Back to Search
Start Over
Synthesis of 8-aryl-3,5,7,3′,4′-penta-O-methylcyanidins from the corresponding quercetin derivatives by reduction with LiAlH4.
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Mar2017, Vol. 58 Issue 10, p919-922. 4p. - Publication Year :
- 2017
-
Abstract
- Synthesis of 8-aryl-3,5,7,3′,4′- penta - O -methylcyanidins from the corresponding quercetin derivatives by reduction with LiAlH 4 is reported. Regioselective iodination at the 8-position of penta - O -methylquercetin followed by a Suzuki-Miyaura reaction gave the 8-arylated quercetin derivatives. By the reduction of 8-arylated quercetins using 4 equiv. of LiAlH 4 at room temperature for 30 min, the corresponding anthocyanidins were obtained with a good yield. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 58
- Issue :
- 10
- 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 :
- 121242042
- Full Text :
- https://doi.org/10.1016/j.tetlet.2017.01.065