메뉴 건너뛰기




Volumn , Issue 2, 2000, Pages 201-204

Heck reactions using aryldiazonium salts towards phosphonic derivatives

Author keywords

Arenediazonium salts; Heck reaction; Hydrogenation; Palladium; Vinylphosphonates; Wadsworth Emmons reactives

Indexed keywords

ARYLDIAZONIUM; PALLADIUM; PHOSPHOLIPID; PHOSPHONIC ACID DERIVATIVE; POLYMER; SUGAR PHOSPHATE; UNCLASSIFIED DRUG;

EID: 0033957059     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-6482     Document Type: Article
Times cited : (74)

References (55)
  • 1
    • 1542690351 scopus 로고
    • Engel, R. Chem. Rev. 1977, 77, 349-367. Klachburn, G.M.; Perree, T.D. Chem. Scr. 1986, 26, 21.
    • (1977) Chem. Rev. , vol.77 , pp. 349-367
    • Engel, R.1
  • 3
    • 84913150907 scopus 로고
    • Kafarski, P.; Lejczak, B. Phosphorus, Sulfur Silicon Relat. Elem. 1991, 63, 193-215. O'Donnell, M.J.; Lawley, L.K.; Pushpavanam, P.B.; Burger, A.; Bordwell, F.G.; Zhang, X.-M. Tetrahedron Lett. 1994, 35, 6421-6424 and literature cited therein; for a recent review on racemic and optically active synthesis of α-aminophosphonic acids see Uziel, J.; Genêt, J.-P. Russ. J. Org. Chem. 1997, 33, 1521-1542.
    • (1991) Phosphorus, Sulfur Silicon Relat. Elem. , vol.63 , pp. 193-215
    • Kafarski, P.1    Lejczak, B.2
  • 4
    • 0027997597 scopus 로고
    • Kafarski, P.; Lejczak, B. Phosphorus, Sulfur Silicon Relat. Elem. 1991, 63, 193-215. O'Donnell, M.J.; Lawley, L.K.; Pushpavanam, P.B.; Burger, A.; Bordwell, F.G.; Zhang, X.-M. Tetrahedron Lett. 1994, 35, 6421-6424 and literature cited therein; for a recent review on racemic and optically active synthesis of α-aminophosphonic acids see Uziel, J.; Genêt, J.-P. Russ. J. Org. Chem. 1997, 33, 1521-1542.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 6421-6424
    • O'Donnell, M.J.1    Lawley, L.K.2    Pushpavanam, P.B.3    Burger, A.4    Bordwell, F.G.5    Zhang, X.-M.6
  • 5
    • 0008307835 scopus 로고    scopus 로고
    • Kafarski, P.; Lejczak, B. Phosphorus, Sulfur Silicon Relat. Elem. 1991, 63, 193-215. O'Donnell, M.J.; Lawley, L.K.; Pushpavanam, P.B.; Burger, A.; Bordwell, F.G.; Zhang, X.-M. Tetrahedron Lett. 1994, 35, 6421-6424 and literature cited therein; for a recent review on racemic and optically active synthesis of α-aminophosphonic acids see Uziel, J.; Genêt, J.-P. Russ. J. Org. Chem. 1997, 33, 1521-1542.
    • (1997) Russ. J. Org. Chem. , vol.33 , pp. 1521-1542
    • Uziel, J.1    Genêt, J.-P.2
  • 7
    • 0343965670 scopus 로고    scopus 로고
    • US 5,627,173 (Hoechst AG 1997)
    • several examples of pharmaceutical active arylated vinylphosphonates are published in the literature of patents e.g. Graeve, R.; Thorwart, W.; Raiss, R.; Weithmann, K.U.; Mullner, S., US 5,627,173 (Hoechst AG 1997). Lennon, P.J., US 5,434,288 (Monsanto Company 1995).
    • Graeve, R.1    Thorwart, W.2    Raiss, R.3    Weithmann, K.U.4    Mullner, S.5
  • 8
    • 0342659541 scopus 로고    scopus 로고
    • US 5,434,288 (Monsanto Company 1995)
    • several examples of pharmaceutical active arylated vinylphosphonates are published in the literature of patents e.g. Graeve, R.; Thorwart, W.; Raiss, R.; Weithmann, K.U.; Mullner, S., US 5,627,173 (Hoechst AG 1997). Lennon, P.J., US 5,434,288 (Monsanto Company 1995).
