Wolfe / Chen Science of Synthesis: Cross Coupling and Heck-Type Reactions Vol. 2

Carbon-Heteroatom Cross Coupling and C-C Cross Coupling of Acidic C-H Nucleophiles
1. Auflage 2014
ISBN: 978-3-13-179071-2
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 744 Seiten, PDF, Format (B × H): 170 mm x 240 mm

In Science of Synthesis: Cross Coupling and Heck-Type Reactions, expert authors present and discuss the best and most reliable methods currently available for the formation of new carbon-carbon and carbon-heteroatom bonds using these reactions, highlighted with representative experimental procedures. Together, the three volumes of Cross Coupling and Heck-Type Reactions provide an extensive overview of the current state of the art in this field of central importance in modern chemistry, and are an invaluable resource for the practicing synthetic organic chemist.

This volume is focused on the formation of carbon-heteroatom bonds and carbon-carbon bonds of acidic C-H nucleophiles. The chapters are intended to provide the reader with a practical guide to the most efficient, reliable, and useful metal-catalyzed cross-coupling reactions that generate C-N, C-P, C-O, C-S, C-B, C-Si, C-CN, and C-F bonds, and C-C bonds adjacent to carbonyl functional groups. The most up-to-date and modern methods are included, including those that facilitate replacement of typically unreactive C-H bonds with carbon-heteroatom bonds.

This volume is part of a 3-volume set:

Cross Coupling and Heck-Type Reactions Workbench Edition

General information about Science of Synthesis

Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Chen, Hao

Wolfe, John

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

2.1 C-N Bond-Forming Reactions
2.1.1 C-N Bond-Forming Reactions of Alkylamines
2.1.1.1 Alkylamines with Aryl and Alkenyl Electrophiles
2.1.1.2 Alkylamines with Hetaryl Electrophiles
2.1.2 C-N Bond-Forming Reactions of Aryl- and Hetarylamines
2.1.2.1 Aryl- and Hetarylamines with Aryl and Alkenyl Electrophiles
2.1.2.2 Aryl- and Hetarylamines with Hetaryl Electrophiles
2.1.3 C-N Bond-Forming Reactions of Hetarenes
2.1.4 C-N Bond-Forming Reactions of Amides and Carbamates
2.1.5 C-N Bond-Forming Reactions of Sulfonamides, Sulfoximides, and Other Nitrogen Nucleophiles
2.1.6 C-N Bond-Forming Reactions of C-H Electrophiles
2.2 C-P Bond-Forming Reactions
2.3 C-O and C-S Bond-Forming Reactions
2.3.1 C-O and C-S Bond-Forming Reactions of C-X Electrophiles
2.3.2 C-O and C-S Bond-Forming Reactions of C—H Electrophiles
2.4 C-B and C-Si Bond-Forming Reactions
2.4.1 C-B and C-Si Bond-Forming Reactions of C-X Electrophiles
2.4.2 C-B and C-Si Bond-Forming Reactions by C-H Functionalization
2.5 C-CN Bond-Forming Reactions
2.6 C-F Bond-Forming Reactions
2.7 C-C Cross-Coupling Reactions of Acidic C-H Nucleophiles
2.7.1 C-C Cross-Coupling Reactions of Acidic C-H Nucleophiles with One Activating Group
2.7.2 C-C Cross-Coupling Reactions of Acidic C-H Nucleophiles with Two Activating Groups