메뉴 건너뛰기




Volumn 14, Issue 3, 2012, Pages 224-230

4-Dimethylamino pyridine-promoted one-pot three-component regioselective synthesis of highly functionalized 4 H -thiopyrans via heteroannulation of β-oxodithioesters

Author keywords

oxodithioesters; 4 dimethylaminopyridine; 4H Thiopyrans; ethyl methyl cyanoacetate; malononitrile; regioselective heteroannulation

Indexed keywords

AMINE; ESTER; PYRAN DERIVATIVE; PYRIDINE DERIVATIVE; THIOL DERIVATIVE; THIOPYRAN;

EID: 84858120143     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co200203e     Document Type: Article
Times cited : (45)

References (82)
  • 1
    • 0034678033 scopus 로고    scopus 로고
    • Target-oriented and diversity-oriented organic synthesis in drug discovery
    • DOI 10.1126/science.287.5460.1964
    • Schreiber, S. L. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery Science 2000, 287, 1964-1969 (Pubitemid 30158663)
    • (2000) Science , vol.287 , Issue.5460 , pp. 1964-1969
    • Schreiber, S.L.1
  • 3
    • 33750309194 scopus 로고
    • Atom Economy-A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
    • Trost, B. M. Atom Economy-A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way Angew. Chem., Int. Ed. Engl. 1995, 34, 259-281
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 259-281
    • Trost, B.M.1
  • 4
    • 7044235263 scopus 로고    scopus 로고
    • Domino reactions in organic synthesis
    • Tietze, L. F. Domino Reactions in Organic Synthesis Chem. Rev. 1996, 96, 115-136 (Pubitemid 126637714)
    • (1996) Chemical Reviews , vol.96 , Issue.1 , pp. 115-136
    • Tietze, L.F.1
  • 5
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • DOI 10.1021/cr0505728
    • Domling, A. Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry Chem. Rev. 2006, 106, 17-89 (Pubitemid 43159621)
    • (2006) Chemical Reviews , vol.106 , Issue.1 , pp. 17-89
    • Domling, A.1
  • 6
    • 34250627489 scopus 로고    scopus 로고
    • Multicomponent Syntheses of Heterocycles by Transition-Metal Catalysis
    • D'Souza, D. M.; Muller, T. J. J. Multicomponent Syntheses of Heterocycles by Transition-Metal Catalysis Chem. Soc. Rev. 2007, 36, 1095-1108
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1095-1108
    • D'Souza, D.M.1    Muller, T.J.J.2
  • 7
    • 58049196954 scopus 로고    scopus 로고
    • Rapid Synthesis of 1,3,4,4-Tetrasubstituted Beta-Lactams from Methyleneaziridines using a Four-Component Reaction
    • Cariou, C. C. A.; Clarkson, G. J.; Shipman, M. Rapid Synthesis of 1,3,4,4-Tetrasubstituted Beta-Lactams from Methyleneaziridines using a Four-Component Reaction J. Org. Chem. 2008, 73, 9762-9764
    • (2008) J. Org. Chem. , vol.73 , pp. 9762-9764
    • Cariou, C.C.A.1    Clarkson, G.J.2    Shipman, M.3
  • 8
    • 77958034343 scopus 로고    scopus 로고
    • Boronic Acids and Esters in the Petasis-Borono Mannich Multicomponent Reaction
    • Pedro, M. P. G; Pedro, M. S. D. C.; Montalbano, F.; Candeias, N. R. Boronic Acids and Esters in the Petasis-Borono Mannich Multicomponent Reaction Chem. Rev. 2010, 110, 6169-6193
    • (2010) Chem. Rev. , vol.110 , pp. 6169-6193
    • Pedro, M.P.G.1    Pedro, M.S.D.C.2    Montalbano, F.3    Candeias, N.R.4
  • 9
    • 78249272919 scopus 로고    scopus 로고
    • One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multicomponent Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium, and Amines
    • Artemev, A. V.; Gusarova, N. K.; Malysheva, S. F.; Mamatyuk, V. I.; Gatilov, Y. V.; Ushakov, I. A.; Trofimov, B. A. One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multicomponent Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium, and Amines Eur. J. Org. Chem. 2010, 6157-6160
    • (2010) Eur. J. Org. Chem. , pp. 6157-6160
    • Artemev, A.V.1    Gusarova, N.K.2    Malysheva, S.F.3    Mamatyuk, V.I.4    Gatilov, Y.V.5    Ushakov, I.A.6    Trofimov, B.A.7
  • 10
    • 78650822243 scopus 로고    scopus 로고
    • Tandem Ugi MCR/Mitsunobu Cyclization as a Short, Protecting-Group-Free Route to Benzoxazinones with Four Diversity Points
    • Banfi, L.; Basso, A.; Giardini, L.; Riva, R.; Rocca, V.; Guanti, G. Tandem Ugi MCR/Mitsunobu Cyclization as a Short, Protecting-Group-Free Route to Benzoxazinones with Four Diversity Points Eur. J. Org. Chem. 2011, 100-109
    • (2011) Eur. J. Org. Chem. , pp. 100-109
