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-Reference-Cited by-同舟云学术

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

Published:1992 Issue:12 Volume: Page:870-873
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Ando Kaori,Hatano Chiharu,Akadegawa Naoki,Shigihara Atsushi,Takayama Hiroaki

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1992/C3/C39920000870

Reference13 articles.

1. 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

2. Novel building block, furan-annelated 3-sulpholene; Diels–Alder reactions of 4,6-dihydrothieno[3,4-c]furan s,s-dioxide

3. New stereoselective method for synthesizing dienes using 3-sulfolenes as masked diene synthons and its application to organic syntheses.

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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