Recent developments in multicomponent synthesis of structurally diversified tetrahydropyridines
暂无分享,去创建一个
[1] T. Kam,et al. Aspidofractinine and Eburnane Alkaloids from a North Borneo Kopsia. Ring-Contracted, Additional Ring-Fused, and Paucidactine-Type Aspidofractinine Alkaloids from K. pauciflora. , 2016, Journal of natural products.
[2] S. D. Guggilapu,et al. B(C6F5)3 as versatile catalyst: an efficient and mild protocol for the one-pot synthesis of functionalized piperidines and 2-substituted benzimidazole derivatives , 2015 .
[3] R. Bharti,et al. One-pot Synthesis of Highly Functionalized Tetrahydropyridines: A Camphoresulfonic Acid Catalyzed Multicomponent Reaction , 2015 .
[4] R. Bussmann,et al. Curare Alkaloids: Constituents of a Matis Dart Poison. , 2015, Journal of natural products.
[5] Xue Yang,et al. Supramolecular Inhibition of Neurodegeneration by a Synthetic Receptor. , 2015, ACS medicinal chemistry letters.
[6] M. Hou,et al. Alkaloids from Pandanus amaryllifolius: Isolation and Their Plausible Biosynthetic Formation. , 2015, Journal of natural products.
[7] J. Menéndez,et al. Expedient, catalyst-free, three-component synthesis of fused tetrahydropyridines in water , 2015 .
[8] Y. Wan,et al. The first example of glucose-containing carbene Brønsted acid synthesis and catalysis: efficient synthesis of five substituted tetrahydropyridines , 2015 .
[9] Yunyun Liu,et al. Enaminone-Based Three-Component Reactions for the Diastereoselective Synthesis of Fused Tetrahydropyridines , 2015 .
[10] Sanjio S. Zade,et al. L-Proline nitrate: a recyclable and green catalyst for the synthesis of highly functionalized piperidines , 2015 .
[11] O. Shishkin,et al. One-pot three-component synthesis of 3-cyano-4-methyl-2,6-dioxopyridine amino enones , 2015 .
[12] K. El-Bayouki,et al. Silica Sulfuric Acid: An Efficient, Reusable, Heterogeneous Catalyst for the One-Pot, Five-Component Synthesis of Highly Functionalized Piperidine Derivatives , 2015 .
[13] Xavier Bugaut,et al. Organocatalytic multicomponent synthesis of enantioenriched polycyclic 1,2,3,4-tetrahydropyridines: key substrate selection enabling regio- and stereoselectivities. , 2015, Chemical communications.
[14] Melinda M. Mulvihill,et al. Selective inhibitor of platelet-activating factor acetylhydrolases 1b2 and 1b3 that impairs cancer cell survival. , 2015, ACS chemical biology.
[15] M. Maghsoodlou,et al. Tartaric acid: a natural, green and highly efficient catalyst for the one-pot synthesis of functionalized piperidines , 2015, Research on Chemical Intermediates.
[16] S. Santra,et al. Solvent-free silica-promoted multicomponent condensation: synthesis of highly functionalized piperidines , 2015, Research on Chemical Intermediates.
[17] D. Enders,et al. Asymmetric Synthesis of Tetrahydropyridines via an Organocatalytic One-Pot Multicomponent Michael/Aza-Henry/Cyclization Triple Domino Reaction , 2014, Organic letters.
[18] V. Dotsenko,et al. Design and synthesis of pyrido[2,1-b][1,3,5]thiadiazine library via uncatalyzed Mannich-type reaction. , 2014, ACS combinatorial science.
[19] Yunyun Liu,et al. Diastereoselective construction of tetrahydropyridine fused bicyclic structures via three-component domino reaction. , 2014, The Journal of organic chemistry.
[20] V. Kouznetsov,et al. Diastereoselective synthesis of dihydroisoindolo[2,1-a]quinolin-11-ones by solvent-free AMCell-SO₃H-catalyzed imino Diels-Alder/intramolecular amide cyclization cascade reactions. , 2014, The Journal of organic chemistry.
[21] K. Sundaramoorthy,et al. Metal-Free, One-Pot, Rapid Synthesis of Tetrahydropyridines Using Acetic Acid as Solvent and Catalyst at Room Temperature , 2014 .
[22] S. M. Baghbanian,et al. H(3)PW(12)O(40)-catalyzed multicomponent reaction for efficient synthesis of highly substituted piperidines. , 2013, Combinatorial chemistry & high throughput screening.
[23] S. Patra,et al. Synthesis of fused tetrahydropyrido[2,3-c]coumarin derivatives as potential inhibitors for dopamine d3 receptors, catalyzed by hydrated ferric sulfate , 2014 .