    • Banfi, L.1    Basso, A.2    Giardini, L.3    Riva, R.4    Rocca, V.5    Guanti, G.6
  • 11
    • 73349112251 scopus 로고    scopus 로고
    • Four-Component Synthesis of Fully Substituted 1,2,4-Triazoles
    • Staben, S. T.; Blaquiere, N. Four-Component Synthesis of Fully Substituted 1,2,4-Triazoles Angew. Chem., Int. Ed. 2010, 49, 325-328
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 325-328
    • Staben, S.T.1    Blaquiere, N.2
  • 12
    • 70350728705 scopus 로고    scopus 로고
    • Catalytic Asymmetric Passerini-Type Reaction: Chiral Aluminum- Organophosphate-Catalyzed Enantioselective Alpha-addition of Isocyanides to Aldehydes
    • Yue, T.; Wang, M.-X.; Wang, D.-X.; Masson, G.; Zhu, J. Catalytic Asymmetric Passerini-Type Reaction: Chiral Aluminum-Organophosphate-Catalyzed Enantioselective Alpha-addition of Isocyanides to Aldehydes J. Org. Chem. 2009, 74, 8396-8399
    • (2009) J. Org. Chem. , vol.74 , pp. 8396-8399
    • Yue, T.1    Wang, M.-X.2    Wang, D.-X.3    Masson, G.4    Zhu, J.5
  • 14
    • 77955220034 scopus 로고    scopus 로고
    • New Multicomponent Domino Reactions (MDRs) in Water: Highly Chemo-, Regio- and Stereoselective Synthesis of Spiro{[1,3]dioxanopyridine}-4,6-diones and Pyrazolo[3,4-b]pyridines
    • Ma, N.; Jiang, B.; Zhang, G.; Tu, S.-J.; Wever, W.; Li, G. New Multicomponent Domino Reactions (MDRs) in Water: Highly Chemo-, Regio- and Stereoselective Synthesis of Spiro{[1,3]dioxanopyridine}-4,6-diones and Pyrazolo[3,4-b]pyridines Green Chem. 2010, 12, 1357-1361
    • (2010) Green Chem. , vol.12 , pp. 1357-1361
    • Ma, N.1    Jiang, B.2    Zhang, G.3    Tu, S.-J.4    Wever, W.5    Li, G.6
  • 15
    • 79959907066 scopus 로고    scopus 로고
    • Multicomponent Reaction Design in the Quest for Molecular Complexity and Diversity
    • Ruijter, E.; Scheffelaar, R.; Orru, R. V. A. Multicomponent Reaction Design in the Quest for Molecular Complexity and Diversity Angew. Chem., Int. Ed. 2011, 50, 6234-6246
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6234-6246
    • Ruijter, E.1    Scheffelaar, R.2    Orru, R.V.A.3
  • 16
    • 23744449320 scopus 로고    scopus 로고
    • Palladium-catalyzed one-pot synthesis of highly substituted furans by a three-component annulation reaction
    • DOI 10.1021/jo050908d
    • Duan, X.-H.; Liu, X.-Y.; Guo, L.-N.; Liao, M.-C.; Liu, W.-M.; Liang, Y.-M. Palladium-Catalyzed One-Pot Synthesis of Highly Substituted Furans by a Three-Component Annulation Reaction J. Org. Chem. 2005, 70, 6980-6983 (Pubitemid 41135942)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.17 , pp. 6980-6983
    • Duan, X.-H.1    Liu, X.-Y.2    Guo, L.-N.3    Liao, M.-C.4    Liu, W.-M.5    Liang, Y.-M.6
  • 17
    • 35548982665 scopus 로고    scopus 로고
    • New light on an old story: Facile and efficient synthesis of 1,3-diaryl-5-spirohexahydropyrimidines via a six-molecule, three-component mannich-type reaction
    • DOI 10.1021/jo7016235
    • Wei, H.-L.; Yan, Z.-Y.; Niu, Y.-N.; Li, G.-Q.; Liang, Y.-M. New Light on an Old Story: Facile and Efficient Synthesis of 1,3-Diaryl-5- spirohexahydropyrimidines via a Six-Molecule, Three-Component Mannich-Type Reaction J. Org. Chem. 2007, 72, 8600-8603 (Pubitemid 350012889)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.22 , pp. 8600-8603
    • Wei, H.-L.1    Yan, Z.-Y.2    Niu, Y.-N.3    Li, G.-Q.4    Liang, Y.-M.5
  • 18
    • 45549084559 scopus 로고    scopus 로고
    • Copper-Catalyzed Multicomponent Reaction: Facile Access to Novel Phosphorus Amidines
    • Cui, S.-L.; Wang, J.; Wang, Y.-G. Copper-Catalyzed Multicomponent Reaction: Facile Access to Novel Phosphorus Amidines Org. Lett. 2008, 10, 1267-1269
    • (2008) Org. Lett. , vol.10 , pp. 1267-1269
    • Cui, S.-L.1    Wang, J.2    Wang, Y.-G.3
  • 19
    • 77249090233 scopus 로고    scopus 로고
    • Bronsted Base-Catalyzed One-Pot Three-Component Biginelli-Type Reaction: An Efficient Synthesis of 4,5,6-Triaryl-3,4-dihydropyrimidin-2(1H)-one and Mechanistic Study
    • Shen, Z.-L.; Xu, X.-P.; Ji, S.-J. Bronsted Base-Catalyzed One-Pot Three-Component Biginelli-Type Reaction: An Efficient Synthesis of 4,5,6-Triaryl-3,4-dihydropyrimidin-2(1H)-one and Mechanistic Study J. Org. Chem. 2010, 75, 1162-1167
    • (2010) J. Org. Chem. , vol.75 , pp. 1162-1167
