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Photoredox-catalyzed cross-coupling of N-indolylacetic acids with nitrones: Access to indole-N-ethylamines.
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Sep2023, Vol. 128, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- [Display omitted] Herein, we report a photoredox-catalyzed cross-coupling reaction of N -indolylacetic acids with nitrones to generate indole- N -ethylamines under mild reaction conditions. This reaction has the characteristics of simple operation, mild conditions, easy to obtain biologically relevant indole- N -ethylamines structural motifs not readily accessible by other methods. [ABSTRACT FROM AUTHOR]
- Subjects :
- *NITRONES
*ACIDS
*SUZUKI reaction
*ETHYLAMINES
*ISOXAZOLIDINES
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 128
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 171391358
- Full Text :
- https://doi.org/10.1016/j.tetlet.2023.154712