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Volumn 9, Issue 1, 1999, Pages 49-54

Toxicity and osmoprotective activities of analogues of glycine betaine obtained by solid phase organic synthesis towards Sinorhizobium meliloti

Author keywords

[No Author keywords available]

Indexed keywords

BETAINE DERIVATIVE;

EID: 0032896906     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(98)00679-9     Document Type: Article
Times cited : (7)

References (26)
  • 3
    • 0026006215 scopus 로고    scopus 로고
    • Csonka, L.N.; Hanson, A.D. Annu. Rev. Microbiol. 1991, 45, 569. Csonka, L.N.; Epstein, W. In Escherichia Coli and Salmonella, Cellular and Molecular Biology 1996, 1210.
    • (1991) Annu. Rev. Microbiol. , vol.45 , pp. 569
    • Csonka, L.N.1    Hanson, A.D.2
  • 15
    • 33748237769 scopus 로고    scopus 로고
    • Früchtel, J.S.; Jung, G. Angew. Chem. Int. Ed. Engl. 1996, 35, 17. Thompson, L.A.; Ellman, J.A. Chem. Rev. 1996, 96, 555. Hermkens, P.H.H.; Ottenheijn, H.C.J.; Rees, D.C. Tetrahedron 1997, 53, 5643.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 17
    • Früchtel, J.S.1    Jung, G.2
  • 16
    • 7044263277 scopus 로고    scopus 로고
    • Früchtel, J.S.; Jung, G. Angew. Chem. Int. Ed. Engl. 1996, 35, 17. Thompson, L.A.; Ellman, J.A. Chem. Rev. 1996, 96, 555. Hermkens, P.H.H.; Ottenheijn, H.C.J.; Rees, D.C. Tetrahedron 1997, 53, 5643.
    • (1996) Chem. Rev. , vol.96 , pp. 555
    • Thompson, L.A.1    Ellman, J.A.2
  • 17
    • 0031001699 scopus 로고    scopus 로고
    • Früchtel, J.S.; Jung, G. Angew. Chem. Int. Ed. Engl. 1996, 35, 17. Thompson, L.A.; Ellman, J.A. Chem. Rev. 1996, 96, 555. Hermkens, P.H.H.; Ottenheijn, H.C.J.; Rees, D.C. Tetrahedron 1997, 53, 5643.
    • (1997) Tetrahedron , vol.53 , pp. 5643
    • Hermkens, P.H.H.1    Ottenheijn, H.C.J.2    Rees, D.C.3
  • 19
    • 0013513422 scopus 로고    scopus 로고
    • note
    • 2. Then, water was evaporated and the chlorhydrate salt of the synthetic betaine was obtained by stirring the dry residue for 2 h in 5 ml of 2 M aqueous HC1. Finally, the synthetic betaine hydrochloride was purified further by triturating the white solid in dimethylketone. Seven GB analogues [N°: name (yield%)] were synthesised in this study: 61: carboxymethyldimethylethyl ammonium chloride (100%), 62: carboxymethyldiethylmethyl ammonium chloride (95%), 63: carboxymethyltriethyl ammonium chloride (65%), 64: carboxymethyldimethylisopropyl ammonium chloride (95%), 65: carboxymethylbutyldimethyl ammonium chloride (80%), 66: carboxymethylmethylpyrrolidinyl ammonium chloride (75%) and 67: carboxymethylmethylmorpholinyl ammonium chloride (65%).
  • 20
    • 0030727607 scopus 로고    scopus 로고
    • In contrast to the situation observed in procedures using bromacetic derivatives no reaction of pyridine with the polymer 4 was observed in our protocol
    • In contrast to the situation observed in procedures using bromacetic derivatives (Vo, N.H.; Eyermann, C.J.; Hodge, C.N. Tetrahedron Lett. 1997, 38, 7951 ), no reaction of pyridine with the polymer 4 was observed in our protocol.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7951
    • Vo, N.H.1    Eyermann, C.J.2    Hodge, C.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.