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Synthesis of the EFG Framework of Tamulamides A and B
Name
nihms-1051446.pdf
Description
Accepted version
Size
643.76 KB
Format
Adobe PDF
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fb1b7ba45fc967180d2f48c925077acd
Author(s) •
Kelley, Elizabeth H
Jamison, Timothy F
Journal
Organic Letters
Publisher
American Chemical Society (ACS)
Version
Author's final manuscript
Abstract
© 2019 American Chemical Society. Synthesis of the fused polycyclic ether motif comprising the EFG rings of the marine ladder polyethers tamulamides A and B has been achieved via two different etherification strategies. Ultimately, a reductive etherification approach proved most successful due to tolerance of the G ring substitution and provided the EFG 6,7,6 ring system in 58% yield.
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
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DOI of Published Version
10.1021/ACS.ORGLETT.9B03015