FLP catalysis: main group hydrogenations of organic unsaturated substrates
J Lam, KM Szkop, E Mosaferi… - Chemical Society Reviews, 2019 - pubs.rsc.org
This article is focused on recent developments in main group mediated hydrogenation
chemistry and catalysis using “frustrated Lewis pairs”(FLPs). The broading range of …
chemistry and catalysis using “frustrated Lewis pairs”(FLPs). The broading range of …
Metallomimetic chemistry of boron
The study of main-group molecules that behave and react similarly to transition-metal (TM)
complexes has attracted significant interest in recent decades. Most notably, the attractive …
complexes has attracted significant interest in recent decades. Most notably, the attractive …
Diverse uses of the reaction of frustrated Lewis pair (FLP) with hydrogen
DW Stephan - Journal of the American Chemical Society, 2021 - ACS Publications
The articulation of the notion of “frustrated Lewis pairs”(FLPs) emerged from the discovery
that H2 can be reversibly activated by combinations of sterically encumbered main group …
that H2 can be reversibly activated by combinations of sterically encumbered main group …
Introducing Frustrated Lewis Pairs to Metal–Organic Framework for Selective Hydrogenation of N-Heterocycles
ZM Xu, Z Hu, Y Huang, SJ Bao, Z Niu… - Journal of the …, 2023 - ACS Publications
Hydrogenated nitrogen heterocyclic compounds play a critical role in the pharmaceutical,
polymer, and agrochemical industries. Recent studies on partial hydrogenation of nitrogen …
polymer, and agrochemical industries. Recent studies on partial hydrogenation of nitrogen …
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 …
Chiral frustrated Lewis pair@ metal‐organic framework as a new platform for heterogeneous asymmetric hydrogenation
Asymmetric hydrogenation, a seminal strategy for the synthesis of chiral molecules, remains
largely unmet in terms of activation by non‐metal sites of heterogeneous catalysts. Herein …
largely unmet in terms of activation by non‐metal sites of heterogeneous catalysts. Herein …
Halogenated triarylboranes: synthesis, properties and applications in catalysis
JL Carden, A Dasgupta, RL Melen - Chemical Society Reviews, 2020 - pubs.rsc.org
Halogenated triarylboranes (BAr3) have been known for decades, however it has only been
since the surge of interest in main group catalysis that their application as strong Lewis acid …
since the surge of interest in main group catalysis that their application as strong Lewis acid …
Enabling catalytic ketone hydrogenation by frustrated Lewis pairs
T Mahdi, DW Stephan - Journal of the American Chemical Society, 2014 - ACS Publications
Enabling Catalytic Ketone Hydrogenation by Frustrated Lewis Pairs | Journal of the American
Chemical Society ACS ACS Publications C&EN CAS Find my institution Log In Journal of the …
Chemical Society ACS ACS Publications C&EN CAS Find my institution Log In Journal of the …
Metal-Free Heterogeneous Asymmetric Hydrogenation of Olefins Promoted by Chiral Frustrated Lewis Pair Framework
The development of metal-free and recyclable catalysts for significant yet challenging
transformations of naturally abundant feedstocks has long been sought after. In this work, we …
transformations of naturally abundant feedstocks has long been sought after. In this work, we …
Designing effective 'frustrated Lewis pair'hydrogenation catalysts
DJ Scott, MJ Fuchter, AE Ashley - Chemical Society Reviews, 2017 - pubs.rsc.org
The past decade has seen the subject of transition metal-free catalytic hydrogenation
develop incredibly rapidly, transforming from a largely hypothetical possibility to a well …
develop incredibly rapidly, transforming from a largely hypothetical possibility to a well …