A facile one-pot ultrasound assisted for an efficient synthesis of 1H-spiro[furo[3,4-b]pyridine-4,3'-indoline]-3-carbonitriles.

[1]  A. S. Al-Bogami,et al.  Divergent reaction pathways for one-pot, three-component synthesis of novel 4H-pyrano[3,2-h]quinolines under ultrasound irradiation. , 2013, Ultrasonics sonochemistry.

[2]  R. Prasad,et al.  Carbon–SO3H: a novel and recyclable solid acid catalyst for the synthesis of spiro[4H-pyran-3,3′-oxindoles] , 2013 .

[3]  Andrew M Haidle,et al.  A one-step, multi-component reaction for the synthesis of fully substituted 5-amino-4-carboxamidthiazoles , 2013 .

[4]  D. Shi,et al.  Efficient synthesis of functionalized dihydro-1H-indol-4(5H)-ones via one-pot three-component reaction under catalyst-free conditions. , 2013, ACS combinatorial science.

[5]  S. Paul,et al.  Dual role of the polymer supported catalyst PEG-OSO3H in aqueous reaction medium: synthesis of highly substituted structurally diversified coumarin and uracil fused spirooxindoles , 2013 .

[6]  S. Tu,et al.  Three-component domino reactions for regioselective formation of bis-indole derivatives. , 2013, ACS combinatorial science.

[7]  Ruby Singh,et al.  New multicomponent domino reaction on water: highly diastereoselective synthesis of spiro[indoline-3,4′-pyrazolo[3,4-b]pyridines] catalyzed by NaCl , 2012 .

[8]  A. Villinger,et al.  One-pot, three-component synthesis of 7-azaindole derivatives from N-substituted 2-amino-4-cyanopyrroles, various aldehydes, and active methylene compounds. , 2012, ACS combinatorial science.

[9]  Lihong Hu,et al.  An Unexpected Multicomponent Reaction to Synthesis of 3-(5-Amino-3-methyl-1H-pyrazol-4-yl)-3-arylpropanoic Acids in Ionic Liquid , 2012 .

[10]  H. Naeimi,et al.  Sonocatalyzed facile and mild one pot synthesis of gem-dichloroaziridine derivatives under alkaline conditions. , 2012, Ultrasonics sonochemistry.

[11]  Lihong Hu,et al.  An unexpected multi-component reaction to synthesis of 3-(5-amino-3-methyl-1H-pyrazol-4-yl)-3-arylpropanoic acids in ionic liquid , 2011 .

[12]  F. Shi,et al.  Facile synthesis of new 4-aza-podophyllotoxin analogs via microwave-assisted multi-component reactions and evaluation of their cytotoxic activity. , 2011, Bioorganic & medicinal chemistry letters.

[13]  S. Tu,et al.  Microwave-Assisted Aqueous Synthesis: A Rapid Approach to Poly-functionalized Indoline-Spiro Benzofurodiazepines , 2011 .

[14]  M. Dabiri,et al.  Sonochemical multi-component synthesis of spirooxindoles. , 2011, Ultrasonics sonochemistry.

[15]  Guigen Li,et al.  Microwave-assisted multicomponent reaction in water leading to highly regioselective formation of benzo[f]azulen-1-ones. , 2011, Tetrahedron.

[16]  Qing Zhu,et al.  One‐Pot Synthesis of Spirooxindole Derivatives Catalyzed by Lipase in the Presence of Water , 2011 .

[17]  Guigen Li,et al.  [4+2+1] Domino cyclization in water for chemo- and regioselective synthesis of spiro-substituted benzo[b]furo[3,4-e][1,4]diazepine derivatives , 2011 .

[18]  P. Mirzaei,et al.  Ultrasound-assisted synthesis of 2,2'-(2-oxoindoline-3,3-diyl)bis(1H-indene-1,3(2H)-dione) derivatives. , 2011, Ultrasonics sonochemistry.

[19]  P. Yogeeswari,et al.  A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of novel spiro-pyrrolothiazolyloxindoles and their antitubercular evaluation. , 2010, European journal of medicinal chemistry.

