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Volumn 16, Issue 4, 2011, Pages 3252-3314

From polymer to small organic molecules: A tight relationship between radical chemistry and solid-phase organic synthesis

Author keywords

Polymer assisted synthesis; Polymer supported reagents; Radical; Solid phase; SPS

Indexed keywords

DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; ORGANIC COMPOUND; POLYMER;

EID: 79955543571     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16043252     Document Type: Review
Times cited : (15)

References (138)
  • 1
    • 33947345669 scopus 로고
    • An instance of trivalent carbon: Triphenylmethyl
    • Gomberg, M. An Instance of Trivalent Carbon: Triphenylmethyl. J. Am. Chem. Soc. 1900, 22, 757-771.
    • (1900) J. Am. Chem. Soc. , vol.22 , pp. 757-771
    • Gomberg, M.1
  • 2
    • 33845223520 scopus 로고    scopus 로고
    • Grafting short peptides onto polybutadiene-block-poly(ethylene oxide): A platform for self-assembling hybrid amphiphiles
    • DOI 10.1002/anie.200602739
    • Geng, Y.; Discher, D.E.; Justynska, J.; Schlaad, H. Grafting Short Peptides onto Polybutadieneblock- poly(ethylene oxide): A Platform for Self-Assembling Hybrid Amphiphiles. Angew. Chem. Int. Ed. Engl. 2006, 45, 7578-7581. (Pubitemid 44851687)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.45 , pp. 7578-7581
    • Geng, Y.1    Discher, D.E.2    Justynska, J.3    Schlaad, H.4
  • 3
    • 34248531614 scopus 로고    scopus 로고
    • Chemical surface modification via radical C-C bond-forming reactions
    • DOI 10.1021/ja0686716
    • Siegenthaler, K.O.; Schäfer, A.; Studer, A. Chemical Surface Modification via Radical C-C Bond-Forming Reactions. J. Am. Chem. Soc. 2007, 129, 5826-5827. (Pubitemid 46748480)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.18 , pp. 5826-5827
    • Siegenthaler, K.O.1    Schafer, A.2    Studer, A.3
  • 4
    • 70350052777 scopus 로고    scopus 로고
    • Clicking polymer brushes with thiolyne chemistry: Indoors and out
    • Hensarling, R.M.; Doughty, V.A.; Chan, J.W.; Patton, D.L. Clicking Polymer Brushes with Thiolyne Chemistry: Indoors and Out. J. Am. Chem. Soc. 2009, 131, 14673-14675.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 14673-14675
    • Hensarling, R.M.1    Doughty, V.A.2    Chan, J.W.3    Patton, D.L.4
  • 5
    • 0000457911 scopus 로고
    • Some properties of radical reactions important in synthesis
    • Walling, C. Some properties of radical reactions important in synthesis. Tetrahedron 1985, 41, 3887-3900.
    • (1985) Tetrahedron , vol.41 , pp. 3887-3900
    • Walling, C.1
  • 6
    • 0027538424 scopus 로고
    • Competition methods and scales for alkyl radical reaction kinetics
    • Newcomb, M. Competition Methods and Scales for Alkyl Radical Reaction Kinetics. Tetrahedron 1993, 49, 1151-1176.
    • (1993) Tetrahedron , vol.49 , pp. 1151-1176
    • Newcomb, M.1
  • 7
    • 33748848564 scopus 로고    scopus 로고
    • Radical chemistry on solid support
    • DOI 10.1007/128-023, Radicals in Synthesis II
    • Gansäuer, A.; McGhee, A.; Procter, D. Radical Chemistry on Solid Support, In Radicals in Synthesis II, Springer: Berlin/Heidelberg, Germany, 2006; Vol. 264, pp. 93-134. (Pubitemid 44420768)
    • (2006) Topics in Current Chemistry , vol.264 , pp. 93-134
    • McGhee, A.M.1    Procter, D.J.2
  • 8
    • 0037132579 scopus 로고    scopus 로고
    • Relative rates and approximate rate constants for inter- and intramolecular hydrogen transfer reactions of polymer-bound radicals
    • DOI 10.1021/ja028249z
    • Curran, D.P.; Yang, F.; Cheong, J.H. Relative Rates and Approximate Rate Constants for Interand Intramolecular Hydrogen Transfer Reactions of Polymer-Bound Radicals. J. Am. Chem. Soc. 2002, 124, 14993-15000. (Pubitemid 36014106)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.50 , pp. 14993-15000
    • Curran, D.P.1    Yang, F.2    Cheong, J.-H.3
  • 9
    • 0027373903 scopus 로고
    • Convergent solid-phase peptide synthesis
    • DOI 10.1016/S0040-4020(01)81800-7
    • Lloyd-Williams, P.; Albericio, F.; Giralt, E. Convergent solid-phase peptide synthesis. Tetrahedron 1993, 49, 11065-11133. (Pubitemid 23361312)
    • (1993) Tetrahedron , vol.49 , Issue.48 , pp. 11065-11133
    • Lloyd-Williams, P.1    Albericio, F.2    Giralt, E.3
  • 12
    • 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
  • 13
    • 33646733929 scopus 로고    scopus 로고
    • Diversity linker units for solid-phase organic synthesis
    • Scott, P.J.H.; Steel, P.G. Diversity Linker Units for Solid-Phase Organic Synthesis. Eur. J. Org. Chem. 2006, 2006, 2251-2268.
    • (2006) Eur. J. Org. Chem. , vol.2006 , pp. 2251-2268
    • Scott, P.J.H.1    Steel, P.G.2
  • 14
    • 0030565531 scopus 로고    scopus 로고
    • A linker that allows efficient formation of aliphatic C-H bonds on polymeric supports
    • DOI 10.1016/0040-4039(96)01419-0
    • Jung, K.W.; Zhao, X.Y.; Janda, K.D. A linker that allows efficient formation of aliphatic C-H bonds on polymeric supports. Tetrahedron Lett. 1996, 37, 6491-6494. (Pubitemid 26278270)
    • (1996) Tetrahedron Letters , vol.37 , Issue.36 , pp. 6491-6494
    • Jung, K.W.1    Zhao, X.-Y.2    Janda, K.D.3
  • 16
    • 0030005645 scopus 로고    scopus 로고
    • A radical approach to N-desulfonylation
    • DOI 10.1016/0040-4039(96)00086-X
    • Parsons, A.F.; Pettifer, R.M. A radical approach to N-desulfonylation. Tetrahedron Lett. 1996, 37, 1667-1670. (Pubitemid 26078534)
    • (1996) Tetrahedron Letters , vol.37 , Issue.10 , pp. 1667-1670
    • Parsons, A.F.1    Pettifer, R.M.2
  • 17
    • 0043238901 scopus 로고    scopus 로고
    • A new strategy for solid phase synthesis of a secondary amide library using sulfonamide linker via radical traceless cleavage
    • DOI 10.1023/A:1024800915201
    • Luo, J.; Huang, W. A new strategy for solid phase synthesis of a secondary amide library using sulfonamide linker via radical traceless cleavage. Mol. Divers. 2003, 6, 33-41. (Pubitemid 36994179)
    • (2003) Molecular Diversity , vol.6 , Issue.1 , pp. 33-41
    • Luo, J.1    Huang, W.2
  • 18
    • 0043172256 scopus 로고    scopus 로고
    • Carbon-carbon bond formation on solid support. Application of the classical Julia-Lythgoe olefination
    • DOI 10.1016/S0040-4039(03)01637-X
    • D'Herde, J.N.P.; J. de Clercq, P. Carbon-carbon bond formation on solid support. Application of the classical Julia-Lythgoe olefination. Tetrahedron Lett. 2003, 44, 6657-6659. (Pubitemid 36945108)
    • (2003) Tetrahedron Letters , vol.44 , Issue.35 , pp. 6657-6659
    • D'herde, J.N.P.1    De Clercq, P.J.2
  • 19
    • 33748847738 scopus 로고    scopus 로고
    • Aromatic homolytic substitution using solid phase synthesis
    • DOI 10.1016/j.tet.2006.02.071, PII S0040402006003553
    • Allin, S.M.; Bowman, W.R.; Karim, R.; Rahman, S.S. Aromatic homolytic substitution using solid phase synthesis. Tetrahedron 2006, 62, 4306-4316. (Pubitemid 44419324)
    • (2006) Tetrahedron , vol.62 , Issue.18 , pp. 4306-4316
    • Allin, S.M.1    Bowman, W.R.2    Karim, R.3    Rahman, S.S.4
  • 20
    • 0033484573 scopus 로고    scopus 로고
    • Polarity-reversal catalysis of hydrogen-atom abstraction reactions: Concepts and applications in organic chemistry
    • Roberts, B.P. Polarity-reversal catalysis of hydrogen-atom abstraction reactions: concepts and applications in organic chemistry. Chem. Soc. Rev. 1999, 28, 25-35.
