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Volumn 48, Issue 23, 2009, Pages 4114-4133

Palladium-catalyzed carbonylation reactions of aryl halides and related compounds

Author keywords

Aryl halides; Carbon monoxide; Carbonylation; Homogeneous catalysis; Palladium

Indexed keywords

AGRO-CHEMICALS; AROMATIC HALIDE; ARYL HALIDES; CARBONYLATION REACTIONS; CARBOXYLIC ACID DERIVATIVES; HOMOGENEOUS CATALYSIS; INDUSTRIAL PROCESSS; INDUSTRIAL PRODUCT; PALLADIUM CATALYST; RAPID DEVELOPMENT; RELATED COMPOUNDS;

EID: 70349967850     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200900013     Document Type: Review
Times cited : (1274)

References (392)
  • 2
    • 20544450502 scopus 로고    scopus 로고
    • 2nd ed, Eds, A. de Meijere, F. Diederich, Wiley-VCH, Weinheim
    • b) Metal-catalyzed Cross-Coupling Reactions, 2nd ed. (Eds.: A. de Meijere, F. Diederich), Wiley-VCH, Weinheim, 2004;
    • (2004) Metal-catalyzed Cross-Coupling Reactions
  • 3
    • 0003779363 scopus 로고    scopus 로고
    • 2nd ed, Eds, M. Better, C. Bolm, Wiley-VCH, Weinheim
    • c) Transition Metals for Organic Synthesis, 2nd ed. (Eds.: M. Better, C. Bolm), Wiley-VCH, Weinheim, 2004.
    • (2004) Transition Metals for Organic Synthesis
  • 9
    • 53149135000 scopus 로고    scopus 로고
    • For some more special carbonylation reviews, see: a
    • For some more special carbonylation reviews, see: a) A. S. Veige, Polyhedron 2008, 27, 3177-3189;
    • (2008) Polyhedron , vol.27 , pp. 3177-3189
    • Veige, A.S.1
  • 31
    • 30944444443 scopus 로고    scopus 로고
    • See, for example: a
    • See, for example: a) N.-W Jan, H.-J. Liu, Org. Lett. 2006, 8, 151-153;
    • (2006) Org. Lett , vol.8 , pp. 151-153
    • Jan, N.-W.1    Liu, H.-J.2
  • 50
    • 0035804408 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 779-781;
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 779-781
  • 102
    • 18844381854 scopus 로고    scopus 로고
    • For a review on carbonylation reactions using carbon monoxide equivalents, see
    • For a review on carbonylation reactions using carbon monoxide equivalents, see T. Morimoto, K. Kakiuchi, Angew. Chem. 2004, 116, 5698-5706;
    • (2004) Angew. Chem , vol.116 , pp. 5698-5706
    • Morimoto, T.1    Kakiuchi, K.2
  • 103
    • 8444233969 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 5580-5588.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 5580-5588
  • 126
    • 0034680642 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 4153-4155;
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 4153-4155
  • 230
    • 0035800382 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 2856-2859;
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 2856-2859
  • 250
    • 70349951292 scopus 로고    scopus 로고
    • According to a study of Bayer AG, approximately 75 % of all current pharmaceuticals contain benzene rings and/or heteroarenes as integral parts of their structure: J. Stetter, F. Lieb, Angew. Chem. 2000, 112, 1792-1812;
    • According to a study of Bayer AG, approximately 75 % of all current pharmaceuticals contain benzene rings and/or heteroarenes as integral parts of their structure: J. Stetter, F. Lieb, Angew. Chem. 2000, 112, 1792-1812;
  • 251
    • 0001608560 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1724-1744.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 1724-1744
  • 252
    • 0002890460 scopus 로고    scopus 로고
    • For a short review on carbonylations of halopyridines and related derivatives, see
    • For a short review on carbonylations of halopyridines and related derivatives, see: M. Beller, W. Mägerlein, A. F. Indolese, C. Fischer, Synthesis 2001, 1098-1109.