    • Lennon, P.J.1
  • 9
    • 0004297233 scopus 로고    scopus 로고
    • Georg Thieme Verlag: Stuttgart
    • Römpp Lexikon Chemie 10; Falbe, J.; Regitz, M., Eds.; Georg Thieme Verlag: Stuttgart; Vol. 6 1999. Jin, S.; Gonsalves, K.E., Macromolecules 1998, 31, 1010-1015 and literature cited therein. Davies, K.P.; Walker, D.R.E.; Woodward, G.; Smith, A.C., EP 861846 A2 (Albright & Wilson Ltd 1998). For applications in the field of flame retardancy in styrenic and acrylic polymers with covalently bound phosphorous-containing groups see Ebdon, J.R, Recent Adv. Flame Retard. Polym. Materials 1997, 8, 161.
    • (1999) Römpp Lexikon Chemie 10 , vol.6
    • Falbe, J.1    Regitz, M.2
  • 10
    • 0031997839 scopus 로고    scopus 로고
    • and literature cited therein
    • Römpp Lexikon Chemie 10; Falbe, J.; Regitz, M., Eds.; Georg Thieme Verlag: Stuttgart; Vol. 6 1999. Jin, S.; Gonsalves, K.E., Macromolecules 1998, 31, 1010-1015 and literature cited therein. Davies, K.P.; Walker, D.R.E.; Woodward, G.; Smith, A.C., EP 861846 A2 (Albright & Wilson Ltd 1998). For applications in the field of flame retardancy in styrenic and acrylic polymers with covalently bound phosphorous-containing groups see Ebdon, J.R, Recent Adv. Flame Retard. Polym. Materials 1997, 8, 161.
    • (1998) Macromolecules , vol.31 , pp. 1010-1015
    • Jin, S.1    Gonsalves, K.E.2
  • 11
    • 0343529834 scopus 로고    scopus 로고
    • EP 861846 A2 (Albright & Wilson Ltd 1998)
    • Römpp Lexikon Chemie 10; Falbe, J.; Regitz, M., Eds.; Georg Thieme Verlag: Stuttgart; Vol. 6 1999. Jin, S.; Gonsalves, K.E., Macromolecules 1998, 31, 1010-1015 and literature cited therein. Davies, K.P.; Walker, D.R.E.; Woodward, G.; Smith, A.C., EP 861846 A2 (Albright & Wilson Ltd 1998). For applications in the field of flame retardancy in styrenic and acrylic polymers with covalently bound phosphorous-containing groups see Ebdon, J.R, Recent Adv. Flame Retard. Polym. Materials 1997, 8, 161.
    • Davies, K.P.1    Walker, D.R.E.2    Woodward, G.3    Smith, A.C.4
  • 12
    • 0007668710 scopus 로고    scopus 로고
    • Römpp Lexikon Chemie 10; Falbe, J.; Regitz, M., Eds.; Georg Thieme Verlag: Stuttgart; Vol. 6 1999. Jin, S.; Gonsalves, K.E., Macromolecules 1998, 31, 1010-1015 and literature cited therein. Davies, K.P.; Walker, D.R.E.; Woodward, G.; Smith, A.C., EP 861846 A2 (Albright & Wilson Ltd 1998). For applications in the field of flame retardancy in styrenic and acrylic polymers with covalently bound phosphorous-containing groups see Ebdon, J.R, Recent Adv. Flame Retard. Polym. Materials 1997, 8, 161.
    • (1997) Recent Adv. Flame Retard. Polym. Materials , vol.8 , pp. 161
    • Ebdon, J.R.1
  • 14
    • 84984265463 scopus 로고
    • Ahlbrecht, H.; Farnung, W. Synthesis 1977, 336-338. Venugopalan, B.; Bevin Hamlet, A.; Durst, T. Tetrahedron Lett. 1981, 22, 191-194.
