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2009, 1st ed., ISBN 9780470033944, xix, 587
Exploring the importance of Richard F. Heck’s carbon coupling reaction, this book highlights the subject of the 2010 Nobel Prize in Chemistry for... 
Palladium catalysts | Heck reaction | Synthesis | Organic compounds | Chemistry | SCIENCE | Physical & Theoretical
Book
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2016, Volume 55, Issue 2, pp. 494 - 499
Transfer hydrogenation is without question a common technology in industry and academia. Unlike its countless varieties, conceptually related transfer... 
hydrosilylation | cations | silane transfer | cyclohexa‐1,4‐dienes | radicals | cyclohexa-1,4-dienes | SILYLATED CYCLOHEXADIENES | HYDROGENATION | REAGENTS | MECHANISM | FRUSTRATED LEWIS-PAIR | CHEMISTRY, MULTIDISCIPLINARY | H BOND ACTIVATION | SI-H | CHEMISTRY | HYDROSILATION | B(C6F5)-CATALYZED HYDROSILYLATION | Silane | Silicon | Hydrosilylation | Hydrogenation | Fission | Intermediates
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2014, Volume 53, Issue 9, pp. 2282 - 2285
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2008, Volume 47, Issue 32, pp. 5997 - 6000
Just ask silicon: An experimentally straightforward yet effective Walden‐type analysis showcases the usefulness of silanes with a stereogenic silicon center as... 
hydrosilylation | Lewis acids | reaction mechanisms | silicon | nucleophilic substitution | Hydrosilylation | Silicon | Nucleophilic substitution | Reaction mechanisms
Journal Article
Nature Chemistry, ISSN 1755-4330, 10/2015, Volume 7, Issue 10, pp. 816 - 822
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2005, Volume 44, Issue 16, pp. 2324 - 2327
Mission possible: Today, catalytic asymmetric variants of nearly all fundamental bond‐forming reactions are known, yet catalyst‐controlled enantioselective... 
Lewis acids | halogenation | asymmetric catalysis | homogeneous catalysis | carbonyl compounds | Carbonyl compounds | Asymmetric catalysis | Homogeneous catalysis | Halogenation
Journal Article
11/2013, ISBN 3527655581, Volume 3, 1
This three volume book is the follow-up handbook to the bestselling volume "Metal-Catalyzed Cross-Coupling Reactions", the definitive reference in the field.... 
Metal catalysts | Organic compounds
Book
Angewandte Chemie - International Edition, ISSN 1433-7851, 08/2015, Volume 54, Issue 35, pp. 10276 - 10279
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2013, Volume 52, Issue 45, pp. 11905 - 11907
Set Me3SiH free! The strong Lewis acid B(C6F5)3 catalyzes the release of hydrosilanes from 3‐silylated cyclohexa‐1,4‐dienes with concomitant formation of... 
boranes | hydrosilylation | Lewis acids | silane transfer | SiH bond activation | Si-H bond activation
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 05/2013, Volume 52, Issue 20, pp. 5216 - 5218
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 1, pp. 52 - 59
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2017, Volume 56, Issue 38, pp. 11649 - 11652
A decarboxylative silylation of aliphatic N‐hydroxyphthalimide (NHPI) esters using Si−B reagents as silicon pronucleophiles is reported. This C(sp3)−Si... 
cross-coupling | radical reactions | copper | decarboxylation | silicon | ACTIVATION | VISIBLE-LIGHT PHOTOCATALYSIS | NUCLEOPHILIC-SUBSTITUTION | BOND FORMATION | QUATERNARY CARBONS | SILICON NUCLEOPHILES | CHEMISTRY, MULTIDISCIPLINARY | NICKEL | ESTERS | ALKYL ELECTROPHILES | BORYLATION | Copper | Esters | Couplings | Cross coupling | Amines | Reagents | Amino acids | Silicon | Carboxylic acids | Substrates | Aliphatic compounds
Journal Article
Organic Letters, ISSN 1523-7060, 05/2016, Volume 18, Issue 10, pp. 2463 - 2466
Cyclohexa-1,4-dienes are introduced to Brønsted acid-catalyzed transfer hydrogenation as an alternative to the widely used Hantzsch dihydropyridines. While... 
Journal Article
Synlett, ISSN 0936-5214, 11/2017, Volume 28, Issue 18, pp. 2394 - 2395
Martin Oestreich is Professor of Organic Chemistry at the Technische Universität Berlin. His appointment was supported by the Einstein Foundation Berlin. He... 
cluster | H BOND ACTIVATION | ALCOHOLS | TRANSFER HYDROSILYLATION | REDUCTION | SI-H | CHEMISTRY, ORGANIC | COPPER | ELECTROPHILES | SILYLATION
Journal Article
Organic Letters, ISSN 1523-7060, 04/2017, Volume 19, Issue 7, pp. 1898 - 1901
Various cyclohexa-2,5-dien-1-yl-substituted germanes are shown to serve as easy-to-handle surrogates of hydrogermanes, including gaseous MeGeH3 and Me2GeH2.... 
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2014, Volume 53, Issue 48, pp. 13278 - 13281
The hydrogenation of oximes and oxime ethers is usually hampered by NO bond cleavage, hence affording amines rather than hydroxylamines. The boron Lewis acid... 
Lewis acids | homogeneous catalysis | reduction | boron | hydrogenation | Boron | Reduction | Hydrogenation | Homogeneous catalysis
Journal Article
NATURE CHEMISTRY, ISSN 1755-4330, 10/2015, Volume 7, Issue 10, pp. 816 - 822
Monosilane (SiH4) is far less well behaved than its carbon analogue methane (CH4). It is a colourless gas that is industrially relevant as a source of... 
SILANE EXPLOSION | THIN-FILMS | MONOSILANE | ACTIVATION | CHEMICAL-VAPOR-DEPOSITION | SILICON NANOWIRES | OLEFINS | CHEMISTRY, MULTIDISCIPLINARY | SILYLATION | MONOLAYERS | B(C6F5)-CATALYZED HYDROSILYLATION | Lewis acid | Methane | Organic chemistry | Transition metals | Hydrogen bonds | Silicon | Hydrogen atoms | Hydrosilylation
Journal Article
Synthesis, ISSN 0039-7881, 10/2017, Volume 49, Issue 20, pp. 4698 - 4702
Abstract B(C 6 F 5 ) 3 is shown to catalyze the deoxygenation of sulfoxides and sulfones to the corresponding sulfides with Et 3 SiH as the stoichiometric... 
paper | Lewis acids | silicon | reduction | boron | Si-H activation
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2018, Volume 24, Issue 21, pp. 5613 - 5622
A detailed experimental analysis of the 1,4‐selective reduction of pyridine with hydrosilanes catalyzed by a coordinatively unsaturated RuII thiolate complex... 
hydrosilylation | metal hydrides | silylium ions | pyridinium ions | cooperative catalysis | Alkaloids | Pyridine | Catalysis | Analysis | Pyridines | Reduction | Transformation | Cations | Hydrides | Hydrosilylation | Dihydropyridine | Chemical synthesis | Intermediates
Journal Article