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Jonas Faghtmann

Showing results (1-10 of 9) with videos related to

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Organic Letters|February 16, 2024
Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] CycloadditionsCasper Larsen Barløse, Jonas Faghtmann, Mikk Kaasik, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 29, 2024
Enantioselective Cascade Reactions of Aminocatalytic Dienamines and Trienamines Initiated by a Cycloaddition ReactionJonas Faghtmann, Signe Sofie Pladsbjerg Andresen, Anne Rask Østergaard, et al.
Organic Letters|May 14, 2025
Enantioselective and Divergent Trienamine-Mediated Reactions of Halogenated MaleimidesJonas Faghtmann, Anne Rask Østergaard, Fabien Fritz, et al.
Organic Letters|February 14, 2023
Asymmetric Organocatalyzed Cascade Reactions─Merging the <i>pseudo</i>-Halogen and Halogen Effect with Dienamine CatalysisCasper Larsen Barløse, Jonas Faghtmann, René Slot Bitsch, et al.
Chemical Science|August 21, 2025
Aminocatalytic enantioselective [2 + 2] cycloaddition of Bicyclo[1.1.0]butanes and α,β-unsaturated aldehydesRené Slot Bitsch, Enrico Marcantonio, Erlaitz Basabe Obregón, et al.
Journal of the American Chemical Society|November 28, 2024
Mechanistic Investigation of the Pseudo-Halogen Effect in Enantioselective Aminocatalyzed [6 + 4] and [10 + 6] Cycloadditions: Enabling Unique Favorskii-Like RearrangementsCasper Džabbarov Barløse, René Slot Bitsch, Jonas Faghtmann, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 17, 2024
Enantioselective Synthesis of α-Quaternary Isochromanes by Oxidative Aminocatalysis and Gold CatalysisPhilipp Waser, Jonas Faghtmann, Marta Gil-Ordóñez, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 14, 2026
Stereoselective Higher-Order [10+4]- and [10+6] Cycloadditions Between Two Highly Unsaturated and Ambiphilic π-AddendsJonas Faghtmann, Anne Kristensen, Fabien Fritz, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 2, 2024
An Enantioselective Aminocatalytic Cascade Reaction Affording Bioactive Hexahydroazulene ScaffoldsJonas Faghtmann, Macarena Eugui, Johannes Nygaard Lamhauge, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Organic Letters|February 16, 2024
Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] CycloadditionsCasper Larsen Barløse, Jonas Faghtmann, Mikk Kaasik, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 29, 2024
Enantioselective Cascade Reactions of Aminocatalytic Dienamines and Trienamines Initiated by a Cycloaddition ReactionJonas Faghtmann, Signe Sofie Pladsbjerg Andresen, Anne Rask Østergaard, et al.
Organic Letters|May 14, 2025
Enantioselective and Divergent Trienamine-Mediated Reactions of Halogenated MaleimidesJonas Faghtmann, Anne Rask Østergaard, Fabien Fritz, et al.
Organic Letters|February 14, 2023
Asymmetric Organocatalyzed Cascade Reactions─Merging the <i>pseudo</i>-Halogen and Halogen Effect with Dienamine CatalysisCasper Larsen Barløse, Jonas Faghtmann, René Slot Bitsch, et al.
Chemical Science|August 21, 2025
Aminocatalytic enantioselective [2 + 2] cycloaddition of Bicyclo[1.1.0]butanes and α,β-unsaturated aldehydesRené Slot Bitsch, Enrico Marcantonio, Erlaitz Basabe Obregón, et al.
Journal of the American Chemical Society|November 28, 2024
Mechanistic Investigation of the Pseudo-Halogen Effect in Enantioselective Aminocatalyzed [6 + 4] and [10 + 6] Cycloadditions: Enabling Unique Favorskii-Like RearrangementsCasper Džabbarov Barløse, René Slot Bitsch, Jonas Faghtmann, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 17, 2024
Enantioselective Synthesis of α-Quaternary Isochromanes by Oxidative Aminocatalysis and Gold CatalysisPhilipp Waser, Jonas Faghtmann, Marta Gil-Ordóñez, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 14, 2026
Stereoselective Higher-Order [10+4]- and [10+6] Cycloadditions Between Two Highly Unsaturated and Ambiphilic π-AddendsJonas Faghtmann, Anne Kristensen, Fabien Fritz, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 2, 2024
An Enantioselective Aminocatalytic Cascade Reaction Affording Bioactive Hexahydroazulene ScaffoldsJonas Faghtmann, Macarena Eugui, Johannes Nygaard Lamhauge, et al.
Pageof 1