Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-6837
Main Title: Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
Author(s): Keess, Sebastian
Oestreich, Martin
Type: Article
Language Code: en
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.
URI: https://depositonce.tu-berlin.de//handle/11303/7647
http://dx.doi.org/10.14279/depositonce-6837
Issue Date: 2017
Date Available: 19-Apr-2018
DDC Class: 540 Chemie und zugeordnete Wissenschaften
Sponsor/Funder: DFG, EXC 314, Unifying Concepts in Catalysis
DFG, Oe 249/11-1, 3-Silylierte Cyclohexa-1,4-diene als Surrogate für gasförmige und gesundheitsschädliche Hydrosilane in der Lewis-Säure-Katalyse
License: https://creativecommons.org/licenses/by/3.0/
Journal Title: Chemical Science
Publisher: Royal Society of Chemistry (RSC)
Publisher Place: Cambridge
Volume: 8
Issue: 7
Publisher DOI: 10.1039/c7sc01657c
Page Start: 4688
Page End: 4695
EISSN: 2041-6539
ISSN: 2041-6520
Appears in Collections:FG Organische Chemie / Synthese und Katalyse » Publications

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