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An easy approach to dihydrofurans by one-step cyclisation of 2-alkenyl substituted 1,3-dicarbonyl compounds

โœ Scribed by Roberto Antonioletti; Giuliana Righi; Lia Oliveri; Paolo Bovicelli


Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
59 KB
Volume
41
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


Dihydrofuran derivatives were obtained by a simple one-step procedure involving an easy epoxidation of 2-alkenyl-1,3-dicarbonyl compounds by dimethyldioxirane prepared in situ and a subsequent cyclisation under the same basic reaction conditions.


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A convenient approach to furan derivativ
โœ R. Antonioletti; F. Bonadies; A. Scettri ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 202 KB

## 5-iodoalkyl-4,5-dihydrofurans & 5-alXylldene-4,5-dihydrofurans 3 and 2,3,5\_trisubstituted furans 4 are obtained through a simple sequence, involving, in the Key-step, a regio-and stereoselective iodoenoletherification of P-alXeny1 substituted i,3-dfcarbonyl compounds i.