메뉴 건너뛰기




Volumn 43, Issue 8, 1996, Pages 1719-1734

A convenient synthesis of n-substituted 2,3-dihydro-3-oxoisothiazolo[5,4-b]pyridines in acidic conditions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0042576572     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-96-7505     Document Type: Article
Times cited : (8)

References (18)
  • 4
    • 3643078913 scopus 로고
    • U. S. Patent, 3,965,107
    • Some N-substituted 2,3-dihydro-3-oxoisothiazolo[5,4-b]pyridines have been reported in several patents and described as fungicides, bactericides, inhibitors of blood platelet aggregation, and antiacne agents: J. L. Rainey and M. C. Seidel, U. S. Patent, 3,965,107 (Chem. Abst.,1976, 85, 160072h); K. H. Baggaley, German Patent 2,718,707 (Chem. Abst., 1978, 88, 50843q); J. Maignam and B. Shroot, German Patent 3,313, 778 (Chem. Abst., 1984, 100, 121052k).
    • (1976) Chem. Abst. , vol.85
    • Rainey, J.L.1    Seidel, M.C.2
  • 5
    • 4244190464 scopus 로고
    • German Patent 2,718,707
    • Some N-substituted 2,3-dihydro-3-oxoisothiazolo[5,4-b]pyridines have been reported in several patents and described as fungicides, bactericides, inhibitors of blood platelet aggregation, and antiacne agents: J. L. Rainey and M. C. Seidel, U. S. Patent, 3,965,107 (Chem. Abst.,1976, 85, 160072h); K. H. Baggaley, German Patent 2,718,707 (Chem. Abst., 1978, 88, 50843q); J. Maignam and B. Shroot, German Patent 3,313, 778 (Chem. Abst., 1984, 100, 121052k).
    • (1978) Chem. Abst. , vol.88
    • Baggaley, K.H.1
  • 6
    • 84986450761 scopus 로고
    • German Patent 3,313, 778
    • Some N-substituted 2,3-dihydro-3-oxoisothiazolo[5,4-b]pyridines have been reported in several patents and described as fungicides, bactericides, inhibitors of blood platelet aggregation, and antiacne agents: J. L. Rainey and M. C. Seidel, U. S. Patent, 3,965,107 (Chem. Abst.,1976, 85, 160072h); K. H. Baggaley, German Patent 2,718,707 (Chem. Abst., 1978, 88, 50843q); J. Maignam and B. Shroot, German Patent 3,313, 778 (Chem. Abst., 1984, 100, 121052k).
    • (1984) Chem. Abst. , vol.100
    • Maignam, J.1    Shroot, B.2
  • 7
    • 2742524039 scopus 로고    scopus 로고
    • Unpublished data from our research laboratories. We will report elsewhere
    • Unpublished data from our research laboratories. We will report elsewhere.
  • 13
    • 37049089075 scopus 로고
    • It was reported that the nucleophilicity of the nitrogen atom on the carbamoyl moiety of N-substituted (Z)-3-benzylsulfinylpropenamides had also influence on their conversion into N-substituted isothiazol-3(2H)-ones by treating with TCAA: N. R. A. Beeley, L. M. Harwood, and P. C. Hedger, J. Chem. Soc., Perkin Trans, 1, 1994, 2245.
    • (1994) J Chem Soc Perkin Trans 1 , pp. 2245
    • Beeley, N.R.A.1    Harwood, L.M.2    Hedger, P.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.