    • Shen, Z.-L.1    Xu, X.-P.2    Ji, S.-J.3
  • 20
    • 77949402431 scopus 로고    scopus 로고
    • Cooperative Catalysis in Multicomponent Reactions: Highly Enantioselective Synthesis of γ-Hydroxyketones with a Quaternary Carbon Stereocenter
    • Guan, X.-Y.; Yang, L.-P.; Hu, W. Cooperative Catalysis in Multicomponent Reactions: Highly Enantioselective Synthesis of γ-Hydroxyketones with a Quaternary Carbon Stereocenter Angew. Chem., Int. Ed. 2010, 49, 2190-2192
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 2190-2192
    • Guan, X.-Y.1    Yang, L.-P.2    Hu, W.3
  • 21
    • 77956483548 scopus 로고    scopus 로고
    • A Cobalt-Catalyzed Multicomponent Approach to Novel 2,3-Di- and 2,2,3-Trisubstituted 3-Methoxycarbonyl-γ-butyrolact-ones
    • Floch, C. L.; Gall, E. L.; Léonel, E.; Koubaa, J.; Martens, T.; Retailleau, P. A Cobalt-Catalyzed Multicomponent Approach to Novel 2,3-Di- and 2,2,3-Trisubstituted 3-Methoxycarbonyl-γ-butyrolact-ones Eur. J. Org. Chem. 2010, 5279-5286
    • (2010) Eur. J. Org. Chem. , pp. 5279-5286
    • Floch, C.L.1    Gall, E.L.2    Léonel, E.3    Koubaa, J.4    Martens, T.5    Retailleau, P.6
  • 22
    • 35548975293 scopus 로고    scopus 로고
    • Applications of Multicomponent Reactions for the Synthesis of Diverse Heterocyclic Scaffolds
    • Sunderhaus, J. D.; Dockendorff, C.; Martin, S. F. Applications of Multicomponent Reactions for the Synthesis of Diverse Heterocyclic Scaffolds Org. Lett. 2007, 9, 4223-4226
    • (2007) Org. Lett. , vol.9 , pp. 4223-4226
    • Sunderhaus, J.D.1    Dockendorff, C.2    Martin, S.F.3
  • 23
    • 77951002240 scopus 로고    scopus 로고
    • A Straight-forward Three-Component Synthesis of α-Amino Esters Containing a Phenylalanine or a Phenylglycine Scaffold
    • Haurena, C.; Gall, E. L.; Sengmany, S.; Martens, T.; Troupel, M. A Straight-forward Three-Component Synthesis of α-Amino Esters Containing a Phenylalanine or a Phenylglycine Scaffold J. Org. Chem. 2010, 75, 2645-2650
    • (2010) J. Org. Chem. , vol.75 , pp. 2645-2650
    • Haurena, C.1    Gall, E.L.2    Sengmany, S.3    Martens, T.4    Troupel, M.5
  • 24
    • 52249112156 scopus 로고    scopus 로고
    • Regioselective Three-Component Synthesis of Highly Fluorescent 1,3,5-Trisubstituted Pyrazoles
    • Willy, B.; Muller, T. J. J. Regioselective Three-Component Synthesis of Highly Fluorescent 1,3,5-Trisubstituted Pyrazoles Eur. J. Org. Chem. 2008, 4157-4168
    • (2008) Eur. J. Org. Chem. , pp. 4157-4168
    • Willy, B.1    Muller, T.J.J.2
  • 25
    • 50849126505 scopus 로고    scopus 로고
    • A Novel and Facile Synthesis of 2-(Cyclohexylamino)-6,7-dihydro-3-aryl- 1H-indol-4(5 H)-ones via a One-pot Multicomponent Reaction
    • Heravi, M. M.; Baghernejad, B.; Oskooie, H. A.; Hekmatshoar, R. A Novel and Facile Synthesis of 2-(Cyclohexylamino)-6,7-dihydro-3-aryl-1H-indol-4(5 H)-ones via a One-pot Multicomponent Reaction Tetrahedron Lett. 2008, 49, 6101-6103
    • (2008) Tetrahedron Lett. , vol.49 , pp. 6101-6103
    • Heravi, M.M.1    Baghernejad, B.2    Oskooie, H.A.3    Hekmatshoar, R.4
  • 26
    • 78049299019 scopus 로고    scopus 로고
    • Synthesis of 2-(Alkylamino)-5-{alkyl[(2-oxo-2 H -chromen-3-yl)carbonyl] amino}-3,4-furandicarboxylates using a Multicomponent Reaction in Water
    • Adib, M.; Sheikhi, E.; Kavoosi, A.; Bijanzadeh, H. R. Synthesis of 2-(Alkylamino)-5-{alkyl[(2-oxo-2 H -chromen-3-yl)carbonyl]amino}-3,4- furandicarboxylates using a Multicomponent Reaction in Water Tetrahedron 2010, 66, 9263-9269
    • (2010) Tetrahedron , vol.66 , pp. 9263-9269
    • Adib, M.1    Sheikhi, E.2    Kavoosi, A.3    Bijanzadeh, H.R.4
  • 27
    • 77954560523 scopus 로고    scopus 로고
    • Highly Enantioselective Construction of Spiro[4 H -pyran-3,3′- oxindoles] Through a Domino Knoevenagel/Michael/Cyclization Sequence Catalyzed by Cupreine
    • Chen, W.-B.; Wu, Z.-J.; Pei, Q.-L.; Cun, L.-F.; Zhang, X.-M.; Yuan, W.-C. Highly Enantioselective Construction of Spiro[4 H -pyran-3,3′-oxindoles] Through a Domino Knoevenagel/Michael/Cyclization Sequence Catalyzed by Cupreine Org. Lett. 2010, 12, 3132-3135
    • (2010) Org. Lett. , vol.12 , pp. 3132-3135
    • Chen, W.-B.1    Wu, Z.-J.2    Pei, Q.-L.3    Cun, L.-F.4    Zhang, X.-M.5    Yuan, W.-C.6
  • 28
    • 65249100749 scopus 로고    scopus 로고
    • Strategies for Innovation in Multicomponent Reaction Design
    • Ganem, B. Strategies for Innovation in Multicomponent Reaction Design Acc. Chem. Res. 2009, 42, 463-472
    • (2009) Acc. Chem. Res. , vol.42 , pp. 463-472
    • Ganem, B.1
  • 29
    • 70349156384 scopus 로고    scopus 로고
    • Natural Product Synthesis Using Multicomponent Reaction Strategies
    • Toure, B. B.; Hall, D. G. Natural Product Synthesis Using Multicomponent Reaction Strategies Chem. Rev. 2009, 109, 4439-4486
    • (2009) Chem. Rev. , vol.109 , pp. 4439-4486
    • Toure, B.B.1    Hall, D.G.2
  • 30
    • 74049098278 scopus 로고    scopus 로고
    • Use of Cyclohexylisocyanide and Methyl 2-Isocyanoacetate as Convertible Isocyanides for Microwave-Assisted Fluorous Synthesis of 1,4-Benzodiazepine-2,5- dione Library
    • Zhou, H.; Zhang, W.; Yan, B. Use of Cyclohexylisocyanide and Methyl 2-Isocyanoacetate as Convertible Isocyanides for Microwave-Assisted Fluorous Synthesis of 1,4-Benzodiazepine-2,5-dione Library J. Comb. Chem. 2010, 12, 206-214
    • (2010) J. Comb. Chem. , vol.12 , pp. 206-214
    • Zhou, H.1    Zhang, W.2    Yan, B.3
  • 31
    • 69049086649 scopus 로고    scopus 로고
    • Four-Component Domino Reaction Leading to Multifunctionalized Quinazolines
    • Jiang, B.; Tu, S.-J.; Kaur, P.; Wever, W.; Li, G. Four-Component Domino Reaction Leading to Multifunctionalized Quinazolines J. Am. Chem. Soc. 2009, 131, 11660-11661
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 11660-11661
    • Jiang, B.1    Tu, S.-J.2    Kaur, P.3    Wever, W.4    Li, G.5
  • 32
    • 78049510211 scopus 로고    scopus 로고
    • Efficient Generation of Biologically Active H-pyrazolo[5,1-a] isoquinolines via Multicomponent Reaction
    • Chen, Z.; Wu, J. Efficient Generation of Biologically Active H-pyrazolo[5,1-a]isoquinolines via Multicomponent Reaction Org. Lett. 2010, 12, 4856-4859
    • (2010) Org. Lett. , vol.12 , pp. 4856-4859
    • Chen, Z.1    Wu, J.2
  • 34
    • 78049517805 scopus 로고    scopus 로고
    • Green Synthesis of α, β - and β, β -Dipeptides under Solvent-Free Conditions
    • Hernández, J. G.; Juaristi, E. Green Synthesis of α, β-and β, β -Dipeptides under Solvent-Free Conditions J. Org. Chem. 2010, 75, 7107-7111
    • (2010) J. Org. Chem. , vol.75 , pp. 7107-7111
    • Hernández, J.G.1    Juaristi, E.2
  • 35
    • 78651366998 scopus 로고    scopus 로고
    • Mild and Efficient Barbier Allylation Reaction Mediated by Magnesium Powder under Solvent-free Conditions
    • Li, S.; Wang, J.-X.; Wen, X.; Ma, X. Mild and Efficient Barbier Allylation Reaction Mediated by Magnesium Powder Under Solvent-free Conditions Tetrahedron 2011, 67, 849-855
    • (2011) Tetrahedron , vol.67 , pp. 849-855
    • Li, S.1    Wang, J.-X.2    Wen, X.3    Ma, X.4
  • 37
    • 79751497330 scopus 로고    scopus 로고
    • An Expeditious, Highly Efficient, Catalyst-free and Solvent-free Synthesis of Nitroamines and Nitrosulfides by Michael Addition
    • Choudhary, G.; Peddinti, R. K. An Expeditious, Highly Efficient, Catalyst-free and Solvent-free Synthesis of Nitroamines and Nitrosulfides by Michael Addition Green Chem. 2011, 13, 276-282
    • (2011) Green Chem. , vol.13 , pp. 276-282
    • Choudhary, G.1    Peddinti, R.K.2
  • 38
    • 33746751482 scopus 로고    scopus 로고
    • Solvent and catalyst-free synthesis of polyphosphates
    • DOI 10.1039/b602462a
    • Iliescu, S.; Ilia, G.; Plesu, N.; Popa, A.; Pascariu, A. Solvent and Catalyst-free Synthesis of Polyphosphates Green Chem. 2006, 8, 727-730 (Pubitemid 44166514)
    • (2006) Green Chemistry , vol.8 , Issue.8 , pp. 727-730
    • Iliescu, S.1    Ilia, G.2    Plesu, N.3    Popa, A.4    Pascariu, A.5
  • 39
    • 78049381254 scopus 로고    scopus 로고
    • Three-Component Solvent-Free Synthesis of Highly Substituted Bicyclic Pyridines Containing a Ring-Junction Nitrogen
    • Yan, S.; Chen, Y.; Liu, L.; He, N.; Lin, J. Three-Component Solvent-Free Synthesis of Highly Substituted Bicyclic Pyridines Containing a Ring-Junction Nitrogen Green Chem. 2010, 12, 2043-2052
    • (2010) Green Chem. , vol.12 , pp. 2043-2052
    • Yan, S.1    Chen, Y.2    Liu, L.3    He, N.4    Lin, J.5
  • 40
    • 1542400198 scopus 로고
    • In; Katritzky, A. R. Rees, C. W. Pergamon: Oxford, U.K. Vol. p, and previous references cited therein.
