Catalytic asymmetric diels-alder reaction of quinone imine ketals: a site-divergent approach.

Angew Chem Int Ed Engl

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto, 606-8502, (Japan).

Published: April 2015

The catalytic asymmetric Diels-Alder reaction of quinone imine ketals with diene carbamates catalyzed by axially chiral dicarboxylic acids is reported herein. A variety of primary and secondary alkyl-substituted quinone derivatives which have not been applied in previous asymmetric quinone Diels-Alder reactions could be employed using this method. More importantly, we succeeded in developing a strategy to divert the reaction site in unsymmetrical 3-alkyl quinone imine ketals from the inherently favored unsubstituted C=C bond to the disfavored alkyl-substituted C=C bond.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201410957DOI Listing

Publication Analysis

Top Keywords

quinone imine
12
imine ketals
12
catalytic asymmetric
8
asymmetric diels-alder
8
diels-alder reaction
8
reaction quinone
8
c=c bond
8
quinone
5
ketals site-divergent
4
site-divergent approach
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!