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ChemInform Abstract: Proximal Ester Assistance vs. Stereoelectronic Prohibition in Catalytic N‐Acyliminium Ion Reactions: Stereoselective Formation of Aza‐Heterocycles with Two Contiguous Quaternary‐Tertiary Stereocenters.

Identifieur interne : 000675 ( Main/Exploration ); précédent : 000674; suivant : 000676

ChemInform Abstract: Proximal Ester Assistance vs. Stereoelectronic Prohibition in Catalytic N‐Acyliminium Ion Reactions: Stereoselective Formation of Aza‐Heterocycles with Two Contiguous Quaternary‐Tertiary Stereocenters.

Auteurs : Moussa Saber ; Sebastien Comesse ; Vincent Dalla ; Pierre Netchitailo ; Adam Daich

Source :

RBID : ISTEX:64546A04FB3A62923A0205C63199529EC7F2446C

English descriptors

Abstract

The intermolecular and intramolecular α‐amidoalkylation of hemicyclic N,O‐acetals proceeds in the presence of NHTf2.

Url:
DOI: 10.1002/chin.201206098


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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   |texte=   ChemInform Abstract: Proximal Ester Assistance vs. Stereoelectronic Prohibition in Catalytic N‐Acyliminium Ion Reactions: Stereoselective Formation of Aza‐Heterocycles with Two Contiguous Quaternary‐Tertiary Stereocenters.
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