Image Année : 2024

Padlocking dihydrofurannulation for the control of small degree of helicity built on a fused-tetracyclic core

Résumé

An organocatalyzed enantioselective domino reaction has been developed for the synthesis of configurationally locked helically chiral fused tetracyclic cores. This methodology allows the modulation of the helicity in the final molecule.

HAL

Décrit hal-04616826 Article Arthur Gaucherand, Expédite Yen-Pon, Diego García-López, Jean-Valère Naubron, Sara Chentouf, et al.. Padlocking dihydrofurannulation for the control of small degree of helicity built on a fused-tetracyclic core. Chemical Science, 2024, 15 (19), pp.7300 - 7307. ⟨10.1039/d4sc00745j⟩. ⟨hal-04616826⟩

HAL

Cite hal-04616826 Article Arthur Gaucherand, Expédite Yen-Pon, Diego García-López, Jean-Valère Naubron, Sara Chentouf, et al.. Padlocking dihydrofurannulation for the control of small degree of helicity built on a fused-tetracyclic core. Chemical Science, 2024, 15 (19), pp.7300 - 7307. ⟨10.1039/d4sc00745j⟩. ⟨hal-04616826⟩

Dates et versions

hal-04616840 , version 1 (19-06-2024)

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Identifiants

  • HAL Id : hal-04616840 , version 1

Citer

Arthur Gaucherand, Expédite Yen-Pon, Diego García-López, Jean-Valère Naubron, Sara Chentouf, et al.. Padlocking dihydrofurannulation for the control of small degree of helicity built on a fused-tetracyclic core. France. 2024. ⟨hal-04616840⟩
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