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Volumn 21, Issue 23, 2011, Pages 7189-7192

Transformation of quercitols into 4-methylenecyclohex-5-ene-1,2,3-triol derivatives, precursors for the chemical chaperones N-octyl-4-epi-β- valienamine (NOEV) and N-octyl-β-valienamine (NOV)

Author keywords

Carbasugar; Carbohydrate mimics; Chemical chaperone; Glycosidase inhibitors; Quercitol; Structure activity relationship; Valienamine

Indexed keywords

4 METHYLENECYCLOHEX 5 ENE 1,2,3 TRIOL DERIVATIVE; GLYCOSIDASE INHIBITOR; N OCTYL 4 EPI BETA VALIENAMINE; N OCTYL BETA VALIENAMINE; QUERCITOL; UNCLASSIFIED DRUG;

EID: 80255138767     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2011.09.067     Document Type: Article
Times cited : (15)

References (34)
  • 30
    • 80255137326 scopus 로고
    • U.S. Patent 3,865,848 This reagent was purchased from Sigma-Aldrich Co. (St. Louis, MO, USA)
    • Nysted, L. N. U.S. Patent 3,865,848, 1975. This reagent was purchased from Sigma-Aldrich Co. (St. Louis, MO, USA).
    • (1975)
    • Nysted, L.N.1
  • 33
    • 0020840748 scopus 로고
    • The formation of the single β-amine through direct amination of α- and β-bromo compounds was mechanistically explained by presuming a neighboring group participation (Ref. 6e, and also see: Toyokuni, T.; Ogawa, S.; Suami, T. Bull. Chem. Soc. Jpn. 1983, 56, 2999)
    • (1983) Bull. Chem. Soc. Jpn. , vol.56 , pp. 2999
    • Toyokuni, T.1    Ogawa, S.2    Suami, T.3
  • 34
    • 79960228405 scopus 로고    scopus 로고
    • In contrast, without neighboring group participation, the amination of the relevant bromo compounds resulted in the generation of the nonstereospecific products (Cumpstey, I.; Ramstadius, C.; Borbas, K. E. Synlett, 2011, 12, 1701).
    • (2011) Synlett , vol.12 , pp. 1701
    • Cumpstey, I.1    Ramstadius, C.2    Borbas, K.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.