    • (1977) Synthesis , pp. 336-338
    • Ahlbrecht, H.1    Farnung, W.2
  • 19
  • 22
    • 0002969490 scopus 로고
    • Xu, Y.; Jin, X.; Huang, G.; Huang, Y. Synthesis 1983, 556-558. Demik, N.N.; Kabachnik, M.M.; Novikova, Z.S.; Beletskaya, I.P. Russ. J. Org. Chem. 1995, 31, 57-60. and Zh. Org. Khim. 1995, 31, 64-68. Ortwine, D.F.; Malone, T.C.; Bigge, C.F.; Drummond, J.T.; Humblet, C.; Johnson, G.; Pinter, G.W. J.Med.Chem. 1992, 35, 1345-1370. Bigge, C.F; Johnson, G.; Ortwine, D.F.; Drummond, J.T.; Retz, D.M.; Brahce, L.J.; Coughenour, L.L.; Marcoux, F.W.; Probert, A.W., Jr. J. Med. Chem. 1992, 35, 1371-1384.
    • (1983) Synthesis , pp. 556-558
    • Xu, Y.1    Jin, X.2    Huang, G.3    Huang, Y.4
  • 23
    • 0343965663 scopus 로고
    • Xu, Y.; Jin, X.; Huang, G.; Huang, Y. Synthesis 1983, 556-558. Demik, N.N.; Kabachnik, M.M.; Novikova, Z.S.; Beletskaya, I.P. Russ. J. Org. Chem. 1995, 31, 57-60. and Zh. Org. Khim. 1995, 31, 64-68. Ortwine, D.F.; Malone, T.C.; Bigge, C.F.; Drummond, J.T.; Humblet, C.; Johnson, G.; Pinter, G.W. J.Med.Chem. 1992, 35, 1345-1370. Bigge, C.F; Johnson, G.; Ortwine, D.F.; Drummond, J.T.; Retz, D.M.; Brahce, L.J.; Coughenour, L.L.; Marcoux, F.W.; Probert, A.W., Jr. J. Med. Chem. 1992, 35, 1371-1384.
    • (1995) Russ. J. Org. Chem. , vol.31 , pp. 57-60
    • Demik, N.N.1    Kabachnik, M.M.2    Novikova, Z.S.3    Beletskaya, I.P.4
  • 24
    • 0343965662 scopus 로고
    • Xu, Y.; Jin, X.; Huang, G.; Huang, Y. Synthesis 1983, 556-558. Demik, N.N.; Kabachnik, M.M.; Novikova, Z.S.; Beletskaya, I.P. Russ. J. Org. Chem. 1995, 31, 57-60. and Zh. Org. Khim. 1995, 31, 64-68. Ortwine, D.F.; Malone, T.C.; Bigge, C.F.; Drummond, J.T.; Humblet, C.; Johnson, G.; Pinter, G.W. J.Med.Chem. 1992, 35, 1345-1370. Bigge, C.F; Johnson, G.; Ortwine, D.F.; Drummond, J.T.; Retz, D.M.; Brahce, L.J.; Coughenour, L.L.; Marcoux, F.W.; Probert, A.W., Jr. J. Med. Chem. 1992, 35, 1371-1384.
    • (1995) Zh. Org. Khim. , vol.31 , pp. 64-68
  • 25
    • 0026681096 scopus 로고
    • Xu, Y.; Jin, X.; Huang, G.; Huang, Y. Synthesis 1983, 556-558. Demik, N.N.; Kabachnik, M.M.; Novikova, Z.S.; Beletskaya, I.P. Russ. J. Org. Chem. 1995, 31, 57-60. and Zh. Org. Khim. 1995, 31, 64-68. Ortwine, D.F.; Malone, T.C.; Bigge, C.F.; Drummond, J.T.; Humblet, C.; Johnson, G.; Pinter, G.W. J.Med.Chem. 1992, 35, 1345-1370. Bigge, C.F; Johnson, G.; Ortwine, D.F.; Drummond, J.T.; Retz, D.M.; Brahce, L.J.; Coughenour, L.L.; Marcoux, F.W.; Probert, A.W., Jr. J. Med. Chem. 1992, 35, 1371-1384.
