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Volumn 6, Issue 12, 2004, Pages 1931-1934

Interesting behavior of α,β-unsaturated oximes in intramolecular [4 + 2] cycloaddition reactions

Author keywords

[No Author keywords available]

Indexed keywords

OXIME;

EID: 3042835371     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol049640n     Document Type: Article
Times cited : (19)

References (30)
  • 1
    • 0036259981 scopus 로고    scopus 로고
    • For reviews on Diels-Alder reaction, see: (a) Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. Angew. Chem., Int. Ed. 2002, 41, 1668. (b) Bear, B. R.; Sparks, S. M.; Shea, K. J. Angew. Chem., Int. Ed. 2001, 40, 820. (c) Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 513-550.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1668
    • Nicolaou, K.C.1    Snyder, S.A.2    Montagnon, T.3    Vassilikogiannakis, G.4
  • 2
    • 0035793788 scopus 로고    scopus 로고
    • For reviews on Diels-Alder reaction, see: (a) Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. Angew. Chem., Int. Ed. 2002, 41, 1668. (b) Bear, B. R.; Sparks, S. M.; Shea, K. J. Angew. Chem., Int. Ed. 2001, 40, 820. (c) Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 513-550.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 820
    • Bear, B.R.1    Sparks, S.M.2    Shea, K.J.3
  • 3
    • 0000048482 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • For reviews on Diels-Alder reaction, see: (a) Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. Angew. Chem., Int. Ed. 2002, 41, 1668. (b) Bear, B. R.; Sparks, S. M.; Shea, K. J. Angew. Chem., Int. Ed. 2001, 40, 820. (c) Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 513-550.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-550
    • Roush, W.R.1
  • 5
    • 0034698152 scopus 로고    scopus 로고
    • For a general discussion of Diels-Alder reactions of 1-azadienes, see: (a) Behforouz, M.; Ahmadian, M. Tetrahedron 2000, 56, 5259. (b) Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic Press: San Diego, 1987; Chapter 9.
    • (2000) Tetrahedron , vol.56 , pp. 5259
    • Behforouz, M.1    Ahmadian, M.2
  • 6
    • 0034698152 scopus 로고    scopus 로고
    • Academic Press: San Diego, Chapter 9
    • For a general discussion of Diels-Alder reactions of 1-azadienes, see: (a) Behforouz, M.; Ahmadian, M. Tetrahedron 2000, 56, 5259. (b) Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic Press: San Diego, 1987; Chapter 9.
    • (1987) Hetero Diels-Alder Methodology in Organic Synthesis
    • Boger, D.L.1    Weinreb, S.M.2
  • 24
    • 23044526507 scopus 로고    scopus 로고
    • For reviews of 1,3-dipolar cycloadditions, see: (a) Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products; Padwa, A., Pearson, W. H., Eds.; Wiley: New York, 2003; Vol. 59. (b) Karlsson, S.; Hogberg, H.-E. Org. Prep. Proced. Int. 2001, 33, 103. (c) Gothelf, K. V.; Jørgensen, K. A. Chem. Rev. 1998, 98, 863. (d) Frederickson, M. Tetrahedron 1997, 53, 403.
    • (2001) Org. Prep. Proced. Int. , vol.33 , pp. 103
    • Karlsson, S.1    Hogberg, H.-E.2
  • 25
    • 11544346529 scopus 로고    scopus 로고
    • For reviews of 1,3-dipolar cycloadditions, see: (a) Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products; Padwa, A., Pearson, W. H., Eds.; Wiley: New York, 2003; Vol. 59. (b) Karlsson, S.; Hogberg, H.-E. Org. Prep. Proced. Int. 2001, 33, 103. (c) Gothelf, K. V.; Jørgensen, K. A. Chem. Rev. 1998, 98, 863. (d) Frederickson, M. Tetrahedron 1997, 53, 403.
    • (1998) Chem. Rev. , vol.98 , pp. 863
    • Gothelf, K.V.1    Jørgensen, K.A.2
  • 26
    • 0031012571 scopus 로고    scopus 로고
    • For reviews of 1,3-dipolar cycloadditions, see: (a) Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products; Padwa, A., Pearson, W. H., Eds.; Wiley: New York, 2003; Vol. 59. (b) Karlsson, S.; Hogberg, H.-E. Org. Prep. Proced. Int. 2001, 33, 103. (c) Gothelf, K. V.; Jørgensen, K. A. Chem. Rev. 1998, 98, 863. (d) Frederickson, M. Tetrahedron 1997, 53, 403.
    • (1997) Tetrahedron , vol.53 , pp. 403
    • Frederickson, M.1
  • 27
    • 85039529929 scopus 로고    scopus 로고
    • note
    • It is worth noting that a simple treatment of 4a in acetic acid at room temperature does not produce any cycloadduct.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.