(1S, 3R, 4R)-2-Azanorbornyl-3-methanol oxazaborolidines in the asymmetric reduction of ketones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. An Efficient Catalytic Stereoselective Route to a Key Intermediate for the Synthesis of the Long-Lived PGI2 Analog ZK 96480 (CicaprostTM)
2. Asymmetric reduction of aromatic ketones with chiral alkoxy-amineborane complexes
3. Asymmetric synthesis using chirally modified borohydrides. Part 1. Enantioselective reduction of aromatic ketones with the reagent prepared from borane and (S)-valinol
4. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
5. A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses
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1. 2-Azanorbornane-Based Amino Alcohol Organocatalysts for Asymmetric Michael Reaction of β-Keto Esters with Nitroolefins;European Journal of Organic Chemistry;2019-06-13
2. Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids;Organic Chemistry Frontiers;2019
3. 2-Azanorbornane-based amine organocatalyst for enantioselective aldol reaction of isatins with ketones;Tetrahedron: Asymmetry;2016-11
4. 2-Azanorbornane – a versatile chiral aza-Diels–Alder cycloadduct: preparation, applications in stereoselective synthesis and biological activity;Organic & Biomolecular Chemistry;2015
5. Synthesis of Nitrogenated Heterocycles by Asymmetric Transfer Hydrogenation of N-(tert-Butylsulfinyl)haloimines;The Journal of Organic Chemistry;2013-08-30
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