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Physics / Proton NMR / Nuclear magnetic resonance spectroscopy / Chemical shift / 1H / Deuterated DMSO / Ethylene / Vitexin / Chemistry / Nuclear magnetic resonance / Spectroscopy


New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum Qun Göthel and Matthias Köck*
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City

Washington / DC / San Salvador / Berlin / Stuttgart / Wilmington / Bremerhaven / /

Company

Wright A. E. / Figure / Smithsonian Institution Press / Shimizu / Creative Commons / /

Country

United States / Bahamas / /

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Facility

University of North Carolina / /

IndustryTerm

Functional / sulfate ester groups / natural products / chemical shifts / terminal methyl groups / chemical investigation / identical sesquiterpene acyclic chain / /

Organization

Alfred-Wegener-Institut / University of North Carolina / Beilstein-Institut / Smithsonian / Helmholtz Center for Infection Research / Universidad Nacional de Colombia / /

Person

Joseph R. Pawlik / Qun Göthel / Florenz Sasse / Faulkner / Matthias Köck / Achim Grube / Woods Hole / CHO OH / Galina Sergeev / Sven Zea / Gesine Schmidt / Georg Thieme Verlag / /

Position

D. J. / Editor / Corresponding author / /

ProvinceOrState

North Carolina / Massachusetts / /

PublishedMedium

the Beilstein Journal / Environmental Chemistry / /

Region

Caribbean / /

Technology

pdf / /

URL

http /

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