메뉴 건너뛰기




Volumn 52, Issue 48, 1996, Pages 15267-15288

(Alkoxyallyl)sulfones as enal β-anion equivalents. Synthesis of 5-substituted 2(5H)-furanones

Author keywords

[No Author keywords available]

Indexed keywords

FURANONE DERIVATIVE;

EID: 0030602252     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)00931-3     Document Type: Article
Times cited : (15)

References (36)
  • 1
    • 0000036801 scopus 로고
    • Pergamon: Oxford
    • 1. Simpkins, N. S. Sulphones in Organic Synthesis; Pergamon: Oxford 1993. For a review of the chemistry of vinylic sulfones, See: Simpkins, N. S. Tetrahedron 1990, 46, 6951.
    • (1993) Sulphones in Organic Synthesis
    • Simpkins, N.S.1
  • 2
    • 0000036801 scopus 로고
    • 1. Simpkins, N. S. Sulphones in Organic Synthesis; Pergamon: Oxford 1993. For a review of the chemistry of vinylic sulfones, See: Simpkins, N. S. Tetrahedron 1990, 46, 6951.
    • (1990) Tetrahedron , vol.46 , pp. 6951
    • Simpkins, N.S.1
  • 4
    • 0026555217 scopus 로고
    • 3. Craig, D.; Smith, A. M. Tetrahedron Lett. 1992, 33, 695; Craig, D.; Ikin, N. J.; Mathews, N.; Smith, A. M. Tetrahedron Lett. 1995, 36, 7531.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 695
    • Craig, D.1    Smith, A.M.2
  • 6
    • 0029054699 scopus 로고
    • 4. For studies on related cyclic systems, see: Kim, S. H.; Jin, Z. D.; Fuchs, P. L. Tetrahedron Lett. 1995, 36, 4537; Jin, Z. D.; Fuchs, P. L. J. Am. Chem. Soc. 1995, 117, 3022.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4537
    • Kim, S.H.1    Jin, Z.D.2    Fuchs, P.L.3
  • 7
    • 0000204525 scopus 로고
    • 4. For studies on related cyclic systems, see: Kim, S. H.; Jin, Z. D.; Fuchs, P. L. Tetrahedron Lett. 1995, 36, 4537; Jin, Z. D.; Fuchs, P. L. J. Am. Chem. Soc. 1995, 117, 3022.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 3022
    • Jin, Z.D.1    Fuchs, P.L.2
  • 14
    • 84972949066 scopus 로고
    • 7. For an analogous one-pot method for the preparation of vinylic sulfones, see: Lee, J. W.; Oh, D. Y. Synth. Commun. 1989, 19, 2209; we thank a referee for bringing this work to our attention. For related methodology applied to the synthesis of vinylic sulfoxides and sulfoximines, see respectively: Craig, D.; Daniels, K.; Marsh, A.; Rainford, D.; Smith, A. M. Synlett 1990, 531, and Craig, D.; Geach, N. J. Synlett 1992, 299.
    • (1989) Synth. Commun. , vol.19 , pp. 2209
    • Lee, J.W.1    Oh, D.Y.2
  • 15
    • 33750249701 scopus 로고
    • 7. For an analogous one-pot method for the preparation of vinylic sulfones, see: Lee, J. W.; Oh, D. Y. Synth. Commun. 1989, 19, 2209; we thank a referee for bringing this work to our attention. For related methodology applied to the synthesis of vinylic sulfoxides and sulfoximines, see respectively: Craig, D.; Daniels, K.; Marsh, A.; Rainford, D.; Smith, A. M. Synlett 1990, 531, and Craig, D.; Geach, N. J. Synlett 1992, 299.
    • (1990) Synlett , pp. 531
    • Craig, D.1    Daniels, K.2    Marsh, A.3    Rainford, D.4    Smith, A.M.5
  • 16
