Alkylation of 4H,6H-thieno[3,4-c]furan 5,5-dioxide and its use as a 3,4-dimethylenefuran synthon in intramolecular Diels–Alder reaction
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930002263
Reference31 articles.
1. Novel formation of dienes with greater steric congestion resulting from the Diels–Alder reaction–desulfonylation sequence of 4-acyl-4H,6H-thieno[3,4-c]furan 5,5-dioxides
2. Diels-Alder reaction of 4,6-dihydrothieno(3,4-c)furan-5,5-dioxide with quinones: Stereoselective synthesis of quinone-annelated 2,3-bis(methylene)-7-oxabicyclo(2.2.1)heptanes.
3. Novel building block, furan-annelated 3-sulpholene; Diels–Alder reactions of 4,6-dihydrothieno[3,4-c]furan s,s-dioxide
4. Stereoselective synthesis of (E)-, (E,Z)- and (E,E)-conjugated dienes via alkylation of 3-sulfolenes as the key step
5. Stereoselective synthesis of (E)-α-hydroxy-1,3-dienes via the reaction of 2,5-dihydrothiophene S,S-dioxides with carbonyl compounds
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