Statements (49)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chemical reaction
|
| gptkbp:application |
synthesis of agrochemicals
synthesis of natural products synthesis of polymers |
| gptkbp:awards |
gptkb:Akira_Suzuki
|
| gptkbp:base |
sodium hydroxide
potassium carbonate |
| gptkbp:chemicalFormula |
oxidative addition
reductive elimination transmetalation |
| gptkbp:climate |
room temperature to elevated temperatures
|
| gptkbp:collaborations |
gptkb:Richard_F._Heck
gptkb:Ei-ichi_Negishi |
| gptkbp:condition |
base required
|
| gptkbp:dissolved |
ethanol
water toluene |
| gptkbp:firstPublished |
1979
|
| gptkbp:hasDepartment |
requires anhydrous conditions
sensitive to functional groups |
| https://www.w3.org/2000/01/rdf-schema#label |
Suzuki coupling
|
| gptkbp:industry |
widely used in agrochemicals
widely used in materials science widely used in pharmaceuticals |
| gptkbp:ingredients |
aryl halides
organoboranes |
| gptkbp:involves |
cross-coupling reaction
|
| gptkbp:is_used_in |
material science
pharmaceutical development |
| gptkbp:judgingCriteria |
high regioselectivity
high stereoselectivity |
| gptkbp:notableWork |
gptkb:Nobel_Prize_in_Chemistry_2010
|
| gptkbp:produces |
gptkb:Akira_Suzuki
generally high yields |
| gptkbp:products |
biaryl compounds
|
| gptkbp:related_to |
gptkb:Negishi_coupling
Heck reaction Stille_coupling |
| gptkbp:research_focus |
developing greener methods
expanding substrate scope improving catalyst efficiency |
| gptkbp:responseTime |
typically short reaction times
|
| gptkbp:safety |
handling of organoboranes
handling of palladium compounds |
| gptkbp:suitableFor |
organic synthesis
|
| gptkbp:uses |
palladium catalyst
|
| gptkbp:was_a_catalyst_for |
Palladium nanoparticles
Palladium(0) complexes Palladium(II) complexes |