Expanding the Boundaries of Water-Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls

2017 ◽  
Vol 129 (32) ◽  
pp. 9640-9644 ◽  
Author(s):  
Éva Dorkó ◽  
Márk Szabó ◽  
Bianka Kótai ◽  
Imre Pápai ◽  
Attila Domján ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Reductive Amination ◽  
Frustrated Lewis Pair

scholarly journals Expanding the Boundaries of Water-Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls

2017 ◽  
Vol 56 (32) ◽  
pp. 9512-9516 ◽  
Author(s):  
Éva Dorkó ◽  
Márk Szabó ◽  
Bianka Kótai ◽  
Imre Pápai ◽  
Attila Domján ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Reductive Amination ◽  
Frustrated Lewis Pair

Living polymerization of naturally renewable butyrolactone-based vinylidenes mediated by a frustrated Lewis pair

2021 ◽  
Vol 12 (38) ◽  
pp. 5548-5555
Author(s):  
Yun Bai ◽  
Huaiyu Wang ◽  
Jianghua He ◽  
Yuetao Zhang
Keyword(s):  
Lewis Acid ◽  
Living Polymerization ◽  
Controlled Polymerization ◽  
Frustrated Lewis Pair

The frustrated Lewis pair composed of an organophosphorus(iii) superbase and a bulky organoaluminum Lewis acid promoted the living/controlled polymerization of naturally renewable butyrolactone-based vinylidenes.

Developing carbon Lewis base/boron Lewis acid frustrated Lewis pair chemistry derived from conjugated dienamines

Tetrahedron ◽  
2019 ◽  
Vol 75 (5) ◽  
pp. 571-579 ◽  
Author(s):  
Jennifer Möricke ◽  
Florian Rehwinkel ◽  
Tobias Danelzik ◽  
Constantin G. Daniliuc ◽  
Birgit Wibbeling ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Lewis Base ◽  
Frustrated Lewis Pair

Intermolecular Redox-Neutral Amine C−H Functionalization Induced by the Strong Boron Lewis Acid B(C6 F5 )3 in the Frustrated Lewis Pair Regime

2017 ◽  
Vol 23 (19) ◽  
pp. 4723-4729 ◽  
Author(s):  
Guo-Qiang Chen ◽  
Gerald Kehr ◽  
Constantin G. Daniliuc ◽  
Markus Bursch ◽  
Stefan Grimme ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Frustrated Lewis Pair

scholarly journals Exploiting the Electronic Tuneability of Carboranes as Supports for Frustrated Lewis Pairs

Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3099 ◽  
Author(s):  
Amanda Benton ◽  
Zachariah Copeland ◽  
Stephen M. Mansell ◽  
Georgina M. Rosair ◽  
Alan J. Welch
Keyword(s):  
Lewis Acid ◽  
Michael Addition ◽  
Coupling Constants ◽  
Frustrated Lewis Pairs ◽  
Acid Component ◽  
Frustrated Lewis Pair ◽  
Lewis Pairs

The first example of a carborane with a catecholborolyl substituent, [1-Bcat-2-Ph-closo-1,2-C2B10H10] (1), has been prepared and characterized and shown to act as the Lewis acid component of an intermolecular frustrated Lewis pair in catalyzing a Michael addition. In combination with B(C6F5)3 the C-carboranylphosphine [1-PPh2-closo-1,2-C2B10H11] (IVa) is found to be comparable with PPh2(C6F5) in its ability to catalyze hydrosilylation, whilst the more strongly basic B-carboranylphosphine [9-PPh2-closo-1,7-C2B10H11] (V) is less effective and the very weakly basic species [μ-2,2ʹ-PPh-{1-(1ʹ-1ʹ,2ʹ-closo-C2B10H10)-1,2-closo-C2B10H10}] (IX) is completely ineffective. Base strengths are rank-ordered via measurement of the 1J 31P-77Se coupling constants of the phosphineselenides [1-SePPh2-closo-1,2-C2B10H11] (2), [9-SePPh2-closo-1,7-C2B10H11] (3), and [SePPh2(C6F5)] (4).

scholarly journals Direct Reductive Amination of Carbonyl Compounds Catalyzed by a Moisture Tolerant Tin(IV) Lewis Acid

2018 ◽  
Vol 360 (6) ◽  
pp. 1066-1071 ◽  
Author(s):  
Joshua S. Sapsford ◽  
Daniel J. Scott ◽  
Nathan J. Allcock ◽  
Matthew J. Fuchter ◽  
Christopher J. Tighe ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Carbonyl Compounds ◽  
Reductive Amination

Gold catalyzed hydrogenations of small imines and nitriles: enhanced reactivity of Au surface toward H2via collaboration with a Lewis base

2014 ◽  
Vol 5 (3) ◽  
pp. 1082-1090 ◽  
Author(s):  
Gang Lu ◽  
Peng Zhang ◽  
Dongqing Sun ◽  
Lei Wang ◽  
Kebin Zhou ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Lewis Base ◽  
Frustrated Lewis Pair

Au (111) surface can serve as a Lewis acid to couple with a Lewis base (e.g. imine or nitrile) to form the Au-coupled FLP (frustrated Lewis pair, left) which can cleave H2, further achieving hydrogenation of small imines and nitriles.

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