    • (1999) Chem. Soc. Rev. , vol.28 , pp. 25-35
    • Roberts, B.P.1
  • 21
    • 0141790801 scopus 로고    scopus 로고
    • The first Pummerer cyclisations on solid phase. Convenient construction of oxindoles enabled by a sulfur-link to resin
    • McAllister, L.A.; Brand, S.; de Gentile, R.; Procter, D.J. The first Pummerer cyclisations on solid phase. Convenient construction of oxindoles enabled by a sulfur-link to resin. Chem. Commun. (Camb.) 2003, 2380-2381. (Pubitemid 37163984)
    • (2003) Chemical Communications , Issue.18 , pp. 2380-2381
    • McAllister, L.A.1    Brand, S.2    De Gentile, R.3    Procter, D.J.4
  • 24
    • 27644478441 scopus 로고    scopus 로고
    • Sulfide- and selenide-based linkers in phase tag-assisted synthesis
    • DOI 10.1016/j.tet.2005.08.056, PII S0040402005014511
    • McAllister, L.A.; McCormick, R.A.; Procter, D.J. Sulfide- and selenide-based linkers in phase tag-assisted synthesis. Tetrahedron 2005, 61, 11527-11576. (Pubitemid 41573690)
    • (2005) Tetrahedron , vol.61 , Issue.49 , pp. 11527-11576
    • McAllister, L.A.1    McCormick, R.A.2    Procter, D.J.3
  • 25
    • 0032509385 scopus 로고    scopus 로고
    • Selenium-linking strategy for traceless solid-phase synthesis: Direct loading, aliphatic C-H bond formation upon cleavage and reaction monitoring by gradient MAS NMR spectroscopy
    • DOI 10.1021/jo9806310
    • Ruhland, T.; Andersen, K.; Pedersen, H. Selenium-Linking Strategy for Traceless Solid-Phase Synthesis: Direct Loading, Aliphatic C-H Bond Formation upon Cleavage and Reaction Monitoring by Gradient MAS NMR Spectroscopy. J. Org. Chem. 1998, 63, 9204-9211. (Pubitemid 29008980)
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.25 , pp. 9204-9211
    • Ruhland, T.1    Andersen, K.2    Pedersen, H.3
  • 26
    • 5644223245 scopus 로고    scopus 로고
    • Traceless solid phase synthesis with polystyrene-bound tellurium and in comparison with polystyrene-bound selenium
    • DOI 10.1055/s-2004-831202
    • Ruhland, T.; Torang, J.; Pedersen, H.; Madsen, J.C.; Bang, K.S. Traceless Solid Phase Synthesis with Polystyrene-Bound Tellurium and in Comparison with Polystyrene-Bound Selenium. Synthesis 2004, 2323-2328. (Pubitemid 39371661)
    • (2004) Synthesis , Issue.14 , pp. 2323-2328
    • Ruhland, T.1    Torang, J.2    Pedersen, H.3    Madsen, J.C.4    Bang, K.S.5
  • 29
    • 0034678005 scopus 로고    scopus 로고
    • 1,2-seleno migrations in carbohydrate chemistry: Solution and solid- phase synthesis of 2-deoxy glycosides, orthoesters, and allyl orthoesters
    • DOI 10.1002/(SICI)1521-3773(20000317)39:6<1089::AID-ANIE1089>3.0. CO;2-V
    • Nicolaou, K.C.; Mitchell, H.J.; Fylaktakidou, K.C.; Suzuki, H.; Rodríguez, R.M. 1, 2-Seleno Migrations in Carbohydrate Chemistry: Solution and Solid-Phase Synthesis of 2-Deoxy Glycosides, Orthoesters, and Allyl Orthoesters. Angew. Chem. Int. Ed. Engl. 2000, 39, 1089-1093. (Pubitemid 30217253)
    • (2000) Angewandte Chemie - International Edition , vol.39 , Issue.6 , pp. 1089-1093
    • Nicolaou, K.C.1    Mitchell, H.J.2    Fylaktakidou, K.C.3    Suzuki, H.4    Rodriguez, R.M.5
  • 30
    • 0034282645 scopus 로고    scopus 로고
    • Total synthesis of everninomicin 13, 384-1-Part 4: Explorations of methodology; stereocontrolled synthesis of 1, 1′-disaccharides, 1, 2-seleno migrations in carbohydrates, and solution- and solid-phase synthesis of 2-deoxy glycosides and orthoesters
    • Nicolaou, K.C.; Fylaktakidou, K.C.; Mitchell, H.J.; van Delft, F.L.; Rodríguez, R.M.; Conley, S.R.; Jin, Z. Total Synthesis of Everninomicin 13, 384-1-Part 4: Explorations of Methodology; Stereocontrolled Synthesis of 1, 1′-Disaccharides, 1, 2-Seleno Migrations in Carbohydrates, and Solution- and Solid-Phase Synthesis of 2-Deoxy Glycosides and Orthoesters. Chem. Eur. J. 2000, 6, 3166-3185.
    • (2000) Chem. Eur. J. , vol.6 , pp. 3166-3185
    • Nicolaou, K.C.1    Fylaktakidou, K.C.2    Mitchell, H.J.3    Van Delft, F.L.4    Rodríguez, R.M.5    Conley, S.R.6    Jin, Z.7
  • 33
    • 0001027385 scopus 로고    scopus 로고
    • A facile method for the solution and solid-phase synthesis of substituted [3.3.1] bicycles
    • Nicolaou, K.C.; Pfefferkorn, J.A.; Cao, G.Q.; Kim, S.; Kessabi, J. A Facile Method for the Solution and Solid-Phase Synthesis of Substituted [3.3.1] Bicycles. Org. Lett. 1999, 1, 807-810.
    • (1999) Org. Lett. , vol.1 , pp. 807-810
    • Nicolaou, K.C.1    Pfefferkorn, J.A.2    Cao, G.Q.3    Kim, S.4    Kessabi, J.5
  • 34
    • 0142196886 scopus 로고    scopus 로고
    • Radical Carbonylation/Reductive Cyclization for the Construction of Tetrahydrofuran-3-ones and Pyrrolidin-3-ones
    • DOI 10.1021/jo030153f
    • Berlin, S.; Ericsson, C.; Engman, L. Radical Carbonylation/Reductive Cyclization for the Construction of Tetrahydrofuran-3-ones and Pyrrolidin-3-ones. J. Org. Chem. 2003, 68, 8386-8396. (Pubitemid 37329096)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.22 , pp. 8386-8396
    • Berlin, S.1    Ericsson, C.2    Engman, L.3
  • 35
    • 0032731879 scopus 로고    scopus 로고
    • Preparation of polymer-supported selenocyanates and their application to solid-phase oxyselenenylation-deselenenylation
    • Fujita, K.I.; Watanabe, K.; Oishi, A.; Ikeda, Y.; Taguchi, Y. Preparation of Polymer-Supported Selenocyanates and their Application to Solid-Phase Oxyselenenylation-Deselenylation. Synlett 1999, 1999, 1760-1762. (Pubitemid 29529442)
    • (1999) Synlett , Issue.11 , pp. 1760-1762
    • Fujita, K.-I.1    Watanabe, K.2    Oishi, A.3    Ikeda, Y.4    Taguchi, Y.5
  • 36
    • 0035211801 scopus 로고    scopus 로고
    • Polystyrene-supported selenosulfonates: Efficient reagents for regio- and stereocontrolled synthesis of vinyl sulfones
    • Qian, H.; Huang, X. Polystyrene-Supported Selenosulfonates: Efficient Reagents for Regio- and Stereocontrolled Synthesis of Vinyl Sulfones. Synlett 2001, 1913-1916. (Pubitemid 33135277)
    • (2001) Synlett , Issue.12 , pp. 1913-1916
    • Qian, H.1    Huang, X.2
  • 37
    • 0037016988 scopus 로고    scopus 로고
    • Polystyrene-supported selenosulfonates: Efficient reagents for the synthesis of acetylenic sulfones
    • DOI 10.1016/S0040-4039(01)02330-9, PII S0040403901023309
    • Qian, H.; Huang, X. Polystyrene-supported selenosulfonates: efficient reagents for the synthesis of acetylenic sulfones. Tetrahedron Lett. 2002, 43, 1059-1061. (Pubitemid 34119254)
    • (2002) Tetrahedron Letters , vol.43 , Issue.6 , pp. 1059-1061
    • Qian, H.1    Huang, X.2
  • 38
    • 33745763733 scopus 로고    scopus 로고
    • Solid-phase synthesis of alpha-keto sulfones
    • Qian, H.; Huang, X. Solid-Phase Synthesis of alpha-Keto Sulfones. Synthesis 2006, 1934-1936.
