메뉴 건너뛰기




Volumn 41, Issue 11, 2008, Pages 1512-1522

Catalytic sequential reactions involving palladacycle-directed aryl coupling steps

Author keywords

[No Author keywords available]

Indexed keywords


EID: 57549092674     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar800040u     Document Type: Review
Times cited : (466)

References (52)
  • 3
    • 57549100910 scopus 로고    scopus 로고
    • Diederich, F, de Meijere, A, Eds, 2nd ed, Wiley-VCH: Weinheim, Germany
    • (a) Diederich, F., de Meijere, A., Eds. Metal-Catalyzed Cross-Coupling Reactions, 2nd ed.; Wiley-VCH: Weinheim, Germany, 2004.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions
  • 4
    • 0036589259 scopus 로고    scopus 로고
    • Aryl-Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
    • (b) Hassan, J.; Sévignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Aryl-Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction. Chem. Rev. 2002, 102, 1359-1469.
    • (2002) Chem. Rev , vol.102 , pp. 1359-1469
    • Hassan, J.1    Sévignon, M.2    Gozzi, C.3    Schulz, E.4    Lemaire, M.5
  • 5
    • 33846918696 scopus 로고    scopus 로고
    • Aryl-Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
    • (a) Alberico, D.; Scott, M. E.; Lautens, M. Aryl-Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation. Chem. Rev. 2007, 107, 174-238.
    • (2007) Chem. Rev , vol.107 , pp. 174-238
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 6
    • 33744510833 scopus 로고    scopus 로고
    • Dyker, G, Ed, Wiley-VCH Verlag: Weinheim, Germany
    • (b) Dyker, G., Ed. Handbook of C-H Transformations; Wiley-VCH Verlag: Weinheim, Germany, 2005.
    • (2005) Handbook of C-H Transformations
  • 7
    • 0037288964 scopus 로고    scopus 로고
    • Catalytic Multistep Reactions via Palladacycles
    • (a) Catellani, M. Catalytic Multistep Reactions via Palladacycles. Synlett 2003, 298-313.
    • (2003) Synlett , pp. 298-313
    • Catellani, M.1
  • 8
    • 33745455671 scopus 로고    scopus 로고
    • Novel Methods of Aromatic Functionalization Using Palladium and Norbornene as a Unique Catalytic System
    • Tsuji, J, Ed, Springer: Berlin
    • (b) Catellani, M. Novel Methods of Aromatic Functionalization Using Palladium and Norbornene as a Unique Catalytic System. In Palladium in Organic Synthesis: Tsuji, J., Ed.; Springer: Berlin, 2005, pp 21-53.
    • (2005) Palladium in Organic Synthesis , pp. 21-53
    • Catellani, M.1
  • 9
    • 50849151376 scopus 로고
    • Addition of Aryl Halides to Tetrakis(triphenylphosphine)palladium(0)
    • (a) Fitton, P.; Rick, E. A. Addition of Aryl Halides to Tetrakis(triphenylphosphine)palladium(0). J. Organomet. Chem. 1971, 28, 287-291.
    • (1971) J. Organomet. Chem , vol.28 , pp. 287-291
    • Fitton, P.1    Rick, E.A.2
  • 10
    • 0242498414 scopus 로고    scopus 로고
    • Roy, A. H.; Hartwig, J. F. Directly Observed Reductive Elimination of Aryl Halides from Monomeric Arylpalladium(II) Halide Complexes. J. Am. Chem. Soc. 2003, 125, 13944-13945.
    • (b) Roy, A. H.; Hartwig, J. F. Directly Observed Reductive Elimination of Aryl Halides from Monomeric Arylpalladium(II) Halide Complexes. J. Am. Chem. Soc. 2003, 125, 13944-13945.
  • 11
    • 0001940158 scopus 로고
    • Reaction of Norbornenes with Phenylpalladium Chloride
    • (a) Horino, H.; Arai, M.; Inoue, N. Reaction of Norbornenes with Phenylpalladium Chloride. Tetrahedron Lett. 1974, 647-650.
