Multi-Component Reactions in Heterocyclic Chemistry
暂无分享,去创建一个
R. R. Khairullina | I. V. Paramonov | Alexey P. Ilyn | Alexey P. Ilyin | M. Naimi-Jamal | S. Ng, | A. Basso | A. Shaabani | S. Tkachenko | S. Desenko | V. A. Chebanov | M. Taddei | O. Fedorova | A. Rezayan | R. Orru | R. Riva | I. Magedov | T. Müller | L. Banfi | E. Muravyova | V. Mokrushin | Afshin Sarvary | A. N. Maslivets | L. Voskressensky | I. N. Vladimirov | E. Petricci | D. Kravchenko | A. Khvat | V. Kysil | A. Ivachtchenko | M. Heidary | A. Sharifi | G. P. Sagitullina | R. S. Sagitullin | Sergey Tsirulnikov | G. Guanti | G. R. Khabibullina | V. Akhmetova | V. L. Gein | Nikolai A. Beliaev | Sara Mashkouri | E. B. Rakhimova | Yana I Sakhno | G. Danagulyan | A. K. Garkushenko | M. I. Vahrin | A. A. Zorina | G. Tokmakov | M. A. Dushek | E. Rozhkova | F. Moliner | Z. T. Niatshina | V. Saraev | Anastasia Yu. Andrushchenko | R. A. Vagapov | N. N. Murzakova | Armen D. Murtchyan | A. K. Tumanyan | Nikolai M. Przhevalski | M. N. Armisheva | N. A. Rassudihina | O. S. Panova | V. V. Potapov | V. N. Vichegjanina | E. B. Levandovskaya | N. V. Nosova
[1] I. Magedov. Structural Simplification of Bioactive Natural Products with Multicomponent Synthesis. Part 4. 4H-Pyrano-[2,3-b]naphthoquinones with Anticancer Activity. , 2012 .
[2] M. Khalilzadeh,et al. A novel isocyanide-based three-component reaction: a facile synthesis of substituted 2H-pyran-3,4-dicarboxylates , 2010 .
[3] Z. G. Aliev,et al. Five-membered 2,3-dioxo heterocycles: LXIX. Direct heterocyclization of [3,4-dihydroisoquinolin-1(2H)-ylidene]-acetamides with 5-arylfuran-2,3-diones. Crystalline and molecular structure of (3E,5Z)-3-[3,3-dimethyl-3,4-dihydroisoquinolin-1(2H)-ylidene]-5-(2-oxo-2-phenylethylidene)pyrrolidine-2,4-dion , 2010 .
[4] A. N. Maslivets,et al. Five-membered 2.3-dioxo heterocycles: LXVIII. Three pathways in the reaction of methyl 3-aroyl-1-aryl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with 3-amino-5,5-dimethylcyclohex-2-en-1-one , 2010 .
[5] Z. G. Aliev,et al. Five-membered 2,3-dioxoheterocycles: LXVII. Pyrroledione-pyrroledion recyclization of isopropyl 2-(1-aryl-4,5-dioxo-2-phenyl-4,5-dihydro-1H-pyrrol-3-yl)-2-oxoacetates under the action of arylamines. Crystal and molecular structure of (z)-isopropyl 2-hydroxy-4,5-dioxo-1-phenyl-3-[phenyl(phenylamino)- , 2010 .
[6] D. Aitken,et al. Passerini reaction-amine deprotection-acyl migration peptide assembly: efficient formal synthesis of cyclotheonamide C. , 2009, Organic letters.
[7] A. V. Varlamov,et al. Synthesis of Heteroannulated Azocine Derivatives , 2009 .
[8] A. Maleki,et al. Novel Multicomponent One‐Pot Synthesis of Tetrahydro‐1H‐1,5‐benzodiazepine‐2‐carboxamide Derivatives. , 2008 .
[9] C. Kappe,et al. Multicomponent cyclocondensation reactions of aminoazoles, arylpyruvic acids and aldehydes with controlled chemoselectivity , 2008 .
[10] R. Orru,et al. 1-Azadienes in cycloaddition and multicomponent reactions towards N-heterocycles. , 2008, Chemical communications.
[11] William E. Kemnitzer,et al. Discovery of 4-aryl-2-oxo-2H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. , 2008, Bioorganic & medicinal chemistry letters.
[12] Benjamin Willy,et al. Consecutive multi-component syntheses of heterocycles via palladium-copper catalyzed generation of alkynones , 2008 .
[13] V. N. Chernenko,et al. Tuning of chemo- and regioselectivities in multicomponent condensations of 5-aminopyrazoles, dimedone, and aldehydes. , 2008, The Journal of organic chemistry.
[14] S. Rogelj,et al. Structural simplification of bioactive natural products with multicomponent synthesis. 2. antiproliferative and antitubulin activities of pyrano[3,2-c]pyridones and pyrano[3,2-c]quinolones. , 2008, Journal of medicinal chemistry.
[15] A. Maleki,et al. A novel one-pot pseudo-five-component synthesis of 4,5,6,7-tetrahydro-1H-1,4-diazepine-5-carboxamide derivatives. , 2008, The Journal of organic chemistry.
[16] R. Brun,et al. Rapid One-Pot Synthesis of Antiparasitic Quinolines Based upon the Microwave-Assisted Coupling-Isomerization Reaction (MACIR) , 2008 .
[17] R. Orru,et al. A multicomponent synthesis of triazinane diones. , 2008, The Journal of organic chemistry.
