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Volumn 39, Issue 14, 1998, Pages 2013-2016

Cycloadditions with clays and alumina without solvents

Author keywords

Alumina; Cycloaddition; Diels Alder; Montmorillonite; Solid slate reactions

Indexed keywords

ALUMINUM OXIDE; SOLVENT;

EID: 0032473907     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00159-2     Document Type: Article
Times cited : (16)

References (37)
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    • 3. For a timely and excellent review on organic reactions on alumina: Kabalka, G. W.; Pagni, R. M. Tetrahedron 1997, 53, 7999-8065.
    • (1997) Tetrahedron , vol.53 , pp. 7999-8065
    • Kabalka, G.W.1    Pagni, R.M.2
  • 20
    • 0342347746 scopus 로고
    • 7. Hoang Van, C.; Ghorbel, A.; Teichner, S. J. Bull. Soc. Chim. Fr. 1972, 437-442. The catalytic activity of alumina, however, can be chiefly attributed to the coexistence of basic and acidic sites, which may also act cooperatively. See for instance: a) Dawson, W. H.; Kaiser, S. W; Ellis,P. D.; Inners, R. R. J. Am. Chem. Soc. 1981, 103, 6780-6781.
    • (1972) Bull. Soc. Chim. Fr. , pp. 437-442
    • Van Hoang, C.1    Ghorbel, A.2    Teichner, S.J.3
  • 21
    • 0010621035 scopus 로고
    • 7. Hoang Van, C.; Ghorbel, A.; Teichner, S. J. Bull. Soc. Chim. Fr. 1972, 437-442. The catalytic activity of alumina, however, can be chiefly attributed to the coexistence of basic and acidic sites, which may also act cooperatively. See for instance: a) Dawson, W. H.; Kaiser, S. W; Ellis,P. D.; Inners, R. R. J. Am. Chem. Soc. 1981, 103, 6780-6781.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 6780-6781
    • Dawson, W.H.1    Kaiser, S.W.2    Ellis, P.D.3    Inners, R.R.4
  • 23
    • 84877031806 scopus 로고
    • 8. For solid-state organic reactions: a) Toda, F. Synlett 1993, 303-312.
    • (1993) Synlett , pp. 303-312
    • Toda, F.1
  • 25
    • 84985579944 scopus 로고
    • 9. Some Diels-Alder reactions on supports, mainly alumina, without solvent have been reported: a) Parlar, H.; Baumann, R. Angew. Chem., Int. Ed. Engl. 1981, 20, 1014.
    • (1981) Angew. Chem., Int. Ed. Engl. , vol.20 , pp. 1014
    • Parlar, H.1    Baumann, R.2
  • 32
    • 0010586471 scopus 로고    scopus 로고
    • Parallel experiments were also conducted either with K-10 or alumina activated at 200 °C, but yields and selectivities were similar to those of unactivated minerals
    • 10. Parallel experiments were also conducted either with K-10 or alumina activated at 200 °C, but yields and selectivities were similar to those of unactivated minerals.
  • 36
    • 0000048258 scopus 로고
    • Trost, B. M.; Fleming, I.; Paquette, L. A., Eds.; Pergamon Press: Oxford
    • d) For a comprehensive treatment of intermolecular [4+2] Diels-Alder reactions: Oppolzer, W. in Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Paquette, L. A., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 315-399.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 315-399
    • Oppolzer, W.1
  • 37
    • 0010621438 scopus 로고    scopus 로고
    • The endo/exo selectivity of the dimethyl maleate reaction can be enhanced by activating alumina at very high temperatures. Moreover, such transformations were run at room temperature: see ref. 9d
    • 12. The endo/exo selectivity of the dimethyl maleate reaction can be enhanced by activating alumina at very high temperatures. Moreover, such transformations were run at room temperature: see ref. 9d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.