    • (1974) Tetrahedron Lett , pp. 647-650
    • Horino, H.1    Arai, M.2    Inoue, N.3
  • 13
    • 0000051004 scopus 로고
    • Reactions of Electron-Rich Arylpalladium Complexes with Olefins. Origin of the Chelate Effect in Vinylation Catalysis
    • (c) Portnoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Reactions of Electron-Rich Arylpalladium Complexes with Olefins. Origin of the Chelate Effect in Vinylation Catalysis. Organometallics 1994, 13, 3465-3479.
    • (1994) Organometallics , vol.13 , pp. 3465-3479
    • Portnoy, M.1    Ben-David, Y.2    Rousso, I.3    Milstein, D.4
  • 15
    • 84981922386 scopus 로고
    • The syn and anti Steric Course in Bimolecular Olefin-Forming Eliminations
    • Sicher, J. The syn and anti Steric Course in Bimolecular Olefin-Forming Eliminations. Angew. Chem., Int. Ed Engl. 1972, 11, 200-214.
    • (1972) Angew. Chem., Int. Ed Engl , vol.11 , pp. 200-214
    • Sicher, J.1
  • 17
    • 0002406804 scopus 로고
    • Palladium-(II) and -(IV) Complexes as Intermediates in Catalytic C-C Bond-Forming Reactions
    • (b) Catellani, M.; Chiusoli, G. P. Palladium-(II) and -(IV) Complexes as Intermediates in Catalytic C-C Bond-Forming Reactions. J. Organomet. Chem. 1988, 346, C27-C30.
    • (1988) J. Organomet. Chem , vol.346
    • Catellani, M.1    Chiusoli, G.P.2
  • 18
    • 33748217906 scopus 로고
    • Palladacycles as Intermediates for Selective Dialkylation of Arenes and Subsequent Fragmentation
    • Catellani, M.; Fagnola, M. C. Palladacycles as Intermediates for Selective Dialkylation of Arenes and Subsequent Fragmentation. Angew. Chem., Int. Ed Engl. 1994, 33, 2421-2422.
    • (1994) Angew. Chem., Int. Ed Engl , vol.33 , pp. 2421-2422
    • Catellani, M.1    Fagnola, M.C.2
  • 19
    • 0007689590 scopus 로고
    • Reversible Insertion of Norbornene into a Nickel-Methallyl Bond
    • Gallazzi, M. C.; Porri, L.; Vitulli, G. Reversible Insertion of Norbornene into a Nickel-Methallyl Bond. J. Organomet. Chem. 1975, 97, 131-138.
    • (1975) J. Organomet. Chem , vol.97 , pp. 131-138
    • Gallazzi, M.C.1    Porri, L.2    Vitulli, G.3
  • 20
    • 0030745436 scopus 로고    scopus 로고
    • A Complex Catalytic Cycle Leading to a Regioselective Synthesis of o,o′-Disubstituted Vinylarenes
    • (a) Catellani, M.; Frignani, F.; Rangoni, A. A Complex Catalytic Cycle Leading to a Regioselective Synthesis of o,o′-Disubstituted Vinylarenes. Angew. Chem., Int. Ed. Engl. 1997, 36, 119-122.
    • (1997) Angew. Chem., Int. Ed. Engl , vol.36 , pp. 119-122
    • Catellani, M.1    Frignani, F.2    Rangoni, A.3
  • 21
    • 0034695701 scopus 로고    scopus 로고
    • Symmetrical and Unsymmetrical 2,6-Dialkyl-1,1′-Biaryls by Combined Catalysis of Aromatic Alkylation via Palladacycles and Suzuki-Type Coupling
    • (b) Catellani, M.; Motti, E.; Minari, M. Symmetrical and Unsymmetrical 2,6-Dialkyl-1,1′-Biaryls by Combined Catalysis of Aromatic Alkylation via Palladacycles and Suzuki-Type Coupling. Chem. Commun. 2000, 157-158.
    • (2000) Chem. Commun , pp. 157-158
    • Catellani, M.1    Motti, E.2    Minari, M.3
  • 22
    • 18744372924 scopus 로고    scopus 로고
    • Palladium Catalyzed Multicomponent Reactions in Ordered Sequence: New Syntheses of o,o′-Dialkylsubstituted Diarylacetylenes and Diarylalkylidenehexahydromethanofluorenes
    • (c) Motti, E.; Rossetti, M.; Bocelli, G.; Catellani, M. Palladium Catalyzed Multicomponent Reactions in Ordered Sequence: New Syntheses of o,o′-Dialkylsubstituted Diarylacetylenes and Diarylalkylidenehexahydromethanofluorenes. J. Organomet. Chem. 2004, 689, 3741-3749.
