Synthesis and insect antifeedant activity of 2-substituted 2,3- dihydrofuran-3-ols and butenolides (Part II)

DOI: 10.1016/S0040-4020(99)00612-2

Source and publish data:

Tetrahedron p. 11077 - 11094 (1999)

Update date:2022-08-02

Topics:

Authors:

Klein Gebbinck, Edwin A.

Stork, Gerrit A.

Jansen, Ben J. M.

De Groot, Aede

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Article abstract of DOI:10.1016/S0040-4020(99)00612-2

The introduction of a hydroxy group at C-13 of the clerodane skeleton is proposed as a strategy to potentially increase the antifeedant activity of simple analogs. This idea is applied to clerodane analogs with furan or butenolide type sidechains and ther

Full text of DOI:10.1016/S0040-4020(99)00612-2

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