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Regioselective Reaction of 2-Indolylmethanols with Enamides.
- Source :
-
Molecules . Apr2023, Vol. 28 Issue 8, p3341. 16p. - Publication Year :
- 2023
-
Abstract
- A highly regioselective reaction of 2-indolylmethanols with enamides has been developed at room temperature by using AlCl3 as a catalyst. A wide range of hybrids (40 examples) of indoles and enamides were obtained in moderate to good yields (up to 98% yield). This transformation represents the efficient way to introduce biologically important indoles and enamides skeleton into structurally complex hybrids. [ABSTRACT FROM AUTHOR]
- Subjects :
- *REGIOSELECTIVITY (Chemistry)
*INDOLE compounds
*SKELETON
Subjects
Details
- Language :
- English
- ISSN :
- 14203049
- Volume :
- 28
- Issue :
- 8
- Database :
- Academic Search Index
- Journal :
- Molecules
- Publication Type :
- Academic Journal
- Accession number :
- 163455598
- Full Text :
- https://doi.org/10.3390/molecules28083341