Frustrated Lewis pair chemistry: development and perspectives
DW Stephan, G Erker - Angewandte Chemie International …, 2015 - Wiley Online Library
Abstract Frustrated Lewis pairs (FLPs) are combinations of Lewis acids and Lewis bases in
solution that are deterred from strong adduct formation by steric and/or electronic factors …
solution that are deterred from strong adduct formation by steric and/or electronic factors …
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 …
Chemie frustrierter Lewis‐Paare: Entwicklung und Perspektiven
DW Stephan, G Erker - Angewandte Chemie, 2015 - Wiley Online Library
Abstract Der Begriff “frustrierte Lewis‐Paare”(FLPs) bezeichnet Kombinationen von Lewis‐
Säuren und Lewis‐Basen in Lösung, die aufgrund sterischer oder elektronischer Faktoren …
Säuren und Lewis‐Basen in Lösung, die aufgrund sterischer oder elektronischer Faktoren …
Organoelement chemistry: Promising growth areas and challenges
GA Abakumov, AV Piskunov… - Russian Chemical …, 2018 - iopscience.iop.org
The chemistry of organoelement compounds is now one of the most rapidly developing
fields of research, regarding both fundamental science and solution of applied problems …
fields of research, regarding both fundamental science and solution of applied problems …
Catalytic Dearomatization of N‐Heteroarenes with Silicon and Boron Compounds
Dearomatized N‐heterocycles are an important class of structural motifs for organic
synthesis and chemical biology. The catalytic dearomative reduction of unactivated N …
synthesis and chemical biology. The catalytic dearomative reduction of unactivated N …
Frustrated Lewis pair catalyzed dehydrogenative oxidation of indolines and other heterocycles
AFG Maier, S Tussing, T Schneider… - Angewandte Chemie …, 2016 - Wiley Online Library
An acceptorless dehydrogenation of heterocycles catalyzed by frustrated Lewis pairs (FLPs)
was developed. Oxidation with concomitant liberation of molecular hydrogen proceeded in …
was developed. Oxidation with concomitant liberation of molecular hydrogen proceeded in …
Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations
J Paradies - Accounts of Chemical Research, 2023 - ACS Publications
Conspectus The activation of molecular hydrogen by main-group element catalysts is an
extremely important approach to metal-free hydrogenations. These so-called frustrated …
extremely important approach to metal-free hydrogenations. These so-called frustrated …
Catalytic Access to Bridged Sila-N-heterocycles from Piperidines via Cascade sp3 and sp2 C–Si Bond Formation
Described herein is the development of an unprecedented route to bridged sila-N-
heterocycles via B (C6F5) 3-catalyzed cascade silylation of N-aryl piperidines with …
heterocycles via B (C6F5) 3-catalyzed cascade silylation of N-aryl piperidines with …
Borane‐Catalyzed Tandem Cyclization/Hydrosilylation Towards Enantio‐ and Diastereoselective Construction of trans‐2,3‐Disubstituted‐1,2,3,4 …
Z Luo, Z Li, H Zhao, J Yang, L Xu, M Lei… - Angewandte …, 2023 - Wiley Online Library
Recent years have witnessed marked progress in the efficient synthesis of various
enantioenriched 1, 2, 3, 4‐tetrahydroquinoxalines. However, enantio‐and diastereoselective …
enantioenriched 1, 2, 3, 4‐tetrahydroquinoxalines. However, enantio‐and diastereoselective …
Dehydrocoupling routes to element–element bonds catalysed by main group compounds
RL Melen - Chemical Society Reviews, 2016 - pubs.rsc.org
Dehydrocoupling reactions, ie reactions involving elimination of H2 between two E–H
bonds, provide a clean route to E–E bonds within the main group. The products afforded …
bonds, provide a clean route to E–E bonds within the main group. The products afforded …