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Volumn 65, Issue 14, 2000, Pages 4423-4430

Solvolyses of 2-deoxy-α- and β-D-glucopyranosyl 4'-bromoisoquinolinium tetrafluoroborates

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE DERIVATIVE; ISOQUINOLINE DERIVATIVE;

EID: 0034647523     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0004106     Document Type: Article
Times cited : (20)

References (59)
  • 1
    • 0030799390 scopus 로고    scopus 로고
    • For some recent examples, see: Liras, J. L.; Lynch, V. M.; Anslyn, E. V. J. Am. Chem. Soc. 1997, 119, 8191-8200. Horenstein, B. A.; Bruner, M. J. Am. Chem. Soc. 1996, 118, 10371-10379. Jagannadham, V.; Amyes, T. L.; Richard, J. P. J. Am. Chem. Soc. 1993, 115, 8465- 8466.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8191-8200
    • Liras, J.L.1    Lynch, V.M.2    Anslyn, E.V.3
  • 2
    • 0029820801 scopus 로고    scopus 로고
    • For some recent examples, see: Liras, J. L.; Lynch, V. M.; Anslyn, E. V. J. Am. Chem. Soc. 1997, 119, 8191-8200. Horenstein, B. A.; Bruner, M. J. Am. Chem. Soc. 1996, 118, 10371-10379. Jagannadham, V.; Amyes, T. L.; Richard, J. P. J. Am. Chem. Soc. 1993, 115, 8465- 8466.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 10371-10379
    • Horenstein, B.A.1    Bruner, M.2
  • 3
    • 0001659252 scopus 로고
    • For some recent examples, see: Liras, J. L.; Lynch, V. M.; Anslyn, E. V. J. Am. Chem. Soc. 1997, 119, 8191-8200. Horenstein, B. A.; Bruner, M. J. Am. Chem. Soc. 1996, 118, 10371-10379. Jagannadham, V.; Amyes, T. L.; Richard, J. P. J. Am. Chem. Soc. 1993, 115, 8465-8466.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 8465-8466
    • Jagannadham, V.1    Amyes, T.L.2    Richard, J.P.3
  • 4
  • 13
    • 0343763611 scopus 로고    scopus 로고
    • note
    • SOH) are correct.
  • 18
    • 0342892601 scopus 로고    scopus 로고
    • note
    • The IUPAC name for 2-deoxy-D-glucose is 2-deoxy-D-arabino-hexose (ref 16).
  • 30
    • 0342892596 scopus 로고    scopus 로고
    • note
    • + values for aqueous trifluoroethanol (v/v) were interpolated from the values given in ref 20 that were measured using a weight-weight basis.
  • 32
    • 0343327672 scopus 로고    scopus 로고
    • note
    • These observations also rule out the possibility that N-methylmorpholine could act as a nucleophile.
  • 38
    • 0342458296 scopus 로고    scopus 로고
    • note
    • The solvolytic rates for 1-adamantylpyridinium perchlorate, quoted in ref 28, were monitored at 190 °C.
  • 42
    • 0343327666 scopus 로고    scopus 로고
    • note
    • In aqueous EtOH and MeOH solvent mixtures that had a water content of >20% (v/v), a small (≤0.9%) but detectable quantity of 1,6-anhydro-2-deoxy-β-D-glucopyranose was generated.
  • 53
    • 0342458282 scopus 로고    scopus 로고
    • note
    • The solvolysis studies reported in ref 12 were performed in equimolar TFE/EtOH, which is equivalent to approximately 56% v/v TFE/EtOH.
  • 54
    • 0342892574 scopus 로고    scopus 로고
    • note
    • +) = 3.31.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.