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Record W7133030721

Application of carbamoylimidazolium salts in small molecule and combinatorial synthesis

2004· dissertation· W7133030721 on OpenAlexaboutno aff
Justyna A. Grzyb

Bibliographic record

VenueTSpace · 2004
Typedissertation
Language
FieldChemistry
TopicQuinazolinone synthesis and applications
Canadian institutionsnot available
Fundersnot available
KeywordsNucleophileReactivity (psychology)AlkylAldehydeSelectivityAqueous solutionCarboxylic acidBicyclic molecule
DOInot available

Abstract

fetched live from OpenAlex

This thesis is a summary of research conducted since February 2000 in the laboratories of Professor Robert A. Batey at the University of Toronto and is continuation of work performed here on carbamoylimidazolium salts. Chapter A covers the synthesis of the imidazolium salts, as well as their application in small molecule preparation. The salts are prepared in two steps with minimal purification, and have been successfully applied to the generation of amides from carboxylic acids. The amides are generated under mild conditions in excellent yields and are pure after aqueous work-up. Previous work in our laboratory has shown that derivatized anilines are unreactive towards the salts. Here the conditions were optimized for the reaction of salts with derivatized anilines to generate substituted ureas. Since imidazolium salts are capable of reacting with various nucleophiles a comparative study was carried out to determine the order of reactivity of the nucleophiles towards the salts. It was shown that sulfur based nucleophiles react significantly faster than any other nucleophile, while aliphatic alcohols and anilines do not react to any significant amount under weakly basic conditions. Synthetically useful selectivity levels between alkyl amines, phenols and carboxylic acids were not obtained. Chapter C covers the application of carbamoylimidazolium salts in the generation of heterocyclic alkaloids. Very poor reactivity of anilines under mild basic conditions allowed for a 4-component Povarov reaction of unprotected p-aminophenol with carbamoylimidazolium salt, aldehyde and 2,3-dihydrofuran. Lastly, the imidazolium salts were used in a short synthesis of fused bicyclic lactams. Chapter B focuses on combinatorial synthesis. Firstly, a semicarbazide library was generated. Hydrazides were reacted with N, N '-carbonyldiimidazole to generate 1,3,4-oxadiazol-2-ones, which were ring opened with amines to generate semicarbazides. Secondly, N, N'-diacylated imidazolidines exhibit herbicidal activity. Thus, we attempted to create a combinatorially friendly method for their synthesis. A common imidazolium salt intermediate was generated from monoacylated imidazolidine, which was then reacted with various amines. Lastly, a small library of ureas, carbamates, thiocarbamates and amides was synthesized to demonstrate the utility of the salts as a common precursor to various functionalities, which can be synthesized in parallel and under same conditions with minimal purification.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.058
Threshold uncertainty score0.999

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.010
GPT teacher head0.279
Teacher spread0.268 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2004
Admission routes1
Has abstractyes

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