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Synthesis of 8-aryl-3,5,7,3′,4′-penta-O-methylcyanidins from the corresponding quercetin derivatives by reduction with LiAlH4.

Authors :
Kimura, Yuki
Oyama, Kin-ichi
Kondo, Tadao
Yoshida, Kumi
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