A Highly Efficient and Enantioselective Access to Tetrahydroisoquinoline Alkaloids: Asymmetric Hydrogenation with an Iridium Catalyst
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Title
A Highly Efficient and Enantioselective Access to Tetrahydroisoquinoline Alkaloids: Asymmetric Hydrogenation with an Iridium Catalyst
Authors
Keywords
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Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 50, Issue 45, Pages 10679-10681
Publisher
Wiley
Online
2011-09-20
DOI
10.1002/anie.201104476
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- An N-Linked Bidentate Phosphoramidite Ligand (N-Me-BIPAM) for Rhodium-Catalyzed Asymmetric Addition of Arylboronic Acids to N-Sulfonylarylaldimines
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- A Highly Enantioselective Access to Tetrahydroisoquinoline and β-Carboline Alkaloids with Simple Noyori-Type Catalysts in Aqueous Media
- (2009) Laurent Evanno et al. CHEMISTRY-A EUROPEAN JOURNAL
- Enantioselective Hydrogenation of N−H Imines
- (2009) Guohua Hou et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Ru(II) Complexes of N-Alkylated TsDPEN Ligands in Asymmetric Transfer Hydrogenation of Ketones and Imines
- (2009) José E. D. Martins et al. ORGANIC LETTERS
- Asymmetric Transfer Hydrogenation of CO and CN Bonds by Tethered RhIIICatalysts
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- Asymmetric Hydrogenation of Cyclic Imines with an Ionic Cp*Rh(III) Catalyst
- (2008) Chaoqun Li et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- A Versatile Cyclodehydration Reaction for the Synthesis of Isoquinoline and β-Carboline Derivatives
- (2008) Mohammad Movassaghi et al. ORGANIC LETTERS
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