Classics in Total Synthesis
E1027562
Classics in Total Synthesis is a highly influential chemistry book that showcases landmark strategies and case studies in the total synthesis of complex natural products.
All labels observed (3)
| Label | Occurrences |
|---|---|
| Classics in Total Synthesis canonical | 1 |
| Classics in Total Synthesis II | 1 |
| Classics in Total Synthesis III | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T13176856 — 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: Classics in Total Synthesis Context triple: [K. C. Nicolaou, notableWork, Classics in Total Synthesis]
-
A.
The Logic of Chemical Synthesis
The Logic of Chemical Synthesis is a seminal book by chemist Elias J. Corey that systematically presents the principles and strategies of retrosynthetic analysis for designing complex organic molecule syntheses.
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B.
Enantioselective Chemical Synthesis
Enantioselective Chemical Synthesis is a foundational work in organic chemistry that systematically presents strategies and methods for constructing chiral molecules with high stereocontrol.
-
C.
Corey–Nicolaou macrolactonization
Corey–Nicolaou macrolactonization is a widely used organic synthesis reaction that forms large-ring lactones from hydroxy acids via an activated ester intermediate.
-
D.
Corey–Winter olefin synthesis
Corey–Winter olefin synthesis is an organic reaction that converts 1,2-diols into alkenes via cyclic thiocarbonate intermediates, widely used for stereospecific formation of double bonds.
-
E.
Evans auxiliary-based asymmetric synthesis
Evans auxiliary-based asymmetric synthesis is a widely influential chiral auxiliary strategy developed by David A. Evans that enables highly stereoselective construction of complex molecules in organic synthesis.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Target entity: Classics in Total Synthesis Target entity description: Classics in Total Synthesis is a highly influential chemistry book that showcases landmark strategies and case studies in the total synthesis of complex natural products.
-
A.
The Logic of Chemical Synthesis
The Logic of Chemical Synthesis is a seminal book by chemist Elias J. Corey that systematically presents the principles and strategies of retrosynthetic analysis for designing complex organic molecule syntheses.
-
B.
Enantioselective Chemical Synthesis
Enantioselective Chemical Synthesis is a foundational work in organic chemistry that systematically presents strategies and methods for constructing chiral molecules with high stereocontrol.
-
C.
Corey–Nicolaou macrolactonization
Corey–Nicolaou macrolactonization is a widely used organic synthesis reaction that forms large-ring lactones from hydroxy acids via an activated ester intermediate.
-
D.
Corey–Winter olefin synthesis
Corey–Winter olefin synthesis is an organic reaction that converts 1,2-diols into alkenes via cyclic thiocarbonate intermediates, widely used for stereospecific formation of double bonds.
-
E.
Evans auxiliary-based asymmetric synthesis
Evans auxiliary-based asymmetric synthesis is a widely influential chiral auxiliary strategy developed by David A. Evans that enables highly stereoselective construction of complex molecules in organic synthesis.
- F. None of above. chosen
Statements (44)
| Predicate | Object |
|---|---|
| instanceOf |
chemistry book
ⓘ
non-fiction book ⓘ scientific monograph ⓘ |
| academicDiscipline |
chemistry
ⓘ
natural products chemistry ⓘ |
| author |
Erik J. Sorensen
NERFINISHED
ⓘ
Kurt Peter C. Nicolaou NERFINISHED ⓘ |
| countryOfPublication | Germany NERFINISHED ⓘ |
| describedAs | highly influential in synthetic organic chemistry ⓘ |
| educationalUse |
graduate-level teaching
ⓘ
research reference ⓘ |
| field |
organic chemistry
ⓘ
total synthesis ⓘ |
| focusesOn |
complex natural products
ⓘ
structure elucidation and synthesis planning ⓘ |
| genre |
reference work
ⓘ
textbook ⓘ |
| hasPart |
mechanistic discussions
ⓘ
retrosynthetic analyses ⓘ step-by-step synthetic routes ⓘ strategy-oriented commentary ⓘ |
| hasSequel |
Classics in Total Synthesis II
NERFINISHED
ⓘ
Classics in Total Synthesis III NERFINISHED ⓘ |
| influenced |
education in synthetic organic chemistry
ⓘ
research in total synthesis ⓘ |
| language | English ⓘ |
| mainSubject |
synthetic organic chemistry
ⓘ
total synthesis of natural products ⓘ |
| notableFor |
case studies of complex natural product synthesis
ⓘ
landmark total synthesis strategies ⓘ |
| partOf | Classics in Total Synthesis series NERFINISHED ⓘ |
| publisher | Wiley-VCH NERFINISHED ⓘ |
| targetAudience |
advanced students of organic chemistry
ⓘ
professional synthetic chemists ⓘ |
| teaches |
retrosynthetic analysis
ⓘ
stereoselective synthesis ⓘ strategy in total synthesis design ⓘ |
| topic |
methodology in organic synthesis
ⓘ
strategy in complex molecule construction ⓘ |
| usesConcept |
asymmetric catalysis
ⓘ
cascade reactions ⓘ chiral pool synthesis ⓘ convergent synthesis ⓘ protecting-group strategies ⓘ |
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: Classics in Total Synthesis Description of subject: Classics in Total Synthesis is a highly influential chemistry book that showcases landmark strategies and case studies in the total synthesis of complex natural products.
Referenced by (3)
Full triples — surface form annotated when it differs from this entity's canonical label.