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Volumn 130, Issue 47, 2008, Pages 15982-15989

Rhodium-catalyzed silylation and intramolecular arylation of nitriles via the silicon-assisted cleavage of carbon-cyano bonds

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CYANIDES; FUNCTIONAL GROUPS; RHODIUM; SILICON;

EID: 56749173730     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja804992n     Document Type: Article
Times cited : (160)

References (117)
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    • A similar stoichiometric reaction has been reported, although the mechanism is proposed to be oxidative addition: Klei, S. R.; Tilley, T. D.; Bergman, R. G. Organometallics 2002, 21, 4648.
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    • One catalytic C-CN bond cleavage reaction that proceeds through neither of the processes shown in Schemes 1 and 2 has also been reported: Luo, F.-H, Chu, C.-I, Cheng, C.-H. Organometallics 1998, 17, 1025
    • One catalytic C-CN bond cleavage reaction that proceeds through neither of the processes shown in Schemes 1 and 2 has also been reported: Luo, F.-H.; Chu, C.-I.; Cheng, C.-H. Organometallics 1998, 17, 1025.
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    • Pd-catalyzed silylation of aryl halides using disilanes has been reported: (a) Shirakawa, E.; Kurahashi, T.; Yoshida, H.; Hiyama, T. Chem. Commun. 2000, 1895.
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    • A similar electronic effect was also observed in mechanistically related rhodium-catalyzed decarbonylation of aldehydes: Fristrup, P.; Kreis, M.; Palmelund, A.; Norrby, P.-O.; Madsen, R. J. Am. Chem. Soc. 2008, 130, 5206.
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    • The reaction of arylrhodium species, generated from arylboron compounds, with aryl halides leading to biaryls has been reported: Ueura, K.; Satoh, T.; Miura, M. Org. Lett. 2005, 7, 2229.
    • The reaction of arylrhodium species, generated from arylboron compounds, with aryl halides leading to biaryls has been reported: Ueura, K.; Satoh, T.; Miura, M. Org. Lett. 2005, 7, 2229.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.