[24] G. Georg,et al. Lithium Perchlorate-, Acetic Anhydride-, and Triphenylphosphine-assisted Multicomponent Syntheses of 4-Unsubstituted 2,5-Dioxooctahydroquinoline-3-carboxylates and 3-carbonitriles. , 2013, Tetrahedron.
[25] E. Rajanarendar,et al. Green Chemistry Approach to Fast and Highly Efficient One-Pot Synthesis of Bis-Isoxazolyl-1,2,5,6-Tetrahydro Pyridine-3-Carboxylates , 2013 .
[26] Hong Wang,et al. Sc(OTf)3-catalyzed three-component cyclization of arylamines, β,γ-unsaturated α-ketoesters, and 1,3-dicarbonyl compounds for the synthesis of highly substituted 1,4-dihydropyridines and tetrahydropyridines. , 2013, The Journal of organic chemistry.
[27] L. Dwoskin,et al. Structural modifications to tetrahydropyridine-3-carboxylate esters en route to the discovery of M5-preferring muscarinic receptor orthosteric antagonists. , 2013, Journal of medicinal chemistry.
[28] M. Ghashang,et al. Multicomponent preparation of highly functionalized piperidines using magnesium hydrogen sulfate as an efficient catalyst , 2013, Research on Chemical Intermediates.
[29] N. Jain,et al. Synthesis and Antiproliferative Activity of Polysubstituted Tetrahydropyridine and Piperidin‐4‐one‐3‐carboxylate Derivatives , 2012 .
[30] M. Ghashang. Zinc Hydrogen Sulfate Promoted Multi-component Preparation of Highly Functionalized Piperidines , 2012 .
[31] S. Perumal,et al. Facile domino reactions in the statistically controlled product- and stereoselective synthesis of densely functionalized cis-1,4-cyclohexa-1,4-dienes and trans,trans-trisubstituted-1,2,5,6-tetrahydropyridines , 2012 .
[32] V. Sathesh,et al. LaCl3·7H2O as an Efficient Catalyst for One-Pot Synthesis of Highly Functionalized Piperidines via Multi-component Organic Reactions , 2012, Catalysis Letters.
[33] Ming Li,et al. Modulating the reactivity of functionalized N,S-ketene acetal in MCR: selective synthesis of tetrahydropyridines and thiochromeno[2,3-b]pyridines via DABCO-catalyzed tandem annulation. , 2012, The Journal of organic chemistry.
[34] G. Brahmachari,et al. Bismuth nitrate-catalyzed multicomponent reaction for efficient and one-pot synthesis of densely functionalized piperidine scaffolds at room temperature , 2012 .
[35] S. Martin,et al. Libraries of 2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-amine derivatives via a multicomponent assembly process/1,3-dipolar cycloaddition strategy. , 2012, ACS combinatorial science.
[36] Y. Jeong,et al. One-pot synthesis of highly diversified tetrahydropyridines by tandem condensation of aldehydes, amines, and β-ketoesters , 2012 .
[37] Lokman H. Choudhury,et al. VCl3 catalyzed imine-based multicomponent reactions for the facile access of functionalized tetrahydropyridines and β-amino carbonyls , 2012, Molecular Diversity.
[38] C. Mukhopadhyay,et al. First report of syn isomers in the diastereoselective synthesis of highly functionalized piperidines catalysed by wet picric acid: factors influencing the syn–anti ratios , 2011 .
[39] Qun-yan Wu,et al. Molecular Diversity of Three‐Component Reactions of Aromatic Aldehydes, Arylamines, and Acetylenedicarboxylates , 2011 .
[40] R. Ghosh,et al. Efficient one-pot synthesis of functionalized piperidine scaffolds via ZrOCl2·8H2O catalyzed tandem reactions of aromatic aldehydes with amines and acetoacetic esters , 2011 .
[41] Peng‐Fei Xu,et al. Organocatalytic enantioselective multicomponent cascade reaction: facile access to tetrahydropyridines with C3 all-carbon quaternary stereocenters , 2011 .
[42] S. Martin,et al. Facile and unified approach to skeletally diverse, privileged scaffolds. , 2011, Organic letters.
[43] Hong-juan Wang,et al. Cerium ammonium nitrate-catalyzed multicomponent reaction for efficient synthesis of functionalized tetrahydropyridines. , 2011, ACS combinatorial science.
[44] Huanfeng Jiang,et al. l-Proline-catalyzed five-component domino reaction leading to multifunctionalized 1,2,3,4-tetrahydropyridines , 2010 .
[45] A. T. Khan,et al. Iodine catalyzed one-pot five-component reactions for direct synthesis of densely functionalized piperidines , 2010 .
