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Palladium and nickel catalyzed trans...

Yoon, Hyung.

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Palladium and nickel catalyzed transformations forming functionalized heterocycles

Record Type:	Electronic resources : Monograph/item
Title/Author:	Palladium and nickel catalyzed transformations forming functionalized heterocycles/ by Hyung Yoon.
Author:	Yoon, Hyung.
Published:	Cham :Springer International Publishing : : 2020.,
Description:	xxix, 212 p. :ill., digital ;24 cm.
[NT 15003449]:	Chapter 1. Carbohalogenation Catalyzed by Palladium and Nickel -- Chapter 2. Diastereoselective Pd-Catalyzed Aryl Cyanation and Aryl Borylation -- Chapter 3. Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne/Alkyne Insertion.
Contained By:	Springer Nature eBook
Subject:	Heterocyclic compounds. -
Online resource:	https://doi.org/10.1007/978-3-030-54077-7
ISBN:	9783030540777

Palladium and nickel catalyzed transformations forming functionalized heterocycles
Yoon, Hyung.

Palladium and nickel catalyzed transformations forming functionalized heterocycles[electronic resource] /by Hyung Yoon. - Cham :Springer International Publishing :2020. - xxix, 212 p. :ill., digital ;24 cm. - Springer theses,2190-5053. - Springer theses..

Chapter 1. Carbohalogenation Catalyzed by Palladium and Nickel -- Chapter 2. Diastereoselective Pd-Catalyzed Aryl Cyanation and Aryl Borylation -- Chapter 3. Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne/Alkyne Insertion.

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, and highlights 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 describes the mechanistic studies performed on these reactions.

ISBN: 9783030540777

Standard No.: 10.1007/978-3-030-54077-7doiSubjects--Topical Terms:

621046
Heterocyclic compounds.

LC Class. No.: QD505 / .Y666 2020

Dewey Class. No.: 541.395

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520 $a 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, and highlights 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 describes the mechanistic studies performed on these reactions.
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