Heterocycles via Cross Dehydrogenative Coupling Synthesis and Functi
This book discusses the developments in the synthesis and functionalization of different heterocycles based on the formation of carbon-carbon (C-C) and carbon-heteroatom (C-X) bonds using cross-dehydrogenative coupling (CDC). Consisting of 13 chapters, th
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erocycles via Cross Dehydrogenative Coupling Synthesis and Functionalization
Heterocycles via Cross Dehydrogenative Coupling
Ananya Srivastava Chandan K. Jana •
Editors
Heterocycles via Cross Dehydrogenative Coupling Synthesis and Functionalization
123
Editors Ananya Srivastava National Institute of Pharmaceutical Education and Research Guwahati, Assam, India
Chandan K. Jana Indian Institute of Technology Guwahati Guwahati, Assam, India
ISBN 978-981-13-9143-9 ISBN 978-981-13-9144-6 https://doi.org/10.1007/978-981-13-9144-6
(eBook)
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Preface
Carbon–carbon and carbon–heteroatom bond formation plays a central role in many chemical syntheses, and revolutions in these reactions will intensely improve the overall synthetic efficiency. This book describes the studies of past several years for the synthesis and functionalization of different heterocycles by making carbon– carbon (C-C) and carbon–heteroatom (C-X) bonds via cross-dehydrogenative coupling (CDC) of C-H and C-H or X-H. CDC, representing a new state of the art in the field of organic chemistry, expedites the synthesis and functionalization of heterocycles to provide architecturally more complex heterocyclic molecules which are the important constituents of most of the biologically active molecules, agrochemicals, etc. These methods offer an alternative to the separate steps of prefunctionalization and defunctionalization that have traditionally been part of the synthetic design. Therefore, in view of step and atom economies, direct utilization of C-H and X-H bonds without preactivation has gained enormous attention