    • (2006) Synthesis , pp. 1934-1936
    • Qian, H.1    Huang, X.2
  • 39
    • 0141683736 scopus 로고    scopus 로고
    • Radical cyclization of 1,6-diene using polystyrene-supported selenosulfones
    • DOI 10.1021/cc030013j
    • Qian, H.; Huang, X. Radical Cyclization of 1, 6-Diene Using Polystyrene-Supported Selenosulfones. J. Comb. Chem. 2003, 5, 569-576. (Pubitemid 37206161)
    • (2003) Journal of Combinatorial Chemistry , vol.5 , Issue.5 , pp. 569-576
    • Qian, H.1    Huang, X.2
  • 40
    • 0000966664 scopus 로고    scopus 로고
    • Reductive cleavage of N-O bonds using samarium(II) iodide in a traceless release strategy for solid-phase synthesis
    • Myers, R.M.; Langston, S.P.; Conway, S.P.; Abell, C. Reductive Cleavage of N-O Bonds Using Samarium(II) Iodide in a Traceless Release Strategy for Solid-Phase Synthesis. Org. Lett. 2000, 2, 1349-1352.
    • (2000) Org. Lett. , vol.2 , pp. 1349-1352
    • Myers, R.M.1    Langston, S.P.2    Conway, S.P.3    Abell, C.4
  • 41
    • 0035180617 scopus 로고    scopus 로고
    • General combinatorial synthesis of tertiary amines on solid support. A novel conditional release strategy based on traceless linking at nitrogen
    • DOI 10.1016/S0040-4039(00)01902-X, PII S004040390001902X
    • Gustafsson, M.; Olsson, R.; Andersson, C.M. General combinatorial synthesis of tertiary amines on solid support. A novel conditional release strategy based on traceless linking at nitrogen. Tetrahedron Lett. 2001, 42, 133-136. (Pubitemid 32011724)
    • (2001) Tetrahedron Letters , vol.42 , Issue.1 , pp. 133-136
    • Gustafsson, M.1    Olsson, R.2    Andersson, C.-M.3
  • 42
    • 0035825754 scopus 로고    scopus 로고
    • Solid-Phase Synthesis of β-Lactams via the Miller Hydroxamate Approach
    • DOI 10.1021/ol006779z
    • Meloni, M.M.; Taddei, M. Solid-Phase Synthesis of beta-Lactams via the Miller Hydroxamate Approach. Org. Lett. 2001, 3, 337-340. (Pubitemid 33692989)
    • (2001) Organic Letters , vol.3 , Issue.3 , pp. 337-340
    • Meloni, M.M.1    Taddei, M.2
  • 43
    • 0038717199 scopus 로고    scopus 로고
    • Application of an ephedrine chiral linker in a solid-phase, 'asymmetric catch-release' approach to γ-butyrolactones
    • Kerrigan, N.J.; Hutchison, P.C.; Heightman, T.D.; Procter, D.J. Application of an ephedrine chiral linker in a solid-phase, 'asymmetric catch-release' approach to gamma-butyrolactones. Chem. Commun. (Camb.) 2003, 21, 1402-1403. (Pubitemid 36734949)
    • (2003) Chemical Communications , Issue.12 , pp. 1402-1403
    • Kerrigan, N.J.1    Hutchison, P.C.2    Heightman, T.D.3    Procter, D.J.4
  • 44
    • 4744346554 scopus 로고    scopus 로고
    • Development of a solid-phase 'asymmetric resin-capture-release' process: Application of an ephedrine chiral resin in an approach to gamma-butyrolactones
    • Kerrigan, N.J.; Hutchison, P.C.; Heightman, T.D.; Procter, D.J. Development of a solid-phase 'asymmetric resin-capture-release' process: application of an ephedrine chiral resin in an approach to gamma-butyrolactones. Org. Biomol. Chem. 2004, 2, 2476-2482.
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 2476-2482
    • Kerrigan, N.J.1    Hutchison, P.C.2    Heightman, T.D.3    Procter, D.J.4
  • 45
    • 33645027432 scopus 로고    scopus 로고
    • 2-mediated reductive coupling of aldehydes with crotonates of atropisomeric 1-naphthamides
    • 2-Mediated Reductive Coupling of Aldehydes with Crotonates of Atropisomeric 1-Naphthamides. J. Org. Chem. 2006, 71, 2445-2455.
    • (2006) J. Org. Chem. , vol.71 , pp. 2445-2455
    • Zhang, Y.1    Wang, Y.2    Dai, W.M.3
  • 46
    • 0037149426 scopus 로고    scopus 로고
    • Reduction of α-aryloxy carbonyl compounds with samarium(II) iodide. A new traceless linker for the solid phase synthesis of carbonyl compounds
    • McKerlie, F.; Procter, D.J.; Wynne, G. Reduction of alpha-aryloxy carbonyl compounds with samarium(II) iodide. A new traceless linker for the solid phase synthesis of carbonyl compounds. Chem. Commun. (Camb.) 2002, 21, 584-585. (Pubitemid 34259057)
    • (2002) Chemical Communications , Issue.6 , pp. 584-585
    • McKerlie, F.1    Procter, D.J.2    Wynne, G.3
  • 47
    • 23844511244 scopus 로고    scopus 로고
    • Evaluation of a new linker system cleaved using samarium(II) iodide. Application in the solid phase synthesis of carbonyl compounds
    • DOI 10.1039/b506294b
    • McKerlie, F.; Rudkin, I.M.; Wynne, G.; Procter, D.J. Evaluation of a new linker system cleaved using samarium(II) iodide. Application in the solid phase synthesis of carbonyl compounds. Org. Biomol. Chem. 2005, 3, 2805-2816. (Pubitemid 41156400)
    • (2005) Organic and Biomolecular Chemistry , vol.3 , Issue.15 , pp. 2805-2816
    • McKerlie, F.1    Rudkin, I.M.2    Wynne, G.3    Procter, D.J.4
  • 48
    • 18744401913 scopus 로고    scopus 로고
    • Oxidative cyclorelease from soluble polymeric supports
    • DOI 10.1021/jo0480951
    • Liu, H.; Wan, S.; Floreancig, P.E. Oxidative Cyclorelease from Soluble Polymeric Supports. J. Org. Chem. 2005, 70, 3814-3818. (Pubitemid 40675307)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.10 , pp. 3814-3818
    • Liu, H.1    Wan, S.2    Floreancig, P.E.3
  • 49
    • 33847021240 scopus 로고    scopus 로고
    • Development and applications of electron-transfer-initiated cyclization reactions
    • Floreancig, P.E. Development and Applications of Electron-Transfer- Initiated Cyclization Reactions. Synlett 2007, 38, 191-203.
    • (2007) Synlett , vol.38 , pp. 191-203
    • Floreancig, P.E.1
  • 50
    • 70350569334 scopus 로고    scopus 로고
    • Synthesis, chemical stability and application of a thiohydroxamic acid linker (THA) for solid-phase organic synthesis
    • Whitehead, D.M.; Helliwell, P.A.; McKeown, S.C.; Routledge, A. Synthesis, chemical stability and application of a thiohydroxamic acid linker (THA) for solid-phase organic synthesis. React. Funct. Polym. 2009, 69, 884-890.
    • (2009) React. Funct. Polym. , vol.69 , pp. 884-890
    • Whitehead, D.M.1    Helliwell, P.A.2    McKeown, S.C.3    Routledge, A.4
  • 51
    • 0034684515 scopus 로고    scopus 로고
    • A photolabile 'traceless' linker for solid-phase organic synthesis
    • Horton, J.R.; Stamp, L.M.; Routledge, A. A photolabile 'traceless' linker for solid-phase organic synthesis. Tetrahedron Lett. 2000, 41, 9181-9184.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9181-9184
    • Horton, J.R.1    Stamp, L.M.2    Routledge, A.3
  • 52
    • 0040077867 scopus 로고    scopus 로고
    • Application of X-ray photoelectron spectroscopy in determining the structure of solid-phase bound substrates
    • Whitehead, D.M.; Jackson, T.; McKeown, S.C.; Wilson, K.; Routledge, A. Application of X-ray Photoelectron Spectroscopy in Determining the Structure of Solid-Phase Bound Substrates. J. Comb. Chem. 2002, 4, 255-257.
    • (2002) J. Comb. Chem. , vol.4 , pp. 255-257
    • Whitehead, D.M.1    Jackson, T.2    McKeown, S.C.3    Wilson, K.4    Routledge, A.5
  • 53
    • 85082712806 scopus 로고
    • Polymer-supported organotin hydrides as immobilized reagents for free radical synthesis
    • Gerigk, U.; Gerlach, M.; Neumann, W.P.; Vieler, R.; Weintritt, V. Polymer-Supported Organotin Hydrides as Immobilized Reagents for Free Radical Synthesis. Synthesis 1990, 1990, 448-452.
    • (1990) Synthesis , vol.1990 , pp. 448-452
    • Gerigk, U.1    Gerlach, M.2    Neumann, W.P.3    Vieler, R.4    Weintritt, V.5
  • 54
    • 0001023798 scopus 로고
    • A polymer-supported organotin hydride and its multipurpose application in radical organic synthesis
    • Gerlach, M.; Joerdens, F.; Kuhn, H.; Neumann, W.P.; Peterseim, M. A polymer-supported organotin hydride and its multipurpose application in radical organic synthesis. J. Org. Chem. 1991, 56, 5971-5972.
