Organocatalytic Enantioselective Friedel−Crafts Alkylation of 4,7-Dihydroindoles with α,β-Unsaturated Aldehydes: An Easy Access to 2-Substituted Indoles
Organic Letters2009Vol. 11(10), pp. 2177–2180
Citations Over TimeTop 10% of 2009 papers
Abstract
An enantioselective Friedel-Crafts alkylation of 4,7-dihydroindoles and alpha,beta-unsaturated aldehydes has been developed. The process is promoted by diphenylprolinol ether to afford 2-substituted 4,7-dihydroindoles in high yields and enantioselectivities. After a subsequent oxidation of the products, the optically active 2-substituted indoles could be obtained smoothly in high yields without any loss of enantioselectivity.
Related Papers
- → Recent developments in enantioselective iron-catalyzed transformations(2019)58 cited
- → Organocatalytic Enantioselective Desymmetrization of Prochiral 2,2‐Disubstituted Cyclic 1,3‐Diones(2021)26 cited
- → Methods of Asymmetric Synthesis—Enantioselective Catalytic Hydrogenation(1971)142 cited
- → The First Catalytic Enantioselective Synthesis of (R)-(+) Lasiodiplodin(1993)18 cited
- → Chiral B(III) Lewis Acids(2000)19 cited