Corey–Mitsunobu reaction
GPTKB entity
Statements (46)
Predicate | Object |
---|---|
gptkbp:instanceOf |
chemical reaction
|
gptkbp:application |
synthesis of amines
synthesis of esters synthesis of ethers synthesis of thioethers |
gptkbp:developedBy |
gptkb:E._J._Corey
T. Mitsunobu |
gptkbp:field |
materials science
pharmaceutical chemistry medicinal chemistry polymer chemistry |
gptkbp:gameMechanics |
formation of an intermediate
involves inversion of configuration |
gptkbp:hasDepartment |
requires excess reagents
sensitive to sterics side reactions possible |
gptkbp:historicalSignificance |
important in synthetic organic chemistry
contributed to the development of new methodologies recognized_in_Nobel_Prize-winning_work |
https://www.w3.org/2000/01/rdf-schema#label |
Corey–Mitsunobu reaction
|
gptkbp:interactsWith |
depends on substrate
high yields possible optimization required |
gptkbp:internationalClassification |
temperature control
anhydrous conditions non-aqueous solvents |
gptkbp:involves |
azodicarboxylates
phosphine_reagents |
gptkbp:isPortrayedBy |
1981
|
gptkbp:namedAfter |
gptkb:E._J._Corey
T. Mitsunobu |
gptkbp:produces |
alkylated products
|
gptkbp:relatedTo |
organic synthesis
functional group transformations alkylation reactions Mitsunobu_reaction |
gptkbp:requires |
base
|
gptkbp:safetyFeatures |
proper ventilation required
flammable solvents toxic_reagents |
gptkbp:supplyChain |
carboxylic acid
phosphine oxide |
gptkbp:type |
nucleophilic substitution
|
gptkbp:usedFor |
conversion of alcohols to other functional groups
|
gptkbp:was_a_catalyst_for |
triphenylphosphine
diethyl azodicarboxylate |