Copper‐Catalyzed Domino Reaction Involving Nitro as an Unexpected Leaving Group: Construction of Dibenzo‐Fused Azepinone Ring
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Rajnikanth Sunke | E. V. V. S. Ramarao | Ramudu Bankala | K. Parsa | M. Pal | P. Kulkarni | S. Nallapati | R. Kapavarapu | Raghavender Medisetti | E. S. Ramarao
[1] I. Namboothiri,et al. Hauser–Kraus Annulation of Phthalides with Nitroalkenes for the Synthesis of Fused and Spiro Heterocycles , 2016 .
[2] I. Namboothiri,et al. Enantioselective Synthesis of Quaternary α-Amino Acids via l-tert-Leucine-Derived Squaramide-Catalyzed Conjugate Addition of α-Nitrocarboxylates to Enones. , 2016, The Journal of organic chemistry.
[3] E. Doris,et al. Carbon Nanotube–Ruthenium Hybrids for the Partial Reduction of 2‐Nitrochalcones: Easy Access to Quinoline N‐Oxides , 2016 .
[4] C. Dey,et al. Synthesis of hydrazinoheterocycles from Morita-Baylis-Hillman adducts of nitroalkenes with azodicarboxylates. , 2016, Organic & biomolecular chemistry.
[5] V. Wadhai,et al. CuI catalyzed CS bond formation by using nitroarenes , 2013 .
[6] M. Pal,et al. AlCl3-mediated hydroarylation-heteroarylation in a single pot: a direct access to densely functionalized olefins of pharmacological interest. , 2013, Chemical communications.
[7] M. Binaschi,et al. Set-up of a new series of HDAC inhibitors: the 5,11-dihydrodibenzo[b,e]azepin-6-ones as privileged structures. , 2012, Bioorganic & medicinal chemistry letters.
[8] Haijun Yang,et al. Copper‐Catalyzed Domino Synthesis of Isoquinolino[2,3‐a]quinazolinones , 2012 .
[9] J. Li,et al. A facile copper-catalyzed one-pot domino synthesis of 5,12-dihydroindolo[2,1-b]quinazolines. , 2012, Organic letters.
[10] R. Rossi,et al. Synthesis of pyrrole and indole quinoxalinone and oxazinone derivatives by intramolecular copper-catalyzed reactions. , 2011, Organic & biomolecular chemistry.
[11] Haijun Yang,et al. Concise copper-catalyzed one-pot tandem synthesis of benzimidazo[1,2-b]isoquinolin-11-one derivatives. , 2010, Chemical communications.
[12] M. Pal,et al. Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease. , 2008, Journal of medicinal chemistry.
[13] D. Ma,et al. Synthesis of 1,2-disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination/condensation process. , 2007, Angewandte Chemie.
[14] R. Bunce,et al. Dibenzo‐fused seven‐membered nitrogen heterocycles by a tandem reduction‐lactamization reaction , 2006 .
[15] Kam Y. J. Zhang,et al. Structural basis for the activity of drugs that inhibit phosphodiesterases. , 2004, Structure.
[16] M. Streiff,et al. Inhibition of PDE4 phosphodiesterase activity induces growth suppression, apoptosis, glucocorticoid sensitivity, p53, and p21(WAF1/CIP1) proteins in human acute lymphoblastic leukemia cells. , 2002, Blood.
[17] E. Keinan,et al. A new class of antiarrhythmic-defibrillatory agents. , 2001, Bioorganic & medicinal chemistry letters.
[18] G. Meinhardt,et al. Phosphodiesterase type 4 inhibitor suppresses expression of anti-apoptotic members of the Bcl-2 family in B-CLL cells and induces caspase-dependent apoptosis , 2001, Leukemia.
[19] R. Horuk,et al. Discovery of novel non-peptide CCR1 receptor antagonists. , 1999, Journal of medicinal chemistry.
[20] M. Billah,et al. Expression, purification, and characterization of human cAMP-specific phosphodiesterase (PDE4) subtypes A, B, C, and D. , 1997, Biochemical and biophysical research communications.
[21] A. Alvarez-Larena,et al. Synthesis, conformational analysis, and molecular structure of 5-ethyl-5,6-dihydro-11H-dibenzo[b,e]azepine-6-thione , 1994 .
[22] J. Prost,et al. New triazine derivatives as potent modulators of multidrug resistance. , 1992, Journal of medicinal chemistry.
[23] D. Mcneil,et al. Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 2. Tricyclic pyridobenzoxazepinones and dibenzoxazepinones. , 1992, Journal of medicinal chemistry.