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Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 3, pp. 728 - 732
A method for the decarboxylative macrocyclization of peptides bearing N‐terminal Michael acceptors has been developed. This synthetic method enables the... 
Michael addition | peptides | photoredox catalysis | decarboxylation | macrocycles | DRUG | MERGING PHOTOREDOX | STABILITY | ARYLATION | ALPHA-AMINO-ACIDS | N-METHYLATION | CHEMISTRY, MULTIDISCIPLINARY | CYCLIC-PEPTIDES | DISCOVERY | STRATEGIES | CARBOXYLIC-ACIDS | Peptides | Amino acids | Catalysis
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2016, Volume 55, Issue 12, pp. 4040 - 4043
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2015, Volume 54, Issue 5, pp. 1625 - 1628
An unprecedented α‐allylation of amines was achieved by combining palladium catalysis and visible‐light photoredox catalysis. In this dual catalysis process,... 
palladium | radicals | photochemistry | synthetic methods | allylic compounds | Palladium | Synthetic methods | Allylic compounds | Radicals | Photochemistry | TRANSITION-METAL CATALYSIS | ORGANIC-SYNTHESIS | GOLD | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ALKENES | ALLYLIC ACETATES | C-H ARYLATION | MICHAEL ACCEPTORS | DUAL CATALYSIS | Amines | Catalysts | Merging | Derivatives | Catalysis | Allyl compounds
Journal Article
SCIENCE, ISSN 0036-8075, 05/2019, Volume 364, Issue 6439, pp. 450 - 450
Visible-light photoredox catalysis offers a distinct activation mode complementary to thermal transition metal catalyzed reactions. The vast majority of... 
MERGING PHOTOREDOX | CROSS-COUPLINGS | COOPERATIVE PHOTOREDOX | ELECTRON-TRANSFER | CU-BASED SENSITIZERS | MULTIDISCIPLINARY SCIENCES | REGIOSELECTIVE SYNTHESIS | TERMINAL ALKYNES | AEROBIC OXIDATION | TRANSFER RADICAL-ADDITION | METAL-COMPLEXES
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2015, Volume 54, Issue 38, pp. 11196 - 11199
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2017, Volume 56, Issue 11, pp. 3080 - 3084
Herein, the first acceptorless dehydrogenation of tetrahydroquinolines (THQs), indolines, and other related N‐heterocycles, by merging visible‐light photoredox... 
reaction mechanisms | cobalt | dehydrogenation | heterocycles | photochemistry | SYSTEM | NITROGEN-HETEROCYCLES | IRIDIUM CATALYST | COMPLEXES | EVOLUTION REACTION | CHEMISTRY, MULTIDISCIPLINARY | EXTERNAL OXIDANT | AMBIENT CONDITIONS | ALCOHOLS | MILD CONDITIONS | REVERSIBLE HYDROGEN STORAGE | Dehydrogenation | Catalysis | Hydrogen storage | Merging | Ambient temperature | Heterocyclic compounds | Cobalt | Quenching
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2015, Volume 137, Issue 35, pp. 11340 - 11348
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 04/2016, Volume 138, Issue 16, pp. 5451 - 5464
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2015, Volume 54, Issue 38, pp. 11200 - 11204
Journal Article
Organic Letters, ISSN 1523-7060, 10/2015, Volume 17, Issue 19, pp. 4830 - 4833
Enabled by iridium photoredox catalysis, 2-oxo-2-(hetero)­arylacetic acids were decarboxylatively added to various Michael acceptors including α,β-unsaturated... 
ARYL BROMIDES | HALIDES | MERGING PHOTOREDOX | NICKEL CATALYSIS | ARYLATION | KETO ACIDS | CHEMISTRY, ORGANIC | POTASSIUM POLYFLUOROBENZOATES | COUPLINGS | ALKYNYLATION | CARBOXYLIC-ACIDS
Journal Article
Organic Letters, ISSN 1523-7060, 2019, Volume 21, Issue 7, pp. 2077 - 2080
The first visible-light-induced acyl radical Smiles rearrangement to transform biaryl ethers to hydroxybenzophenones under mild and metal-free conditions is... 
MERGING PHOTOREDOX | REAGENTS | ARYL MIGRATION REACTIONS | NICKEL CATALYSIS | ALKYLATION | ARYLATION | CHEMISTRY, ORGANIC | ALPHA-KETO ACIDS | DERIVATIVES | CARBOXYLIC-ACIDS | DECARBOXYLATIVE ALKYNYLATION
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 2017, Volume 56, Issue 27, pp. 8004 - 8008
An unprecedented method that makes use of the cooperative interplay between molecular iodine and photo-redox catalysis has been developed for dual... 
amination | photoredox catalysis | iodine catalysis | 1,5-HAT processes | cooperative catalysis | MERGING PHOTOREDOX | NICKEL CATALYSIS | COMPLEXES | IONS | CHEMISTRY, MULTIDISCIPLINARY | OXYGEN | C-H ARYLATION | AMINES | DENSITY-FUNCTIONAL THEORY
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2015, Volume 21, Issue 50, pp. 18080 - 18084
The direct and controlled activation of a C(sp3)H bond adjacent to an O atom is of particular synthetic value for the conventional derivatization of ethers or... 
oxonium | CH activation | photoredox catalysis | isochromans | C-H activation | 9-MESITYL-10-METHYLACRIDINIUM ION | MERGING PHOTOREDOX | STRATEGY | ARYLATION | ORGANOCATALYSIS | ALDEHYDES | ADJACENT | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | BENZYLIC ETHERS | VISIBLE-LIGHT CATALYSIS | Cross coupling | Photocatalysis | Chemical bonds | Esters | Activation | Transformations | Catalysis | Ethers
Journal Article