    • (2004) J. Organomet. Chem , vol.689 , pp. 3741-3749
    • Motti, E.1    Rossetti, M.2    Bocelli, G.3    Catellani, M.4
  • 24
    • 0000182523 scopus 로고
    • Conformational Effects in Elementary Steps in Catalytic Reactions. Oxidative Addition of 3-Bromoprop-1-ene to a Palladium(II) Metallacyclic Complex
    • (a) Catellani, M.; Mann, B. E. Conformational Effects in Elementary Steps in Catalytic Reactions. Oxidative Addition of 3-Bromoprop-1-ene to a Palladium(II) Metallacyclic Complex. J. Organomet. Chem. 1990, 390, 251-255.
    • (1990) J. Organomet. Chem , vol.390 , pp. 251-255
    • Catellani, M.1    Mann, B.E.2
  • 25
    • 0002083534 scopus 로고
    • Regioselective Ring Opening of a Palladium(IV) Alkylaromatic Metallacycle by Benzyl Group Migration tram Palladium to the Aromatic Carbon and X-ray Structure of the Resulting Palladium(II) Complex
    • (b) Bocelli, G.; Catellani, M.; Ghelli, S. Regioselective Ring Opening of a Palladium(IV) Alkylaromatic Metallacycle by Benzyl Group Migration tram Palladium to the Aromatic Carbon and X-ray Structure of the Resulting Palladium(II) Complex. J. Organomet. Chem. 1993, 458, C12-C15.
    • (1993) J. Organomet. Chem , vol.458
    • Bocelli, G.1    Catellani, M.2    Ghelli, S.3
  • 26
    • 0002521519 scopus 로고    scopus 로고
    • For Pd(IV), see: Canty, A. J. Development of Organopalladium(IV) Chemistry: Fundamental Aspects and Systems for Studies of Mechanism in Organometallic Chemistry and Catalysis. Acc. Chem. Res. 1992, 25, 83-90.
    • (c) For Pd(IV), see: Canty, A. J. Development of Organopalladium(IV) Chemistry: Fundamental Aspects and Systems for Studies of Mechanism in Organometallic Chemistry and Catalysis. Acc. Chem. Res. 1992, 25, 83-90.
  • 27
    • 9344257648 scopus 로고    scopus 로고
    • Catellani, M.; Chiusoli, G. P. Palladium-Catalyzed Synthesis of 1,2,3,4,4a, 12b-Hexahydro-1,4-methanotriphenylenes. J. Organomet. Chem. 1985, 286, C13-C16.
    • Catellani, M.; Chiusoli, G. P. Palladium-Catalyzed Synthesis of 1,2,3,4,4a, 12b-Hexahydro-1,4-methanotriphenylenes. J. Organomet. Chem. 1985, 286, C13-C16.
  • 28
    • 0000879572 scopus 로고    scopus 로고
    • Selective Aryl Coupling via Palladacycles: A New Route to m-Alkylbiphenyls or m-Terphenyls
    • Catellani, M.; Motti, E. Selective Aryl Coupling via Palladacycles: A New Route to m-Alkylbiphenyls or m-Terphenyls. New J. Chem. 1998, 22, 759-761.
    • (1998) New J. Chem , vol.22 , pp. 759-761
    • Catellani, M.1    Motti, E.2
  • 29
    • 0348013280 scopus 로고    scopus 로고
    • Synthesis of Selectively Substituted ortho-Vinylbiphenyls by Palladium-Catalysed Reaction of ortho-Substituted Aryl Iodides with Olefins
    • Motti, E.; Ippomei, G.; Deledda, S.; Catellani, M. Synthesis of Selectively Substituted ortho-Vinylbiphenyls by Palladium-Catalysed Reaction of ortho-Substituted Aryl Iodides with Olefins. Synthesis 2003, 2671-2678.
