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Volumn 10, Issue 1, 2008, Pages 73-75

The benzil rearrangement reaction: Trapping of a hitherto minor product and its application to the development of a selective cyanide anion indicator

Author keywords

[No Author keywords available]

Indexed keywords

ANION; BENZIL; CYANIDE; DRUG DERIVATIVE; PHENYLGLYOXAL; UNCLASSIFIED DRUG;

EID: 38349129171     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7027306     Document Type: Article
Times cited : (146)

References (26)
  • 7
    • 0037024174 scopus 로고    scopus 로고
    • The basicity of the anions in question (including cyanide) could be contributing to the observed sensing and competition effects. See: (a) Anzenbacher, P., Jr.; Tyson, D. S.; Jursíková, K.; Castellano, F. N. J. Am. Chem. Soc. 2002, 124, 6232-6233.
    • The basicity of the anions in question (including cyanide) could be contributing to the observed sensing and competition effects. See: (a) Anzenbacher, P., Jr.; Tyson, D. S.; Jursíková, K.; Castellano, F. N. J. Am. Chem. Soc. 2002, 124, 6232-6233.
  • 13
    • 34848826861 scopus 로고    scopus 로고
    • An interesting reaction-based approach to developing fluorescent (but non-colorimetric) cyanide anion receptors, involving the use of ammonium boranes, was reported during the time this work was being written up for publication. See: Hudnall, T. W, Gabbai, F. P. J. Am. Chem. Soc. 2007, 129, 11978-11986
    • An interesting reaction-based approach to developing fluorescent (but non-colorimetric) cyanide anion receptors, involving the use of ammonium boranes, was reported during the time this work was being written up for publication. See: Hudnall, T. W.; Gabbai, F. P. J. Am. Chem. Soc. 2007, 129, 11978-11986.
  • 19
    • 5044231098 scopus 로고    scopus 로고
    • Previous workers isolated la in 18% yield while recovering benzil in 60% yield: Clerici, A.; Porta, O. J. Org. Chem. 1994, 59, 1591-1592.
    • Previous workers isolated la in 18% yield while recovering benzil in 60% yield: Clerici, A.; Porta, O. J. Org. Chem. 1994, 59, 1591-1592.
  • 21
    • 0141618497 scopus 로고    scopus 로고
    • N,N-Dimethyl-4-ethynylbenzenamine is commercially available. N,N-Diethyl-4-ethynylbenzenamine was synthesized according to a literature procedure: Miki, Y.; Momotake, A.; Arai, T. Org. Biomol. Chem. 2003, 1, 2655-2660.
    • N,N-Dimethyl-4-ethynylbenzenamine is commercially available. N,N-Diethyl-4-ethynylbenzenamine was synthesized according to a literature procedure: Miki, Y.; Momotake, A.; Arai, T. Org. Biomol. Chem. 2003, 1, 2655-2660.
  • 25
    • 33746590750 scopus 로고    scopus 로고
    • There is increasing interest in the development of reaction-based sensors and indicators within the generalized molecular recognition field. For recent work, see, for instance: (a) Albers, A. E, Okreglak, V. S, Chang, C. J. J. Am. Chem. Soc. 2006, 128, 9640-9641
    • There is increasing interest in the development of reaction-based sensors and indicators within the generalized molecular recognition field. For recent work, see, for instance: (a) Albers, A. E.; Okreglak, V. S.; Chang, C. J. J. Am. Chem. Soc. 2006, 128, 9640-9641.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.