    • (1992) J.Med.Chem. , vol.35 , pp. 1345-1370
    • Ortwine, D.F.1    Malone, T.C.2    Bigge, C.F.3    Drummond, J.T.4    Humblet, C.5    Johnson, G.6    Pinter, G.W.7
  • 26
    • 0026717063 scopus 로고
    • Xu, Y.; Jin, X.; Huang, G.; Huang, Y. Synthesis 1983, 556-558. Demik, N.N.; Kabachnik, M.M.; Novikova, Z.S.; Beletskaya, I.P. Russ. J. Org. Chem. 1995, 31, 57-60. and Zh. Org. Khim. 1995, 31, 64-68. Ortwine, D.F.; Malone, T.C.; Bigge, C.F.; Drummond, J.T.; Humblet, C.; Johnson, G.; Pinter, G.W. J.Med.Chem. 1992, 35, 1345-1370. Bigge, C.F; Johnson, G.; Ortwine, D.F.; Drummond, J.T.; Retz, D.M.; Brahce, L.J.; Coughenour, L.L.; Marcoux, F.W.; Probert, A.W., Jr. J. Med. Chem. 1992, 35, 1371-1384.
    • (1992) J. Med. Chem. , vol.35 , pp. 1371-1384
    • Bigge, C.F.1    Johnson, G.2    Ortwine, D.F.3    Drummond, J.T.4    Retz, D.M.5    Brahce, L.J.6    Coughenour, L.L.7    Marcoux, F.W.8    Probert A.W., Jr.9
  • 30
    • 0001582686 scopus 로고
    • Burini, A.; Cacchi, S.; Pace, P.; Pietroni, B.R. Synlett 1995, 677-679. Holt, D.A.; Erb, J.M. Tetrahedron Lett. 1989, 30, 5393-5396.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 5393-5396
    • Holt, D.A.1    Erb, J.M.2
  • 31
    • 85064671573 scopus 로고
    • For some recent works in this area : see Beller, M., Kühlein, K., Synlett 1995, 441-442. Ikenaga, K.; Matsumoto, S.; Kikukawa, K.; Matsuda, T., Chem.Lett. 1988, 873-876. Sengupta, S., Sadhukhan, S.K., Tetrahedron Lett. 1998; 39, 715-718. Sengupta, S., Sadhukan, S.K., Bhattacharyya, S., Guha, J., J. Chem. Soc., Perkin Trans I 1998, 407-410.
    • (1995) Synlett , pp. 441-442
    • Beller, M.1    Kühlein, K.2
  • 32
    • 0013568123 scopus 로고
    • For some recent works in this area : see Beller, M., Kühlein, K., Synlett 1995, 441-442. Ikenaga, K.; Matsumoto, S.; Kikukawa, K.; Matsuda, T., Chem.Lett. 1988, 873-876. Sengupta, S., Sadhukhan, S.K., Tetrahedron Lett. 1998; 39, 715-718. Sengupta, S., Sadhukan, S.K., Bhattacharyya, S., Guha, J., J. Chem. Soc., Perkin Trans I 1998, 407-410.
    • (1988) Chem.Lett. , pp. 873-876
    • Ikenaga, K.1    Matsumoto, S.2    Kikukawa, K.3    Matsuda, T.4
  • 33
    • 0032509945 scopus 로고    scopus 로고
    • For some recent works in this area : see Beller, M., Kühlein, K., Synlett 1995, 441-442. Ikenaga, K.; Matsumoto, S.; Kikukawa, K.; Matsuda, T., Chem.Lett. 1988, 873-876. Sengupta, S., Sadhukhan, S.K., Tetrahedron Lett. 1998; 39, 715-718. Sengupta, S., Sadhukan, S.K., Bhattacharyya, S., Guha, J., J. Chem. Soc., Perkin Trans I 1998, 407-410.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 715-718
    • Sengupta, S.1    Sadhukhan, S.K.2
  • 34
    • 33748651904 scopus 로고    scopus 로고
    • For some recent works in this area : see Beller, M., Kühlein, K., Synlett 1995, 441-442. Ikenaga, K.; Matsumoto, S.; Kikukawa, K.; Matsuda, T., Chem.Lett. 1988, 873-876. Sengupta, S., Sadhukhan, S.K., Tetrahedron Lett. 1998; 39, 715-718. Sengupta, S., Sadhukan, S.K., Bhattacharyya, S., Guha, J., J. Chem. Soc., Perkin Trans I 1998, 407-410.
