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Record W2315321368 · doi:10.14288/1.0061780

The chemistry of thujone : new enantioselective syntheses of Ambrox[Registered trade mark] and Epi-Ambrox

2008· article· en· W2315321368 on OpenAlexaff
Carles Cirera

Bibliographic record

VenuecIRcle (University of British Columbia) · 2008
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicPlant biochemistry and biosynthesis
Canadian institutionsUniversity of British Columbia
Fundersnot available
KeywordsEnantioselective synthesisChemistryOrganic chemistryCatalysis

Abstract

fetched live from OpenAlex

This thesis is concerned with the development of a new synthetic approach to(-)-Ambrox® (2) and epi-Ambrox (3) using thujone (1) as an enantiopure building block. Thujone (1), a readily available starting material obtained from Western red cedar, can be efficiently converted to D-cyperone (144), which can be chemically elaborated to obtain the key intermediate, enone 143. As a model study for the synthesis of racemic 2 and 3, a synthetic sequence starting with a cyclohexanone derivative has also been developed to afford the racemic intermediate143. Acid catalyzed Robinson annelation of 2-methylcyclohexanone with1-chloropentan-3-one gave enone 165. Methylation of 165 to 166 with methyl iodide and potassium tert-amylate proceeded in high yield. Wolff-Kishner reduction of 166 gave 167which was then oxidized to racemic 143 with sodium dichromate. At this stage, enantiopure 143, obtained via 144, from thujone (1) was prepared and compared with racemic 143. A novel method for the transposition of the carbonyl function in enantiopure 143 to the isomeric enantiopure enone 172 was developed. Treatment of 143 with manganese(III) acetate allowed introduction of an acetoxy function at the C8 position, to afford a mixture of isomers (185 and 186 4:1 ratio) in excellent yield (86 %). Reduction of 185and 186 with lithium aluminum hydride provided a mixture of alcohols, which without separation, was treated with p-toluenesulfonic acid to yield 172. This 3 step process, 143to 172, could be performed without isolation of intermediates and in an overall yield of64 %. Stereoselective alkylation of 172 with ethyl iodoacetate yielded compound 201exclusively with entry of the side chain in an axial orientation. Hydrogenation of 201 to205 and then ketalization, afforded 215. Reduction of the ester, protection of the alcohol functionality, and deprotection of the carbonyl, finally gave compound 219 in excellent yields. Reaction of 219 with the cerium chloride-methyllithium reagent gave 220, which yielded, after hydrogenolysis, diol 221. p-Toluenesulfonic acid catalyzed cyclization ofdiol 221 provided the potent ambergris odorant (-)-epi-Ambrox (3). Epimerization of the side chain in 219 with sodium methoxide in methanol gave compound 225 which was further converted into (-)-Ambrox® (2) by an identical sequence as for (-)-epi-Ambrox (3).

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 score0.003
Threshold uncertainty score0.010

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 communication0.0000.001
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0030.002

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 head0.164
Teacher spread0.155 · 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
Published2008
Admission routes1
Has abstractyes

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