Non-Biaryl Atropisomers in Organocatalysis

A new class of 6′‐hydroxy cinchona alkaloids, with a non‐biaryl atropisomeric functionalisation at position 5′ of the quinoline core can be prepared by an easy amination procedure. These are the first derivatives for which the principle of atropisomerism is engrafted in the classical core of the cin...

Full description

Saved in:

Bibliographic Details
Published in:	Chemistry : a European journal Vol. 12; no. 23; pp. 6039 - 6052
Main Authors:	Brandes, Sebastian, Niess, Barbara, Bella, Marco, Prieto, Auxiliadora, Overgaard, Jacob, Jørgensen, Karl Anker
Format:	Journal Article
Language:	English
Published:	Weinheim WILEY-VCH Verlag 07.08.2006 WILEY‐VCH Verlag Wiley
Subjects:	amination asymmetric catalysis atropisomerism Chemistry Chemistry, Multidisciplinary fluorination Michael addition Physical Sciences Science & Technology Michael addition fluorination BAYLIS-HILLMAN REACTION QUATERNARY STEREOCENTERS EFFICIENT SYNTHESIS asymmetric catalysis AXIALLY CHIRAL ANILIDES atropisomerism CINCHONA ALKALOIDS ENANTIOSELECTIVE CONJUGATE ADDITION ASYMMETRIC MICHAEL REACTIONS amination STEREOSELECTIVE-SYNTHESIS ALPHA-FLUORINATION CARBON-NITROGEN BONDS
ISSN:	0947-6539, 1521-3765
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!