    • (1998) J. Chem. Soc., Perkin Trans I , pp. 407-410
    • Sengupta, S.1    Sadhukan, S.K.2    Bhattacharyya, S.3    Guha, J.4
  • 36
    • 0343093877 scopus 로고
    • Wada, Y.; Oda, R. Kogyo Kagaku Zasshi 1964, 67, 2093. C.A. 1965, 62, 13177.
    • (1965) Kogyo Kagaku Zasshi , vol.62 , pp. 13177
  • 38
    • 0001590919 scopus 로고
    • 3 were suspended in 5 mL of solvent at room temperature. Subsequently 0.85 mmol of the vinylphosphonate was added at room temperature and the resulting mixture was stirred at 50 °C. The progress of the reaction was monitored by measuring the volume of given off gas (5 min - 2 h). After the reaction was completed the solvent was evaporated and the residue was purified by flash chromatography on silica.
    • (1949) Org. React. , vol.5 , pp. 193-228
    • Roe, A.1
  • 39
    • 33845561098 scopus 로고
    • 3 were suspended in 5 mL of solvent at room temperature. Subsequently 0.85 mmol of the vinylphosphonate was added at room temperature and the resulting mixture was stirred at 50 °C. The progress of the reaction was monitored by measuring the volume of given off gas (5 min - 2 h). After the reaction was completed the solvent was evaporated and the residue was purified by flash chromatography on silica
    • 3 were suspended in 5 mL of solvent at room temperature. Subsequently 0.85 mmol of the vinylphosphonate was added at room temperature and the resulting mixture was stirred at 50 °C. The progress of the reaction was monitored by measuring the volume of given off gas (5 min - 2 h). After the reaction was completed the solvent was evaporated and the residue was purified by flash chromatography on silica.
    • (1979) J. Org. Chem. , vol.44 , pp. 1572-1574
    • Doyle, M.P.1    Bryker, W.J.2
  • 40
    • 0342659535 scopus 로고    scopus 로고
    • note
    • CP = 4.5 Hz), 60.39 (t), 16.1 (q), 13.9 (q).
  • 41
    • 0343965656 scopus 로고    scopus 로고
    • EP 0 102 925 A2 and EP 0 248 245 A2 (Ciba-Geigy 1983)
    • 3 were suspended in 5 mL of solvent at room temperature. Subsequently 0.85 mmol of the vinylphosphonate was added at room temperature and the resulting mixture was stirred at 50 °C. The progress of the reaction was monitored by measuring the volume of given off gas (15 min - 2 h). After the Heck reaction was completed the mixture was cooled to room temperature and stirred at room temperature under hydrogen (1 atm). The progress of the reaction was monitored TLC (1 - 2 days). After the hydrogenation was completed the solvent was evaporated and the residue was purified by flash chromatography on silica.
    • Meyer, W.1    Reinehr, D.2    Oertle, K.3    Schurter, R.4
  • 42
    • 0033583489 scopus 로고    scopus 로고
    • 3 were suspended in 5 mL of solvent at room temperature. Subsequently 0.85 mmol of the vinylphosphonate was added at room temperature and the resulting mixture was stirred at 50 °C. The progress of the reaction was monitored by measuring the volume of given off gas (15 min - 2 h). After the Heck reaction was completed the mixture was cooled to room temperature and stirred at room temperature under hydrogen (1 atm). The progress of the reaction was monitored TLC (1 - 2 days). After the hydrogenation was completed the solvent was evaporated and the residue was purified by flash chromatography on silica