    • (1991) J. Org. Chem. , vol.56 , pp. 5971-5972
    • Gerlach, M.1    Joerdens, F.2    Kuhn, H.3    Neumann, W.P.4    Peterseim, M.5
  • 55
    • 0344902741 scopus 로고
    • A new method for the deoxygenation of secondary alcohols
    • Barton, D.H.R.; McCombie, S.W. A new method for the deoxygenation of secondary alcohols. J. Chem. Soc., Perkin Trans. 1 1975, 1574-1585.
    • (1975) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1574-1585
    • Barton, D.H.R.1    McCombie, S.W.2
  • 56
    • 84989517967 scopus 로고
    • Elegant improvement of the deoxygenation of alcohols using a polystyrene-supported organotin hydride
    • Neumann, W.P.; Peterseim, M. Elegant Improvement of the Deoxygenation of Alcohols Using a Polystyrene-Supported Organotin Hydride. Synlett 1992, 1992, 801-802.
    • (1992) Synlett , vol.1992 , pp. 801-802
    • Neumann, W.P.1    Peterseim, M.2
  • 59
    • 0032565936 scopus 로고    scopus 로고
    • In situ generated, polymer-supported organotin hydrides as clean reducing agents
    • DOI 10.1016/S0040-4039(98)00873-9, PII S0040403998008739
    • Dumartin, G.; Pourcel, M.; Delmond, B.; Donard, O.; Pereyre, M. In situ generated, polymersupported organotin hydrides as clean reducing agents. Tetrahedron Lett. 1998, 39, 4663-4666. (Pubitemid 28267017)
    • (1998) Tetrahedron Letters , vol.39 , Issue.26 , pp. 4663-4666
    • Dumartin, G.1    Pourcel, M.2    Delmond, B.3    Donard, O.4    Pereyre, M.5
  • 60
    • 0001316748 scopus 로고    scopus 로고
    • Preparation and reactivity of a macroporous polymer-supported organotin hydride catalyst
    • PII S0014305797002863
    • Chemin, A.; Deleuze, H.; Maillard, B. Preparation and reactivity of a macroporous polymersupported organotin hydride catalyst. Eur. Polym. J. 1998, 34, 1395-1404. (Pubitemid 128425244)
    • (1998) European Polymer Journal , vol.34 , Issue.10 , pp. 1395-1404
    • Chemin, A.1    Deleuze, H.2    Maillard, B.3
  • 61
    • 0034728945 scopus 로고    scopus 로고
    • Catalytic and supported Barton-McCombie deoxygenation of secondary alcohols: A clean reaction
    • DOI 10.1016/S0040-4039(00)00418-4, PII S0040403900004184
    • Boussaguet, P.; Delmond, B.; Dumartin, G.; Pereyre, M. Catalytic and supported Barton- McCombie deoxygenation of secondary alcohols: a clean reaction. Tetrahedron Lett. 2000, 41, 3377-3380. (Pubitemid 30307818)
    • (2000) Tetrahedron Letters , vol.41 , Issue.18 , pp. 3377-3380
    • Boussaguet, P.1    Delmond, B.2    Dumartin, G.3    Pereyre, M.4
  • 62
    • 0030800209 scopus 로고    scopus 로고
    • 3SnH-catalyzed Barton-McCombie deoxygenation of alcohols
    • 3SnH-Catalyzed Barton-McCombie Deoxygenation of Alcohols. J. Am. Chem. Soc. 1997, 119, 6949-6950.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6949-6950
    • Lopez, R.M.1    Hays, D.S.2    Fu, G.C.3
  • 63
    • 78649713640 scopus 로고
    • A polymer-supported distannane as photochemical, regenerable source of stannyl radicals for organic synthesis
    • Harendza, M.; Lessmann, K.; Neumann, W.P. A Polymer-Supported Distannane as Photochemical, Regenerable Source of Stannyl Radicals for Organic Synthesis. Synlett 1993, 1993, 283-285.
    • (1993) Synlett , vol.1993 , pp. 283-285
    • Harendza, M.1    Lessmann, K.2    Neumann, W.P.3
  • 64
    • 0031038144 scopus 로고    scopus 로고
    • An improved synthesis of a polymer-supported distannane and its application to radical formation
    • DOI 10.1016/S0040-4020(96)01078-2, PII S0040402096010782
    • Junggebauer, J.; Neumann, W.P. An improved synthesis of a polymer-supported distannane and its application to radical formation. Tetrahedron 1997, 53, 1301-1310. (Pubitemid 27042977)
    • (1997) Tetrahedron , vol.53 , Issue.4 , pp. 1301-1310
    • Junggebauer, J.1    Neumann, W.P.2
  • 66
    • 0000211886 scopus 로고    scopus 로고
    • Convenient catalytic free radical reductions of alkyl halides using an organotin reagent on non-cross-linked polystyrene support
    • Enholm, E.J.; Schulte, J.P. Convenient Catalytic Free Radical Reductions of Alkyl Halides Using an Organotin Reagent on Non-Cross-Linked Polystyrene Support. Org. Lett. 1999, 1, 1275-1277.
    • (1999) Org. Lett. , vol.1 , pp. 1275-1277
    • Enholm, E.J.1    Schulte, J.P.2
  • 67
    • 33847802299 scopus 로고
    • Method for catalytic dehalogenations via trialkyltin hydrides
    • Corey, E.J.; Suggs, J.W. Method for catalytic dehalogenations via trialkyltin hydrides. J. Org. Chem. 1975, 40, 2554-2555.
    • (1975) J. Org. Chem. , vol.40 , pp. 2554-2555
    • Corey, E.J.1    Suggs, J.W.2
  • 68
    • 2742528871 scopus 로고
    • Homolytic carbocyclization by use of a heterogeneous supported organotin catalyst. A new synthetic route to 2-alkoxytetrahydrofurans and gamma-butyrolactones
    • Ueno, Y.; Chino, K.; Watanabe, M.; Moriya, O.; Okawara, M. Homolytic carbocyclization by use of a heterogeneous supported organotin catalyst. A new synthetic route to 2-alkoxytetrahydrofurans and gamma-butyrolactones. J. Am. Chem. Soc. 1982, 104, 5564-5566.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5564-5566
    • Ueno, Y.1    Chino, K.2    Watanabe, M.3    Moriya, O.4    Okawara, M.5
  • 69
    • 0001240267 scopus 로고    scopus 로고
    • First polymer-supported organogermanium hydrides and their reduction of organic halides
    • PII S027753879600469X
    • Mochida, K.; Sugimoto, H.; Yasuo, Y. First polymer-supported organogermanium hydrides and their reduction of organic halides. Polyhedron 1997, 16, 1767-1770. (Pubitemid 127350591)
    • (1997) Polyhedron , vol.16 , Issue.10 , pp. 1767-1770
    • Mochida, K.1    Sugimoto, H.2    Yokoyama, Y.3
  • 70
    • 2942704237 scopus 로고    scopus 로고
    • New solid phase triorganogermanium hydrides for radical synthesis
    • Bowman, W.R.; Krintel, S.L.; Schilling, M.B. New Solid Phase Triorganogermanium Hydrides for Radical Synthesis. Synlett 2004, 2004, 1215-1218. (Pubitemid 38797663)
    • (2004) Synlett , Issue.7 , pp. 1215-1218
    • Bowman, W.R.1    Krintel, S.L.2    Schilling, M.B.3
  • 71
    • 0033615771 scopus 로고    scopus 로고
    • Radical-polar crossover reactions with polymer-supported tetrathiafulvalene
    • DOI 10.1016/S0040-4039(99)01679-2, PII S0040403999016792
    • Patro, B.; Merrett, M.; Murphy, J.A.; Sherrington, D.C.; Morrison, M.G.J.T. Radical-polar crossover reactions with polymer-supported tetrathiafulvalene. Tetrahedron Lett. 1999, 40, 7857-7860. (Pubitemid 29487939)
    • (1999) Tetrahedron Letters , vol.40 , Issue.44 , pp. 7857-7860
    • Patro, B.1    Merrett, M.2    Murphy, J.A.3    Sherrington, D.C.4    Morrison, M.G.J.T.5
  • 72
    • 0032484067 scopus 로고    scopus 로고
    • Flight from the tyranny of tin: The quest for practical radical sources free from metal encumbrances
    • Baguley, P.A.; Walton, J.C. Flight from the Tyranny of Tin: The Quest for Practical Radical Sources Free from Metal Encumbrances. Angew. Chem. Int. Ed. Engl. 1998, 37, 3072-3082.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 3072-3082
    • Baguley, P.A.1    Walton, J.C.2
  • 73
    • 33748725566 scopus 로고    scopus 로고
    • Tetrathiafulvalene-mediated stereoselective synthesis of the tetracyclic core of Aspidosperma alkaloids
    • Fletcher, R.; Kizil, M.; Lampard, C.; Murphy, J.A.; Roome, S.J. Tetrathiafulvalene-mediated stereoselective synthesis of the tetracyclic core of Aspidosperma alkaloids. J. Chem. Soc., Perkin Trans. 1 1998, 2341-2352.
