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Volumn 52, Issue 14, 1996, Pages 4983-4994

An efficient functionalization of [60]fullerene. Diels-Alder reaction using 1,3-butadienes substituted with electron-withdrawing and electron-donating (silyloxy) groups

Author keywords

[No Author keywords available]

Indexed keywords

FULLERENE DERIVATIVE; POLYCYCLIC HYDROCARBON;

EID: 0029933196     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00106-8     Document Type: Article
Times cited : (50)

References (51)
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    • g) Diederich, F.; Isaacs, L.; Philp, D. Chem. Soc. Rev. 1994, 243. For [8+2]cycloaddition, see: Beer, E.; Feuerer, M.; Knorr, A.; Daub, M. J. Angew. Chem. Int. Ed. Engl. 1994, 33, 1087.
    • (1994) Chem. Soc. Rev. , pp. 243
    • Diederich, F.1    Isaacs, L.2    Philp, D.3
  • 22
    • 0008520555 scopus 로고
    • e) Ohno, M.; Koide, N.; Eguchi, S. Heterocyclic Commun. 1995, 1, 125. For the hetero version of o-quinodimethane, see: Ohno, M.; Azuma, T.; Eguchi, S. Chem. Lett. 1993, 1833.
    • (1995) Heterocyclic Commun. , vol.1 , pp. 125
    • Ohno, M.1    Koide, N.2    Eguchi, S.3
  • 23
    • 0003091351 scopus 로고
    • e) Ohno, M.; Koide, N.; Eguchi, S. Heterocyclic Commun. 1995, 1, 125. For the hetero version of o-quinodimethane, see: Ohno, M.; Azuma, T.; Eguchi, S. Chem. Lett. 1993, 1833.
    • (1993) Chem. Lett. , pp. 1833
    • Ohno, M.1    Azuma, T.2    Eguchi, S.3
  • 33
    • 0026469324 scopus 로고
    • 60, being consistent with the observed trend of reactivity, and this fact might be explained also by an orbital effect.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 7097
    • Naim, A.1    Shevlin, P.B.2
  • 41
    • 0028197521 scopus 로고
    • b) Byun, H.-S.; Reddy, K. C.; Bittman, R. Tetrahedron Lett. 1994, 35, 1371. For microwave conditions, see: Kundu, M. K.; Mukherjee, S. B.; Balu, N.; Padmakumar, R.; Bhat, S. V. Synlett 1994, 444.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 1371
    • Byun, H.-S.1    Reddy, K.C.2    Bittman, R.3
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    • note
    • -1; however, the detailed structure was not determined.
  • 51
    • 85030195708 scopus 로고    scopus 로고
    • note
    • Ketone 8 was prepared by employing aqueous conditions as described in ref. 15, but it was difficult to obtain it in a pure form. Therefore, the reaction was conducted using a large excess of crude reagent which was first purified as far as possible by chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.