Mary Garson, PhD

Affiliations: 
University of Queensland, Saint Lucia, Queensland, Australia 
Area:
natural product chemistry
Website:
http://researchers.uq.edu.au/researcher/102
Google:
"Mary Garson"
Bio:

http://staff.scmb.uq.edu.au/staff/mary-garson

Mean distance: 9.21
 
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Publications

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Cheney KL, White A, Mudianta IW, et al. (2016) Choose Your Weaponry: Selective Storage of a Single Toxic Compound, Latrunculin A, by Closely Related Nudibranch Molluscs. Plos One. 11: e0145134
Hirayama Y, Katavic PL, White AM, et al. (2016) New Cytotoxic Norditerpenes from the Australian Nudibranchs Goniobranchus Splendidus and Goniobranchus Daphne Australian Journal of Chemistry. 69: 136-144
Alghazwi M, Kan YQ, Zhang W, et al. (2016) Neuroprotective activities of natural products from marine macroalgae during 1999–2015 Journal of Applied Phycology. 1-18
Rudiyansyaha, Panthong K, Garson MJ. (2015) Chemistry and Pharmacognosy of the Genus Durio. Natural Product Communications. 10: 1853-60
White AM, Pierens GK, Forster LC, et al. (2015) Rearranged Diterpenes and Norditerpenes from Three Australian Goniobranchus Mollusks. Journal of Natural Products
Mándi A, Mudianta IW, Kurtán T, et al. (2015) Absolute Configuration and Conformational Study of Psammaplysins A and B from the Balinese Marine Sponge Aplysinella strongylata. Journal of Natural Products. 78: 2051-6
White AM, Pierens GK, Skinner-Adams T, et al. (2015) Antimalarial Isocyano and Isothiocyanato Sesquiterpenes with Tri- and Bicyclic Skeletons from the Nudibranch Phyllidia ocellata. Journal of Natural Products
Yong KWL, Mudianta IW, Cheney KL, et al. (2015) Isolation of norsesterterpenes and spongian diterpenes from dorisprismatica (= Glossodoris) atromarginata Journal of Natural Products. 78: 421-430
Bolte B, Basutto JA, Bryan CS, et al. (2015) Modular total syntheses of the marine-derived resorcylic Acid lactones cochliomycins a and B using a late-stage nozaki-hiyama-kishi macrocyclization reaction. The Journal of Organic Chemistry. 80: 460-70
Suciati, Garson MJ. (2014) Isolation of the tetrapeptide apicidins G, H and I from the fungus Fusarium semitectum Natural Product Communications. 9: 233-236
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