Convergent total synthesis of (±) myricanol, a cyclic natural diarylheptanoid
Author:
Affiliation:
1. Department of Science
2. University of Basilicata
3. 85100 Potenza
4. Italy
5. Laboratoire d'Innovation Moléculaire et Applications (UMR CNRS 7042)
6. Université de Strasbourg/Université de haute Alsace
7. ECPM
8. Strasbourg
9. France
Abstract
Third total synthesis of the meta, meta-bridged diarylheptanoid: myricanol with remarkable anti-tau properties.
Funder
Centre National de la Recherche Scientifique
Ministero dell’Istruzione, dell’Università e della Ricerca
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB02052C
Reference41 articles.
1. Constitution and absolute configuration of meta,meta-bridged, strained biphenyls from Myrica nagi; X-ray analysis of 16-bromomyricanol
2. Tannins and other phenolics from Myrica esculenta bark
3. Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene
4. Anti-androgenic Activity of Myricae Cortex. Isolation of Active Constituents from Bark of Myrica rubra.
5. Bioactive Constituents of Chinese Natural Medicines. VII. Inhibitors of Degranulation in RBL-2H3 Cells and Absolute Stereostructures of Three New Diarylheptanoid Glycosides from the Bark of Myrica rubra.
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