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kw.\*:("Pyrido\[3,4-b\]indole dérivé")

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SYNTHESIS OF 3,4-DIHYDROPYRIDO (3,4-B) BENZINDOLES USING POLYPHOSPHATE ESTER AS A CYCLISING AGENTHIREMATH SP; KADDARGI SS.1975; J. INDIAN CHEM. SOC.; INDIA; DA. 1975; VOL. 52; NO 9; PP. 866-868; BIBL. 11 REF.Article

Oxazolo[3',2':1,2]pyrido[3,4-b]indole und [1,3]-oxazino[3',2':1,2]pyrido[3,4-b]indole durch eine einfache Kondensationsreaktion von 3,4-dihydro-β-carbolin mit α- bzw. β-Hydroxy-carbonsäuren = Oxazolo[3',2':1,2]pyrido[3,4-b]indoles and [1,3]-oxazino[3',2':1,2]pyrido[3,4-b]indoles by a simple condensation reaction of 3,4-dihydro-β-carbolin with α- and β-hydroxycarboxylic acidsWANNER, K. T; WEBER, U.Synthesis (Stuttgart). 1994, Num 4, pp 387-390, issn 0039-7881Article

The 1H- and 13C-nuclear magnetic resonance spectra of manzamine C and related compoundsSEKI, H; NAKAGAWA, M; HASHIMOTO, A et al.Chemical and pharmaceutical bulletin. 1993, Vol 41, Num 6, pp 1173-1176, issn 0009-2363Article

Alkyl anhydronium bases of harmaline: a β-carboline alkaloid of Peganum harmalaBINA SHAHEEN SIDDIQUI; SHAHID BADER USMANI; SABIRA BEGUN et al.Heterocycles (Sendai). 1994, Vol 38, Num 6, pp 1257-1264, issn 0385-5414Article

The 1H- and 13C-nuclear magnetic resonance spectra of harman. Reinvestigation of the assignments by one- and two-dimensional methodsSEKI, H; HASHIMOTO, A; HINO, T et al.Chemical and pharmaceutical bulletin. 1993, Vol 41, Num 6, pp 1169-1172, issn 0009-2363Article

Meisenheimer rearrangement of azetopyridoindoles. VI: Synthesis of 12-carbaeudistomin and related compoundsKURIHARA, T; SAKAMOTO, Y; MATSUMOTO, H et al.Chemical and pharmaceutical bulletin. 1994, Vol 42, Num 3, pp 475-480, issn 0009-2363Article

Synthesis of enantiomeric pure E-Nor-15-azayohimbinesVALLS, N; BONJOCH, J; DEL ALAMO, C et al.Helvetica chimica acta. 1992, Vol 75, Num 1, pp 137-144, issn 0018-019XArticle

Design, synthesis, and evaluation of a novel class of 2,3-disubstituted-tetrahydro-β-carboline derivativesLI ZENG; JIANWEI ZHANG.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 11, pp 3718-3722, issn 0960-894X, 5 p.Article

A New Cytotoxic β-Carboline Alkaloid from Galianthe thalictroidesFIGUEIREDO, Patricia O; GARCEZ, Fernanda R; MATOS, Maria De Fátima C et al.Planta medica. 2011, Vol 77, Num 16, pp 1852-1854, issn 0032-0943, 3 p.Article

Influence of reaction conditions on products of the Pictet—Spengler condensationPULKA, Karolina; MISICKA, Aleksandra.Tetrahedron (Oxford. Print). 2011, Vol 67, Num 10, issn 0040-4020, 1723, 1955-1959 [6 p.]Article

Development of the pictet-spengler reaction catalyzed by AuCl3/AgOTfSO WON YOUN.Journal of organic chemistry. 2006, Vol 71, Num 6, pp 2521-2523, issn 0022-3263, 3 p.Article

Catalytic Ν-sulfonyliminium ion-mediated cyclizations to α-vinyl-substituted isoquinolines and β-carbolines and applications in metathesisKINDERMAN, Sape S; WEKKING, Monique M. T; VAN MAARSEVEEN, Jan H et al.Journal of organic chemistry. 2005, Vol 70, Num 14, pp 5519-5527, issn 0022-3263, 9 p.Article