    • (2003) Synthesis , pp. 2671-2678
    • Motti, E.1    Ippomei, G.2    Deledda, S.3    Catellani, M.4
  • 30
    • 0000702671 scopus 로고
    • Palladium-Catalyzed Vinylation of Organic Halides
    • (a) Heck, R. F. Palladium-Catalyzed Vinylation of Organic Halides. Org. React. 1982, 27, 345-390.
    • (1982) Org. React , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 31
    • 0038584673 scopus 로고
    • Recent Developments and New Perspectives in the Heck Reaction
    • (b) Cabri, W.; Candiani, I. Recent Developments and New Perspectives in the Heck Reaction. Acc. Chem. Res. 1995, 28, 2-7.
    • (1995) Acc. Chem. Res , vol.28 , pp. 2-7
    • Cabri, W.1    Candiani, I.2
  • 32
    • 0029846361 scopus 로고    scopus 로고
    • An Improved Synthesis of 1,4-cis,exo-Hexa- or Tetrahydromethano- or -Ethanobiphenylene Derivatives Catalyzed by Palladium Complexes
    • Catellani, M.; Ferioli, L. An Improved Synthesis of 1,4-cis,exo-Hexa- or Tetrahydromethano- or -Ethanobiphenylene Derivatives Catalyzed by Palladium Complexes. Synthesis 1996, 769-772.
    • (1996) Synthesis , pp. 769-772
    • Catellani, M.1    Ferioli, L.2
  • 33
    • 33646152128 scopus 로고    scopus 로고
    • Aryl Transfer between Pd(II) Centers or Pd(IV) Intermediates in Pd-Catalyzed Domino Reactions
    • Cárdenas, D. J.; Martín-Matute, B.; Echavarren, A. M. Aryl Transfer between Pd(II) Centers or Pd(IV) Intermediates in Pd-Catalyzed Domino Reactions. J. Am. Chem. Soc. 2006, 128, 5033-5040.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 5033-5040
    • Cárdenas, D.J.1    Martín-Matute, B.2    Echavarren, A.M.3
  • 34
    • 0042388114 scopus 로고    scopus 로고
    • Motti, E.; Mignozzi, A.; Catellani, M. A. New Type of Palladium-Catalysed Aromatic Cross-Coupling Combined with a Suzuki Reaction: Synthesis of Selectively 2,3′-Substituted 1,1′:2′,1″-Terphenyl Derivatives. J. Mol. Catal. A: Chem. 2003, 204-205, 115-124.
    • Motti, E.; Mignozzi, A.; Catellani, M. A. New Type of Palladium-Catalysed Aromatic Cross-Coupling Combined with a Suzuki Reaction: Synthesis of Selectively 2,3′-Substituted 1,1′:2′,1″-Terphenyl Derivatives. J. Mol. Catal. A: Chem. 2003, 204-205, 115-124.
  • 35
    • 34249074441 scopus 로고    scopus 로고
    • Aryl to Aryl Palladium Migration in the Heck and Suzuki Coupling of o-Halobiaryls
    • For a similar behavior, see: a
    • For a similar behavior, see: (a) Campo, M. A.; Zhang, H.; Yao, T.; Ibdah, A.; McCulla, R. D.; Huang, Q.; Zhao, J.; Jenks, W. S.; Larock, R. C. Aryl to Aryl Palladium Migration in the Heck and Suzuki Coupling of o-Halobiaryls. J. Am. Chem. Soc. 2007, 129, 6298-6307.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 6298-6307
    • Campo, M.A.1    Zhang, H.2    Yao, T.3    Ibdah, A.4    McCulla, R.D.5    Huang, Q.6    Zhao, J.7    Jenks, W.S.8    Larock, R.C.9
  • 36
    • 0345411906 scopus 로고    scopus 로고
    • A New Catalytic Method for the Synthesis of Selectively Substituted Biphenyls Containing an Oxoalkyl Chain
    • Catellani, M.; Deledda, S.; Ganchegui, B.; Hénin, F.; Motti, E.; Muzart, J. A New Catalytic Method for the Synthesis of Selectively Substituted Biphenyls Containing an Oxoalkyl Chain. J. Organomet. Chem. 2003, 687, 473-482.
