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Total Synthesis of Tedarene A.

Authors :
Maurent K
Vanucci-BacquƩ C
Saffon-Merceron N
Baltas M
Bedos-Belval F
Source :
Journal of natural products [J Nat Prod] 2017 May 26; Vol. 80 (5), pp. 1623-1630. Date of Electronic Publication: 2017 May 02.
Publication Year :
2017

Abstract

Tedarene A is a macrocyclic diaryl ether heptanoid isolated from the marine sponge Tedania ignis showing an inhibitory effect against nitric oxide production. The first total synthesis of tedarene A was achieved starting from the commercially available 3-(4-methoxyphenyl)propan-1-ol in nine steps and 15.3% overall yield. The synthetic sequence featured an E,Z-dienic bond introduction and a macrocyclization under Ullman conditions. During the synthesis, the E,E-isomer of tedarene A was also obtained and fully characterized.

Details

Language :
English
ISSN :
1520-6025
Volume :
80
Issue :
5
Database :
MEDLINE
Journal :
Journal of natural products
Publication Type :
Academic Journal
Accession number :
28463511
Full Text :
https://doi.org/10.1021/acs.jnatprod.7b00199