Fr. 134.00

Studies on Green Synthetic Reactions Based on Formic Acid from Biomass

English · Paperback / Softback

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Description

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This book introduces readers to the use of formic acid for efficient organic synthesis. It describes the N-methylation of aromatic and aliphatic amines with formic acid using a boron-based catalyst [B(C6F5)3] in combination with silanes and without the need for an expensive transition metal catalyst. It also shows that formic acid interacts with alkynes and allyl alcohols through a carbonylation process that generates carbon monoxide in situ from nickel and palladium catalysis, respectively, doing away with the need to use high-pressure CO gas and offering a user-friendly and practical method for preparing functionalized , beta- and beta, Gamma-unsaturated carboxylic acids. The findings presented not only enrich the field of 'C1 chemistry,' but also support the advancement of green and sustainable chemistry. 

List of contents

Introduction.- Conversion of Formic Acid as C1 building block on Organic Synthesis.- Non-Metal Boron-Catalyzed N-methylation Conversion of Amines with Formic Acid.- Nickel-Catalyzed Hydrocarboxylation of Alkynes with Formic Acid through Catalytic CO Recycling.- Efficient Pd-Catalyzed Carboxylation of Allylic Alcohols with Formic Acid.- Conclusions.

About the author










Dr. Ming-Chen Fu received his B.Sc. degree from Hefei University of Technology in 2013, and doctoral degree from The University of Science and Technology of China (USTC) under the supervision of Prof. Yao Fu in 2018. He then worked as a postdoctoral fellow at USTC. His research interests are focused on green synthetic reactions based on formic acid, and development of novel catalytic systems in visible light-induced decarboxylative coupling reactions.

Product details

Authors Ming-Chen Fu
Publisher Springer, Berlin
 
Languages English
Product format Paperback / Softback
Released 25.08.2021
 
EAN 9789811576256
ISBN 978-981-1576-25-6
No. of pages 105
Dimensions 155 mm x 6 mm x 235 mm
Illustrations XIV, 105 p. 189 illus., 24 illus. in color.
Series Springer Theses
Subject Natural sciences, medicine, IT, technology > Chemistry > Physical chemistry

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