    • 3 were suspended in 5 mL of solvent at room temperature. Subsequently 0.85 mmol of the vinylphosphonate was added at room temperature and the resulting mixture was stirred at 50 °C. The progress of the reaction was monitored by measuring the volume of given off gas (15 min - 2 h). After the Heck reaction was completed the mixture was cooled to room temperature and stirred at room temperature under hydrogen (1 atm). The progress of the reaction was monitored TLC (1 - 2 days). After the hydrogenation was completed the solvent was evaporated and the residue was purified by flash chromatography on silica.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1071-1073
    • Bräse, S.1    Schroen, M.2
  • 45
    • 0029793732 scopus 로고    scopus 로고
    • The spectroscopical data were identical to previously reported data. 24
    • For the reaction conditions see Yue, X.; Li, Y. Synthesis 1996, 736-740. The spectroscopical data were identical to previously reported data. 24
    • (1996) Synthesis , pp. 736-740
    • Yue, X.1    Li, Y.2
  • 46
    • 33750236967 scopus 로고
    • Herrmann, W.A.; Broßmer, C.; Öfele, K.; Reisinger, C.-P.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. Int. Ed. Engl. 1995, 34, 1844-1848. Beller, M.; Fischer, H.; Herrmann, W.A.; Öfele, K.; Broßmer, C. Angew. Chem. Int. Ed. Engl. 1995, 37, 1848-1849. Herrmann, W.A; Broßmer, C.; Reisinger, C.-P.; Riermeier, T.H.; Öfele, K.; Beller, M. Chem. Eur. J. 1997, 3, 1357-1364. Herrmann, W.A.; Reissinger, C.-P.; Öfele, K.; Broßmer, C.; Beller, M.; Fischer, H. J. Mol. Catal. 1996, 103, 133-146. Beller, M.; Riermeier, H. Tetrahedron Lett. 1996, 37, 6535-6538. Beller, M.; Riermeier, H.; Haber, S.; Kleiner, H.J.; Herrmann, W.A. Chem. Ber. 1996, 129, 1259-1264.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1844-1848
    • Herrmann, W.A.1    Broßmer, C.2    Öfele, K.3    Reisinger, C.-P.4    Priermeier, T.5    Beller, M.6    Fischer, H.7
  • 47
    • 33748233333 scopus 로고
    • Herrmann, W.A.; Broßmer, C.; Öfele, K.; Reisinger, C.-P.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. Int. Ed. Engl. 1995, 34, 1844-1848. Beller, M.; Fischer, H.; Herrmann, W.A.; Öfele, K.; Broßmer, C. Angew. Chem. Int. Ed. Engl. 1995, 37, 1848-1849. Herrmann, W.A; Broßmer, C.; Reisinger, C.-P.; Riermeier, T.H.; Öfele, K.; Beller, M. Chem. Eur. J. 1997, 3, 1357-1364. Herrmann, W.A.; Reissinger, C.-P.; Öfele, K.; Broßmer, C.; Beller, M.; Fischer, H. J. Mol. Catal. 1996, 103, 133-146. Beller, M.; Riermeier, H. Tetrahedron Lett. 1996, 37, 6535-6538. Beller, M.; Riermeier, H.; Haber, S.; Kleiner, H.J.; Herrmann, W.A. Chem. Ber. 1996, 129, 1259-1264.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 1848-1849
    • Beller, M.1    Fischer, H.2    Herrmann, W.A.3    Öfele, K.4    Broßmer, C.5
  • 48
    • 0030767352 scopus 로고    scopus 로고
    • Herrmann, W.A.; Broßmer, C.; Öfele, K.; Reisinger, C.-P.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. Int. Ed. Engl. 1995, 34, 1844-1848. Beller, M.; Fischer, H.; Herrmann, W.A.; Öfele, K.; Broßmer, C. Angew. Chem. Int. Ed. Engl. 1995, 37, 1848-1849. Herrmann, W.A; Broßmer, C.; Reisinger, C.-P.; Riermeier, T.H.; Öfele, K.; Beller, M. Chem. Eur. J. 1997, 3, 1357-1364. Herrmann, W.A.; Reissinger, C.-P.; Öfele, K.; Broßmer, C.; Beller, M.; Fischer, H. J. Mol. Catal. 1996, 103, 133-146. Beller, M.; Riermeier, H. Tetrahedron Lett. 1996, 37, 6535-6538. Beller, M.; Riermeier, H.; Haber, S.; Kleiner, H.J.; Herrmann, W.A. Chem. Ber. 1996, 129, 1259-1264.
