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National Institutes of Health
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A Strategy for the Convergent and Stereoselective Assembly of Polycyclic Molecules.
E. E. Robinson
R. J. Thomson
Journal of the American Chemical Society
Corpus ID: 39913545
The stereoselective oxidative coupling of cyclic ketones via silyl bis-enol ethers followed by ring-closing metathesis is shown…
Terpenes in sponge cell membranes: Cell separation and membrane fractionation studies with the tropical marine spongeAmphimedon sp.
Janice E. Thompson
R. M. Larsen
P. R. Bergquist
Corpus ID: 24082845
The differing sponge and symbiotic microbial cell types in the tropical marine spongeAmphimedon sp. were fractionated according…
A formal total synthesis of the marine diterpenoid diisocyanoadociane.
Corpus ID: 33203585
[Structure: see text] A formal total synthesis of diisocyanoadociane, a marine diterpenoid with potent antimalarial properties…
Biosynthetic pathways to isocyanides and isothiocyanates; precursor incorporation studies on terpene metabolites in the tropical marine sponges Amphimedon terpenensis and Axinyssa n.sp.
Organic & biomolecular chemistry
Corpus ID: 21056152
The biosynthetic origins of the isocyanide and isothiocyanate functional groups in the marine sponge metabolites…
Inhibition of heme detoxification processes underlies the antimalarial activity of terpene isonitrile compounds from marine sponges.
Journal of medicinal chemistry
Corpus ID: 70236
A series of terpene isonitriles, isolated from marine sponges, have previously been shown to exhibit antimalarial activities…
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