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The New England Journal of Medicine, ISSN 0028-4793, 06/2017, Volume 376, Issue 24, pp. 2388 - 2389
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 02/2018, Volume 57, Issue 6, pp. 1458 - 1473
Solid magnesium hydride [MgH2]∞ has been pursued as a potential hydrogen‐storage material. Organic chemists were rather interested in soluble magnesium hydride... 
magnesium | molecular hydrides | clusters | hydrogen storage | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Hydrogen | Chemical properties | Hydrogen storage | Reagents | Chemists | Chemical bonds | Hydrides | Magnesium | Catalysis | Atomic structure | Chemical synthesis | Hydrogen ion concentration | Structural analysis
Journal Article
Journal of the American Heart Association, ISSN 2047-9980, 07/2019, Volume 8, Issue 14, pp. e013361 - e013361
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 2018, Volume 54, Issue 22, pp. 2701 - 2714
The mono(amido) triamine macrocyclic ligand Me TACD [(Me TACD)H = 1,4,7-trimethyl-1,4,7,10-tetraazacyclododecane] is a versatile supporting ligand for a... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Ligands | Amides | Transition metals | Coordination compounds | Electropositivity
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2018, Volume 57, Issue 31, pp. 9590 - 9602
The application of solid calcium hydride CaH2 has been mostly confined to its use as a desiccant, although its catalytic activity has long been known. Since... 
H2 activation | hydrides | catalysis | reactivity | calcium | activation | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Reviews | Calcium | Desiccants | Metal compounds | Calcium compounds | Catalytic activity | Hydrides | Catalysis | Chemical synthesis | Molecular chains
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2016, Volume 55, Issue 42, pp. 13326 - 13329
Triphenylborane (BPh3) was found to catalyze the reduction of tertiary amides with hydrosilanes to give amines under mild condition with high chemoselectivity... 
hydrosilylation | chemoselectivity | triphenylborane | amide reduction | Schiff bases | Cytokinins | Amides | Amines | Reduction | Ketones | Imines | Esters | Hydrosilylation
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 03/2012, Volume 59, Issue 13, pp. 1200 - 1254
Journal Article