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Mary J Garson

Showing results (11-20 of 69) with videos related to

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Journal of Natural Products|November 13, 2018
Elucidation of Relative and Absolute Configurations of Highly Rearranged Diterpenoids and Evidence for a Putative Biosynthetic Intermediate from the Australian Nudibranch Goniobranchus geometricusLouise C Forster, Gregory K Pierens, Mary J Garson
Molecules (Basel, Switzerland)|March 25, 2017
Revision of the Structure of Acremine P from a Marine-Derived Strain of Acremonium persicinumMary J Garson, Warren Hehre, Gregory K Pierens, et al.
Journal of Natural Products|October 23, 2004
New indole alkaloids from the roots of Ochrosia acuminataAngela A Salim, Mary J Garson, David J Craik
Natural Product Communications|July 23, 2015
Oxygenated Terpenes from Indo-Pacific Nudibranchs: Scalarane Sesterterpenes from Glossodoris hikuerensis and 12-Acetoxy Dendrillolide A from Goniobranchus albonaresI Wayan Mudianta, Andrew M White, Mary J Garson
Journal of Natural Products|September 25, 2004
New indole alkaloids from the bark of Alstonia scholarisAngela A Salim, Mary J Garson, David J Craik
Environmental Microbiology|April 9, 2005
Marine actinomycetes related to the "Salinospora" group from the Great Barrier Reef sponge Pseudoceratina clavataTae Kyung Kim, Mary J Garson, John A Fuerst
Microbial Ecology|October 11, 2005
Culturable bacterial symbionts isolated from two distinct sponge species (Pseudoceratina clavata and Rhabdastrella globostellata) from the Great Barrier Reef display similar phylogenetic diversityFeras F Lafi, Mary J Garson, John A Fuerst
Journal of Natural Products|January 24, 2004
New alkaloids from Pandanus amaryllifoliusAngela A Salim, Mary J Garson, David J Craik
Acta Crystallographica. Section C, Crystal Structure Communications|April 1, 2010
The 293 K structure of tetradehydrohaliclonacyclamine AI Wayan Mudianta, Mary J Garson, Paul V Bernhardt
Journal of Natural Products|November 21, 2012
Confirmation of the configuration of 10-isothiocyanato-4-cadinene diastereomers through synthesisKeisuke Nishikawa, Taiki Umezawa, Mary J Garson, et al.
Pageof 7

Showing results (11-20 of 69) with videos related to

Sort By:
Pageof 7
Journal of Natural Products|November 13, 2018
Elucidation of Relative and Absolute Configurations of Highly Rearranged Diterpenoids and Evidence for a Putative Biosynthetic Intermediate from the Australian Nudibranch Goniobranchus geometricusLouise C Forster, Gregory K Pierens, Mary J Garson
Molecules (Basel, Switzerland)|March 25, 2017
Revision of the Structure of Acremine P from a Marine-Derived Strain of Acremonium persicinumMary J Garson, Warren Hehre, Gregory K Pierens, et al.
Journal of Natural Products|October 23, 2004
New indole alkaloids from the roots of Ochrosia acuminataAngela A Salim, Mary J Garson, David J Craik
Natural Product Communications|July 23, 2015
Oxygenated Terpenes from Indo-Pacific Nudibranchs: Scalarane Sesterterpenes from Glossodoris hikuerensis and 12-Acetoxy Dendrillolide A from Goniobranchus albonaresI Wayan Mudianta, Andrew M White, Mary J Garson
Journal of Natural Products|September 25, 2004
New indole alkaloids from the bark of Alstonia scholarisAngela A Salim, Mary J Garson, David J Craik
Environmental Microbiology|April 9, 2005
Marine actinomycetes related to the "Salinospora" group from the Great Barrier Reef sponge Pseudoceratina clavataTae Kyung Kim, Mary J Garson, John A Fuerst
Microbial Ecology|October 11, 2005
Culturable bacterial symbionts isolated from two distinct sponge species (Pseudoceratina clavata and Rhabdastrella globostellata) from the Great Barrier Reef display similar phylogenetic diversityFeras F Lafi, Mary J Garson, John A Fuerst
Journal of Natural Products|January 24, 2004
New alkaloids from Pandanus amaryllifoliusAngela A Salim, Mary J Garson, David J Craik
Acta Crystallographica. Section C, Crystal Structure Communications|April 1, 2010
The 293 K structure of tetradehydrohaliclonacyclamine AI Wayan Mudianta, Mary J Garson, Paul V Bernhardt
Journal of Natural Products|November 21, 2012
Confirmation of the configuration of 10-isothiocyanato-4-cadinene diastereomers through synthesisKeisuke Nishikawa, Taiki Umezawa, Mary J Garson, et al.
Pageof 7