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Volumn 129, Issue 26, 2007, Pages 8080-8081

Rh-catalyzed arylation and alkenylation of C60 using organoboron compounds

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ALKYNE; BORONIC ACID DERIVATIVE; FULLERENE; ORGANOBORON DERIVATIVE; RHODIUM COMPLEX;

EID: 34447115833     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja073042x     Document Type: Article
Times cited : (104)

References (44)
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    • Pioneering works: (a) Sakai, M.; Hayashi, H.; Miyaura, N. Organometallics 1997, 16, 4229.
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    • Selected recent examples in this area: (e) Paquin, J.-F.; Defieber, C.; Stephenson, C. R. J.; Carreira, E. M. J. Am. Chem. Soc. 2005, 127, 10850.
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    • Boronic acid derivatives are air-stable, storable, and easily accessible by various methods. For general views for boronic acid derivatives, see:, Ed, Wiley-VCH: Weinheim, Germany, Over 750 boronic acid derivatives are now commercially available from Sigma-Aldrich
    • Boronic acid derivatives are air-stable, storable, and easily accessible by various methods. For general views for boronic acid derivatives, see: Hall, D. G., Ed. Boronic Acids; Wiley-VCH: Weinheim, Germany, 2005. Over 750 boronic acid derivatives are now commercially available from Sigma-Aldrich (http://www.sigmaaldrich.com).
    • (2005) Boronic Acids
  • 33
    • 84890711311 scopus 로고    scopus 로고
    • Throughout this paper, selectivity stands for a ratio of the quantity of desired product over the quantity of substrate converted (Orchin, M.; Macomber, R. S.; Pinhas, A. R.; Wilson, R. M., The Vocabulary and Concepts of Organic Chemistry, 2nd ed.; Wiley-Interscience: New Jersey, 2005).
    • Throughout this paper, "selectivity" stands for a ratio of the quantity of desired product over the quantity of substrate converted (Orchin, M.; Macomber, R. S.; Pinhas, A. R.; Wilson, R. M., The Vocabulary and Concepts of Organic Chemistry, 2nd ed.; Wiley-Interscience: New Jersey, 2005).
  • 34
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    • For an exception in this regard, see ref 3f
    • For an exception in this regard, see ref 3f.
  • 35
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    • Potassium trifluoro(organo)borates in rhodium-catalyzed conjugate additions: (a) Navarre, L.; Pucheault, M.; Darses, S.; Genet, J.-P. Tetrahedron Lett. 2005, 46, 4247.
    • Potassium trifluoro(organo)borates in rhodium-catalyzed conjugate additions: (a) Navarre, L.; Pucheault, M.; Darses, S.; Genet, J.-P. Tetrahedron Lett. 2005, 46, 4247.
  • 38
    • 33847312744 scopus 로고    scopus 로고
    • Recently, Hartwig also found a similar ortho-substitution effect in transmetalation from boron to rhodium, which might be closely related to the present reaction: (a) Zhao, P.; Incarvito, C. D.; Hartwig, J. F. J. Am. Chem. Soc. 2007, 129, 1876.
    • Recently, Hartwig also found a similar ortho-substitution effect in transmetalation from boron to rhodium, which might be closely related to the present reaction: (a) Zhao, P.; Incarvito, C. D.; Hartwig, J. F. J. Am. Chem. Soc. 2007, 129, 1876.
  • 39
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    • Kakiuchi also observed a seemingly similar effect in ruthenium catalysis using arylboronates: (b) Kakiuchi, F.; Matsuura, Y.; Kan, S.; Chatani, N. J. Am. Chem. Soc. 2005, 127, 5936.
    • Kakiuchi also observed a seemingly similar effect in ruthenium catalysis using arylboronates: (b) Kakiuchi, F.; Matsuura, Y.; Kan, S.; Chatani, N. J. Am. Chem. Soc. 2005, 127, 5936.
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  • 44
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    • For catalytic transformation of functionalized fullerenes, see: e
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    • (2006) Chem. Lett , vol.35 , pp. 858
    • Matsuo, Y.1    Iwashita, A.2    Nakamura, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.