Multicomponent approach for the synthesis of non-natural tryptophan, tryptamine and β-carboline derivativesJEANNIN, Laurent; BOISBRUN, Michel; NEMES, Csaba et al.Comptes rendus. Chimie. 2003, Vol 6, Num 5-6, pp 517-528, issn 1631-0748, 12 p.Article

(1H-indol-3-yl)alcanamides et dérivés: synthèse et évaluation pharmacologique = (1H-indol-3-yl)alcanamides and derivatives/synthesis and pharmacological evaluationFouchard, Fabienne; Le Baut, G.1994, 300 p.Thesis

Convenient Synthesis of a Library of Lactam-Fused β-Carbolines via the Ugi ReactionHUTAIT, Samiran; NAYAK, Maloy; PENTA, Ashok et al.Synthesis (Stuttgart). 2011, Num 3, pp 419-430, issn 0039-7881, 12 p.Article

Efficient and Practical One-Pot Conversions of N-Tosyltetrahydroisoquinolines into Isoquinolines and of N-Tosyltetrahydro-β-carbolines into β-Carbolines through Tandem β-Elimination and AromatizationJING DONG; SHI, Xiao-Xin; YAN, Jing-Jing et al.European journal of organic chemistry (Print). 2010, Num 36, pp 6987-6992, issn 1434-193X, 6 p.Article

The Pictet-Spengler reaction and biogenic tryptamines : formation of tetrahydro-β-carbolines at physiological pHCALLAWAY, J. C; GYNTHER, J; POSO, A et al.Journal of heterocyclic chemistry. 1994, Vol 31, Num 2, pp 431-435, issn 0022-152XArticle

Development of a Two-Step Route to 3-PBC and βCCt, Two Agents Active against Alcohol Self-Administration in Rodent and Primate ModelsNAMJOSHI, Ojas A; GRYBOSKI, Angelica; FONSECA, German O et al.Journal of organic chemistry. 2011, Vol 76, Num 11, pp 4721-4727, issn 0022-3263, 7 p.Article

Nonsymmetrical β-Carboline Dimers from an Ascidian, Didemnum spKEARNS, Philip S; RIDEOUT, John A.Journal of natural products (Print). 2008, Vol 71, Num 7, pp 1280-1282, issn 0163-3864, 3 p.Article

Synthesis and biological studies of 1-amino β-carbolinesBOURSEREAU, Yohan; COLDHAM, Iain.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 23, pp 5841-5844, issn 0960-894X, 4 p.Article

Studies towards streptonigrinoids : formal synthesis of lavendamycin methyl esterCIUFOLINI, M. A; BISHOP, M. J.Journal of the Chemical Society. Chemical communications. 1993, Num 18, pp 1463-1464, issn 0022-4936Article

Beta-carboline alkaloids derived from the ascidian Synoicum spTAE HYUNG WON; JEON, Ju-Eun; LEE, So-Hyoung et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 13, pp 4082-4087, issn 0968-0896, 6 p.Article

Design and synthesis of Pictet―Spengler condensation products that exhibit oncogenic-RAS synthetic lethality and induce non-apoptotic cell deathSKOUTA, Rachid; HAYANO, Miki; SHIMADA, Kenichi et al.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 17, pp 5707-5713, issn 0960-894X, 7 p.Article

Structure―activity relationship in the antitumor activity of 6-, 8- or 6,8-substituted 3-benzylamino-β-carboline derivativesIKEDA, Reiko; KIMURA, Takanori; TSUTSUMI, Tatsuya et al.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 10, pp 3506-3515, issn 0960-894X, 10 p.Article

β-Carboline alkaloids from the leaves of Trigonostemon lii Y.T. ChangLIA, Shi-Fei; YU ZHANG; YAN LI et al.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 6, pp 2296-2299, issn 0960-894X, 4 p.Article

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