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Record W2294498551 · doi:10.14288/1.0060579

Syntheses of selected heme protein model compounds

2010· article· en· W2294498551 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenuecIRcle (University of British Columbia) · 2010
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicHemoglobin structure and function
Canadian institutionsUniversity of British Columbia
Fundersnot available
KeywordsHemeChemistryComputer scienceBiochemistry

Abstract

fetched live from OpenAlex

Strapped porphyrins may be defined as those compounds in which some bridging group is covalently attached to opposite edges of the porphyrin macrocycle. This class of compound has been extensively studied as models for the active sites of heme proteins such as hemoglobins, cytochrome P450 etc. Two avenues of approach to the synthesis of strapped porphyrins have been used. The strap may be covalently attached to opposite edges of a preformed porphyrin, or the two halves of the porphyrin macrocycle may be assembled at each, end of the strap with a final intramolecular cyclization fitting the strap into place. The latter approach has been adopted here to provide a general route to those strapped porphyrins bearing functional groups in the bridging straps. Compounds 87a, 87b and 118a, 118b have been prepared as possible models for cytochrome c and catalase, while the porphyrin-quinone compounds 143a, 143b may be used to study electron transfer in donor/acceptor complexes. The syntheses of the various strapped porphyrins all originate from the α-free-iodoalkyl pyrroles 44, 64 which, are readily available via Friedel-Crafts acylation of β-free pyrrole 1, followed by reduction and iodination of the alkyl chain and modification of the α-methyl group. For the sulfide-strap porphyrins, reaction with, sodium sulfide to give the bis[(pyrrol-3-yl)alkyl]sulfides 75a, 75b formed the strap. Elaboration to the his-dipyrromethanes 77a, 77b provided all the units necessary for porphyrin synthesis. Saponification and decarboxylation followed by high-dilution acid-catalyzed intramolecular cyclization yielded the strapped porphyrins 87a (9-19%) and 87b (10-18%). Exposure to light during work-up is believed to be responsible for the formation of the corresponding sulfoxide-strap porphyrins 88a, 88b. [See Thesis for Diagrams] Conversion of 44 and 64 to the corresponding phosphonium salts 94a, 94b followed by a double Wittig reaction under phase-transfer conditions with either of the dialdehydes 95 or 131 gave the bis-alkenes. Catalytic hydrogenation yielded the bis(pyrrol-3-yl) compounds 113a, 113b and 138a, 138b. Elaboration to the bis-dipyrromethanes was followed by saponification, decarboxylation and intramolecular cyclization to furnish the strapped porphyrins. These relatively unstrained compounds were obtained in good yield: 117a (30-44%), 117b (21-53%), 140a (41-60%), 140b (20-40%). Treatment of the anisole-porphyrin 117a, 117b with boron tribromide furnished the phenol-strapped porphyrin ,118a (76-89%) , 118b (89-95%). Demethylation of the dimethoxybenzene-porphyrin 140a, 140b also with boron tribromide yielded the hydroquinone which was oxidized to the quinone-strapped porphyrin 143a (.82-87%), 143b (70%). An attempt was made to incorporate a suitably substituted imidazole into the bridging strap using the same procedure. However production of the required 1,5-disubstituted imidazole intermediates was hampered by low yields and difficulty in purification. The failure to prepare the necessary imidazole bis-aldehyde 170 led to cancellation of this attempt. All the porphyrins were subjected to elemental analysis, high resolution mass spectrometry, and visible absorption and ¹H- and ¹³C-NMR spectroscopy. A simplistic attempt was made to correlate the spectral characteristics to the structure, length and conformation of the strap. [See Thesis for Diagrams]

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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 categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.963
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

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 integrity0.0000.000
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 head0.005
GPT teacher head0.166
Teacher spread0.161 · 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