    • (1998) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2341-2352
    • Fletcher, R.1    Kizil, M.2    Lampard, C.3    Murphy, J.A.4    Roome, S.J.5
  • 75
    • 0000158583 scopus 로고    scopus 로고
    • A new supported reagent for the photochemical generation of radicals in solution
    • DOI 10.1021/ol007032b
    • de Luca, L.; Giacomelli, G.; Porcu, G.; Taddei, M. A New Supported Reagent for the Photochemical Generation of Radicals in Solution. Org. Lett. 2001, 3, 855-857. (Pubitemid 33629410)
    • (2001) Organic Letters , vol.3 , Issue.6 , pp. 855-857
    • De Luca, L.1    Giacomelli, G.2    Porcu, G.3    Taddei, M.4
  • 76
    • 11644264856 scopus 로고
    • The invention of new radical chain reactions. Part VIII. Radical chemistry of thiohydroxamic esters; A new method for the generation of carbon radicals from carboxylic acids
    • Barton, D.H.R.; Crich, D.; Motherwell, W.B. The invention of new radical chain reactions. Part VIII. Radical chemistry of thiohydroxamic esters; A new method for the generation of carbon radicals from carboxylic acids. Tetrahedron 1985, 41, 3901-3924.
    • (1985) Tetrahedron , vol.41 , pp. 3901-3924
    • Barton, D.H.R.1    Crich, D.2    Motherwell, W.B.3
  • 78
    • 33644506756 scopus 로고    scopus 로고
    • Solid-supported copper catalysts for atom-transfer radical cyclizations: Assessment of support type and ligand structure on catalyst performance in the synthesis of nitrogen heterocycles
    • Clark, A.J.; Geden, J.V.; Thom, S. Solid-Supported Copper Catalysts for Atom-Transfer Radical Cyclizations: Assessment of Support Type and Ligand Structure on Catalyst Performance in the Synthesis of Nitrogen Heterocycles. J. Org. Chem. 2006, 71, 1471-1479.
    • (2006) J. Org. Chem. , vol.71 , pp. 1471-1479
    • Clark, A.J.1    Geden, J.V.2    Thom, S.3
  • 81
    • 0033521154 scopus 로고    scopus 로고
    • Efficient room temperature copper(I) mediated 5-endo radical cyclisations
    • DOI 10.1016/S0040-4039(99)01806-7, PII S0040403999018067
    • Clark, A.J.; Dell, C.P.; Ellard, J.M.; Hunt, N.A.; McDonagh, J.P. Efficient room temperature copper(I) mediated 5-endo radical cyclisations. Tetrahedron Lett. 1999, 40, 8619-8623. (Pubitemid 29531074)
    • (1999) Tetrahedron Letters , vol.40 , Issue.49 , pp. 8619-8623
    • Clark, A.J.1    Dell, C.P.2    Ellard, J.M.3    Hunt, N.A.4    McDonagh, J.P.5
  • 82
    • 77949637062 scopus 로고    scopus 로고
    • Catalytic atom-transfer radical cyclization by copper/bipyridine species encapsulated in polysiloxane
    • Motoyama, Y.; Kamo, K.; Yuasa, A.; Nagashima, H. Catalytic atom-transfer radical cyclization by copper/bipyridine species encapsulated in polysiloxane. Chem. Commun. (Camb.) 2010, 46, 2256-2258.
    • (2010) Chem. Commun. (Camb.) , vol.46 , pp. 2256-2258
    • Motoyama, Y.1    Kamo, K.2    Yuasa, A.3    Nagashima, H.4
  • 83
    • 17144416808 scopus 로고    scopus 로고
    • 2-mediated photochemical preparation of 2-substituted 1,3-dioxolanes and tetrahydrofurans from alcohols with polymer-supported hypervalent iodine reagent, PSDIB
    • DOI 10.1055/s-2005-864802, U02605ST
    • Teduka, T.; Togo, H. I2-Mediated Photochemical Preparation of 2-Substituted 1, 3-Dioxolanes and Tetrahydrofurans from Alcohols with Polymer-Supported Hypervalent Iodine Reagent, PSDIB. Synlett 2005, 2005, 923-926. (Pubitemid 40524257)
    • (2005) Synlett , Issue.6 , pp. 923-926
    • Teduka, T.1    Togo, H.2
  • 84
    • 30544437488 scopus 로고    scopus 로고
    • Oxidation of alcohols with nitroxyl radical resins under two-phase conditions
    • DOI 10.1055/s-2005-922775, U28805ST
    • Kashiwagi, Y.; Ikezoe, H.; Ono, T. Oxidation of Alcohols with Nitroxyl Radical Resins under Two-Phase Conditions. Synlett 2006, 2006, 69-72. (Pubitemid 43082391)
    • (2006) Synlett , Issue.1 , pp. 69-72
    • Kashiwagi, Y.1    Ikezoe, H.2    Ono, T.3
  • 85
    • 0030819770 scopus 로고    scopus 로고
    • Intermolecular free radical reactions on solid support. Allylation of esters
    • PII S0040403997104452
    • Sibi, M.P.; Chandramouli, S.V. Intermolecular free radical reactions on solid support. Allylation of esters. Tetrahedron Lett. 1997, 38, 8929-8932. (Pubitemid 27526183)
    • (1997) Tetrahedron Letters , vol.38 , Issue.52 , pp. 8929-8932
    • Sibi, M.P.1    Chandramouli, S.V.2
  • 86
    • 0000780387 scopus 로고    scopus 로고
    • Free radical allyl transfers utilizing soluble non-cross-linked polystyrene and carbohydrate scaffold supports
    • Enholm, E.J.; Gallagher, M.E.; Jiang, S.; Batson, W.A. Free Radical Allyl Transfers Utilizing Soluble Non-Cross-Linked Polystyrene and Carbohydrate Scaffold Supports. Org. Lett. 2000, 2, 3355-3357.
    • (2000) Org. Lett. , vol.2 , pp. 3355-3357
    • Enholm, E.J.1    Gallagher, M.E.2    Jiang, S.3    Batson, W.A.4
  • 87
    • 0000809126 scopus 로고    scopus 로고
    • Free radical reactions on soluble supports from ring-opening metathesis
    • DOI 10.1021/ol016632n
    • Enholm, E.J.; Gallagher, M.E. Free Radical Reactions on Soluble Supports from Ring-Opening Metathesis. Org. Lett. 2001, 3, 3397-3399. (Pubitemid 33625370)
    • (2001) Organic Letters , vol.3 , Issue.21 , pp. 3397-3399
    • Enholm, E.J.1    Gallagher, M.E.2
  • 89
    • 0000063548 scopus 로고    scopus 로고
    • Intermolecular conjugate addition of alkyl radicals on solid phase
    • Zhu, X.; Ganesan, A. Intermolecular Conjugate Addition of Alkyl Radicals on Solid Phase. J. Comb. Chem. 1999, 1, 157-162.
    • (1999) J. Comb. Chem. , vol.1 , pp. 157-162
    • Zhu, X.1    Ganesan, A.2
  • 90
    • 0037152292 scopus 로고    scopus 로고
    • Free radical addition of haloalkanes to polymer bound olefins and its application to the solid-phase synthesis of pyrethroids
    • Kumar, H.M.S.; Chakravarthy, P.P.; Rao, M.S.; Reddy, P.S.R.; Yadav, J.S. Free radical addition of haloalkanes to polymer bound olefins and its application to the solid-phase synthesis of pyrethroids. Tetrahedron Lett. 2002, 43, 7817-7819.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 7817-7819
    • Kumar, H.M.S.1    Chakravarthy, P.P.2    Rao, M.S.3    Reddy, P.S.R.4    Yadav, J.S.5
  • 91
    • 0033546094 scopus 로고    scopus 로고
    • Solid-phase synthesis of α-amino acids by radical addition to a dehydroalanine derivative
    • DOI 10.1016/S0040-4039(99)00799-6, PII S0040403999007996
    • Yim, A.M.; Vidal, Y.; Viallefont, P.; Martinez, J. Solid-phase synthesis of alpha-amino acids by radical addition to adehydroalanine derivative. Tetrahedron Lett. 1999, 40, 4535-4538. (Pubitemid 29251661)
    • (1999) Tetrahedron Letters , vol.40 , Issue.24 , pp. 4535-4538
    • Yim, A.-M.1    Vidal, Y.2    Viallefont, P.3    Martinez, J.4
  • 92
    • 0037118327 scopus 로고    scopus 로고
    • Solid-phase intermolecular radical reactions 2: Synthesis of C-glycopeptide mimetics via a novel acrylate acceptor
    • Caddick, S.; Hamza, D.; Wadman, S.N.; Wilden, J.D. Solid-Phase Intermolecular Radical Reactions 2: Synthesis of C-Glycopeptide Mimetics via a Novel Acrylate Acceptor. Org. Lett. 2002, 4, 1775-1777.
