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Rearrangements of ketols by hydriodic acid

SR

Membre a labase

Sumanas Rakhit

Résumé du colloque

The reduction of α-ketols (the alcoholic function being exclusively on a tertiary carbon) by treatment with hydriodic acid in acetic acid has been investigated. It will be shown that many representatives lead to rearrangements while similar analogs suffer straight reduction. The reason for the differences in the reaction paths and the underlying mechanisms will be discussed.

Contexte

Section :
Chimie organique
news icon Thème du colloque :
Chimie organique
manager icon Responsables :
Peter Morand
host icon Hôte : Université d’Ottawa

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Chimie organique

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Thème du colloque :

Chimie organique