Corey– Ziegler– Hoffmann reaction
GPTKB entity
Statements (53)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:chemical_compound
|
| gptkbp:bfsLayer |
5
|
| gptkbp:bfsParent |
gptkb:Elias_James_Corey
gptkb:E._J._Corey |
| gptkbp:applies_to |
pharmaceutical chemistry
ketones chemical industry |
| gptkbp:can_lead_to |
new carbon-carbon bonds
|
| gptkbp:developed_by |
1970s
|
| https://www.w3.org/2000/01/rdf-schema#label |
Corey– Ziegler– Hoffmann reaction
|
| gptkbp:ingredients |
gptkb:sodium_bromide
gptkb:sodium_hypochlorite acetic acid |
| gptkbp:involves |
oxidation
|
| gptkbp:is_associated_with |
E. J. Corey’s work
|
| gptkbp:is_considered |
a key reaction in organic synthesis
a versatile reaction a foundational reaction |
| gptkbp:is_documented_in |
gptkb:literary_work
|
| gptkbp:is_explored_in |
research studies
new applications |
| gptkbp:is_influenced_by |
reaction conditions
|
| gptkbp:is_noted_for |
selectivity
its selectivity and efficiency |
| gptkbp:is_optimized_for |
yield
|
| gptkbp:is_part_of |
organic chemistry
reaction mechanisms reaction pathways synthetic methodology |
| gptkbp:is_recognized_for |
its efficiency
|
| gptkbp:is_related_to |
Wittig reaction
oxidative cleavage functionalization of hydrocarbons |
| gptkbp:is_studied_in |
mechanistic chemistry
mechanistic insights |
| gptkbp:is_used_by |
aldehydes from alcohols
|
| gptkbp:is_used_for |
functional group transformations
convert alcohols to aldehydes |
| gptkbp:is_used_in |
synthesis of complex molecules
synthesis of natural products synthesis of intermediates |
| gptkbp:is_utilized_in |
gptkb:academic_research
synthesis of complex structures |
| gptkbp:named_after |
gptkb:E._J._Corey
gptkb:H._Ziegler gptkb:R._Hoffmann |
| gptkbp:performed_by |
various substrates
|
| gptkbp:produced_by |
aldehydes
|
| gptkbp:significance |
total synthesis
|
| gptkbp:training |
organic chemistry courses
|
| gptkbp:type |
organic synthesis
|
| gptkbp:uses |
gptkb:lithium_diisopropylamide
|
| gptkbp:was_a_catalyst_for |
copper salts
|