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Information Journal Paper

Title

A SHORT METHOD FOR THE SYNTHESIS OF A (ALPHA)-TOCOPHEROL SIDE CHAIN

Pages

  1-10

Abstract

 The enzymatic hydrolysis of meso-1, 7-diacetoxy-2,6-dimethylheptane 5, prepared from 2,6-dimethylhepta-1,6-diene 6, gave the (2S,6R)-7-acetoxy-2,6-dimethyl-1-heptanol 1, which was transformed to the (2R,6R)-2,6,10-trimethyl-1-undecanol 7. In this manner, the C14 side chain of a-Tocopherol was synthesized from 2,6-dimethylhepta-1,6-diene 6 in only 5 steps.

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  • Cite

    APA: Copy

    MOHAMMADI ZIARANI, GH., CHENEVERT, R., & BADIEI, A.R.. (2007). A SHORT METHOD FOR THE SYNTHESIS OF A (ALPHA)-TOCOPHEROL SIDE CHAIN . IRANIAN JOURNAL OF CHEMISTRY AND CHEMICAL ENGINEERING (IJCCE), 26(4), 1-10. SID. https://sid.ir/paper/548266/en

    Vancouver: Copy

    MOHAMMADI ZIARANI GH., CHENEVERT R., BADIEI A.R.. A SHORT METHOD FOR THE SYNTHESIS OF A (ALPHA)-TOCOPHEROL SIDE CHAIN . IRANIAN JOURNAL OF CHEMISTRY AND CHEMICAL ENGINEERING (IJCCE)[Internet]. 2007;26(4):1-10. Available from: https://sid.ir/paper/548266/en

    IEEE: Copy

    GH. MOHAMMADI ZIARANI, R. CHENEVERT, and A.R. BADIEI, “A SHORT METHOD FOR THE SYNTHESIS OF A (ALPHA)-TOCOPHEROL SIDE CHAIN ,” IRANIAN JOURNAL OF CHEMISTRY AND CHEMICAL ENGINEERING (IJCCE), vol. 26, no. 4, pp. 1–10, 2007, [Online]. Available: https://sid.ir/paper/548266/en

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