    • 0002256265 scopus 로고
    • 7. For an analogous one-pot method for the preparation of vinylic sulfones, see: Lee, J. W.; Oh, D. Y. Synth. Commun. 1989, 19, 2209; we thank a referee for bringing this work to our attention. For related methodology applied to the synthesis of vinylic sulfoxides and sulfoximines, see respectively: Craig, D.; Daniels, K.; Marsh, A.; Rainford, D.; Smith, A. M. Synlett 1990, 531, and Craig, D.; Geach, N. J. Synlett 1992, 299.
    • (1992) J. Synlett , pp. 299
    • Craig, D.1    Geach, N.2
  • 21
    • 0039273708 scopus 로고
    • 12. 2-Benzyloxyethanal has been prepared using a variety of methods. See: (i) Palfray, S. Bull. Soc. Chim. Fr. 1937, 5, 950; Shiao, M.-J.; Yang, C.-Y.; Lee, S.-H.; Wu, T.-C. Synth. Commun. 1988, 18, 359 (oxidative cleavage of 3-benzyloxy-1,2-propanediol);
    • (1937) Bull. Soc. Chim. Fr. , vol.5 , pp. 950
    • Palfray, S.1
  • 22
    • 0001631888 scopus 로고
    • (oxidative cleavage of 3-benzyloxy-1,2-propanediol)
    • 12. 2-Benzyloxyethanal has been prepared using a variety of methods. See: (i) Palfray, S. Bull. Soc. Chim. Fr. 1937, 5, 950; Shiao, M.-J.; Yang, C.-Y.; Lee, S.-H.; Wu, T.-C. Synth. Commun. 1988, 18, 359 (oxidative cleavage of 3-benzyloxy-1,2-propanediol);
    • (1988) Synth. Commun. , vol.18 , pp. 359
    • Shiao, M.-J.1    Yang, C.-Y.2    Lee, S.-H.3    Wu, T.-C.4
  • 24
    • 3142632523 scopus 로고
    • ozone addition to benzyl vinyl ether followed by Zn-mediated reduction
    • (iii) Danishefsky, S. J.; DeNinno, M. P. J. Org. Chem. 1986, 51, 2615 (ozone addition to benzyl vinyl ether followed by Zn-mediated reduction);
    • (1986) J. Org. Chem. , vol.51 , pp. 2615
    • Danishefsky, S.J.1    DeNinno, M.P.2
  • 25
    • 0026513813 scopus 로고
    • DIBAL-H-mediated reduction of methyl 2-benzyloxyacetate
    • (iv) Kobayashi, Y.; Ito, Y.; Terashima, S. Tetrahedron 1992, 48; 55 (DIBAL-H-mediated reduction of methyl 2-benzyloxyacetate);
    • (1992) Tetrahedron , vol.48 , pp. 55
    • Kobayashi, Y.1    Ito, Y.2    Terashima, S.3
  • 26
    • 0019989994 scopus 로고
    • activated DMSO-mediated oxidation of 2-benzyloxyethanol
    • (v) Parry, R. J.; Naidu, M. V. J. Am. Chem. Soc. 1982, 104, 3217 (activated DMSO-mediated oxidation of 2-benzyloxyethanol);
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 3217
    • Parry, R.J.1    Naidu, M.V.2
  • 27
    • 0027312320 scopus 로고
    • (ozonolytic cleavage of (Z)-1,4-bis(benzyloxy)-2-butene)
    • (vi) Jones, K.; Storey, J. M. D. Tetrahedron 1993, 49, 4901-4906 (ozonolytic cleavage of (Z)-1,4-bis(benzyloxy)-2-butene);
    • (1993) Tetrahedron , vol.49 , pp. 4901-4906
    • Jones, K.1    Storey, J.M.D.2
  • 28
    • 0039697372 scopus 로고
    • hydrolysis-oxidative cleavage of syn-1,2-bis(benzyloxymethyl)oxirane
    • (vii) Garner, P.; Park, J. M. Synth. Commun. 1987, 17, 189 (hydrolysis-oxidative cleavage of syn-1,2-bis(benzyloxymethyl)oxirane.
    • (1987) Synth. Commun. , pp. 189
    • Garner, P.1    Park, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.