Synthesis of lupiwighteone via a para-Claisen–Cope rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Prenylated isoflavonoids—An update
2. Effects of naturally occurring prenylated flavonoids on enzymes metabolizing arachidonic acid: Cyclooxygenases and lipoxygenases11Abbreviations: AA, arachidonic acid; COX, cyclooxygenase; LOX, lipoxygenase; PG, prostaglandin; TX, thromboxane; HETE, hydroxyeicosatetraenoic acid; NDGA, nordihydroguaiaretic acid; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; LPS, lipopolysaccharide; DMEM, Dulbecco’s modified Eagle’s medium; FBS, fetal bovine serum; and PMN, polymorphonuclear leukocyte.
3. Constitution of luteone and parvisoflavones-A and -B and synthesis of their methyl ethers and related isoflavones
4. A study of claisen rearrangements of (1,1-dimethyl-3-prop-2-prop-2-ynyloxy)-[4H]-1-benzopyran-4-one derivatives.
5. HPLC Analysis of White Lupin Isoflavonoids
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