    • Ingall, A. H. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R.; Rees, C. W., Eds.; Pergamon: Oxford, U.K., 1984; Vol. 3, p 885, and previous references cited therein.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 885
    • Ingall, A.H.1
  • 41
    • 0344258043 scopus 로고
    • Monocyclic Sulphur Containing Pyrones
    • previous references cited therein
    • Mayer, R.; Broy, W.; Zahradnik, R. Monocyclic Sulphur Containing Pyrones Adv. Heterocycl. Chem. 1967, 8, 219-276, and previous references cited therein
    • (1967) Adv. Heterocycl. Chem. , vol.8 , pp. 219-276
    • Mayer, R.1    Broy, W.2    Zahradnik, R.3
  • 42
  • 43
    • 0028223855 scopus 로고
    • AA1, a newly synthesized monovalent lipophilic cation, expresses potent in vivo antitumor activity
    • Sun, X.; Wong, J. R.; Song, K.; Hu, J.; Garlid, K. D.; Chen, L. B. AA1, a Newly Synthesized Monovalent Lipophilic Cation, Expresses Potent in vivo Antitumor Activity Cancer Res. 1994, 54, 1465-1471 (Pubitemid 24106407)
    • (1994) Cancer Research , vol.54 , Issue.6 , pp. 1465-1471
    • Sun, X.1    Wong, J.R.2    Song, K.3    Hu, J.4    Garlid, K.D.5    Chen, L.B.6
  • 45
    • 84891829198 scopus 로고
    • Chem. Abstr. 1994, 123, 169509.
    • (1994) Chem. Abstr. , vol.123 , pp. 169509
  • 47
    • 84906461238 scopus 로고    scopus 로고
    • Chem. Abstr. 2005, 142, 219151.
    • (2005) Chem. Abstr. , vol.142 , pp. 219151
  • 48
    • 84891826497 scopus 로고
    • Study of nitro derivatives with biological interest.XXXVII. Some pyran analogs of nitrobenzofurans and nitronaphthofurans
    • Daniel, D.; Rene, R. Study of nitro derivatives with biological interest.XXXVII. Some pyran analogs of nitrobenzofurans and nitronaphthofurans Eur. J. Med. Chem. 1984, 19, 477-479
    • (1984) Eur. J. Med. Chem. , vol.19 , pp. 477-479
    • Daniel, D.1    Rene, R.2
  • 50
    • 84891830648 scopus 로고
    • Chem. Abstr. 1978, 89, 43112.
    • (1978) Chem. Abstr. , vol.89 , pp. 43112
  • 51
    • 0035605816 scopus 로고    scopus 로고
    • Iodination and Metal Halogen Exchange of Aromatic Compounds: An Improved Preparation of a Key Oxazolidinone Antibiotic Intermediate
    • Herrinton, P. M.; Owen, C. E.; Gage, J. R. Iodination and Metal Halogen Exchange of Aromatic Compounds: An Improved Preparation of a Key Oxazolidinone Antibiotic Intermediate Org. Process Res. Dev. 2001, 5, 80-83
    • (2001) Org. Process Res. Dev. , vol.5 , pp. 80-83
    • Herrinton, P.M.1    Owen, C.E.2    Gage, J.R.3
  • 52
    • 84944041948 scopus 로고    scopus 로고
    • In; Katritzky, A. R. Rees, C. W. Scriven, E. F. V. Pergamon Press: Oxford, U.K. Vol.
