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J Procter

Showing results (51-60 of 200) with videos related to

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The Journal of Organic Chemistry|October 22, 2024
Computational Study of SmI<sub>2</sub>-Catalyzed Intermolecular Couplings of Cyclopropyl Ketones: Links between the Structure and ReactivitySong Yu, Ciro Romano, David J Procter, et al.
The Journal of Organic Chemistry|April 12, 2003
The remarkable effect of cosolvent on a samarium(II)-mediated 4-exo-trig cyclization: further synthetic studies on pestalotiopsin ADavid J Edmonds, Kenneth W Muir, David J Procter
Journal of the American Chemical Society|April 13, 2022
Asymmetric Total Synthesis of (-)-Phaeocaulisin AÁron Péter, Giacomo E M Crisenza, David J Procter
Organic & Biomolecular Chemistry|March 23, 2007
Synthesis and evaluation of a new polymer-supported pseudoephedrine auxiliary for asymmetric alkylations on solid phaseAndrea M McGhee, Jean-Claude Kizirian, David J Procter
Chemical Communications (Cambridge, England)|January 26, 2007
Exploring a new, connective Pummerer reaction: formation of oxindoles by the reaction of thiols with glyoxamidesMarc Miller, William Tsang, Andrew Merritt, et al.
Organic Letters|December 5, 2003
Switching between novel samarium(II)-mediated cyclizations by a simple change in alcohol cosolventThomas K Hutton, Kenneth W Muir, David J Procter
The Journal of Organic Chemistry|January 31, 2004
Application of a recyclable pseudoephedrine resin in asymmetric alkylations on solid phasePanee C Hutchison, Tom D Heightman, David J Procter
Organic Letters|December 20, 2002
Evaluation of a pseudoephedrine linker for asymmetric alkylations on solid phasePanee C Hutchison, Tom D Heightman, David J Procter
Organic Letters|October 18, 2011
Nucleophilic ortho allylation of aryl and heteroaryl sulfoxidesAndrew J Eberhart, Jason E Imbriglio, David J Procter
Organic Letters|October 25, 2014
Switching between reaction pathways by an alcohol cosolvent effect: SmI2-ethylene glycol vs SmI2-H2O mediated synthesis of uracilsMichal Szostak, Malcolm Spain, Brice Sautier, et al.
Pageof 20

Showing results (51-60 of 200) with videos related to

Sort By:
Pageof 20
The Journal of Organic Chemistry|October 22, 2024
Computational Study of SmI<sub>2</sub>-Catalyzed Intermolecular Couplings of Cyclopropyl Ketones: Links between the Structure and ReactivitySong Yu, Ciro Romano, David J Procter, et al.
The Journal of Organic Chemistry|April 12, 2003
The remarkable effect of cosolvent on a samarium(II)-mediated 4-exo-trig cyclization: further synthetic studies on pestalotiopsin ADavid J Edmonds, Kenneth W Muir, David J Procter
Journal of the American Chemical Society|April 13, 2022
Asymmetric Total Synthesis of (-)-Phaeocaulisin AÁron Péter, Giacomo E M Crisenza, David J Procter
Organic & Biomolecular Chemistry|March 23, 2007
Synthesis and evaluation of a new polymer-supported pseudoephedrine auxiliary for asymmetric alkylations on solid phaseAndrea M McGhee, Jean-Claude Kizirian, David J Procter
Chemical Communications (Cambridge, England)|January 26, 2007
Exploring a new, connective Pummerer reaction: formation of oxindoles by the reaction of thiols with glyoxamidesMarc Miller, William Tsang, Andrew Merritt, et al.
Organic Letters|December 5, 2003
Switching between novel samarium(II)-mediated cyclizations by a simple change in alcohol cosolventThomas K Hutton, Kenneth W Muir, David J Procter
The Journal of Organic Chemistry|January 31, 2004
Application of a recyclable pseudoephedrine resin in asymmetric alkylations on solid phasePanee C Hutchison, Tom D Heightman, David J Procter
Organic Letters|December 20, 2002
Evaluation of a pseudoephedrine linker for asymmetric alkylations on solid phasePanee C Hutchison, Tom D Heightman, David J Procter
Organic Letters|October 18, 2011
Nucleophilic ortho allylation of aryl and heteroaryl sulfoxidesAndrew J Eberhart, Jason E Imbriglio, David J Procter
Organic Letters|October 25, 2014
Switching between reaction pathways by an alcohol cosolvent effect: SmI2-ethylene glycol vs SmI2-H2O mediated synthesis of uracilsMichal Szostak, Malcolm Spain, Brice Sautier, et al.
Pageof 20