    • (2001) Synthesis , pp. 1098-1109
    • Beller, M.1    Mägerlein, W.2    Indolese, A.F.3    Fischer, C.4
  • 253
    • 70349968926 scopus 로고    scopus 로고
    • M. Scalone, P. Vogt, Hoffmann-La Roche, Switzerland, EP 0385210, 1990, A2
    • M. Scalone, P. Vogt, (Hoffmann-La Roche, Switzerland), EP 0385210, 1990, A2.
  • 258
    • 36148950591 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 8460-8463.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 8460-8463
  • 272
    • 36949000797 scopus 로고    scopus 로고
    • For formylation reactions in natural product synthesis employing silanes, see a
    • For formylation reactions in natural product synthesis employing silanes, see a) D. C. Behenna, J. L. Stockdill, B. M. Stoltz, Angew. Chem. 2007, 119, 4155-4158;
    • (2007) Angew. Chem , vol.119 , pp. 4155-4158
    • Behenna, D.C.1    Stockdill, J.L.2    Stoltz, B.M.3
  • 273
    • 34250721043 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 4077-4080;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 4077-4080
  • 279
    • 37049085765 scopus 로고    scopus 로고
    • Formylations of aryl chlorides have been realized by: a Y. Ben-David, M. Portnoy, D. Milstein, J. Chem. Soc. Chem. Commun. 1989, 1816-1817;
    • Formylations of aryl chlorides have been realized by: a) Y. Ben-David, M. Portnoy, D. Milstein, J. Chem. Soc. Chem. Commun. 1989, 1816-1817;
  • 280
    • 70349949701 scopus 로고    scopus 로고
    • see reference [54f
    • b) see reference [54f].
  • 292
    • 33748292412 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 154-158;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 154-158
  • 293
    • 70349957186 scopus 로고    scopus 로고
    • J. J. Almena Perea, A. Monsees, R. Kadyrov, T. Riermeier, K. Rossen, W.-R. Krahnert, M. Beller, S. Klaus, A. Zapf, (Degussa AG, Germany), PCT Int. Appl. WO 2006/103148, 2006, Al.
    • b) J. J. Almena Perea, A. Monsees, R. Kadyrov, T. Riermeier, K. Rossen, W.-R. Krahnert, M. Beller, S. Klaus, A. Zapf, (Degussa AG, Germany), PCT Int. Appl. WO 2006/103148, 2006, Al.
  • 294
    • 38949209091 scopus 로고    scopus 로고
    • For the synthesis and characterization of palladium(0) and aryl palladium(II) bromide complexes of cataCX ium A, see A. G. Sergeev, A. Zapf, A. Spannenberg, M. Beller, Organometallics 2008, 27, 297-300.
    • For the synthesis and characterization of palladium(0) and aryl palladium(II) bromide complexes of cataCX ium A, see A. G. Sergeev, A. Zapf, A. Spannenberg, M. Beller, Organometallics 2008, 27, 297-300.
  • 320
    • 28744458623 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 7674-7684;
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 7674-7684
  • 371
    • 14644427201 scopus 로고    scopus 로고
    • For synthetic applications of indium organometallic compounds in (carbonylative) cross-coupling reactions, see
    • For synthetic applications of indium organometallic compounds in (carbonylative) cross-coupling reactions, see M. A. Pena, J. Pérez Sestelo, L. A. Sarandeses, Synthesis 2005, 485-492.
    • (2005) Synthesis , pp. 485-492
    • Pena, M.A.1    Pérez Sestelo, J.2    Sarandeses, L.A.3
  • 385
    • 27544431953 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6951-6956.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 6951-6956
  • 392
    • 56049086113 scopus 로고    scopus 로고
    • While this article was in preparation, a related summary was published, see: C. F. J. Barnard, Organometallics 2008, 27, 5402-5422
    • While this article was in preparation, a related summary was published, see: C. F. J. Barnard, Organometallics 2008, 27, 5402-5422.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.