Article
Synthesis of the C1–C23 Fragment of the Archazolids and Evidence for V-ATPase but not COX Inhibitory Activity
Synlett
(2017)
Abstract
A convergent synthesis of a C₁–C₂₃ fragment of the archazolids has been completed based on a high-yielding Stille coupling to construct the substituted Z,Z,E-conjugated triene. After removal of the protecting groups, the resulting tetrol exhibited evidence for inhibition of the vacuolar-type ATPase (V-ATPase) but not cyclooxygenase (COX) inhibitory activity.
Keywords
- archazolid,
- natural product,
- Stille reaction,
- V-ATPase,
- cyclooxygenase,
- total synthesis
Disciplines
Publication Date
February 8, 2017
DOI
10.1055/s-0036-1588413
Publisher Statement
Published by Thieme
Citation Information
Gregory W. O’Neil, Alexander M. Craig, John R. Williams, Jeffrey C. Young, et al.. "Synthesis of the C1–C23 Fragment of the Archazolids and Evidence for V-ATPase but not COX Inhibitory Activity" Synlett Vol. 28 Iss. 9 (2017) p. 1101 - 1105 Available at: http://works.bepress.com/pc_spiegel/17/