David A. Petrone Petrone Stereoselective Heterocycle Synthesis via Alkene Difunctionalization

Stereoselective Heterocycle Synthesis via Alkene Difunctionalization

von David A. Petrone

Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation

Preis unbekannt

Buch in deiner Nähe kaufen


...oder deine aktuelle Postleitzahl eingeben:
oder

Beschreibung

This book investigates the use of palladium modified by bulky ligands as catalysts for new chemical transformations that rapidly assemble several classes of complex heterocyles. It documents the development of new chemical reactions involving carbon–carbon (C‒C) and carbon–halogen (C‒X) bond formation in the context of alkene difunctionalization and dearomatization reactions. Due to the ubiquity of heterocycles in bioactive natural products and life-improving pharmaceutical treatments, a long-term goal for synthetic organic chemists has been to develop novel and creative heterocycle syntheses that illicit a high degree of product diversity and are characterized by mild reaction conditions and limited waste production. A considerable fraction of leading pharmaceutical drugs contain at least one heterocycle within their chemical structure, and their prevalence in these technologies is strong evidence that the fundamental curiosities of organic chemistry lead to real-world solutions for the health and wellness of the global population.


This book investigates the use of palladium modified by bulky ligands as catalysts for new chemical transformations that rapidly assemble several classes of complex heterocyles. It documents the development of new chemical reactions involving carbon–carbon (C‒C) and carbon–halogen (C‒X) bond formation in the context of alkene difunctionalization and dearomatization reactions. Due to the ubiquity of heterocycles in bioactive natural products and life-improving pharmaceutical treatments, a long-term goal for synthetic organic chemists has been to develop novel and creative heterocycle syntheses that illicit a high degree of product diversity and are characterized by mild reaction conditions and limited waste production. A considerable fraction of leading pharmaceutical drugs contain at least one heterocycle within their chemical structure, and their prevalence in these technologies is strong evidence that the fundamental curiosities of organic chemistry lead to real-world solutions for the health and wellness of the global population.


Nominated as an outstanding Ph.D. thesis by the University of Toronto, Canada Includes extensive background literature on Pd-catalyzed cross-coupling chemistry and catalytic carbon–halogen bond formation Presents clear figures and schematics that provide the reader with an intuitive guide

Autor*in

David A. Petrone

Themen in »Stereoselective Heterocycle Synthesis via Alkene Difunctionalization«

Palladium Catalysis Stereoselective Synthesis Catalyst Development Halogenation Reactions Suzuki Coupling Cyanation Reactions Phosphine Ligands Natural Product Synthesis Reaction Progress Heck Reaction

Stimmen zu »Stereoselective Heterocycle Synthesis via Alkene Difunctionalization«

Details

ISBN: 9783319775074
Verlag: Springer International Publishing
Erscheinung: 02.04.2018

Link teilen


Über buchnah.de | Die Buchhandlungen | Die Verlage | Impressum & Kontakt | Datenschutz | Presse


Auf dieser Seite kannst Du Buchhandlungen in der Nähe finden