[46] A. T. Khan,et al. Synthesis of highly functionalized piperidines by one-pot multicomponent reaction using tetrabutylammonium tribromide (TBATB) , 2010 .
[47] Pedro M. P. Gois,et al. Boronic acids and esters in the Petasis-borono Mannich multicomponent reaction. , 2010, Chemical reviews.
[48] M. Hayashi,et al. Leucoridines A-D, cytotoxic Strychnos-Strychnos bisindole alkaloids from Leuconotis. , 2010, Journal of natural products.
[49] Y. Perumal,et al. A facile synthesis and discovery of highly functionalized tetrahydro-pyridines and pyridines as antimycobacterial agents. , 2010, Chemical & pharmaceutical bulletin.
[50] Miguel Peña‐López,et al. A versatile enantioselective synthesis of barrenazines. , 2010, Organic letters.
[51] Kan Wang,et al. Cyanoacetamide MCR (III): three-component Gewald reactions revisited. , 2010, Journal of combinatorial chemistry.
[52] J. Menéndez,et al. Efficient generation of highly functionalized fused oxazepine frameworks based on a CAN-catalyzed four-component tetrahydropyridine synthesis/ring-closing metathesis sequence. , 2009, The Journal of organic chemistry.
[53] Huanfeng Jiang,et al. Hydroalkylation leading to heterocyclic compounds (Part 2): practical synthesis of polysubstituted 1,2,3,4-tetrahydropyridines through multicomponent reactions (MCRs) , 2009 .
[54] S. Katsumura,et al. Efficient synthesis of 2,4,5-trisubstituted 2,5-chiral tetrahydropyridines using a one-pot asymmetric azaelectrocyclization protocol. , 2009, Chemical communications.
[55] J. Menéndez,et al. A very efficient cerium(IV) ammonium nitrate catalyzed, four-component synthesis of tetrahydropyridines and its application in the concise generation of functionalized homoquinolizine frameworks. , 2009, Chemistry.
[56] S. Khanum,et al. Benzophenone-N-ethyl piperidine ether analogues--synthesis and efficacy as anti-inflammatory agent. , 2009, Bioorganic & medicinal chemistry letters.
[57] J. Pandey,et al. Organocatalyzed highly atom economic one pot synthesis of tetrahydropyridines as antimalarials. , 2009, Bioorganic & medicinal chemistry.
[58] Y. Sasson,et al. Phase transfer methodology for the synthesis of substituted stilbenes under Knoevenagel condensation condition , 2008 .
[59] A. T. Khan,et al. Effects of substituents in the beta-position of 1,3-dicarbonyl compounds in bromodimethylsulfonium bromide-catalyzed multicomponent reactions: a facile access to functionalized piperidines. , 2008, The Journal of organic chemistry.
[60] B. Ganem,et al. Multicomponent reaction design: a one-pot route to substituted di-O-acylglyceric acid amides from α-diazoketones , 2008 .
[61] David O. Miller,et al. Povarov reactions involving 3-aminocoumarins: synthesis of 1,2,3,4-tetrahydropyrido[2,3-c]coumarins and pyrido[2,3-c]coumarins. , 2008, The Journal of organic chemistry.
[62] M. Thompson,et al. Versatile assembly of 5-aminothiazoles based on the Ugi four-component coupling , 2008 .
[63] M. Rueping,et al. A highly enantioselective Brønsted acid catalyzed reaction cascade. , 2008, Angewandte Chemie.
[64] 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.
[65] B. Kaafarani,et al. Synthesis and metal-binding studies of a novel pyrene discotic , 2008 .
[66] M. Shi,et al. Lewis acid-catalyzed Prins-type reactions of methylenecyclopropylcarbinols with aldehydes and aldimines , 2008 .
[67] A. Whitwood,et al. Pot, atom and step economic (PASE) synthesis of highly functionalized piperidines: a five-component condensation , 2007 .
[68] T. Müller,et al. Multi-component syntheses of heterocycles by transition-metal catalysis. , 2007, Chemical Society reviews.
[69] H. Waldmann,et al. Optimization of three- and four-component reactions for polysubstituted piperidines: application to the synthesis and preliminary biological screening of a prototype library. , 2007, Journal of combinatorial chemistry.
[70] C. Avendaño,et al. The first aza Diels-Alder reaction involving an alpha,beta-unsaturated hydrazone as the dienophile: stereoselective synthesis of C-4 functionalized 1,2,3,4-tetrahydroquinolines containing a quaternary stereocenter. , 2007, Organic & biomolecular chemistry.
[71] Thomas Hermann,et al. Synthesis and SAR of 3,5-diamino-piperidine derivatives: novel antibacterial translation inhibitors as aminoglycoside mimetics. , 2007, Bioorganic & medicinal chemistry letters.