    • Ingall, A. H. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R., Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon Press: Oxford, U.K., 1996; Vol. 5, p 501.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.5 , pp. 501
    • Ingall, A.H.1
  • 53
    • 0013424606 scopus 로고
    • Cyclic Sulfides in Organic Synthesis
    • Vedejs, E.; Krafft, G. A. Cyclic Sulfides in Organic Synthesis Tetrahedron 1982, 38, 2857-2881
    • (1982) Tetrahedron , vol.38 , pp. 2857-2881
    • Vedejs, E.1    Krafft, G.A.2
  • 54
    • 0001109658 scopus 로고
    • The Synthesis of 2,3-Disubstituted Cyclopentenones Using the Ramberg-Baecklund Reaction in Conjunction with Organocopper Chemistry
    • Casy, G.; Taylor, R. J. K. The Synthesis of 2,3-Disubstituted Cyclopentenones Using the Ramberg-Baecklund Reaction in Conjunction with Organocopper Chemistry Tetrahedron 1989, 45, 455-466
    • (1989) Tetrahedron , vol.45 , pp. 455-466
    • Casy, G.1    Taylor, R.J.K.2
  • 55
    • 33750878006 scopus 로고    scopus 로고
    • Thiopyran route to polypropionates: An efficient synthesis of serricornin
    • DOI 10.1021/jo061747w
    • Ward, D. E.; Jheengut, V.; Beye, G. E. Thiopyran Route to Polypropionates: An Efficient Synthesis of Serricornin J. Org. Chem. 2006, 71, 8989-8992 (Pubitemid 44721982)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.23 , pp. 8989-8992
    • Ward, D.E.1    Jheengut, V.2    Beye, G.E.3
  • 57
    • 37049077081 scopus 로고
    • Preparation of Thiathromboxane Analogs and Formal Total Synthesis of Dithiathromboxane A2 Based on Conjugate Addition Reactions of Thiin-4-ones
    • Casy, G.; Lane, S.; Taylor, R. J. K. Preparation of Thiathromboxane Analogs and Formal Total Synthesis of Dithiathromboxane A2 Based on Conjugate Addition Reactions of Thiin-4-ones J. Chem. Soc., Perkin Trans 1 1986, 1397-1404
    • (1986) J. Chem. Soc., Perkin Trans 1 , pp. 1397-1404
    • Casy, G.1    Lane, S.2    Taylor, R.J.K.3
  • 58
    • 0035808969 scopus 로고    scopus 로고
    • The synthesis of polyoxygenated, enantiopure cyclopentene derivatives using the Ramberg-Bäcklund rearrangement
    • DOI 10.1016/S0040-4039(00)02209-7, PII S0040403900022097
    • McAllister, G. D.; Taylor, R. J. K. The Synthesis of Polyoxygenated, Enantiopure Cyclopentene Derivatives Using the Ramberg-Backlund Rearrangement Tetrahedron Lett. 2001, 42, 1197-1200 (Pubitemid 32149877)
    • (2001) Tetrahedron Letters , vol.42 , Issue.6 , pp. 1197-1200
    • McAllister, G.D.1    Taylor, R.J.K.2
  • 60
    • 0033532517 scopus 로고    scopus 로고
    • The first catalytic, highly enantioselective hetero-Diels-Alder reaction of thiabutadienes
    • Saito, T.; Takekawa, K.; Takahashi, T. The First Catalytic, Highly Enantioselective Hetero-Diels-Alder Reaction of Thiabutadienes Chem. Commun. 1999, 1001-1002 (Pubitemid 29259708)
    • (1999) Chemical Communications , Issue.11 , pp. 1001-1002
    • Saito, T.1    Takekawa, K.2    Takahashi, T.3
  • 61
    • 33744781814 scopus 로고    scopus 로고
    • Microwave-promoted one-pot synthesis of 4H-thiopyrans from α,β-unsaturated ketones via a three-component reaction
    • DOI 10.1016/j.tetlet.2006.05.020, PII S0040403906009300
    • Barthakur, M. G.; Chetia, A.; Boruah, R. C. Microwave-Promoted One-Pot Synthesis of 4 H -Thiopyrans from α, β -Unsaturated Ketones via a Three-Component Reaction Tetrahedron Lett. 2006, 47, 4925-4927 (Pubitemid 43831113)
    • (2006) Tetrahedron Letters , vol.47 , Issue.28 , pp. 4925-4927
    • Barthakur, M.G.1    Chetia, A.2    Boruah, R.C.3
  • 63
    • 58849122180 scopus 로고    scopus 로고
    • Ionic Liquid Promoted Preparation of 4 H -Thiopyran and Pyrimidine Nucleoside-Thiopyran Hybrids Through One-Pot Multicomponent Reaction of Thioamide
    • Zhang, X.; Li, X.; Fan, X.; Wang, X.; Li, D.; Qu, G.; Wang, J. Ionic Liquid Promoted Preparation of 4 H -Thiopyran and Pyrimidine Nucleoside-Thiopyran Hybrids Through One-Pot Multicomponent Reaction of Thioamide Mol. Diversity 2009, 13, 57-61
    • (2009) Mol. Diversity , vol.13 , pp. 57-61
    • Zhang, X.1    Li, X.2    Fan, X.3    Wang, X.4    Li, D.5    Qu, G.6    Wang, J.7
  • 64
    • 44549083347 scopus 로고    scopus 로고
    • MWI-Promoted Preparation of 4 H -Thiopyran Derivatives Through One-Pot Multicomponent Reactions
    • Fan, X.; Wang, X.; Zhang, X.; Li, X.; Qu, G. MWI-Promoted Preparation of 4 H -Thiopyran Derivatives Through One-Pot Multicomponent Reactions J. Chem. Res. 2007, 693-695
