Shared posts

20 Jul 16:42

Direct Cross‐Coupling of Allylic C(sp3)−H Bonds with Aryl‐ and Vinylbromides by Combined Nickel and Visible‐Light Catalysis

by Dr. Long Huang , Prof. Dr. Magnus Rueping
Angewandte Chemie International Edition, EarlyView.
20 Jul 16:38

Mechanochemical Activation of Zinc and Application to Negishi Cross‐Coupling

by QunCao , Joseph L.Howard , EmilieWheatley , Duncan L.Browne
Angewandte Chemie International Edition, EarlyView.
19 Jul 06:58

Thermoformed fluoropolymer tubing for in-line mixing

React. Chem. Eng., 2018, 3,707-713
DOI: 10.1039/C8RE00112J, Paper
Open Access Open Access
Creative Commons Licence&nbsp This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Kai Wang, Haomiao Zhang, Yi Shen, Andrea Adamo, Klavs F. Jensen
We present a thermoforming method to make in-line micromixer in commercial fluoropolymer tubing.
The content of this RSS Feed (c) The Royal Society of Chemistry
15 Jul 15:16

[ASAP] Highly Ambiphilic Room Temperature Stable Six-Membered Cyclic (Alkyl)(amino)carbenes

by Cory M. Weinstein, Glen P. Junor, Daniel R. Tolentino, Rodolphe Jazzar, Mohand Melaimi, Guy Bertrand

TOC Graphic

Journal of the American Chemical Society
DOI: 10.1021/jacs.8b05518
13 Jul 20:12

[ASAP] One-Pot Sequential Kinetic Profiling of a Highly Reactive Manganese Catalyst for Ketone Hydroboration: Leveraging s-Bond Metathesis via Alkoxide Exchange Steps

by Vladislav Vasilenko, Clemens K. Blasius, Lutz H. Gade

TOC Graphic

Journal of the American Chemical Society
DOI: 10.1021/jacs.8b05340
13 Jul 19:51

[ASAP] Dearomative Cascade Photocatalysis: Divergent Synthesis through Catalyst Selective Energy Transfer

by Michael J. James, Jonas Luca Schwarz, Felix Strieth-Kalthoff, Birgit Wibbeling, Frank Glorius

TOC Graphic

Journal of the American Chemical Society
DOI: 10.1021/jacs.8b03302
13 Jul 19:34

Radical Trifluoromethoxylation of Arenes Triggered by a Visible‐Light‐Mediated N‐O Redox Fragmentation

by AntonioTogni , Benson J.Jelier , Pascal F.Tripet , EwaPietrasiak , IvanFranzoni , GunnarJeschke
Angewandte Chemie International Edition, Volume 0, Issue ja, -Not available-.
13 Jul 19:14

European Restrictions on 1,2‐Dichloroethane: C−H Activation Research and Development Should Be Liberated and not Limited

by JamesSherwood
Angewandte Chemie International Edition, EarlyView.
13 Jul 18:14

Chromophore Activation of α,β‐Unsaturated Carbonyl Compounds and Its Application to Enantioselective Photochemical Reactions

by M. Sc. Christoph Brenninger , Dr. John D. Jolliffe , Prof. Dr. Thorsten Bach
Angewandte Chemie International Edition, EarlyView.
13 Jul 17:50

Continuous Visible‐Light Photoflow Approach for a Manganese‐Catalyzed (Het)Arene C−H Arylation

by Dr. Yu‐Feng Liang , Ralf Steinbock , Long Yang , Prof. Dr. Lutz Ackermann
Angewandte Chemie International Edition, EarlyView.
13 Jul 17:22

A Fully Automated Continuous‐Flow Platform for Fluorescence Quenching Studies and Stern–Volmer Analysis

by KoenKuijpers , CeciliaBottecchia , DarioCambie , KoenDrummen , NielsKoenig , TimothyNoel
Angewandte Chemie International Edition, EarlyView.
13 Jul 08:38

Rapid and Mild Synthesis of Amino Acid N‐Carboxy Anhydrides: Basic‐to‐Acidic Flash Switching in a Microflow Reactor

by YumaOtake , HiroyukiNakamura , ShinichiroFuse
Angewandte Chemie International Edition, EarlyView.
27 Jun 12:32

