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Information Journal Paper

Title

GREEN AND DIASTEROSELECTIVE OXIDATIVE CYCLIZATION OF BISNAPHTHOLS TO SPIRANS

Pages

  351-358

Abstract

 Hydrogen peroxide/MoO3, as an efficient and clean oxidizing system was used to afford diasteroselective oxidative cyclization of bisnaphthols to SPIRANS in ethanol at 60oC with high yields. Bisnaphthols were prepared by the reaction of a series of aldehydes and 2-naphthol in the presence of a catalytic amount of H3[P(Mo3O10)4].nH2O (HPA) in refluxing dichloromethane.

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  • Cite

    APA: Copy

    ALIZADEH, A., KHODAEI, M.M., & MORADI, K.H.. (2010). GREEN AND DIASTEROSELECTIVE OXIDATIVE CYCLIZATION OF BISNAPHTHOLS TO SPIRANS. JOURNAL OF THE IRANIAN CHEMICAL SOCIETY(JICS), 7(2), 351-358. SID. https://sid.ir/paper/282375/en

    Vancouver: Copy

    ALIZADEH A., KHODAEI M.M., MORADI K.H.. GREEN AND DIASTEROSELECTIVE OXIDATIVE CYCLIZATION OF BISNAPHTHOLS TO SPIRANS. JOURNAL OF THE IRANIAN CHEMICAL SOCIETY(JICS)[Internet]. 2010;7(2):351-358. Available from: https://sid.ir/paper/282375/en

    IEEE: Copy

    A. ALIZADEH, M.M. KHODAEI, and K.H. MORADI, “GREEN AND DIASTEROSELECTIVE OXIDATIVE CYCLIZATION OF BISNAPHTHOLS TO SPIRANS,” JOURNAL OF THE IRANIAN CHEMICAL SOCIETY(JICS), vol. 7, no. 2, pp. 351–358, 2010, [Online]. Available: https://sid.ir/paper/282375/en

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