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Stephen P Marsden

Showing results (51-60 of 62) with videos related to

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Chemical Communications (Cambridge, England)|May 3, 2023
Modular synthesis of bicyclic twisted amides and anilinesAlexandra Hindle, Krzysztof Baj, Jonathan A Iggo, et al.
Organic Letters|April 10, 2009
Synthesis of benzazoles by hydrogen-transfer catalysisA John Blacker, Mohamed M Farah, Michael I Hall, et al.
Chemical Communications (Cambridge, England)|May 6, 2016
A divergent synthetic approach to diverse molecular scaffolds: assessment of lead-likeness using LLAMA, an open-access computational toolIgnacio Colomer, Christopher J Empson, Philip Craven, et al.
Chemical Communications (Cambridge, England)|December 19, 2022
Synthesis of spirocyclic 1,2-diamines by dearomatising intramolecular diamination of phenolsAnthony Aimon, Mark J Dow, Abigail R Hanby, et al.
Beilstein Journal of Organic Chemistry|September 25, 2025
Rhodium-catalysed connective synthesis of diverse reactive probes bearing S(VI) electrophilic warheadsScott Rice, Julian Chesti, William R T Mosedale, et al.
Bioorganic & Medicinal Chemistry|March 6, 2015
Aminomethylhydroxylation of alkenes: Exploitation in the synthesis of scaffolds for small molecule librariesIgnacio Colomer, Ololade Adeniji, George M Burslem, et al.
Bioorganic & Medicinal Chemistry|January 21, 2015
Design, synthesis and decoration of molecular scaffolds for exploitation in the production of alkaloid-like librariesPhilip Craven, Anthony Aimon, Mark Dow, et al.
Communications Chemistry|May 16, 2026
Algorithm-driven, phenotype-directed bioactive molecular discoveryAmalia-Sofia Piticari, Samuel D Griggs, Laura Crawford, et al.
Organic & Biomolecular Chemistry|November 20, 2014
A unified lead-oriented synthesis of over fifty molecular scaffoldsRichard G Doveston, Paolo Tosatti, Mark Dow, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 7, 2017
Synthesis and Demonstration of the Biological Relevance of sp<sup>3</sup> -rich Scaffolds Distantly Related to Natural Product FrameworksDaniel J Foley, Philip G E Craven, Patrick M Collins, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Chemical Communications (Cambridge, England)|May 3, 2023
Modular synthesis of bicyclic twisted amides and anilinesAlexandra Hindle, Krzysztof Baj, Jonathan A Iggo, et al.
Organic Letters|April 10, 2009
Synthesis of benzazoles by hydrogen-transfer catalysisA John Blacker, Mohamed M Farah, Michael I Hall, et al.
Chemical Communications (Cambridge, England)|May 6, 2016
A divergent synthetic approach to diverse molecular scaffolds: assessment of lead-likeness using LLAMA, an open-access computational toolIgnacio Colomer, Christopher J Empson, Philip Craven, et al.
Chemical Communications (Cambridge, England)|December 19, 2022
Synthesis of spirocyclic 1,2-diamines by dearomatising intramolecular diamination of phenolsAnthony Aimon, Mark J Dow, Abigail R Hanby, et al.
Beilstein Journal of Organic Chemistry|September 25, 2025
Rhodium-catalysed connective synthesis of diverse reactive probes bearing S(VI) electrophilic warheadsScott Rice, Julian Chesti, William R T Mosedale, et al.
Bioorganic & Medicinal Chemistry|March 6, 2015
Aminomethylhydroxylation of alkenes: Exploitation in the synthesis of scaffolds for small molecule librariesIgnacio Colomer, Ololade Adeniji, George M Burslem, et al.
Bioorganic & Medicinal Chemistry|January 21, 2015
Design, synthesis and decoration of molecular scaffolds for exploitation in the production of alkaloid-like librariesPhilip Craven, Anthony Aimon, Mark Dow, et al.
Communications Chemistry|May 16, 2026
Algorithm-driven, phenotype-directed bioactive molecular discoveryAmalia-Sofia Piticari, Samuel D Griggs, Laura Crawford, et al.
Organic & Biomolecular Chemistry|November 20, 2014
A unified lead-oriented synthesis of over fifty molecular scaffoldsRichard G Doveston, Paolo Tosatti, Mark Dow, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 7, 2017
Synthesis and Demonstration of the Biological Relevance of sp<sup>3</sup> -rich Scaffolds Distantly Related to Natural Product FrameworksDaniel J Foley, Philip G E Craven, Patrick M Collins, et al.
Pageof 7