메뉴 건너뛰기




Volumn 399, Issue 5, 2011, Pages 1811-1814

The 2010 Chemistry Nobel Prize to R.F. Heck, E. Negishi, and A. Suzuki for palladium-catalyzed cross-coupling reactions

Author keywords

[No Author keywords available]

Indexed keywords

CROSS COUPLING REACTIONS; HECK REACTIONS; HOKKAIDO UNIVERSITY , JAPAN; IN-SITU; NOBEL PRIZES; ORGANIC SYNTHESIS; ORGANOELEMENT COMPOUNDS; PALLADATION; PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS; PRECATALYSTS; TRIPHENYL PHOSPHINES; UNIVERSITY OF DELAWARE; VARIOUS SUBSTRATES;

EID: 79251607310     PISSN: 16182642     EISSN: 16182650     Source Type: Journal    
DOI: 10.1007/s00216-010-4555-1     Document Type: Article
Times cited : (33)

References (34)
  • 1
    • 0000702671 scopus 로고
    • 1:CAS:528:DyaL38XmtFGjtb8%3D
    • RF Heck 1982 Org React 27 345 390 1:CAS:528:DyaL38XmtFGjtb8%3D
    • (1982) Org React , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 3
    • 17144421373 scopus 로고    scopus 로고
    • D. Astruc (eds). Wiley-VCH Weinheim. 10.1002/3527601767.ch3
    • Suzuki A (2002) In: Astruc D (ed) Modern arene chemistry. Wiley-VCH, Weinheim, pp 53-106
    • (2002) Modern Arene Chemistry , pp. 53-106
    • Suzuki, A.1
  • 4
    • 20544450502 scopus 로고    scopus 로고
    • A. de Meyere F. Diederich (eds). Wiley-VCH Weinheim
    • de Meyere A, Diederich F (eds) (2004) Metal-catalyzed cross coupling reactions. Wiley-VCH, Weinheim
    • (2004) Metal-catalyzed Cross Coupling Reactions
  • 8
    • 13044307437 scopus 로고
    • 1:CAS:528:DyaF1MXjsVOl 10.1021/ja01022a034
    • RF Heck 1968 J Am Chem Soc 90 5518 5526 1:CAS:528:DyaF1MXjsVOl 10.1021/ja01022a034
    • (1968) J Am Chem Soc , vol.90 , pp. 5518-5526
    • Heck, R.F.1
  • 9
    • 0000264806 scopus 로고
    • 1:CAS:528:DyaF1MXjsVGi 10.1021/ja01022a035
    • RF Heck 1968 J Am Chem Soc 90 5526 5531 1:CAS:528:DyaF1MXjsVGi 10.1021/ja01022a035
    • (1968) J Am Chem Soc , vol.90 , pp. 5526-5531
    • Heck, R.F.1
  • 10
    • 0013155804 scopus 로고
    • 1:CAS:528:DyaF1MXjtlOh 10.1021/ja01022a036
    • RF Heck 1968 J Am Chem Soc 90 5531 5534 1:CAS:528:DyaF1MXjtlOh 10.1021/ja01022a036
    • (1968) J Am Chem Soc , vol.90 , pp. 5531-5534
    • Heck, R.F.1
  • 11
    • 0001055187 scopus 로고
    • 1:CAS:528:DyaF1MXjtlOj 10.1021/ja01022a038
    • RF Heck 1968 J Am Chem Soc 90 5538 5542 1:CAS:528:DyaF1MXjtlOj 10.1021/ja01022a038
    • (1968) J Am Chem Soc , vol.90 , pp. 5538-5542
    • Heck, R.F.1
  • 12
    • 0642367235 scopus 로고
    • 1:CAS:528:DyaF1MXivFSgtA%3D%3D 10.1021/ja01022a039
    • RF Heck 1968 J Am Chem Soc 90 5542 5546 1:CAS:528:DyaF1MXivFSgtA%3D%3D 10.1021/ja01022a039
    • (1968) J Am Chem Soc , vol.90 , pp. 5542-5546
    • Heck, R.F.1
  • 13
    • 33947328566 scopus 로고
    • 1:CAS:528:DyaF1MXltlGlug%3D%3D 10.1021/ar50011a003
    • L Vaska 1968 Acc Chem Res 1 335 343 1:CAS:528:DyaF1MXltlGlug%3D%3D 10.1021/ar50011a003
    • (1968) Acc Chem Res , vol.1 , pp. 335-343
    • Vaska, L.1
  • 14
    • 4243489506 scopus 로고
    • 1:CAS:528:DyaK3sXmt1Gqu7c%3D 10.1021/cr00022a008
    • P Knochel 1993 Chem Rev 93 2117 2188 1:CAS:528:DyaK3sXmt1Gqu7c%3D 10.1021/cr00022a008
    • (1993) Chem Rev , vol.93 , pp. 2117-2188
    • Knochel, P.1
  • 15
    • 0032537674 scopus 로고    scopus 로고
    • Organozinc mediated reactions
    • DOI 10.1016/S0040-4020(98)00318-4, PII S0040402098003184
    • P Knochel JJ Almena Perea P Jones 1998 Tetrahedron 54 8275 8319 1:CAS:528:DyaK1cXksFCqs7o%3D 10.1016/S0040-4020(98)00318-4 (Pubitemid 28294229)
    • (1998) Tetrahedron , vol.54 , Issue.29 , pp. 8275-8319
    • Knochel, P.1    Almena Perea, J.J.2    Jones, P.3
  • 18
    • 2042507954 scopus 로고
    • 1:CAS:528:DyaK2MXoslGiurg%3D 10.1021/cr00039a007
    • N Miyaura A Suzuki 1995 Chem Rev 95 2457 2483 1:CAS:528: DyaK2MXoslGiurg%3D 10.1021/cr00039a007
    • (1995) Chem Rev , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 20
    • 57549117034 scopus 로고    scopus 로고
    • 1:CAS:528:DC%2BD1cXht1yrtrvO 10.1021/ar800148f
    • GC Fu 2008 Acc Chem Res 41 1555 1564 1:CAS:528:DC%2BD1cXht1yrtrvO 10.1021/ar800148f
    • (2008) Acc Chem Res , vol.41 , pp. 1555-1564
    • Fu, G.C.1
  • 21
    • 57549099215 scopus 로고    scopus 로고
    • 1:CAS:528:DC%2BD1cXosVejs7c%3D 10.1021/ar800036s
    • R Martin SL Buchwald 2008 Acc Chem Res 41 1461 1473 1:CAS:528: DC%2BD1cXosVejs7c%3D 10.1021/ar800036s
    • (2008) Acc Chem Res , vol.41 , pp. 1461-1473
    • Martin, R.1    Buchwald, S.L.2
  • 22
    • 0037090932 scopus 로고    scopus 로고
    • N-heterocyclic carbenes: A new concept in organometallic catalysis
    • DOI 10.1002/1521-3773(20020415)41:8<1290::AID-ANIE1290>3.0.CO;2-Y
    • WA Herrmann 2002 Angew Chem Int Ed 41 1290 1309 1:CAS:528: DC%2BD38Xjt1ertbY%3D 10.1002/1521-3773(20020415)41:8<1290::AID-ANIE1290>3. 0.CO;2-Y (Pubitemid 34437411)
    • (2002) Angewandte Chemie - International Edition , vol.41 , Issue.8 , pp. 1290-1309
    • Herrmann, W.A.1
  • 23
    • 57549115030 scopus 로고    scopus 로고
    • 1:CAS:528:DC%2BD1cXhtV2hs7zN 10.1021/ar800020y
    • N Marion SP Nolan 2008 Acc Chem Res 41 1440 1449 1:CAS:528: DC%2BD1cXhtV2hs7zN 10.1021/ar800020y
    • (2008) Acc Chem Res , vol.41 , pp. 1440-1449
    • Marion, N.1    Nolan, S.P.2
  • 24
    • 36549089582 scopus 로고    scopus 로고
    • 'Homeopathic' catalytic activity and atom-leaching mechanism in Miyaura-Suzuki reactions under ambient conditions with precise dendrimer-stabilized Pd nanoparticles
    • DOI 10.1002/anie.200703067
    • AK Diallo C Ornelas L Salmon J Ruiz D Astruc 2007 Angew Chem Int Ed 46 8644 8648 1:CAS:528:DC%2BD2sXhtl2rsrfO 10.1002/anie.200703067 (Pubitemid 350189084)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.45 , pp. 8644-8648
    • Diallo, A.K.1    Ornelas, C.2    Salmon, L.3    Aranzaes, J.R.4    Astruc, D.5
  • 31
    • 33947091124 scopus 로고
    • 1:CAS:528:DyaE38Xks1Wgu7g%3D 10.1021/ja00767a075
    • K Tamao K Sumitani M Kumada 1972 J Am Chem Soc 94 4374 4375 1:CAS:528:DyaE38Xks1Wgu7g%3D 10.1021/ja00767a075
    • (1972) J Am Chem Soc , vol.94 , pp. 4374-4375
    • Tamao, K.1    Sumitani, K.2    Kumada, M.3
  • 32
    • 0001772484 scopus 로고
    • 1:CAS:528:DyaE2sXltlGrtrc%3D 10.1016/S0022-328X(00)91739-X
    • J-F Fauvarque A Jutand 1977 J Organomet Chem 132 C17 C19 1:CAS:528:DyaE2sXltlGrtrc%3D 10.1016/S0022-328X(00)91739-X
    • (1977) J Organomet Chem , vol.132
    • Fauvarque, J.-F.1    Jutand, A.2
  • 33
    • 0034127063 scopus 로고    scopus 로고
    • 1:CAS:528:DC%2BD3cXhs1Wktrs%3D 10.1021/ar980063a
    • C Amatore A Jutand 2000 Acc Chem Res 33 314 321 1:CAS:528: DC%2BD3cXhs1Wktrs%3D 10.1021/ar980063a
    • (2000) Acc Chem Res , vol.33 , pp. 314-321
    • Amatore, C.1    Jutand, A.2
  • 34
    • 80055002387 scopus 로고    scopus 로고
    • Nobelprize.org
    • Nobelprize.org (2010) The Nobel Prize in chemistry 2010. http://nobelprize.org/nobel-prizes/chemistry/laureates/2010/
    • (2010) The Nobel Prize in Chemistry 2010


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.