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Volumn 75, Issue 8, 2010, Pages 2760-2762

Acetone cyanohydrin as a source of HCN in the Cu-catalyzed hydrocyanation of α-aryl diazoacetates

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE CYANOHYDRIN; FREE CYANIDES; HIGH YIELD; HYDROCYANATION; HYDROGEN CYANIDE; IN-SITU; TRIMETHYLSILYL CYANIDE;

EID: 77951003571     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100356d     Document Type: Article
Times cited : (54)

References (43)
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    • For recent reports on the enantioselective X-H (X = N, O, S, etc) insertion into α-diazocarbonyl compounds, see
    • For recent reports on the enantioselective X-H (X = N, O, S, etc) insertion into α-diazocarbonyl compounds, see: Maier, T. C.; Fu, G. C. J. Am. Chem. Soc. 2006, 128, 4594
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4594
    • Maier, T.C.1    Fu, G.C.2
  • 27
    • 33845278206 scopus 로고
    • For reviews on the weakly coordinating anions to assist the formation of metal cationic species, see
    • For reviews on the weakly coordinating anions to assist the formation of metal cationic species, see: Beck, W.; Snkel, K. Chem. Rev. 1988, 88, 1405
    • (1988) Chem. Rev. , vol.88 , pp. 1405
    • Beck, W.1    Skel, K.2
  • 32
    • 17144389366 scopus 로고    scopus 로고
    • For recent reports of the rhodium-catalyzed carbenoid formation, see
    • For recent reports of the rhodium-catalyzed carbenoid formation, see: Huang, H.; Wang, Y.; Chen, Z.; Hu, W. Adv. Synth. Catal. 2005, 347, 531
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 531
    • Huang, H.1    Wang, Y.2    Chen, Z.3    Hu, W.4
  • 35
    • 77950997631 scopus 로고    scopus 로고
    • See the Supporting Information for the detailed experimental procedures
    • See the Supporting Information for the detailed experimental procedures.
  • 43
    • 77950973134 scopus 로고    scopus 로고
    • One reviewer suggested an alternative mechanistic pathway where TMSCN would be in equilibrium with TMSNC and this isocyanide can accelerate the reaction rate, acting as a similar way to cyanide ion
    • One reviewer suggested an alternative mechanistic pathway where TMSCN would be in equilibrium with TMSNC and this isocyanide can accelerate the reaction rate, acting as a similar way to cyanide ion.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.