1.12 Intermolecular Radical C—H Functionalization

Author(s):  
M. Bietti ◽  
F. Dénès

AbstractThe generation of carbon-centered radicals via intermolecular hydrogen-atom transfer (HAT) from C—H bonds to an abstracting species (HAT reagent) represents a significant challenge in terms of reactivity, site-selectivity and stereoselectivity. The radical species resulting from such a transfer can then engage in carbon—carbon or carbon—heteroatom bond formation, possibly through the intervention of transition-metal catalysts, leading to a variety of functionalized products. This chapter aims to provide the reader with useful guidelines to understand, predict, and design selective radical transformations based upon initial HAT from a C—H bond coupled to different radical-capture strategies. A selection of examples that illustrate different approaches to implement HAT reactions in synthetically useful procedures are presented.

Author(s):  
Xuchong Tang ◽  
Yingwei Zhao

: Transition-metal-catalyzed C−H bond activation employing a directing group is becoming a powerful tool to access C−C or C−hetero bond formation. Oxygen and nitrogen atoms are commonly applied as the electron donor for these directing groups. In contrast, there are only few studies on sulfur-containing groups, probably due to their toxicity to transition-metal catalysts. Nowadays a large amount of C−H activation reactions directed by sulfur-containing auxiliary groups have been successfully achieved. Because these groups can be facilely removed or modified in situ or in further steps, they are of great value in creative synthetic strategies. This paper reviews recent advances in the studies using thioether, thiol/thiophenol/disulfide, sulfoxide, and thiocarbonyl as directing groups for intermolecular C−H functionalizations as well as intramolecular oxidative annulations.


Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 674
Author(s):  
Lou Rocard ◽  
Donghuang Chen ◽  
Adrien Stadler ◽  
Hailong Zhang ◽  
Richard Gil ◽  
...  

This review summarizes the most noteworthy achievements in the field of C–O and C–N bond formation by hydroalkoxylation and hydroamination reactions on unactivated alkenes (including 1,2- and 1,3-dienes) promoted by earth-abundant 3d transition metal catalysts based on manganese, iron, cobalt, nickel, copper and zinc. The relevant literature from 2012 until early 2021 has been covered.


2020 ◽  
Vol 49 (11) ◽  
pp. 3525-3531
Author(s):  
Ana B. Buades ◽  
Zsolt Kelemen ◽  
Víctor S. Arderiu ◽  
Adnana Zaulet ◽  
Clara Viñas ◽  
...  

An electrophilic substitution on metallacarboranes by using a stabilized carbocation that can be made in situ is reported for the first time.


2019 ◽  
Author(s):  
Shiori Date ◽  
Kensei Hamasaki ◽  
Karen Sunagawa ◽  
Hiroki Koyama ◽  
Chikayoshi Sebe ◽  
...  

<div>We report here a catalytic, Markovnikov selective, and scalable synthetic method for the synthesis of saturated sulfur heterocycles, which are found in the structures of pharmaceuticals and natural products, in one step from an alkenyl thioester. Unlike a potentially labile alkenyl thiol, an alkenyl thioester is stable and easy to prepare. The powerful Co catalysis via a cobalt hydride hydrogen atom transfer and radical-polar crossover mechanism enabled simultaneous cyclization and deprotection. The substrate scope was expanded by the extensive optimization of the reaction conditions and tuning of the thioester unit.</div>


Sign in / Sign up

Export Citation Format

Share Document