Amanote Research
Register
Sign In
Mitigating the Risk of Coprecipitation of Pinacol During Isolation From Telescoped Miyaura Borylation and Suzuki Couplings Utilizing Boron Pinacol Esters: Use of Modeling for Process Design
doi 10.1021/acs.oprd.5b00324.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Suzuki-Miyaura Cross-Coupling of 3-Pyridyl Triflates With Alk-1-Enyl-2-Pinacol Boronates
Synthesis
Organic Chemistry
Catalysis
One-Pot Borylation/Suzuki–Miyaura Sp2–sp3 Cross-Coupling
Chemical Communications
Surfaces
Alloys
Materials Chemistry
Coatings
Metals
Optical
Magnetic Materials
Films
Catalysis
Chemistry
Electronic
Composites
Ceramics
ChanEvansLam Amination of Boronic Acid Pinacol (BPin) Esters: Overcoming the Aryl Amine Problem
Microwave-Assisted Suzuki–Miyaura Couplings on Α-Iodoenaminones
Tetrahedron Letters
Organic Chemistry
Biochemistry
Drug Discovery
Pd-Catalyzed Suzuki–Miyaura and Hiyama–Denmark Couplings of Aryl Sulfamates
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Stereoselection in the Prins-Pinacol Synthesis of Acyltetrahydrofurans
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Preparation of 2,3,3-Triarylacrylic Acid Esters Using Suzuki–Miyaura Coupling Reactions
Synthesis
Organic Chemistry
Catalysis
Boron-Masking Strategy for the Selective Synthesis of Oligoarenes via Iterative Suzuki-Miyaura Coupling
Boron-Masking Strategy for the Selective Synthesis of Oligoarenes via Iterative Suzuki-Miyaura Coupling
