نتایج جستجو برای: indeno 12 b quinoline 911 dione

تعداد نتایج: 1411421  

Journal: :Journal of composites and compounds 2022

3,5-Bis(trifluoromethyl) phenyl ammonium triflate(BFPAT) catalyzed one-pot synthesis of indeno[1,2-b]pyridine compound derivatives by four-component condensation aldehyde, aromatic ketones, 1,3-indanedione, and acetate in ethanol. Accessible starting materials, Simplicity operation, green practical catalyst, easy purification, excellent yields are the key benefits current technique.

2010
Arnold R. Romero Bohórquez Vladimir V. Kouznetsov Teresa González Alexander Briceño

The title compound, C(23)H(22)N(2), was obtained using the three-component imino Diels-Alder reaction via a one-pot condensation between anilines, α-pyridine-carboxy-aldehyde and indene using BF(3)·OEt(2) as the catalyst. The mol-ecular structure reveals the cis-form as the unique diastereoisomer. The crystal structure comprises one-dimensional zigzag ribbons connected via N-H⋯N hydrogen bonds....

Journal: :Crystals 2022

New 6-CF3-1H-pyrazolo[3,4-b]quinolines with a methyl and/or phenyl group attached to the pyrazole core (Molx (x = 1, 2, 3, 4)) were synthesized and characterized in terms of their optoelectronic applications: photovoltaic electroluminescence. The fluorescence emissions investigated phenyl-decorated pyrazoloquinolines is caused by photoinduced charge transfer p process occurring between substitu...

Journal: :European journal of medicinal chemistry 2011
Ram Shankar Upadhayaya Popat D Shinde Sandip A Kadam Amit N Bawane Aftab Y Sayyed Ramakant A Kardile Pallavi N Gitay Santosh V Lahore Shailesh S Dixit András Földesi Jyoti Chattopadhyaya

Recently we have reported anti-TB properties of a new class of conformationally-constrained indeno[2,1-c]quinolines, which are although considerably active (MIC 0.39-0.78 μg/mL) suffered from intense solubility problems. We thought of improving their bioavailability by prodrugs approach. Accordingly esters of the "Lead" indeno[2,1-c]quinolines 1, 15 and 27 derivatives were synthesized and their...

Journal: :Antimicrobial agents and chemotherapy 1993
A Fournet A A Barrios V Muñoz R Hocquemiller A Cavé J Bruneton

Ten 2-substituted quinoline alkaloids isolated from a plant used for treatment of New World cutaneous leishmaniasis have antileishmanial in vitro activities against the extracellular forms of Leishmania spp. BALB/c mice infected with Leishmania amazonensis PH8 or H-142 or Leishmania venezuelensis were treated 1 day after the parasitic infection with a quinoline alkaloid (100 mg/kg of body weigh...

Journal: :Chemical & pharmaceutical bulletin 1999
M Cabeza A Quiroz E Bratoeff M E Murillo E Ramírez G Flores

The pharmacological activity of eight pregnane derivatives 17-alpha acetoxyprogesterone 9, 17-alpha acetoxy-4, 5-epoxypregnan-3, 20-dione 10, 17-alpha acetoxy-4-chloro-4-pregnene-3, 20-dione 11, 17-alpha acetoxy-4-bromo-4-pregnene-3, 20-dione 12, 17-alpha hydroxy-4-bromo-4-pregnene-3, 20-dione 13, 4-chloro-17-alpha hydroxy-4-pregnene-3, 20-dione 14, 17-alpha benzoyloxy-4-bromo-4-pregnene-3, 20-...

Journal: :Chemical communications 2011
Takeshi Tanaka Hiromi Inui Hiroshi Kida Takeshi Kodama Takuya Okamoto Aki Takeshima Yoshimitsu Tachi Yoshiki Morimoto

The characteristic indeno-tetrahydropyridine core of cytotoxic haouamine B (2) was efficiently synthesized featuring the diastereoselective construction of a diaryl-substituted stereogenic quaternary center by an intramolecular Pd-catalyzed α-C-arylation and subsequent direct conversion of the vinylogous imide function into the C2-C25 double bond by TsNHNH(2).

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