Issue 7, 2017

Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes

Abstract

Safe- and convenient-to-handle surrogates of hazardous chemicals are always in demand. Recently introduced cyclohexa-1,4-dienes with adequate substitution fulfil this role as El+/H equivalents in B(C6F5)3-catalysed transfer reactions of El–H to π- and σ-donors (C[double bond, length as m-dash]C/C[triple bond, length as m-dash]C and C[double bond, length as m-dash]O/C[double bond, length as m-dash]N). Surrogates of Si–H/Ge–H, H–H and even C–H bonds have been designed and successfully applied to ionic transfer hydrosilylation/hydrogermylation, hydrogenation and hydro-tert-butylation, respectively. These processes and their basic principles are summarised in this Minireview. The similarities and differences between these transfer reactions as well as the challenges associated with these transformations are discussed.

Graphical abstract: Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes

Article information

Article type
Minireview
Submitted
13 Apr 2017
Accepted
20 May 2017
First published
24 May 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2017,8, 4688-4695

Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes

S. Keess and M. Oestreich, Chem. Sci., 2017, 8, 4688 DOI: 10.1039/C7SC01657C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements