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Volumn , Issue 2, 2003, Pages 288-294

Synthesis of polyfunctional organosulfur compounds mediated by azetidinium salts

Author keywords

Alkylation; Heterocycles; Nucleophiles; Ring opening; Sulfonates

Indexed keywords

CHEMICAL BONDS; SALTS; SULFUR COMPOUNDS;

EID: 0037281057     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-36825     Document Type: Article
Times cited : (11)

References (38)
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    • For reviews, see: (a) Davis, D. E.; Storr, R. C. In Comprehensive Heterocyclic Chemistry, Vol. 7; Lwowski, W., Ed.; Pergamon: Oxford, 1984, 238. (b) Cromwell, N. H.; Philips, B. Chem. Rev. 1979, 79, 331.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.7 , pp. 238
    • Davis, D.E.1    Storr, R.C.2
  • 2
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    • For reviews, see: (a) Davis, D. E.; Storr, R. C. In Comprehensive Heterocyclic Chemistry, Vol. 7; Lwowski, W., Ed.; Pergamon: Oxford, 1984, 238. (b) Cromwell, N. H.; Philips, B. Chem. Rev. 1979, 79, 331.
    • (1979) Chem. Rev. , vol.79 , pp. 331
    • Cromwell, N.H.1    Philips, B.2
  • 3
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    • For recent synthetic applications of azetidines, see: (a) Almena, J.; Foubelo, F.; Yus, M. Tetrahedron 1994, 50, 5775. (b) Alcaide, B.; Almendros, P.; Aragoncillo, C.; Salgado, N. R. J. Org. Chem. 1999, 64, 9596. (c) Ungureanu, I.; Klotz, P.; Schoenfelder, A.; Mann, A. Chem. Commun. 2001, 958; and references cited therein.
    • (1994) Tetrahedron , vol.50 , pp. 5775
    • Almena, J.1    Foubelo, F.2    Yus, M.3
  • 4
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    • For recent synthetic applications of azetidines, see: (a) Almena, J.; Foubelo, F.; Yus, M. Tetrahedron 1994, 50, 5775. (b) Alcaide, B.; Almendros, P.; Aragoncillo, C.; Salgado, N. R. J. Org. Chem. 1999, 64, 9596. (c) Ungureanu, I.; Klotz, P.; Schoenfelder, A.; Mann, A. Chem. Commun. 2001, 958; and references cited therein.
    • (1999) J. Org. Chem. , vol.64 , pp. 9596
    • Alcaide, B.1    Almendros, P.2    Aragoncillo, C.3    Salgado, N.R.4
  • 5
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    • and references cited therein
    • For recent synthetic applications of azetidines, see: (a) Almena, J.; Foubelo, F.; Yus, M. Tetrahedron 1994, 50, 5775. (b) Alcaide, B.; Almendros, P.; Aragoncillo, C.; Salgado, N. R. J. Org. Chem. 1999, 64, 9596. (c) Ungureanu, I.; Klotz, P.; Schoenfelder, A.; Mann, A. Chem. Commun. 2001, 958; and references cited therein.
    • (2001) Chem. Commun. , pp. 958
    • Ungureanu, I.1    Klotz, P.2    Schoenfelder, A.3    Mann, A.4
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    • 6
    • 6
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    • note
    • For example: 4b = MOPSO sodium salt: Fluka 69941, Sigma M5914.
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    • US Patent 4169950
    • (c) Ferguson, W. J. US Patent 4169950, 1979; Chem. Abstr. 1979, 92, 75852.
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    • and references cited therein
    • (a) Distler, H. Angew. Chem., Int. Ed. Engl. 1967, 6, 544; Angew. Chem. 1967, 79, 520; and references cited therein.
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  • 38
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    • note
    • The higher than commonly acceptable differences between calculated and found data of some elemental analyses for compounds 2 and 4 can arise from contamination with NaCl which is hard to remove by crystallization. The purified salt 2d (column chromatography) may contain trace amounts of the free acid 6d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.