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kw.\*:("Indolizino\[1,2-b\]quinoléine dérivé")

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Chemical modification of antitumor alkaloids, 20(S)-camptothecin and 7-ethylcamptothecin : reaction of the E-lactone ring portion with hydrazine hydrateYAEGASHI, T; SAWADA, S; FURUTA, T et al.Chemical and pharmaceutical bulletin. 1993, Vol 41, Num 5, pp 971-974, issn 0009-2363Article

Preparation of mappicine ketones from camptothecins : chemistry of the camptothecin E ringFORTUNAK, J. M. D; MASTROCOLA, A. R; MELLINGER, M et al.Tetrahedron letters. 1994, Vol 35, Num 32, issn 0040-4039, 5741, 5763-5764 [3 p.]Article

Chemical modification of an antitumor alkaloid, 20(S)-camptothecin : E-lactone ring-modified water-soluble derivatives of 7-ethylcamptothecinSAWADA, S; YAEGASHI, T; FURUTA, T et al.Chemical and pharmaceutical bulletin. 1993, Vol 41, Num 2, pp 310-313, issn 0009-2363Article

Recent applications of radical reactions in natural product synthesisCURRAN, D. P; SISKO, J; YESKE, P. E et al.Pure and applied chemistry. 1993, Vol 65, Num 6, pp 1153-1159, issn 0033-4545Conference Paper

Synthesis and biological assays of E-ring analogs of camptothecin and homocamptothecinTANGIRALA, Raghuram S; ANTONY, Smitha; AGAMA, Keli et al.Bioorganic & medicinal chemistry. 2006, Vol 14, Num 18, pp 6202-6212, issn 0968-0896, 11 p.Article

New 4+1 radical annulations. A formal total synthesis of (±)-camptothecinCURAN, D. P; HUI LIU.Journal of the American Chemical Society. 1992, Vol 114, Num 14, pp 5863-5864, issn 0002-7863Article

Formaldehyde-induced DNA cross-link of indolizino[1,2-b]quinolines derived from the A-D rings of camptothecinPERZYNA, Aurore; MARTY, Carine; FACOMPRE, Michael et al.Journal of medicinal chemistry (Print). 2002, Vol 45, Num 26, pp 5809-5812, issn 0022-2623, 4 p.Article

Total synthesis of (±)-17-norcamptothecin, a novel E-ring modified camptothecinDEVERT, Marie; SABOT, Cyrille; GIBOREAU, Pascale et al.Tetrahedron (Oxford. Print). 2010, Vol 66, Num 35, issn 0040-4020, 7063, 7227-7231 [6 p.]Article

Regioselective synthesis and cytotoxicities of camptothecin derivatives modified at the 7-, 10- and 20-positionsPAN, Xian-Dao; RUI HAN; SUN, Piao-Yang et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 21, pp 3739-3741, issn 0960-894X, 3 p.Article

Fluorous mixture synthesis : A fluorous-tagging strategy for the synthesis and separation of mixtures of organic compoundsZHIYONG LUO; QISHENG ZHANG; ODERAOTOSHI, Yoji et al.Science (Washington, D.C.). 2001, Vol 291, Num 5509, pp 1766-1769, issn 0036-8075Article

Recent synthetic developments in a powerful imino Diels-Alder reaction (Povarov reaction) : application to the synthesis of N-polyheterocycles and related alkaloidsKOUZNETSOV, Vladimir V.Tetrahedron (Oxford. Print). 2009, Vol 65, Num 14, issn 0040-4020, 2717, 2721-2750 [31 p.]Article

Synthesis of position-specific tritium-labeled 20(S)-camptothecin, 9-amino-20(S)-camptothecin, and 10,11-methylenedioxy-20(S)-camptothecinNICHOLAS, A. W; WANI, M. C; WALL, M. E et al.Journal of labelled compounds & radiopharmaceuticals. 1993, Vol 33, Num 9, pp 839-848, issn 0362-4803Article

A six-step synthesis of (±) camptothecinCOMINS, D. L; HAO HONG; SAHA, J. K et al.Journal of organic chemistry. 1994, Vol 59, Num 18, pp 5120-5121, issn 0022-3263Article

Asymmetric synthesis of camptothecin alkaloids : a nine-step synthesis of (S)-camptothecinCOMINS, D. L; HAO HONG; GAO JIANHUA et al.Tetrahedron letters. 1994, Vol 35, Num 30, issn 0040-4039, 5309, 5331-5334 [5 p.]Article

Regioselective synthesis of camptothecinRAMA RAO, A. V; YADAV, J. S; MURALIKRISHNA VALLURI et al.Tetrahedron letters. 1994, Vol 35, Num 21, issn 0040-4039, 3435, 3613-3616 [5 p.]Article

Thermodynamic Studies of 10-Hydroxy-camptothecin in Aqueous SolutionsKUNADHARAJU, Sasank; SAVVA, Michalakis.Journal of chemical and engineering data (Print). 2010, Vol 55, Num 1, pp 103-112, issn 0021-9568, 10 p.Article

Design, Synthesis, and Biological Evaluation of 14-Substituted Aromathecins as Topoisomerase I InhibitorsCINELLI, Maris A; MORRELL, Andrew; DEXHEIMER, Thomas S et al.Journal of medicinal chemistry (Print). 2008, Vol 51, Num 15, pp 4609-4619, issn 0022-2623, 11 p.Article

Kinetic studies of the hydrolysis and lactonization of camptothecin and its derivatives, CPT-11 and SN-38, in aqueous solutionAKIMOTO, K; KAWAI, A; OHYA, K et al.Chemical and pharmaceutical bulletin. 1994, Vol 42, Num 10, pp 2135-2138, issn 0009-2363Article

Plant antitumor agents. XXX: Synthesis and structure activity of novel camptothecin analogsWALL, M. E; WANI, M. C; NICHOLAS, A. W et al.Journal of medicinal chemistry (Print). 1993, Vol 36, Num 18, pp 2689-2700, issn 0022-2623Article

Drug delivery systems. 2. Camptothecin 20-O-Poly(ethylene glycol) ester transport formsGREENWALD, R. B; PENDRI, A; CONOVER, C et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 10, pp 1938-1940, issn 0022-2623Article

Semi-synthesis and biological activity of γ-lactones analogs of camptothecinMINGZONG LI; WEIDONG TANG; FUXING ZENG et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 24, pp 6441-6443, issn 0960-894X, 3 p.Article

Synthesis and biological evaluation of bis and monocarbonate prodrugs of 10-hydroxycamptothecinsXUNGUI HE; WEI LU; XIQUN JIANG et al.Bioorganic & medicinal chemistry. 2004, Vol 12, Num 15, pp 4003-4008, issn 0968-0896, 6 p.Article

Synthesis and pharmacological evaluation of novel non-lactone analogues of camptothecinHAUTEFAYE, Patrick; CIMETIERE, Bernard; PIERRE, Alain et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 16, pp 2731-2735, issn 0960-894X, 5 p.Article

Novel 20-carbonate linked prodrugs of camptothecin and 9-aminocamptothecin designed for activation by tumour-associated plasminDE GROOT, Franciscus M. H; BUSSCHER, Guuske F; ABEN, René W. M et al.Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 17, pp 2371-2376, issn 0960-894XArticle

Cancer chemotherapy: A SN-38 (7-ethyl-10-hydroxycamptothecin) glucuronide prodrug for treatment by a PMT (prodrug monotherapy) StrategyANGENAULT, Stéphane; THIROT, Sylvie; SCHMIDT, Frédéric et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 5, pp 947-950, issn 0960-894X, 4 p.Article

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