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The Journal of Organic Chemistry
|
February 16, 2008
Highly enantioselective desymmetrization of meso anhydrides by a bifunctional thiourea-based organocatalyst at low catalyst loadings and room temperature
Aldo Peschiulli, Yurii Gun'ko, Stephen J Connon
Nature Chemistry
|
April 24, 2010
Synergistic organocatalysis in the kinetic resolution of secondary thiols with concomitant desymmetrization of an anhydride
Aldo Peschiulli, Barbara Procuranti, Cornelius J O' Connor, et al.
The Journal of Organic Chemistry
|
July 24, 2008
Organocatalytic asymmetric addition of alcohols and thiols to activated electrophiles: efficient dynamic kinetic resolution and desymmetrization protocols
Aldo Peschiulli, Cormac Quigley, Seán Tallon, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 25, 2020
3,3-Difluoro-3,4,5,6-tetrahydropyridin-2-amines: Potent and permeable BACE-1 inhibitors
Aldo Peschiulli, Daniel Oehlrich, Frederik Rombouts, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
July 26, 2012
Direct α-functionalization of saturated cyclic amines
Emily A Mitchell, Aldo Peschiulli, Nicolas Lefevre, et al.
Organic & Biomolecular Chemistry
|
October 13, 2011
The immobilisation of chiral organocatalysts on magnetic nanoparticles: the support particle cannot always be considered inert
Oliver Gleeson, Gemma-Louise Davies, Aldo Peschiulli, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
June 20, 2013
Ruthenium-catalyzed α-(hetero)arylation of saturated cyclic amines: reaction scope and mechanism
Aldo Peschiulli, Veerle Smout, Thomas E Storr, et al.
The Journal of Organic Chemistry
|
September 7, 2013
Removal of the pyridine directing group from α-substituted N-(pyridin-2-yl)piperidines obtained via directed Ru-catalyzed sp3 C-H functionalization
Veerle Smout, Aldo Peschiulli, Stefan Verbeeck, et al.
Journal of the American Chemical Society
|
July 2, 2020
Hydrogen Bonding Phase-Transfer Catalysis with Ionic Reactants: Enantioselective Synthesis of γ-Fluoroamines
Giulia Roagna, David M H Ascough, Francesco Ibba, et al.
European Journal of Medicinal Chemistry
|
December 17, 2021
Modulating physicochemical properties of tetrahydropyridine-2-amine BACE1 inhibitors with electron-withdrawing groups: A systematic study
Frederik J R Rombouts, Chien-Chi Hsiao, Solène Bache, et al.
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Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
The Journal of Organic Chemistry
|
February 16, 2008
Highly enantioselective desymmetrization of meso anhydrides by a bifunctional thiourea-based organocatalyst at low catalyst loadings and room temperature
Aldo Peschiulli, Yurii Gun'ko, Stephen J Connon
Nature Chemistry
|
April 24, 2010
Synergistic organocatalysis in the kinetic resolution of secondary thiols with concomitant desymmetrization of an anhydride
Aldo Peschiulli, Barbara Procuranti, Cornelius J O' Connor, et al.
The Journal of Organic Chemistry
|
July 24, 2008
Organocatalytic asymmetric addition of alcohols and thiols to activated electrophiles: efficient dynamic kinetic resolution and desymmetrization protocols
Aldo Peschiulli, Cormac Quigley, Seán Tallon, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 25, 2020
3,3-Difluoro-3,4,5,6-tetrahydropyridin-2-amines: Potent and permeable BACE-1 inhibitors
Aldo Peschiulli, Daniel Oehlrich, Frederik Rombouts, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
July 26, 2012
Direct α-functionalization of saturated cyclic amines
Emily A Mitchell, Aldo Peschiulli, Nicolas Lefevre, et al.
Organic & Biomolecular Chemistry
|
October 13, 2011
The immobilisation of chiral organocatalysts on magnetic nanoparticles: the support particle cannot always be considered inert
Oliver Gleeson, Gemma-Louise Davies, Aldo Peschiulli, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
June 20, 2013
Ruthenium-catalyzed α-(hetero)arylation of saturated cyclic amines: reaction scope and mechanism
Aldo Peschiulli, Veerle Smout, Thomas E Storr, et al.
The Journal of Organic Chemistry
|
September 7, 2013
Removal of the pyridine directing group from α-substituted N-(pyridin-2-yl)piperidines obtained via directed Ru-catalyzed sp3 C-H functionalization
Veerle Smout, Aldo Peschiulli, Stefan Verbeeck, et al.
Journal of the American Chemical Society
|
July 2, 2020
Hydrogen Bonding Phase-Transfer Catalysis with Ionic Reactants: Enantioselective Synthesis of γ-Fluoroamines
Giulia Roagna, David M H Ascough, Francesco Ibba, et al.
European Journal of Medicinal Chemistry
|
December 17, 2021
Modulating physicochemical properties of tetrahydropyridine-2-amine BACE1 inhibitors with electron-withdrawing groups: A systematic study
Frederik J R Rombouts, Chien-Chi Hsiao, Solène Bache, et al.
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of 2