    • (2003) J. Organomet. Chem , vol.687 , pp. 473-482
    • Catellani, M.1    Deledda, S.2    Ganchegui, B.3    Hénin, F.4    Motti, E.5    Muzart, J.6
  • 37
    • 0000204989 scopus 로고
    • Palladium Chloride-Sodium Bicarbonate-Catalyzed Phenylation of Acyclic Allylic Alcohols. 3. 1,2-Chirality Transfer in a Heck Reaction via a Wacker-type Intermediate
    • Smadja, W.; Czernecki, S.; Ville, G.; Georgoulis, C. Palladium Chloride-Sodium Bicarbonate-Catalyzed Phenylation of Acyclic Allylic Alcohols. 3. 1,2-Chirality Transfer in a Heck Reaction via a Wacker-type Intermediate. Organometallics 1987, 6, 166-169.
    • (1987) Organometallics , vol.6 , pp. 166-169
    • Smadja, W.1    Czernecki, S.2    Ville, G.3    Georgoulis, C.4
  • 38
    • 0000831302 scopus 로고    scopus 로고
    • A Novel Palladium-Catalyzed Synthesis of Phenanthrenes from ortho-Substituted Aryl Iodides and Diphenyl- or Alkylphenylacetylenes
    • Catellani, M.; Motti, E.; Baratta, S. A Novel Palladium-Catalyzed Synthesis of Phenanthrenes from ortho-Substituted Aryl Iodides and Diphenyl- or Alkylphenylacetylenes. Org. Lett. 2001, 23, 3611-3614.
    • (2001) Org. Lett , vol.23 , pp. 3611-3614
    • Catellani, M.1    Motti, E.2    Baratta, S.3
  • 39
    • 29244470332 scopus 로고    scopus 로고
    • Palladium-Catalysed Synthesis of non Symmetrically Disubstituted-1,1′-Biphenyls from o-Substituted Aryl Iodides through Aryl Coupling and Delayed Hydrogenolysis
    • Deledda, S.; Motti, E.; Catellani, M. Palladium-Catalysed Synthesis of non Symmetrically Disubstituted-1,1′-Biphenyls from o-Substituted Aryl Iodides through Aryl Coupling and Delayed Hydrogenolysis. Can. J. Chem. 2005, 83, 741-747.
    • (2005) Can. J. Chem , vol.83 , pp. 741-747
    • Deledda, S.1    Motti, E.2    Catellani, M.3
  • 40
    • 0347720656 scopus 로고    scopus 로고
    • Faccini, F.; Motti, E.; Catellani, M. A New Reaction Sequence Involving Palladium-Catalyzed Unsymmetrical Aryl Coupling. J. Am. Chem. Soc. 2004, 126, 78-79.
    • Faccini, F.; Motti, E.; Catellani, M. A New Reaction Sequence Involving Palladium-Catalyzed Unsymmetrical Aryl Coupling. J. Am. Chem. Soc. 2004, 126, 78-79.
  • 42
    • 37049008699 scopus 로고    scopus 로고
    • A Convergent Synthesis of Polysubstituted Aromatic Nitriles via Palladium-Catalyzed C-H Functionalization
    • Mariampillai, B.; Alliot, J.; Li, M.; Lautens, M. A Convergent Synthesis of Polysubstituted Aromatic Nitriles via Palladium-Catalyzed C-H Functionalization. J. Am. Chem. Soc. 2007, 129, 15372-15379.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 15372-15379
    • Mariampillai, B.1    Alliot, J.2    Li, M.3    Lautens, M.4
  • 44
    • 0000157513 scopus 로고    scopus 로고
    • Practical Palladium Catalysts for C-N and C-O Bond Formation
    • Miyaura, N, Ed, Springer: Berlin
    • (a) Muci, A. R.; Buchwald, S. L. Practical Palladium Catalysts for C-N and C-O Bond Formation. In Cross-Coupling Reactions; Miyaura, N., Ed.; Springer: Berlin, 2002; pp 131-209.