[ASAP] Iron-Catalyzed Methylation Using the Borrowing Hydrogen Approach

by Kurt Polidano, Benjamin D. W. Allen, Jonathan M. J. Williams, Louis C. Morrill

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ACS Catalysis
DOI: 10.1021/acscatal.8b02158
26 Jun 16:52

A Detailed Study of Irradiation Requirements Towards an Efficient Photochemical Wohl‐Ziegler Procedure in Flow

by Holly E. Bonfield , Dr. Jason D. Williams , Wei Xiang Ooi , Dr. Stuart G. Leach , Prof. Dr. William J. Kerr , Lee J. Edwards
ChemPhotoChem A Detailed Study of Irradiation Requirements Towards an Efficient Photochemical Wohl‐Ziegler Procedure in Flow

And then there was light: The significance of defining light power requirements within photochemical reactions has been exemplified using the Wohl–Ziegler reaction in batch and flow. The optimized reaction conditions were subsequently applied to a range of synthetically relevant (hetero)aromatic compounds under continuous flow conditions.


Abstract

A platform has been developed to enable standardization of light sources, allowing consistent scale‐up from high‐throughput screening in batch to flow, using the same pseudo‐monochromatic light source. The impact of wavelength and light intensity on a photochemical reaction was evaluated within this platform using the Wohl‐Ziegler benzylic bromination of 4‐methyl‐3‐(trifluoromethyl)benzonitrile with N‐bromosuccinimide as a model system. It was found that only 40 % of the maximum light intensity was required while still maintaining reaction rate, allowing more reliable temperature control and lower energy consumption. The optimized reaction conditions were subsequently applied to a range of synthetically relevant (hetero)aromatic compounds under continuous conditions, exploring the scope of the process within a mild and scalable procedure.

12 Jun 09:12

Formal Giese addition of C(sp3)–H nucleophiles enabled by visible light mediated Ni catalysis of triplet enone diradicals

Chem. Sci., 2018, 9,5810-5815
DOI: 10.1039/C8SC01827H, Edge Article
Open Access Open Access
Geun Seok Lee, Soon Hyeok Hong
Formal Giese addition of C(sp3)–H substrates is achieved by the unprecedented merger of triplet chemistry and Ni catalysis.
The content of this RSS Feed (c) The Royal Society of Chemistry
08 Jun 16:58

Visible‐Light‐Accelerated Copper(II)‐Catalyzed Regio‐ and Chemoselective Oxo‐Azidation of Vinyl Arenes

by M. Sc. Asik Hossain , Dr. Adiyala Vidyasagar , M. Sc. Christian Eichinger , Dr. Christian Lankes , M. Sc. Jenny Phan , Prof. Dr. Julia Rehbein , Prof. Dr. Oliver Reiser
Angewandte Chemie International Edition, EarlyView.
08 Jun 16:23

The Generation of Diazo Compounds in Continuous‐Flow

by Katharina J. Hock , Prof. Dr. Rene M. Koenigs
Chemistry – A European Journal, EarlyView.
08 Jun 16:19

Synthetic and Mechanistic Investigation of an Oxime Ether Electrocyclization Approach to Heteroaromatic Boronic Acid Derivatives

by Helena Mora‐Radó , Lia Sotorríos , Dr. Matthew P. Ball‐Jones , Dr. Laurent Bialy , Dr. Werngard Czechtizky , Dr. María Méndez , Prof. Enrique Gómez‐Bengoa , Prof. Joseph P. A. Harrity
Chemistry – A European Journal, EarlyView.
01 Jun 08:09

[ASAP] Cooperative Catalysis: A Strategy To Synthesize Trifluoromethyl-thioesters from Aldehydes

by Satobhisha Mukherjee, Tuhin Patra, Frank Glorius

TOC Graphic

ACS Catalysis
DOI: 10.1021/acscatal.8b01519
01 Jun 06:34

Design and construction of an open source-based photometer and its applications in flow chemistry

React. Chem. Eng., 2018, 3,478-486
DOI: 10.1039/C8RE00070K, Paper
Open Access Open Access
Creative Commons Licence&nbsp This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Gabriel Glotz, C. Oliver Kappe
An inexpensive and easy to build photometer using a movable measuring cell for flow chemistry applications was designed with temporal resolution down to 1 ms.
The content of this RSS Feed (c) The Royal Society of Chemistry
30 May 14:14

