Total Synthesis of an Antifouling Marine Furanosesquiterpene

Chad N. Ungarean; Jeremy D. Mason; Benjamin R. Eyer; Nicholas S. Duca; Jaimie M. Mong; S. Shaun Murphree

doi:10.1055/s-0036-1588711

Total Synthesis of an Antifouling Marine Furanosesquiterpene

Chad N. Ungarean
, Jeremy D. Mason
, Benjamin R. Eyer
, Nicholas S. Duca
, Jaimie M. Mong
, S. Shaun Murphree

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

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.

Original language	English (US)
Article number	ss-2016-z0777-op
Pages (from-to)	2177-2181
Number of pages	5
Journal	Synthesis (Germany)
Volume	49
Issue number	10
DOIs	https://doi.org/10.1055/s-0036-1588711
State	Published - May 17 2017

All Science Journal Classification (ASJC) codes

Catalysis
Organic Chemistry

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1055/s-0036-1588711

Cite this

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title = "Total Synthesis of an Antifouling Marine Furanosesquiterpene",

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.",

author = "Ungarean, \{Chad N.\} and Mason, \{Jeremy D.\} and Eyer, \{Benjamin R.\} and Duca, \{Nicholas S.\} and Mong, \{Jaimie M.\} and Murphree, \{S. Shaun\}",

note = "Publisher Copyright: {\textcopyright} Georg Thieme VerlagStuttgart · New York.",

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doi = "10.1055/s-0036-1588711",

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AU - Ungarean, Chad N.

AU - Mason, Jeremy D.

AU - Eyer, Benjamin R.

AU - Duca, Nicholas S.

AU - Mong, Jaimie M.

AU - Murphree, S. Shaun

PY - 2017/5/17

Y1 - 2017/5/17

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/85012134617

UR - https://www.scopus.com/pages/publications/85012134617#tab=citedBy

U2 - 10.1055/s-0036-1588711

DO - 10.1055/s-0036-1588711

M3 - Article

AN - SCOPUS:85012134617

SN - 0039-7881

VL - 49

SP - 2177

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JO - Synthesis (Germany)

JF - Synthesis (Germany)

IS - 10

M1 - ss-2016-z0777-op

ER -

Total Synthesis of an Antifouling Marine Furanosesquiterpene

Abstract

All Science Journal Classification (ASJC) codes

UN SDGs

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