    • (2002) Org. Lett. , vol.4 , pp. 1775-1777
    • Caddick, S.1    Hamza, D.2    Wadman, S.N.3    Wilden, J.D.4
  • 93
    • 0033515460 scopus 로고    scopus 로고
    • Novel synthesis of α-amino acid derivatives through triethylborane- induced solid-phase radical reactions
    • DOI 10.1021/jo982466u
    • Miyabe, H.; Fujishima, Y.; Naito, T. Novel Synthesis of alpha-Amino Acid Derivatives through Triethylborane-Induced Solid-Phase Radical Reactions. J. Org. Chem. 1999, 64, 2174-2175. (Pubitemid 29180422)
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.7 , pp. 2174-2175
    • Miyabe, H.1    Fujishima, Y.2    Naito, T.3
  • 94
    • 0037430574 scopus 로고    scopus 로고
    • Carbon-carbon bond construction on solid support: Triethylborane-induced radical reactions of oxime ethers
    • DOI 10.1016/S0040-4020(03)00154-6
    • Miyabe, H.; Nishimura, A.; Fujishima, Y.; Naito, T. Carbon-carbon bond construction on solid support: triethylborane-induced radical reactions of oxime ethers. Tetrahedron 2003, 59, 1901-1907. (Pubitemid 36255671)
    • (2003) Tetrahedron , vol.59 , Issue.11 , pp. 1901-1907
    • Miyabe, H.1    Nishimura, A.2    Fujishima, Y.3    Naito, T.4
  • 95
    • 2942702314 scopus 로고    scopus 로고
    • Carbon-carbon bond construction based on radical addition to C=N bond
    • Miyabe, H.; Ueda, M.; Naito, T. Carbon-Carbon Bond Construction Based on Radical Addition to C=N Bond. Synlett 2004, 2004, 1140-1157. (Pubitemid 38797650)
    • (2004) Synlett , Issue.7 , pp. 1140-1157
    • Miyabe, H.1    Ueda, M.2    Naito, T.3
  • 96
    • 0033840493 scopus 로고    scopus 로고
    • Development of solid-phase radical reactions using oxime ethers as a radical acceptor
    • Miyabe, H. Development of Solid-Phase Radical Reactions Using Oxime Ethers as a Radical Acceptor. Yakugaku Zasshi 2000, 120, 667-676. (Pubitemid 30662912)
    • (2000) Yakugaku Zasshi , vol.120 , Issue.8 , pp. 667-676
    • Miyabe, H.1
  • 97
    • 0041421054 scopus 로고    scopus 로고
    • Development of carbon radical addition to imine derivatives
    • Miyabe, H. Development of Carbon Radical Addition to Imine Derivatives. Yakugaku Zasshi 2003, 123, 285-294. (Pubitemid 41327456)
    • (2003) Yakugaku Zasshi , vol.123 , Issue.5 , pp. 285-294
    • Miyabe, H.1
  • 98
    • 0000500365 scopus 로고    scopus 로고
    • Stereocontrol in solid-phase radical reactions: Radical addition to oxime ether anchored to polymer support
    • Miyabe, H.; Konishi, C.; Naito, T. Stereocontrol in Solid-Phase Radical Reactions: Radical Addition to Oxime Ether Anchored to Polymer Support. Org. Lett. 2000, 2, 1443-1445.
    • (2000) Org. Lett. , vol.2 , pp. 1443-1445
    • Miyabe, H.1    Konishi, C.2    Naito, T.3
  • 99
    • 0642371240 scopus 로고    scopus 로고
    • Diastereoselective solid-phase radical addition to oxime ether anchored to polymer support
    • Miyabe, H.; Konishi, C.; Naito, T. Diastereoselective Solid-Phase Radical Addition to Oxime Ether Anchored to Polymer Support. Chem. Pharm. Bull. 2003, 51, 540-544. (Pubitemid 41656805)
    • (2003) Chemical and Pharmaceutical Bulletin , vol.51 , Issue.5 , pp. 540-544
    • Miyabe, H.1    Konishi, C.2    Naito, T.3
  • 100
    • 0033972363 scopus 로고    scopus 로고
    • Radical reaction of phenylsulfonyl oxime ethers on solid support: Application to the synthesis of α-amino esters
    • Jeon, G.H.; Yoon, J.Y.; Kim, S.; Kim, S.S. Radical Reaction of Phenylsulfonyl Oxime Ethers on Solid Support: Application to the Synthesis of alpha-Amino Esters. Synlett 2000, 2000, 128-130. (Pubitemid 30056092)
    • (2000) Synlett , Issue.1 , pp. 128-130
    • Jeon, G.-H.1    Yoon, J.-Y.2    Kim, S.3    Kim, S.S.4
  • 101
    • 0033607738 scopus 로고    scopus 로고
    • Triethylborane-induced solid-phase radical cyclization of oxime ethers
    • DOI 10.1016/S0040-4039(99)01788-8, PII S0040403999017888
    • Miyabe, H.; Tanaka, H.; Naito, T. Triethylborane-induced solid-phase radical cyclization of oxime ethers. Tetrahedron Lett. 1999, 40, 8387-8390. (Pubitemid 29524817)
    • (1999) Tetrahedron Letters , vol.40 , Issue.48 , pp. 8387-8390
    • Miyabe, H.1    Tanaka, H.2    Naito, T.3
  • 102
    • 0035821167 scopus 로고    scopus 로고
    • Solid-phase tandem radical addition-cyclisation reaction of oxime ethers
    • Miyabe, H.; Fujii, K.; Tanaka, H.; Naito, T. Solid-phase tandem radical addition-cyclisation reaction of oxime ethers. Chem. Commun. (Camb.) 2001, 831-832. (Pubitemid 32417502)
    • (2001) Chemical Communications , Issue.9 , pp. 831-832
    • Miyabe, H.1    Fujii, K.2    Tanaka, H.3    Naito, T.4
  • 103
    • 16544386947 scopus 로고    scopus 로고
    • Solid-phase tandem radical addition-cyclization reaction: Triethylborane-induced reaction of oxime ethers anchored to polymer support
    • DOI 10.1248/cpb.52.842
    • Miyabe, H.; Tanaka, H.; Naito, T. Solid-Phase Tandem Radical Addition-Cyclization Reaction: Triethylborane-Induced Reaction of Oxime Ethers Anchored to Polymer Support. Chem. Pharm. Bull. 2004, 52, 842-847. (Pubitemid 41679575)
    • (2004) Chemical and Pharmaceutical Bulletin , vol.52 , Issue.7 , pp. 842-847
    • Miyabe, H.1    Tanaka, H.2    Naito, T.3
  • 104
    • 3142692422 scopus 로고    scopus 로고
    • Solid-phase synthesis of indol-2-ones by microwave-assisted radical cyclization
    • Akamatsu, H.; Fukase, K.; Kusumoto, S. Solid-Phase Synthesis of Indol-2-ones by Microwave- Assisted Radical Cyclization. Synlett 2004, 2004, 1049-1053. (Pubitemid 38925061)
    • (2004) Synlett , Issue.6 , pp. 1049-1053
    • Akamatsu, H.1    Fukase, K.2    Kusumoto, S.3
  • 106
    • 13944260490 scopus 로고    scopus 로고
    • Synthetic applications of aryl radical building blocks for cyclisation onto azoles
    • DOI 10.1016/j.tet.2005.01.064
    • Allin, S.M.; Bowman, W.R.; Elsegood, M.R.J.; McKee, V.; Karim, R.; Rahman, S.S. Synthetic applications of aryl radical building blocks for cyclisation onto azoles. Tetrahedron 2005, 61, 2689-2696. (Pubitemid 40267670)
    • (2005) Tetrahedron , vol.61 , Issue.10 , pp. 2689-2696
    • Allin, S.M.1    Bowman, W.R.2    Elsegood, M.R.J.3    McKee, V.4    Karim, R.5    Rahman, S.S.6
  • 107
    • 0032806957 scopus 로고    scopus 로고
    • Functionalization via radical cyclization of cyclohexenediol derivatives bound to polystyrene
    • Berteina, S.; de Mesmaeker, A.; Wendeborn, S. Functionalization via Radical Cyclization of Cyclohexenediol Derivatives Bound to Polystyrene. Synlett 1999, 1999, 1121-1123. (Pubitemid 29360876)
    • (1999) Synlett , Issue.7 , pp. 1121-1123
    • Berteina, S.1    De Mesmaeker, A.2    Wendeborn, S.3
  • 108
    • 0030826980 scopus 로고    scopus 로고
    • 2-mediated radical cyclization
    • 2-Mediated Radical Cyclization. J. Org. Chem. 1997, 62, 5678-5679.
