Continuous flow hydroformylation using supported ionic liquid phase catalysts with carbon dioxide as a carrier.High chemo and regioselective formation of alcohols from the hydrocarbonylation of alkenes using cooperative ligand effects.Continuous flow hydroformylation of alkenes in supercritical fluid-ionic liquid biphasic systems.Continuous flow homogeneous catalysis using supercritical fluids.A single enantiomer (99%) directly from continuous-flow asymmetric hydrogenation.Highly selective formation of linear esters from terminal and internal alkenes catalysed by palladium complexes of bis-(di-tert-butylphosphinomethyl)benzene.Methoxycarbonylation of vinyl acetate catalysed by palladium complexes of bis(ditertiarybutylphosphinomethyl)benzene and related ligands.Homogeneous catalytic hydrogenation of amides to amines.Preparation of phenolic compounds by decarboxylation of hydroxybenzoic acids or desulfonation of hydroxybenzenesulfonic acid, catalysed by electron rich palladium complexes.Novel diazaphospholidine terminated polyhedral oligomeric silsesquioxanes in styrene and vinyl acetate hydroformylation: synthesis and molecular dynamics studies.Hybrid dendritic molecules with confined chromophore architecture to tune fluorescence efficiency.Diphenylphosphine containing macromolecules in the methoxycarbonylation of ethene: the effect of macromolecular architecture on the selectivity of the reaction.Polymer producing palladium complexes of unidentate phosphines in the methoxycarbonylation of ethene.Diazaphospholidine terminated polyhedral oligomeric silsesquioxanes in the hydroformylation of vinyl acetate.Synthesis of functional cubes from octavinylsilsesquioxane (OVS).The methoxycarbonylation of aryl chlorides catalysed by palladium complexes of bis(di-tert-butylphosphinomethyl)benzene.Modelling proposed intermediates in the hydrocarbonylation of alkenes catalysed by rhodium complexes of PBui3 and PPri3.A new route to N-aromatic heterocycles from the hydrogenation of diesters in the presence of anilines.Rhodium catalysed hydroformylation of alkenes using highly fluorophilic phosphines.Highly versatile catalytic hydrogenation of carboxylic and carbonic acid derivatives using a Ru-triphos complex: molecular control over selectivity and substrate scope."Solventless" continuous flow homogeneous hydroformylation of 1-octene.Hydroformylation in fluorous solvents.The design of a continuous reactor for fluorous biphasic reactions under pressure and its use in alkene hydroformylation.A computational study of the methanolysis of palladium-acyl bonds.Ultra-pure organotellurium precursors for the low temperature MOVPE growth of II/VI compound semiconductorsUnusual Stereochemistry in Complexes of the Form [RhH(CO)2(PPri3)2]†The European Chemical Society (EuChemS)The reaction of o-xylylene complexes of ruthenium with alkynes under oxidative conditionsSilsesquioxane dendrimers as catalysts: A bite-sized molecular dynamics studySynthesis and crystal structures of bromo- and ester-functionalised polyhedral silsesquioxanesThe structure of phosphine-functionalised silsesquioxane-based dendrimers: a molecular dynamics studyHydrocarbonylation reactions using alkylphosphine-containing dendrimers based on a polyhedral oligosilsesquioxane corePhosphine containing dendrimers for highly regioselective rhodium catalysed hydroformylation of alkenes: a positive ‘dendritic effect’Formation of