4-Dimethylaminopyridine-catalyzed multi-component one-pot reactions for the convenient synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] derivatives

[1]  Samuel R. Mendes,et al.  Efficient synthesis of 3-selanyl- and 3-sulfanylindoles employing trichloroisocyanuric acid and dichalcogenides , 2012 .

[2]  Z. Khalesi,et al.  A one-pot, three-component synthesis of spiro[indoline-isoxazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine]triones in water , 2012 .

[3]  Y. R. Lee,et al.  Iodine-catalyzed efficient synthesis of azaarene substituted 3-hydroxy-2-oxindole derivatives through sp3 C–H functionalization , 2012 .

[4]  J. Zhao,et al.  Base-catalyzed three-component direct Mannich reaction of enolizable ketones with high syn-selectivities , 2012 .

[5]  H. Liu,et al.  Rapid and efficient ultrasound-assisted method for the combinatorial synthesis of spiro[indoline-3,4'-pyrano[2,3-c]pyrazole] derivatives. , 2012, ACS combinatorial science.

[6]  M. Pal,et al.  A Pd-mediated new strategy to functionalized 2-aminochromenes: their in vitro evaluation as potential anti tuberculosis agents. , 2011, Bioorganic & medicinal chemistry letters.

[7]  Bo Zhou,et al.  An efficient one‐pot three‐component reaction for synthesis of spirooxindole derivatives in water media under catalyst‐free condition , 2011 .

[8]  G. Nandi,et al.  One-pot two-component [3 + 2] cycloaddition/annulation protocol for the synthesis of highly functionalized thiophene derivatives. , 2011, The Journal of organic chemistry.

[9]  M. Hamann,et al.  Marine indole alkaloids: potential new drug leads for the control of depression and anxiety. , 2010, Chemical reviews.

[10]  D. Shi,et al.  Efficient one-pot synthesis of novel spirooxindole derivatives via three-component reaction in aqueous medium. , 2010, Journal of combinatorial chemistry.

[11]  D. Shi,et al.  Efficient one-pot synthesis of spirooxindole derivatives catalyzed by L-proline in aqueous medium. , 2010, Journal of combinatorial chemistry.

[12]  J. Yu,et al.  Sodium stearate-catalyzed multicomponent reactions for efficient synthesis of spirooxindoles in aqueous micellar media , 2010 .

[13]  V. M. Merkulova,et al.  Electrochemically induced multicomponent assembling of isatins, 4-hydroxyquinolin-2(1H)-one and malononitrile: a convenient and efficient way to functionalized spirocyclic [indole-3,4′-pyrano[3,2-c]quinoline] scaffold , 2010, Molecular Diversity.

[14]  Y. Liu,et al.  A Green Efficient Synthesis of spiro[indoline-3,4′(1H‘)-pyrano [2,3-c]pyrazol]-2-one derivatives , 2009 .

[15]  A. Dorofeev,et al.  Electrocatalytic multicomponent assembling of isatins, 3-methyl-2-pyrazolin-5-ones and malononitrile: facile and convenient way to functionalized spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] system , 2009, Molecular Diversity.

[16]  L. A. Shemchuk,et al.  Synthesis of fused 2′-amino-3′-R-spiro-[indole-3,4′-pyran]-2(1H)-ones , 2008 .

[17]  C. Yao,et al.  Fluoride ion catalyzed multicomponent reactions for efficient synthesis of 4H-chromene and N-arylquinoline derivatives in aqueous media , 2008 .

[18]  S. Ji,et al.  A simple and clean procedure for three-component synthesis of spirooxindoles in aqueous medium , 2007 .

[19]  R. Raghunathan,et al.  TiO2–silica mediated one pot three component 1,3-dipolar cycloaddition reaction: a facile and rapid synthesis of dispiro acenaphthenone/oxindole [indanedione/oxindole] pyrroloisoquinoline ring systems , 2007 .

[20]  P. Chauhan,et al.  Bis and tris indole alkaloids from marine organisms: new leads for drug discovery. , 2007, Current medicinal chemistry.

[21]  Anna Ivana Scovassi,et al.  Arylthioindole inhibitors of tubulin polymerization. 3. Biological evaluation, structure-activity relationships and molecular modeling studies. , 2007, Journal of medicinal chemistry.

[22]  P. T. Perumal,et al.  A new InCl3-catalyzed, facile and efficient method for the synthesis of spirooxindoles under conventional and solvent-free microwave conditions , 2007 .

[23]  Helgi B. Schiöth,et al.  Evolutionary conservation of the structural, pharmacological, and genomic characteristics of the melanocortin receptor subtypes , 2005, Peptides.

[24]  C. Funk.  Leukotriene modifiers as potential therapeutics for cardiovascular disease , 2005, Nature Reviews Drug Discovery.

[25]  S. Pednekar,et al.  Large scale Biginelli reaction via water-based biphasic media: a green chemistry strategy , 2005 .

[26]  U. Kusebauch,et al.  Massive parallel catalyst screening: toward asymmetric MCRs. , 2003, Organic letters.

[27]  H. Gröger.  Catalytic enantioselective Strecker reactions and analogous syntheses. , 2003, Chemical reviews.

[28]  Robert M. Williams,et al.  Concise, asymmetric total synthesis of spirotryprostatin A. , 2003, Organic letters.

[29]  U. Pindur,et al.  Chemistry and biology of new marine alkaloids from the indole and annelated indole series. , 2003, Current medicinal chemistry.

[30]  S. Marcaccini,et al.  Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment , 2000 .

[31]  J. Pezzuto,et al.  Pyranoquinoline alkaloids from Zanthoxylum simulans , 1997 .

[32]  H. Greger,et al.  Pyranoquinolones and acridones from Vepris bilocularis , 1996 .

[33]  Tsuneo Sato,et al.  Organotin triflates as functional lewis acids. A new entry to simple and efficient robinson annulation , 1990 .

[34]  M. Kornet,et al.  Oxindole-3-spiropyrrolidines and -piperidines. Synthesis and local anesthetic activity. , 1976, Journal of medicinal chemistry.