    • (1997) J. Org. Chem. , vol.62 , pp. 5678-5679
    • Du, X.1    Armstrong, R.W.2
  • 109
    • 0032537215 scopus 로고    scopus 로고
    • 2-mediated sequential radical cyclization/anionic capture of aryl iodides on solid support
    • DOI 10.1016/S0040-4039(98)00292-5, PII S0040403998002925
    • 2-mediated sequential radical cyclization/anionic capture of aryl iodides on solid support. Tetrahedron Lett. 1998, 39, 2281-2284. (Pubitemid 28167941)
    • (1998) Tetrahedron Letters , vol.39 , Issue.16 , pp. 2281-2284
    • Du, X.1    Armstrong, R.W.2
  • 110
    • 0032490966 scopus 로고    scopus 로고
    • Application of radical chemistry to solid support synthesis
    • DOI 10.1016/S0040-4039(98)01172-1, PII S0040403998011721
    • Berteina, S.; Mesmaeker, A.D. Application of radical chemistry to solid support synthesis. Tetrahedron Lett. 1998, 39, 5759-5762. (Pubitemid 28346310)
    • (1998) Tetrahedron Letters , vol.39 , Issue.32 , pp. 5759-5762
    • Berteina, S.1    De Mesmaeker, A.2
  • 111
    • 0002334207 scopus 로고    scopus 로고
    • Radical and palladium-mediated cyclizations of ortho-iodo benzyl enamines: Application to solid phase synthesis
    • Berteina, S.; Wendeborn, S.; de Mesmaeker, A. Radical and Palladium-Mediated Cyclization of Ortho-Iodo Benzyl Enamines: Application to Solid Phase Synthesis. Synlett 1998, 1998, 1231-1233. (Pubitemid 128694211)
    • (1998) Synlett , Issue.11 , pp. 1231-1233
    • Berteina, S.1    Wendeborn, S.2    De Mesmaeker, A.3
  • 112
    • 14644420179 scopus 로고    scopus 로고
    • A cleaner approach to solid-supported radical chemistry: Application of hypophosphite salts to intramolecular C-C bond formation on the solid-phase
    • DOI 10.1055/s-2005-862376, D19304ST
    • Chevet, C.; Jackson, T.; Santry, B.; Routledge, A. A Cleaner Approach to Solid-Supported Radical Chemistry: Application of Hypophosphite Salts to Intramolecular C-C Bond Formation on the Solid-Phase. Synlett 2005, 2005, 477-480. (Pubitemid 40314120)
    • (2005) Synlett , Issue.3 , pp. 477-480
    • Chevet, C.1    Jackson, T.2    Santry, B.3    Routledge, A.4
  • 114
    • 0002464476 scopus 로고    scopus 로고
    • An Investigation into Solid-Phase Radical Chemistry - Synthesis of Furan Rings
    • Routledge, A.; Abell, C.; Balasubramanian, S. An Investigation into Solid-Phase Radical Chemistry-Synthesis of Furan Rings. Synlett 1997, 1997, 61-62. (Pubitemid 127495740)
    • (1997) Synlett , vol.1997 , Issue.1 , pp. 61-62
    • Routledge, A.1    Abell, C.2    Balasubramanian, S.3
  • 115
    • 0034074359 scopus 로고    scopus 로고
    • Solid-phase synthesis of 1-chloromethyl-1,2-dihydro-3H-benz[e]indole (seco-CBI) and a polyamide conjugate
    • Jia, G.; Iida, H.; Lown, J.W. Solid-Phase Synthesis of 1-Chloromethyl-1, 2-dihydro-3Hbenz[ e]indole (seco-CBI) and a Polyamide Conjugate. Synlett 2000, 2000, 603-606. (Pubitemid 30339869)
    • (2000) Synlett , Issue.5 , pp. 603-606
    • Jia, G.1    Iida, H.2    Lown, J.W.3
  • 116
    • 0033597245 scopus 로고    scopus 로고
    • Radical cyclization on solid support: Synthesis of γ-butyrolactones
    • DOI 10.1016/S0040-4039(99)00503-1, PII S0040403999005031
    • Watanabe, Y.; Ishikawa, S.; Takao, G.; Toru, T. Radical cyclization on solid support: Synthesis of gamma-butyrolactones. Tetrahedron Lett. 1999, 40, 3411-3414. (Pubitemid 29189401)
    • (1999) Tetrahedron Letters , vol.40 , Issue.17 , pp. 3411-3414
    • Watanabe, Y.1    Ishikawa, S.2    Takao, G.3    Toru, T.4
  • 117
    • 0000348093 scopus 로고    scopus 로고
    • Highly diastereoselective radical cyclizations on soluble ring opening metathesis supports
    • Enholm, E.J.; Cottone, J.S. Highly Diastereoselective Radical Cyclizations on Soluble Ring Opening Metathesis Supports. Org. Lett. 2001, 3, 3959-3962.
    • (2001) Org. Lett. , vol.3 , pp. 3959-3962
    • Enholm, E.J.1    Cottone, J.S.2
  • 118
    • 0032538355 scopus 로고    scopus 로고
    • Use of Lewis acids in free radical reactions
    • DOI 10.1002/(SICI)1521-3773(19981016)37:19<2562::AID-ANIE2562>3.0. CO;2-D
    • Renaud, P.; Gerster, M. Use of Lewis Acids in Free Radical Reactions. Angew. Chem. Int. Ed. Engl. 1998, 37, 2562-2579. (Pubitemid 28501503)
    • (1998) Angewandte Chemie - International Edition , vol.37 , Issue.19 , pp. 2562-2579
    • Renaud, P.1    Gerster, M.2
  • 119
    • 0031440150 scopus 로고    scopus 로고
    • Construction of chiral quaternary carbon centers by catalytic enantioselective radical-mediated alkylation of α-iodolactones using allyltributyltin in the presence of a chiral Lewis acid
    • DOI 10.1021/ja972065g
    • Murakata, M.; Jono, T.; Mizuno, Y.; Hoshino, O. Construction of Chiral Quaternary Carbon Centers by Catalytic Enantioselective Radical-Mediated Allylation of alpha-Iodolactones Using Allyltributyltin in the Presence of a Chiral Lewis Acid. J. Am. Chem. Soc. 1997, 119, 11713-11714. (Pubitemid 28006143)
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.48 , pp. 11713-11714
    • Murakata, M.1    Jono, T.2    Mizuno, Y.3    Hoshino, O.4
  • 120
    • 12044254102 scopus 로고
    • Acyclic stereochemical control in free-radical reactions
    • Porter, N.A.; Giese, B.; Curran, D.P. Acyclic stereochemical control in free-radical reactions. Acc. Chem. Res. 1991, 24, 296-304.
    • (1991) Acc. Chem. Res. , vol.24 , pp. 296-304
    • Porter, N.A.1    Giese, B.2    Curran, D.P.3
  • 121
    • 0028850710 scopus 로고
    • A simple preparation of (R)-(2-cyclopentenyl)acetic acid and (R)-(2-cyclohexenyl)acetic acid using beta-diastereoselective radical cyclization in the presence of Lewis acid
    • Nishida, M.; Hayashi, H.; Yamaura, Y.; Yanaginuma, E.; Yonemitsu, O.; Nishida, A.; Kawahara, N. A simple preparation of (R)-(2-cyclopentenyl)acetic acid and (R)-(2-cyclohexenyl)acetic acid using beta-diastereoselective radical cyclization in the presence of Lewis acid. Tetrahedron Lett. 1995, 36, 269-272.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 269-272
    • Nishida, M.1    Hayashi, H.2    Yamaura, Y.3    Yanaginuma, E.4    Yonemitsu, O.5    Nishida, A.6    Kawahara, N.7
  • 123
    • 33748219558 scopus 로고    scopus 로고
    • Diastereoselective Chelation-Controlled Radical Cyclization of Chiral Oxazolidinone-Derived 2-Alkenamides and Modeling of the Transition State
    • Badone, D.; Bernassau, J.M.; Cardamone, R.; Guzzi, U. Diastereoselective Chelation-Controlled Radical Cyclization of Chiral Oxazolidinone-Derived 2-Alkenamides and Modeling of the Transition State. Angew. Chem. Int. Ed. Engl. 1996, 35, 535-538. (Pubitemid 126665338)
    • (1996) Angewandte Chemie (International Edition in English) , vol.35 , Issue.5 , pp. 535-538
    • Badone, D.1    Bernassau, J.-M.2    Cardamone, R.3    Guzzi, U.4
  • 124
    • 5644264941 scopus 로고    scopus 로고
    • Thiol-mediated free radical cyclisations of isocyanides on solid support
    • DOI 10.1016/j.tetlet.2004.09.078, PII S0040403904020362
    • Lamberto, M.; Corbett, D.F.; Kilburn, J.D. Thiol-mediated free radical cyclisations of isocyanides on solid support. Tetrahedron Lett. 2004, 45, 8541-8543. (Pubitemid 39369910)
    • (2004) Tetrahedron Letters , vol.45 , Issue.46 , pp. 8541-8543
    • Lamberto, M.1    Corbett, D.F.2    Kilburn, J.D.3
  • 125
    • 0037433941 scopus 로고    scopus 로고
    • Sulfur-mediated radical cyclisation reactions on solid support
    • DOI 10.1016/S0040-4039(02)02594-7, PII S0040403902025947
    • Harrowven, D.C.; May, P.J.; Bradley, M. Sulfur-mediated radical cyclisation reactions on solid support. Tetrahedron Lett. 2003, 44, 503-506. (Pubitemid 36009243)
    • (2003) Tetrahedron Letters , vol.44 , Issue.3 , pp. 503-506
    • Harrowven, D.C.1    May, P.J.2    Bradley, M.3
  • 126
    • 0000020896 scopus 로고
    • Regio- and stereo-selectivity of alkenyl radical ring closure: A theoretical study
    • Beckwith, A.L.J.; Schiesser, C.H. Regio- and stereo-selectivity of alkenyl radical ring closure: A theoretical study. Tetrahedron 1985, 41, 3925-3941.