    • (2007) J. Chem. Res. , pp. 693-695
    • Fan, X.1    Wang, X.2    Zhang, X.3    Li, X.4    Qu, G.5
  • 65
    • 33744766551 scopus 로고    scopus 로고
    • Reaction of 3-aryl-2-cyanothioacrylamides with dimethyl acetylenecarboxylate, methyl propiolate, and N-phenylmaleimide
    • DOI 10.1007/s11172-006-0204-4
    • Deryabina, T. G.; Demina, M. A.; Belskaya, N. P.; Bakulev, V. A. Reaction of 3-Aryl-2-cyanothioacrylamides with Dimethyl Acetylenecarboxylate, Methyl Propiolate, and N-phenylmaleimide Russ. Chem. Bull. 2005, 54, 2880-2889 (Pubitemid 43823061)
    • (2005) Russian Chemical Bulletin , vol.54 , Issue.12 , pp. 2880-2889
    • Deryabina, T.G.1    Demina, M.A.2    Belskaya, N.P.3    Bakulev, V.A.4
  • 66
    • 77955672329 scopus 로고    scopus 로고
    • Facile and Divergent Synthesis of Substituted Pyridine-2,4(1 H,3 H)-diones and 4 H -Thiopyran-4-ones from α -Alkenoyl- α -carbamoyl Ketene-S,S-acetals
    • Liu, J.; Fu, X.; Zhou, Y.; Zhou, G.; Liang, Y.; Dong, D. Facile and Divergent Synthesis of Substituted Pyridine-2,4(1 H,3 H)-diones and 4 H -Thiopyran-4-ones from α -Alkenoyl- α -carbamoyl Ketene-S,S-acetals Aus. J. Chem. 2010, 63, 1267-1271
    • (2010) Aus. J. Chem. , vol.63 , pp. 1267-1271
    • Liu, J.1    Fu, X.2    Zhou, Y.3    Zhou, G.4    Liang, Y.5    Dong, D.6
  • 67
    • 33751386438 scopus 로고
    • Synthesis of 2,6-Diaryl-4 H -thiopyran-4-ones
    • Boaz, N. W.; Fox, K. M. Synthesis of 2,6-Diaryl-4 H -thiopyran-4-ones J. Org. Chem. 1993, 58, 3042-3045
    • (1993) J. Org. Chem. , vol.58 , pp. 3042-3045
    • Boaz, N.W.1    Fox, K.M.2
  • 68
    • 37049084782 scopus 로고
    • Reaction of 3-Aryl-2-cyanothioacrylamides with Electron-deficient Alkynes: Synthesis of 4-Aryl-4 H -thiopyrans
    • Bloxham, J.; Dell, C. P. Reaction of 3-Aryl-2-cyanothioacrylamides with Electron-deficient Alkynes: Synthesis of 4-Aryl-4 H -thiopyrans J. Chem. Soc., Perkin Trans. 1 1994, 989-993
    • (1994) J. Chem. Soc., Perkin Trans. 1 , pp. 989-993
    • Bloxham, J.1    Dell, C.P.2
  • 69
    • 77950864682 scopus 로고    scopus 로고
    • Novel 3-Alkanoyl/Aroyl/Heteroaroyl-2 H -chromene-2-thiones: Synthesis and Evaluation of their Antioxidant Activities
    • Singh, O. M.; Devi, N. S.; Thokchom, D. S.; Sharma, G. J. Novel 3-Alkanoyl/Aroyl/Heteroaroyl-2 H -chromene-2-thiones: Synthesis and Evaluation of their Antioxidant Activities Eur. J. Med. Chem. 2010, 45, 2250-2257
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 2250-2257
    • Singh, O.M.1    Devi, N.S.2    Thokchom, D.S.3    Sharma, G.J.4
  • 70
    • 65249177954 scopus 로고    scopus 로고
    • Application of β -Oxodithioesters in Domino and Multicomponent Reactions: Facile Route to Dihydropyrimidines and Coumarins
    • Singh, O. M.; Devi, N. S. Application of β -Oxodithioesters in Domino and Multicomponent Reactions: Facile Route to Dihydropyrimidines and Coumarins J. Org. Chem. 2009, 74, 3141-3144
    • (2009) J. Org. Chem. , vol.74 , pp. 3141-3144
    • Singh, O.M.1    Devi, N.S.2
  • 71
    • 43449095015 scopus 로고    scopus 로고
    • Alkylation of Aryl 3-Oxopropanedithioate and 3-Amino-1-aryl-3-thioxo-1- propanones as an Effective Tool for the Construction of Differently Substituted Thiophenes and Annulated Thiophenes
    • Samuel, R.; Chandran, P.; Retnamma, S.; Sasikala, K. A.; Sridevi, N. K.; Anabha, E. R.; Asokan, C. V. Alkylation of Aryl 3-Oxopropanedithioate and 3-Amino-1-aryl-3-thioxo-1-propanones as an Effective Tool for the Construction of Differently Substituted Thiophenes and Annulated Thiophenes Tetrahedron 2008, 64, 5944-5948
    • (2008) Tetrahedron , vol.64 , pp. 5944-5948
    • Samuel, R.1    Chandran, P.2    Retnamma, S.3    Sasikala, K.A.4    Sridevi, N.K.5    Anabha, E.R.6    Asokan, C.V.7
  • 72
    • 35348996543 scopus 로고    scopus 로고
    • A facile method for the synthesis of substituted 2-ylidene-1,3-oxathioles from acetophenones
    • DOI 10.1016/j.tetlet.2007.09.076, PII S0040403907018552
    • Samuel, R.; Asokan, C. V.; Suma, S.; Chandran, A.; Retnamma, S.; Anabha, E. R. A Facile Method for the Synthesis of Substituted 2-Ylidene-1,3-oxathioles from Acetophenones Tetrahedron Lett. 2007, 48, 8376-8378 (Pubitemid 47615083)
    • (2007) Tetrahedron Letters , vol.48 , Issue.47 , pp. 8376-8378
    • Samuel, R.1    Asokan, C.V.2    Suma, S.3    Chandran, P.4    Retnamma, S.5    Anabha, E.R.6
  • 73
    • 28044473878 scopus 로고    scopus 로고