[ASAP] Carbon Dioxide-Mediated C(sp3)–H Arylation of Amine Substrates

by Mohit Kapoor, Daniel Liu, Michael C. Young

TOC Graphic

Journal of the American Chemical Society
DOI: 10.1021/jacs.8b05061
30 May 14:05

Eosin Y as a Direct Hydrogen‐Atom Transfer Photocatalyst for the Functionalization of C−H Bonds

by Xuan‐Zi Fan , Dr. Jia‐Wei Rong , Hao‐Lin Wu , Quan Zhou , Dr. Hong‐Ping Deng , Jin Da Tan , Cheng‐Wen Xue , Dr. Li‐Zhu Wu , Dr. Hai‐Rong Tao , Dr. Jie Wu
Angewandte Chemie International Edition, EarlyView.
28 May 09:32

A continuous flow approach for the C–H functionalization of 1,2,3-triazoles in γ-valerolactone as a biomass-derived medium

Green Chem., 2018, 20,2888-2893
DOI: 10.1039/C8GC01115J, Paper
Francesco Ferlin, Lorenzo Luciani, Stefano Santoro, Assunta Marrocchi, Daniela Lanari, Alexander Bechtoldt, Lutz Ackermann, Luigi Vaccaro
Herein we report an efficient procedure for the C–H functionalization of 1,2,3-triazoles in a continuous flow regime applied to a variety of functionalities and to the inter- or intramolecular versions of the process.
The content of this RSS Feed (c) The Royal Society of Chemistry
16 May 17:12

A General, Activator‐Free Palladium‐Catalyzed Synthesis of Arylacetic and Benzoic Acids from Formic Acid

by Lin Wang , Helfried Neumann , Matthias Beller
Angewandte Chemie International Edition, EarlyView.
16 May 17:04

Catalytic Direct‐Type Addition Reactions of Alkylarenes with Imines and Alkenes

by Dr. Yasuhiro Yamashita , Dr. Hirotsugu Suzuki , Io Sato , Tsubasa Hirata , Prof. Dr. Shū Kobayashi
Angewandte Chemie International Edition, EarlyView.
16 May 17:00

Iron‐Catalyzed Ring‐Closing C−O/C−O Metathesis of Aliphatic Ethers

by Tobias Biberger , Szabolcs Makai , Dr. Zhong Lian , Dr. Bill Morandi
Angewandte Chemie International Edition, EarlyView.
16 May 16:57

Stereospecific Nucleophilic Substitution with Arylboronic Acids as Nucleophiles in the Presence of a CONH Group

by Duanshuai Tian , Dr. Chengxi Li , Dr. Guoxian Gu , Henian Peng , Prof. Dr. Xumu Zhang , Prof. Dr. Wenjun Tang
Angewandte Chemie International Edition, EarlyView.
16 May 16:39

7‐Step Flow Synthesis of the HIV Integrase Inhibitor Dolutegravir

by Dr. Robert E. Ziegler , Dr. Bimbisar K. Desai , Dr. Jo‐Ann Jee , Prof. Dr. B. Frank Gupton , Prof. Dr. Thomas D. Roper , Prof. Dr. Timothy F. Jamison
Angewandte Chemie International Edition, EarlyView.
14 May 16:28

[ASAP] Development of a Safe and High-Throughput Continuous Manufacturing Approach to 4-(2-Hydroxyethyl)thiomorpholine 1,1-Dioxide

by Neil A. Strotman, Yichen Tan, Kyle W. Powers, Maxime Soumeillant, Simon W. Leung

TOC Graphic

Organic Process Research & Development
DOI: 10.1021/acs.oprd.8b00100
11 May 07:52

[ASAP] Transforming Benzylic Amines into Diarylmethanes: Cross-Couplings of Benzylic Pyridinium Salts via C–N Bond Activation

by Jennie Liao, Weiye Guan, Brian P. Boscoe, Joseph W. Tucker, John W. Tomlin, Michelle R. Garnsey, Mary P. Watson

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Organic Letters
DOI: 10.1021/acs.orglett.8b01062