From (phenylsulfanyl)cycloalkanecarbaldehydes to optically active spirocyclic tetrahydrofurans: stereospecific resolution of symmetric aldehydes through (S)-proline-catalysed aldol reaction

SECCI, FRANCESCO;FRONGIA, ANGELO;SARAIS, GIORGIA;ARCA, MASSIMILIANO;
2014-01-01

Abstract

A variety of enantiomerically enriched tetrahydrofuran spirocyclic derivatives have been synthesised by a sequential enantioselective proline-induced stereospecific resolution through aldol reaction of (E/Z)-(phenylsulfanyl)cycloalkane-carbaldehydes followed by a ketone reduction, acid-catalysed [1,2]-SPh stereospecific migration, and ring-closure reaction.
Files in This Item:
File Size Format  
201402653_ftp.pdf

Solo gestori archivio

Size 3.72 MB
Format Adobe PDF
3.72 MB Adobe PDF & nbsp; View / Open   Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Questionnaire and social

Share on:
Impostazioni cookie