Hydroboration (book)
E595506
"Hydroboration" is a seminal chemistry book by Nobel laureate Herbert C. Brown that systematically presents the reactions, mechanisms, and synthetic applications of organoborane chemistry.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Hydroboration (book) canonical | 2 |
How this entity was disambiguated
This entity first appeared as the object of triple T6493423 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
Target entity: Hydroboration (book) Context triple: [Herbert C. Brown, publication, Hydroboration (book)]
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A.
Barton–McCombie deoxygenation
Barton–McCombie deoxygenation is an organic chemistry reaction that converts alcohols into the corresponding hydrocarbons via radical-mediated removal of the hydroxyl group.
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B.
Sharpless aminohydroxylation
Sharpless aminohydroxylation is a stereoselective chemical reaction that converts alkenes into vicinal amino alcohols using a chiral catalyst, widely used in asymmetric synthesis.
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C.
Eschenmoser
Eschenmoser is a Swiss surname most notably associated with Albert Eschenmoser, a prominent organic chemist known for his pioneering work in the synthesis of complex natural products and studies on the origin of life.
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D.
“Superacids”
“Superacids” is a landmark chemistry book by George A. Olah that systematically explores extremely strong acids and their role in stabilizing carbocations and enabling unusual chemical reactions.
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E.
Corey–Bakshi–Shibata reduction
The Corey–Bakshi–Shibata reduction is a widely used asymmetric organic reaction that enantioselectively reduces ketones to chiral alcohols using a chiral oxazaborolidine catalyst and borane.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Target entity: Hydroboration (book) Target entity description: "Hydroboration" is a seminal chemistry book by Nobel laureate Herbert C. Brown that systematically presents the reactions, mechanisms, and synthetic applications of organoborane chemistry.
-
A.
Barton–McCombie deoxygenation
Barton–McCombie deoxygenation is an organic chemistry reaction that converts alcohols into the corresponding hydrocarbons via radical-mediated removal of the hydroxyl group.
-
B.
Sharpless aminohydroxylation
Sharpless aminohydroxylation is a stereoselective chemical reaction that converts alkenes into vicinal amino alcohols using a chiral catalyst, widely used in asymmetric synthesis.
-
C.
Eschenmoser
Eschenmoser is a Swiss surname most notably associated with Albert Eschenmoser, a prominent organic chemist known for his pioneering work in the synthesis of complex natural products and studies on the origin of life.
-
D.
“Superacids”
“Superacids” is a landmark chemistry book by George A. Olah that systematically explores extremely strong acids and their role in stabilizing carbocations and enabling unusual chemical reactions.
-
E.
Corey–Bakshi–Shibata reduction
The Corey–Bakshi–Shibata reduction is a widely used asymmetric organic reaction that enantioselectively reduces ketones to chiral alcohols using a chiral oxazaborolidine catalyst and borane.
- F. None of above. chosen
Statements (42)
| Predicate | Object |
|---|---|
| instanceOf |
book
ⓘ
chemistry book ⓘ |
| author |
Herbert C. Brown
NERFINISHED
ⓘ
Herbert Charles Brown NERFINISHED ⓘ |
| authorNationality | American ⓘ |
| contributesTo |
development of organoborane-based synthetic methods
ⓘ
understanding of hydroboration selectivity ⓘ |
| coversCompoundClass | organoboranes ⓘ |
| coversReactionType |
addition reactions
ⓘ
hydrometallation ⓘ |
| describedAs |
seminal monograph on hydroboration chemistry
ⓘ
systematic presentation of organoborane reactions and mechanisms ⓘ |
| field |
organic chemistry
ⓘ
organometallic chemistry ⓘ synthetic chemistry ⓘ |
| hasDiscipline | chemistry ⓘ |
| hasFormat | print ⓘ |
| hasNobelLaureateAuthor | true ⓘ |
| hasScientificFocus |
kinetics and mechanisms of hydroboration
ⓘ
structure–reactivity relationships in boron chemistry ⓘ synthetic methodology development ⓘ |
| hasSubdiscipline | physical organic chemistry ⓘ |
| influencedBy | Herbert C. Brown’s research on boron chemistry ⓘ |
| intendedAudience |
graduate students in chemistry
ⓘ
research chemists ⓘ |
| language | English ⓘ |
| mainSubject |
hydroboration
ⓘ
organoborane chemistry ⓘ |
| notableFor |
comprehensive treatment of hydroboration reactions
ⓘ
establishing conceptual framework for organoborane chemistry ⓘ |
| publicationEra | 20th century ⓘ |
| relatedTo | Nobel Prize in Chemistry 1979 NERFINISHED ⓘ |
| topic |
addition of boron–hydrogen bonds to multiple bonds
ⓘ
borane reagents ⓘ hydroboration–oxidation ⓘ organoborane intermediates ⓘ reaction mechanisms ⓘ regioselectivity in hydroboration ⓘ stereochemistry of hydroboration ⓘ synthetic applications of organoboranes ⓘ |
| usedBy | synthetic organic chemists ⓘ |
| usedIn | advanced organic chemistry education ⓘ |
How these facts were elicited
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You are a knowledge base construction expert. Given a subject entity and a description of it, return factual statements that you know for the subject as a JSON list of dictionaries(triples), where keys must be "subject", "predicate" and "object". The number of facts may be very high, between 25 to 50 or more, for very popular subjects. For less popular subjects, the number of facts can be very low, like 5 or 10. # Requirements - If you don't know the subject at all, return an empty list. - If the subject is not a named entity, return an empty list. - Include at least one triple where predicate is "instanceOf". - Do not get too wordy. - Separate several objects into multiple triples with one object.
Subject: Hydroboration (book) Description of subject: "Hydroboration" is a seminal chemistry book by Nobel laureate Herbert C. Brown that systematically presents the reactions, mechanisms, and synthetic applications of organoborane chemistry.
Referenced by (2)
Full triples — surface form annotated when it differs from this entity's canonical label.