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Volumn 2, Issue 3, 2005, Pages 231-234

Regioselective synthesis of 3-(aryloxyacetyl)-2,3-dihydrothieno[3,2-c] [1] benzothiopyran-4-ones: A tandem [2,3] and [3,3]sigmatropic rearrangement approach

Author keywords

3 (aryloxyacetyl) 2; 3 dihydrothieno 3,2 c 1 benzothiopyran 4 ones; 4 mercaptothiopyran 2 ones; 2,3 and 3,3 sigmatropic rearrangement

Indexed keywords


EID: 33746139250     PISSN: 15701786     EISSN: None     Source Type: Journal    
DOI: 10.2174/1570178053765294     Document Type: Review
Times cited : (4)

References (36)
  • 9
    • 46149101675 scopus 로고    scopus 로고
    • H. E. Zimmermann, in Molecular Rearrangements, Part 1, ed., P. de Mayo, Interscience, New York, 1963, p. 345.
    • H. E. Zimmermann, in Molecular Rearrangements, Part 1, ed., P. de Mayo, Interscience, New York, 1963, p. 345.
  • 21
    • 0001566960 scopus 로고
    • ed. Elderfield, R. C, Wiley, New York
    • (e) Wawzonek, S. in "Heterocyclic Compounds" ed. Elderfield, R. C., Wiley, New York, 1951, 2, 176.
    • (1951) Heterocyclic Compounds , vol.2 , pp. 176
    • Wawzonek, S.1
  • 23
    • 0000467525 scopus 로고
    • ed. Sammes, P. G. Pergarnon Press, Oxford
    • (a) Staunton, J. in "Comprehensive Organic Chemistry", ed. Sammes, P. G. Pergarnon Press, Oxford, 1979, 4, 646.
    • (1979) Comprehensive Organic Chemistry , vol.4 , pp. 646
    • Staunton, J.1
  • 24
    • 0242671327 scopus 로고
    • ed. Boulton, A. J, A. Mckillop, Pergamon Press, Oxford
    • (b) Hepworth, J. D. in "Comprehensive Heterocyclic Chemistry", ed. Boulton, A. J.; A. Mckillop, Pergamon Press, Oxford, 1984, 3, 1799.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 1799
    • Hepworth, J.D.1
  • 31
    • 46149096644 scopus 로고    scopus 로고
    • 2: C, 68.18; H, 4.54. Found, C, 68.38; H, 4.72.
    • 2: C, 68.18; H, 4.54. Found, C, 68.38; H, 4.72.
  • 32
    • 46149090256 scopus 로고    scopus 로고
    • Compound 4a: Yield: 91, white solid; mp, 125 °C. UV (EtOH, λmax, 343, 284, 274, 236 nm. IR (KBr, γmax, 2921, 1725, 1473, 1047, 816 cm-1. 1H NMR (CDCl3, 300 MHz, δH, 2.28 (s, 3H, CH3, 3.57 (dd, 1H, J, 9, 12 Hz, SCH2, 3.64 (dd, 1H, J, 6, 12 Hz, SCH2, 4.82 (d, 1H, J, 17 Hz, OCH2, 4.88 (d, 1H, J, 17 Hz, OCH2) 4.96 (dd, 1H, J, 6, 9 Hz, 6.81-7.68 (m, 8H, ArH, MS m/z: 367 M, Anal. Calcd. For C20H15 O3S2: C, 65.39; H, 4.08. Found, C, 65.64; H, 4.29
    • 2: C, 65.39; H, 4.08. Found, C, 65.64; H, 4.29.
  • 34
    • 46149123991 scopus 로고    scopus 로고
    • 2: C,60.00; H, 3.07. Found, C, 60.21; H, 3.31.
    • 2: C,60.00; H, 3.07. Found, C, 60.21; H, 3.31.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.