## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Fused oxacycle synthesis via radical cyclization of β-alkoxyacrylates
✍ Scribed by Eun Lee; Jin Sung Tae; You Hoon Chong; Yong Cheol Park; Mikyung Yun; Sangsoo Kim
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 283 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Radical cyclization of I~-alkoxyacrylates is now firmly established as an effective method in forming 5-or 6-membered oxacycles, l The value of this reaction lies in the fact that only cis-2,5-disubstituted tetrahydrofurans and cis-2,6-disubstituted tetrahydropyrans are obtained when [~-alkoxyacryla
trans-Kumausyne was synthesized from D-(+)-xylose. Radical cycLization reaction of a I]-alkoxyacrylate intermediate proceeded stereoselectively to give a tetrahydrofuranyl product with correct stereochemistry.
Radical cyclization reaction of a bis(~-alkoxyacrylate) intermediate prepared from (-)-diethyl D-tartrate proceeded stereoselectively to give a 2,6-dioxabicyclo[3.3.0]octane product, which was converted into a known intermediate in the synthesis of kumausallene.