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Palladium And Nickel Catalyzed Transformations Forming Functionalized Heterocycles 1st Ed Hyung Yoon

  • SKU: BELL-22501966
Palladium And Nickel Catalyzed Transformations Forming Functionalized Heterocycles 1st Ed Hyung Yoon
$ 31.00 $ 45.00 (-31%)

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Palladium And Nickel Catalyzed Transformations Forming Functionalized Heterocycles 1st Ed Hyung Yoon instant download after payment.

Publisher: Springer International Publishing;Springer
File Extension: PDF
File size: 16.28 MB
Author: Hyung Yoon
ISBN: 9783030540760, 9783030540777, 3030540766, 3030540774
Language: English
Year: 2020
Edition: 1st ed.

Product desciption

Palladium And Nickel Catalyzed Transformations Forming Functionalized Heterocycles 1st Ed Hyung Yoon by Hyung Yoon 9783030540760, 9783030540777, 3030540766, 3030540774 instant download after payment.

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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