scispace - formally typeset
Journal ArticleDOI

Symmetrical and unsymmetrical 2,6-dialkyl-1,1′-biaryls by combined catalysis of aromatic alkylation via palladacycles and Suzuki-type coupling

Marta Catellani, +2 more
- 01 Jan 2000 - 
- Iss: 2, pp 157-158
Reads0
Chats0
TLDR
In this article, the title compounds are made readily accessible by a catalytic procedure, occurring under mild conditions, based on palladium-mediated ortho alkylation of aromatic iodides with alkyl bromides followed by reaction with arylboronic acids.
About
This article is published in Chemical Communications.The article was published on 2000-01-01. It has received 88 citations till now. The article focuses on the topics: Alkylation & Catellani reaction.

read more

Citations
More filters
Journal ArticleDOI

Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: mechanism and scope.

TL;DR: This review summarizes the development and scope of carboxylates as cocatalysts in transition-metal-catalyzed C-H functionalizations until autumn 2010 and proposes new acronyms, such as CMD (concerted metalationdeprotonation), IES (internal electrophilic substitution), or AMLA (ambiphilic metal ligand activation), which describe related mechanisms.
Journal ArticleDOI

Towards mild metal-catalyzed C–H bond activation

TL;DR: This critical review summarizes and discusses endeavours towards the development of mild C-H activation methods and wishes to trigger more research towards this goal.
Journal ArticleDOI

Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions.

TL;DR: This Minireview summarizes selected examples of the use of secondary alkyl halides as electrophiles in cross-coupling reactions, with emphasis on the transition metals employed, the mechanistic pathways involved, and implications in terms of the stereochemical outcome of reactions.
Journal ArticleDOI

Organopalladium(IV) chemistry

TL;DR: The stoichiometric reactions of Pd(IV) complexes are described and their potential mechanism in catalytic reactions is discussed, leading to the design and development of novel reactions that could not be accessed by traditional Pd (0)/Pd(II) chemistry.
Related Papers (5)