    • (1985) Tetrahedron , vol.41 , pp. 3925-3941
    • Beckwith, A.L.J.1    Schiesser, C.H.2
  • 127
    • 33845282341 scopus 로고
    • Force-field model for intramolecular radical additions
    • Spellmeyer, D.C.; Houk, K.N. Force-field model for intramolecular radical additions. J. Org. Chem. 1987, 52, 959-974.
    • (1987) J. Org. Chem. , vol.52 , pp. 959-974
    • Spellmeyer, D.C.1    Houk, K.N.2
  • 128
    • 0033153049 scopus 로고    scopus 로고
    • Total synthesis of the CP molecules CP-263,114 and CP-225,917- Part 1: Synthesis of key intermediates and intelligence gathering
    • DOI 10.1002/(SICI)1521-3773(19990601)38:11<1669::AID-ANIE1669>3.0. CO;2-D
    • Nicolaou, K.C.; Baran, P.S.; Zhong, Y.L.; Choi, H.S.; Yoon, W.H.; He, Y.; Fong, K.C. Total Synthesis of the CP Molecules CP-263, 114 and CP-225, 917 - Part 1: Synthesis of Key Intermediates and Intelligence Gathering. Angew. Chem. Int. Ed. Engl. 1999, 38, 1669-1675. (Pubitemid 29288787)
    • (1999) Angewandte Chemie - International Edition , vol.38 , Issue.11 , pp. 1669-1675
    • Nicolaou, K.C.1    Baran, P.S.2    Zhong, Y.-L.3    Choi, H.-S.4    Yoon, W.H.5    He, Y.6    Fong, K.C.7
  • 129
    • 0033152137 scopus 로고    scopus 로고
    • Total synthesis of the cp molecules cp-225,917 and cp-263,114 - Part 2: Evolution of the final strategy
    • DOI 10.1002/(SICI)1521-3773(19990601)38:11<1676::AID-ANIE1676>3.0. CO;2-T
    • Nicolaou, K.C.; Baran, P.S.; Zhong, Y.L.; Fong, K.C.; He, Y.; Yoon, W.H.; Choi, H.S. Total Synthesis of the CP Molecules CP-225, 917 and CP-263, 114 - Part 2: Evolution of the Final Strategy. Angew. Chem. Int. Ed. Engl. 1999, 38, 1676-1678. (Pubitemid 29288788)
    • (1999) Angewandte Chemie - International Edition , vol.38 , Issue.11 , pp. 1676-1678
    • Nicolaou, K.C.1    Baran, P.S.2    Zhong, Y.-L.3    Fong, K.C.4    He, Y.5    Yoon, W.H.6    Choi, H.-S.7
  • 130
    • 0034603046 scopus 로고    scopus 로고
    • New synthetic technology for the rapid construction of novel heterocycles - Part 1: The reaction of Dess - Martin periodinane with anilides and related compounds
    • DOI 10.1002/(SICI)1521-3773(20000204)39:3<622::AID-ANIE622>3.0. CO;2-B
    • Nicolaou, K.C.; Zhong, Y.L.; Baran, P.S. New Synthetic Technology for the Rapid Construction of Novel Heterocycles - Part 1: The Reaction of Dess-Martin Periodinane with Anilides and Related Compounds. Angew. Chem. Int. Ed. Engl. 2000, 39, 622-625. (Pubitemid 30101761)
    • (2000) Angewandte Chemie - International Edition , vol.39 , Issue.3 , pp. 622-625
    • Nicolaou, K.C.1    Zhong, Y.-L.2    Baran, P.S.3
  • 131
    • 0037070584 scopus 로고    scopus 로고
    • Iodine(V) reagents in organic synthesis. Part 3. New routes to heterocyclic compounds via o-iodoxybenzoic acid-mediated cyclizations: Generality, scope, and mechanism
    • DOI 10.1021/ja012126h
    • Nicolaou, K.C.; Baran, P.S.; Zhong, Y.L.; Barluenga, S.; Hunt, K.W.; Kranich, R.; Vega, J.A. Iodine(V) Reagents in Organic Synthesis. Part 3: New Routes to Heterocyclic Compounds via o-Iodoxybenzoic Acid-Mediated Cyclizations: Generality, Scope, and Mechanism. J. Am. Chem. Soc. 2002, 124, 2233-2244. (Pubitemid 34267109)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.10 , pp. 2233-2244
    • Nicolaou, K.C.1    Baran, P.S.2    Zhong, Y.-L.3    Barluenga, S.4    Hunt, K.W.5    Kranich, R.6    Vega, J.A.7
  • 132
    • 0033214241 scopus 로고    scopus 로고
    • Solid-phase intermolecular radical reactions 1. Sulfonyl radical addition to isolated alkenes and alkynes
    • DOI 10.1016/S0040-4039(99)01525-7, PII S0040403999015257
    • Caddick, S.; Hamza, D.; Wadman, S.N. Solid-phase intermolecular radical reactions 1. Sulfonyl radical addition to isolated alkenes and alkynes. Tetrahedron Lett. 1999, 40, 7285-7288. (Pubitemid 29456980)
    • (1999) Tetrahedron Letters , vol.40 , Issue.40 , pp. 7285-7288
    • Caddick, S.1    Hamza, D.2    Wadman, S.N.3
  • 133
    • 0035102971 scopus 로고    scopus 로고
    • Solid-phase free radical addition of thiols to allyl ethers
    • Plourde Jr, R.; Johnson Jr, L.L.; Longo, R.K. Solid-Phase Free Radical Addition of Thiols to Allyl Ethers. Synlett 2001, 2001, 439-441. (Pubitemid 32216055)
    • (2001) Synlett , Issue.3 , pp. 439-441
    • Plourde R., Jr.1    Johnson L.L., Jr.2    Longo, R.K.3
  • 134
    • 0034701512 scopus 로고    scopus 로고
    • Constructing the 2-(thiobenzyl)ethyl carbamate linker via thiyl radical addition
    • DOI 10.1016/S0040-4039(00)00324-5, PII S0040403900003245
    • Timár, Z.; Gallagher, T. Constructing the 2-(thiobenzyl)ethyl carbamate linker via thiyl radical addition. Tetrahedron Lett. 2000, 41, 3173-3176. (Pubitemid 30256766)
    • (2000) Tetrahedron Letters , vol.41 , Issue.17 , pp. 3173-3176
    • Timar, Z.1    Gallagher, T.2
  • 135
    • 0037043176 scopus 로고    scopus 로고
    • Xanthates and solid-phase chemistry. A new soluble polymer analogue of Wang resin
    • DOI 10.1016/S0040-4020(02)00526-4, PII S0040402002005264
    • Dublanchet, A.C.; Lusinchi, M.; Zard, S.Z. Xanthates and solid-phase chemistry. A new soluble polymer analogue of Wang resin. Tetrahedron 2002, 58, 5715-5721. (Pubitemid 34722909)
    • (2002) Tetrahedron , vol.58 , Issue.28 , pp. 5715-5721
    • Dublanchet, A.-C.1    Lusinchi, M.2    Zard, S.Z.3
  • 136
    • 33645457635 scopus 로고    scopus 로고
    • Cyclizations and cycloadditions of acetylenic sulfones on solid supports
    • Back, T.G.; Zhai, H. Cyclizations and cycloadditions of acetylenic sulfones on solid supports. Chem. Commun. (Camb.) 2006, 21, 326-328.
    • (2006) Chem. Commun. (Camb.) , vol.21 , pp. 326-328
    • Back, T.G.1    Zhai, H.2
  • 137
    • 0035858760 scopus 로고    scopus 로고
    • The Barton radical decarboxylation on solid phase. A versatile synthesis of peptides containing modified amino acids
    • DOI 10.1016/S0040-4039(01)00496-8, PII S0040403901004968
    • Attardi, M.E.; Taddei, M. The Barton radical decarboxylation on solid phase. A versatile synthesis of peptides containing modified amino acids. Tetrahedron Lett. 2001, 42, 3519-3522. (Pubitemid 32385753)
    • (2001) Tetrahedron Letters , vol.42 , Issue.20 , pp. 3519-3522
    • Attardi, M.E.1    Taddei, M.2
  • 138
    • 70349140106 scopus 로고    scopus 로고
    • Chemoselective nitration of phenols with tert-butyl nitrite in solution and on solid support
    • Koley, D.; Colon, O.C.; Savinov, S.N. Chemoselective Nitration of Phenols with tert-Butyl Nitrite in Solution and on Solid Support. Org. Lett. 2009, 11, 4172-4175.
    • (2009) Org. Lett. , vol.11 , pp. 4172-4175
    • Koley, D.1    Colon, O.C.2    Savinov, S.N.3


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