z-logo
open-access-imgOpen Access
Total synthesis of (±)-aspercyclide A and its C19 methyl ether
Author(s) -
James L. Carr,
D.A. Offermann,
M.D. Holdom,
Philip Dusart,
Andrew J. P. White,
Andrew J. Beavil,
Robin J. Leatherbarrow,
Stephen D. Lindell,
Brian J. Sutton,
Alan C. Spivey
Publication year - 2009
Publication title -
chemical communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/b923528k
Subject(s) - ether , chemistry , derivative (finance) , stereochemistry , antagonist , medicinal chemistry , organic chemistry , biochemistry , receptor , financial economics , economics
The total syntheses of (+/-)-aspercyclide A (1) and its C19 methyl ether (15a) featuring Heck-Mizoroki macrocyclisation to form the 11-membered (E)-styrenyl biaryl ether lactone core are described.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

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