Spiro-Bicyclic Bisborane Catalysts for Metal-Free Chemoselective and Enantioselective Hydrogenation of Quinolines
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Spiro-Bicyclic Bisborane Catalysts for Metal-Free Chemoselective and Enantioselective Hydrogenation of Quinolines
Authors
Keywords
-
Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 14, Pages 4664-4668
Publisher
Wiley
Online
2019-02-14
DOI
10.1002/anie.201900907
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- B(C 6 F 5 ) 3 -catalyzed metal-free hydrogenations of 2-quinolinecarboxylates
- (2018) Caifang Han et al. TETRAHEDRON LETTERS
- C2-Symmetric Bicyclic Bis-Borane Catalysts: Kinetic or Thermodynamic Products from a Reversible Hydroboration of Dienes
- (2018) Xian-Shuang Tu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Highly Stereoselective Metal-Free Hydrogenations of Pyrrolo[1,2-a]quinoxalines
- (2018) Xiaoqin Liu et al. ORGANIC LETTERS
- From structure to novel reactivity in frustrated Lewis pairs
- (2018) Jan Paradies COORDINATION CHEMISTRY REVIEWS
- Tris(pentafluorophenyl)borane and Beyond: Modern Advances in Borylation Chemistry
- (2017) James R. Lawson et al. INORGANIC CHEMISTRY
- Highly Enantioselective Direct Synthesis of Endocyclic Vicinal Diamines through Chiral Ru(diamine)-Catalyzed Hydrogenation of 2,2′-Bisquinoline Derivatives
- (2016) Wenpeng Ma et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- B(C6F5)3-catalyzed metal-free hydrogenation of 3,6-diarylpyridazines
- (2016) Wei Wang et al. DALTON TRANSACTIONS
- Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines
- (2016) Wei Wang et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- The broadening reach of frustrated Lewis pair chemistry
- (2016) D. W. Stephan SCIENCE
- Strong Brønsted acid promoted asymmetric hydrogenation of isoquinolines and quinolines catalyzed by a Rh–thiourea chiral phosphine complex via anion binding
- (2016) Jialin Wen et al. Chemical Science
- Hydrogenations at Room Temperature and Atmospheric Pressure with Mesoionic Carbene-Stabilized Borenium Catalysts
- (2015) Patrick Eisenberger et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Frustrated Lewis Pair Chemistry: Development and Perspectives
- (2015) Douglas W. Stephan et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- A unified survey of Si–H and H–H bond activation catalysed by electron-deficient boranes
- (2015) Martin Oestreich et al. CHEMICAL SOCIETY REVIEWS
- Cis-Selective and Highly Enantioselective Hydrogenation of 2,3,4-Trisubstituted Quinolines
- (2015) Zhenhua Zhang et al. ORGANIC LETTERS
- Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines
- (2015) Zhenhua Zhang et al. ORGANIC LETTERS
- Palladium-catalyzed asymmetric hydrogenation of 3-phthalimido substituted quinolines
- (2014) Xian-Feng Cai et al. CHEMICAL COMMUNICATIONS
- Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
- (2014) Edon Vitaku et al. JOURNAL OF MEDICINAL CHEMISTRY
- Asymmetric Transfer Hydrogenation of 3-Nitroquinolines: Facile Access to Cyclic Nitro Compounds with Two Contiguous Stereocenters
- (2013) Xian-Feng Cai et al. Chemistry-An Asian Journal
- Metal-Free Borane-Catalyzed Highly Stereoselective Hydrogenation of Pyridines
- (2013) Yongbing Liu et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Metal-Free Hydrogenation of N-Based Heterocycles
- (2013) Tayseer Mahdi et al. ORGANOMETALLICS
- Highly Enantioselective Transfer Hydrogenation of Quinolines Catalyzed by Gold Phosphates: Achiral Ligand Tuning and Chiral-Anion Control of Stereoselectivity
- (2012) Xi-Feng Tu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Bis(tetrafluorophenyl)borane
- (2012) Daniel Winkelhaus et al. DALTON TRANSACTIONS
- Dihydrophenanthridine: A New and Easily Regenerable NAD(P)H Model for Biomimetic Asymmetric Hydrogenation
- (2012) Qing-An Chen et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Highly Active Metal-Free Catalysts for Hydrogenation of Unsaturated Nitrogen-Containing Compounds
- (2011) Victor Sumerin et al. ADVANCED SYNTHESIS & CATALYSIS
- Advances in the Chemistry of Tetrahydroquinolines
- (2011) Vellaisamy Sridharan et al. CHEMICAL REVIEWS
- Asymmetric Hydrogenation of Heteroarenes and Arenes
- (2011) Duo-Sheng Wang et al. CHEMICAL REVIEWS
- Catalytic Hydrogenation with Frustrated Lewis Pairs: Selectivity Achieved by Size-Exclusion Design of Lewis Acids
- (2011) Gábor Erős et al. CHEMISTRY-A EUROPEAN JOURNAL
- Highly Enantioselective Hydrogenation of Quinolines Using Phosphine-Free Chiral Cationic Ruthenium Catalysts: Scope, Mechanism, and Origin of Enantioselectivity
- (2011) Tianli Wang et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Enantioselective Hydrogenation with Chiral Frustrated Lewis Pairs
- (2010) Dianjun Chen et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Metal-free reductions of N-heterocycles via Lewis acid catalyzed hydrogenation
- (2010) Stephen J. Geier et al. CHEMICAL COMMUNICATIONS
- pH-Regulated Asymmetric Transfer Hydrogenation of Quinolines in Water
- (2009) Chao Wang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Highly Enantioselective Iridium-Catalyzed Hydrogenation of 2-Benzylquinolines and 2-Functionalized and 2,3-Disubstituted Quinolines
- (2009) Da-Wei Wang et al. JOURNAL OF ORGANIC CHEMISTRY
- Hydrogenation of Quinolines Using a Recyclable Phosphine-Free Chiral Cationic Ruthenium Catalyst: Enhancement of Catalyst Stability and Selectivity in an Ionic Liquid
- (2008) Haifeng Zhou et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Metal-free catalytic hydrogenation of imines with tris(perfluorophenyl)borane
- (2008) Dianjun Chen et al. CHEMICAL COMMUNICATIONS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started