Progress on All Ends for Carbon-Carbon Bond Formation through Photoredox Catalysis
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Progress on All Ends for Carbon-Carbon Bond Formation through Photoredox Catalysis
Authors
Keywords
-
Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 17, Pages 5006-5008
Publisher
Wiley
Online
2015-03-18
DOI
10.1002/anie.201411513
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Oxidative Photoredox-Catalytic Activation of Aliphatic Nucleophiles for C(sp3)-C(sp2) Cross-Coupling Reactions
- (2014) Emanuela Jahn et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Dual Catalysis Sees the Light: Combining Photoredox with Organo-, Acid, and Transition-Metal Catalysis
- (2014) Matthew N. Hopkinson et al. CHEMISTRY-A EUROPEAN JOURNAL
- Asymmetric photoredox transition-metal catalysis activated by visible light
- (2014) Haohua Huo et al. NATURE
- Reduction of aryl halides by consecutive visible light-induced electron transfer processes
- (2014) I. Ghosh et al. SCIENCE
- A Dual-Catalysis Approach to Enantioselective [2 + 2] Photocycloadditions Using Visible Light
- (2014) J. Du et al. SCIENCE
- Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis
- (2014) J. C. Tellis et al. SCIENCE
- Photoredox Catalysis for Organic Syntheses
- (2013) Melissa Reckenthäler et al. ADVANCED SYNTHESIS & CATALYSIS
- Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
- (2013) Christopher K. Prier et al. CHEMICAL REVIEWS
- Visible-Light-Driven Photoredox Catalysis in the Construction of Carbocyclic and Heterocyclic Ring Systems
- (2013) Jun Xuan et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters
- (2013) Giulia Bergonzini et al. Chemical Science
- Visible-Light-Promoted Stereoselective Alkylation by Combining Heterogeneous Photocatalysis with Organocatalysis
- (2012) Maria Cherevatskaya et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Visible-Light-Induced Photocatalytic Reductive Transformations of Organohalides
- (2012) Hyejin Kim et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis
- (2012) Daniel A. DiRocco et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Synergistic catalysis: A powerful synthetic strategy for new reaction development
- (2012) Anna E. Allen et al. Chemical Science
- Metal-Free, Cooperative Asymmetric Organophotoredox Catalysis with Visible Light
- (2010) Matthias Neumann et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- From Noble Metal to Nobel Prize: Palladium-Catalyzed Coupling Reactions as Key Methods in Organic Synthesis
- (2010) Xiao-Feng Wu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Visible light photoredox catalysis: applications in organic synthesis
- (2010) Jagan M. R. Narayanam et al. CHEMICAL SOCIETY REVIEWS
- Enantioselective α-Benzylation of Aldehydes via Photoredox Organocatalysis
- (2010) Hui-Wen Shih et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Light in Aminocatalysis: The Asymmetric Intermolecular α-Alkylation of Aldehydes
- (2009) Paolo Melchiorre ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Photoredox Catalysis with Visible Light
- (2009) Kirsten Zeitler ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Enantioselective α-Trifluoromethylation of Aldehydes via Photoredox Organocatalysis
- (2009) David A. Nagib et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Merging Photoredox Catalysis with Organocatalysis: The Direct Asymmetric Alkylation of Aldehydes
- (2008) D. A. Nicewicz et al. SCIENCE
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now