Total Synthesis of Altissimacoumarin D, a Small Molecule Sirtuin1 Activator
AUTOR(ES)
Silva, Anna C., Benelkebir, Hanae, Lopes, Rosangela S. C., Lopes, Claudio C., Ganesan, A.
FONTE
J. Braz. Chem. Soc.
DATA DE PUBLICAÇÃO
2018-05
RESUMO
The total synthesis of the plant natural product altissimacoumarin D was achieved by the Mitsunobu alkylation of isofraxidin by geraniol. Isofraxidin was prepared from 2,4-dihydroxybenzaldehyde in five steps. The key reaction was the Knoevenagel condensation of an ortho-hydroxybenzaldehyde with Meldrum's acid under neutral conditions in water and one-pot acid catalyzed cyclization to the coumarin.
Documentos Relacionados
- Identification of small-molecule antagonists that inhibit an activator:coactivator interaction
- Synthesis of the active metabolite of vitamin D, 1,25(OH)2D3, by synovial fluid macrophages in arthritic diseases.
- A formal total synthesis of deoxynojirimycin from D-glucitol
- The noncalcemic analogue of vitamin D, 22-oxacalcitriol, suppresses parathyroid hormone synthesis and secretion.
- Vitamina D, polimorfismos do gene VDR e neurofibromatose 1