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Volumn 131, Issue 34, 2009, Pages 12240-12249

Influence of biaryl phosphine structure on C-N and C-C bond formation

Author keywords

[No Author keywords available]

Indexed keywords

ARYLAMINATION; BIPHENYL LIGAND; BOND-FORMING REACTIONS; C-C BOND FORMATION; C-C BOND FORMING REACTION; CATALYTIC SYSTEM; ORTHO POSITION; PHOSPHINE LIGANDS; ROOM TEMPERATURE; STRUCTURAL CHARACTERISTICS; STRUCTURAL ELEMENTS; STRUCTURAL SIMILARITY; SUPPORT CATALYST; X-RAY ANALYSIS; X-RAY CRYSTALLOGRAPHIC ANALYSIS;

EID: 69349091791     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja902679b     Document Type: Article
Times cited : (54)

References (74)
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    • Christmann, U.1    Vilar, R.2
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    • For reviews see: (a)
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    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1154
  • 41
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    • For examples on Pd-catalyzed Suzuki-Miyaura reactions of nucleosides, see: (a)
    • For examples on Pd-catalyzed Suzuki-Miyaura reactions of nucleosides, see: (a) Jacobsen, M. F.; Ferapontova, E. E.; Gothelf, K. V. Org. Biomol. Chem. 2009, 7, 905-908.
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 905-908
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  • 54
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    • CCDC depositions 689629 and 689630 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Center via
    • CCDC depositions 689629 and 689630 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Center via www.ccdc.cam.ac.uk/data- request/cif.
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    • 6): L1 -14.1 ppm, L2 17.9 ppm, L3 -9.7 ppm, and L4 -13.7 ppm
    • 6): L1) -14.1 ppm, L2 ) 17.9 ppm, L3) -9.7 ppm, and L4) -13.7 ppm.
  • 58
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    • 8): δ 47.6. This complex appears to be somewhat more labile compared to complex 3 during routine operations
    • 8): δ 47.6. This complex appears to be somewhat more labile compared to complex 3 during routine operations.
  • 59
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    • 8): δ 69.7
    • 8): δ 69.7.
  • 60
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    • 8): δ 47.4.
    • 8): δ 47.4.
  • 73
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    • Inhibition of catalytic activity by nucleosides has been reported
    • Inhibition of catalytic activity by nucleosides has been reported: Western, E. C.; Shaughnessy, K. H. J. Org. Chem. 2005, 70, 6378-6388.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.