Total Synthesis of an Antifouling Marine Furanosesquiterpene

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Issue Date
2017-02-10
Authors
Ungarean, Chad N.
Mason, Jeremy D.
Eyer, Benjamin R.
Duca, Nicholas S.
Mong, Jaimie M.
Murphree, S. Shaun
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Post print of this article will be made available to the public after February 10, 2018.
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Keywords
furans , sulfones , natural products , total synthesis , heterocycles
Abstract
An antifouling sesquiterpene isolated from Sinularia sp. was synthesized from citronellyl acetate in eight steps and 9% overall yield. The furan moiety was constructed using a multifunctional sulfone reagent.
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Chemistry
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Publisher's version can be used on author's personal website only. Post print can be used in a repository after a 12 month embargo.
Citation
Ungarean, C.N., et al. (2017). Total Synthesis of an Antifouling Marine Furanosesquiterpene. Synthesis 49(10): 2177-2181. doi: 10.1055/s-0036-1588711.
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Published article
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Thieme
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