New building blocks, 3,5-dihydro-1H-thieno[3,4-c]pyrrole 2,2-dioxides; preparation and their Diels–Alder reaction with dimethyl acetylenedicarboxylate-Reference-Cited by-同舟云学术

New building blocks, 3,5-dihydro-1H-thieno[3,4-c]pyrrole 2,2-dioxides; preparation and their Diels–Alder reaction with dimethyl acetylenedicarboxylate

Published:1992 Issue:16 Volume: Page:1100-1102
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Ando Kaori,Kankake Mutuo,Suzuki Takayoshi,Takayama Hiroaki

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1992/C3/C39920001100

Reference15 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. 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

4. 1-(p-Chlorophenyl)-3,4-dimethylenepyrrolidine, a new pyrrole isomer

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

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