Negishi reaction

GPTKB entity

Statements (59)
Predicate Object
gptkbp:instanceOf chemical reaction
gptkbp:appliesTo heteroaryl compounds
synthesis of complex organic molecules
gptkbp:can_be natural products
mild conditions
aryl halides with aliphatic zinc reagents
gptkbp:enables the discovery of new materials.
the synthesis of challenging targets
gptkbp:enhances synthetic routes
the efficiency of chemical processes
gptkbp:facilitates palladium catalysts
the development of new drugs
the formation of complex structures
gptkbp:generator bioactive compounds
diverse chemical libraries
https://www.w3.org/2000/01/rdf-schema#label Negishi reaction
gptkbp:improves the sustainability of chemical synthesis
yield of products
gptkbp:includes alkyl halides
gptkbp:involves cross-coupling of organozinc reagents
gptkbp:is_a metal-catalyzed coupling reaction
gptkbp:is_a_subject_of modern organic chemistry
gptkbp:is_a_time_for synthesizing biaryl compounds
gptkbp:is_a_tool_for carbon-carbon bond formation
gptkbp:is_essential_for forming new carbon-carbon bonds
gptkbp:is_used_in material science
pharmaceutical chemistry
the synthesis of polymers
the production of agrochemicals
Stille_reaction
gptkbp:previousName gptkb:Akira_Negishi
gptkbp:produces the 1970s
fine chemicals
stereocenters
carbon-carbon bonds
gptkbp:reduces side reactions
gptkbp:relatedTo Suzuki_reaction
gptkbp:requires an inert atmosphere
gptkbp:suitableFor organic synthesis
gptkbp:uses transition metal catalysts
gptkbp:was_a_catalyst_for industrial applications
new synthetic methodologies
pharmaceutical intermediates
specific substrates
gptkbp:was_a_response_to reaction kinetics
reaction mechanisms
reaction rates
organometallic chemistry
catalyst efficiency
the development of new materials
high regioselectivity
other coupling reactions
functionalized materials
access to novel compounds
functionalized organic molecules
new chemical space
selective functionalization
the modification of existing compounds
complex_molecular_architectures