Synthesis of the aminocyclopentenediol fragment of queuosine by way of the stereoselective addition of an organometallic reagent to a N-t -butanesulfinyl glycosylamine - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Organic & Biomolecular Chemistry Année : 2024

Synthesis of the aminocyclopentenediol fragment of queuosine by way of the stereoselective addition of an organometallic reagent to a N-t -butanesulfinyl glycosylamine

Résumé

A concise, stereocontrolled synthesis of the aminocyclopentenediol component of queuosine from l -ribose by way of a N-t -butanesulfinyl glycosylamine is reported.

Domaines

Chimie organique
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Dates et versions

hal-04646213 , version 1 (12-07-2024)

Identifiants

Citer

Floriane Heis, Estelle Gallienne, Olivier Martin. Synthesis of the aminocyclopentenediol fragment of queuosine by way of the stereoselective addition of an organometallic reagent to a N-t -butanesulfinyl glycosylamine. Organic & Biomolecular Chemistry, 2024, 22 (1), pp.106-113. ⟨10.1039/d3ob01713c⟩. ⟨hal-04646213⟩
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