Silylium Ions: From Elusive Reactive Intermediates to Potent Catalysts
HFT Klare, L Albers, L Süsse, S Keess… - Chemical …, 2021 - ACS Publications
The history of silyl cations has all the makings of a drama but with a happy ending. Being
considered reactive intermediates impossible to isolate in the condensed phase for …
considered reactive intermediates impossible to isolate in the condensed phase for …
Synthesis and glycosidation of anomeric halides: evolution from early studies to modern methods of the 21st century
Y Singh, SA Geringer, AV Demchenko - Chemical reviews, 2022 - ACS Publications
Advances in synthetic carbohydrate chemistry have dramatically improved access to
common glycans. However, many novel methods still fail to adequately address challenges …
common glycans. However, many novel methods still fail to adequately address challenges …
Functionalization of fluorinated molecules by transition-metal-mediated C–F bond activation to access fluorinated building blocks
T Ahrens, J Kohlmann, M Ahrens, T Braun - Chemical Reviews, 2015 - ACS Publications
Fluorinated organic compounds increasingly gain importance in numerous areas of
chemistry and everyday life. Building blocks which contain fluorinated entities are of high …
chemistry and everyday life. Building blocks which contain fluorinated entities are of high …
CF bond activation under transition-metal-free conditions
The unique properties of fluorine-containing organic compounds make fluorine substitution
attractive for the development of pharmaceuticals and various specialty materials, which …
attractive for the development of pharmaceuticals and various specialty materials, which …
A unified survey of Si–H and H–H bond activation catalysed by electron-deficient boranes
M Oestreich, J Hermeke, J Mohr - Chemical Society Reviews, 2015 - pubs.rsc.org
The bond activation chemistry of B (C6F5) 3 and related electron-deficient boranes is
currently experiencing a renaissance due to the fascinating development of frustrated Lewis …
currently experiencing a renaissance due to the fascinating development of frustrated Lewis …
Phosphorus Lewis acids: emerging reactivity and applications in catalysis
JM Bayne, DW Stephan - Chemical Society Reviews, 2016 - pubs.rsc.org
Part of the renaissance in main group chemistry has been a result of the focus on reactivity.
This has led to the development of applications in stoichiometric reactivity and catalysis. In …
This has led to the development of applications in stoichiometric reactivity and catalysis. In …
Main-group Lewis acids for C–F bond activation
T Stahl, HFT Klare, M Oestreich - Acs Catalysis, 2013 - ACS Publications
The significant benefits of fluorinated compounds have inspired the development of diverse
techniques for the activation and subsequent (de) functionalization of rather inert C–F …
techniques for the activation and subsequent (de) functionalization of rather inert C–F …
Tris(ortho‐carboranyl)borane: An Isolable, Halogen‐Free, Lewis Superacid
The synthesis of tris (ortho‐carboranyl) borane (BoCb3), a single site neutral Lewis
superacid, in one pot from commercially available materials is achieved. The high fluoride …
superacid, in one pot from commercially available materials is achieved. The high fluoride …
Synthesis of fluorinated building blocks by transition‐metal‐mediated hydrodefluorination reactions
MF Kuehnel, D Lentz, T Braun - … Chemie International Edition, 2013 - Wiley Online Library
The activation and functionalization of carbon–fluorine bonds can be considered as a major
challenge in organometallic chemistry. The growing demand for means to introduce fluorine …
challenge in organometallic chemistry. The growing demand for means to introduce fluorine …
Lewis acidity of organofluorophosphonium salts: hydrodefluorination by a saturated acceptor
Prototypical Lewis acids, such as boranes, derive their reactivity from electronic
unsaturation. Here, we report the Lewis acidity and catalytic application of electronically …
unsaturation. Here, we report the Lewis acidity and catalytic application of electronically …