Novel building block, furan-annelated 3-sulpholene; Diels–Alder reactions of 4,6-dihydrothieno[3,4-c]furan s,s-dioxide
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1990/C3/C39900001687
Reference19 articles.
1. Stereoselective synthesis of (5E)- and (5Z)-vitamin D3 19-alkanoic acids via vitamin D3-sulfur dioxide adducts
2. STEREOSELECTIVE SYNTHESIS OF (E)-, (E,Z)- AND (E,E)-CONJUGATED DIENES VIA ALKYLATION OF 3-SULFOLENES AS KEY STEP
3. Stereoselective synthesis of (E)-, (E,Z)- and (E,E)-conjugated dienes via alkylation of 3-sulfolenes as the key step
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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4. Quantitative preparation of 3,4-di(methylene)tetrahydrothiophene-1,1-dioxide by Zn-induced 1,4-debromination. A valuable 6-C reactive diene in [4+2] cycloadditions with DMAD and [60]fullerene;RSC Advances;2012
5. ChemInform Abstract: Novel Building Block, Furan-Annelated 3-Sulfolene. Diels-Alder Reactions of 4,6-Dihydrothieno(3,4-c)furan S,S-Dioxide.;ChemInform;2010-08-23
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