Issue 35, 2013

Retracted Article: A highly concise and practical route to clavaminols, sphinganine and (+)-spisulosine via indium mediated allylation of α-hydrazino aldehyde and a theoretical insight into the stereochemical aspects of the reaction

Abstract

A conceptually different approach has been employed for the synthesis of 1,2-amino alcohols by proline-catalyzed α-amination of aldehyde and one-pot indium mediated allylation of the crude α-hydrazino aldehydes. DFT based quantum chemical calculations have been performed to obtain a quantitative explanation of the stereoselectivity of the reaction.

Graphical abstract: Retracted Article: A highly concise and practical route to clavaminols, sphinganine and (+)-spisulosine via indium mediated allylation of α-hydrazino aldehyde and a theoretical insight into the stereochemical aspects of the reaction

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
09 Apr 2013
Accepted
01 Jul 2013
First published
01 Jul 2013

RSC Adv., 2013,3, 15442-15448

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