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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Article Doi

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:

Authors:

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

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

Products guided by the article

R&D Labs maybe for 104344-07-2

Relevant to this article

Syntheses, structures, and magnetic properties of heterobimetallic complexes based on tetracyanometallic building blocks

Discovery of N -[(4 R)-6-(4-Chlorophenyl)-7-(2,4-dichlorophenyl)-2,2- dimethyl-3,4-dihydro-2 H -pyrano[2,3- b ]pyridin-4-yl]-5-methyl-1 H -pyrazole-3-carboxamide (MK-5596) as a novel cannabinoid-1 receptor (CB1R) inverse agonist for the treatment of obesity

Discovery of Orally Bioavailable Chromone Derivatives as Potent and Selective BRD4 Inhibitors: Scaffold Hopping, Optimization, and Pharmacological Evaluation

Formal total synthesis of (-)-haouamine A

Synthesis of 10-(4-methyl-1-piperazinyl)thieno[3,2-b][1,5]benzothiazepines

Acid-catalysed hydrolysis of trityl derivatives in strongly acidic aqueous media