    • Regioselective synthesis of 1-aryl-3,4-substituted/annulated-5- (methylthio) pyrazoles and 1-aryl-3-(methylthio)-4,5-substituted/annulated pyrazoles
    • DOI 10.1021/jo051771u
    • Peruncheralathan, S.; Khan, T. A.; Ila, H.; Junjappa, H. Regioselective Synthesis of 1-Aryl-3,4-substituted/annulated-5-(methylthio)pyrazoles and 1-Aryl-3-(methylthio)-4,5-substituted/annulated Pyrazoles J. Org. Chem. 2005, 70, 10030-10035 (Pubitemid 41689169)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.24 , pp. 10030-10035
    • Peruncheralathan, S.1    Khan, T.A.2    Ila, H.3    Junjappa, H.4
  • 74
    • 67650529102 scopus 로고    scopus 로고
    • An Efficient One-Pot Synthesis of Tetrahydrobenzo[ a ]xanthene-11-one and Diazabenzo[ a ]anthracene-9,11-dione Derivatives under Solvent Free Condition
    • Nandi, G. C.; Samai, S.; Kumar, R.; Singh, M. S. An Efficient One-Pot Synthesis of Tetrahydrobenzo[ a ]xanthene-11-one and Diazabenzo[ a ]anthracene-9,11-dione Derivatives under Solvent Free Condition Tetrahedron 2009, 65, 7129-7134
    • (2009) Tetrahedron , vol.65 , pp. 7129-7134
    • Nandi, G.C.1    Samai, S.2    Kumar, R.3    Singh, M.S.4
  • 76
    • 70350516103 scopus 로고    scopus 로고
    • L-Proline: An Efficient Catalyst for the One-Pot Synthesis of 2,4,5-Trisubstituted and 1,2,4,5-Tetrasubstituted Imidazoles
    • Samai, S.; Nandi, G. C.; Singh, P.; Singh, M. S. L-Proline: An Efficient Catalyst for the One-Pot Synthesis of 2,4,5-Trisubstituted and 1,2,4,5-Tetrasubstituted Imidazoles Tetrahedron 2009, 65, 10155-10161
    • (2009) Tetrahedron , vol.65 , pp. 10155-10161
    • Samai, S.1    Nandi, G.C.2    Singh, P.3    Singh, M.S.4
  • 77
    • 77951106045 scopus 로고    scopus 로고
    • 3-Catalyzed, Three-Component Coupling of Aldehydes, β -Naphthol, and 6-Amino-1,3-dimethyluracil to Functionalized Naphthopyranopyrimidines
    • 3-Catalyzed, Three-Component Coupling of Aldehydes, β -Naphthol, and 6-Amino-1,3-dimethyluracil to Functionalized Naphthopyranopyrimidines Synlett 2010, 1133-1137
    • (2010) Synlett , pp. 1133-1137
    • Nandi, G.C.1    Samai, S.2    Singh, M.S.3
  • 78
    • 77957813897 scopus 로고    scopus 로고
    • Application of Cyclic-1,3-diketones in Domino and Multicomponent Reactions: Facile Route to Highly Functionalized Chromeno[2,3- d ]pyrimidinones and Diazabenzo[ b ]fluorenones under Solvent-Free Conditions
    • Kumar, R.; Raghuvanshi, K.; Verma, R. K.; Singh, M. S. Application of Cyclic-1,3-diketones in Domino and Multicomponent Reactions: Facile Route to Highly Functionalized Chromeno[2,3- d ]pyrimidinones and Diazabenzo[ b ]fluorenones under Solvent-Free Conditions Tetrahedron Lett. 2010, 51, 5933-5936
    • (2010) Tetrahedron Lett. , vol.51 , pp. 5933-5936
    • Kumar, R.1    Raghuvanshi, K.2    Verma, R.K.3    Singh, M.S.4
  • 79
    • 79960232606 scopus 로고    scopus 로고
    • L-Proline Catalyzed Synthesis of Densely Functionalized Pyrido[2,3- d ]pyrimidines via Three-Component One-Pot Domino Knoevenagel Aza-Diels-Alder Reaction
    • Samai, S.; Nandi, G. C.; Chowdhury, S.; Singh, M. S. L-Proline Catalyzed Synthesis of Densely Functionalized Pyrido[2,3- d ]pyrimidines via Three-Component One-Pot Domino Knoevenagel Aza-Diels-Alder Reaction Tetrahedron 2011, 67, 5935-5941
    • (2011) Tetrahedron , vol.67 , pp. 5935-5941
    • Samai, S.1    Nandi, G.C.2    Chowdhury, S.3    Singh, M.S.4
  • 80
    • 79960190015 scopus 로고    scopus 로고
    • Regioselective Synthesis of Tetrahydrothiochromen-5-ones via a One-Pot Three-Component Solvent-Free Domino Protocol
    • Chowdhury, S.; Nandi, G. C.; Samai, S.; Singh, M. S. Regioselective Synthesis of Tetrahydrothiochromen-5-ones via a One-Pot Three-Component Solvent-Free Domino Protocol Org. Lett. 2011, 13, 3762-3765
    • (2011) Org. Lett. , vol.13 , pp. 3762-3765
    • Chowdhury, S.1    Nandi, G.C.2    Samai, S.3    Singh, M.S.4
  • 82
    • 78449261907 scopus 로고    scopus 로고
    • Biginelli and Hantzsch-Type Reactions Leading to Highly Functionalized Dihydropyrimidinone, Thiocoumarin, and Pyridopyrimidinone Frameworks via Ring Annulation with β -Oxodithioesters
    • Nandi, G. C.; Samai, S.; Singh, M. S. Biginelli and Hantzsch-Type Reactions Leading to Highly Functionalized Dihydropyrimidinone, Thiocoumarin, and Pyridopyrimidinone Frameworks via Ring Annulation with β -Oxodithioesters J. Org. Chem. 2010, 75, 7785-7795
    • (2010) J. Org. Chem. , vol.75 , pp. 7785-7795
    • Nandi, G.C.1    Samai, S.2    Singh, M.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.