Diels–Alder reaction

GPTKB entity

Properties (57)
Predicate Object
gptkbp:instanceOf chemical reaction
gptkbp:can_be thermal conditions
photochemical conditions
gptkbp:established gptkb:Kurt_Alder
gptkb:Otto_Diels
gptkbp:genus in nature
https://www.w3.org/2000/01/rdf-schema#label Diels–Alder reaction
gptkbp:includes substituted dienes
substituted dienophiles
gptkbp:involves diene
dienophile
gptkbp:is_a certain conditions
pericyclic reaction
[4+2] cycloaddition
gptkbp:is_a_source_of steroids
terpenes
alkaloids
polycyclic compounds
gptkbp:is_a_subject_of organic synthesis
gptkbp:is_characterized_by concerted mechanism
gptkbp:is_essential_for materials science
pharmaceutical chemistry
gptkbp:is_used_in natural products
polymers
synthesis of complex organic molecules
gptkbp:leads cis or trans products
gptkbp:mayHave six-membered rings
Lewis_acids
gptkbp:previousName Otto_Diels_and_Kurt_Alder
gptkbp:produces cyclohexene derivative
gptkbp:was_a_response_to used in organic electronics
used in agrochemicals
used in nanotechnology
used in drug discovery
regioselective
used in synthetic biology
used in green chemistry
used in material science
accelerated by catalysts
new sigma bonds
performed in aqueous media
performed in solvent-free conditions
pi bonds
stereoselective
two unsaturated compounds
used in asymmetric synthesis
used in combinatorial chemistry
used in cosmetic chemistry
used in flavor chemistry
used in food chemistry
used in fragrance chemistry
used in medicinal chemistry
used in polymer additives
used in polymer chemistry
used in supramolecular chemistry
used in total synthesis
chemoselective