6533b86dfe1ef96bd12c9d6b
RESEARCH PRODUCT
Pyrrole Studies. Part 40.1Synthesis of 2- and 3-Substitoted 1-Methylindoles from Vinylpyrroles.
Eugenia Gonzalez-rosendeElena Zaballos-garcíaJosé Sepúlveda-arquesR. A. Jonessubject
chemistry.chemical_compoundChemistryYield (chemistry)Organic ChemistryOrganic chemistryDehydrogenationPyrroledescription
Abstract 4-Substituted-2-vinylpyrroles are more reactive than 2-substituted-4-vinylpyrroles in their reaction with DMAD to yield, respectively, 6/7- and 4,5-dihydroindoles, which are readily dehydrogenated to give indoles possessing electron-withdrawing substitutents at the 3- and 2-positions.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1988-10-01 | Synthetic Communications |