[18] William E. Kemnitzer,et al. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based HTS assay. Part 5: modifications of the 2- and 3-positions. , 2008, Bioorganic & medicinal chemistry letters.
[19] A. V. Varlamov,et al. Chapter 2 Synthesis of Heteroannulated Azocine Derivatives , 2008 .
[20] S. Rogelj,et al. Discovery and investigation of antiproliferative and apoptosis-inducing properties of new heterocyclic podophyllotoxin analogues accessible by a one-step multicomponent synthesis. , 2007, Journal of medicinal chemistry.
[21] R. Orru,et al. A resource-efficient and highly flexible procedure for a three-component synthesis of 2-imidazolines. , 2007, The Journal of organic chemistry.
[22] A. Maleki,et al. A novel isocyanide-based three-component reaction: synthesis of highly substituted 1,6-dihydropyrazine-2,3-dicarbonitrile derivatives. , 2007, The Journal of organic chemistry.
[23] T. Müller,et al. Multi-component syntheses of heterocycles by transition-metal catalysis. , 2007, Chemical Society reviews.
[24] U. Dzhemilev,et al. Thiomethylation of amino alcohols using formaldehyde and hydrogen sulfide , 2007 .
[25] S. Rogelj,et al. Structural simplification of bioactive natural products with multicomponent synthesis: dihydropyridopyrazole analogues of podophyllotoxin. , 2007, Bioorganic & medicinal chemistry letters.
[26] A. Maleki,et al. One-Pot Three-Component Synthesis of 3-Aminoimidazo[1,2-a]pyridines and -pyrazines in the Presence of Silica Sulfuric Acid , 2007 .
[27] A. Maleki,et al. Ionic Liquid Promoted One-Pot Three-Component Reaction: Synthesis of Annulated Imidazo[1,2-a]azines Using Trimethylsilylcyanide , 2007 .
[28] A. Shaabani,et al. Synthesis of tetrahydrobenzimidazo[1,2-b]quinazolin-1(2H)-one and tetrahydro-1,2,4-triazolo[5,1-b]quinazolin-8(4H)-one ring systems under solvent-free conditions. , 2006, Combinatorial chemistry & high throughput screening.
[29] A. Spek,et al. Diastereoselective multicomponent synthesis of dihydropyridones with an isocyanide functionality. , 2006, Organic letters.
[30] G. Danagulyan. Kost—Sagitullin Rearrangement and Other Isomerization Recyclizations of Pyrimidines , 2006 .
[31] C. Kappe,et al. Microwave-assisted three-component synthesis of 7-aryl-2-alkylthio-4,7-dihydro-1,2,4-triazolo[1,5-a]-pyrimidine-6-carboxamides and their selective reduction. , 2006, Journal of combinatorial chemistry.
[32] William E. Kemnitzer,et al. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8-positions. , 2005, Bioorganic & medicinal chemistry letters.
[33] G. Danagulyan. Kost-Sagitullin Rearrangement and Other Isomerization Recyclizations of Pyrimidines. (Review) , 2005 .
[34] Gerd Kaupp,et al. Organic Solid-State Reactions with 100% Yield , 2005 .
[35] David R. Anderson,et al. Aminocyanopyridine inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2). , 2005, Bioorganic & medicinal chemistry letters.
[36] S. Desenko,et al. Three-Component Procedure for the Synthesis of 5-Aryl-5,8-dihydroazolo[1,5-a]pyrimidine-7-carboxylic Acids , 2005 .
[37] R. Bon,et al. Multicomponent synthesis of 2-imidazolines. , 2005, The Journal of organic chemistry.
[38] U. Dzhemilev,et al. Multicomponent condensation of aliphatic amines with formaldehyde and hydrogen sulfide , 2005 .
[39] Jieping Zhu,et al. Multicomponent Reactions: ZHU:MULTICOMPONENT REACTIONS O-BK , 2005 .
[40] U. Dzhemilev,et al. Multicomponent heterocyclization of hydrazine, hydrogen sulfide, and formaldehyde , 2004 .
[41] A. V. Varlamov,et al. Tandem Cleavage of Hydrogenated β‐ and γ‐Carbolines − New Practical Synthesis of Tetrahydroazocino[4,5‐b]indoles and Tetrahydroazocino[5,4‐b]indoles Showing Acetylcholinesterase Inhibitory Activity , 2004 .
[42] S. Schreiber,et al. A planning strategy for diversity-oriented synthesis. , 2004, Angewandte Chemie.
[43] W. Motherwell,et al. A novel isocyanide based three component reaction. , 2003, Chemical communications.
[44] M. Greef,et al. Recent Advances in Solution-Phase Multicomponent Methodology for the Synthesis of Heterocyclic Compounds , 2003 .
[45] W. Darby,et al. 4(5)‐Hydroxymethylimidazole Hydrochloride , 2003 .
[46] A. Katritzky,et al. Exchange Aminations in Conversions of Pyrimidinium Iodides to 2-Alkylaminonicotinic Acids. , 2000 .
[47] A. Katritzky,et al. Exchange Aminations in Conversions of Pyrimidinium Iodides to 2-Alkylaminonicotinic Acids , 2000 .
[48] W. Darby,et al. The Preparation of 4(5)-Hydroxymethyl-imidazole , 1942 .
[49] R. Herrmann,et al. Über neue Abkömmlinge des Imidazols (IV. Mitteil. über Imidazole) , 1937 .