Stereospecific formation of a substituted trans-decaline as an intermediate for the synthesis of clerodane insect antifeedants
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. DIELS–ALDER REACTION OF SUBSTITUTED MALEIC ANHYDRIDES WITH 1-VINYLCYCLOHEXENE AN APPROACH TO THE SYNTHESES OF CLERODANE DITERPENES
2. Diels-alder reactions of substituted maleic anhydrides with 1-vinylcoclohexane
3. Insect antifeedants. 1. Diels-Alders approach to the synthesis of ajugarin I
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1. The Mechanism of RuO4-Mediated Oxidations of Ethers: Isotope Effects, Solvent Effects and Substituent Effects.;Acta Chemica Scandinavica;1995
2. Preparation of α,β-Unsaturated Carbonyl Compounds and Nitriles by Selenoxide Elimination;Organic Reactions;1993-09-29
3. Synthesis of tricyclo[6.2.2.01,6]Dodeca-6,9-dienes. An approach to clerodane diterpenes.;Tetrahedron Letters;1990-01
4. Synthesis of Clerodane Diterpenes via Lewis Acid Catalyzed Cycloadditions;Selectivities in Lewis Acid Promoted Reactions;1989
5. A general method for the synthesis of clerodane diterpenoids. Stereospecific total syntheses of (±)-15, 16-epoxy--cleroda-3, 13(16), 14-triene and (±)-maingayic acid;Tetrahedron;1988-01
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