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Issue 14, 1998
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Using a rigid molecule tricyclodecadienone for the stereospecific synthesis of the chain compound senecivernic acid 1

Abstract

The highly efficient synthesis of a chain compound, senecivernic acid 2, using a rigid molecule, tricyclodecadienone 1, as the starting material via a retro-Diels–Alder reaction as the key step and without using any protecting groups is described in a total of ten steps and in 50% overall yield.

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Article type: Paper
DOI: 10.1039/A802857E
Citation: J. Chem. Soc., Perkin Trans. 1, 1998,0, 2127-2130

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    Using a rigid molecule tricyclodecadienone for the stereospecific synthesis of the chain compound senecivernic acid 1

    Z. Liu, L. Zhao, Y. Xie, Y. Wu, L. Wong and H. Zheng, J. Chem. Soc., Perkin Trans. 1, 1998, 0, 2127
    DOI: 10.1039/A802857E

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