    • (2002) Cross-Coupling Reactions , pp. 131-209
    • Muci, A.R.1    Buchwald, S.L.2
  • 45
    • 0013418182 scopus 로고    scopus 로고
    • Palladium-Catalyzed Amination of Aryl Halides and Related Reactions
    • Negishi, E.-I, Ed, Wiley-Interscience: New York
    • (b) Hartwig, J. F. Palladium-Catalyzed Amination of Aryl Halides and Related Reactions. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-I., Ed.; Wiley-Interscience: New York, 2002; pp 1051-1096.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 1051-1096
    • Hartwig, J.F.1
  • 46
    • 33646198385 scopus 로고    scopus 로고
    • Transition Metal-Catalyzed Arylation of Amines and Alcohols
    • 2nd ed, Beller, M, Bolm, C. Eds, Wiley-VCH: Weinheim, Germany
    • (c) Zapf, A.; Beller, M.; Riermeier, T. H. Transition Metal-Catalyzed Arylation of Amines and Alcohols. In Transition Metals tor Organic Synthesis, 2nd ed.; Beller, M., Bolm, C. Eds.; Wiley-VCH: Weinheim, Germany, 2004; pp 231-256.
    • (2004) Transition Metals tor Organic Synthesis , pp. 231-256
    • Zapf, A.1    Beller, M.2    Riermeier, T.H.3
  • 47
    • 33749003211 scopus 로고    scopus 로고
    • Sequential Unsymmetrical Aryl Coupling of o-Substituited Aryl Iodides with o-Bromophenols and Reaction with Olefins: Palladium-Catalyzed Synthesis of 6H-Dibenzopyran Derivatives
    • Motti, E.; Faccini, F.; Ferrari, I.; Catellani, M.; Ferraccioli, R. Sequential Unsymmetrical Aryl Coupling of o-Substituited Aryl Iodides with o-Bromophenols and Reaction with Olefins: Palladium-Catalyzed Synthesis of 6H-Dibenzopyran Derivatives. Org. Lett. 2006, 8, 3967-3970.
    • (2006) Org. Lett , vol.8 , pp. 3967-3970
    • Motti, E.1    Faccini, F.2    Ferrari, I.3    Catellani, M.4    Ferraccioli, R.5
  • 49
    • 11844306017 scopus 로고    scopus 로고
    • Synthesis of 6-Phenanthridinones and their Heterocyclic Analogues through Palladium-Catalyzed Sequential Aryl-Aryl and N-Aryl Coupling
    • Ferraccioli, R.; Carenzi, D.; Rombolà, O.; Catellani, M. Synthesis of 6-Phenanthridinones and their Heterocyclic Analogues through Palladium-Catalyzed Sequential Aryl-Aryl and N-Aryl Coupling. Org. Lett. 2004, 6, 4759-4762.
    • (2004) Org. Lett , vol.6 , pp. 4759-4762
    • Ferraccioli, R.1    Carenzi, D.2    Rombolà, O.3    Catellani, M.4
  • 50
    • 0035323796 scopus 로고    scopus 로고
    • 2-Furyl Phosphines as Ligands for Transition-Metal-Mediated Organic Synthesis
    • Andersen, N. G.; Keay, B. A. 2-Furyl Phosphines as Ligands for Transition-Metal-Mediated Organic Synthesis. Chem. Rev. 2001, 101, 997-1030.
    • (2001) Chem. Rev , vol.101 , pp. 997-1030
    • Andersen, N.G.1    Keay, B.A.2
  • 51
    • 31544477437 scopus 로고    scopus 로고
    • A Simple Catalytic Synthesis of Condensed Pyridones from o-Bromoarylcarboxamides Involving ipso Substitution via Palladacycles
    • Ferraccioli, R.; Carenzi, D.; Motti, E.; Catellani, M. A Simple Catalytic Synthesis of Condensed Pyridones from o-Bromoarylcarboxamides Involving ipso Substitution via Palladacycles. J. Am. Chem. Soc. 2006, 128, 722-723.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 722-723
    • Ferraccioli, R.1    Carenzi, D.2    Motti, E.3    Catellani, M.4
  • 52
    • 0033564994 scopus 로고    scopus 로고
    • The Development of Efficient Protocols for the Palladium-Catalyzed Cyclization Reactions of Secondary Amides and Carbamates
    • Yang, B. H.; Buchwald, S. L. The Development of Efficient Protocols for the Palladium-Catalyzed Cyclization Reactions of Secondary Amides and Carbamates. Org. Lett. 1999, 1, 35-38.
    • (1999) Org. Lett , vol.1 , pp. 35-38
    • Yang, B.H.1    Buchwald, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.