메뉴 건너뛰기




Volumn 5, Issue 10, 2010, Pages 2168-2172

Development of a second generation palladium catalyst system for the aminocarbonylation of aryl halides with CO and ammonia

Author keywords

Ammonia; Aryl halides; Carbonylation; Palladium; Primary amides

Indexed keywords

ARYL HALIDES; CATALYST SYSTEM; MILD REACTION CONDITIONS; PALLADIUM CATALYST; PRIMARY AMIDES; SECOND GENERATION;

EID: 77957576118     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000418     Document Type: Article
Times cited : (97)

References (157)
  • 2
  • 3
    • 0001383916 scopus 로고
    • (Ed.:J. I. Kroschitz), Wiley, New York
    • D. Lipp in Encyclopedia of Chemical Technology, Vol. 1 (Ed.:J. I. Kroschitz), Wiley, New York, 1991, p. 266-287;
    • (1991) Encyclopedia of Chemical Technology , vol.1 , pp. 266-287
    • Lipp, D.1
  • 4
    • 0012387552 scopus 로고
    • (Ed.: J. I. Kroschwitz), Wiley, New York
    • R. Opsahl in Encyclopedia of Chemical Technology, Vol. 2 (Ed.: J. I. Kroschwitz), Wiley, New York, 1991, p. 346-356.
    • (1991) Encyclopedia of Chemical Technology , vol.2 , pp. 346-356
    • Opsahl, R.1
  • 5
    • 0000221261 scopus 로고
    • For selected examples, see
    • For selected examples, see: a) S. Jenkins, J. Am. Chem. Soc. 1933, 55, 703-706;
    • (1933) J. Am. Chem. Soc. , vol.55 , pp. 703-706
    • Jenkins, S.1
  • 11
    • 54249095056 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 8492-8495;
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8492-8495
  • 16
    • 0000422519 scopus 로고
    • For selected examples on the reduction of primary amides to amines, see
    • For selected examples on the reduction of primary amides to amines, see: a) H. Broadbent, W. Bartley, J. Org. Chem. 1963, 28, 2345-2347;
    • (1963) J. Org. Chem. , vol.28 , pp. 2345-2347
    • Broadbent, H.1    Bartley, W.2
  • 28
    • 0032832459 scopus 로고    scopus 로고
    • For selected samples on the dehydration of primary amides to nitriles, see
    • For selected samples on the dehydration of primary amides to nitriles, see: a) D. Bose, J. Subhas, P. Goud, Synthesis 1999, 1724-1726;
    • (1999) Synthesis , pp. 1724-1726
    • Bose, D.1    Subhas, J.2    Goud, P.3
  • 33
    • 7244229660 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 5375-5377;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5375-5377
  • 49
    • 4544239197 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 1576-1580;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1576-1580
  • 59
    • 44049100990 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 3607-3609;
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3607-3609
  • 71
    • 34447298662 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 5202-5205;
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 5202-5205
  • 79
    • 56449086705 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 9249-9251;
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9249-9251
  • 81
  • 82
    • 70350254143 scopus 로고    scopus 로고
    • For selected reviews involving metal-catalyzed carbonylation of aryl halides, see
    • For selected reviews involving metal-catalyzed carbonylation of aryl halides, see: a) A. Brennführer, H. Neumann, M. Beller, Angew. Chem. 2009, 121, 4176-4196;
    • (2009) M. Beller, Angew. Chem. , vol.121 , pp. 4176-4196
    • Brennführer, A.1    Neumann, H.2
  • 83
    • 70349967850 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 4114-4133;
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4114-4133
  • 85
    • 0037922802 scopus 로고    scopus 로고
    • 'Carbonylation of Benzyl-and Aryl-X Compounds', 2nd ed. (Eds.: B. Cornils, W. A. Herrmann), Wiley-VCH, Weinheim
    • 'Carbonylation of Benzyl-and Aryl-X Compounds' M. Beller in Applied Homogeneous Catalysis with Organometallic Compounds, 2nd ed. (Eds.: B. Cornils, W. A. Herrmann), Wiley-VCH, 2002, Weinheim, 145-156;
    • (2002) Applied Homogeneous Catalysis with Organometallic Compounds , pp. 145-156
    • Beller, M.1
  • 91
    • 0001681767 scopus 로고
    • For selected examples of palladium-catalyzed carbonylations of aryl halides, see
    • For selected examples of palladium-catalyzed carbonylations of aryl halides, see: a) A. Schoenberg, I. Bartoletti, R. F. Heck, J. Org. Chem. 1974, 39, 3318-3326;
    • (1974) J. Org. Chem. , vol.39 , pp. 3318-3326
    • Schoenberg, A.1    Bartoletti, I.2    Heck, R.F.3
  • 96
    • 36148950591 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 8460-8463;
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 8460-8463
  • 99
    • 76249094922 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 1139-1142;
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1139-1142
  • 110
    • 77951672796 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 3371-3374.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 3371-3374
  • 124
  • 129
    • 34250860782 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3402-3404;
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 3402-3404
  • 135
    • 0035800382 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 2856-2859;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2856-2859
  • 140
    • 0033677599 scopus 로고    scopus 로고
    • For other selected application of cataCXiumA, see
    • For other selected application of cataCXiumA, see: a) A. Ehrentraut, A. Zapf, M. Beller, Synlett 2000, 1589-1592;
    • (2000) Synlett , pp. 1589-1592
    • Ehrentraut, A.1    Zapf, A.2    Beller, M.3
  • 142
    • 0034680642 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 4153-4155;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 4153-4155
  • 146
    • 0037416368 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 1056-1058;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1056-1058
  • 151
  • 155
    • 34547775774 scopus 로고    scopus 로고
    • For an excellent review on ferrocenylphosphine ligands see
    • For an excellent review on ferrocenylphosphine ligands see: A. Fihri, P. Meunier, J.-C. Hierso, Coord. Chem. Rev. 2007, 251, 2017-2055.
    • (2007) Coord. Chem. Rev. , vol.251 , pp. 2017-2055
    • Fihri, A.1    Meunier, P.2    Hierso, J.-C.3
  • 156
    • 56449129254 scopus 로고    scopus 로고
    • For mechanic studies on palladium-catalyzed carbonylations, see
    • For mechanic studies on palladium-catalyzed carbonylations, see: a) A. G. Sergeev, A. Spannenberg, M. Beller, J. Am. Chem. Soc. 2008, 130, 15549-15563;
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 15549-15563
    • Sergeev, A.G.1    Spannenberg, A.2    Beller, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.