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Record W7071732491

Synthetic studies towards the spiroimine unit of the spirolides

2010· dissertation· en· W7071732491 on OpenAlexaboutno aff

Bibliographic record

VenueResearchSpace (University of Auckland) · 2010
Typedissertation
Languageen
FieldEnvironmental Science
TopicMarine Toxins and Detection Methods
Canadian institutionsnot available
Fundersnot available
KeywordsMoietyBicyclic moleculePharmacophoreEnantiopure drugBioassay
DOInot available

Abstract

fetched live from OpenAlex

The spirolides (A-D) were isolated from the digestive glands of mussels, scallops and toxic plankton from the east coast of Nova Scotia in Canada. These toxins are metabolites of the dinoflagellate Alexandrium ostenfeldii and A. peruvianum. To date fourteen members of this family have been identified from around the world. The spirolides are considered fast acting neurotoxins due to their effect in the mouse bioassay and activate L-type calcium channels. They also represents the most potent non-peptidic nicotinic acetylcholine antagonists, rendering them attractive candidates for the treatment of cardiovascular disorders and candidates for the development as antagonists of specific receptor sub-types. The total synthesis of the spirolides has not yet been reported. Their structure can be divided in two parts; an upper novel 6,7-spiroimine unit and a lower 5,5,6- bis-spiroacetal moiety which was previously synthesised by the Ishira and Brimble groups. However, the spiroimine unit has not yet been synthesised, representing a synthetic challenge of great interest due to the fact that this part has been established as the putative pharmacophore of this family of marine biotoxins. This study provides two approaches to the bicyclic spiroimine moiety of the spirolides A and B. The first proposed retrosynthesis accesses the C29 quaternary stereocentre using a highly diastereoselective Birch reductive alkylation. Further studies on the diastereoselective hydrogenation of the resulting double bonds, cleavage of the auxiliary and cyclisation studies afforded a range of enantiopure bicyclic spirolactams. During these studies, a synthetic approach to the challenging A ring of the spirolides A and B has been established via diastereoselective Myers alkylation of an amide derived from (S,S)-pseudoephedrine. Unfortunately, the lactam functionality could not be converted to an imine. Subsequently, an improved retrosynthetic pathway, making use of a Diels-Alder reaction to simultaneously establish the C7 and C29 stereocentres of the spirolides was extensively studied. Further transformation of the Diels-Alder adduct afforded the advanced azido-aldehyde or azidoketone in good overall yield. Studies of the cyclisation using various phosphines with the two different substrates afforded the surprising crystallographic structure of a stable 14-membered diimine ring and also the successful synthesis of the 6,7-spiroketimine unit of the spirolide. This new strategy has lead to a better understanding of the stability of the imine unit and allowed the development of a viable pathway for the synthesis of the 7,6-spiroimine unit of the spirolides.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
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 score0.001
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

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

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 head0.054
GPT teacher head0.321
Teacher spread0.267 · 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 source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
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
Published2010
Admission routes1
Has abstractyes

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