z-logo
Premium
Total Synthesis of Kaempferol and Methylated Kaempferol Derivatives
Author(s) -
Lee YeanJang,
Wu TsaoDong
Publication year - 2001
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.200100033
Subject(s) - chemistry , kaempferol , hydroxylation , natural product , total synthesis , organic chemistry , oxidative phosphorylation , stereochemistry , quercetin , biochemistry , antioxidant , enzyme
Kaempferol ( 1 ), a natural product from various plants, was synthesized in which the longest linear sequence is only seven steps in over all yields of 47% from commercially avail able 1,3,5‐trimethoxybenzene (10). The methylated kaempferols 2–5 were also pre pared by use of this concise synthetic methodology. The key transformations in this synthesis involved the I 2 oxidative‐promoting‐cyclization and DDO oxidative hydroxylation. Several strategies to achieve 1 are provided.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom