett. 41:2000;2309-2312
    • (2000) Tetrahedron Lett. , vol.41 , pp. 2309-2312
    • Jones, W.1    Kiselyov, A.S.2
  • 12
    • 0034929896 scopus 로고    scopus 로고
    • A solid-phase approach to tetrahydrochromano[4,3-b]quinolines
    • Zhang D, Kiselyov AS. A solid-phase approach to tetrahydrochromano[4, 3-b]quinolines. Synlett 2001;1173-5.
    • (2001) Synlett , pp. 1173-1175
    • Zhang, D.1    Kiselyov, A.S.2
  • 13
    • 0030021298 scopus 로고    scopus 로고
    • Evidence for a stepwise mechanism in formal hetero-Diels-Alder reactions of N-arylimines
    • Linkert F., Laschat S., Kotila S., Fox T. Evidence for a stepwise mechanism in formal hetero-Diels-Alder reactions of N-arylimines. Tetrahedron. 52:1996;955-970
    • (1996) Tetrahedron , vol.52 , pp. 955-970
    • Linkert, F.1    Laschat, S.2    Kotila, S.3    Fox, T.4
  • 14
    • 84943920736 scopus 로고
    • SHELXS, program for structure solution
    • Sheldrick GM. SHELXS, program for structure solution. Acta Crystallogr Sect A 1990;46:467-73.
    • (1990) Acta Crystallogr Sect A , vol.46 , pp. 467-473
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.