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 reactions
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910001765
Reference11 articles.
1. Novel building block, furan-annelated 3-sulpholene; Diels–Alder reactions of 4,6-dihydrothieno[3,4-c]furan s,s-dioxide
2. Stereoselective synthesis of (E)-, (E,Z)- and (E,E)-conjugated dienes via alkylation of 3-sulfolenes as the key step
3. Stereoselective synthesis of (E)-α-hydroxy-1,3-dienes via the reaction of 2,5-dihydrothiophene S,S-dioxides with carbonyl compounds
4. Novel, readily occurring, and stereoselective synthesis of conjugated trienes using 2-trialkylstannyl-2,5-dihydrothiophene S,S-dioxides
5. New stereoselective method for synthesizing dienes using 3-sulfolenes as masked diene synthons and its application to organic syntheses.
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3. ChemInform Abstract: 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 Reactions.;ChemInform;2010-08-22
4. Synthesis of 2,5-Disubstituted Thienosultines and Their Thermal Reactions with Dienophiles and Nucleophiles;The Journal of Organic Chemistry;2002-12-01
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