[20]  A. Thangamani Regiospecific synthesis and biological evaluation of spirooxindolopyrrolizidines via [3+2] cycloaddition of azomethine ylide. , 2010, European journal of medicinal chemistry.

[21]  M. N. Ponnuswamy,et al.  One-pot multicomponent synthesis and anti-microbial evaluation of 2'-(indol-3-yl)-2-oxospiro(indoline-3,4'-pyran) derivatives. , 2010, Bioorganic & medicinal chemistry letters.

[22]  A. Bazgir,et al.  One‐pot and three‐component synthesis of spiro[chromeno[2,3‐d] pyrimidine‐5,3′‐indoline]‐diones and spiro[chromeno[2,3‐c] pyrazole‐4,3′‐indoline]‐diones , 2010 .

[23]  B. Cheng,et al.  Ionic liquid [EMIM]OAc under ultrasonic irradiation towards the first synthesis of trisubstituted imidazoles. , 2010, Ultrasonics sonochemistry.

[24]  A. Karimi,et al.  Novel Mono- and Bis(spiro-2-amino-4H-pyrans): Alum-Catalyzed Reaction of 4-Hydroxycoumarinand Malononitrile with Isatins, Quinones, or Ninhydrin , 2010 .

[25]  H. Khavasi,et al.  Ultrasound-assisted one-pot, three-component synthesis of spiro[indoline-3,4'-pyrazolo[3,4-b]pyridine]-2,6'(1'H)-diones in water. , 2010, Ultrasonics sonochemistry.

[26]  A. Bazgir,et al.  One-pot, pseudo four-component synthesis of a spiro[diindeno[1,2-b:2',1'-e]pyridine-11,3'-indoline]-trione library. , 2010, Journal of combinatorial chemistry.

[27]  P. Mirzaei,et al.  Synthesis of spiro[benzopyrazolonaphthyridine-indoline]-diones and spiro[chromenopyrazolopyridine-indoline]-diones by one-pot, three-component methods in water , 2009 .

[28]  M. Ranson,et al.  An investigation into the cytotoxicity and mode of action of some novel N-alkyl-substituted isatins. , 2007, Journal of medicinal chemistry.

[29]  N. Afza,et al.  Isatinones A and B, new antifungal oxindole alkaloids from Isatis costata. , 2007, Molecules.

[30]  R. Raghunathan,et al.  Ultrasonic assisted-silica mediated [3+2] cycloaddition of azomethine ylides—a facile multicomponent one-pot synthesis of novel dispiroheterocycles , 2006 .

[31]  Su Qiu,et al.  Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction. , 2006, Journal of medicinal chemistry.

[32]  A. Loupy,et al.  Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro [indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3H-indole-3,2'-thiazolidine]-3'(1,2,4-triazol-3-yl)-2,4'(1H)-dione. , 2006, Bioorganic & medicinal chemistry.

[33]  S. Hecht,et al.  Javaniside, a novel DNA cleavage agent from Alangium javanicum having an unusual oxindole skeleton. , 2004, Chemical communications.

[34]  J. Stables,et al.  Anticonvulsant activity of Schiff bases of isatin derivatives. , 2004, Acta pharmaceutica.

[35]  Timothy J Mason,et al.  Sonochemistry and sonoprocessing: the link, the trends and (probably) the future. , 2003, Ultrasonics sonochemistry.

[36]  Kinzo Matsumoto,et al.  Pteropodine and isopteropodine positively modulate the function of rat muscarinic M(1) and 5-HT(2) receptors expressed in Xenopus oocyte. , 2002, European journal of pharmacology.

[37]  H. Itokawa,et al.  A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans chinensin, justicidin B, and Taiwanin C , 1997 .

[38]  H. Kakeya,et al.  Novel mammalian cell cycle inhibitors, spirotryprostatins A and B, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase☆ , 1997 .

[39]  M. Medic-Saric,et al.  BIOLOGICALLY ACTIVE MANNICH BASES DERIVED FROM ISATIN AND 5-NITROISATIN , 1978 .