Stereoselective syntheses of 2-subtituted perhydrofuro[2,3b]furans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Synthesis of a hydroxy dihydrofuran acetal related to azadirachtin: A potent insect antifeedant
2. Synthesis of the furo-pyran moiety of azadirachtin.
3. General synthetic route to γ-butyrolactones via stereoselective radical cyclization by organotin species
4. Synthesis of perhydrofuro [2,3-b] furan compounds and the structure-activity relationships of the antifeeding active compounds.
5. Stereocontrolled synthesis of clerodin homolog
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1. Direct Formylation of Enol Ethers Using Cyanuric Chloride andN,N-Dimethylformamide;Journal of the Chinese Chemical Society;2004-06
2. A model synthetic approach towards the furanacetal component of azadirachtin: a potent insect antifeedant;Arkivoc;2003-01-03
3. An Unprecedented CoII-Tetraphenylporphyrin-Catalyzed Decomposition of Bicyclic Endoperoxides: A New Approach to Substituted Furofuran Systems;European Journal of Organic Chemistry;2000-04
4. Total Synthesis of Dihydroclerodin from (R)-(−)-Carvone;The Journal of Organic Chemistry;1999-11-20
5. 2-methoxy-5-alkoxy-2,5-dihydrofurans: New useful polyfunctionalized C4 building blocks;Tetrahedron Letters;1998-07
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