[72] D. Tejedor,et al. Chemo-differentiating ABB' multicomponent reactions. Privileged building blocks. , 2007, Chemical Society reviews.
[73] C. Ramalingan,et al. Synthesis, stereochemistry, and antimicrobial evaluation of substituted piperidin-4-one oxime ethers. , 2006, European journal of medicinal chemistry.
[74] S. Perumal,et al. Synthesis, stereochemistry, and antimicrobial activity of 2,6-diaryl-3-(arylthio)piperidin-4-ones. , 2006, Chemical & pharmaceutical bulletin.
[75] Madhavi Gangapuram,et al. Synthesis of 1-(Substituted Phenylcarbonyl/sulfonylamino)-1,2,3,6-tetrahydropyridine-5-carboxylic acid diethylamides as Potential Anti-inflammatory Agents. , 2006, Journal of heterocyclic chemistry.
[76] Alexander Dömling,et al. Recent developments in isocyanide based multicomponent reactions in applied chemistry. , 2006, Chemical reviews.
[77] P. Ramachandran,et al. Chiral synthesis of functionalized tetrahydropyridines: gamma-aminobutyric acid uptake inhibitor analogues. , 2005, The Journal of organic chemistry.
[78] J. Díaz,et al. Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines. , 2005, Journal of combinatorial chemistry.
[79] J. Moseley. Alternative esters in the synthesis of ZD0947 , 2005 .
[80] J. Díaz,et al. Dihydropyridine-based MCRs. New reaction pathways in the interaction with ethyl glyoxalate and non-aromatic amines , 2003 .
[81] David A. Powell,et al. Lanthanide(III)-catalyzed multi-component aza-Diels–Alder reaction of aliphatic N-arylaldimines with cyclopentadiene , 2003 .
[82] D. Hall,et al. A three-component reaction for diversity-oriented synthesis of polysubstituted piperidines: solution and solid-phase optimization of the first tandem aza[4+2]/allylboration. , 2003, Chemistry.
[83] A J Elliott,et al. Systematic structure-based design and stereoselective synthesis of novel multisubstituted cyclopentane derivatives with potent antiinfluenza activity. , 2001, Journal of medicinal chemistry.
[84] J. Peyronel,et al. A new multicomponent domino reaction of 1,3-dicarbonyl compounds: one-pot access to polycyclic N/O-, N/S-, and N/N-aminals. , 2001, Organic letters.
[85] J. Stables,et al. Synthesis and structure-activity relationships of potential anticonvulsants based on 2-piperidinecarboxylic acid and related pharmacophores. , 2001, European journal of medicinal chemistry.
[86] I. Ugi,et al. Multicomponent Reactions with Isocyanides. , 2000, Angewandte Chemie.
[87] Michael D B Swedberg,et al. 3-(5-Alkylamino-4-isoxazolyl)-1,2,5,6-tetrahydropyridines: a novel class of central nicotinic receptor ligands. , 1998, Bioorganic & medicinal chemistry.
[88] T. Heffner,et al. Aryl 1-but-3-ynyl-4-phenyl-1,2,3,6-tetrahydropyridines as potential antipsychotic agents: synthesis and structure-activity relationships. , 1996, Journal of medicinal chemistry.
[89] K. Redda,et al. Synthesis of some N‐[pyridyl(phenyl)carbonylamino]hydroxyalkyl‐(benzyl)‐1,2,3,6‐tetrahydropyridines as potential anti‐inflammatory agents , 1995 .
[90] Y. Kita,et al. Stereochemistry of the 2-hydroxy-1,2,3,4-tetrahydropyridine intermediate of hantzsch cyclization , 1993 .
[91] P. Simon,et al. Synthèses et activités psychotropes de 3,4-diarylpipéridines. Corrélation structure-activité et recherche d'une activité antihypertensive , 1991 .
[92] M. Taylor,et al. 2-(2-Aryl-2-oxoethylidene)-1,2,3,4-tetrahydropyridines. Novel isomers of 1,4-dihydropyridine calcium channel blockers. , 1988, Journal of medicinal chemistry.
[93] A. Brossi,et al. Synthesis and dihydropteridine reductase inhibitory effects of potential metabolites of the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. , 1985, Journal of medicinal chemistry.
[94] E. Knaus,et al. Synthesis of N-[[(substituted-phenyl)carbonyl]amino]-1,2,3,6-tetrahydropyridines with analgesic and hyperglycemic activity. , 1982, Journal of medicinal chemistry.
[95] K. Gewald,et al. Heterocyclen aus CH‐aciden Nitrilen, VIII. 2‐Amino‐thiophene aus methylenaktiven Nitrilen, Carbonylverbindungen und Schwefel , 1966 .