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Chemical Record (New York, N.Y.)
|
December 4, 2021
Synthesis of Pyrrolidine- and γ-Lactam-Containing Natural Products and Related Compounds from Pyrrole Scaffolds
Wesley J Olivier, Jason A Smith, Alex C Bissember
Organic & Biomolecular Chemistry
|
February 2, 2018
Methods for the synthesis of annulated pyrroles via cyclisation strategies
Wesley J Olivier, Jason A Smith, Alex C Bissember
Organic Letters
|
April 13, 2021
Unified Total Syntheses of (±)-Sessilifoliamides B, C, and D
Wesley J Olivier, Alex C Bissember, Jason A Smith
Organic Letters
|
July 28, 2022
Structural Revision of Parvistemoamide: Informing Biosynthetic Proposals of <i>Stemona</i> Alkaloids
Wesley J Olivier, Jason A Smith, Alex C Bissember
Angewandte Chemie (International Ed. in English)
|
March 17, 2026
Near-Infrared-Light-Driven Photochemistry and Photocatalysis: Mechanisms, Recent Applications, and Opportunities in Organic Synthesis and Biology
Santosh K Pagire, Wesley J Olivier, Debabrata Maiti, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 24, 2021
Revised Structures of Dehydrostenines A and B: Total Syntheses of (±)-Dehydrostenine A and Structure Assigned to Dehydrostenine B
Wesley J Olivier, Nigel T Lucas, Alex C Bissember, et al.
Journal of Natural Products
|
December 24, 2016
ent-Labdane Diterpenoids from Dodonaea viscosa
Wesley J Olivier, Nathan L Kilah, James Horne, et al.
Fitoterapia
|
October 17, 2017
Extraction of carboxylic acid-containing diterpenoids from Dodonaea viscosa via pressurised hot water extraction
Bianca J Deans, Wesley J Olivier, David Girbino, et al.
Natural Product Reports
|
October 11, 2022
Strategies for the synthesis of <i>Stemona</i> alkaloids: an update
Wesley J Olivier, Jackson S Henneveld, Jason A Smith, et al.
Organic Letters
|
October 22, 2021
Exploring Cyclization Strategies to Access <i>Stemona</i> Alkaloids: Subtle Effects Influencing Reactivity in Intramolecular Michael Additions
Wesley J Olivier, Rasool BabaAhmadi, Nigel T Lucas, et al.
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Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Chemical Record (New York, N.Y.)
|
December 4, 2021
Synthesis of Pyrrolidine- and γ-Lactam-Containing Natural Products and Related Compounds from Pyrrole Scaffolds
Wesley J Olivier, Jason A Smith, Alex C Bissember
Organic & Biomolecular Chemistry
|
February 2, 2018
Methods for the synthesis of annulated pyrroles via cyclisation strategies
Wesley J Olivier, Jason A Smith, Alex C Bissember
Organic Letters
|
April 13, 2021
Unified Total Syntheses of (±)-Sessilifoliamides B, C, and D
Wesley J Olivier, Alex C Bissember, Jason A Smith
Organic Letters
|
July 28, 2022
Structural Revision of Parvistemoamide: Informing Biosynthetic Proposals of <i>Stemona</i> Alkaloids
Wesley J Olivier, Jason A Smith, Alex C Bissember
Angewandte Chemie (International Ed. in English)
|
March 17, 2026
Near-Infrared-Light-Driven Photochemistry and Photocatalysis: Mechanisms, Recent Applications, and Opportunities in Organic Synthesis and Biology
Santosh K Pagire, Wesley J Olivier, Debabrata Maiti, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 24, 2021
Revised Structures of Dehydrostenines A and B: Total Syntheses of (±)-Dehydrostenine A and Structure Assigned to Dehydrostenine B
Wesley J Olivier, Nigel T Lucas, Alex C Bissember, et al.
Journal of Natural Products
|
December 24, 2016
ent-Labdane Diterpenoids from Dodonaea viscosa
Wesley J Olivier, Nathan L Kilah, James Horne, et al.
Fitoterapia
|
October 17, 2017
Extraction of carboxylic acid-containing diterpenoids from Dodonaea viscosa via pressurised hot water extraction
Bianca J Deans, Wesley J Olivier, David Girbino, et al.
Natural Product Reports
|
October 11, 2022
Strategies for the synthesis of <i>Stemona</i> alkaloids: an update
Wesley J Olivier, Jackson S Henneveld, Jason A Smith, et al.
Organic Letters
|
October 22, 2021
Exploring Cyclization Strategies to Access <i>Stemona</i> Alkaloids: Subtle Effects Influencing Reactivity in Intramolecular Michael Additions
Wesley J Olivier, Rasool BabaAhmadi, Nigel T Lucas, et al.
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