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Titlebook: Palladium and Nickel Catalyzed Transformations Forming Functionalized Heterocycles; Hyung Yoon Book 2020 The Editor(s) (if applicable) and

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书目名称Palladium and Nickel Catalyzed Transformations Forming Functionalized Heterocycles
编辑Hyung Yoon
视频video
概述Nominated as an outstanding PhD thesis by the University of Toronto, Ontario, Canada.Describes Pd-catalyzed domino reactions in a concise manner.Provides a general overview of C-H activation.Presents
丛书名称Springer Theses
图书封面Titlebook: Palladium and Nickel Catalyzed Transformations Forming Functionalized Heterocycles;  Hyung Yoon Book 2020 The Editor(s) (if applicable) and
描述.This book presents Pd- and Ni-catalyzed transformations generating functionalized heterocycles. Transition metal catalysis is at the forefront of synthetic organic chemistry since it offers new and powerful methods to forge carbon–carbon bonds in high atom- and step-economy. .In Chapter 1, the author describes a Pd- and Ni-catalyzed cycloisomerization of aryl iodides to alkyl iodides, known as carboiodination. In the context of the Pd-catalyzed variant, the chapter explores the production of enantioenriched carboxamides through diastereoselective Pd-catalyzed carboiodination. It then discusses Ni-catalyzed reactions to generate oxindoles and an enantioselective variant employing a dual ligand system. .Chapter 2 introduces readers to a Pd-catalyzed diastereoselective anion-capture cascade. It also examines diastereoselective Pd-catalyzed aryl cyanation to synthesize alkyl nitriles, a method that generates high yields of borylated chromans as a single diastereomer, andhighlights its synthetic utility.  . .Lastly, Chapter 3 presents a Pd-catalyzed domino process harnessing carbopalladation, C–H activation and π-system insertion (benzynes and alkynes) to generate spirocycles. It also
出版日期Book 2020
关键词Carboiodination; Domino Reaction; C-H Activation; Cyanation; Borylation; Pd-Catalyzed Spirocyclization; Ca
版次1
doihttps://doi.org/10.1007/978-3-030-54077-7
isbn_softcover978-3-030-54079-1
isbn_ebook978-3-030-54077-7Series ISSN 2190-5053 Series E-ISSN 2190-5061
issn_series 2190-5053
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

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