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Chemistry – A European Journal, ISSN 0947-6539, 12/2018, Volume 24, Issue 67, pp. 17823 - 17831
Journal Article
Journal Article
Angewandte Chemie International Edition, ISSN 1521-3773, 2009, Volume 48, Issue 36, pp. 6643 - 6646
Frustrated Lewis pairs comprising phosphine and borane react to reversibly bind and release CO2, offering a rare example of metal-free CO2 sequestration. The... 
phosphines | boranes | frustrated Lewis pairs | carbon dioxide fixation | Frustrated lewis pairs | Boranes | Carbon dioxide fixation | Phosphines | HETEROLYTIC DIHYDROGEN ACTIVATION | ACID | IMINES | CO2 | FREE CATALYTIC-HYDROGENATION | N-HETEROCYCLIC CARBENES | ZETA-VALENCE QUALITY | BORANE | CHEMISTRY, MULTIDISCIPLINARY | CHEMISTRY | GAUSSIAN-BASIS SETS
Journal Article
Angewandte Chemie International Edition in English, ISSN 1433-7851, 2011, Volume 50, Issue 17, pp. 3925 - 3928
Catch it! Geminal phosphorus/aluminum-based frustrated Lewis pairs (FLPs) are easily obtained by hydroalumination of alkynylphosphines. These FLPs can activate... 
phosphines | density functional calculations | alanes | carbon dioxide fixation | frustrated Lewis pairs
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2010, Volume 49, Issue 49, pp. 9475 - 9478
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2012, Volume 18, Issue 17, pp. 5184 - 5187
Frustrated partners: Based on an initial mechanistic investigation, enantioselective hydrosilylation of various imines was accomplished for the first time by... 
hydrosilylation | asymmetric catalysis | homogeneous catalysis | frustrated Lewis pairs | FREE HYDROGEN ACTIVATION | MECHANISM | IMINES | B(C6F5)-CATALYZED HYDROSILATION | REACTIVITY | BORANE | CHEMISTRY, MULTIDISCIPLINARY | KETONES | CHEMISTRY | BIS(PENTAFLUOROPHENYL)BORANE | Transformations | Hydrosilylation | Imines | Catalysts
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 06/2017, Volume 23, Issue 31, pp. 7422 - 7427
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2014, Volume 53, Issue 42, pp. 11306 - 11309
N‐methylacridinium salts are Lewis acids with high hydride ion affinity but low oxophilicity. The cation forms a Lewis adduct with... 
Lewis acids | silanes | reduction | synthetic methods | frustrated Lewis pairs | Silanes | Frustrated lewis pairs | Reduction | Synthetic methods
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2015, Volume 21, Issue 4, pp. 1454 - 1457
The “η2‐formylborane” moiety formed by CO reduction with HB(C6F5)2 at a P/B frustrated Lewis pair template undergoes a hydroxymethylation reaction at the... 
pyridine | boron | hydroxymethylation | frustrated Lewis pairs | phosphorus | Phosphorus | Boron | Hydroxymethylation | Pyridine | Frustrated Lewis pairs | Frustrated lewis pairs | CHEMISTRY, MULTIDISCIPLINARY | Pyridines | Reduction | Pyrimidines | Pathways
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2012, Volume 51, Issue 40, pp. 10164 - 10168
Weak nucleophiles for strong activation: The reversible activation of dihydrogen by an electron‐deficient phosphine, (C6F5)PPh2, in combination with the Lewis... 
olefin | alkenes | phosphanes | hydrogenation | frustrated Lewis pairs | HETEROLYTIC DIHYDROGEN ACTIVATION | IMINES | HYDROSILYLATION | REACTIVITY | H-2 ACTIVATION | CHEMISTRY, MULTIDISCIPLINARY | REDUCTION | SCALES | CHEMISTRY | NUCLEOPHILICITY | SILYL
Journal Article