β-Sulfonylnitroolefins as very reactive alkyne-equivalents in Diels-Alder reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Regioselective construction of cyclohexene derivatives by Diels–Alder reactions of nitro-olefins with dienes and subsequent denitration with tributyltin hydride
2. Use of phenyl vinyl sulfoxide as an acetylene equivalent in Diels-Alder cycloadditions
3. An ethylene and terminal olefin equivalent in [4 + 2] .pi. cycloadditions. General synthetic application of phenyl vinyl sulfone to the construction of functionalized six-membered rings
4. Dienophilic reactivity of Trans-1,2-bis(phenylsulphonyl)ethylene: A valid alternative to maleic anhydride
5. cis-1,2-Bis(phenylsulphonyl)ethylene: a novel, convenient acetylene synthon in Diels–Alder reactions
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