Results 161 to 170 of about 5,572 (222)

Electrifying Hydroformylation Catalysts Exposes Voltage-Driven C-C Bond Formation. [PDF]

open access: yesJ Am Chem Soc
Zeng JS   +6 more
europepmc   +1 more source

Electrolyte-Guided Selectivity Unlocks Pathway Control in Electrochemical Olefin Functionalization. [PDF]

open access: yesJ Am Chem Soc
Gordon-Levitan D   +11 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

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Applied Hydroformylation

Chemical Reviews, 2012
Robert Franke   +2 more
exaly   +3 more sources

Hydroformylation

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Klaus-Diether Wiese, Dietmar Obst
openaire   +2 more sources

Fluorous Hydroformylation

2011
The application of fluorous phosphine-modified catalysts for the hydroformylation of olefins is reviewed.
Xi, Zhao   +3 more
openaire   +2 more sources

Asymmetric Hydroformylation

2013
Rhodium is currently the metal of choice to achieve high enantioselectivities in the hydroformylation of a relatively wide variety of alkene substrates. The elucidation of the different steps of the catalytic cycle and the characterization of the resting state, together with the discovery of several types of ligands that are able to provide high ...
Bernabé F, Perandones   +2 more
openaire   +2 more sources

The Retro‐Hydroformylation Reaction

Angewandte Chemie International Edition, 2015
AbstractHydroformylation, a reaction that adds carbon monoxide and dihydrogen across an unsaturated carbon–carbon multiple bond, has been widely employed in the chemical industry since its discovery in 1938. In contrast, the reverse reaction, retro‐hydroformylation, has seldom been studied.
Shuhei, Kusumoto   +2 more
openaire   +2 more sources

Hydroformylation of [1-14C]propene

Journal of the Chemical Society, Chemical Communications, 1976
The hydroformylation of [1-14C]propene under high CO and H2 pressure in the presence of Co2(CO)8 gave [214C]-n-butanal (48%), [4-14C]-n-butanal (32%), and 2-methyl[3-14C]propanal (20%).
PIACENTI, FRANCO   +4 more
openaire   +3 more sources

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