acrylic acid derivatives from the reaction of carbon dioxide with ethylene complexes of molybdenum and tungstenContinuous flow asymmetric cyclopropanation reactions using Cu(i) complexes of Pc-L* ligands supported on silica as catalysts with carbon dioxide as a carrierSuper Critical Drying: A New Method for Conserving Waterlogged Archaeological MaterialsComparison between phosphine and NHC-modified Pd catalysts in the telomerization of butadiene with methanol – A kinetic study combined with model-based experimental analysisElectronic Grade Alkyls of Group 12 and 13 ElementsBis(phosphine) derivatives of diaminesThe preparation and complexation of 5,10-bis(diphenylphosphino)phenazine
P50
Q43045711-AA84B6C1-6E23-4643-96BC-86569A2A6D03Q43126970-1731A2D3-766D-4B3D-899E-42480BCD9E8BQ44686018-2C878EA1-95C4-40F7-B129-B6260A1AA9E2Q44770397-0F0C1422-BAE0-4B29-AAE4-DCC25BE9871FQ44917519-5137DCAF-57E2-456A-A33E-285B7BD07F0EQ44996267-711DFD70-2BA5-4D0D-AA20-ACDB9E8F5982Q45279028-4A5BCC4E-56A3-4EEE-AF7D-D19DDD134365Q45712646-3A972784-3F52-4A6B-BC78-976687478A95Q45975459-6F8CD4CF-591A-404B-B32B-BA05918A96A9Q46043395-827B3ED1-5FD2-4DE3-98A7-70072235AEC7Q46050489-61175BB5-2BD6-4C61-86E7-3A410F2EB297Q46094043-A2F518EF-4DCA-480D-A9F6-2B5AAE6258ACQ46155537-871BE60D-91D6-430E-B870-925772AAEC4DQ46198814-D1A29657-9662-42B4-A852-005E7CD395D3Q46224820-E91F990C-24DC-4136-9EB0-7C0057A5820EQ46475168-FDE9D7C3-6380-4105-8E79-BA29212C3883Q46608894-7A404CD0-3D7B-48DA-89F3-4D50844555EDQ46720120-746117E3-2B2F-4A4E-A5C3-9CC17DA41612Q46823401-3AFC568A-D577-4594-A68C-BF5C6E5AF633Q46840739-BA670418-6211-4F6A-AC78-97AEB83A5A35Q46878453-E6D59146-B0A7-48D5-B138-D0F5AC4F456FQ47569404-BC434AAB-52CE-4131-9576-43078768FC0AQ47632419-398BBE04-610D-4055-A458-E0F8DB09C8C0Q51076810-D5FF775E-E1FF-4BFE-BA21-74EC8E50F251Q53938553-30F27134-FA4F-4B29-9292-BE213BFBE694Q56744368-6290B19A-A070-4BC4-84F8-12A514EF91D7Q57169407-18673771-023D-4993-8427-34A166001EEDQ57331191-41D194C7-F985-487D-86CE-5224C03F5C1AQ57385273-12B161BD-6759-40CD-A8D2-6131B1A4D7B7Q57385282-C2C02E4B-DBCD-4D0E-8545-77A0706ABFABQ57385290-63E0C569-5847-4627-B58D-F193EC7D5A48Q57385295-F91698AD-E2E3-4F08-8DC4-51BC3284DDE8Q57385297-FFF351FF-3404-42E9-BEDC-AD911ADB4177Q57405335-446D46F0-3421-471F-B403-AA0ED97683B4Q57600126-6A41F3C6-7FEA-44CC-AB63-DCC6261D223BQ58510486-4D4B615F-299E-46E2-9F46-4A5FB43AF66BQ59020936-A850611F-270E-49E7-BACE-4C93CBDFFF8CQ59344733-F1EFD085-5081-40A6-B6D9-33408D0396BCQ59763213-B8A2CBF4-001E-4191-BC9D-5F3222315421Q59763349-2B0A0AD3-29AE-45D4-9793-59590BD310A0
P50
description
Brits universitair docent (1948-)
@nl
English chemist
@en
chimiste britannique
@fr
englischer Chemiker
@de
name
David J. Cole-Hamilton
@ast
David J. Cole-Hamilton
@ca
David J. Cole-Hamilton
@de
David J. Cole-Hamilton
@en
David J. Cole-Hamilton
@es
David J. Cole-Hamilton
@fr
David J. Cole-Hamilton
@sl
type
label
David J. Cole-Hamilton
@ast
David J. Cole-Hamilton
@ca
David J. Cole-Hamilton
@de
David J. Cole-Hamilton
@en
David J. Cole-Hamilton
@es
David J. Cole-Hamilton
@fr
David J. Cole-Hamilton
@sl
prefLabel
David J. Cole-Hamilton
@ast
David J. Cole-Hamilton
@ca
David J. Cole-Hamilton
@de
David J. Cole-Hamilton
@en
David J. Cole-Hamilton
@es
David J. Cole-Hamilton
@fr
David J. Cole-Hamilton
@sl
P166
P1006
P214
P244
P268
P269
P1006
P1412
P21
P213
0000 0001 1578 0810
P214
P244
P268
P269
P31
P496
0000-0003-4994-8612
P569
1948-05-22T00:00:00Z
P735
P7859
lccn-n88201021