    • (1997) Chem. Eur. J. , vol.3 , pp. 1357-1364
    • Herrmann, W.A.1    Broßmer, C.2    Reisinger, C.-P.3    Riermeier, T.H.4    Öfele, K.5    Beller, M.6
  • 49
    • 0000242501 scopus 로고    scopus 로고
    • Herrmann, W.A.; Broßmer, C.; Öfele, K.; Reisinger, C.-P.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. Int. Ed. Engl. 1995, 34, 1844-1848. Beller, M.; Fischer, H.; Herrmann, W.A.; Öfele, K.; Broßmer, C. Angew. Chem. Int. Ed. Engl. 1995, 37, 1848-1849. Herrmann, W.A; Broßmer, C.; Reisinger, C.-P.; Riermeier, T.H.; Öfele, K.; Beller, M. Chem. Eur. J. 1997, 3, 1357-1364. Herrmann, W.A.; Reissinger, C.-P.; Öfele, K.; Broßmer, C.; Beller, M.; Fischer, H. J. Mol. Catal. 1996, 103, 133-146. Beller, M.; Riermeier, H. Tetrahedron Lett. 1996, 37, 6535-6538. Beller, M.; Riermeier, H.; Haber, S.; Kleiner, H.J.; Herrmann, W.A. Chem. Ber. 1996, 129, 1259-1264.
    • (1996) J. Mol. Catal. , vol.103 , pp. 133-146
    • Herrmann, W.A.1    Reissinger, C.-P.2    Öfele, K.3    Broßmer, C.4    Beller, M.5    Fischer, H.6
  • 50
    • 0030565564 scopus 로고    scopus 로고
    • Herrmann, W.A.; Broßmer, C.; Öfele, K.; Reisinger, C.-P.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. Int. Ed. Engl. 1995, 34, 1844-1848. Beller, M.; Fischer, H.; Herrmann, W.A.; Öfele, K.; Broßmer, C. Angew. Chem. Int. Ed. Engl. 1995, 37, 1848-1849. Herrmann, W.A; Broßmer, C.; Reisinger, C.-P.; Riermeier, T.H.; Öfele, K.; Beller, M. Chem. Eur. J. 1997, 3, 1357-1364. Herrmann, W.A.; Reissinger, C.-P.; Öfele, K.; Broßmer, C.; Beller, M.; Fischer, H. J. Mol. Catal. 1996, 103, 133-146. Beller, M.; Riermeier, H. Tetrahedron Lett. 1996, 37, 6535-6538. Beller, M.; Riermeier, H.; Haber, S.; Kleiner, H.J.; Herrmann, W.A. Chem. Ber. 1996, 129, 1259-1264.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 6535-6538
    • Beller, M.1    Riermeier, H.2
  • 51
    • 0001684422 scopus 로고    scopus 로고
    • Herrmann, W.A.; Broßmer, C.; Öfele, K.; Reisinger, C.-P.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. Int. Ed. Engl. 1995, 34, 1844-1848. Beller, M.; Fischer, H.; Herrmann, W.A.; Öfele, K.; Broßmer, C. Angew. Chem. Int. Ed. Engl. 1995, 37, 1848-1849. Herrmann, W.A; Broßmer, C.; Reisinger, C.-P.; Riermeier, T.H.; Öfele, K.; Beller, M. Chem. Eur. J. 1997, 3, 1357-1364. Herrmann, W.A.; Reissinger, C.-P.; Öfele, K.; Broßmer, C.; Beller, M.; Fischer, H. J. Mol. Catal. 1996, 103, 133-146. Beller, M.; Riermeier, H. Tetrahedron Lett. 1996, 37, 6535-6538. Beller, M.; Riermeier, H.; Haber, S.; Kleiner, H.J.; Herrmann, W.A. Chem. Ber. 1996, 129, 1259-1264.
    • (1996) Chem. Ber. , vol.129 , pp. 1259-1264
    • Beller, M.1    Riermeier, H.2    Haber, S.3    Kleiner, H.J.4    Herrmann, W.A.5
  • 52
    • 0347155021 scopus 로고    scopus 로고
    • A new review article concerning the catalytic applications of the palladacycle trans-di(μ-acetato)-bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) in cross couplings was recently published by Speicher, A; Schulz, T.; Eicher, T. J. Prakt. Chem. 1999, 341, 605.
    • (1999) J. Prakt. Chem. , vol.341 , pp. 605
    • Speicher, A.1    Schulz, T.2    Eicher, T.3
  • 53
    • 0343093872 scopus 로고    scopus 로고
    • note
    • +, 6).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.